| Year |
Citation |
Score |
| 2023 |
Morra A, Mavaddat N, Muranen TA, Ahearn TU, Allen J, Andrulis IL, Auvinen P, Becher H, Behrens S, Blomqvist C, Bojesen SE, Bolla MK, Brauch H, Camp NJ, Carvalho S, et al. The impact of coding germline variants on contralateral breast cancer risk and survival. American Journal of Human Genetics. PMID 36827971 DOI: 10.1016/j.ajhg.2023.02.003 |
0.313 |
|
| 2023 |
Figlioli G, Billaud A, Ahearn TU, Antonenkova NN, Becher H, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Blok MJ, Bogdanova NV, Bonanni B, Burwinkel B, Camp NJ, Campbell A, et al. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. European Journal of Human Genetics : Ejhg. PMID 36707629 DOI: 10.1038/s41431-022-01257-w |
0.34 |
|
| 2022 |
Berndt SI, Vijai J, Benavente Y, Camp NJ, Nieters A, Wang Z, Smedby KE, Kleinstern G, Hjalgrim H, Besson C, Skibola CF, Morton LM, Brooks-Wilson AR, Teras LR, Breeze C, et al. Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Leukemia. PMID 36273105 DOI: 10.1038/s41375-022-01711-0 |
0.361 |
|
| 2022 |
Dicanio M, Giaccherini M, Clay-Gilmour A, Macauda A, Sainz J, Machiela MJ, Rybicka-Ramos M, Norman AD, Tyczyńska A, Chanock SJ, Barington T, Kumar SK, Bhatti P, Cozen W, Brown EE, ... ... Camp NJ, et al. A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk. International Journal of Cancer. PMID 36082445 DOI: 10.1002/ijc.34278 |
0.401 |
|
| 2022 |
Dorling L, Carvalho S, Allen J, Parsons MT, Fortuno C, González-Neira A, Heijl SM, Adank MA, Ahearn TU, Andrulis IL, Auvinen P, Becher H, Beckmann MW, Behrens S, Bermisheva M, ... ... Camp NJ, et al. Breast cancer risks associated with missense variants in breast cancer susceptibility genes. Genome Medicine. 14: 51. PMID 35585550 DOI: 10.1186/s13073-022-01052-8 |
0.314 |
|
| 2022 |
Mavaddat N, Dorling L, Carvalho S, Allen J, González-Neira A, Keeman R, Bolla MK, Dennis J, Wang Q, Ahearn TU, Andrulis IL, Beckmann MW, Behrens S, Benitez J, ... ... Camp NJ, et al. Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes. Jama Oncology. PMID 35084436 DOI: 10.1001/jamaoncol.2021.6744 |
0.353 |
|
| 2021 |
Griffin Waller R, Madsen MJ, Gardner J, Sborov DW, Camp NJ. Duo Shared Genomic Segment analysis identifies a genome-wide significant risk locus at 18q21.33 in myeloma pedigrees. Journal of Translational Genetics and Genomics. 5: 112-123. PMID 34888494 DOI: 10.20517/jtgg.2021.09 |
0.34 |
|
| 2021 |
DiBlasi E, Shabalin AA, Monson ET, Keeshin BR, Bakian AV, Kirby AV, Ferris E, Chen D, William N, Gaj E, Klein M, Jerominski L, Callor WB, Christensen E, Smith KR, ... ... Camp NJ, et al. Rare protein-coding variants implicate genes involved in risk of suicide death. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34042246 DOI: 10.1002/ajmg.b.32861 |
0.302 |
|
| 2021 |
Waller RG, Klein RJ, Vijai J, McKay JD, Clay-Gilmour A, Wei X, Madsen MJ, Sborov DW, Curtin K, Slager SL, Offit K, Vachon CM, Lipkin SM, Dumontet C, Camp NJ. Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes. Human Molecular Genetics. PMID 33751038 DOI: 10.1093/hmg/ddab066 |
0.371 |
|
| 2021 |
Macauda A, Piredda C, Clay-Gilmour AI, Sainz J, Buda G, Markiewicz M, Barington T, Ziv E, Hildebrandt MAT, Belachew AA, Varkonyi J, Prejzner W, Druzd-Sitek A, Spinelli J, Andersen NF, ... ... Camp NJ, et al. Expression quantitative trait loci of genes predicting outcome are associated with survival of multiple myeloma patients. International Journal of Cancer. PMID 33675538 DOI: 10.1002/ijc.33547 |
0.316 |
|
| 2021 |
Dorling L, Carvalho S, Allen J, González-Neira A, Luccarini C, Wahlström C, Pooley KA, Parsons MT, Fortuno C, Wang Q, Bolla MK, Dennis J, Keeman R, Alonso MR, ... ... Camp NJ, et al. Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women. The New England Journal of Medicine. PMID 33471991 DOI: 10.1056/NEJMoa1913948 |
0.305 |
|
| 2020 |
