| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2000 |
Scott RJ. Small-Scale Dynamics of Large-Scale Processes The American Historical Review. 105: 472. DOI: 10.2307/1571462 |
0.275 |
|
| 2017 |
Scott RJ, Barbosa LAdA, Haddad CHB. How Does the Law Put a Historical Analogy to Work?: Defining the Imposition of "A Condition Analogous to That of a Slave" in Modern Brazil Duke Journal of Constitutional Law & Public Policy. 13: 1-46. DOI: 10.2139/Ssrn.3058191 |
0.269 |
|
| 2011 |
Scott RJ. Slavery and the Law in Atlantic Perspective: Jurisdiction, Jurisprudence, and Justice Law and History Review. 29: 915-924. DOI: 10.1017/S0738248011000496 |
0.267 |
|
| 1994 |
Scott RJ. Defining the Boundaries of Freedom in the World of Cane: Cuba, Brazil, and Louisiana after Emancipation The American Historical Review. 99: 70. DOI: 10.2307/2166163 |
0.266 |
|
| 1984 |
Scott RJ. Explaining Abolition: Contradiction, Adaptation, and Challenge in Cuban Slave Society, 1860–1886 Comparative Studies in Society and History. 26: 83-111. DOI: 10.1017/S0010417500010781 |
0.261 |
|
| 1983 |
Scott RJ. Gradual Abolition and the Dynamics of Slave Emancipation in Cuba, 1868-86 Americas. 63: 449-477. DOI: 10.1215/00182168-63.3.449 |
0.256 |
|
| 2007 |
Scott RJ. Public rights and private commerce: A nineteenth-century Atlantic creole itinerary Current Anthropology. 48: 237-256. DOI: 10.1086/510475 |
0.256 |
|
| 2007 |
Scott RJ. The Atlantic World and the road to Plessy v. Ferguson The Journal of American History. 94: 726-733. DOI: 10.2307/25095133 |
0.247 |
|
| 1988 |
Scott RJ. Exploring the Meaning of Freedom: Postemancipation Societies in Comparative Perspective Americas. 68: 407-428. DOI: 10.1215/00182168-68.3.407 |
0.246 |
|
| 2011 |
Scott RJ. Paper Thin: Freedom and Re-enslavement in the Diaspora of the Haitian Revolution Law and History Review. 29: 1061-1087. DOI: 10.1017/S0738248011000538 |
0.242 |
|
| 1999 |
Scott RJ. Reclamando la mula de Gregoria Quesada: El significado de la libertad en los valles del Arimao y del Caunao, Cienfuegos, Cuba Illes I Imperis. 89-110. DOI: 10.2436/69216 |
0.238 |
|
| 1982 |
Scott RJ. Odious Commerce, Britain, Spain and the Abolition of the Cuban Slave Trace. By David Murray. (New York: Cambridge University Press, 1981. Pp. xi, 423. Abbreviations. Notes. Bibliography. Index. $44.40.) Americas. 39: 138-140. DOI: 10.2307/981278 |
0.237 |
|
| 2002 |
Scott RJ, Zeuske M. Property in Writing, Property on the Ground: Pigs, Horses, Land, and Citizenship in the Aftermath of Slavery, Cuba, 1880-1909 Comparative Studies in Society and History. 44: 669-699. DOI: 10.1017/S0010417502000324 |
0.237 |
|
| 2013 |
Scott RJ. Derechos públicos y comercio privado: un itinerario criollo en el Atlántico del siglo XIX Historia Critica. 205-235. DOI: 10.7440/Histcrit49.2013.10 |
0.236 |
|
| 2017 |
Scott RJ, Hébrard J. Trabalho escravo : l’esclavage contemporain au Brésil BréSil(S). DOI: 10.4000/Bresils.2250 |
0.234 |
|
| 1998 |
Scott RJ. Race, Labor, and Citizenship in Cuba: A View from the Sugar District of Cienfuegos, 1886–1909 Americas. 78: 687-728. DOI: 10.1215/00182168-78.4.687 |
0.233 |
|
| 2004 |
Scott RJ, Zeuske M. Le 'droit d'avoir des droits': Les revendications des ex-esclaves à Cuba (1872-1909) Annales. Histoire, Sciences Sociales. 59: 521-545. DOI: 10.1017/S0395264900017704 |
0.23 |
|
| 2001 |
Scott RJ, Zeuske M. Demandas de propiedad y ciudadanía: los exesclavos y sus descendientes en la región central de Cuba Illes I Imperis. 109-134. DOI: 10.2436/69413 |
0.225 |
|
| 2017 |
Scott RJ. Social Facts, Legal Fictions, and the Attribution of Slave Status: The Puzzle of Prescription Law and History Review. 35: 1-22. DOI: 10.1017/S0738248016000560 |
0.212 |
|
| 1999 |
Scott RJ. ‘Stubborn and disposed to stand their ground’: Black militia, sugar workers and the dynamics of collective action in the Louisiana sugar bowl, 1863–87 Slavery & Abolition. 20: 103-126. DOI: 10.1080/01440399908575271 |
0.211 |
|
| 2019 |
Scott RJ, Fornias CV. María Coleta and the Capuchin Friar: Slavery, Salvation, and the Adjudication of Status William and Mary Quarterly. 76: 727-762. DOI: 10.5309/Willmaryquar.76.4.0727 |
0.208 |
|
| 1987 |
Maingot AP, Scott RJ. Slave Emancipation in Cuba: The Transition to Free Labor, 1860-1899 Journal of Interdisciplinary History. 17: 883. DOI: 10.2307/204660 |
0.199 |
|
| 1986 |
Abel C, Scott RJ. Slave Emancipation in Cuba; The Transition to Free Labor, 1860-1899 Bulletin of Latin American Research. 5: 123. DOI: 10.2307/3338658 |
0.199 |
|
| 2006 |
Debniak T, Cybulski C, Kurzawski G, Górski B, Huzarski T, Byrski T, Gronwald J, Suchy J, Masojć B, Mierzejewski M, Lener M, Teodorczyk U, Medrek K, Złowocka E, Grabowska-Kłujszo E, ... ... Scott R, et al. Low-risk Genes and Multi-organ Cancer Risk in the Polish Population. Hereditary Cancer in Clinical Practice. 4: 52-5. PMID 20223005 DOI: 10.1186/1897-4287-4-1-52 |
0.182 |
|
| 2009 |
Ashton KA, Proietto A, Otton G, Symonds I, Scott RJ. Genetic variants in MUTYH are not associated with endometrial cancer risk. Hereditary Cancer in Clinical Practice. 7: 3. PMID 19338676 DOI: 10.1186/1897-4287-7-3 |
0.178 |
|
| 2014 |
Zyluk A, Paszkowska-Szczur K, Gupta S, Scott RJ, Lubi?ski J, D?bniak T. Dupuytren's disease and the risk of malignant neoplasms. Hereditary Cancer in Clinical Practice. 12: 6. PMID 24598251 DOI: 10.1186/1897-4287-12-6 |
0.175 |
|
| 2016 |
Talseth-Palmer BA, Bauer DC, Sjursen W, Evans TJ, McPhillips M, Proietto A, Otton G, Spigelman AD, Scott RJ. Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Cancer Medicine. PMID 26811195 DOI: 10.1002/cam4.628 |
0.174 |
|
| 2016 |
Li N, Thompson ER, Rowley SM, McInerny S, Devereux L, Goode D, Investigators L, Wong-Brown MW, Scott RJ, Trainer AH, Gorringe KL, James PA, Campbell IG. Reevaluation of RINT1 as a breast cancer predisposition gene. Breast Cancer Research and Treatment. PMID 27544226 DOI: 10.1007/s10549-016-3944-3 |
0.174 |
|
| 2021 |
Li N, Lim BWX, Thompson ER, McInerny S, Zethoven M, Cheasley D, Rowley SM, Wong-Brown MW, Devereux L, Gorringe KL, Sloan EK, Trainer A, Scott RJ, James PA, Campbell IG. Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study. Npj Breast Cancer. 7: 76. PMID 34117267 DOI: 10.1038/s41523-021-00279-9 |
0.173 |
|
| 2018 |
O'Mara TA, Glubb DM, Amant F, Annibali D, Ashton K, Attia J, Auer PL, Beckmann MW, Black A, Bolla MK, Brauch H, Brenner H, Brinton L, Buchanan DD, Burwinkel B, ... ... Scott RJ, et al. Identification of nine new susceptibility loci for endometrial cancer. Nature Communications. 9: 3166. PMID 30093612 DOI: 10.1038/S41467-018-05427-7 |
0.172 |
|
| 2009 |
Shi Z, Johnstone D, Talseth-Palmer BA, Evans TJ, Spigelman AD, Groombridge C, Milward EA, Olynyk JK, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age International Journal of Cancer. 125: 78-83. PMID 19291797 DOI: 10.1002/ijc.24304 |
0.171 |
|
| 2018 |
Wu L, Shi W, Long J, Guo X, Michailidou K, Beesley J, Bolla MK, Shu XO, Lu Y, Cai Q, Al-Ejeh F, Rozali E, Wang Q, Dennis J, Li B, ... ... Scott RJ, et al. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer. Nature Genetics. PMID 29915430 DOI: 10.1038/S41588-018-0132-X |
0.17 |
|
| 2018 |
Ten Broeke SW, van der Klift HM, Tops CMJ, Aretz S, Bernstein I, Buchanan DD, de la Chapelle A, Capella G, Clendenning M, Engel C, Gallinger S, Gomez Garcia E, Figueiredo JC, Haile R, Hampel HL, ... ... Scott R, et al. Cancer Risks for PMS2-Associated Lynch Syndrome. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO2018784777. PMID 30161022 DOI: 10.1200/JCO.2018.78.4777 |
0.169 |
|
| 2013 |
Chen J, Pande M, Huang YJ, Wei C, Amos CI, Talseth-Palmer BA, Meldrum CJ, Chen WV, Gorlov IP, Lynch PM, Scott RJ, Frazier ML. Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients. Carcinogenesis. 34: 299-306. PMID 23125224 DOI: 10.1093/Carcin/Bgs344 |
0.169 |
|
| 2014 |
Masson AL, Talseth-Palmer BA, Evans TJ, Grice DM, Hannan GN, Scott RJ. Expanding the genetic basis of copy number variation in familial breast cancer. Hereditary Cancer in Clinical Practice. 12: 15. PMID 24955146 DOI: 10.1186/1897-4287-12-15 |
0.169 |
|
| 2006 |
Talseth BA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53. International Journal of Cancer. 118: 2479-84. PMID 16353134 DOI: 10.1002/ijc.21661 |
0.169 |
|
| 2017 |
Hansen MF, Johansen J, Sylvander AE, Bjørnevoll I, Talseth-Palmer BA, Lavik LA, Xavier A, Engebretsen LF, Scott RJ, Drabløs F, Sjursen W. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics. PMID 28195393 DOI: 10.1111/cge.12994 |
0.168 |
|
| 2006 |
Ashton KA, Meldrum CJ, McPhillips ML, Suchy J, Kurzawski G, Lubinski J, Scott RJ. The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria. Hereditary Cancer in Clinical Practice. 4: 94-102. PMID 20223014 DOI: 10.1186/1897-4287-4-2-94 |
0.167 |
|
| 2014 |
Rudnicka H, Masojc B, van de Wetering T, Debniak T, Cybulski C, Gronwald J, Scott R, Lubinski J, Gorski B. First recurrent large genomic rearrangement in the BRCA1 gene found in Poland. Cancer Epidemiology. 38: 382-5. PMID 24947589 DOI: 10.1016/j.canep.2014.05.010 |
0.167 |
|
| 2012 |
Wong-Brown M, Li S, Wilkins M, Avery-Kiejda K, Bowden N, Scott R. Abstract P4-10-02: Targeted resequencing of BRCA1 and BRCA2 in inherited breast cancer Cancer Research. 72. DOI: 10.1158/0008-5472.Sabcs12-P4-10-02 |
0.166 |
|
| 2015 |
O'Mara TA, Glubb DM, Painter JN, Cheng T, Dennis J, Attia J, Holliday EG, McEvoy M, Scott RJ, Ashton K, Proietto T, Otton G, Shah M, Ahmed S, et al. Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer. Endocrine-Related Cancer. 22: 851-61. PMID 26330482 DOI: 10.1530/Erc-15-0319 |
0.162 |
|
| 2007 |
Talseth BA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Genetic polymorphisms in xenobiotic clearance genes and their influence on disease expression in hereditary nonpolyposis colorectal cancer patients. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 2307-10. PMID 17119063 DOI: 10.1158/1055-9965.EPI-06-0040 |
0.162 |
|
| 2017 |
Michailidou K, Lindström S, Dennis J, Beesley J, Hui S, Kar S, Lemaçon A, Soucy P, Glubb D, Rostamianfar A, Bolla MK, Wang Q, Tyrer J, Dicks E, Lee A, ... ... Scott RJ, et al. Association analysis identifies 65 new breast cancer risk loci. Nature. PMID 29059683 DOI: 10.1038/Nature24284 |
0.161 |
|
| 2009 |
Reeves SG, Meldrum C, Groombridge C, Spigelman AD, Suchy J, Kurzawski G, Lubinski J, McElduff P, Scott RJ. MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer. European Journal of Human Genetics : Ejhg. 17: 629-35. PMID 19156174 DOI: 10.1038/ejhg.2008.239 |
0.161 |
|
| 2016 |
Chen MM, O'Mara TA, Thompson DJ, Painter JN, Attia J, Black A, Brinton L, Chanock S, Chen C, Cheng TH, Cook LS, Crous-Bou M, Doherty J, Friedenreich CM, ... ... Scott RJ, et al. GWAS meta-analysis of 16,852 women identifies new susceptibility locus for endometrial cancer. Human Molecular Genetics. PMID 27008869 DOI: 10.1093/Hmg/Ddw092 |
0.161 |
|
| 2004 |
Lim W, Olschwang S, Keller JJ, Westerman AM, Menko FH, Boardman LA, Scott RJ, Trimbath J, Giardiello FM, Gruber SB, Gille JJP, Offerhaus GJA, De Rooij FWM, Wilson JHP, Spigelman AD, et al. Relative frequency and morphology of cancers in STK11 mutation carriers Gastroenterology. 126: 1788-1794. PMID 15188174 DOI: 10.1053/J.Gastro.2004.03.014 |
0.161 |
|
| 1995 |
Müller H, Scott R, Weber W, Meier R. Colorectal cancer: lessons for genetic counselling and care for families. Clinical Genetics. 46: 106-14. PMID 7988067 DOI: 10.1111/j.1399-0004.1994.tb04212.x |
0.161 |
|
| 2006 |
Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJP, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJA, De Rooij FWM, et al. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome Clinical Cancer Research. 12: 3209-3215. PMID 16707622 DOI: 10.1158/1078-0432.Ccr-06-0083 |
0.16 |
|
| 2004 |
Kurzawski G, Suchy J, Kładny J, Grabowska E, Mierzejewski M, Jakubowska A, Debniak T, Cybulski C, Kowalska E, Szych Z, Domagała W, Scott RJ, Lubiński J. The NOD2 3020insC mutation and the risk of colorectal cancer. Cancer Research. 64: 1604-6. PMID 14996717 DOI: 10.1158/0008-5472.CAN-03-3791 |
0.16 |
|
| 2004 |
Scott RJ, Ashton KA. Familial breast and bowel cancer: does it exist? Hereditary Cancer in Clinical Practice. 2: 25-9. PMID 20233481 DOI: 10.1186/1897-4287-2-1-25 |
0.16 |
|
| 2008 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Benner A, Lubiński J, Scott RJ, Hamann U. Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism. Bmc Cancer. 8: 90. PMID 18397521 DOI: 10.1186/1471-2407-8-90 |
0.16 |
|
| 2014 |
De Vivo I, Prescott J, Setiawan VW, Olson SH, Wentzensen N, Attia J, Black A, Brinton L, Chen C, Chen C, Cook LS, Crous-Bou M, Doherty J, Dunning AM, ... ... Scott RJ, et al. Genome-wide association study of endometrial cancer in E2C2. Human Genetics. 133: 211-24. PMID 24096698 DOI: 10.1007/S00439-013-1369-1 |
0.16 |
|
| 2008 |
Talseth BA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer. Scandinavian Journal of Gastroenterology. 42: 628-32. PMID 17454884 DOI: 10.1080/00365520601106699 |
0.16 |
|
| 1999 |
Scott RJ, Sobol HH. Prognostic implications of cancer susceptibility genes: any news? Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer. 151: 71-84. PMID 10337719 DOI: 10.1007/978-3-642-59945-3_5 |
0.159 |
|
| 2008 |
Talseth BA, Ashton KA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer. International Journal of Cancer. 122: 1273-7. PMID 18027856 DOI: 10.1002/ijc.23177 |
0.159 |
|
| 2010 |
Tomlinson IP, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, Koessler T, Pharoah PD, Niittymäki I, Niittymäkix I, Tuupanen S, Tuupanenx S, Aaltonen LA, Hemminki K, Lindblom A, ... ... Scott R, et al. COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. British Journal of Cancer. 102: 447-54. PMID 19920828 DOI: 10.1038/Sj.Bjc.6605338 |
0.159 |
|
| 1996 |
Hutter P, Couturier A, Scott RJ, Alday P, Delozier-Blanchet C, Cachat F, Antonarakis SE, Joris F, Gaudin M, D'Amato L, Buerstedde JM. Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation. Journal of Medical Genetics. 33: 636-40. PMID 8863153 DOI: 10.1136/Jmg.33.8.636 |
0.159 |
|
| 2015 |
Cheng TH, Thompson D, Painter J, O'Mara T, Gorman M, Martin L, Palles C, Jones A, Buchanan DD, Ko Win A, Hopper J, Jenkins M, Lindor NM, Newcomb PA, Gallinger S, ... ... Scott RJ, et al. Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Scientific Reports. 5: 17369. PMID 26621817 DOI: 10.1038/Srep17369 |
0.159 |
|
| 2021 |
Li N, Zethoven M, McInerny S, Devereux L, Huang YK, Thio N, Cheasley D, Gutiérrez-Enríquez S, Moles-Fernández A, Diez O, Nguyen-Dumont T, Southey MC, Hopper JL, Simard J, Dumont M, ... ... Scott RJ, et al. Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects. Npj Breast Cancer. 7: 52. PMID 33980861 DOI: 10.1038/s41523-021-00255-3 |
0.159 |
|
| 2014 |
Gromowski T, Masojć B, Scott RJ, Cybulski C, Górski B, Kluźniak W, Paszkowska-Szczur K, Rozmiarek A, Dębniak B, Maleszka R, Kładny J, Lubiński J, Dębniak T. Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study. Cancer Genetics. 207: 128-32. PMID 24767713 DOI: 10.1016/j.cancergen.2014.03.003 |
0.159 |
|
| 2009 |
Scott RJ, Lubinski J. Genetic epidemiology studies in hereditary non-polyposis colorectal cancer. Methods in Molecular Biology (Clifton, N.J.). 472: 89-102. PMID 19107430 DOI: 10.1007/978-1-60327-492-0_4 |
0.158 |
|
| 2021 |
Wiik MU, Evans TJ, Belhadj S, Bolton KA, Dymerska D, Jagmohan-Changur S, Capellá G, Kurzawski G, Wijnen JT, Valle L, Vasen HFA, Lubinski J, Scott RJ, Talseth-Palmer BA. A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants. Scientific Reports. 11: 11401. PMID 34059744 DOI: 10.1038/s41598-021-90501-2 |
0.158 |
|
| 2007 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Edler L, Lubinski J, Scott RJ, Hamann U. Integrin beta3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk. Journal of Medical Genetics. 44: 408-11. PMID 17220212 DOI: 10.1136/jmg.2006.047498 |
0.158 |
|
| 2002 |
Jakubowska A, Nej K, Huzarski T, Scott RJ, Lubiński J. BRCA2 gene mutations in families with aggregations of breast and stomach cancers. British Journal of Cancer. 87: 888-91. PMID 12373604 DOI: 10.1038/sj.bjc.6600562 |
0.157 |
|
| 2010 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Tołoczko-Grabarek A, Gilbert M, Edler L, Zapatka M, Eils R, Lubiński J, Scott RJ, Hamann U. BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms. Breast Cancer Research and Treatment. 119: 201-11. PMID 19360465 DOI: 10.1007/s10549-009-0390-5 |
0.157 |
|
| 2008 |
Złowocka E, Cybulski C, Górski B, Debniak T, Słojewski M, Wokołorczyk D, Serrano-Fernández P, Matyjasik J, van de Wetering T, Sikorski A, Scott RJ, Lubiński J. Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancer. International Journal of Cancer. 122: 583-6. PMID 17918154 DOI: 10.1002/ijc.23099 |
0.157 |
|
| 2011 |
Spurdle AB, Thompson DJ, Ahmed S, Ferguson K, Healey CS, O'Mara T, Walker LC, Montgomery SB, Dermitzakis ET, Fahey P, Montgomery GW, Webb PM, Fasching PA, Beckmann MW, ... ... Scott RJ, et al. Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Nature Genetics. 43: 451-4. PMID 21499250 DOI: 10.1038/Ng.812 |
0.157 |
|
| 2016 |
Campbell I, Thompson E, Rowely S, Li N, McInerny S, Devereux L, Wong-Brown M, Trainer A, Mitchell G, Scott R, James P. Abstract P2-09-02: Panel testing for familial breast cancer: Tension at the boundary of research and clinical care Cancer Research. 76. DOI: 10.1158/1538-7445.Sabcs15-P2-09-02 |
0.157 |
|
| 2015 |
Thompson ER, Gorringe KL, Rowley SM, Li N, McInerny S, Wong-Brown MW, Devereux L, Li J, Trainer AH, Mitchell G, Scott RJ, James PA, Campbell IG. Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context. Scientific Reports. 5: 14800. PMID 26455428 DOI: 10.1038/srep14800 |
0.157 |
|
| 2013 |
Masson AL, Talseth-Palmer BA, Evans TJ, Grice DM, Duesing K, Hannan GN, Scott RJ. Copy number variation in hereditary non-polyposis colorectal cancer. Genes. 4: 536-55. PMID 24705261 DOI: 10.3390/genes4040536 |
0.156 |
|
| 2018 |
Dębniak T, Scott RJ, Górski B, Masojć B, Kram A, Maleszka R, Cybulski C, Paszkowska-Szczur K, Kashyap A, Murawa D, Malińska K, Kiedrowicz M, Rogoża-Janiszewska E, Rudnicka H, Deptuła J, et al. BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population. Plos One. 13: e0204768. PMID 30286154 DOI: 10.1371/journal.pone.0204768 |
0.156 |
|
| 2009 |
