| Year |
Citation |
Score |
| 2021 |
Graff M, Justice AE, Young KL, Marouli E, Zhang X, Fine RS, Lim E, Buchanan V, Rand K, Feitosa MF, Wojczynski MK, Yanek LR, Shao Y, Rohde R, Adeyemo AA, ... ... Gillanders EM, et al. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. American Journal of Human Genetics. PMID 33713608 DOI: 10.1016/j.ajhg.2021.02.011 |
0.306 |
|
| 2020 |
Rotunno M, Barajas R, Clyne M, Hoover E, Simonds NI, Lam TK, Mechanic LE, Goldstein AM, Gillanders E. A systematic literature review of whole exome and genome sequencing population studies of genetic susceptibility to cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 32467344 DOI: 10.1158/1055-9965.EPI-19-1551 |
0.325 |
|
| 2019 |
Barajas R, Hoover E, Clyne M, Lam T, Mechanic L, Goldstein A, Gillanders E, Rotunno M. Abstract 1600: A literature review of whole exome and genome sequencing population studies for identifying novel germline mutations in relation to cancer risk Epidemiology. DOI: 10.1158/1538-7445.Sabcs18-1600 |
0.381 |
|
| 2018 |
Huyghe JR, Bien SA, Harrison TA, Kang HM, Chen S, Schmit SL, Conti DV, Qu C, Jeon J, Edlund CK, Greenside P, Wainberg M, Schumacher FR, Smith JD, Levine DM, ... ... Gillanders E, et al. Discovery of common and rare genetic risk variants for colorectal cancer. Nature Genetics. PMID 30510241 DOI: 10.1038/S41588-018-0286-6 |
0.366 |
|
| 2017 |
Rotunno M, Clyne M, Lam T, Mechanic L, Daee D, Nelson S, Gillanders E, Goldstein A. Abstract 2589: Identifying cancer susceptibility variants and genes using whole exome and genome sequencing: a literature review Cancer Research. 77: 2589-2589. DOI: 10.1158/1538-7445.Am2017-2589 |
0.411 |
|
| 2016 |
Amos CI, Dennis J, Wang Z, Byun J, Schumacher FR, Gayther SA, Casey G, Hunter DJ, Sellers TA, Gruber SB, Dunning AM, Michailidou K, Fachal L, Doheny K, Spurdle AB, ... ... Gillanders E, et al. The OncoArray Consortium: a Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 27697780 DOI: 10.1158/1055-9965.Epi-16-0106 |
0.488 |
|
| 2015 |
Barrett JH, Taylor JC, Bright C, Harland M, Dunning AM, Akslen LA, Andresen PA, Avril MF, Azizi E, Bianchi Scarrà G, Brossard M, Brown KM, Dębniak T, Elder DE, Friedman E, ... ... Gillanders EM, et al. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. International Journal of Cancer. Journal International Du Cancer. 136: 1351-60. PMID 25077817 DOI: 10.1002/Ijc.29099 |
0.316 |
|
| 2014 |
Al Olama AA, Kote-Jarai Z, Berndt SI, Conti DV, Schumacher F, Han Y, Benlloch S, Hazelett DJ, Wang Z, Saunders E, Leongamornlert D, Lindstrom S, Jugurnauth-Little S, Dadaev T, Tymrakiewicz M, ... ... Gillanders EM, et al. A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. Nature Genetics. 46: 1103-9. PMID 25217961 DOI: 10.1038/Ng.3094 |
0.416 |
|
| 2014 |
Wang Z, Zhu B, Zhang M, Parikh H, Jia J, Chung CC, Sampson JN, Hoskins JW, Hutchinson A, Burdette L, Ibrahim A, Hautman C, Raj PS, Abnet CC, Adjei AA, ... ... Gillanders EM, et al. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33. Human Molecular Genetics. 23: 6616-33. PMID 25027329 DOI: 10.1093/Hmg/Ddu363 |
0.337 |
|
| 2013 |
Hutter CM, Mechanic LE, Chatterjee N, Kraft P, Gillanders EM. Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report. Genetic Epidemiology. 37: 643-57. PMID 24123198 DOI: 10.1002/Gepi.21756 |
0.43 |
|
| 2013 |
Peng B, Chen HS, Mechanic LE, Racine B, Clarke J, Clarke L, Gillanders E, Feuer EJ. Genetic Simulation Resources: a website for the registration and discovery of genetic data simulators. Bioinformatics (Oxford, England). 29: 1101-2. PMID 23435068 DOI: 10.1093/Bioinformatics/Btt094 |