Gulbahce HE, White S, Herget KA, Stoddard G, Camp NJ, Buys SS, Sweeney C. 21-gene recurrence score testing utilization among older women from different races: A population-based study. Journal of Geriatric Oncology. PMID 32646620 DOI: 10.1016/J.Jgo.2020.06.004 |
0.393 |
|
| 2020 |
Zhang YD, Hurson AN, Zhang H, Choudhury PP, Easton DF, Milne RL, Simard J, Hall P, Michailidou K, Dennis J, Schmidt MK, Chang-Claude J, Gharahkhani P, Whiteman D, Campbell PT, ... ... Camp NJ, et al. Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers. Nature Communications. 11: 3353. PMID 32620889 DOI: 10.1038/S41467-020-16483-3 |
0.432 |
|
| 2020 |
Clay-Gilmour AI, Hildebrandt MAT, Brown EE, Hofmann JN, Spinelli JJ, Giles GG, Cozen W, Bhatti P, Wu X, Waller RG, Belachew AA, Robinson DP, Norman AD, Sinnwell JP, Berndt SI, ... ... Camp NJ, et al. Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance. Blood Advances. 4: 2789-2797. PMID 32569378 DOI: 10.1182/Bloodadvances.2020001435 |
0.397 |
|
| 2020 |
Kleinstern G, Camp NJ, Berndt SI, Birmann BM, Nieters A, Bracci PM, McKay JD, Ghesquières H, Lan Q, Hjalgrim H, Benavente Y, Monnereau A, Wang SS, Zhang Y, Purdue MP, et al. Lipid trait variants and the risk of non-Hodgkin lymphoma subtypes: A Mendelian Randomization Study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 32108027 DOI: 10.1158/1055-9965.Epi-19-0803 |
0.351 |
|
| 2020 |
Hanson HA, Leiser CL, Madsen MJ, Gardner J, Knight S, Cessna M, Sweeney C, Doherty JA, Smith KR, Bernard PS, Camp NJ. Family Study Designs Informed by Tumor Heterogeneity and Multi-Cancer Pleiotropies: The Power of the Utah Population Database. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 32098891 DOI: 10.1158/1055-9965.Epi-19-0912 |
0.386 |
|
| 2020 |
Hanson HA, Leiser CL, O'Neil B, Martin C, Gupta S, Smith KR, Dechet C, Lowrance WT, Madsen MJ, Camp NJ. Harnessing Population Pedigree Data and Machine Learning Methods to Identify Patterns of Familial Bladder Cancer Risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 32098890 DOI: 10.1158/1055-9965.Epi-19-0681 |
0.351 |
|
| 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, ... ... Camp NJ, 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 |
0.369 |
|
| 2020 |
Waller RG, Madsen MJ, Gardner J, Sborov D, Camp NJ. Abstract A40: Characterization of quantitative gene-expression dimensions in myeloma tumors Cancer Epidemiology and Prevention Biomarkers. 29. DOI: 10.1158/1538-7755.Modpop19-A40 |
0.321 |
|
| 2020 |
Wei M, Pappas L, Guinto E, Sweeney C, Camp N, Freer P, Buys S, Henry NL, Curtin K. Abstract P2-08-10: Mammographic breast density changes with endocrine therapy (ET) in women with hormone receptor positive (HR+) breast cancer in a Utah population Cancer Research. 80. DOI: 10.1158/1538-7445.Sabcs19-P2-08-10 |
0.302 |
|
| 2020 |
Feusier JE, Madsen MJ, Voelkerding K, Glenn M, Camp N. Abstract 2119: Gene mapping in high-risk chronic lymphocytic leukemia pedigree identifies risk locus at chromosome 2q22.1 Cancer Research. 80: 2119-2119. DOI: 10.1158/1538-7445.Am2020-2119 |
0.489 |
|
| 2019 |
Moore A, Kane E, Wang Z, Panagiotou OA, Teras LR, Monnereau A, Wong Doo N, Machiela MJ, Skibola CF, Slager SL, Salles G, Camp NJ, Bracci PM, Nieters A, Vermeulen RCH, et al. Genetically Determined Height and Risk of Non-hodgkin Lymphoma. Frontiers in Oncology. 9: 1539. PMID 32064237 DOI: 10.3389/Fonc.2019.01539 |
0.432 |
|
| 2019 |
Din L, Sheikh M, Kosaraju N, Smedby KE, Bernatsky S, Berndt SI, Skibola CF, Nieters A, Wang S, McKay JD, Cocco P, Maynadié M, Foretová L, Staines A, Mack TM, ... ... Camp NJ, et al. Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Genetic Epidemiology. PMID 31407831 DOI: 10.1002/Gepi.22242 |
0.401 |
|
| 2019 |
Feldkamp ML, Krikov S, Gardner J, Madsen MJ, Darlington T, Sargent R, Camp NJ. Shared genomic segments in high-risk multigenerational pedigrees with gastroschisis. Birth Defects Research. PMID 31385443 DOI: 10.1002/Bdr2.1567 |
0.382 |
|
| 2019 |