Lubiński J, Korzeń M, Górski B, Cybulski C, Dębniak T, Jakubowska A, Jaworska K, Wokołorczyk D, Mędrek K, Matyjasik J, Huzarski T, Byrski T, Gronwald J, Masojć B, Lener M, ... ... Scott R, et al. Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology Breast Cancer Research and Treatment. 114: 121-126. PMID 18415014 DOI: 10.1007/S10549-008-9974-8 |
0.154 |
|
| 2015 |
Carvajal-Carmona LG, O'Mara TA, Painter JN, Lose FA, Dennis J, Michailidou K, Tyrer JP, Ahmed S, Ferguson K, Healey CS, Pooley K, Beesley J, Cheng T, Jones A, Howarth K, ... ... Scott RJ, et al. Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. Human Genetics. 134: 231-45. PMID 25487306 DOI: 10.1007/S00439-014-1515-4 |
0.154 |
|
| 2014 |
Purrington KS, Slettedahl S, Bolla MK, Michailidou K, Czene K, Nevanlinna H, Bojesen SE, Andrulis IL, Cox A, Hall P, Carpenter J, Yannoukakos D, Haiman CA, Fasching PA, Mannermaa A, ... ... Scott R, et al. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade. Human Molecular Genetics. 23: 6034-46. PMID 24927736 DOI: 10.1093/Hmg/Ddu300 |
0.154 |
|
| 2013 |
Picelli S, Lorenzo Bermejo J, Chang-Claude J, Hoffmeister M, Fernández-Rozadilla C, Carracedo A, Castells A, Castellví-Bel S, Naccarati A, Pardini B, Vodickova L, Müller H, Talseth-Palmer BA, Stibbard G, ... ... Scott RJ, et al. Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility. Plos One. 8: e72091. PMID 24039736 DOI: 10.1371/Journal.Pone.0072091 |
0.153 |
|
| 2006 |
Hitchins M, Williams R, Cheong K, Halani N, Lin VA, Packham D, Ku S, Buckle A, Hawkins N, Burn J, Gallinger S, Goldblatt J, Kirk J, Tomlinson I, Scott R, et al. MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer. Gastroenterology. 129: 1392-9. PMID 16285940 DOI: 10.1053/J.GASTRO.2005.09.003 |
0.153 |
|
| 2016 |
Bolton KA, Avery-Kiejda KA, Holliday EG, Attia J, Bowden NA, Scott RJ. A polymorphic repeat in the IGF1 promoter influences the risk of endometrial cancer. Endocrine Connections. PMID 27090263 DOI: 10.1530/EC-16-0003 |
0.152 |
|
| 2021 |
Xavier A, Scott RJ, Talseth-Palmer B. Exome sequencing of FAP-like individuals identifies both known and novel causative genes. Clinical Genetics. PMID 34259353 DOI: 10.1111/cge.14029 |
0.152 |
|
| 2020 |
Ahadova A, Seppälä TT, Engel C, Gallon R, Burn J, Holinski-Feder E, Steinke-Lange V, Möslein G, Nielsen M, Ten Broeke S, Laghi L, Dominguez-Valentin M, Capella G, Macrae F, Scott R, et al. The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance. International Journal of Cancer. PMID 32683684 DOI: 10.1002/ijc.33224 |
0.152 |
|
| 2017 |
Milne RL, Kuchenbaecker KB, Michailidou K, Beesley J, Kar S, Lindström S, Hui S, Lemaçon A, Soucy P, Dennis J, Jiang X, Rostamianfar A, Finucane H, Bolla MK, McGuffog L, ... ... Scott RJ, et al. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Nature Genetics. PMID 29058716 DOI: 10.1038/Ng.3785 |
0.152 |
|
| 2003 |
Górski B, Debniak T, Masojć B, Mierzejewski M, Medrek K, Cybulski C, Jakubowska A, Kurzawski G, Chosia M, Scott R, Lubiński J. Germline 657del5 mutation in the NBS1 gene in breast cancer patients. International Journal of Cancer. 106: 379-81. PMID 12845677 DOI: 10.1002/ijc.11231 |
0.151 |
|
| 2015 |
Painter JN, O'Mara TA, Batra J, Cheng T, Lose FA, Dennis J, Michailidou K, Tyrer JP, Ahmed S, Ferguson K, Healey CS, Kaufmann S, Hillman KM, Walpole C, Moya L, ... ... Scott RJ, et al. Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics. 24: 1478-92. PMID 25378557 DOI: 10.1093/Hmg/Ddu552 |
0.151 |
|
| 2004 |
Debniak T, Górski B, Scott RJ, Cybulski C, Medrek K, Zowocka E, Kurzawski G, Debniak B, Kadny J, Bielecka-Grzela S, Maleszka R, Lubiński J. Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer. International Journal of Cancer. 110: 558-62. PMID 15122588 DOI: 10.1002/ijc.20163 |
0.151 |
|
| 2006 |
Dębniak T, Scott RJ, Huzarski T, Byrski T, Rozmiarek A, Dębniak B, Górski B, Cybulski C, Mędrek K, Mierzejewski M, Masojc B, Matyjasik J, Złowocka E, Teodorczyk U, Lener M, et al. CDKN2A common variant and multi‐organ cancer risk—a population‐based study International Journal of Cancer. 118: 3180-3182. PMID 16395703 DOI: 10.1002/Ijc.21760 |
0.151 |
|
| 2016 |
Bolton KA, Holliday EG, Attia J, Bowden NA, Avery-Kiejda KA, Scott RJ. A novel polymorphic repeat in the upstream regulatory region of the estrogen-induced gene EIG121 is not associated with the risk of developing breast or endometrial cancer. Bmc Research Notes. 9: 287. PMID 27230222 DOI: 10.1186/s13104-016-2086-3 |
0.151 |
|
| 2007 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Edler L, Lubiñski J, Scott RJ, Hamann U. The RAD51 135 G>C polymorphism modifies breast cancer and ovarian cancer risk in Polish BRCA1 mutation carriers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 270-5. PMID 17301259 DOI: 10.1158/1055-9965.EPI-06-0562 |
0.15 |
|
| 2018 |
Painter JN, O'Mara TA, Morris AP, Cheng THT, Gorman M, Martin L, Hodson S, Jones A, Martin NG, Gordon S, Henders AK, Attia J, McEvoy M, Holliday EG, Scott RJ, et al. Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Medicine. PMID 29608257 DOI: 10.1002/Cam4.1445 |
0.15 |
|
| 2016 |
Southey MC, Goldgar DE, Winqvist R, Pylkäs K, Couch F, Tischkowitz M, Foulkes WD, Dennis J, Michailidou K, van Rensburg EJ, Heikkinen T, Nevanlinna H, Hopper JL, Dörk T, Claes KB, ... ... Scott RJ, et al. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Journal of Medical Genetics. PMID 27595995 DOI: 10.1136/jmedgenet-2016-103839 |
0.15 |
|
| 2020 |
Fachal L, Aschard H, Beesley J, Barnes DR, Allen J, Kar S, Pooley KA, Dennis J, Michailidou K, Turman C, Soucy P, Lemaçon A, Lush M, Tyrer JP, Ghoussaini M, ... ... Scott RJ, et al. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes. Nature Genetics. PMID 31911677 DOI: 10.1038/s41588-019-0537-1 |
0.15 |
|
| 2006 |
Debniak T, Scott R, Masojc B, Serrano-Fernández P, Huzarski T, Byrski T, Debniak B, Górski B, Cybulski C, Medrek K, Kurzawski G, van de Wetering T, Maleszka R, Kładny J, Lubinski J. MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk. International Journal of Cancer. 119: 2597-602. PMID 16988943 DOI: 10.1002/ijc.22210 |
0.15 |
|
| 2006 |
Jakubowska A, Gronwald J, Górski B, Huzarski T, Byrski T, Benner A, Lubiński J, Scott RJ, Hamann U. The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutation. Breast Cancer Research and Treatment. 104: 67-74. PMID 17004108 DOI: 10.1007/s10549-006-9389-3 |
0.149 |
|
| 2006 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Edler L, Lubiński J, Scott RJ, Hamann U. Methylenetetrahydrofolate reductase polymorphisms modify BRCA1-associated breast and ovarian cancer risks. Breast Cancer Research and Treatment. 104: 299-308. PMID 17063264 DOI: 10.1007/s10549-006-9417-3 |
0.149 |
|
| 2016 |
Painter JN, Kaufmann S, O'Mara TA, Hillman KM, Sivakumaran H, Darabi H, Cheng TH, Pearson J, Kazakoff S, Waddell N, Hoivik EA, Goode EL, Scott RJ, Tomlinson I, Dunning AM, et al. A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 Binding. American Journal of Human Genetics. 98: 1159-1169. PMID 27259051 DOI: 10.1016/j.ajhg.2016.04.012 |
0.148 |
|
| 2013 |
Talseth-Palmer BA, Wijnen JT, Andreassen EK, Barker D, Jagmohan-Changur S, Tops CM, Meldrum C, Spigelman A, Hes FJ, Van Wezel T, Vasen HF, Scott RJ. The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients. Hereditary Cancer in Clinical Practice. 11: 20. PMID 24373140 DOI: 10.1186/1897-4287-11-20 |
0.148 |
|
| 2011 |
Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, ... ... Scott RJ, et al. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature. 476: 214-9. PMID 21833088 DOI: 10.1038/Nature10251 |
0.148 |
|
| 2014 |
Kurlapska A, Serrano-Fernández P, Baszuk P, Gupta S, Starzy?ska T, Ma?ecka-Panas E, Dabrowski A, D?bniak T, Kurzawski G, Suchy J, Rogoza-Mateja W, Scott RJ, Lubi?ski J. Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening. Clinical Genetics. PMID 25117299 DOI: 10.1111/cge.12481 |
0.148 |
|
| 2018 |
Morten BC, Chiu S, Oldmeadow C, Lubinski J, Scott RJ, Avery-Kiejda KA. The intron 3 16 bp duplication polymorphism of p53 (rs17878362) is not associated with increased risk of developing triple-negative breast cancer. Breast Cancer Research and Treatment. PMID 30430302 DOI: 10.1007/s10549-018-5039-9 |
0.148 |
|
| 2004 |
Liu X, Sinn HP, Ulmer HU, Scott RJ, Hamann U. Intronic TP53 Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer Families. Hereditary Cancer in Clinical Practice. 2: 139-45. PMID 20233468 DOI: 10.1186/1897-4287-2-3-139 |
0.147 |
|
| 2016 |
Lener MR, Scott RJ, Kluźniak W, Baszuk P, Cybulski C, Wiechowska-Kozłowska A, Huzarski T, Byrski T, Kładny J, Pietrzak S, Soluch A, Jakubowska A, Lubiński J. Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer? International Journal of Cancer. 139: 601-6. PMID 27038244 DOI: 10.1002/ijc.30116 |
0.147 |
|
| 2013 |
Talseth-Palmer BA, Holliday EG, Evans TJ, McEvoy M, Attia J, Grice DM, Masson AL, Meldrum C, Spigelman A, Scott RJ. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients. Bmc Medical Genomics. 6: 10. PMID 23531357 DOI: 10.1186/1755-8794-6-10 |
0.146 |
|
| 2012 |
Jakubowska A, Rozkrut D, Antoniou A, Hamann U, Scott RJ, McGuffog L, Healy S, Sinilnikova OM, Rennert G, Lejbkowicz F, Flugelman A, Andrulis IL, Glendon G, Ozcelik H, et al. Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study. British Journal of Cancer. 106: 2016-24. PMID 22669161 DOI: 10.1038/Bjc.2012.160 |
0.146 |
|
| 2011 |
Wong MW, Nordfors C, Mossman D, Pecenpetelovska G, Avery-Kiejda KA, Talseth-Palmer B, Bowden NA, Scott RJ. BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer. Breast Cancer Research and Treatment. 127: 853-9. PMID 21409391 DOI: 10.1007/s10549-011-1443-0 |
0.146 |
|
| 2013 |
Talseth-Palmer BA, Wijnen JT, Brenne IS, Jagmohan-Changur S, Barker D, Ashton KA, Tops CM, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G, Spigelman A, Møller P, ... ... Scott RJ, et al. Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers. International Journal of Cancer. Journal International Du Cancer. 132: 1556-64. PMID 22987364 DOI: 10.1002/ijc.27843 |
0.145 |
|
| 2006 |
Hitchins M, Suter C, Wong J, Cheong K, Hawkins N, Leggett B, Scott R, Spigelman A, Tomlinson I, Martin D, Ward R. Germline epimutations of APC are not associated with inherited colorectal polyposis. Gut. 55: 586-7. PMID 16531545 DOI: 10.1136/Gut.2005.087486 |
0.145 |
|
| 2015 |
Thompson ER, Gorringe KL, Rowley SM, Wong-Brown MW, McInerny S, Li N, Trainer AH, Devereux L, Doyle MA, Li J, Lupat R, Delatycki MB, Mitchell G, James PA, ... Scott RJ, et al. Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls. Breast Cancer Research : Bcr. 17: 111. PMID 26283626 DOI: 10.1186/s13058-015-0627-7 |
0.145 |
|
| 2004 |
Scott RJ. DNA double strand break repair and its association with inherited predispositions to breast cancer. Hereditary Cancer in Clinical Practice. 2: 37-43. PMID 20233482 DOI: 10.1186/1897-4287-2-1-37 |
0.145 |
|
| 2001 |
Scott RJ, Meldrum C, Crooks R, Spigelman AD, Kirk J, Tucker K, Koorey D. Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity Gut. 48: 508-514. PMID 11247895 DOI: 10.1136/Gut.48.4.508 |
0.144 |
|
| 2015 |
Thompson DJ, O'Mara TA, Glubb DM, Painter JN, Cheng T, Folkerd E, Doody D, Dennis J, Webb PM, Gorman M, Martin L, Hodgson S, Michailidou K, Tyrer JP, Maranian MJ, ... ... Scott RJ, et al. CYP19A1 fine-mapping and Mendelian randomisation: estradiol is causal for endometrial cancer. Endocrine-Related Cancer. PMID 26574572 DOI: 10.1530/Erc-15-0386 |
0.144 |
|
| 2017 |
Fazekas-Lavu M, Parker A, Spigelman AD, Scott RJ, Epstein RJ, Jensen M, Samaras K. Thyroid cancer in a patient with Lynch syndrome - case report and literature review. Therapeutics and Clinical Risk Management. 13: 915-918. PMID 28769567 DOI: 10.2147/TCRM.S121812 |
0.144 |
|
| 2005 |
Jaworowska E, Masojć B, Tarnowska C, Brzosko M, Fliciński J, Serrano-Fernandez P, Matyjasik J, Amernik K, Scott RJ, Lubiński J. Association between early-onset breast and laryngeal cancers. Breast Cancer Research and Treatment. 97: 215-9. PMID 16331346 DOI: 10.1007/s10549-005-9116-5 |
0.144 |
|
| 2007 |
Talseth BA, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott RJ. MDM2 SNP309 T>G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients. International Journal of Cancer. 120: 563-5. PMID 17096342 DOI: 10.1002/ijc.22339 |
0.144 |
|
| 2012 |
Long J, Zheng W, Xiang YB, Lose F, Thompson D, Tomlinson I, Yu H, Wentzensen N, Lambrechts D, Dörk T, Dubrowinskaja N, Goodman MT, Salvesen HB, Fasching PA, Scott RJ, et al. Genome-wide association study identifies a possible susceptibility locus for endometrial cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 980-7. PMID 22426144 DOI: 10.1158/1055-9965.Epi-11-1160 |
0.143 |
|
| 2020 |
Feng H, Gusev A, Pasaniuc B, Wu L, Long J, Abu-Full Z, Aittomäki K, Andrulis IL, Anton-Culver H, Antoniou AC, Arason A, Arndt V, Aronson KJ, Arun BK, Asseryanis E, ... ... Scott RJ, et al. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status. Genetic Epidemiology. PMID 32115800 DOI: 10.1002/gepi.22288 |
0.143 |
|
| 2005 |
Weber W, Scott RJ. Case report: familial gastric cancer and chordoma in the same family. Hereditary Cancer in Clinical Practice. 3: 81-4. PMID 20223035 DOI: 10.1186/1897-4287-3-2-81 |
0.143 |
|
| 1998 |
Lakhani SR, Jacquemier J, Sloane JP, Gusterson BA, Anderson TJ, van de Vijver MJ, Farid LM, Venter D, Antoniou A, Storfer-Isser A, Smyth E, Steel CM, Haites N, Scott RJ, Goldgar D, et al. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. Journal of the National Cancer Institute. 90: 1138-45. PMID 9701363 DOI: 10.1093/Jnci/90.15.1138 |
0.143 |
|
| 2015 |
Wong-Brown MW, Meldrum CJ, Carpenter JE, Clarke CL, Narod SA, Jakubowska A, Rudnicka H, Lubinski J, Scott RJ. Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer. Breast Cancer Research and Treatment. 150: 71-80. PMID 25682074 DOI: 10.1007/S10549-015-3293-7 |
0.143 |
|
| 2005 |
McPhillips M, Meldrum CJ, Creegan R, Edkins E, Scott RJ. Deletion Mutations in an Australian Series of HNPCC Patients. Hereditary Cancer in Clinical Practice. 3: 43-7. PMID 20223028 DOI: 10.1186/1897-4287-3-1-43 |
0.142 |
|
| 2006 |
Lener MR, Oszutowska D, Castaneda J, Kurzawski G, Suchy J, Nej-Wołosiak K, Byrski T, Huzarski T, Gronwald J, Szymańska A, Szymańska-Pasternak J, Grodzki T, Serwatowski P, Bre Borowicz G, Scott RJ, et al. Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer. Breast Cancer Research and Treatment. 95: 141-5. PMID 16267612 DOI: 10.1007/s10549-005-9057-z |
0.142 |
|
| 1999 |
Heinimann K, Scott RJ, Buerstedde JM, Weber W, Siebold K, Attenhofer M, Müller H, Dobbie Z. Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer. Cancer. 85: 2512-8. PMID 10375096 DOI: 10.1002/(SICI)1097-0142(19990615)85:12<2512::AID-CNCR4>3.0.CO;2-G |
0.142 |
|
| 2008 |
Froyen G, Corbett M, Vandewalle J, Jarvela I, Lawrence O, Meldrum C, Bauters M, Govaerts K, Vandeleur L, Van Esch H, Chelly J, Sanlaville D, van Bokhoven H, Ropers HH, Laumonnier F, ... ... Scott R, et al. Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. American Journal of Human Genetics. 82: 432-43. PMID 18252223 DOI: 10.1016/j.ajhg.2007.11.002 |
0.142 |
|
| 2015 |
Nead KT, Sharp SJ, Thompson DJ, Painter JN, Savage DB, Semple RK, Barker A, Perry JR, Attia J, Dunning AM, Easton DF, Holliday E, Lotta LA, O'Mara T, ... ... Scott RJ, ... ... Scott RA, et al. Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis. Journal of the National Cancer Institute. 107. PMID 26134033 DOI: 10.1093/jnci/djv178 |
0.142 |
|
| 2016 |
Couch FJ, Kuchenbaecker KB, Michailidou K, Mendoza-Fandino GA, Nord S, Lilyquist J, Olswold C, Hallberg E, Agata S, Ahsan H, Aittomäki K, Ambrosone C, Andrulis IL, Anton-Culver H, Arndt V, ... ... Scott R, et al. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nature Communications. 7: 11375. PMID 27117709 DOI: 10.1038/Ncomms11375 |
0.141 |
|
| 2015 |
Darabi H, McCue K, Beesley J, Michailidou K, Nord S, Kar S, Humphreys K, Thompson D, Ghoussaini M, Bolla MK, Dennis J, Wang Q, Canisius S, Scott CG, Apicella C, ... ... Scott RJ, et al. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. American Journal of Human Genetics. 97: 22-34. PMID 26073781 DOI: 10.1016/J.Ajhg.2015.05.002 |
0.141 |
|
| 2015 |
Moir-Meyer GL, Pearson JF, Lose F, Scott RJ, McEvoy M, Attia J, Holliday EG, Pharoah PD, Dunning AM, Thompson DJ, Easton DF, Spurdle AB, et al. Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition. Human Genetics. 134: 269-78. PMID 25381466 DOI: 10.1007/s00439-014-1507-4 |
0.141 |
|
| 2010 |
Tomlinson IPM, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, Koessler T, Pharoah PD, Niittymäki I, Tuupanen S, Aaltonen LA, Hemminki K, Lindblom A, Försti A, Sieber O, ... ... Scott R, et al. Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338)) British Journal of Cancer. 102. DOI: 10.1038/Sj.Bjc.6605518 |
0.141 |
|
| 2005 |
Scott RJ, Meldrum CJ. Missense mutations in cancer predisposing genes: can we make sense of them? Hereditary Cancer in Clinical Practice. 3: 123-7. PMID 20223037 DOI: 10.1186/1897-4287-3-3-123 |
0.141 |
|
| 1996 |
Garvin AM, Spycher M, Häner M, Torhorst J, Müller H, Herrmann R, Rochlitz C, Weber W, Scott RJ. BRCA1 mutations in a selected series of breast/ovarian cancer patients Journal of Medical Genetics. 33: 721-725. PMID 8880569 DOI: 10.1136/jmg.33.9.721 |
0.141 |
|
| 2016 |
Easton DF, Lesueur F, Decker B, Michailidou K, Li J, Allen J, Luccarini C, Pooley KA, Shah M, Bolla MK, Wang Q, Dennis J, Ahmad J, Thompson ER, Damiola F, ... ... Scott RJ, et al. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Journal of Medical Genetics. PMID 26921362 DOI: 10.1136/Jmedgenet-2015-103529 |
0.139 |
|
| 2008 |
Reeves SG, Rich D, Meldrum CJ, Colyvas K, Kurzawski G, Suchy J, Lubinski J, Scott RJ. IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer. International Journal of Cancer. Journal International Du Cancer. 123: 1339-43. PMID 18623088 DOI: 10.1002/ijc.23668 |
0.139 |
|
| 2008 |
Debniak T, van de Wetering T, Scott R, Nagay L, Cybulski C, Górski B, Jakubowska A, Gronwald J, Masojć B, Huzarski T, Byrski T, Nej-Wołosiak K, Kładny J, Maleszka R, Lubinski J. Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland. European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (Ecp). 17: 389-91. PMID 18714178 DOI: 10.1097/CEJ.0b013e3282f75eb1 |
0.139 |
|