0.324 |
|
| 2013 |
Melin B, Dahlin AM, Andersson U, Wang Z, Henriksson R, Hallmans G, Bondy ML, Johansen C, Feychting M, Ahlbom A, Kitahara CM, Wang SS, Ruder AM, Carreón T, Butler MA, ... ... Gillanders E, et al. Known glioma risk loci are associated with glioma with a family history of brain tumours -- a case-control gene association study. International Journal of Cancer. Journal International Du Cancer. 132: 2464-8. PMID 23115063 DOI: 10.1002/Ijc.27922 |
0.386 |
|
| 2012 |
Jacobs KB, Yeager M, Zhou W, Wacholder S, Wang Z, Rodriguez-Santiago B, Hutchinson A, Deng X, Liu C, Horner MJ, Cullen M, Epstein CG, Burdett L, Dean MC, Chatterjee N, ... ... Gillanders EM, et al. Detectable clonal mosaicism and its relationship to aging and cancer. Nature Genetics. 44: 651-8. PMID 22561519 DOI: 10.1038/Ng.2270 |
0.306 |
|
| 2012 |
Mechanic LE, Chen HS, Amos CI, Chatterjee N, Cox NJ, Divi RL, Fan R, Harris EL, Jacobs K, Kraft P, Leal SM, McAllister K, Moore JH, Paltoo DN, Province MA, ... ... Gillanders EM, et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genetic Epidemiology. 36: 22-35. PMID 22147673 DOI: 10.1002/Gepi.20652 |
0.309 |
|
| 2012 |
MacGregor S, Brown K, Stark M, Gartside M, Woods S, Bonazzi V, Aoude L, Dutton-Regester K, Tyagi S, Liu J, Duffy D, Palmer J, Cust A, Schmid H, Symmons J, ... ... Gillanders E, et al. From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes Hereditary Cancer in Clinical Practice. 10: A46. DOI: 10.1186/1897-4287-10-S2-A46 |
0.416 |
|
| 2012 |
Kaminski BM, Amos CI, DeRycke E, Gillanders EM, Gruber SB, Henderson BE, Hunter DJ, Lepage PK, Sellers TA, Seminara D. Abstract 78: Genetic Associations and Mechanisms in Oncology (GAME-ON): A network approach to post-GWAS research. Cancer Epidemiology Biomarkers & Prevention. 21: 78-78. DOI: 10.1158/1055-9965.Gwas-78 |
0.373 |
|
| 2011 |
Hinch AG, Tandon A, Patterson N, Song Y, Rohland N, Palmer CD, Chen GK, Wang K, Buxbaum SG, Akylbekova EL, Aldrich MC, Ambrosone CB, Amos C, Bandera EV, Berndt SI, ... ... Gillanders EM, et al. The landscape of recombination in African Americans. Nature. 476: 170-5. PMID 21775986 DOI: 10.1038/Nature10336 |
0.312 |
|
| 2011 |
Hindorff LA, Gillanders EM, Manolio TA. Genetic architecture of cancer and other complex diseases: lessons learned and future directions. Carcinogenesis. 32: 945-54. PMID 21459759 DOI: 10.1093/Carcin/Bgr056 |
0.427 |
|
| 2011 |
Bookman EB, McAllister K, Gillanders E, Wanke K, Balshaw D, Rutter J, Reedy J, Shaughnessy D, Agurs-Collins T, Paltoo D, Atienza A, Bierut L, Kraft P, Fallin MD, Perera F, et al. Gene-environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop. Genetic Epidemiology. 35: 217-25. PMID 21308768 DOI: 10.1002/Gepi.20571 |
0.33 |
|
| 2010 |
Demenais F, Mohamdi H, Chaudru V, Goldstein AM, Newton Bishop JA, Bishop DT, Kanetsky PA, Hayward NK, Gillanders E, Elder DE, Avril MF, Azizi E, van Belle P, Bergman W, Bianchi-Scarrà G, et al. Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. Journal of the National Cancer Institute. 102: 1568-83. PMID 20876876 DOI: 10.1093/Jnci/Djq363 |
0.311 |
|
| 2010 |
Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl PO, Gillanders EM, Agnarsson BA, Jönsson G, Pylkäs K, Mustonen A, Heikkinen T, Aittomäki K, Blomqvist C, Melin B, Johannsson OT, et al. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families. Breast Cancer Research : Bcr. 12: R50. PMID 20637093 DOI: 10.1186/bcr2608 |
0.457 |
|
| 2010 |
Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl P, Gillanders E, Agnarsson BA, Jönsson G, Pylkäs K, Johannsson OT, Møller P, Winqvist R, Nevanlinna H, Borg Å, Barkardottir RB. Abstract 1855: Genome-wide search for linkage in Icelandic high-risk breast cancer families Cancer Research. 70: 1855-1855. DOI: 10.1158/1538-7445.Am10-1855 |
0.559 |
|
| 2009 |
Weyandt J, Snyder C, Lynch H, Gillanders E, Holmes T, Bailey-Wilson J, Ellsworth R. Identification of BRCA1 and BRCA2 genetic modifiers. Cancer Research. 69: 1040. DOI: 10.1158/0008-5472.Sabcs-1040 |
0.643 |
|
| 2008 |
Duggal P, Gillanders EM, Holmes TN, Bailey-Wilson JE. Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies. Bmc Genomics. 9: 516. PMID 18976480 DOI: 10.1186/1471-2164-9-516 |
0.536 |
|
| 2008 |
Gunnarsson H, Arason A, Gillanders EM, Agnarsson BA, Johannesdottir G, Johannsson OT, Barkardottir RB. Evidence against PALB2 involvement in Icelandic breast cancer susceptibility. Journal of Negative Results in Biomedicine. 7: 5. PMID 18637200 DOI: 10.1186/1477-5751-7-5 |
0.317 |
|
| 2008 |
de Snoo FA, Hottenga JJ, Gillanders EM, Sandkuijl LA, Jones MP, Bergman W, van der Drift C, van Leeuwen I, van Mourik L, Huurne JA, Frants RR, Willemze R, Breuning MH, Trent JM, Gruis NA. Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families. European Journal of Human Genetics : Ejhg. 16: 1135-41. PMID 18398432 DOI: 10.1038/ejhg.2008.72 |
0.377 |
|
| 2008 |
Kim Y, Duggal P, Gillanders EM, Kim H, Bailey-Wilson JE. Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype data. Genetic Epidemiology. 32: 41-51. PMID 17685456 DOI: 10.1002/Gepi.20260 |
0.491 |
|
| 2007 |
Lange EM, Robbins CM, Gillanders EM, Zheng SL, Xu J, Wang Y, White KA, Chang BL, Ho LA, Trent JM, Carpten JD, Isaacs WB, Cooney KA. Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis. Human Genetics. 121: 49-55. PMID 17120048 DOI: 10.1007/S00439-006-0274-2 |
0.453 |
|
| 2007 |
Baffoe-Bonnie AB, Kittles RA, Gillanders E, Ou L, George A, Robbins C, Ahaghotu C, Bennett J, Boykin W, Hoke G, Mason T, Pettaway C, Vijayakumar S, Weinrich S, Jones MP, et al. Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer study (AAHPC). The Prostate. 67: 22-31. PMID 17031815 DOI: 10.1002/Pros.20456 |
0.662 |
|
| 2006 |
Gillanders EM, Pearson JV, Sorant AJ, Trent JM, O'Connell JR, Bailey-Wilson JE. The value of molecular haplotypes in a family-based linkage study. American Journal of Human Genetics. 79: 458-68. PMID 16909384 DOI: 10.1086/506626 |
0.552 |
|
| 2006 |
Lange EM, Ho LA, Beebe-Dimmer JL, Wang Y, Gillanders EM, Trent JM, Lange LA, Wood DP, Cooney KA. Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12. Human Genetics. 119: 400-7. PMID 16508751 DOI: 10.1007/S00439-006-0149-6 |
0.517 |
|
| 2006 |
Chang BL, Lange EM, Dimitrov L, Valis CJ, Gillanders EM, Lange LA, Wiley KE, Isaacs SD, Wiklund F, Baffoe-Bonnie A, Langefeld CD, Zheng SL, Matikainen MP, Ikonen T, Fredriksson H, et al. Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect. Human Genetics. 118: 716-24. PMID 16328469 DOI: 10.1007/S00439-005-0099-4 |
0.628 |
|
| 2005 |
Duggal P, Gillanders EM, Mathias RA, Ibay GP, Klein AP, Baffoe-Bonnie AB, Ou L, Dusenberry IP, Tsai YY, Chines PS, Doan BQ, Bailey-Wilson JE. Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium. Bmc Genetics. 6: S73. PMID 16451687 DOI: 10.1186/1471-2156-6-S1-S73 |
0.507 |
|
| 2005 |
Klein AP, Tsai YY, Duggal P, Gillanders EM, Barnhart M, Mathias RA, Dusenberry IP, Turiff A, Chines PS, Goldstein J, Wojciechowski R, Hening W, Pugh EW, Bailey-Wilson JE. Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits. Bmc Genetics. 6: S20. PMID 16451629 DOI: 10.1186/1471-2156-6-S1-S20 |