Clay-Gilmour AI, Rishi AR, Goldin LR, Greenberg-Worisek AJ, Achenbach SJ, Rabe KG, Maurer MJ, Kay NE, Shanafelt TD, Call TG, Brice Weinberg J, Camp NJ, Cerhan JR, Leis J, Norman A, et al. Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. Blood Cancer Journal. 9: 59. PMID 31383849 DOI: 10.1038/S41408-019-0220-X |
0.305 |
|
| 2019 |
Glenn MJ, Madsen MJ, Davis E, Garner CD, Curtin K, Jones B, Williams JA, Tomasson MH, Camp NJ. Elevated IgM and abnormal free light chain ratio are increased in relatives from high-risk chronic lymphocytic leukemia pedigrees. Blood Cancer Journal. 9: 25. PMID 30808891 DOI: 10.1038/S41408-019-0186-8 |
0.362 |
|
| 2019 |
Millar MM, Kinney AY, Camp NJ, Cannon-Albright LA, Hashibe M, Penson DF, Kirchhoff AC, Neklason DW, Gilsenan AW, Dieck GS, Stroup AM, Edwards SL, Bateman C, Carter ME, Sweeney C. Predictors of Response Outcomes for Research Recruitment Through a Central Cancer Registry: Evidence From 17 Population-Based Studies. American Journal of Epidemiology. PMID 30689685 DOI: 10.1093/Aje/Kwz011 |
0.384 |
|
| 2019 |
Camp NJ, Madsen MJ, Herranz J, Rodríguez-Lescure Á, Ruiz A, Martín M, Bernard PS. Re-interpretation of PAM50 gene expression as quantitative tumor dimensions shows utility for clinical trials: application to prognosis and response to paclitaxel in breast cancer. Breast Cancer Research and Treatment. PMID 30673970 DOI: 10.1007/S10549-018-05097-5 |
0.365 |
|
| 2019 |
Clay-Gilmour AI, Hildebrandt M, Asmann Y, Brown EE, Hofmann JN, Spinelli J, Giles G, Bhatti P, Cozen W, Robinson DP, O'Brien DR, Rajkumar SV, Tian S, Berndt SI, Chanock SJ, ... ... Camp NJ, et al. Association between a Polygenic Risk Score for Multiple Myeloma Risk and Overall Survival Blood. 134: 4366-4366. DOI: 10.1182/Blood-2019-126088 |
0.423 |
|
| 2019 |
Barnard ME, Camp NJ, Doherty JA. Abstract 4174: Familiality of ovarian cancer histotypes in the Utah Population Database Cancer Research. 79: 4174-4174. DOI: 10.1158/1538-7445.Sabcs18-4174 |
0.357 |
|
| 2019 |
Clay-Gilmour AI, Hildebrandt MA, Camp NJ, Ziv E, Brown EE, Hofmann JN, Spinelli JJ, Giles GG, Bhatti P, Cozen W, Wu X, Robinson DP, Norman AD, Sinnwell JP, Kumar SK, et al. Abstract 2686: Associations between a polygenic risk score and risk of multiple myeloma and its precursor Cancer Research. 79: 2686-2686. DOI: 10.1158/1538-7445.Am2019-2686 |
0.443 |
|
| 2019 |
Coon H, Ferris E, Darlington T, Morgan J, Sargent R, Fraser A, Smith KR, Camp NJ, Gregg C. Sa18Significant Overlap Of Genomic Regions From Extended High-Risk Autism Families With Evolutionarily Accelerated Regions In A Species With Highly Unusual Social Behavior European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.240 |
0.317 |
|
| 2019 |
DiBlasi E, Li Q, Anderson J, Callor WB, Christensen E, Jerominski L, Sargent R, Gray D, Camp N, Shabalin A, Docherty A, Coon H. 66Analyses Of Disease-Associated And Likely Functional Variants From Psycharray Implicate Genes Involved In Risk For Completed Suicide European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.073 |
0.385 |
|
| 2018 |
Coon H, Darlington TM, DiBlasi E, Callor WB, Ferris E, Fraser A, Yu Z, William N, Das SC, Crowell SE, Chen D, Anderson JS, Klein M, Jerominski L, Cannon D, ... ... Camp NJ, et al. Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. Molecular Psychiatry. PMID 30353169 DOI: 10.1038/S41380-018-0282-3 |
0.436 |
|
| 2018 |
Wang SS, Carrington M, Berndt SI, Slager SL, Bracci PM, Voutsinas J, Cerhan JR, Ekström Smedby K, Hjalgrim H, Vijai J, Morton LM, Vermeulen R, Paltiel O, Vajdic CM, Linet MS, ... ... Camp NJ, et al. HLA class I and II diversity contributes to the etiologic heterogeneity of non-Hodgkin lymphoma subtypes. Cancer Research. PMID 29735552 DOI: 10.1158/0008-5472.Can-17-2900 |
0.33 |
|
| 2018 |
Kleinstern G, Camp NJ, Goldin LR, Vachon CM, Vajdic CM, de Sanjose S, Weinberg JB, Benavente Y, Casabonne D, Liebow M, Nieters A, Hjalgrim H, Melbye M, Glimelius B, Adami HO, et al. Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. Blood. PMID 29674426 DOI: 10.1182/Blood-2017-11-814608 |