| 2008 |
Jakubowska A, Gronwald J, Menkiszak J, Górski B, Huzarski T, Byrski T, Edler L, Lubiński J, Scott RJ, Hamann U. The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women. Cancer Letters. 262: 71-6. PMID 18171601 DOI: 10.1016/j.canlet.2007.11.029 |
0.139 |
|
| 2009 |
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J, Gilbert M, Hamann U, Scott RJ. Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer. Gynecologic Oncology. 113: 109-14. PMID 19193430 DOI: 10.1016/j.ygyno.2008.12.036 |
0.139 |
|
| 2015 |
Serrano-Fernandez P, Dymerska D, Kurzawski G, Derkacz R, Sobieszcza?ska T, Banaszkiewicz Z, Roomere H, Oitmaa E, Metspalu A, Janavi?ius R, Elsakov P, Razumas M, Petrulis K, Irmejs A, Miklaševi?s E, ... Scott RJ, et al. Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia. Gastroenterology Research and Practice. 2015: 204089. PMID 26101521 DOI: 10.1155/2015/204089 |
0.138 |
|
| 1994 |
Scott RJ, Müller H. Familial and genetic aspects of colorectal carcinogenesis. European Journal of Cancer (Oxford, England : 1990). 2163-7. PMID 8297659 DOI: 10.1016/0959-8049(93)90056-L |
0.138 |
|
| 2016 |
Thompson ER, Rowley SM, Li N, McInerny S, Devereux L, Wong-Brown MW, Trainer AH, Mitchell G, Scott RJ, James PA, Campbell IG. Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. PMID 26786923 DOI: 10.1200/JCO.2015.63.7454 |
0.138 |
|
| 1998 |
Neuhausen SL, Godwin AK, Gershoni-Baruch R, Schubert E, Garber J, Stoppa-Lyonnet D, Olah E, Csokay B, Serova O, Lalloo F, Osorio A, Stratton M, Offit K, Boyd J, Caligo MA, ... Scott RJ, et al. Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. American Journal of Human Genetics. 62: 1381-8. PMID 9585613 DOI: 10.1086/301885 |
0.138 |
|
| 1997 |
Scott RJ, Froggatt NJ, Trembath RC, Evans DG, Hodgson SV, Maher ER. Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation. Human Molecular Genetics. 5: 1921-4. PMID 8968744 DOI: 10.1093/HMG/5.12.1921 |
0.138 |
|
| 2018 |
Mavaddat N, Michailidou K, Dennis J, Lush M, Fachal L, Lee A, Tyrer JP, Chen TH, Wang Q, Bolla MK, Yang X, Adank MA, Ahearn T, Aittomäki K, Allen J, ... ... Scott RJ, et al. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes. American Journal of Human Genetics. PMID 30554720 DOI: 10.1016/J.Ajhg.2018.11.002 |
0.137 |
|
| 2015 |
Stirzaker C, Zotenko E, Song JZ, Qu W, Nair SS, Locke WJ, Stone A, Armstong NJ, Robinson MD, Dobrovic A, Avery-Kiejda KA, Peters KM, French JD, Stein S, Korbie DJ, ... ... Scott RJ, et al. Methylome sequencing in triple-negative breast cancer reveals distinct methylation clusters with prognostic value. Nature Communications. 6: 5899. PMID 25641231 DOI: 10.1038/Ncomms6899 |
0.137 |
|
| 2014 |
Mirecka A, Paszkowska-Szczur K, Scott RJ, Górski B, van de Wetering T, Wokołorczyk D, Gromowski T, Serrano-Fernandez P, Cybulski C, Kashyap A, Gupta S, Gołąb A, Słojewski M, Sikorski A, Lubiński J, et al. Common variants of xeroderma pigmentosum genes and prostate cancer risk. Gene. 546: 156-61. PMID 24933002 DOI: 10.1016/j.gene.2014.06.026 |
0.137 |
|
| 2014 |
Wong-Brown MW, Avery-Kiejda KA, Bowden NA, Scott RJ. Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer International Journal of Cancer. 134: 301-305. PMID 23824750 DOI: 10.1002/ijc.28361 |
0.137 |
|
| 2011 |
Reeves SG, Meldrum C, Groombridge C, Spigelman A, Suchy J, Kurzawski G, Lubinski J, Scott RJ. DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome. Cancer Epidemiology. 36: 183-9. PMID 21974800 DOI: 10.1016/j.canep.2011.09.003 |
0.137 |
|
| 2016 |
Sjursen W, McPhillips M, Scott RJ, Talseth-Palmer BA. Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Molecular Genetics & Genomic Medicine. 4: 223-31. PMID 27064304 DOI: 10.1002/mgg3.198 |
0.137 |
|
| 2009 |
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J, Gilbert M, Hamann U, Scott RJ. Estrogen receptor polymorphisms and the risk of endometrial cancer. Bjog : An International Journal of Obstetrics and Gynaecology. 116: 1053-61. PMID 19438492 DOI: 10.1111/j.1471-0528.2009.02185.x |
0.137 |
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| 2020 |
Rogoża-Janiszewska E, Malińska K, Górski B, Scott RJ, Cybulski C, Kluźniak W, Lener M, Jakubowska A, Gronwald J, Huzarski T, Lubiński J, Dębniak T. Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population. Breast Cancer (Tokyo, Japan). PMID 32888145 DOI: 10.1007/s12282-020-01151-7 |
0.137 |
|
| 2015 |
Paszkowska-Szczur K, Scott RJ, Górski B, Cybulski C, Kurzawski G, Dymerska D, Gupta S, van de Wetering T, Masoj? B, Kashyap A, Gapska P, Gromowski T, K?adny J, Lubi?ski J, D?bniak T. Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population. Molecular Biology Reports. 42: 755-64. PMID 25391773 DOI: 10.1007/s11033-014-3824-z |
0.136 |
|
| 2015 |
Mavaddat N, Pharoah PD, Michailidou K, Tyrer J, Brook MN, Bolla MK, Wang Q, Dennis J, Dunning AM, Shah M, Luben R, Brown J, Bojesen SE, Nordestgaard BG, Nielsen SF, ... ... Scott R, et al. Prediction of breast cancer risk based on profiling with common genetic variants. Journal of the National Cancer Institute. 107. PMID 25855707 DOI: 10.1093/Jnci/Djv036 |
0.136 |
|
| 2011 |
Jaworowska E, Trubicka J, Lener MR, Masojć B, Złowocka-Perłowska E, McKay JD, Renard H, Oszutowska D, Wokołorczyk D, Lubiński J, Grodzki T, Serwatowski P, Nej-Wołosiak K, Tołoczko-Grabarek A, Sikorski A, ... ... Scott RJ, et al. Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population. Plos One. 6: e25057. PMID 21966413 DOI: 10.1371/journal.pone.0025057 |
0.136 |
|
| 2020 |
Glubb DM, Thompson DJ, Aben KK, Alsulimani A, Amant F, Annibali D, Attia J, Barricarte A, Beckmann MW, Berchuck A, Bermisheva M, Bernardini MQ, Bischof K, Bjørge L, Bodelon C, ... ... Scott RJ, et al. Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 33144283 DOI: 10.1158/1055-9965.EPI-20-0739 |
0.136 |
|
| 2019 |
Shu X, Bao J, Wu L, Long J, Shu XO, Guo X, Yang Y, Michailidou K, Bolla MK, Wang Q, Dennis J, Andrulis IL, Castelao JE, Dörk T, Gago-Dominguez M, ... ... Scott RJ, et al. Evaluation of Associations between Genetically Predicted Circulating Protein Biomarkers and Breast Cancer Risk. International Journal of Cancer. PMID 31265136 DOI: 10.1002/Ijc.32542 |
0.136 |
|
| 2007 |
Jaworowska E, Serrano-Fernández P, Tarnowska C, Lubiński J, Brzosko M, Flicinski J, Masojc B, Matyjasik J, Scott RJ, Narod SA, Lubiński J. Familial association of laryngeal, lung, stomach and early-onset breast cancer. Breast Cancer Research and Treatment. 112: 359-61. PMID 18097745 DOI: 10.1007/S10549-007-9869-0 |
0.135 |
|
| 2007 |
Matyjasik J, Cybulski C, Masojć B, Jakubowska A, Serrano-Fernandez P, Górski B, Debniak T, Huzarski T, Byrski T, Gronwald J, Złowocka E, Narod SA, Scott R, Lubinski J. CYP1B1 and predisposition to breast cancer in Poland. Breast Cancer Research and Treatment. 106: 383-8. PMID 17458695 DOI: 10.1007/S10549-007-9500-4 |
0.135 |
|
| 2010 |
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J, Scott RJ. Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk. Bmc Cancer. 10: 382. PMID 20646321 DOI: 10.1186/1471-2407-10-382 |
0.135 |
|
| 2006 |
Masojć B, Mierzejewski M, Cybulski C, van de Wetering T, Debniak T, Górski B, Jaworowska E, Tarnowska C, Lenner M, Scott RJ, Lubiński J. Cancer Familial Aggregation (CFA) and G446A polymorphism in ARLTS1 gene. Breast Cancer Research and Treatment. 99: 59-62. PMID 16570116 DOI: 10.1007/s10549-006-9180-5 |
0.134 |
|
| 1997 |
Garvin AM, Attenhofer-Haner M, Scott RJ. BRCA1 and BRCA2 mutation analysis in 86 early onset breast/ovarian cancer patients Journal of Medical Genetics. 34: 990-995. PMID 9429140 DOI: 10.1136/jmg.34.12.990 |
0.134 |
|
| 2010 |
Trubicka J, Grabowska-Kłujszo E, Suchy J, Masojć B, Serrano-Fernandez P, Kurzawski G, Cybulski C, Górski B, Huzarski T, Byrski T, Gronwald J, Złowocka E, Kładny J, Banaszkiewicz Z, Wiśniowski R, ... ... Scott RJ, et al. Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility. Bmc Cancer. 10: 420. PMID 20701755 DOI: 10.1186/1471-2407-10-420 |
0.134 |
|
| 2010 |
Scott RJ. Have the roles of two functional polymorphisms in breast cancer, R72P in P53 and MDM2-309 in MDM2, become clearer? Breast Cancer Research : Bcr. 12: 102. PMID 20156327 DOI: 10.1186/bcr2474 |
0.133 |
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| 2013 |
Talseth-Palmer BA, Wijnen JT, Grice DM, Scott RJ. Genetic modifiers of cancer risk in Lynch syndrome: a review. Familial Cancer. 12: 207-16. PMID 23471748 DOI: 10.1007/s10689-013-9614-2 |
0.133 |
|
| 2014 |
Avery-Kiejda KA, Morten B, Wong-Brown MW, Mathe A, Scott RJ. The relative mRNA expression of p53 isoforms in breast cancer is associated with clinical features and outcome. Carcinogenesis. 35: 586-96. PMID 24336193 DOI: 10.1093/carcin/bgt411 |
0.133 |
|
| 2006 |
Reeves S, Meldrum C, Scott RJ. Re: IGF-1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer. Journal of the National Cancer Institute. 98: 1664-5; author reply. PMID 17105989 DOI: 10.1093/JNCI/DJJ452 |
0.133 |
|
| 2016 |
Cheng TH, Thompson DJ, O'Mara TA, Painter JN, Glubb DM, Flach S, Lewis A, French JD, Freeman-Mills L, Church D, Gorman M, Martin L, Hodgson S, Webb PM, ... ... Scott RJ, et al. Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics. PMID 27135401 DOI: 10.1038/Ng.3562 |
0.132 |
|
| 2020 |
Kho PF, Amant F, Annibali D, Ashton K, Attia J, Auer PL, Beckmann MW, Black A, Brinton L, Buchanan DD, Chanock SJ, Chen C, Chen MM, Cheng THT, Cook LS, ... ... Scott RJ, et al. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer. International Journal of Cancer. PMID 32851660 DOI: 10.1002/Ijc.33206 |
0.132 |
|
| 2020 |
Kapoor PM, Mavaddat N, Choudhury PP, Wilcox AN, Lindström S, Behrens S, Michailidou K, Dennis J, Bolla MK, Wang Q, Jung A, Abu-Ful Z, Ahearn T, Andrulis IL, Anton-Culver H, ... ... Scott RJ, et al. Combined associations of a polygenic risk score and classical risk factors with breast cancer risk. Journal of the National Cancer Institute. PMID 32359158 DOI: 10.1093/Jnci/Djaa056 |
0.132 |
|
| 2001 |
Guldenschuh I, Hurlimann R, Muller A, Ammann R, Mullhaupt B, Dobbie Z, Zala GF, Flury R, Seelentag W, Roth J, Meyenberger C, Fried M, Hoppeler T, Spigelman AD, Scott RJ. Relationship between APC genotype, polyp distribution, and oral sulindac treatment in the colon and rectum of patients with familial adenomatous polyposis. Diseases of the Colon and Rectum. 44: 1090-7; discussion 1. PMID 11535846 DOI: 10.1007/BF02234627 |
0.131 |
|
| 2014 |
Oldmeadow C, Mossman D, Evans TJ, Holliday EG, Tooney PA, Cairns MJ, Wu J, Carr V, Attia JR, Scott RJ. Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci. Journal of Psychiatric Research. 52: 44-9. PMID 24507884 DOI: 10.1016/j.jpsychires.2014.01.011 |
0.131 |
|
| 2010 |
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J, Gilbert M, Hamann U, Scott RJ. Polymorphisms in genes of the steroid hormone biosynthesis and metabolism pathways and endometrial cancer risk. Cancer Epidemiology. 34: 328-37. PMID 20381444 DOI: 10.1016/j.canep.2010.03.005 |
0.131 |
|
| 2009 |
Attia J, Ioannidis JP, Thakkinstian A, McEvoy M, Scott RJ, Minelli C, Thompson J, Infante-Rivard C, Guyatt G. How to use an article about genetic association: A: Background concepts. Jama. 301: 74-81. PMID 19126812 DOI: 10.1001/jama.2008.901 |
0.13 |
|
| 2013 |
Holliday EG, Smith AV, Cornes BK, Buitendijk GH, Jensen RA, Sim X, Aspelund T, Aung T, Baird PN, Boerwinkle E, Cheng CY, van Duijn CM, Eiriksdottir G, Gudnason V, Harris T, ... ... Scott RJ, et al. Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. Plos One. 8: e53830. PMID 23326517 DOI: 10.1371/Journal.Pone.0053830 |
0.13 |
|
| 2019 |
Seppälä TT, Ahadova A, Dominguez-Valentin M, Macrae F, Evans DG, Therkildsen C, Sampson J, Scott R, Burn J, Möslein G, Bernstein I, Holinski-Feder E, Pylvänäinen K, Renkonen-Sinisalo L, Lepistö A, et al. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report. Hereditary Cancer in Clinical Practice. 17: 8. PMID 30858900 DOI: 10.1186/s13053-019-0106-8 |
0.13 |
|
| 2018 |
Li N, Rowley SM, Goode DL, Amarasinghe KC, McInerny S, Devereux L, Wong-Brown MW, Lupat R, Lee JEA, Hughes S, Thompson ER, Zethoven M, Li J, Trainer AH, ... ... Scott RJ, et al. Mutations in RECQL are not associated with breast cancer risk in an Australian population. Nature Genetics. PMID 30224651 DOI: 10.1038/s41588-018-0206-9 |
0.13 |
|
| 1998 |
Hamann U, Häner M, Stosiek U, Bastert G, Scott RJ. Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families. Journal of Medical Genetics. 34: 884-8. PMID 9391879 DOI: 10.1136/jmg.34.11.884 |
0.129 |
|
| 2017 |
Gromowski T, Gapska P, Scott RJ, Kąklewski K, Marciniak W, Durda K, Lener M, Górski B, Cybulski C, Sukiennicki G, Kaczmarek K, Jaworska-Bieniek K, Paszkowska-Szczur K, Waloszczyk P, Lubiński J, et al. Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence. International Journal of Cancer. PMID 28411367 DOI: 10.1002/ijc.30740 |
0.129 |
|
| 2014 |
Bolton K, Holliday E, Bowden N, Avery-Kiejda K, Scott R. 939: A highly polymorphic AG repeat in the upstream regulatory region of the estrogen-induced gene EIG121 is a modifier of disease risk in endometrial cancer European Journal of Cancer. 50: S230. DOI: 10.1016/S0959-8049(14)50835-0 |
0.129 |
|
| 2008 |
Suchy J, Kłujszo-Grabowska E, Kładny J, Cybulski C, Wokołorczyk D, Szymańska-Pasternak J, Kurzawski G, Scott RJ, Lubiński J. Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk. Bmc Cancer. 8: 112. PMID 18433468 DOI: 10.1186/1471-2407-8-112 |
0.128 |
|
| 2007 |
Bowden NA, Croft A, Scott RJ. Gene expression profiling in familial adenomatous polyposis adenomas and desmoid disease. Hereditary Cancer in Clinical Practice. 5: 79-96. PMID 19725988 DOI: 10.1186/1897-4287-5-2-79 |
0.128 |
|
| 2003 |
Meldrum CJ, McPhillips M, Crooks R, Thomas L, Edkins T, Creegan R, Miller E, Agrez M, Scott RJ. A Comparison Between Denaturing Gradient Gel Electrophoresis and Denaturing High Performance Liquid Chromatography in Detecting Mutations in Genes Associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC) and the Identification of 9 New Mutations Previously Unidentified by DGGE Hereditary Cancer in Clinical Practice. 1: 39. DOI: 10.1186/1897-4287-1-1-39 |
0.128 |
|
| 2016 |
Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, et al. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Nature Communications. 7: 10635. PMID 26868379 DOI: 10.1038/Ncomms10635 |
0.128 |
|
| 2018 |
Campbell I, Li N, Rowley S, Goode D, Devereux L, McInerny S, Grewal N, Lee A, Trainer A, Wong-Brown M, Scott R, Gorringe K, James P. Abstract PD1-04: The contribution of rare variants, polygenic risk, and novel candidate genes to the hereditary risk of breast cancer in a large cohort of breast cancer families Cancer Research. 78. DOI: 10.1158/1538-7445.Sabcs17-Pd1-04 |
0.128 |
|
| 2013 |
Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, ... ... Scott RJ, et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Human Molecular Genetics. 22: 2754-64. PMID 23474815 DOI: 10.1093/Hmg/Ddt116 |
0.127 |
|
| 2019 |
Xavier A, Olsen MF, Lavik LA, Johansen J, Singh AK, Sjursen W, Scott RJ, Talseth-Palmer BA. Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome. Molecular Genetics & Genomic Medicine. e850. PMID 31297992 DOI: 10.1002/mgg3.850 |
0.127 |
|
| 2002 |
Kurzawski G, Safranow K, Suchy J, Chlubek D, Scott RJ, Lubiński J. Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography. Journal of Biochemical and Biophysical Methods. 51: 89-100. PMID 11879922 DOI: 10.1016/S0165-022X(02)00003-9 |
0.127 |
|
| 2019 |
Escala-Garcia M, Guo Q, Dörk T, Canisius S, Keeman R, Dennis J, Beesley J, Lecarpentier J, Bolla MK, Wang Q, Abraham J, Andrulis IL, Anton-Culver H, Arndt V, Auer PL, ... ... Scott RJ, et al. Genome-wide association study of germline variants and breast cancer-specific mortality. British Journal of Cancer. PMID 30787463 DOI: 10.1038/S41416-019-0393-X |
0.127 |
|
| 2014 |
Evans TJ, Milne E, Anderson D, de Klerk NH, Jamieson SE, Talseth-Palmer BA, Bowden NA, Holliday EG, Rudant J, Orsi L, Richardson E, Lavis L, Catchpoole D, Attia JR, Armstrong BK, ... ... Scott RJ, et al. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. Plos One. 9: e110255. PMID 25310577 DOI: 10.1371/journal.pone.0110255 |
0.127 |
|
| 1996 |
Dobbie Z, Müller H, Scott RJ. Secretory phospholipase A2 does not appear to be associated with phenotypic variation in familial adenomatous polyposis. Human Genetics. 98: 386-90. PMID 8707313 DOI: 10.1007/s004390050226 |
0.125 |
|
| 2010 |
Out AA, Tops CM, Nielsen M, Weiss MM, van Minderhout IJ, Fokkema IF, Buisine MP, Claes K, Colas C, Fodde R, Fostira F, Franken PF, Gaustadnes M, Heinimann K, Hodgson SV, ... ... Scott RJ, et al. Leiden Open Variation Database of the MUTYH gene. Human Mutation. 31: 1205-15. PMID 20725929 DOI: 10.1002/humu.21343 |
0.125 |
|
| 1992 |
Müller H, Scott R. Hereditary conditions in which the loss of heterozygosity may be important. Mutation Research. 284: 15-24. PMID 1279387 DOI: 10.1016/0027-5107(92)90021-S |
0.125 |
|
| 2009 |
Attia J, Ioannidis JP, Thakkinstian A, McEvoy M, Scott RJ, Minelli C, Thompson J, Infante-Rivard C, Guyatt G. How to use an article about genetic association: B: Are the results of the study valid? Jama. 301: 191-7. PMID 19141767 DOI: 10.1001/jama.2008.946 |
0.125 |
|
| 2014 |
Cox AJ, Moscovis SM, Blackwell CC, Scott RJ. Cytokine gene polymorphism among Indigenous Australians. Innate Immunity. 20: 431-9. PMID 23940076 DOI: 10.1177/1753425913498911 |
0.125 |
|
| 2009 |
Kładny J, Suchy J, Kłujszo-Grabowska E, Kacperski T, Scott RJ, Kurzawski G, Lubiński J. Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism. Cancer Epidemiology. 33: 161-3. PMID 19679065 DOI: 10.1016/j.canep.2009.06.004 |
0.124 |
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| 2011 |
Avery-Kiejda KA, Bowden NA, Croft AJ, Scurr LL, Kairupan CF, Ashton KA, Talseth-Palmer BA, Rizos H, Zhang XD, Scott RJ, Hersey P. P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation. Bmc Cancer. 11: 203. PMID 21615965 DOI: 10.1186/1471-2407-11-203 |
0.123 |
|
| 1997 |
van der Luijt RB, Meera Khan P, Vasen HF, Breukel C, Tops CM, Scott RJ, Fodde R. Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli. Human Genetics. 98: 727-34. PMID 8931709 DOI: 10.1007/s004390050293 |
0.123 |
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| 2015 |