0.512 |
|
| 2005 |
Baffoe-Bonnie AB, Smith JR, Stephan DA, Schleutker J, Carpten JD, Kainu T, Gillanders EM, Matikainen M, Teslovich TM, Tammela T, Sood R, Balshem AM, Scarborough SD, Xu J, Isaacs WB, et al. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region. Human Genetics. 117: 307-16. PMID 15906096 DOI: 10.1007/S00439-005-1306-Z |
0.62 |
|
| 2005 |
Chang BL, Isaacs SD, Wiley KE, Gillanders EM, Zheng SL, Meyers DA, Walsh PC, Trent JM, Xu J, Isaacs WB. Genome-wide screen for prostate cancer susceptibility genes in men with clinically significant disease. The Prostate. 64: 356-61. PMID 15754351 DOI: 10.1002/Pros.20249 |
0.393 |
|
| 2005 |
Chang BL, Gillanders EM, Isaacs SD, Wiley KE, Adams T, Turner AR, Zheng SL, Meyers DA, Carpten JD, Walsh PC, Trent JM, Xu J, Isaacs WB. Evidence for a general cancer susceptibility locus at 3p24 in families with hereditary prostate cancer. Cancer Letters. 219: 177-82. PMID 15723717 DOI: 10.1016/J.Canlet.2004.10.005 |
0.447 |
|
| 2005 |
Rökman A, Baffoe-Bonnie AB, Gillanders E, Fredriksson H, Autio V, Ikonen T, Gibbs KD, Jones M, Gildea D, Freas-Lutz D, Markey C, Matikainen MP, Koivisto PA, Tammela TL, Kallioniemi OP, et al. Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus. Human Genetics. 116: 43-50. PMID 15549392 DOI: 10.1007/S00439-004-1214-7 |
0.687 |
|
| 2005 |
Baffoe-Bonnie AB, Smith JR, Stephan DA, Schleutker J, Carpten JD, Kainu T, Gillanders EM, Matikainen M, Teslovich TM, Tammela T, Sood R, Balshem AM, Scarborough SD, Xu J, Isaacs WB, et al. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region Human Genetics. 118: 307-307. DOI: 10.1007/S00439-005-0050-8 |
0.583 |
|
| 2004 |
Gillanders EM, Masiello A, Gildea D, Umayam L, Duggal P, Jones MP, Klein AP, Freas-Lutz D, Ibay G, Trout K, Wolfsberg TG, Trent JM, Bailey-Wilson JE, Baxevanis AD. GeneLink: a database to facilitate genetic studies of complex traits. Bmc Genomics. 5: 81. PMID 15491493 DOI: 10.1186/1471-2164-5-81 |
0.532 |
|
| 2004 |
Gillanders EM, Xu J, Chang BL, Lange EM, Wiklund F, Bailey-Wilson JE, Baffoe-Bonnie A, Jones M, Gildea D, Riedesel E, Albertus J, Isaacs SD, Wiley KE, Mohai CE, Matikainen MP, et al. Combined genome-wide scan for prostate cancer susceptibility genes. Journal of the National Cancer Institute. 96: 1240-7. PMID 15316059 DOI: 10.1093/Jnci/Djh228 |
0.597 |
|
| 2004 |
Xu J, Langefeld CD, Zheng SL, Gillanders EM, Chang BL, Isaacs SD, Williams AH, Wiley KE, Dimitrov L, Meyers DA, Walsh PC, Trent JM, Isaacs WB. Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage. Human Genetics. 115: 255-62. PMID 15185141 DOI: 10.1007/S00439-004-1144-4 |
0.469 |
|
| 2004 |
Friedrichsen DM, Stanford JL, Isaacs SD, Janer M, Chang BL, Deutsch K, Gillanders E, Kolb S, Wiley KE, Badzioch MD, Zheng SL, Walsh PC, Jarvik GP, Hood L, Trent JM, et al. Identification of a prostate cancer susceptibility locus on chromosome 7q11-21 in Jewish families. Proceedings of the National Academy of Sciences of the United States of America. 101: 1939-44. PMID 14769943 DOI: 10.1073/Pnas.0308336100 |
0.574 |
|
| 2004 |
Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, et al. Genome-wide scanning for linkage in Finnish breast cancer families. European Journal of Human Genetics : Ejhg. 12: 98-104. PMID 14560309 DOI: 10.1038/Sj.Ejhg.5201091 |
0.677 |
|
| 2004 |
Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, et al. Erratum: Genome-wide scanning for linkage in Finnish breast cancer families European Journal of Human Genetics. 12: 256-256. DOI: 10.1038/Sj.Ejhg.5201140 |
0.607 |
|
| 2003 |
Lange EM, Gillanders EM, Davis CC, Brown WM, Campbell JK, Jones M, Gildea D, Riedesel E, Albertus J, Freas-Lutz D, Markey C, Giri V, Dimmer JB, Montie JE, Trent JM, et al. Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1. The Prostate. 57: 326-34. PMID 14601029 DOI: 10.1002/Pros.10307 |
0.461 |
|
| 2003 |
Xu J, Gillanders EM, Isaacs SD, Chang BL, Wiley KE, Zheng SL, Jones M, Gildea D, Riedesel E, Albertus J, Freas-Lutz D, Markey C, Meyers DA, Walsh PC, Trent JM, et al. Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families. The Prostate. 57: 320-5. PMID 14601028 DOI: 10.1002/Pros.10306 |
0.449 |
|
| 2003 |
Wiklund F, Gillanders EM, Albertus JA, Bergh A, Damber JE, Emanuelsson M, Freas-Lutz DL, Gildea DE, Göransson I, Jones MS, Jonsson BA, Lindmark F, Markey CJ, Riedesel EL, Stenman E, et al. Genome-wide scan of Swedish families with hereditary prostate cancer: suggestive evidence of linkage at 5q11.2 and 19p13.3. The Prostate. 57: 290-7. PMID 14601025 DOI: 10.1002/pros.10303 |
0.477 |
|
| 2003 |
Schleutker J, Baffoe-Bonnie AB, Gillanders E, Kainu T, Jones MP, Freas-Lutz D, Markey C, Gildea D, Riedesel E, Albertus J, Gibbs KD, Matikainen M, Koivisto PA, Tammela T, Bailey-Wilson JE, et al. Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26. The Prostate. 57: 280-9. PMID 14601024 DOI: 10.1002/Pros.10302 |
0.672 |
|
| 2003 |
Gillanders E, Juo SH, Holland EA, Jones M, Nancarrow D, Freas-Lutz D, Sood R, Park N, Faruque M, Markey C, Kefford RF, Palmer J, Bergman W, Bishop DT, Tucker MA, et al. Localization of a novel melanoma susceptibility locus to 1p22. American Journal of Human Genetics. 73: 301-13. PMID 12844286 DOI: 10.1086/377140 |
0.61 |
|
| 2003 |
Tranebjaerg L, Teslovich TM, Jones M, Barmada MM, Fagerheim T, Dahl A, Escolar DM, Trent JM, Gillanders EM, Stephan DA. Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13. Human Genetics. 113: 293-5. PMID 12811539 DOI: 10.1007/s00439-003-0967-8 |
0.377 |
|
| 2002 |
Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nature Genetics. 32: 676-80. PMID 12434154 DOI: 10.1038/Ng1048 |
0.516 |
|
| 2002 |
Stephan DA, Howell GR, Teslovich TM, Coffey AJ, Smith L, Bailey-Wilson JE, Malechek L, Gildea D, Smith JR, Gillanders EM, Schleutker J, Hu P, Steingruber HE, Dhami P, Robbins CM, et al. Physical and transcript map of the hereditary prostate cancer region at xq27. Genomics. 79: 41-50. PMID 11827456 DOI: 10.1006/Geno.2001.6681 |
0.541 |
|
| 2002 |
Carpten J, Nupponen N, Isaacs S, Sood R, Robbins C, Xu J, Faruque M, Moses T, Ewing C, Gillanders E, Hu P, Bujnovszky P, Makalowska I, Baffoe-Bonnie A, Faith D, et al. Germline mutations in the ribonuclease L gene in families showing linkage with HPC1. Nature Genetics. 30: 181-4. PMID 11799394 DOI: 10.1038/Ng823 |
0.638 |
|
| 2002 |
Matikainen M, Schleutker J, Gillanders E, Baffoe-Bonnie A, Jones MP, Kainu T, Markey C, Koivisto P, Tammela T, Bailey-Wilson J, Trent J, Kallioniemi O. Novel region of interest in chromosome 11 and other putative regions identified in a genome-wide scan in finnish hereditary prostate cancer families European Urology Supplements. 1: 8. DOI: 10.1016/S1569-9056(02)80020-3 |
0.656 |
|
| 2001 |
Douglas JA, Boehnke M, Gillanders E, Trent JM, Gruber SB. Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies Nature Genetics. 28: 361-364. PMID 11443299 DOI: 10.1038/Ng582 |
0.407 |
|
| 2001 |