0.453 |
|
| 2018 |
Madsen MJ, Knight S, Sweeney C, Factor RE, Salama ME, Stijleman IJ, Rajamanickam V, Welm BE, Arunachalam S, Jones B, Rachamadugu R, Rowe K, Cessna M, Thomas A, Kushi LH, ... ... Camp NJ, et al. Reparameterization of PAM50 expression identifies novel breast tumor dimensions and leads to discovery of a genomewide significant breast cancer locus at 12q15. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 29650789 DOI: 10.1158/1055-9965.Epi-17-0887 |
0.315 |
|
| 2018 |
Waller RG, Darlington TM, Wei X, Madsen MJ, Thomas A, Curtin K, Coon H, Rajamanickam V, Musinsky J, Jayabalan D, Atanackovic D, Rajkumar SV, Kumar S, Slager S, Middha M, ... ... Camp NJ, et al. Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. Plos Genetics. 14: e1007111. PMID 29389935 DOI: 10.1371/Journal.Pgen.1007111 |
0.442 |
|
| 2018 |
Clay-Gilmour AI, Camp NJ, Wei X, Norman AD, Sinnwell JP, Demangel D, Waller RG, Dumontet C, McKay J, Offit K, Chen S, O'Brien DR, Rajkumar SV, Klein R, Kumar SK, et al. Large-Scale Linkage Analysis of Multiple Myeloma (MM) and Monoclonal Gammopathy of Undetermined Significance (MGUS) Families Blood. 132: 4501-4501. DOI: 10.1182/Blood-2018-99-119320 |
0.428 |
|
| 2018 |
Hanson H, Leiser C, Martin C, O'Neil B, Lowrance W, Alter O, Gupta S, Kohlmann W, Greenberg S, Smith K, Camp N. MP06-15 REDEFINING THE BLADDER CANCER PHENOTYPE USING PATTERNS OF FAMILIAL RISK Journal of Urology. 199. DOI: 10.1016/J.Juro.2018.02.207 |
0.353 |
|
| 2017 |
Li J, Li H, Makunin I, Thompson BA, Tao K, Young EL, Lopez J, Camp NJ, Tavtigian SV, John EM, Andrulis IL, Khanna KK, Goldgar D, Chenevix-Trench G. Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families. Breast Cancer Research and Treatment. PMID 28840378 DOI: 10.1007/S10549-017-4469-0 |
0.387 |
|
| 2017 |
Law PJ, Berndt SI, Speedy HE, Camp NJ, Sava GP, Skibola CF, Holroyd A, Joseph V, Sunter NJ, Nieters A, Bea S, Monnereau A, Martin-Garcia D, Goldin LR, Clot G, et al. Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Nature Communications. 8: 14175. PMID 28165464 DOI: 10.1038/Ncomms14175 |
0.399 |
|
| 2017 |
Besson C, Moore A, Wu W, Camp NJ, Vajdic C, Morton LM, Smedby KE, Sanjose Sd, Shanafelt TD, Brewer J, Zablotska L, Engels EA, Cerhan JR, Slager SL, Han J, et al. Common Genetic Polymorphisms Contribute to the Association between Non-Melanoma Skin Cancer and Chronic Lymphocytic Leukemia Blood. 130: 1454-1454. DOI: 10.1182/Blood.V130.Suppl_1.1454.1454 |
0.383 |
|
| 2017 |
Kleinstern G, Sanjosé Sd, Camp N, Vajdic CM, Call TG, Liebow M, Robinson D, Kay NE, Cunningham J, Benavente Y, Monnereau A, Spinelli J, Cerhan JR, Slager SL. Abstract 4267: Association of polygenic risk scores and family history with the risk of chronic lymphocytic leukemia (CLL) Epidemiology. 77: 4267-4267. DOI: 10.1158/1538-7445.Am2017-4267 |
0.345 |
|
| 2016 |
Bradford JR, Cox A, Bernard P, Camp NJ. Consensus Analysis of Whole Transcriptome Profiles from Two Breast Cancer Patient Cohorts Reveals Long Non-Coding RNAs Associated with Intrinsic Subtype and the Tumour Microenvironment. Plos One. 11: e0163238. PMID 27685983 DOI: 10.1371/Journal.Pone.0163238 |
0.354 |
|
| 2016 |
Rand KA, Song C, Dean E, Serie DJ, Curtin K, Sheng X, Hu D, Huff CA, Bernal-Mizrachi L, Tomasson MH, Ailwadhi S, Singhal S, Pawlish KS, Peters ES, BLock CH, ... ... Camp NJ, et al. A meta-analysis of multiple myeloma risk regions in African and European ancestry populations identifies putatively functional loci. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 27587788 DOI: 10.1158/1055-9965.Epi-15-1193 |
0.442 |
|
| 2016 |