Ibrahim-Verbaas CA, Bressler J, Debette S, Schuur M, Smith AV, Bis JC, Davies G, Trompet S, Smith JA, Wolf C, Chibnik LB, Liu Y, Vitart V, Kirin M, Petrovic K, ... ... Scott RJ, et al. GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Molecular Psychiatry. PMID 25869804 DOI: 10.1038/Mp.2015.37 |
0.123 |
|
| 2011 |
Talseth-Palmer BA, Brenne IS, Ashton KA, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G, Spigelman A, Lubinski J, Scott RJ. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome. Journal of Medical Genetics. 48: 279-84. PMID 21097774 DOI: 10.1136/jmg.2010.079962 |
0.123 |
|
| 2018 |
Chatterjee G, Pai T, Hardiman T, Avery-Kiejda K, Scott RJ, Spencer J, Pinder SE, Grigoriadis A. Molecular patterns of cancer colonisation in lymph nodes of breast cancer patients. Breast Cancer Research : Bcr. 20: 143. PMID 30458865 DOI: 10.1186/s13058-018-1070-3 |
0.123 |
|
| 2018 |
Holmes M, Connor T, Oldmeadow C, Pockney PG, Scott RJ, Talseth-Palmer BA. CD36 - a plausible modifier of disease phenotype in familial adenomatous polyposis. Hereditary Cancer in Clinical Practice. 16: 14. PMID 30065793 DOI: 10.1186/s13053-018-0096-y |
0.123 |
|
| 2015 |
Morten BC, Wong-Brown MW, Scott RJ, Avery-Kiejda KA. The presence of the intron 3 16bp duplication polymorphism of p53 (rs17878362) in breast cancer is associated with a low Δ40p53:p53 ratio and better outcome. Carcinogenesis. PMID 26586794 DOI: 10.1093/carcin/bgv164 |
0.123 |
|
| 2015 |
Mathe A, Wong-Brown M, Morten B, Forbes JF, Braye SG, Avery-Kiejda KA, Scott RJ. Novel genes associated with lymph node metastasis in triple negative breast cancer. Scientific Reports. 5: 15832. PMID 26537449 DOI: 10.1038/srep15832 |
0.123 |
|
| 2014 |
Avery-Kiejda KA, Braye SG, Mathe A, Forbes JF, Scott RJ. Decreased expression of key tumour suppressor microRNAs is associated with lymph node metastases in triple negative breast cancer. Bmc Cancer. 14: 51. PMID 24479446 DOI: 10.1186/1471-2407-14-51 |
0.122 |
|
| 2015 |
D?bniak T, Gromowski T, Scott RJ, Gronwald J, Huzarski T, Byrski T, Kurzawski G, Dymerska D, Górski B, Paszkowska-Szczur K, Cybulski C, Serrano-Fernandez P, Lubi?ski J. Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families. Hereditary Cancer in Clinical Practice. 13: 3. PMID 25606063 DOI: 10.1186/s13053-015-0025-2 |
0.122 |
|
| 1997 |
Garvin AM, Eppenberger U, Müller H, Eppenberger-Castori S, Scott RJ. BRCA1 mutations found in archived early onset breast tumours European Journal of Cancer Part A. 33: 683-686. PMID 9274454 DOI: 10.1016/S0959-8049(96)00499-6 |
0.122 |
|
| 2001 |
Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, Sart Dd, Tucker K, Kirk J. Hereditary Nonpolyposis Colorectal Cancer in 95 Families: Differences and Similarities between Mutation-Positive and Mutation-Negative Kindreds American Journal of Human Genetics. 68: 118-127. PMID 11112663 DOI: 10.1086/316942 |
0.122 |
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| 2016 |
Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF, Oskarsson S, Pickrell JK, Thom K, Timshel P, de Vlaming R, ... ... Scott RJ, et al. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 533: 539-42. PMID 27225129 DOI: 10.1038/Nature17671 |
0.122 |
|
| 2011 |
Burn J, Gerdes AM, Macrae F, Mecklin JP, Moeslein G, Olschwang S, Eccles D, Evans DG, Maher ER, Bertario L, Bisgaard ML, Dunlop MG, Ho JW, Hodgson SV, Lindblom A, ... ... Scott RJ, et al. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial. Lancet (London, England). 378: 2081-7. PMID 22036019 DOI: 10.1016/S0140-6736(11)61049-0 |
0.122 |
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| 2009 |
Attia J, Ioannidis JP, Thakkinstian A, McEvoy M, Scott RJ, Minelli C, Thompson J, Infante-Rivard C, Guyatt G. How to use an article about genetic association: C: What are the results and will they help me in caring for my patients? Jama. 301: 304-8. PMID 19155457 DOI: 10.1001/jama.2008.993 |
0.121 |
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| 2015 |
Thompson ER, Gorringe KL, Rowley SM, Wong-Brown MW, McInerny S, Li N, Trainer AH, Devereux L, Doyle MA, Li J, Lupat R, Delatycki MB, Mitchell G, James PA, Scott RJ, et al. Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls Breast Cancer Research. 17. DOI: 10.1186/s13058-015-0627-7 |
0.121 |
|
| 2008 |
Jaworowska E, Serrano-Fernández P, Tarnowska C, Lubiński J, Kram A, Masojc B, Scott R, Lubiński J. Clinical and epidemiological features of familial laryngeal cancer in Poland. Cancer Detection and Prevention. 31: 270-5. PMID 17935913 DOI: 10.1016/J.CDP.2006.06.007 |
0.121 |
|
| 1995 |
Scott RJ, Van der Luijt R, Spycher M, Mary JL, Muller A, Hoppeler TH, Haner M, Muller HJ, Martinoli S, Brazzola PL, Khan PM. Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes Gut. 36: 731-736. PMID 7797123 DOI: 10.1136/gut.36.5.731 |
0.121 |
|
| 2013 |
Bolton KA, Ross JP, Grice DM, Bowden NA, Holliday EG, Avery-Kiejda KA, Scott RJ. STaRRRT: a table of short tandem repeats in regulatory regions of the human genome. Bmc Genomics. 14: 795. PMID 24228761 DOI: 10.1186/1471-2164-14-795 |
0.121 |
|
| 2014 |
Spurdle AB, Couch FJ, Parsons MT, McGuffog L, Barrowdale D, Bolla MK, Wang Q, Healey S, Schmutzler R, Wappenschmidt B, Rhiem K, Hahnen E, Engel C, Meindl A, Ditsch N, ... ... Scott R, et al. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia. Breast Cancer Research : Bcr. 16: 3419. PMID 25857409 DOI: 10.1186/S13058-014-0474-Y |
0.12 |
|
| 2015 |
Movahedi M, Bishop DT, Macrae F, Mecklin JP, Moeslein G, Olschwang S, Eccles D, Evans DG, Maher ER, Bertario L, Bisgaard ML, Dunlop MG, Ho JW, Hodgson SV, Lindblom A, ... ... Scott RJ, et al. Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. PMID 26282643 DOI: 10.1200/JCO.2014.58.9952 |
0.12 |
|
| 2013 |
Paszkowska-Szczur K, Scott RJ, Serrano-Fernandez P, Mirecka A, Gapska P, Górski B, Cybulski C, Maleszka R, Sulikowski M, Nagay L, Lubinski J, Dębniak T. Xeroderma pigmentosum genes and melanoma risk. International Journal of Cancer. Journal International Du Cancer. 133: 1094-100. PMID 23436679 DOI: 10.1002/ijc.28123 |
0.12 |
|
| 2015 |
Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, ... ... Scott RJ, et al. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Molecular Psychiatry. 20: 183-92. PMID 25644384 DOI: 10.1038/Mp.2014.188 |
0.12 |
|
| 2004 |
Smith CJ, Crock PA, King BR, Meldrum CJ, Scott RJ. Phenotype-genotype correlations in a series of wolfram syndrome families. Diabetes Care. 27: 2003-9. PMID 15277431 DOI: 10.2337/DIACARE.27.8.2003 |
0.12 |
|
| 1994 |
Müller H, Scott RJ. How common is hereditary cancer? Annals of Medicine. 26: 173-5. PMID 8074835 DOI: 10.3109/07853899409147886 |
0.119 |
|
| 2012 |
Scott RJ. Overview of genetic markers for hereditary colorectal cancer Hereditary Cancer in Clinical Practice. 10: A22. DOI: 10.1186/1897-4287-10-S4-A22 |
0.119 |
|
| 2010 |
Talseth-Palmer BA, McPhillips M, Groombridge C, Spigelman A, Scott RJ. MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer. Hereditary Cancer in Clinical Practice. 8: 5. PMID 20487569 DOI: 10.1186/1897-4287-8-5 |
0.119 |
|
| 2011 |
Yotova V, Lefebvre JF, Moreau C, Gbeha E, Hovhannesyan K, Bourgeois S, Bédarida S, Azevedo L, Amorim A, Sarkisian T, Avogbe PH, Chabi N, Dicko MH, Kou' Santa Amouzou ES, Sanni A, ... ... Scott RJ, et al. An X-linked haplotype of Neandertal origin is present among all non-African populations. Molecular Biology and Evolution. 28: 1957-62. PMID 21266489 DOI: 10.1093/molbev/msr024 |
0.119 |
|
| 2015 |
Chan JP, Thalamuthu A, Oldmeadow C, Armstrong NJ, Holliday EG, McEvoy M, Kwok JB, Assareh AA, Peel R, Hancock SJ, Reppermund S, Menant J, Trollor JN, Brodaty H, Schofield PR, ... ... Scott RJ, et al. Genetics of hand grip strength in mid to late life. Age (Dordrecht, Netherlands). 37: 9745. PMID 25637336 DOI: 10.1007/S11357-015-9745-5 |
0.119 |
|
| 1997 |
Heinimann K, Müller H, Weber W, Scott RJ. Disease expression in Swiss hereditary non-polyposis colorectal cancer (HNPCC) kindreds. International Journal of Cancer. 74: 281-5. PMID 9221805 DOI: 10.1002/(SICI)1097-0215(19970620)74:3<281::AID-IJC8>3.0.CO;2-V |
0.118 |
|
| 2012 |
Mathers JC, Movahedi M, Macrae F, Mecklin JP, Moeslein G, Olschwang S, Eccles D, Evans G, Maher ER, Bertario L, Bisgaard ML, Dunlop M, Ho JW, Hodgson S, Lindblom A, ... ... Scott RJ, et al. Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial. The Lancet. Oncology. 13: 1242-9. PMID 23140761 DOI: 10.1016/S1470-2045(12)70475-8 |
0.118 |
|
| 2003 |
Jakubowska A, Scott R, Menkiszak J, Gronwald J, Byrski T, Huzarski T, Górski B, Cybulski C, Debniak T, Kowalska E, Starzy?ska T, ?awniczak M, Narod S, Lubinski J. A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer. European Journal of Human Genetics : Ejhg. 11: 955-8. PMID 14647210 DOI: 10.1038/Sj.Ejhg.5201064 |
0.118 |
|
| 2015 |
Bowden NA, Beveridge NJ, Ashton KA, Baines KJ, Scott RJ. Understanding Xeroderma Pigmentosum Complementation Groups Using Gene Expression Profiling after UV-Light Exposure. International Journal of Molecular Sciences. 16: 15985-96. PMID 26184184 DOI: 10.3390/ijms160715985 |
0.118 |
|
| 2015 |
Wong-Brown M, Avery-Kiejda K, Scott RJ. Genetic insights into breast cancer risk Hereditary Cancer in Clinical Practice. 13. DOI: 10.1186/1897-4287-13-S1-A1 |
0.118 |
|
| 2017 |
Thompson ER, Wong-Brown M, Rowley SM, Dooley S, Lil N, Hipwell M, McInerny S, Meldrum C, Devereux L, Mossman D, Trainer AH, Millar B, Mitchell G, Smith C, James PA, ... ... Scott RJ, et al. Meeting abstracts from the Annual Conference on Hereditary Cancers 2015 Hereditary Cancer in Clinical Practice. 15. DOI: 10.1186/s13053-017-0074-9 |
0.118 |
|
| 2002 |
Ward R, Meldrum C, Williams R, Mokany E, Scott R, Turner J, Hawkins N, Burgess B, Groombridge C, Spigelman A. Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer. Journal of Cancer Research and Clinical Oncology. 128: 403-11. PMID 12200596 DOI: 10.1007/s00432-002-0361-2 |
0.117 |
|
| 2016 |
Wong SQ, Scott R, Fox SB. KRAS mutation testing in colorectal cancer: the model for molecular pathology testing in the future Colorectal Cancer. 5: 73-80. DOI: 10.2217/CRC-2015-0009 |
0.117 |
|
| 1996 |
Buerstedde JM, Alday P, Torhorst J, Weber W, Müller H, Scott R. Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes. Journal of Medical Genetics. 32: 909-12. PMID 8592341 DOI: 10.1136/jmg.32.11.909 |
0.117 |
|
| 2014 |
Avery-Kiejda KA, Braye SG, Forbes JF, Scott RJ. The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer. Bmc Cancer. 14: 253. PMID 24725360 DOI: 10.1186/1471-2407-14-253 |
0.117 |
|
| 2002 |
Hamann U, Liu X, Lange S, Ulmer HU, Benner A, Scott RJ. Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany. Journal of Medical Genetics. 39: E12. PMID 11897832 DOI: 10.1136/jmg.39.3.e12 |
0.116 |
|
| 2009 |
Dymerska D, Serrano-Fernández P, Suchy J, Pławski A, Słomski R, Kaklewski K, Scott RJ, Gronwald J, Kładny J, Byrski T, Huzarski T, Lubiński J, Kurzawski G. Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients. The Journal of Molecular Diagnostics : Jmd. 12: 82-90. PMID 20007843 DOI: 10.2353/JMOLDX.2010.090063 |
0.116 |
|
| 2009 |
Whitehall V, Tran K, Umapathy A, Grieu F, Hewitt C, Evans TJ, Ismail T, Wei QL, Collins P, Ravetto P, Leggett B, Salto-Tellez M, Soong R, Fox S, Scott RJ, et al. A multicenter blinded study to evaluate KRAS mutation testing methodologies in the clinical setting Journal of Molecular Diagnostics. 11: 543-552. PMID 19815694 DOI: 10.2353/jmoldx.2009.090057 |
0.116 |
|
| 2011 |
Oldmeadow C, Riveros C, Holliday EG, Scott R, Moscato P, Wang JJ, Mitchell P, Buitendijk GH, Vingerling JR, Klaver CC, Klein R, Attia J. Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods. Genetic Epidemiology. 35: 745-54. PMID 22125219 DOI: 10.1002/gepi.20622 |
0.116 |
|
| 2015 |
Lener M, Muszy?ska M, Jakubowska A, Jaworska-Bieniek K, Sukiennicki G, Kaczmarek K, Durda K, Gromowski T, Serrano-Fernández P, K?adny J, Wiechowska-Koz?owska A, Grodzki T, Jaworowska E, Lubi?ski J, Górecka-Szyld B, ... ... Scott RJ, et al. Selenium as a marker of cancer risk and of selection for control examinations in surveillance. Contemporary Oncology (Poznań, Poland). 19: A60-1. PMID 25691823 DOI: 10.5114/wo.2014.47131 |
0.116 |
|
| 2004 |
Gawdis-Wojnarska B, Brzosko M, Fliciński J, Marlicz K, Starzyńska T, Scott RJ, Lubiński J. Nuclear pedigree criteria for the identification of individuals suspected to be at risk of an inherited predisposition to gastric cancer. Hereditary Cancer in Clinical Practice. 2: 65-8. PMID 20233472 DOI: 10.1186/1897-4287-2-2-65 |
0.115 |
|
| 2018 |
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, ... ... Scott RA, ... ... Scott RJ, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706. PMID 30388399 DOI: 10.1016/J.Ajhg.2018.09.009 |
0.115 |
|
| 2004 |
Scott RJ, Crooks R, Rose L, Attia J, Thakkinstian A, Thomas L, Spigelman AD, Meldrum CJ. Germline Missense Changes in the APC Gene and Their Relationship to Disease. Hereditary Cancer in Clinical Practice. 2: 81-91. PMID 20233475 DOI: 10.1186/1897-4287-2-2-81 |
0.115 |
|
| 2005 |
Ashton KA, Meldrum CJ, McPhillips ML, Kairupan CF, Scott RJ. Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients. Hereditary Cancer in Clinical Practice. 3: 65-70. PMID 20223032 DOI: 10.1186/1897-4287-3-2-65 |
0.115 |
|
| 2019 |
Revelas M, Thalamuthu A, Oldmeadow C, Evans TJ, Armstrong NJ, Riveros C, Kwok JB, Schofield PR, Brodaty H, Scott RJ, Attia JR, Sachdev PS, Mather KA. Exceptional Longevity and Polygenic Risk for Cardiovascular Health. Genes. 10. PMID 30889929 DOI: 10.3390/Genes10030227 |
0.114 |
|
| 2012 |
Nyholt DR, Low SK, Anderson CA, Painter JN, Uno S, Morris AP, MacGregor S, Gordon SD, Henders AK, Martin NG, Attia J, Holliday EG, McEvoy M, Scott RJ, Kennedy SH, et al. Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics. 44: 1355-9. PMID 23104006 DOI: 10.1038/Ng.2445 |
0.114 |
|
| 2015 |
Guo ST, Chi MN, Yang RH, Guo XY, Zan LK, Wang CY, Xi YF, Jin L, Croft A, Tseng HY, Yan XG, Farrelly M, Wang FH, Lai F, Wang JF, ... ... Scott R, et al. INPP4B is an oncogenic regulator in human colon cancer. Oncogene. PMID 26411369 DOI: 10.1038/Onc.2015.361 |
0.114 |
|
| 1997 |
Scott RJ. Cancer genes: Functional aspects European Journal of Cancer. 33: 1706-1707. DOI: 10.1016/S0959-8049(97)00259-1 |
0.113 |
|
| 2008 |
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J, Gilbert M, Hamann U, Scott RJ. The influence of the Cyclin D1 870 G>A polymorphism as an endometrial cancer risk factor. Bmc Cancer. 8: 272. PMID 18822177 DOI: 10.1186/1471-2407-8-272 |
0.113 |
|
| 2014 |
Scott RJ, Fox SB, Desai J, Grieu F, Amanuel B, Garrett K, Harraway J, Cheetham G, Pattle N, Haddad A, Byron K, Rudzki B, Waring P, Iacopetta B. KRAS mutation testing of metastatic colorectal cancer in Australia: where are we at? Asia-Pacific Journal of Clinical Oncology. 10: 261-5. PMID 24811330 DOI: 10.1111/ajco.12201 |
0.113 |
|
| 2018 |
Petit J, Carroll G, Gould T, Pockney P, Dun M, Scott RJ. Cell-free DNA as a Diagnostic Blood-Based Biomarker for Colorectal Cancer: A Systematic Review. The Journal of Surgical Research. 236: 184-197. PMID 30694754 DOI: 10.1016/j.jss.2018.11.029 |
0.113 |
|
| 2020 |
Baszuk P, Janasik B, Pietrzak S, Marciniak W, Reszka E, Białkowska K, Jabłońska E, Muszyńska M, Lesicka M, Derkacz R, Grodzki T, Wójcik J, Wojtyś M, Dębniak T, Cybulski C, ... ... Scott RJ, et al. Lung Cancer Occurrence-Correlation with Serum Chromium Levels and Genotypes. Biological Trace Element Research. PMID 32648197 DOI: 10.1007/s12011-020-02240-6 |
0.112 |
|
| 2013 |
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, ... ... Scott RJ, et al. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics. 45: 145-54. PMID 23263486 DOI: 10.1038/Ng.2500 |
0.112 |
|
| 2006 |
Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, Rooij FW, et al. STK11 status and intussusception risk in Peutz-Jeghers syndrome Journal of Medical Genetics. 43. PMID 16882735 DOI: 10.1136/Jmg.2005.040535 |
0.111 |
|
| 2005 |
Kairupan CF, Meldrum CJ, Crooks R, Milward EA, Spigelman AD, Burgess B, Groombridge C, Kirk J, Tucker K, Ward R, Williams R, Scott RJ. Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations International Journal of Cancer. 116: 73-77. PMID 15761860 DOI: 10.1002/Ijc.20983 |
0.111 |
|
| 2013 |
Sim X, Jensen RA, Ikram MK, Cotch MF, Li X, MacGregor S, Xie J, Smith AV, Boerwinkle E, Mitchell P, Klein R, Klein BE, Glazer NL, Lumley T, McKnight B, ... ... Scott RJ, et al. Genetic loci for retinal arteriolar microcirculation. Plos One. 8: e65804. PMID 23776548 DOI: 10.1371/Journal.Pone.0065804 |
0.111 |
|
| 2015 |
Greenop KR, Bailey HD, Miller M, Scott RJ, Attia J, Ashton LJ, Downie P, Armstrong BK, Milne E. Breastfeeding and nutrition to 2 years of age and risk of childhood acute lymphoblastic leukemia and brain tumors. Nutrition and Cancer. 67: 431-41. PMID 25646650 DOI: 10.1080/01635581.2015.998839 |
0.111 |
|
| 2017 |
Avery-Kiejda KA, Mathe A, Scott RJ. Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases. Genomics Data. 14: 1-4. PMID 28736703 DOI: 10.1016/j.gdata.2017.07.004 |
0.11 |
|
| 2019 |
Dominguez-Valentin M, Seppälä TT, Sampson JR, Macrae F, Winship I, Evans DG, Scott RJ, Burn J, Möslein G, Bernstein I, Pylvänäinen K, Renkonen-Sinisalo L, Lepistö A, Lindblom A, Plazzer JP, et al. Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report. Hereditary Cancer in Clinical Practice. 17: 28. PMID 31636762 DOI: 10.1186/s13053-019-0127-3 |
0.11 |
|
| 2008 |
Alberici P, Gaspar C, Franken P, Gorski MM, de Vries I, Scott RJ, Ristimäki A, Aaltonen LA, Fodde R. Smad4 haploinsufficiency: a matter of dosage. Pathogenetics. 1: 2. PMID 19014666 DOI: 10.1186/1755-8417-1-2 |
0.11 |
|
| 1996 |
GARVIN AM, HANER M, MULLER H, WEBER W, TORHORST J, SCOTT RJ. BRCA1 AND BRCA2 MUTATION DETECTION IN A SELECTED SERIES OF BREAST CANCER PATIENTS European Journal of Cancer Prevention. 5: 101. DOI: 10.1097/00008469-199612002-00016 |
0.109 |
|
| 2014 |
Abdullah N, Attia J, Oldmeadow C, Scott RJ, Holliday EG. The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings. International Journal of Endocrinology. 2014: 593982. PMID 24744783 DOI: 10.1155/2014/593982 |
0.109 |
|
| 2014 |
Loth DW, Artigas MS, Gharib SA, Wain LV, Franceschini N, Koch B, Pottinger TD, Smith AV, Duan Q, Oldmeadow C, Lee MK, Strachan DP, James AL, Huffman JE, Vitart V, ... ... Scott RA, ... ... Scott RJ, et al. Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nature Genetics. 46: 669-77. PMID 24929828 DOI: 10.1038/Ng.3011 |