Gillanders E, Douglas J, Gruber S, Yan H, Vogelstein B, Sood R, Carpten J, Dennis T, Boehnke M, Trent J. Use of experimentally constructed haplotypes in gene mapping studies of hereditary cancers Nature Genetics. 27: 56-56. DOI: 10.1038/87094 |
0.406 |
|
| 2000 |
Schleutker J, Matikainen M, Smith J, Koivisto P, Baffoe-Bonnie A, Kainu T, Gillanders E, Sankila R, Pukkala E, Carpten J, Stephan D, Tammela T, Brownstein M, Bailey-Wilson J, Trent J, et al. A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 6: 4810-5. PMID 11156239 |
0.484 |
|
| 2000 |
Bergthorsson JT, Johannesdottir G, Arason A, Benediktsdottir KR, Agnarsson BA, Bailey-Wilson JE, Gillanders E, Smith J, Trent J, Barkardottir RB. Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer. Human Genetics. 107: 372-5. PMID 11129338 DOI: 10.1007/S004390000384 |
0.689 |
|
| 2000 |
Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, Gillanders E, Syrjäkoski K, Kainu T, Vahteristo P, Krahe R, Pääkkönen K, Hartikainen J, Blomqvist C, Löppönen T, et al. Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland. European Journal of Human Genetics : Ejhg. 8: 757-63. PMID 11039575 DOI: 10.1038/Sj.Ejhg.5200529 |
0.447 |
|
| 2000 |
Bittner M, Meltzer P, Chen Y, Jiang Y, Seftor E, Hendrix M, Radmacher M, Simon R, Yakhini Z, Ben-Dor A, Sampas N, Dougherty E, Wang E, Marincola F, Gooden C, ... ... Gillanders E, et al. Molecular classification of cutaneous malignant melanoma by gene expression profiling. Nature. 406: 536-40. PMID 10952317 DOI: 10.1038/35020115 |
0.316 |
|
| 2000 |
Kainu T, Juo SHH, Desper R, Schäffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi T, Koivisto P, et al. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus Proceedings of the National Academy of Sciences of the United States of America. 97: 9603-9608. PMID 10944226 DOI: 10.1073/Pnas.97.17.9603 |
0.629 |
|
| 1999 |
Lange EM, Chen H, Brierley K, Perrone EE, Bock CH, Gillanders E, Ray ME, Cooney KA. Linkage analysis of 153 prostate cancer families over a 30-cM region containing the putative susceptibility locus HPCX Clinical Cancer Research. 5: 4013-4020. PMID 10632333 |
0.485 |
|
| 1999 |
Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken A, Bailey-Wilson J, Wang X, Patel RJ, Robbins CM, Chung M, Annett G, Weinberg K, Borchert MS, et al. Localization of a gene for Duane retraction syndrome to chromosome 2q31. American Journal of Human Genetics. 65: 1639-46. PMID 10577917 DOI: 10.1086/302656 |
0.599 |
|
| 1999 |
Stephan DA, Gillanders E, Vanderveen D, Freas-Lutz D, Wistow G, Baxevanis AD, Robbins CM, VanAuken A, Quesenberry MI, Bailey-Wilson J, Juo SH, Trent JM, Smith L, Brownstein MJ. Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. Proceedings of the National Academy of Sciences of the United States of America. 96: 1008-12. PMID 9927684 DOI: 10.1073/Pnas.96.3.1008 |
0.557 |
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| 1999 |
Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova G, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, ... ... Gillanders E, et al. Evidence for a Prostate Cancer Susceptibility Locus on the X Chromosome Journal of Urology. 161: 1386-1386. DOI: 10.1016/S0022-5347(01)61689-6 |
0.355 |
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| 1998 |
Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, ... ... Gillanders E, et al. Evidence for a prostate cancer susceptibility locus on the X chromosome. Nature Genetics. 20: 175-9. PMID 9771711 DOI: 10.1016/S0022-5347(01)61689-6 |
0.67 |
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