Schinasi LH, Brown EE, Camp NJ, Wang SS, Hofmann JN, Chiu BC, Miligi L, Beane Freeman LE, de Sanjose S, Bernstein L, Monnereau A, Clavel J, Tricot GJ, Atanackovic D, Cocco P, et al. Multiple myeloma and family history of lymphohaematopoietic cancers: Results from the International Multiple Myeloma Consortium. British Journal of Haematology. PMID 27330041 DOI: 10.1111/Bjh.14199 |
0.389 |
|
| 2016 |
Machiela MJ, Lan Q, Slager SL, Vermeulen RC, Teras LR, Camp NJ, Cerhan JR, Spinelli JJ, Wang SS, Nieters A, Vijai J, Yeager M, Wang Z, Ghesquières H, McKay J, et al. Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. Human Molecular Genetics. 25: 1663-76. PMID 27008888 DOI: 10.1093/Hmg/Ddw027 |
0.412 |
|
| 2016 |
Berndt SI, Camp NJ, Skibola CF, Vijai J, Wang Z, Gu J, Nieters A, Kelly RS, Smedby KE, Monnereau A, Cozen W, Cox A, Wang SS, Lan Q, Teras LR, et al. Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. Nature Communications. 7: 10933. PMID 26956414 DOI: 10.1038/Ncomms10933 |
0.42 |
|
| 2016 |
Camp NJ, Lin WY, Bigelow A, Burghel GJ, Mosbruger T, Parry M, Waller RG, Rigas SH, Tai PY, Berrett K, Rajamanickam V, Cosby R, Brock IW, Jones B, Connley D, et al. Discordant Haplotype Sequencing Identifies Functional Variants at the 2q33 Breast Cancer Risk Locus. Cancer Research. PMID 26795348 DOI: 10.1158/0008-5472.Can-15-1629 |
0.725 |
|
| 2016 |
Clark E, Esplin S, Manuck T, Neklason D, Wu W, Jorde L, Camp N, Varner M. 397: Mapping genetic susceptibility to preterm birth: Analysis of Utah pedigrees using shared genomic segment analysis American Journal of Obstetrics and Gynecology. 214: S218-S219. DOI: 10.1016/J.Ajog.2015.10.438 |
0.361 |
|
| 2015 |
Ziv E, Dean E, Hu D, Martino A, Serie D, Curtin K, Campa D, Aftab B, Bracci P, Buda G, Zhao Y, Caswell-Jin J, Diasio R, Dumontet C, Dudziński M, ... ... Camp NJ, et al. Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Nature Communications. 6: 10203. PMID 26648255 DOI: 10.1038/Ncomms10203 |
0.363 |
|
| 2015 |
Ziv E, Dean E, Hu D, Martino A, Serie D, Curtin K, Campa D, Aftab B, Bracci P, Buda G, Zhao Y, Caswell-Jin J, Diasio R, Dumontet C, Dudzi?ski M, ... ... Camp NJ, et al. Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Nature Communications. 6: 7539. PMID 26198393 DOI: 10.1038/Ncomms8539 |
0.414 |
|
| 2015 |
Lin WY, Camp NJ, Ghoussaini M, Beesley J, Michailidou K, Hopper JL, Apicella C, Southey MC, Stone J, Schmidt MK, Broeks A, Van't Veer LJ, Th Rutgers EJ, Muir K, Lophatananon A, et al. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. Human Molecular Genetics. 24: 285-98. PMID 25168388 DOI: 10.1093/Hmg/Ddu431 |
0.485 |
|
| 2015 |
Curtin K, Zhao Y, Hu D, Tricot GJ, Ziv E, Atanackovic D, Camp NJ. A Genome-Wide Association Study of Myeloma Survival in Utah Uncovers Germline Variants That May Influence Survival of Multiple Myeloma Patients Blood. 126: 2993-2993. DOI: 10.1182/Blood.V126.23.2993.2993 |
0.459 |
|
| 2015 |
Waller RG, Curtin K, Atanackovic D, Tricot GJ, Lipkin SM, Camp NJ. Exome Sequencing in Myeloma Pedigrees Implicates RAS1 and NOTCH Signaling Are Involved in Inherited Myeloma Risk Blood. 126: 2976-2976. DOI: 10.1182/Blood.V126.23.2976.2976 |
0.468 |
|
| 2015 |
Garner C, Glenn M, Waller RG, Rajamanickam V, Darlington T, Sargent R, Camp NJ. Disruption of the SUMO Pathway in a High-Risk B-Cell Non-Hodgkin Lymphoma Pedigree Blood. 126: 2682-2682. DOI: 10.1182/Blood.V126.23.2682.2682 |
0.468 |
|
| 2015 |
Camp NJ, Waller RG, Garner C, Tricot GJ, Tomasson M, Atanackovic D, Glenn M. Elevated Rates of Monoclonal Gammopathy in High-Risk Chronic Lymphocytic Leukemia Pedigrees Blood. 126: 1449-1449. DOI: 10.1182/Blood.V126.23.1449.1449 |
0.386 |
|
| 2015 |
Curtin K, Neumayer L, Morgan MB, Stein MA, Camp NJ, Mineau GP, Rowe KG, Buys SS. Abstract P3-07-07: Familial risk of breast density in extended Utah pedigrees Cancer Research. 75. DOI: 10.1158/1538-7445.Sabcs14-P3-07-07 |
0.368 |
|
| 2015 |
Rand KA, Song C, Dean E, Serie D, Curtin K, Hazelett D, Hwang AE, Sheng X, Stram A, Berg DJVD, Huff CA, Bernal-Mizrachi L, Tomasson MH, Ailawadhi S, Roos AD, ... ... Camp N, et al. Abstract 4629: Multiple myeloma susceptibility loci examined in African and European ancestry populations Cancer Research. 75: 4629-4629. DOI: 10.1158/1538-7445.Am2015-4629 |