0.109 |
|
| 2019 |
Xavier A, Scott RJ, Talseth-Palmer BA. TAPES: A tool for assessment and prioritisation in exome studies. Plos Computational Biology. 15: e1007453. PMID 31613886 DOI: 10.1371/journal.pcbi.1007453 |
0.108 |
|
| 2018 |
Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, ... ... Scott RJ, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976. PMID 30061609 DOI: 10.1038/S41467-018-05369-0 |
0.108 |
|
| 2018 |
Sina AA, Carrascosa LG, Liang Z, Grewal YS, Wardiana A, Shiddiky MJA, Gardiner RA, Samaratunga H, Gandhi MK, Scott RJ, Korbie D, Trau M. Epigenetically reprogrammed methylation landscape drives the DNA self-assembly and serves as a universal cancer biomarker. Nature Communications. 9: 4915. PMID 30514834 DOI: 10.1038/s41467-018-07214-w |
0.108 |
|
| 2019 |
Berry NK, Scott RJ, Rowlings P, Enjeti AK. Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignancies. Critical Reviews in Oncology/Hematology. 142: 58-67. PMID 31377433 DOI: 10.1016/j.critrevonc.2019.07.016 |
0.108 |
|
| 2017 |
Gorski M, van der Most PJ, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, ... ... Scott RJ, et al. 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific Reports. 7: 45040. PMID 28452372 DOI: 10.1038/Srep45040 |
0.108 |
|
| 2016 |
Mather KA, Thalamuthu A, Oldmeadow C, Song F, Armstrong NJ, Poljak A, Holliday EG, McEvoy M, Kwok JB, Assareh AA, Reppermund S, Kochan NA, Lee T, Ames D, Wright MJ, ... ... Scott RJ, et al. Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults. Scientific Reports. 6: 23675. PMID 27030319 DOI: 10.1038/Srep23675 |
0.107 |
|
| 2013 |
Lener MR, Gupta S, Scott RJ, Tootsi M, Kulp M, Tammesoo ML, Viitak A, Metspalu A, Serrano-Fernández P, Kładny J, Jaworska-Bieniek K, Durda K, Muszyńska M, Sukiennicki G, Jakubowska A, et al. Can selenium levels act as a marker of colorectal cancer risk? Bmc Cancer. 13: 214. PMID 23627542 DOI: 10.1186/1471-2407-13-214 |
0.106 |
|
| 2009 |
Cotton RG, Al Aqeel AI, Al-Mulla F, Carrera P, Claustres M, Ekong R, Hyland VJ, Macrae FA, Marafie MJ, Paalman MH, Patrinos GP, Qi M, Ramesar RS, Scott RJ, Sijmons RH, et al. Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 843-9. PMID 20010362 DOI: 10.1097/GIM.0b013e3181c371c5 |
0.105 |
|
| 2020 |
Berry NK, Scott RJ, Sutton R, Law T, Trahair TN, Dalla-Pozza L, Ritchie P, Barbaric D, Enjeti AK. Enrichment of atypical hyperdiploidy and IKZF1 deletions detected by SNP-microarray in high-risk Australian AIEOP-BFM B-cell acute lymphoblastic leukaemia cohort. Cancer Genetics. 242: 8-14. PMID 32058318 DOI: 10.1016/j.cancergen.2020.01.051 |
0.105 |
|
| 1999 |
Heinimann K, Müllhaupt B, Weber W, Attenhofer M, Scott RJ, Fried M, Martinoli S, Müller H, Dobbie Z. Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status. Gut. 43: 675-9. PMID 9824350 DOI: 10.1136/gut.43.5.675 |
0.104 |
|
| 2014 |
Thompson BA, Spurdle AB, Plazzer JP, Greenblatt MS, Akagi K, Al-Mulla F, Bapat B, Bernstein I, Capellá G, den Dunnen JT, du Sart D, Fabre A, Farrell MP, Farrington SM, Frayling IM, ... ... Scott RJ, et al. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database. Nature Genetics. 46: 107-15. PMID 24362816 DOI: 10.1038/Ng.2854 |
0.104 |
|
| 2013 |
Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, Abdellaoui A, Agrawal A, Albrecht E, Alizadeh BZ, Amin N, Barnard J, Baumeister SE, ... ... Scott RJ, et al. GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (New York, N.Y.). 340: 1467-71. PMID 23722424 DOI: 10.1126/Science.1235488 |
0.104 |
|
| 1995 |
Dobbie Z, Spycher M, Hürliman R, Ammann R, Ammann T, Roth J, Müller A, Müller H, Scott RJ. Mutational analysis of the first 14 exons of the adenomatous polyposis coli (APC) gene. European Journal of Cancer (Oxford, England : 1990). 1709-13. PMID 7833149 DOI: 10.1016/0959-8049(94)00294-F |
0.104 |
|
| 2015 |
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V, Hottenga JJ, Trompet S, Müller-Nurasyid M, Zhao JH, Brody JA, ... ... Scott R, ... ... Scott RJ, et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics. PMID 26561523 DOI: 10.1093/Hmg/Ddv454 |
0.103 |
|
| 2015 |
Jaworska-Bieniek K, Lener M, Muszyńska M, Serrano-Fernández P, Sukiennicki G, Durda K, Gromowski T, Gupta S, Kładny J, Wiechowska-Kozłowska A, Grodzki T, Jaworowska E, Lubiński J, Górecka-Szyld B, Wilk G, ... ... Scott RJ, et al. Selenium and Cancer Food and Nutritional Components in Focus. 2015: 377-390. DOI: 10.1039/9781782622215-00377 |
0.103 |
|
| 2014 |
Moayyeri A, Hsu YH, Karasik D, Estrada K, Xiao SM, Nielson C, Srikanth P, Giroux S, Wilson SG, Zheng HF, Smith AV, Pye SR, Leo PJ, Teumer A, Hwang JY, ... ... Scott R, et al. Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Human Molecular Genetics. 23: 3054-68. PMID 24430505 DOI: 10.1093/Hmg/Ddt675 |
0.103 |
|
| 2019 |
Hnatyszyn A, Hryhorowicz S, Kaczmarek-Ryś M, Lis E, Słomski R, Scott RJ, Pławski A. Colorectal carcinoma in the course of inflammatory bowel diseases. Hereditary Cancer in Clinical Practice. 17: 18. PMID 31338130 DOI: 10.1186/s13053-019-0118-4 |
0.103 |
|
| 2017 |
Wain LV, Vaez A, Jansen R, Joehanes R, van der Most PJ, Erzurumluoglu AM, O'Reilly PF, Cabrera CP, Warren HR, Rose LM, Verwoert GC, Hottenga JJ, Strawbridge RJ, Esko T, Arking DE, ... ... Scott R, ... ... Scott RA, et al. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension (Dallas, Tex. : 1979). PMID 28739976 DOI: 10.1161/Hypertensionaha.117.09438 |
0.102 |
|
| 2004 |
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, ... ... Scott R, et al. Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American Journal of Human Genetics. 75: 161-73. PMID 15185170 DOI: 10.1086/422475 |
0.102 |
|
| 2004 |
Blackwell CC, Moscovis SM, Gordon AE, Al Madani OM, Hall ST, Gleeson M, Scott RJ, Roberts-Thomson J, Weir DM, Busuttil A. Ethnicity, infection and sudden infant death syndrome. Fems Immunology and Medical Microbiology. 42: 53-65. PMID 15325398 DOI: 10.1016/j.femsim.2004.06.007 |
0.102 |
|
| 2019 |
Yari H, Jin L, Teng L, Wang Y, Wu Y, Liu GZ, Gao W, Liang J, Xi Y, Feng YC, Zhang C, Zhang YY, Tabatabaee H, La T, Yang RH, ... ... Scott R, et al. LncRNA REG1CP promotes tumorigenesis through an enhancer complex to recruit FANCJ helicase for REG3A transcription. Nature Communications. 10: 5334. PMID 31767869 DOI: 10.1038/S41467-019-13313-Z |
0.102 |
|
| 2016 |
Mathe A, Wong-Brown M, Locke WJ, Stirzaker C, Braye SG, Forbes JF, Clark SJ, Avery-Kiejda KA, Scott RJ. DNA methylation profile of triple negative breast cancer-specific genes comparing lymph node positive patients to lymph node negative patients. Scientific Reports. 6: 33435. PMID 27671774 DOI: 10.1038/srep33435 |
0.102 |
|
| 2015 |
Greenop KR, Scott RJ, Attia J, Bower C, de Klerk NH, Norris MD, Haber M, Jamieson SE, van Bockxmeer FM, Gottardo NG, Ashton LJ, Armstrong BK, Milne E. Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 24: 931-7. PMID 25809864 DOI: 10.1158/1055-9965.EPI-14-1248 |
0.102 |
|
| 2001 |
Nasioulas S, Jones IT, St John DJ, Scott RJ, Forrest SM, McKinlay Gardner RJ. Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutation. Familial Cancer. 1: 3-7. PMID 14574009 DOI: 10.1023/A:1011570523343 |
0.101 |
|
| 2012 |
Cheng YC, Anderson CD, Bione S, Keene K, Maguire JM, Nalls M, Rasheed A, Zeginigg M, Attia J, Baker R, Barlera S, Biffi A, Bookman E, Brott TG, Brown RD, ... ... Scott RJ, et al. Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke? Stroke; a Journal of Cerebral Circulation. 43: 980-6. PMID 22363065 DOI: 10.1161/Strokeaha.111.632075 |
0.1 |
|
| 2015 |
Mathe A, Scott RJ, Avery-Kiejda KA. miRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer. International Journal of Molecular Sciences. 16: 28347-76. PMID 26633365 DOI: 10.3390/ijms161226090 |
0.1 |
|
| 1997 |
Dobbie Z, Heinimann K, Bishop DT, Müller H, Scott RJ. Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis. Human Genetics. 99: 653-7. PMID 9150735 DOI: 10.1007/s004390050423 |
0.099 |
|
| 2016 |
Purrington KS, Visscher DW, Wang C, Yannoukakos D, Hamann U, Nevanlinna H, Cox A, Giles GG, Eckel-Passow JE, Lakis S, Kotoula V, Fountzilas G, Kabisch M, Rüdiger T, Heikkilä P, ... ... Scott R, et al. Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes. Breast Cancer Research and Treatment. PMID 27083182 DOI: 10.1007/S10549-016-3775-2 |
0.099 |
|
| 2012 |
Kurzawski G, Dymerska D, Serrano-Fernández P, Trubicka J, Masojć B, Jakubowska A, Scott RJ. DNA and RNA analyses in detection of genetic predisposition to cancer. Hereditary Cancer in Clinical Practice. 10: 17. PMID 23206658 DOI: 10.1186/1897-4287-10-17 |
0.099 |
|
| 2007 |
Scott RJ. Response to “Variability in the clinical phenotype among families with HNPCC”: The potential importance of the location of the mutation in the gene by Dr. Prathap Bandipalliam International Journal of Cancer. 120: 2278-2278. DOI: 10.1002/ijc.22347 |
0.099 |
|
| 2006 |
Bowden NA, Tooney PA, Scott RJ. Gene expression profiling of xeroderma pigmentosum. Hereditary Cancer in Clinical Practice. 4: 103-10. PMID 20223010 DOI: 10.1186/1897-4287-4-2-103 |
0.099 |
|
| 2010 |
Ikram MK, Sim X, Xueling S, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, ... ... Scott RJ, et al. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. Plos Genetics. 6: e1001184. PMID 21060863 DOI: 10.1371/Journal.Pgen.1001184 |
0.099 |
|
| 1996 |
Dobbie Z, Spycher M, Mary JL, Häner M, Guldenschuh I, Hürliman R, Amman R, Roth J, Müller H, Scott RJ. Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene. Journal of Medical Genetics. 33: 274-80. PMID 8730280 DOI: 10.1136/jmg.33.4.274 |
0.099 |
|
| 2016 |
Painter JN, O'Mara TA, Marquart L, Webb PM, Attia J, Medland SE, Cheng T, Dennis J, Holliday EG, McEvoy M, Scott RJ, Ahmed S, Healey CS, Shah M, Gorman M, et al. Genetic risk score Mendelian randomization shows that obesity measured as body mass index, but not waist:hip ratio, is causal for endometrial cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 27550749 DOI: 10.1158/1055-9965.Epi-16-0147 |
0.099 |
|
| 2018 |
Xavier MJ, Mitchell LA, McEwan KE, Scott R, Aitken RJ. Genomic integrity in the male germ line: evidence in support of the disposable soma hypothesis. Reproduction (Cambridge, England). PMID 29921625 DOI: 10.1530/REP-18-0202 |
0.098 |
|
| 2016 |
Okbay A, Baselmans BM, De Neve JE, Turley P, Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, Derringer J, Gratten J, Lee JJ, Liu JZ, de Vlaming R, Ahluwalia TS, ... ... Scott RJ, et al. Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics. 48: 1591. PMID 27898078 DOI: 10.1038/Ng1216-1587B |
0.098 |
|
| 2009 |
Kaput J, Cotton RG, Hardman L, Watson M, Al Aqeel AI, Al-Aama JY, Al-Mulla F, Alonso S, Aretz S, Auerbach AD, Bapat B, Bernstein IT, Bhak J, Bleoo SL, Blöcker H, ... ... Scott RJ, et al. Planning the human variome project: the Spain report. Human Mutation. 30: 496-510. PMID 19306394 DOI: 10.1002/Humu.20972 |
0.098 |
|
| 2014 |
Cox MB, Bowden NA, Scott RJ, Lechner-Scott J. Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis Multiple Sclerosis Journal. 20: 489-491. PMID 23897640 DOI: 10.1177/1352458513498127 |
0.098 |
|
| 2017 |
Berry NK, Dixon-McIver A, Scott RJ, Rowlings P, Enjeti AK. Detection of complex genomic signatures associated with risk in plasma cell disorders. Cancer Genetics. 218: 1-9. PMID 29153091 DOI: 10.1016/j.cancergen.2017.08.004 |
0.098 |
|
| 2015 |
Dun MD, Chalkley RJ, Faulkner S, Keene S, Avery-Kiejda K, Scott RJ, Falkenby LG, Cairns MJ, Larsen MR, Bradshaw RA, Hondermarck H. Proteotranscriptomic Profiling of 231-BR Breast Cancer Cells: Identification of Potential Biomarkers and Therapeutic Targets for Brain Metastasis. Molecular & Cellular Proteomics : McP. PMID 26041846 DOI: 10.1074/Mcp.M114.046110 |
0.098 |
|
| 2011 |
Mossman D, Scott RJ. Long term transcriptional reactivation of epigenetically silenced genes in colorectal cancer cells requires DNA hypomethylation and histone acetylation. Plos One. 6: e23127. PMID 21829702 DOI: 10.1371/journal.pone.0023127 |
0.098 |
|
| 2018 |
Dębniak T, Scott RJ, Lea RA, Górski B, Masojć B, Cybulski C, Kram A, Maleszka R, Gromowski T, Paszkowska-Szczur K, Kashyap A, Lener MR, Malińska K, Rogoża E, Murawa D, et al. Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland. Cancer Research and Treatment : Official Journal of Korean Cancer Association. PMID 29764119 DOI: 10.4143/crt.2018.157 |
0.098 |
|
| 2019 |
Davies G, Lam M, Harris SE, Trampush JW, Luciano M, Hill WD, Hagenaars SP, Ritchie SJ, Marioni RE, Fawns-Ritchie C, Liewald DCM, Okely JA, Ahola-Olli AV, Barnes CLK, Bertram L, ... ... Scott RJ, et al. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications. 10: 2068. PMID 31043617 DOI: 10.1038/S41467-019-10160-W |
0.098 |
|
| 2014 |
Mathe A, Avery-Kiejda K, Wong-Brown M, Forbes J, Braye S, Scott R. 130: Eight microRNAs as biomarkers for metastatic spread in triple negative breast cancer European Journal of Cancer. 50: S29. DOI: 10.1016/S0959-8049(14)50110-4 |
0.097 |
|
| 2021 |
Lubiński J, Jaworowska E, Derkacz R, Marciniak W, Białkowska K, Baszuk P, Scott RJ, Lubiński JA. Survival of Laryngeal Cancer Patients Depending on Zinc Serum Level and Oxidative Stress Genotypes. Biomolecules. 11. PMID 34200699 DOI: 10.3390/biom11060865 |
0.097 |
|
| 2008 |
Burn J, Bishop DT, Mecklin JP, Macrae F, Möslein G, Olschwang S, Bisgaard ML, Ramesar R, Eccles D, Maher ER, Bertario L, Jarvinen HJ, Lindblom A, Evans DG, Lubinski J, ... ... Scott RJ, et al. Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome. The New England Journal of Medicine. 359: 2567-78. PMID 19073976 DOI: 10.1056/NEJMoa0801297 |
0.097 |
|
| 2013 |
Johnstone DM, Riveros C, Heidari M, Graham RM, Trinder D, Berretta R, Olynyk JK, Scott RJ, Moscato P, Milward EA. Evaluation of Different Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes. Microarrays (Basel, Switzerland). 2: 131-52. PMID 27605185 DOI: 10.3390/microarrays2020131 |
0.097 |
|
| 2018 |
Białkowska K, Marciniak W, Muszyńska M, Baszuk P, Gupta S, Jaworska-Bieniek K, Sukiennicki G, Durda K, Gromowski T, Prajzendanc K, Cybulski C, Huzarski T, Gronwald J, Dębniak T, Scott RJ, et al. Association of zinc level and polymorphism in MMP-7 gene with prostate cancer in Polish population. Plos One. 13: e0201065. PMID 30036379 DOI: 10.1371/journal.pone.0201065 |
0.097 |
|
| 2011 |
Hondow HL, Fox SB, Mitchell G, Scott RJ, Beshay V, Wong SQ, Dobrovic A. A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. Bmc Cancer. 11: 265. PMID 21702907 DOI: 10.1186/1471-2407-11-265 |
0.097 |
|
| 2017 |
Najdawi F, Crook A, Maidens J, McEvoy C, Fellowes A, Pickett J, Ho M, Nevell D, McIlroy K, Sheen A, Sioson L, Ahadi M, Turchini J, Clarkson A, Hogg R, ... ... Scott RJ, et al. Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy. Pathology. PMID 28669579 DOI: 10.1016/j.pathol.2017.05.004 |
0.096 |
|
| 2021 |
Pariyar M, Johns A, Thorne RF, Scott RJ, Avery-Kiejda KA. Copy number variation in triple negative breast cancer samples associated with lymph node metastasis. Neoplasia (New York, N.Y.). 23: 743-753. PMID 34225099 DOI: 10.1016/j.neo.2021.05.016 |
0.096 |
|
| 2017 |
Maltby VE, Lea RA, Sanders KA, White N, Benton MC, Scott RJ, Lechner-Scott J. Differential methylation at MHC in CD4(+) T cells is associated with multiple sclerosis independently of HLA-DRB1. Clinical Epigenetics. 9: 71. PMID 28729889 DOI: 10.1186/s13148-017-0371-1 |
0.096 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Scott RA, ... ... Scott RJ, et al. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30429575 DOI: 10.1038/S41588-018-0297-3 |
0.095 |
|
| 2017 |
Strumidło A, Skiba S, Scott RJ, Lubiński J. The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation. Hereditary Cancer in Clinical Practice. 15: 15. PMID 29021870 DOI: 10.1186/s13053-017-0076-7 |
0.095 |
|
| 2014 |
Smith G, James CA, Scott R, Woolf E. Ask the experts: chromatographic baselines. Bioanalysis. 6: 1167-70. PMID 24946917 DOI: 10.4155/bio.14.67 |
0.095 |
|
| 2019 |
Pietrzak S, Wójcik J, Scott RJ, Kashyap A, Grodzki T, Baszuk P, Bielewicz M, Marciniak W, Wójcik N, Dębniak T, Masojć B, Pieróg J, Cybulski C, Gronwald J, Wojtyś M, et al. Influence of the selenium level on overall survival in lung cancer. Journal of Trace Elements in Medicine and Biology : Organ of the Society For Minerals and Trace Elements (Gms). 56: 46-51. PMID 31442953 DOI: 10.1016/j.jtemb.2019.07.010 |
0.095 |
|
| 2018 |
Kamien B, Ronan A, Poke G, Sinnerbrink I, Baynam G, Ward M, Gibson WT, Dudding-Byth T, Scott RJ. A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing. Molecular Syndromology. 9: 70-82. PMID 29593474 DOI: 10.1159/000484532 |
0.094 |
|
| 2017 |
Abdullah N, Abdul Murad NA, Mohd Haniff EA, Syafruddin SE, Attia J, Oldmeadow C, Kamaruddin MA, Abd Jalal N, Ismail N, Ishak M, Jamal R, Scott RJ, Holliday EG. Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort. Public Health. 149: 31-38. PMID 28528225 DOI: 10.1016/j.puhe.2017.04.003 |
0.094 |
|
| 2015 |
Green MJ, Raudino A, Cairns MJ, Wu J, Tooney PA, Scott RJ, Carr VJ. Do common genotypes of FK506 binding protein 5 (FKBP5) moderate the effects of childhood maltreatment on cognition in schizophrenia and healthy controls? Journal of Psychiatric Research. 70: 9-17. PMID 26424418 DOI: 10.1016/j.jpsychires.2015.07.019 |
0.094 |
|
| 2015 |
Gu BJ, Field J, Dutertre S, Ou A, Kilpatrick TJ, Lechner-Scott J, Scott R, Lea R, Taylor BV, Stankovich J, Butzkueven H, Gresle M, Laws SM, Petrou S, Hoffjan S, et al. A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human Molecular Genetics. PMID 26188005 DOI: 10.1093/hmg/ddv278 |
0.093 |
|
| 2019 |
Liu X, Low SK, Atkins JR, Wu JQ, Reay WR, Cairns HM, Green MJ, Schall U, Jablensky A, Mowry B, Michie PT, Catts SV, Henskens F, Pantelis C, Loughland C, ... ... Scott RJ, et al. Wnt receptor gene was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort. The Australian and New Zealand Journal of Psychiatry. 4867419885443. PMID 31735061 DOI: 10.1177/0004867419885443 |
0.093 |
|
| 2015 |
Moscovis SM, Cox A, Hall ST, Burns CJ, Scott RJ, Blackwell CC. Effects of gender, cytokine gene polymorphisms and environmental factors on inflammatory responses. Innate Immunity. 21: 523-30. PMID 25432967 DOI: 10.1177/1753425914553645 |