0.416 |
|
| 2014 |
Darlington TM, Pimentel R, Smith K, Bakian AV, Jerominski L, Cardon J, Camp NJ, Callor WB, Grey T, Singleton M, Yandell M, Renshaw PF, Yurgelun-Todd DA, Gray D, Coon H. Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. Translational Psychiatry. 4: e471. PMID 25335167 DOI: 10.1038/Tp.2014.111 |
0.368 |
|
| 2014 |
Teerlink CC, Thibodeau SN, McDonnell SK, Schaid DJ, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, ... ... Camp NJ, et al. Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease. Human Genetics. 133: 347-56. PMID 24162621 DOI: 10.1007/S00439-013-1384-2 |
0.42 |
|
| 2014 |
Glenn MJ, Waller RG, Camp NJ. Exome Sequencing in a Family with Chronic Lymphocytic Leukemia, Mantle Cell Lymphoma and Autoimmune Disease Uncovers Potential Germline Risk-Alleles Blood. 124: 5629-5629. DOI: 10.1182/Blood.V124.21.5629.5629 |
0.459 |
|
| 2014 |
Lorenzo FR, Tashi T, Koul P, Camp NJ, Thiagarajan P, Prchal JT. Inherited Giant Platelet Disorder, Kashmiri Thrombocytopenia, a Common Syndrome Found in Srinagar, India Blood. 124: 4211-4211. DOI: 10.1182/Blood.V124.21.4211.4211 |
0.364 |
|
| 2014 |
Camp NJ, Lin W, Bigelow A, Parry MA, Mosbruger T, Burghel G, Rajamanickam V, Rigas SH, Cosby R, Connley D, Wang G, George T, Waller R, Cannon-Albright LA, Jones B, et al. Abstract 3267: Targeted DNA and RNA sequencing identifies breast cancer risk variants associated with differential expression of CASP8 and CFLAR/CASP10 Cancer Research. 74: 3267-3267. DOI: 10.1158/1538-7445.Am2014-3267 |
0.434 |
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| 2013 |
Coon H, Darlington T, Pimentel R, Smith KR, Huff CD, Hu H, Jerominski L, Hansen J, Klein M, Callor WB, Byrd J, Bakian A, Crowell SE, McMahon WM, Rajamanickam V, ... Camp NJ, et al. Genetic risk factors in two Utah pedigrees at high risk for suicide. Translational Psychiatry. 3: e325. PMID 24252905 DOI: 10.1038/Tp.2013.100 |
0.425 |
|
| 2013 |
Lin WY, Brock IW, Connley D, Cramp H, Tucker R, Slate J, Reed MW, Balasubramanian SP, Cannon-Albright LA, Camp NJ, Cox A. Associations of ATR and CHEK1 single nucleotide polymorphisms with breast cancer. Plos One. 8: e68578. PMID 23844225 DOI: 10.1371/Journal.Pone.0068578 |
0.479 |
|
| 2013 |
Berndt SI, Skibola CF, Joseph V, Camp NJ, Nieters A, Wang Z, Cozen W, Monnereau A, Wang SS, Kelly RS, Lan Q, Teras LR, Chatterjee N, Chung CC, Yeager M, et al. Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Nature Genetics. 45: 868-76. PMID 23770605 DOI: 10.1038/Ng.2652 |
0.362 |
|
| 2013 |
Slager SL, Achenbach SJ, Asmann YW, Camp NJ, Rabe KG, Goldin LR, Call TG, Shanafelt TD, Kay NE, Cunningham JM, Wang AH, Weinberg JB, Norman AD, Link BK, Leis JF, et al. Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypes. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 22: 461-6. PMID 23307532 DOI: 10.1158/1055-9965.Epi-12-1217 |
0.507 |
|
| 2013 |
Xu J, Lange EM, Lu L, Zheng SL, Wang Z, Thibodeau SN, Cannon-Albright LA, Teerlink CC, Camp NJ, Johnson AM, Zuhlke KA, Stanford JL, Ostrander EA, Wiley KE, Isaacs SD, et al. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics. 132: 5-14. PMID 23064873 DOI: 10.1007/S00439-012-1229-4 |
0.376 |
|
| 2013 |
Rand KA, Camp N, Martino A, Dean EW, Serie DJ, Edlund CK, Hu D, Curtin K, Huntsman S, Van Den Berg DJ, De Roos A, Brown EE, Giles GG, Spinelli JJ, Ailawadhi S, et al. A Meta-Analysis Of Genome-Wide Association Studies Of Multiple Myeloma In Cases and Controls Of European Origin Identifies a Risk Locus In 12q23.1 Blood. 122: 3111-3111. DOI: 10.1182/Blood.V122.21.3111.3111 |
0.498 |
|
| 2013 |