0.093 |
|
| 2016 |
Pringle KG, Delforce SJ, Wang Y, Ashton K, Proietto A, Otton G, Blackwell CC, Scott RJ, Lumbers ER. Renin angiotensin system gene polymorphisms and endometrial cancer. Endocrine Connections. PMID 27068935 DOI: 10.1530/EC-15-0112 |
0.093 |
|
| 2010 |
Mossman D, Kim KT, Scott RJ. Demethylation by 5-aza-2'-deoxycytidine in colorectal cancer cells targets genomic DNA whilst promoter CpG island methylation persists. Bmc Cancer. 10: 366. PMID 20618997 DOI: 10.1186/1471-2407-10-366 |
0.093 |
|
| 2009 |
Bahlo M, Booth DR, Simon A Broadley, Brown MA, Foote SJ, Griffiths LR, Kilpatrick TJ, Lechner-Scott J, Moscato P, Perreau VM, Rubio JP, Scott RJ, Stankovich J, Stewart GJ, Taylor BV, et al. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Nature Genetics. 41: 824-828. PMID 19525955 DOI: 10.1038/Ng.396 |
0.093 |
|
| 2018 |
Fullerton JM, Klauser P, Lenroot RK, Shaw AD, Overs B, Heath A, Cairns MJ, Atkins J, Scott R, Schofield PR, Weickert CS, Pantelis C, Fornito A, Whitford TJ, et al. Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls. Translational Psychiatry. 8: 21. PMID 29353880 DOI: 10.1038/S41398-017-0052-Z |
0.092 |
|
| 2018 |
Rhead B, Brorson IS, Berge T, Adams C, Quach H, Moen SM, Berg-Hansen P, Celius EG, Sangurdekar DP, Bronson PG, Lea RA, Burnard S, Maltby VE, Scott RJ, Lechner-Scott J, et al. Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients. Plos One. 13: e0206511. PMID 30379917 DOI: 10.1371/Journal.Pone.0206511 |
0.092 |
|
| 2017 |
Smith-Anttila CJA, Bensing S, Alimohammadi M, Dalin F, Oscarson M, Zhang MD, Perheentupa J, Husebye ES, Gustafsson J, Björklund P, Fransson A, Nordmark G, Rönnblom L, Meloni A, Scott RJ, et al. Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1. Autoimmunity. 1-9. PMID 28557628 DOI: 10.1080/08916934.2017.1332183 |
0.092 |
|
| 2013 |
Yadav S, Cotlarciuc I, Munroe PB, Khan MS, Nalls MA, Bevan S, Cheng YC, Chen WM, Malik R, McCarthy NS, Holliday EG, Speed D, Hasan N, Pucek M, Rinne PE, ... ... Scott RJ, et al. Genome-wide analysis of blood pressure variability and ischemic stroke. Stroke; a Journal of Cerebral Circulation. 44: 2703-9. PMID 23929743 DOI: 10.1161/Strokeaha.113.002186 |
0.092 |
|
| 2000 |
Scott RJ, Spigelman AD. Tumour site, sex, and survival in colorectal cancer. Lancet (London, England). 356: 857; author reply 85. PMID 11022958 DOI: 10.1016/S0140-6736(05)73439-5 |
0.092 |
|
| 2015 |
Greenop KR, Miller M, Bailey HD, Scott RJ, Attia J, Bower C, van Bockxmeer FM, Ashton LJ, Armstrong BK, Milne E. Paternal dietary folate, B6 and B12 intake, and the risk of childhood brain tumors. Nutrition and Cancer. 67: 224-30. PMID 25625505 DOI: 10.1080/01635581.2015.990571 |
0.091 |
|
| 2010 |
Talseth-Palmer B, Brenne I, Ashton K, Evans T, McPhillips M, Groombridge C, Kurzawski G, Spigelman A, Lubinski J, Scott R. 83 Colorectal cancer susceptibility loci on chr 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome European Journal of Cancer Supplements. 8: 22. DOI: 10.1016/S1359-6349(10)70892-2 |
0.091 |
|
| 2007 |
Kairupan C, Scott RJ. Base excision repair and the role of MUTYH. Hereditary Cancer in Clinical Practice. 5: 199-209. PMID 19725997 DOI: 10.1186/1897-4287-5-4-199 |
0.091 |
|
| 2006 |
Bowden NA, Weidenhofer J, Scott RJ, Schall U, Todd J, Michie PT, Tooney PA. Preliminary investigation of gene expression profiles in peripheral blood lymphocytes in schizophrenia. Schizophrenia Research. 82: 175-83. PMID 16414245 DOI: 10.1016/j.schres.2005.11.012 |
0.091 |
|
| 2021 |
Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, ... ... Scott RJ, et al. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. PMID 34002096 DOI: 10.1038/s41588-021-00857-4 |
0.09 |
|
| 1997 |
Scott R. DNA Mismatch Repair and Hereditary Nonpolyposis Colorectal Cancer Oncology Research and Treatment. 20: 42-47. DOI: 10.1159/000218895 |
0.09 |
|
| 2015 |
Grimson S, Cox AJ, Pringle K, Burns C, Lumbers E, Blackwell C, Scott RJ. The prevalence of unique SNPs in the renin-angiotensin system highlights the need for pharmacogenetics in Indigenous Australians. Clinical and Experimental Pharmacology & Physiology. PMID 26667052 DOI: 10.1111/1440-1681.12525 |
0.09 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, ... ... Scott RJ, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.09 |
|
| 2018 |
Abdullah N, Murad NAA, Attia J, Oldmeadow C, Kamaruddin MA, Jalal NA, Ismail N, Jamal R, Scott RJ, Holliday EG. Differing Contributions of Classical Risk Factors to Type 2 Diabetes in Multi-Ethnic Malaysian Populations. International Journal of Environmental Research and Public Health. 15. PMID 30544761 DOI: 10.3390/ijerph15122813 |
0.09 |
|
| 2017 |
Jamaluddin MFB, Ko YA, Kumar M, Brown Y, Bajwa P, Nagendra PB, Skerrett-Byrne D, Hondermarck H, Baker MA, Dun MD, Scott RJ, Nahar P, Tanwar PS. Proteomic profiling of human uterine fibroids reveals upregulation of the extracellular matrix protein periostin. Endocrinology. PMID 29244110 DOI: 10.1210/en.2017-03018 |
0.089 |
|
| 2015 |
Sapkota Y, Attia J, Gordon SD, Henders AK, Holliday EG, Rahmioglu N, MacGregor S, Martin NG, McEvoy M, Morris AP, Scott RJ, Zondervan KT, Montgomery GW, Nyholt DR. Genetic burden associated with varying degrees of disease severity in endometriosis. Molecular Human Reproduction. 21: 594-602. PMID 25882541 DOI: 10.1093/Molehr/Gav021 |
0.089 |
|
| 2021 |
Mouchahoir T, Schiel JE, Rogers R, Heckert A, Place BJ, Ammerman A, Li X, Robinson T, Schmidt B, Chumsae CM, Li X, Manuilov AV, Yan B, Staples GO, Ren D, ... ... Scott R, et al. New Peak Detection Performance Metrics from the MAM Consortium Interlaboratory Study. Journal of the American Society For Mass Spectrometry. PMID 33710905 DOI: 10.1021/jasms.0c00415 |
0.089 |
|
| 2016 |
Hess JL, Tylee DS, Barve R, de Jong S, Ophoff RA, Kumarasinghe N, Tooney P, Schall U, Gardiner E, Beveridge NJ, Scott RJ, Yasawardene S, Perera A, Mendis J, Carr V, et al. Transcriptome-wide mega-analyses reveal joint dysregulation of immunologic genes and transcription regulators in brain and blood in schizophrenia. Schizophrenia Research. PMID 27450777 DOI: 10.1016/J.Schres.2016.07.006 |
0.089 |
|
| 2016 |
Mehta D, Tropf FC, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson PK, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, ... ... Scott RJ, et al. Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. Jama Psychiatry. PMID 27007234 DOI: 10.1001/Jamapsychiatry.2016.0129 |
0.089 |
|
| 2014 |
Mather KA, Thalamuthu A, Oldmeadow C, Song F, Armstrong NJ, Poljak A, Holliday L, McEvoy M, Kwok J, Assareh A, Reppermund S, Ames D, Wright M, Trollor JN, Schofield PW, ... ... Scott RJ, et al. Genome-Wide Significant Results Identified For Plasma Apolipoprotein H Levels Alzheimers & Dementia. 10: 788. DOI: 10.1016/J.Jalz.2014.05.1526 |
0.089 |
|
| 2011 |
Bailey HD, Armstrong BK, de Klerk NH, Fritschi L, Attia J, Scott RJ, Smibert E, Milne E. Exposure to professional pest control treatments and the risk of childhood acute lymphoblastic leukemia. International Journal of Cancer. Journal International Du Cancer. 129: 1678-88. PMID 21080443 DOI: 10.1002/ijc.25769 |
0.088 |
|
| 2015 |
Blackwell C, Moscovis S, Hall S, Burns C, Scott RJ. Exploring the risk factors for sudden infant deaths and their role in inflammatory responses to infection. Frontiers in Immunology. 6: 44. PMID 25798137 DOI: 10.3389/fimmu.2015.00044 |
0.088 |
|
| 1993 |
Scott RJ, Itin P, Kleijer WJ, Kolb K, Arlett C, Muller H. Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair. Journal of the American Academy of Dermatology. 29: 883-9. PMID 8408834 DOI: 10.1016/0190-9622(93)70263-S |
0.087 |
|
| 2020 |
Maltby VE, Lea RA, Burnard S, Xavier A, Van Cao T, White N, Kennedy D, Groen K, Sanders KA, Seeto R, Bray S, Gresle M, Laverick L, Butzkueven H, Scott RJ, et al. Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients. Scientific Reports. 10: 22217. PMID 33335118 DOI: 10.1038/s41598-020-78809-x |
0.087 |
|
| 2019 |
Hess JL, Tylee DS, Barve R, de Jong S, Ophoff RA, Kumarasinghe N, Tooney P, Schall U, Gardiner E, Beveridge NJ, Scott RJ, Yasawardene S, Perera A, Mendis J, Carr V, et al. Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses. Schizophrenia Research. PMID 31391148 DOI: 10.1016/J.Schres.2019.07.036 |
0.087 |
|
| 2005 |
Gronwald J, Jauch A, Cybulski C, Schoell B, Böhm-Steuer B, Lener M, Grabowska E, Górski B, Jakubowska A, Domagała W, Chosia M, Scott RJ, Lubiński J. Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization. International Journal of Cancer. 114: 230-6. PMID 15540206 DOI: 10.1002/ijc.20723 |
0.087 |
|
| 2014 |
Oldmeadow C, Holliday EG, McEvoy M, Scott R, Kwok JB, Mather K, Sachdev P, Schofield P, Attia J. Concordance between direct and imputed APOE genotypes using 1000 Genomes data. Journal of Alzheimer's Disease : Jad. 42: 391-3. PMID 24903779 DOI: 10.3233/Jad-140846 |
0.087 |
|
| 2006 |
Mossman D, Scott RJ. Epimutations, inheritance and causes of aberrant DNA methylation in cancer. Hereditary Cancer in Clinical Practice. 4: 75-80. PMID 20223011 DOI: 10.1186/1897-4287-4-2-75 |
0.087 |
|
| 2008 |
Mendes A, Scott RJ, Moscato P. Microarrays--identifying molecular portraits for prostate tumors with different Gleason patterns. Methods in Molecular Medicine. 141: 131-51. PMID 18453088 DOI: 10.1007/978-1-60327-148-6_8 |
0.087 |
|
| 2010 |
Gandhi KS, McKay FC, Cox M, Riveros C, Armstrong N, Heard RN, Vucic S, Williams DW, Stankovich J, Brown M, Danoy P, Stewart GJ, Broadley S, Moscato P, Lechner-Scott J, ... Scott RJ, et al. The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Human Molecular Genetics. 19: 2134-43. PMID 20190274 DOI: 10.1093/Hmg/Ddq090 |
0.086 |
|
| 2020 |
Feng YC, Liu XY, Teng L, Ji Q, Wu Y, Li JM, Gao W, Zhang YY, La T, Tabatabaee H, Yan XG, Jamaluddin MFB, Zhang D, Guo ST, Scott RJ, et al. c-Myc inactivation of p53 through the pan-cancer lncRNA MILIP drives cancer pathogenesis. Nature Communications. 11: 4980. PMID 33020477 DOI: 10.1038/s41467-020-18735-8 |
0.086 |
|
| 2021 |
Frampton D, Rampling T, Cross A, Bailey H, Heaney J, Byott M, Scott R, Sconza R, Price J, Margaritis M, Bergstrom M, Spyer MJ, Miralhes PB, Grant P, Kirk S, et al. Genomic characteristics and clinical effect of the emergent SARS-CoV-2 B.1.1.7 lineage in London, UK: a whole-genome sequencing and hospital-based cohort study. The Lancet. Infectious Diseases. PMID 33857406 DOI: 10.1016/S1473-3099(21)00170-5 |
0.086 |
|
| 2014 |
Milne E, Greenop KR, Fritschi L, Attia J, Bailey HD, Scott RJ, Ashton LJ, Smibert E, Armstrong BK. Childhood and parental diagnostic radiological procedures and risk of childhood brain tumors. Cancer Causes & Control : Ccc. 25: 375-83. PMID 24445596 DOI: 10.1007/s10552-014-0338-x |
0.086 |
|
| 2015 |
Hancock DB, Levy JL, Gaddis NC, Glasheen C, Saccone NL, Page GP, Hulse GK, Wildenauer D, Kelty EA, Schwab SG, Degenhardt L, Martin NG, Montgomery GW, Attia J, Holliday EG, ... ... Scott RJ, et al. Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1. Biological Psychiatry. PMID 25744370 DOI: 10.1016/J.Biopsych.2015.01.003 |
0.086 |
|
| 2016 |
Delforce SJ, Lumbers ER, Corbisier de Meautsart C, Wang Y, Proietto A, Otton G, Scurry J, Verrills NM, Scott RJ, Pringle KG. Expression of renin angiotensin system (RAS) components in endometrial cancer. Endocrine Connections. PMID 27956412 DOI: 10.1530/EC-16-0082 |
0.085 |
|
| 2018 |
Morten B, Scott R, Avery-Kiejda K. PO-107 A potential role for DELTA40P53 in the regulation of breast cancer stem cells Esmo Open. 3: A62. DOI: 10.1136/esmoopen-2018-EACR25.148 |
0.085 |
|
| 2014 |
McCarthy-Jones S, Green MJ, Scott RJ, Tooney PA, Cairns MJ, Wu JQ, Oldmeadow C, Carr V. Preliminary evidence of an interaction between the FOXP2 gene and childhood emotional abuse predicting likelihood of auditory verbal hallucinations in schizophrenia. Journal of Psychiatric Research. 50: 66-72. PMID 24360035 DOI: 10.1016/j.jpsychires.2013.11.012 |
0.084 |
|
| 2013 |
Graves M, Benton M, Lea R, Boyle M, Tajouri L, Macartney-Coxson D, Scott R, Lechner-Scott J. Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 20: 1033-1041. PMID 24336351 DOI: 10.1177/1352458513516529 |
0.084 |
|
| 2015 |
Lener MR, Scott RJ, Wiechowska-Kozłowska A, Serrano-Fernandez P, Baszuk P, Jaworska-Bieniek K, Sukiennicki G, Marciniak W, Muszynska M, Kładny J, Gromowski T, Kaczmarek K, Jakubowska A, Lubinski J. Serum Concentrations of Se and Cu in Patients Diagnosed with Pancreatic Cancer. Cancer Research and Treatment : Official Journal of Korean Cancer Association. PMID 26727715 DOI: 10.4143/crt.2015.282 |
0.084 |
|
| 2019 |
Zhang X, Morten BC, Scott RJ, Avery-Kiejda KA. A Simple Migration/Invasion Workflow Using an Automated Live-cell Imager. Journal of Visualized Experiments : Jove. PMID 30774141 DOI: 10.3791/59042 |
0.084 |
|
| 2015 |
Milne E, Greenop KR, Scott RJ, Haber M, Norris MD, Attia J, Jamieson SE, Miller M, Bower C, Bailey HD, Dawson S, McCowage GB, de Klerk NH, van Bockxmeer FM, Armstrong BK. Folate pathway gene polymorphisms, maternal folic acid use, and risk of childhood acute lymphoblastic leukemia. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 24: 48-56. PMID 25395472 DOI: 10.1158/1055-9965.EPI-14-0680 |
0.083 |
|
| 2014 |
Greenop KR, Peters S, Fritschi L, Glass DC, Ashton LJ, Bailey HD, Scott RJ, Daubenton J, de Klerk NH, Armstrong BK, Milne E. Exposure to household painting and floor treatments, and parental occupational paint exposure and risk of childhood brain tumors: results from an Australian case-control study. Cancer Causes & Control : Ccc. 25: 283-91. PMID 24337771 DOI: 10.1007/s10552-013-0330-x |
0.083 |
|
| 2017 |
Daneshi N, Holliday E, Hancock S, Schneider JJ, Scott RJ, Attia J, Milward EA. Prevalence of clinically actionable genotypes and medication exposure of older adults in the community. Pharmacogenomics and Personalized Medicine. 10: 17-27. PMID 28203101 DOI: 10.2147/PGPM.S123719 |
0.083 |
|
| 2013 |
Barzideh J, Scott RJ, Aitken RJ. Analysis of the global methylation status of human spermatozoa and its association with the tendency of these cells to enter apoptosis Andrologia. 45: 424-429. PMID 23121197 DOI: 10.1111/and.12033 |
0.083 |
|
| 2020 |
Lener MR, Reszka E, Marciniak W, Lesicka M, Baszuk P, Jabłońska E, Białkowska K, Muszyńska M, Pietrzak S, Derkacz R, Grodzki T, Wójcik J, Wojtyś M, Dębniak T, Cybulski C, ... ... Scott RJ, et al. Blood cadmium levels as a marker for early lung cancer detection. Journal of Trace Elements in Medicine and Biology : Organ of the Society For Minerals and Trace Elements (Gms). 64: 126682. PMID 33249371 DOI: 10.1016/j.jtemb.2020.126682 |
0.083 |
|
| 2015 |
O'Brien AR, Saunders NF, Guo Y, Buske FA, Scott RJ, Bauer DC. VariantSpark: population scale clustering of genotype information. Bmc Genomics. 16: 1052. PMID 26651996 DOI: 10.1186/s12864-015-2269-7 |
0.082 |
|
| 2010 |
Bowden NA, Ashton KA, Avery-Kiejda KA, Zhang XD, Hersey P, Scott RJ. Nucleotide excision repair gene expression after Cisplatin treatment in melanoma. Cancer Research. 70: 7918-26. PMID 20807809 DOI: 10.1158/0008-5472.CAN-10-0161 |
0.082 |
|
| 2009 |
Lubiński J, Sijmons RH, Scott RJ. Hereditary Cancer in Clinical Practice transfers to BioMed Central Hereditary Cancer in Clinical Practice. 7. DOI: 10.1186/1897-4287-7-1 |
0.082 |
|
| 2005 |
Blackwell CC, Moscovis SM, Gordon AE, Al Madani OM, Hall ST, Gleeson M, Scott RJ, Roberts-Thomson J, Weir DM, Busuttil A. Cytokine responses and sudden infant death syndrome: genetic, developmental, and environmental risk factors. Journal of Leukocyte Biology. 78: 1242-54. PMID 16204631 DOI: 10.1189/jlb.0505253 |
0.082 |
|
| 2016 |
McKenzie R, Scott RJ, Otton G, Scurry J. Early changes of endometrial neoplasia revealed by loss of mismatch repair gene protein expression in a patient diagnosed with Lynch syndrome. Pathology. 48: 78-80. PMID 27020214 DOI: 10.1016/j.pathol.2015.11.003 |
0.082 |
|
| 2016 |
Lubinski J, Scott RJ, Sijmons R, Theissen SM. Thank you to all our manuscript reviewers in 2015. Hereditary Cancer in Clinical Practice. 14: 7. PMID 26933466 DOI: 10.1186/s13053-016-0047-4 |
0.082 |
|
| 2001 |
Connor JR, Milward EA, Moalem S, Sampietro M, Boyer P, Percy ME, Vergani C, Scott RJ, Chorney M. Is hemochromatosis a risk factor for Alzheimer's disease? Journal of Alzheimer's Disease : Jad. 3: 471-477. PMID 12214033 DOI: 10.3233/Jad-2001-3506 |
0.082 |
|
| 2014 |
Greenop KR, Miller M, de Klerk NH, Scott RJ, Attia J, Ashton LJ, Dalla-Pozza L, Bower C, Armstrong BK, Milne E. Maternal dietary intake of folate and vitamins B6 and B12 during pregnancy and risk of childhood brain tumors. Nutrition and Cancer. 66: 800-9. PMID 24897174 DOI: 10.1080/01635581.2014.916326 |
0.082 |
|
| 2015 |
Rush A, Christiansen JH, Farrell JP, Goode SM, Scott RJ, Spring KJ, Byrne JA. Biobank classification in an Australian setting. Biopreservation and Biobanking. 13: 212-8. PMID 26035012 DOI: 10.1089/bio.2015.0007 |
0.082 |
|
| 2019 |
Schmidt AF, Holmes MV, Preiss D, Swerdlow DI, Denaxas S, Fatemifar G, Faraway R, Finan C, Valentine D, Fairhurst-Hunter Z, Hartwig FP, Horta BL, Hypponen E, Power C, Moldovan M, ... ... Scott RA, ... ... Scott R, et al. Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. Bmc Cardiovascular Disorders. 19: 240. PMID 31664920 DOI: 10.1186/S12872-019-1187-Z |
0.082 |
|
| 2018 |
Maltby VE, Lea RA, Graves MC, Sanders KA, Benton MC, Tajouri L, Scott RJ, Lechner-Scott J. Genome-wide DNA methylation changes in CD19 B cells from relapsing-remitting multiple sclerosis patients. Scientific Reports. 8: 17418. PMID 30479356 DOI: 10.1038/s41598-018-35603-0 |
0.081 |
|
| 2003 |
Lubiński W, Kurzawski G, Suchy J, Szych Z, Penkala K, Palacz O, Scott RJ, Lubiński J. Electro-oculographic and electroretinographic studies in HNPCC gene mutation carriers. Ophthalmic Research. 35: 281-94. PMID 12920342 DOI: 10.1159/000072149 |
0.081 |
|
| 2012 |
Holliday EG, Maguire JM, Evans TJ, Koblar SA, Jannes J, Sturm JW, Hankey GJ, Baker R, Golledge J, Parsons MW, Malik R, McEvoy M, Biros E, Lewis MD, Lincz LF, ... ... Scott RJ, et al. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nature Genetics. 44: 1147-51. PMID 22941190 DOI: 10.1038/Ng.2397 |
0.081 |
|
| 2016 |
Masson AL, Talseth-Palmer BA, Evans TJ, McElduff P, Spigelman AD, Hannan GN, Scott RJ. Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients Meta Gene. 7: 95-104. DOI: 10.1016/j.mgene.2015.12.005 |
0.081 |
|
| 2001 |
Macrae F, Ives P, Leggett B, Scott R, Burn J. CAPP2: A RANDOMIZED CONTROLLED TRIAL (RCT) OF ASPIRIN & RESISTANT STARCH IN HEREDITARY NON POLYPOSIS COLORECTAL CANCER Journal of Gastroenterology and Hepatology. 16: 14-14. DOI: 10.1111/j.1440-1746.2001.ca01-14.x |
0.08 |
|
| 2013 |
Williams FM, Carter AM, Hysi PG, Surdulescu G, Hodgkiss D, Soranzo N, Traylor M, Bevan S, Dichgans M, Rothwell PM, Sudlow C, Farrall M, Silander K, Kaunisto M, Wagner P, ... ... Scott RJ, et al. Ischemic stroke is associated with the ABO locus: the EuroCLOT study. Annals of Neurology. 73: 16-31. PMID 23381943 DOI: 10.1002/Ana.23838 |
0.08 |
|
| 2020 |
Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, ... ... Scott RJ, et al. The genetic architecture of the human cerebral cortex. Science (New York, N.Y.). 367. PMID 32193296 DOI: 10.1126/Science.Aay6690 |
0.08 |
|
| 2015 |
Cropley VL, Scarr E, Fornito A, Klauser P, Bousman CA, Scott R, Cairns MJ, Tooney PA, Pantelis C, Dean B. The effect of a muscarinic receptor 1 gene variant on grey matter volume in schizophrenia. Psychiatry Research. 234: 182-7. PMID 26481978 DOI: 10.1016/j.pscychresns.2015.09.004 |
0.08 |
|
| 2016 |
Okbay A, Baselmans BM, De Neve JE, Turley P, Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, Derringer J, Gratten J, Lee JJ, Liu JZ, de Vlaming R, Ahluwalia TS, ... ... Scott RJ, et al. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics. PMID 27089181 DOI: 10.1038/Ng.3552 |
0.08 |
|
| 2017 |
de Vries PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen MH, Wang JJ, Attia JR, Marioni RE, Steri M, Weng LC, Pool R, Grossmann V, ... ... Scott RJ, et al. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Plos One. 12: e0167742. PMID 28107422 DOI: 10.1371/Journal.Pone.0167742 |
0.079 |
|
| 2013 |
Schache M, Richardson AJ, Mitchell P, Wang JJ, Rochtchina E, Viswanathan AC, Wong TY, Saw SM, Topouzis F, Xie J, Sim X, Holliday EG, Attia J, Scott RJ, Baird PN. Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study cohort. Ophthalmology. 120: 292-7. PMID 23131718 DOI: 10.1016/J.Ophtha.2012.08.006 |
0.079 |
|
| 2012 |
Gardiner EJ, Cairns MJ, Liu B, Beveridge NJ, Carr V, Kelly B, Scott RJ, Tooney PA. Gene expression analysis reveals schizophrenia-associated dysregulation of immune pathways in peripheral blood mononuclear cells. Journal of Psychiatric Research. 47: 425-37. PMID 23218666 DOI: 10.1016/j.jpsychires.2012.11.007 |
0.079 |
|
| 2015 |
Riveros C, Vimieiro R, Holliday EG, Oldmeadow C, Wang JJ, Mitchell P, Attia J, Scott RJ, Moscato PA. Identification of genome-wide SNP-SNP and SNP-clinical Boolean interactions in age-related macular degeneration. Methods in Molecular Biology (Clifton, N.J.). 1253: 217-55. PMID 25403535 DOI: 10.1007/978-1-4939-2155-3_12 |
0.079 |
|
| 2018 |
Davies G, Lam M, Harris SE, Trampush JW, Luciano M, Hill WD, Hagenaars SP, Ritchie SJ, Marioni RE, Fawns-Ritchie C, Liewald DCM, Okely JA, Ahola-Olli AV, Barnes CLK, Bertram L, ... ... Scott RJ, et al. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications. 9: 2098. PMID 29844566 DOI: 10.1038/S41467-018-04362-X |
0.079 |
|
| 2007 |
Scott RJ, Gastony GJ, Weatherford JW, Nakazato T. Characterization of four members of the alpha-tubulin gene family in Ceratopteris richardii American Fern Journal. 97: 47-65. DOI: 10.1640/0002-8444(2007)97[47:Cofmot]2.0.Co;2 |
0.078 |
|
| 2014 |
Baines KJ, Simpson JL, Wood LG, Scott RJ, Fibbens NL, Powell H, Cowan DC, Taylor DR, Cowan JO, Gibson PG. Sputum gene expression signature of 6 biomarkers discriminates asthma inflammatory phenotypes. The Journal of Allergy and Clinical Immunology. 133: 997-1007. PMID 24582314 DOI: 10.1016/j.jaci.2013.12.1091 |
0.078 |
|
| 2014 |
Morten B, Scott R, Avery-Kiejda K. 134: The role of Delta-40p53 and p53 in Estrogen Receptor-a signalling pathways in breast cancer European Journal of Cancer. 50: S30. DOI: 10.1016/S0959-8049(14)50114-1 |
0.078 |
|
| 2013 |
Kumarasinghe N, Beveridge NJ, Gardiner E, Scott RJ, Yasawardene S, Perera A, Mendis J, Suriyakumara K, Schall U, Tooney PA. Gene expression profiling in treatment-naive schizophrenia patients identifies abnormalities in biological pathways involving AKT1 that are corrected by antipsychotic medication. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 16: 1483-503. PMID 23442539 DOI: 10.1017/S1461145713000035 |
0.078 |
|
| 2013 |
Green MJ, Cairns MJ, Wu J, Dragovic M, Jablensky A, Tooney PA, Scott RJ, Carr VJ. Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia. Molecular Psychiatry. 18: 774-80. PMID 22733126 DOI: 10.1038/Mp.2012.84 |
0.077 |
|
| 1997 |
Humar B, Müller H, Scott RJ. Elevated frequency of p53-independent apoptosis after irradiation increases levels of DNA breaks in ataxia telangiectasia lymphoblasts. International Journal of Radiation Biology. 72: 257-69. PMID 9298106 DOI: 10.1080/095530097143257 |
0.077 |
|
| 2015 |
Pan X, Bowman M, Scott RJ, Fitter J, Nicholson RC, Smith R, Zakar T. Methylation of the Corticotropin Releasing Hormone Gene Promoter in BeWo Cells: Relationship to Gene Activity. International Journal of Endocrinology. 2015: 861302. PMID 26457081 DOI: 10.1155/2015/861302 |
0.077 |
|
| 2010 |
Booth DR, Heard RN, Stewart GJ, Cox M, Scott RJ, Lechner-Scott J, Goris A, Dobosi R, Dubois B, Saarela J, Leppä V, Peltonen L, Pirttila T, Cournu-Rebeix I, et al. Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics. 42: 469-70; author reply. PMID 20502484 DOI: 10.1038/Ng0610-469 |
0.077 |
|
| 2013 |
Milne E, Greenop KR, Scott RJ, Ashton LJ, Cohn RJ, de Klerk NH, Armstrong BK. Parental smoking and risk of childhood brain tumors. International Journal of Cancer. Journal International Du Cancer. 133: 253-9. PMID 23280760 DOI: 10.1002/ijc.28004 |
0.076 |
|
| 2014 |
Atkins JR, Wu JQ, Tooney PA, Scott RJ, Carr VJ, Cairns MJ. Poster #S132 COPY NUMBER VARIANT ANALYSIS ON 401 CASES OF SCHIZOPHRENIA: A SEARCH FOR CAUSAL GENES FINDS DISRUPTION IN THE NEUROGENESIS REGULATOR JAGGED 2 Schizophrenia Research. 153: S136. DOI: 10.1016/S0920-9964(14)70411-6 |
0.076 |
|
| 2013 |
Milne E, Greenop KR, Scott RJ, de Klerk NH, Bower C, Ashton LJ, Heath JA, Armstrong BK. Parental alcohol consumption and risk of childhood acute lymphoblastic leukemia and brain tumors. Cancer Causes & Control : Ccc. 24: 391-402. PMID 23247637 DOI: 10.1007/s10552-012-0125-5 |
0.076 |
|
| 2019 |
Sukiennicki GM, Marciniak W, Muszyńska M, Baszuk P, Gupta S, Białkowska K, Jaworska-Bieniek K, Durda K, Lener M, Pietrzak S, Gromowski T, Prajzendanc K, Łukomska A, Waloszczyk P, Wójcik JZ, ... Scott R, et al. Iron levels, genes involved in iron metabolism and antioxidative processes and lung cancer incidence. Plos One. 14: e0208610. PMID 30640897 DOI: 10.1371/journal.pone.0208610 |
0.076 |
|
| 2009 |
Milne E, Royle JA, de Klerk NH, Blair E, Bailey H, Cole C, Attia J, Scott RJ, Armstrong BK. Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study. American Journal of Epidemiology. 170: 221-8. PMID 19478236 DOI: 10.1093/aje/kwp117 |
0.076 |
|
| 2019 |
Geaghan MP, Atkins JR, Brichta AM, Tooney PA, Scott RJ, Carr VJ, Cairns MJ. Alteration of miRNA-mRNA interactions in lymphocytes of individuals with schizophrenia. Journal of Psychiatric Research. 112: 89-98. PMID 30870714 DOI: 10.1016/J.Jpsychires.2019.02.023 |
0.075 |
|
| 2017 |
Ko YA, Jamaluddin M, Adebayo M, Bajwa P, Scott R, Dharmarajan A, Nahar P, Tanwar PS. Extracellular Matrix (ECM) Activates β-catenin Signaling in Uterine Fibroids. Reproduction (Cambridge, England). PMID 29066531 DOI: 10.1530/REP-17-0339 |
0.075 |
|
| 2008 |
Scott RJ. Modifier genes and HNPCC: variable phenotypic expression in HNPCC and the search for modifier genes. European Journal of Human Genetics : Ejhg. 16: 531-2. PMID 18301442 DOI: 10.1038/ejhg.2008.46 |
0.075 |
|
| 2013 |
Bowden NA, Ashton KA, Vilain RE, Avery-Kiejda KA, Davey RJ, Murray HC, Budden T, Braye SG, Zhang XD, Hersey P, Scott RJ. Regulators of Global Genome Repair Do Not Respond to DNA Damaging Therapy but Correlate with Survival in Melanoma Plos One. 8. PMID 23940574 DOI: 10.1371/journal.pone.0070424 |
0.074 |
|
| 2012 |
Johnstone D, Graham RM, Trinder D, Delima RD, Riveros C, Olynyk JK, Scott RJ, Moscato P, Milward EA. Brain transcriptome perturbations in the Hfe(-/-) mouse model of genetic iron loading. Brain Research. 1448: 144-52. PMID 22370144 DOI: 10.1016/j.brainres.2012.02.006 |
0.074 |
|
| 2014 |
Holliday EG, Attia J, Hancock S, Koloski N, McEvoy M, Peel R, D'Amato M, Agréus L, Nyhlin H, Andreasson A, Almazar AE, Saito YA, Scott RJ, Talley NJ. Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome. The American Journal of Gastroenterology. 109: 770-2. PMID 24797007 DOI: 10.1038/ajg.2014.56 |
0.074 |
|
| 2012 |
Vilain RE, Braye SG, Scott RJ. BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma Pathology. 44: S99. DOI: 10.1016/S0031-3025(16)32887-2 |
0.074 |
|
| 2015 |
Pundavela J, Roselli S, Faulkner S, Attia J, Scott RJ, Thorne RF, Forbes JF, Bradshaw RA, Walker MM, Jobling P, Hondermarck H. Nerve fibers infiltrate the tumor microenvironment and are associated with nerve growth factor production and lymph node invasion in breast cancer. Molecular Oncology. PMID 26009480 DOI: 10.1016/J.Molonc.2015.05.001 |
0.073 |
|
| 2014 |
Greenop KR, Hinwood AL, Fritschi L, Scott RJ, Attia J, Ashton LJ, Heath JA, Armstrong BK, Milne E. Vehicle refuelling, use of domestic wood heaters and the risk of childhood brain tumours: Results from an Australian case-control study. Pediatric Blood & Cancer. PMID 25283072 DOI: 10.1002/pbc.25268 |
0.073 |
|
| 2012 |
Wu JQ, Wang X, Beveridge NJ, Tooney PA, Scott RJ, Carr VJ, Cairns MJ. Transcriptome sequencing revealed significant alteration of cortical promoter usage and splicing in schizophrenia. Plos One. 7: e36351. PMID 22558445 DOI: 10.1371/journal.pone.0036351 |
0.073 |
|
| 2015 |
Scott R, Dooley S, Lewis W, Meldrum C, Pockney P, Draganic B, Smith S, Jones F, Hewitt C, Phillimore H, Lucas A, Shi E, Namdarian K, Chan T, Acosta D, et al. P-273 Concordance of RAS mutation status in CRC patients by comparison of results from circulating tumour DNA and tissue-based testing Annals of Oncology. 26: iv80. DOI: 10.1093/ANNONC/MDV233.270 |
0.073 |
|
| 2005 |
Weidenhofer J, Bowden NA, Scott RJ, Tooney PA. Altered gene expression in the amygdala in schizophrenia: up-regulation of genes located in the cytomatrix active zone. Molecular and Cellular Neurosciences. 31: 243-50. PMID 16236523 DOI: 10.1016/j.mcn.2005.09.013 |
0.073 |
|
| 2013 |
Titmarsh CJ, Moscovis SM, Hall S, Tzanakaki G, Kesanopoulos K, Xirogianni A, Scott RJ, Blackwell CC. Comparison of cytokine gene polymorphisms among Greek patients with invasive meningococcal disease or viral meningitis. Journal of Medical Microbiology. 62: 694-700. PMID 23378564 DOI: 10.1099/jmm.0.058073-0 |
0.072 |
|
| 2014 |
Dymerska D, Kurzawski G, Suchy J, Roomere H, Toome K, Metspalu A, Janavičius R, Elsakov P, Irmejs A, Berzina D, Miklaševičs E, Gardovskis J, Rebane E, Kelve M, Kładny J, ... ... Scott RJ, et al. Lynch syndrome mutations shared by the Baltic States and Poland Clinical Genetics. 86: 190-193. PMID 24032978 DOI: 10.1111/cge.12251 |
0.072 |
|
| 2019 |
Söderholm M, Pedersen A, Lorentzen E, Stanne TM, Bevan S, Olsson M, Cole JW, Fernandez-Cadenas I, Hankey GJ, Jimenez-Conde J, Jood K, Lee JM, Lemmens R, Levi C, Mitchell BD, ... ... Scott R, et al. Genome-wide association meta-analysis of functional outcome after ischemic stroke. Neurology. PMID 30796134 DOI: 10.1212/Wnl.0000000000007138 |
0.072 |
|
| 2022 |
Mouchahoir T, Schiel JE, Rogers R, Heckert A, Place BJ, Ammerman A, Li X, Robinson T, Schmidt B, Chumsae CM, Li X, Manuilov AV, Yan B, Staples GO, Ren D, ... ... Scott R, et al. Attribute Analytics Performance Metrics from the MAM Consortium Interlaboratory Study. Journal of the American Society For Mass Spectrometry. PMID 36018776 DOI: 10.1021/jasms.2c00129 |
0.072 |
|
| 2017 |
Gorski M, Most PJV, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, ... ... Scott RJ, et al. Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific Reports. 7: 46835. PMID 28548086 DOI: 10.1038/Srep46835 |
0.072 |
|
| 2022 |
Grey ADR, Scott R, Shah B, Acher P, Liyanage S, Pavlou M, Omar R, Chinegwundoh F, Patki P, Shah TT, Hamid S, Ghei M, Gilbert K, Campbell D, Brew-Graves C, et al. Multiparametric ultrasound versus multiparametric MRI to diagnose prostate cancer (CADMUS): a prospective, multicentre, paired-cohort, confirmatory study. The Lancet. Oncology. 23: 428-438. PMID 35240084 DOI: 10.1016/S1470-2045(22)00016-X |
0.072 |
|
| 2015 |
Sapkota Y, Low SK, Attia J, Gordon SD, Henders AK, Holliday EG, MacGregor S, Martin NG, McEvoy M, Morris AP, Takahashi A, Scott RJ, Kubo M, Zondervan KT, Montgomery GW, et al. Association between endometriosis and the interleukin 1A (IL1A) locus. Human Reproduction (Oxford, England). 30: 239-48. PMID 25336714 DOI: 10.1093/Humrep/Deu267 |
0.072 |
|
| 2008 |
Dudding T, Heron J, Thakkinstian A, Nurk E, Golding J, Pembrey M, Ring SM, Attia J, Scott RJ. Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis. Journal of Thrombosis and Haemostasis : Jth. 6: 1869-75. PMID 18752569 DOI: 10.1111/j.1538-7836.2008.03134.x |
0.071 |
|
| 2006 |
Scott R, Moscovis S, Hall S, Gleeson M, Roberts-Thomson J, Blackwell C. The influence of infection on cytokine gene polymorphisms in evolution Before Farming. 2006: 1-7. DOI: 10.3828/BFARM.2006.2.1 |
0.071 |
|
| 2008 |
Weidenhofer J, Scott RJ, Tooney PA. Investigation of the expression of genes affecting cytomatrix active zone function in the amygdala in schizophrenia: effects of antipsychotic drugs. Journal of Psychiatric Research. 43: 282-90. PMID 18490030 DOI: 10.1016/j.jpsychires.2008.04.001 |
0.071 |
|
| 2015 |
Scott RJ, Wong-Brown M, McPhillips M, Dooley S, Spigelman A, Gleeson M, Meldrum C. The curious case of a woman with two BRCA1 mutations in trans Hereditary Cancer in Clinical Practice. 13. DOI: 10.1186/1897-4287-13-S2-A11 |
0.07 |
|
| 2014 |
Green MJ, Chia TY, Cairns MJ, Wu J, Tooney PA, Scott RJ, Carr VJ. Catechol-O-methyltransferase (COMT) genotype moderates the effects of childhood trauma on cognition and symptoms in schizophrenia. Journal of Psychiatric Research. 49: 43-50. PMID 24252819 DOI: 10.1016/j.jpsychires.2013.10.018 |
0.07 |
|
| 2012 |
Orsi L, Rudant J, Bonaventure A, Goujon-Bellec S, Corda E, Evans TJ, Petit A, Bertrand Y, Nelken B, Robert A, Michel G, Sirvent N, Chastagner P, Ducassou S, Rialland X, ... ... Scott RJ, et al. Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE). Leukemia. 26: 2561-4. PMID 22660188 DOI: 10.1038/leu.2012.148 |
0.07 |
|
| 2019 |
Gill D, James NE, Monori G, Lorentzen E, Fernandez-Cadenas I, Lemmens R, Thijs V, Rost NS, Scott R, Hankey GJ, Lindgren A, Jern C, Maguire JM. Genetically Determined Risk of Depression and Functional Outcome After Ischemic Stroke. Stroke. STROKEAHA119026089. PMID 31238828 DOI: 10.1161/STROKEAHA.119.026089 |
0.07 |
|
| 2007 |
Attia J, Thakkinstian A, Wang Y, Lincz L, Parsons M, Sturm J, McGettigan P, Scott R, Meldrum C, Levi C. The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis. Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association. 16: 173-9. PMID 17689414 DOI: 10.1016/j.jstrokecerebrovasdis.2007.03.002 |
0.07 |
|
| 1991 |
Scott RJ, Hickok LG. Inheritance and characterization of a dark-germinating, light-inhibited mutant in the fern Ceratopteris richardii Canadian Journal of Botany. 69: 2616-2619. DOI: 10.1139/B91-326 |
0.07 |
|
| 2015 |
Bergon A, Belzeaux R, Comte M, Pelletier F, Hervé M, Gardiner EJ, Beveridge NJ, Liu B, Carr V, Scott RJ, Kelly B, Cairns MJ, Kumarasinghe N, Schall U, Blin O, et al. CX3CR1 is dysregulated in blood and brain from schizophrenia patients. Schizophrenia Research. 168: 434-43. PMID 26285829 DOI: 10.1016/J.Schres.2015.08.010 |
0.07 |
|
| 2016 |
Tan AG, Kifley A, Mitchell P, Rochtchina E, Flood VM, Cumming RG, Jun G, Holliday EG, Scott RJ, Teo YY, Klein BE, Cheng CY, Iyengar SK, Wang JJ. Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract. Jama Ophthalmology. PMID 26986182 DOI: 10.1001/Jamaophthalmol.2016.0167 |
0.07 |
|
| 2015 |
Li Y, Scott RJ, Doughty J, Grant M, Qi B. Protein S-acyltransferase 14: a specific role for palmitoylation in leaf senescence in Arabidopsis. Plant Physiology. PMID 26537563 DOI: 10.1104/pp.15.00448 |
0.069 |
|
| 2020 |
Malińska K, Deptuła J, Rogoża-Janiszewska E, Górski B, Scott R, Rudnicka H, Kashyap A, Domagała P, Hybiak J, Masojć B, Cybulski C, Kram A, Boer M, Kiedrowicz M, Lubiński J, et al. Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population. European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (Ecp). PMID 32976206 DOI: 10.1097/CEJ.0000000000000633 |
0.069 |
|
| 2015 |
Ahmed HU, Dickinson L, Charman S, Weir S, McCartan N, Hindley RG, Freeman A, Kirkham AP, Sahu M, Scott R, Allen C, Van der Meulen J, Emberton M. Focal Ablation Targeted to the Index Lesion in Multifocal Localised Prostate Cancer: a Prospective Development Study. European Urology. PMID 25682339 DOI: 10.1016/j.eururo.2015.01.030 |
0.068 |
|
| 2017 |
Kelly S, Jahanshad N, Zalesky A, Kochunov P, Agartz I, Alloza C, Andreassen OA, Arango C, Banaj N, Bouix S, Bousman CA, Brouwer RM, Bruggemann J, Bustillo J, Cahn W, ... ... Scott RJ, et al. Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group. Molecular Psychiatry. PMID 29038599 DOI: 10.1038/Mp.2017.170 |
0.068 |
|
| 2015 |
Maltby VE, Graves MC, Lea RA, Benton MC, Sanders KA, Tajouri L, Scott RJ, Lechner-Scott J. Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients. Clinical Epigenetics. 7: 118. PMID 26550040 DOI: 10.1186/s13148-015-0152-7 |
0.068 |
|
| 2015 |
Moscovis SM, Gordon AE, Al Madani OM, Gleeson M, Scott RJ, Hall ST, Burns C, Blackwell C. Genetic and Environmental Factors Affecting TNF-α Responses in Relation to Sudden Infant Death Syndrome. Frontiers in Immunology. 6: 374. PMID 26284064 DOI: 10.3389/fimmu.2015.00374 |
0.067 |
|
| 2015 |
Holliday EG, Traylor M, Malik R, Bevan S, Falcone G, Hopewell JC, Cheng YC, Cotlarciuc I, Bis JC, Boerwinkle E, Boncoraglio GB, Clarke R, Cole JW, Fornage M, Furie KL, ... ... Scott RJ, et al. Genetic overlap between diagnostic subtypes of ischemic stroke. Stroke; a Journal of Cerebral Circulation. 46: 615-9. PMID 25613305 DOI: 10.1161/Strokeaha.114.007930 |