Berndt SI, Skibola CF, Joseph V, Camp NJ, Nieters A, Wang Z, Cozen W, Monnereau A, Kelly RS, Sanjose Sd, Linet MS, Riboli E, Vineis P, Hjalgrim H, Cerhan JR, et al. Abstract LB-23: Meta-analysis of genome-wide association studies identifies multiple loci associated with chronic lymphocytic leukemia. Cancer Research. 73. DOI: 10.1158/1538-7445.Am2013-Lb-23 |
0.431 |
|
| 2012 |
Cai Z, Thomas A, Teerlink C, Farnham JM, Cannon-Albright LA, Camp NJ. Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees. Bmc Genomics. 13: 676. PMID 23190577 DOI: 10.1186/1471-2164-13-676 |
0.435 |
|
| 2012 |
Arrington CB, Bleyl SB, Matsunami N, Bowles NE, Leppert TI, Demarest BL, Osborne K, Yoder BA, Byrne JL, Schiffman JD, Null DM, DiGeronimo R, Rollins M, Faix R, Comstock J, ... Camp NJ, et al. A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia. American Journal of Medical Genetics. Part A. 158: 3137-47. PMID 23165927 DOI: 10.1002/Ajmg.A.35664 |
0.424 |
|
| 2012 |
Slager SL, Camp NJ, Conde L, Shanafelt TD, Achenbach SJ, Rabe KG, Kay NE, Novak AJ, Call TG, Bracci PM, Sille FM, Sanchez S, Akers NK, Cunningham JM, Serie DJ, et al. Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes. British Journal of Haematology. 159: 572-6. PMID 23025533 DOI: 10.1111/Bjh.12070 |
0.45 |
|
| 2012 |
Knight S, Abo RP, Abel HJ, Neklason DW, Tuohy TM, Burt RW, Thomas A, Camp NJ. Shared genomic segment analysis: the power to find rare disease variants. Annals of Human Genetics. 76: 500-9. PMID 22989048 DOI: 10.1111/J.1469-1809.2012.00728.X |
0.71 |
|
| 2012 |
Bailey-Wilson JE, Childs EJ, Cropp CD, Schaid DJ, Xu J, Camp NJ, Cannon-Albright LA, Farnham JM, George A, Powell I, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, et al. Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families. Bmc Medical Genetics. 13: 46. PMID 22712434 DOI: 10.1186/1471-2350-13-46 |
0.409 |
|
| 2012 |
Slager SL, Skibola CF, Di Bernardo MC, Conde L, Broderick P, McDonnell SK, Goldin LR, Croft N, Holroyd A, Harris S, Riby J, Serie DJ, Kay NE, Call TG, Bracci PM, ... ... Camp NJ, et al. Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. Blood. 120: 843-6. PMID 22700719 DOI: 10.1182/Blood-2012-03-413591 |
0.458 |
|
| 2012 |
Jin G, Lu L, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Cannon-Albright LA, Camp NJ, Teerlink CC, Fitzgerald LM, Stanford JL, Wiley KE, Isaacs SD, Walsh PC, Foulkes WD, et al. Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics. 131: 1095-103. PMID 22198737 DOI: 10.1007/S00439-011-1136-0 |
0.46 |
|
| 2012 |
Camp NJ, Parry M, Knight S, Abo R, Elliott G, Rigas SH, Balasubramanian SP, Reed MW, McBurney H, Latif A, Newman WG, Cannon-Albright LA, Evans DG, Cox A. Fine-mapping CASP8 risk variants in breast cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 176-81. PMID 22056502 DOI: 10.1158/1055-9965.Epi-11-0845 |
0.732 |
|
| 2012 |
Campa D, Butterbach K, Slager SL, Skibola CF, de Sanjosé S, Benavente Y, Becker N, Foretova L, Maynadie M, Cocco P, Staines A, Kaaks R, Boffetta P, Brennan P, Conde L, ... ... Camp NJ, et al. A comprehensive study of polymorphisms in the ABCB1, ABCC2, ABCG2, NR1I2 genes and lymphoma risk. International Journal of Cancer. Journal International Du Cancer. 131: 803-12. PMID 21918980 DOI: 10.1002/Ijc.26436 |
0.438 |
|
| 2012 |
Lu L, Cancel-Tassin G, Valeri A, Cussenot O, Lange EM, Cooney KA, Farnham JM, Camp NJ, Cannon-Albright LA, Tammela TL, Schleutker J, Hoegel J, Herkommer K, Maier C, Vogel W, et al. Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG. The Prostate. 72: 410-26. PMID 21748754 DOI: 10.1002/Pros.21443 |
0.435 |
|
| 2012 |
Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L. A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Human Genetics. 131: 77-85. PMID 21706340 DOI: 10.1007/S00439-011-1048-Z |
0.711 |
|
| 2011 |
Cai Z, Knight S, Thomas A, Camp NJ. Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data. Bmc Proceedings. 5: S9. PMID 22373081 DOI: 10.1186/1753-6561-5-S9-S9 |
0.479 |
|
| 2011 |