0.067 |
|
| 2019 |
Scott R, Hawarden A, Russell B, Edmondson RJ. Decision-Making in Gynaecological Oncology Multidisciplinary Team Meetings: A Cross-Sectional, Observational Study of Ovarian Cancer Cases. Oncology Research and Treatment. 1-6. PMID 31743932 DOI: 10.1159/000504260 |
0.067 |
|
| 2016 |
Schmiegel W, Scott RJ, Dooley S, Lewis W, Meldrum CJ, Pockney P, Draganic B, Smith S, Hewitt C, Philimore H, Lucas A, Shi E, Namdarian K, Chan T, Acosta D, et al. Blood-based detection of RAS mutations to guide anti-EGFR therapy in colorectal cancer patients: concordance of results from circulating tumor DNA and tissue-based RAS testing. Molecular Oncology. PMID 28106345 DOI: 10.1002/1878-0261.12023 |
0.066 |
|
| 2017 |
Pan X, Bowman M, Scott RJ, Fitter J, Smith R, Zakar T. Promoter Methylation Pattern Controls Corticotropin Releasing Hormone Gene Activity in Human Trophoblasts. Plos One. 12: e0170671. PMID 28151936 DOI: 10.1371/journal.pone.0170671 |
0.066 |
|
| 2011 |
Cox MB, Ban M, Bowden NA, Baker A, Scott RJ, Lechner-Scott J. Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 18: 16-22. PMID 21816760 DOI: 10.1177/1352458511415562 |
0.066 |
|
| 2016 |
Morten BC, Scott RJ, Avery-Kiejda KA. Comparison of the QuantiGene 2.0 Assay and Real-Time RT-PCR in the Detection of p53 Isoform mRNA Expression in Formalin-Fixed Paraffin-Embedded Tissues- A Preliminary Study. Plos One. 11: e0165930. PMID 27832134 DOI: 10.1371/journal.pone.0165930 |
0.066 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Scott RA, ... ... Scott RJ, et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30224653 DOI: 10.1038/S41588-018-0205-X |
0.065 |
|
| 2012 |
Johnstone DM, Graham RM, Trinder D, Riveros C, Olynyk JK, Scott RJ, Moscato P, Milward EA. Changes in brain transcripts related to Alzheimer's disease in a model of HFE hemochromatosis are not consistent with increased Alzheimer's disease risk. Journal of Alzheimer's Disease : Jad. 30: 791-803. PMID 22466002 DOI: 10.3233/JAD-2012-112183 |
0.065 |
|
| 2012 |
Smith CJ, Bensing S, Burns C, Robinson PJ, Kasperlik-Zaluska AA, Scott RJ, Kämpe O, Crock PA. Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis: immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays. European Journal of Endocrinology / European Federation of Endocrine Societies. 166: 391-8. PMID 22193973 DOI: 10.1530/EJE-11-1015 |
0.065 |
|
| 1993 |
Rey JP, Scott R, Müller H. Induction and removal of interstrand crosslinks in the ribosomal RNA genes of lymphoblastoid cell lines from patients with Fanconi anemia. Mutation Research. 289: 171-80. PMID 7690885 DOI: 10.1016/0027-5107(93)90067-P |
0.064 |
|
| 2017 |
Naudin C, Smith B, Bond DR, Dun MD, Scott RJ, Ashman LK, Weidenhofer J, Roselli S. Characterization of the early molecular changes in the glomeruli of Cd151 (-/-) mice highlights induction of mindin and MMP-10. Scientific Reports. 7: 15987. PMID 29167507 DOI: 10.1038/s41598-017-15993-3 |
0.064 |
|
| 2012 |
Ahmed HU, Hindley RG, Dickinson L, Freeman A, Kirkham AP, Sahu M, Scott R, Allen C, Van der Meulen J, Emberton M. Focal therapy for localised unifocal and multifocal prostate cancer: a prospective development study. The Lancet. Oncology. 13: 622-32. PMID 22512844 DOI: 10.1016/S1470-2045(12)70121-3 |
0.064 |
|
| 2015 |
Moscovis SM, Gordon AE, Al Madani OM, Gleeson M, Scott RJ, Hall ST, Burns C, Blackwell C. Virus Infections and Sudden Death in Infancy: The Role of Interferon-γ. Frontiers in Immunology. 6: 107. PMID 25814991 DOI: 10.3389/fimmu.2015.00107 |
0.063 |
|
| 2016 |
Wong-Brown M, McPhillips M, Gleeson M, Spigelman AD, Meldrum CJ, Dooley S, Scott RJ. When is a mutation not a mutation: The case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans Hereditary Cancer in Clinical Practice. 14. DOI: 10.1186/s13053-015-0045-y |
0.063 |
|
| 2018 |
Groen K, Lea RA, Maltby VE, Scott RJ, Lechner-Scott J. Letter to the editor: blood processing and sample storage have negligible effects on methylation. Clinical Epigenetics. 10: 22. PMID 29456766 DOI: 10.1186/s13148-018-0455-6 |
0.063 |
|
| 2015 |
Abdullah N, Abdul Murad NA, Attia J, Oldmeadow C, Mohd Haniff EA, Syafruddin SE, Abd Jalal N, Ismail N, Ishak M, Jamal R, Scott RJ, Holliday EG. Characterizing the genetic risk for Type 2 diabetes in a Malaysian multi-ethnic cohort. Diabetic Medicine : a Journal of the British Diabetic Association. PMID 25711284 DOI: 10.1111/dme.12735 |
0.063 |
|
| 2020 |
Groen K, Maltby VE, Scott RJ, Tajouri L, Lechner-Scott J. Erythrocyte microRNAs show biomarker potential and implicate multiple sclerosis susceptibility genes. Clinical and Translational Medicine. 10: 74-90. PMID 32508012 DOI: 10.1002/ctm2.22 |
0.063 |
|
| 2018 |
Groen K, Maltby VE, Lea RA, Sanders KA, Fink JL, Scott RJ, Tajouri L, Lechner-Scott J. Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis. Bmc Medical Genomics. 11: 48. PMID 29783973 DOI: 10.1186/s12920-018-0365-7 |
0.062 |
|
| 2019 |
Wilson RP, Börger L, Holton MD, Scantlebury DM, Gómez-Laich A, Quintana F, Rosell F, Graf PM, Williams H, Gunner R, Hopkins L, Marks N, Geraldi NR, Duarte CM, Scott R, et al. Estimates for energy expenditure in free-living animals using acceleration proxies; a reappraisal. The Journal of Animal Ecology. PMID 31173339 DOI: 10.1111/1365-2656.13040 |
0.062 |
|
| 2011 |
Baines KJ, Simpson JL, Wood LG, Scott RJ, Gibson PG. Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples Journal of Allergy and Clinical Immunology. 127. PMID 21211650 DOI: 10.1016/j.jaci.2010.10.024 |
0.062 |
|
| 2010 |
Holliday EG, Scott RJ, Attia J. Evidence-based medicine in the era of biomarkers: teaching a new dog old tricks? Clinical Pharmacology and Therapeutics. 88: 740-2. PMID 21081940 DOI: 10.1038/clpt.2010.214 |
0.062 |
|
| 2007 |
Mhaidat NM, Zhang XD, Allen J, Avery-Kiejda KA, Scott RJ, Hersey P. Temozolomide induces senescence but not apoptosis in human melanoma cells. British Journal of Cancer. 97: 1225-33. PMID 17968428 DOI: 10.1038/sj.bjc.6604017 |
0.062 |
|
| 1988 |
WARNE TR, HICKOK LG, SCOTT RJ. Characterization and genetic analysis of antheridiogen-insensitive mutants in the fern Ceratopteris Botanical Journal of the Linnean Society. 96: 371-379. DOI: 10.1111/J.1095-8339.1988.TB00692.X |
0.062 |
|
| 2018 |
Kennedy DW, White NM, Benton MC, Fox A, Scott RJ, Griffiths LR, Mengersen K, Lea RA. Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA. Plos One. 13: e0208915. PMID 30571772 DOI: 10.1371/journal.pone.0208915 |
0.061 |
|
| 2017 |
Grey A, Scott R, Charman S, van der Meulen J, Frinking P, Acher P, Liyanage S, Madaan S, Constantinescu G, Shah B, Graves CB, Freeman A, Jameson C, Ramachandran N, Emberton M, et al. The CADMUS trial - Multi-parametric ultrasound targeted biopsies compared to multi-parametric MRI targeted biopsies in the diagnosis of clinically significant prostate cancer. Contemporary Clinical Trials. PMID 29108869 DOI: 10.1016/j.cct.2017.10.011 |
0.061 |
|
| 2004 |
Moscovis SM, Gordon AE, Hall ST, Gleeson M, Scott RJ, Roberts-Thomsom J, Weir DM, Busuttil A, Blackwell CC. Interleukin 1-beta responses to bacterial toxins and sudden infant death syndrome. Fems Immunology and Medical Microbiology. 42: 139-45. PMID 15325407 DOI: 10.1016/j.femsim.2004.06.005 |
0.061 |
|
| 2012 |
Milne E, Greenop KR, Bower C, Miller M, van Bockxmeer FM, Scott RJ, de Klerk NH, Ashton LJ, Gottardo NG, Armstrong BK. Maternal use of folic acid and other supplements and risk of childhood brain tumors. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 1933-41. PMID 22941336 DOI: 10.1158/1055-9965.EPI-12-0803 |
0.061 |
|
| 2010 |
Milne E, Royle JA, Miller M, Bower C, de Klerk NH, Bailey HD, van Bockxmeer F, Attia J, Scott RJ, Norris MD, Haber M, Thompson JR, Fritschi L, Marshall GM, Armstrong BK. Maternal folate and other vitamin supplementation during pregnancy and risk of acute lymphoblastic leukemia in the offspring. International Journal of Cancer. Journal International Du Cancer. 126: 2690-9. PMID 19839053 DOI: 10.1002/ijc.24969 |
0.061 |
|
| 2004 |
Moscovis SM, Gordon AE, Al Madani OM, Gleeson M, Scott RJ, Roberts-Thomson J, Hall ST, Weir DM, Busuttil A, Blackwell CC. Interleukin-10 and sudden infant death syndrome. Fems Immunology and Medical Microbiology. 42: 130-8. PMID 15325406 DOI: 10.1016/j.femsim.2004.06.020 |
0.06 |
|
| 2008 |
Talseth-Palmer BA, Bowden NA, Hill A, Meldrum C, Scott RJ. Whole genome amplification and its impact on CGH array profiles. Bmc Research Notes. 1: 56. PMID 18710509 DOI: 10.1186/1756-0500-1-56 |
0.06 |
|
| 2017 |
Cox AJ, Zhang P, Evans TJ, Scott RJ, Cripps AW, West NP. Gene expression profiles in whole blood and associations with metabolic dysregulation in obesity. Obesity Research & Clinical Practice. PMID 28755841 DOI: 10.1016/j.orcp.2017.07.001 |
0.06 |
|
| 2020 |
Gunner RM, Wilson RP, Holton MD, Scott R, Hopkins P, Duarte CM. A new direction for differentiating animal activity based on measuring angular velocity about the yaw axis. Ecology and Evolution. 10: 7872-7886. PMID 32760571 DOI: 10.1002/Ece3.6515 |
0.059 |
|
| 2012 |
Milne E, Greenop KR, Scott RJ, Bailey HD, Attia J, Dalla-Pozza L, de Klerk NH, Armstrong BK. Parental prenatal smoking and risk of childhood acute lymphoblastic leukemia. American Journal of Epidemiology. 175: 43-53. PMID 22143821 DOI: 10.1093/aje/kwr275 |
0.059 |
|
| 2021 |
Reay WR, El Shair SI, Geaghan MP, Riveros C, Holliday EG, McEvoy MA, Hancock S, Peel R, Scott RJ, Attia JR, Cairns MJ. Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function. Elife. 10. PMID 33720009 DOI: 10.7554/eLife.63115 |
0.059 |
|
| 2014 |
Thomas S, Fazakarley L, Thomas PW, Brenton S, Collyer S, Perring S, Scott R, Galvin K, Hillier C. Testing the feasibility and acceptability of using the Nintendo Wii in the home to increase activity levels, vitality and well-being in people with multiple sclerosis (Mii-vitaliSe): protocol for a pilot randomised controlled study. Bmj Open. 4: e005172. PMID 24812193 DOI: 10.1136/bmjopen-2014-005172 |
0.059 |
|
| 2012 |
Bailey HD, Miller M, Langridge A, de Klerk NH, van Bockxmeer FM, Attia J, Scott RJ, Armstrong BK, Milne E. Maternal dietary intake of folate and vitamins B6 and B12 during pregnancy and the risk of childhood acute lymphoblastic leukemia. Nutrition and Cancer. 64: 1122-30. PMID 22966944 DOI: 10.1080/01635581.2012.707278 |
0.058 |
|
| 2011 |
Talseth-Palmer BA, Scott RJ, Vasen HF, Wijnen JT. 8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome. European Journal of Human Genetics : Ejhg. 20: 487-8; author reply . PMID 22166948 DOI: 10.1038/ejhg.2011.232 |
0.058 |
|
| 2008 |
Avery-Kiejda KA, Zhang XD, Adams LJ, Scott RJ, Vojtesek B, Lane DP, Hersey P. Small molecular weight variants of p53 are expressed in human melanoma cells and are induced by the DNA-damaging agent cisplatin. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 14: 1659-68. PMID 18310316 DOI: 10.1158/1078-0432.Ccr-07-1422 |
0.058 |
|
| 2015 |
Lener M, Wiechowska-Kozlowska A, Scott RJ, Muszynska M, Kladny J, Waloszczyk P, Rutkowska A, Sukiennicki G, Gromowski T, Jaworska-Bieniek K, van de Wetering T, Kaczmarek K, Jakubowska A, Lubinski J. Serum concentrations of Cu, Se, Fe and Zn in patients diagnosed with pancreatic cancer Hereditary Cancer in Clinical Practice. 13. DOI: 10.1186/1897-4287-13-S1-A14 |
0.058 |
|
| 2017 |
Cuenco J, Minnion J, Tan T, Scott R, Germain N, Ling Y, Chen R, Ghatei M, Bloom S. Degradation paradigm of the Gut Hormone, Pancreatic Polypeptide, by hepatic and renal peptidases. Endocrinology. PMID 28323997 DOI: 10.1210/en.2016-1827 |
0.058 |
|
| 2012 |
Gamble C, McIntosh K, Scott R, Ho KH, Plevin R, Paul A. Inhibitory kappa B Kinases as targets for pharmacological regulation. British Journal of Pharmacology. 165: 802-19. PMID 21797846 DOI: 10.1111/j.1476-5381.2011.01608.x |
0.058 |
|
| 2017 |
Thomas S, Fazakarley L, Thomas PW, Collyer S, Brenton S, Perring S, Scott R, Thomas F, Thomas C, Jones K, Hickson J, Hillier C. Mii-vitaliSe: a pilot randomised controlled trial of a home gaming system (Nintendo Wii) to increase activity levels, vitality and well-being in people with multiple sclerosis. Bmj Open. 7: e016966. PMID 28954791 DOI: 10.1136/bmjopen-2017-016966 |
0.058 |
|
| 2013 |
Greenop KR, Peters S, Bailey HD, Fritschi L, Attia J, Scott RJ, Glass DC, de Klerk NH, Alvaro F, Armstrong BK, Milne E. Exposure to pesticides and the risk of childhood brain tumors. Cancer Causes & Control : Ccc. 24: 1269-78. PMID 23558445 DOI: 10.1007/s10552-013-0205-1 |
0.058 |
|
| 2015 |
Bowden NA, Beveridge NJ, Ashton KA, Baines KJ, Scott RJ. Understanding xeroderma pigmentosum complementation groups using gene expression profiling after UV-light exposure International Journal of Molecular Sciences. 16: 15985-15996. DOI: 10.3390/ijms160715985 |
0.058 |
|
| 2016 |
Tharakan G, Scott R, Szepietowski O, Miras AD, Blakemore AI, Purkayastha S, Ahmed A, Chahal H, Tan T. Limitations of the DiaRem Score in Predicting Remission of Diabetes Following Roux-En-Y Gastric Bypass (RYGB) in an ethnically Diverse Population from a Single Institution in the UK. Obesity Surgery. PMID 27613192 DOI: 10.1007/s11695-016-2368-9 |
0.057 |
|
| 2011 |
Maguire J, Thakkinstian A, Levi C, Lincz L, Bisset L, Sturm J, Scott R, Whyte S, Attia J. Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: a novel finding. Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association. 20: 134-44. PMID 20472470 DOI: 10.1016/j.jstrokecerebrovasdis.2009.10.011 |
0.056 |
|
| 2013 |
Jensen RA, Sim X, Li X, Cotch MF, Ikram MK, Holliday EG, Eiriksdottir G, Harris TB, Jonasson F, Klein BE, Launer LJ, Smith AV, Boerwinkle E, Cheung N, Hewitt AW, ... ... Scott R, et al. Genome-wide association study of retinopathy in individuals without diabetes. Plos One. 8: e54232. PMID 23393555 DOI: 10.1371/Journal.Pone.0054232 |
0.056 |
|
| 2010 |
Attia J, Thakkinstian A, McElduff P, Milne E, Dawson S, Scott RJ, Klerk Nd, Armstrong B, Thompson J. Detecting genotyping error using measures of degree of Hardy-Weinberg disequilibrium. Statistical Applications in Genetics and Molecular Biology. 9: Article 5. PMID 20196755 DOI: 10.2202/1544-6115.1463 |
0.056 |
|
| 2003 |
Scott RJ. Familial Adenomatous Polyposis (FAP) and Other Polyposis Syndromes Hereditary Cancer in Clinical Practice. 1: 19. DOI: 10.1186/1897-4287-1-1-19 |
0.056 |
|
| 2014 |
Smith CJ, Bensing S, Maltby VE, Zhang M, Scott RJ, Smith R, Kämpe O, Hökfelt T, Crock PA. Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysitis. Pituitary. 17: 22-9. PMID 23329361 DOI: 10.1007/s11102-013-0461-9 |
0.056 |
|
| 2010 |
Loughland C, Draganic D, McCabe K, Richards J, Nasir A, Allen J, Catts S, Jablensky A, Henskens F, Michie P, Mowry B, Pantelis C, Schall U, Scott R, Tooney P, et al. Australian Schizophrenia Research Bank: a database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia. The Australian and New Zealand Journal of Psychiatry. 44: 1029-35. PMID 21034186 DOI: 10.3109/00048674.2010.501758 |
0.056 |
|
| 2012 |
Monzón-Argüello C, Dell'Amico F, Morinière P, Marco A, López-Jurado LF, Hays GC, Scott R, Marsh R, Lee PL. Lost at sea: genetic, oceanographic and meteorological evidence for storm-forced dispersal. Journal of the Royal Society, Interface / the Royal Society. 9: 1725-32. PMID 22319111 DOI: 10.1098/rsif.2011.0788 |
0.056 |
|
| 2014 |
Holliday EG, Traylor M, Malik R, Bevan S, Maguire J, Koblar SA, Sturm J, Hankey GJ, Oldmeadow C, McEvoy M, Sudlow C, Rothwell PM, Coresh J, Hamet P, Tremblay J, ... ... Scott RJ, et al. Polygenic overlap between kidney function and large artery atherosclerotic stroke. Stroke; a Journal of Cerebral Circulation. 45: 3508-13. PMID 25352485 DOI: 10.1161/Strokeaha.114.006609 |
0.055 |
|
| 1997 |
Maier D, Comparone D, Taylor E, Zhang Z, Gratzl O, Van Meir EG, Scott RJ, Merlo A. New deletion in low-grade oligodendroglioma at the glioblastoma suppressor locus on chromosome 10q25-26. Oncogene. 15: 997-1000. PMID 9285695 DOI: 10.1038/sj.onc.1201209 |
0.055 |
|
| 2017 |
Maguire JM, Bevan S, Stanne TM, Lorenzen E, Fernandez-Cadenas I, Hankey GJ, Jimenez-Conde J, Jood K, Lee JM, Lemmens R, Levi C, Norrving B, Rannikmae K, Rost N, Rosand J, ... ... Scott R, et al. GISCOME - Genetics of Ischaemic Stroke Functional Outcome network: A protocol for an international multicentre genetic association study. European Stroke Journal. 2: 229-237. PMID 31008316 DOI: 10.1177/2396987317704547 |
0.055 |
|
| 2014 |
Tzoulis P, Evans R, Falinska A, Barnard M, Tan T, Woolman E, Leyland R, Martin N, Edwards R, Scott R, Gurazada K, Parsons M, Nair D, Khoo B, Bouloux PM. Multicentre study of investigation and management of inpatient hyponatraemia in the UK. Postgraduate Medical Journal. 90: 694-8. PMID 25398584 DOI: 10.1136/Postgradmedj-2014-132885 |
0.055 |
|
| 2018 |
Dias T, Biswas M, Daneshi N, Holliday E, Hancock S, Kerr K, Munro I, Attia J, Scott R, Milward L. Potential Clinically Significant Drug and Gene Interactions Involving Cytochrome P450 Family 2 Subfamily D Member 6 (CYP2D6) Relevant to Opioids Used for Chronic Pain in Community-dwelling Older Australians Frontiers in Pharmacology. 9. DOI: 10.3389/CONF.FPHAR.2018.63.00002 |
0.054 |
|
| 1987 |
Scott RJ, Hickok LG. GENETIC ANALYSIS OF ANTHERIDIOGEN SENSITIVITY IN CERATOPTERIS RICHARDII American Journal of Botany. 74: 1872-1877. DOI: 10.1002/J.1537-2197.1987.TB08789.X |
0.054 |
|
| 2017 |
Burnard S, Lechner-Scott J, Scott RJ. EBV and MS: Major cause, minor contribution or red-herring? Multiple Sclerosis and Related Disorders. 16: 24-30. PMID 28755681 DOI: 10.1016/j.msard.2017.06.002 |
0.054 |
|
| 2010 |
Riveros C, Mellor D, Gandhi KS, McKay FC, Cox MB, Berretta R, Vaezpour SY, Inostroza-Ponta M, Broadley SA, Heard RN, Vucic S, Stewart GJ, Williams DW, Scott RJ, Lechner-Scott J, et al. A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis. Plos One. 5: e14176. PMID 21152067 DOI: 10.1371/journal.pone.0014176 |
0.054 |
|
| 2008 |
Zacharakis E, Ahmed HU, Ishaq A, Scott R, Illing R, Freeman A, Allen C, Emberton M. The feasibility and safety of high-intensity focused ultrasound as salvage therapy for recurrent prostate cancer following external beam radiotherapy. Bju International. 102: 786-92. PMID 18564135 DOI: 10.1111/j.1464-410X.2008.07775.x |
0.054 |
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