Carlquist JF, McKinney JT, Horne BD, Camp NJ, Cannon-Albright L, Muhlestein JB, Hopkins P, Clarke JL, Mower CP, Park JJ, Nicholas ZP, Huntinghouse JA, Anderson JL. Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids. Journal of Clinical & Experimental Cardiology. 2. PMID 22229114 DOI: 10.4172/2155-9880.1000138 |
0.603 |
|
| 2011 |
Lin WY, Camp NJ, Cannon-Albright LA, Allen-Brady K, Balasubramanian S, Reed MW, Hopper JL, Apicella C, Giles GG, Southey MC, Milne RL, Arias-Pérez JI, Menéndez-Rodríguez P, Benítez J, Grundmann M, et al. A role for XRCC2 gene polymorphisms in breast cancer risk and survival. Journal of Medical Genetics. 48: 477-84. PMID 21632523 DOI: 10.1136/Jmedgenet-2011-100018 |
0.672 |
|
| 2011 |
Catalona WJ, Bailey-Wilson JE, Camp NJ, Chanock SJ, Cooney KA, Easton DF, Eeles RA, FitzGerald LM, Freedman ML, Gudmundsson J, Kittles RA, Margulies EH, McGuire BB, Ostrander EA, Rebbeck TR, et al. National Cancer Institute Prostate Cancer Genetics Workshop. Cancer Research. 71: 3442-6. PMID 21558387 DOI: 10.1158/0008-5472.Can-11-0314 |
0.384 |
|
| 2011 |
Knight S, Camp NJ. Validity and power of association testing in family-based sampling designs: evidence for and against the common wisdom. Genetic Epidemiology. 35: 174-81. PMID 21328615 DOI: 10.1002/Gepi.20565 |
0.329 |
|
| 2011 |
Cai Z, Camp NJ, Cannon-Albright L, Thomas A. Identification of regions of positive selection using Shared Genomic Segment analysis. European Journal of Human Genetics : Ejhg. 19: 667-71. PMID 21304558 DOI: 10.1038/Ejhg.2010.257 |
0.361 |
|
| 2011 |
Curtin K, Camp NJ. Fine-scale structure of the genome and markers used in association mapping. Methods in Molecular Biology (Clifton, N.J.). 713: 71-88. PMID 21153612 DOI: 10.1007/978-1-60327-416-6_6 |
0.465 |
|
| 2011 |
Allen-Brady K, Camp NJ. Genetic distance and markers used in linkage mapping. Methods in Molecular Biology (Clifton, N.J.). 713: 43-53. PMID 21153610 DOI: 10.1007/978-1-60327-416-6_4 |
0.646 |
|
| 2011 |
Slager SL, Rabe KG, Achenbach SJ, Vachon CM, Goldin LR, Strom SS, Lanasa MC, Spector LG, Rassenti LZ, Leis JF, Camp NJ, Glenn M, Kay NE, Cunningham JM, Hanson CA, et al. Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. Blood. 117: 1911-6. PMID 21131588 DOI: 10.1182/Blood-2010-09-308205 |
0.465 |
|
| 2011 |
Abo R, Knight S, Thomas A, Camp NJ. Automated construction and testing of multi-locus gene-gene associations. Bioinformatics (Oxford, England). 27: 134-6. PMID 21076150 DOI: 10.1093/Bioinformatics/Btq616 |
0.709 |
|
| 2011 |
Andreotti G, Benhaim-Luzon V, Brennan P, Sanjose Sd, Caudet LC, Costantini AS, Cocco P, Becker N, Foretova L, Maynadie M, Nieters A, Birmann B, Staines A, Miliken K, Weisenburger D, ... ... Camp N, et al. Abstract B115: A pooled analysis of smoking and alcohol drinking and risk of multiple myeloma in the International Multiple Myeloma Consortium Cancer Prevention Research. 4. DOI: 10.1158/1940-6207.Prev-11-B115 |
0.314 |
|
| 2010 |
Abo R, Wong J, Thomas A, Camp NJ. Haplotype association analyses in resources of mixed structure using Monte Carlo testing. Bmc Bioinformatics. 11: 592. PMID 21143908 DOI: 10.1186/1471-2105-11-592 |
0.735 |
|
| 2010 |
Goldin LR, Lanasa MC, Slager SL, Cerhan JR, Vachon CM, Strom SS, Camp NJ, Spector LG, Leis JF, Morrison VA, Glenn M, Rabe KG, Achenbach SJ, Algood SD, Abbasi F, et al. Common occurrence of monoclonal B-cell lymphocytosis among members of high-risk CLL families. British Journal of Haematology. 151: 152-8. PMID 20738309 DOI: 10.1111/J.1365-2141.2010.08339.X |
0.316 |
|
| 2010 |
Anderson JL, Horne BD, Camp NJ, Muhlestein JB, Hopkins PN, Cannon-Albright LA, Mower CP, Park JJ, Clarke JL, Nicholas ZP, McKinney JT, Carlquist JF. Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery disease. American Heart Journal. 160: 250-256.e3. PMID 20691829 DOI: 10.1016/J.Ahj.2010.05.031 |
0.571 |
|
| 2010 |
Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM. Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Molecular Autism. 1: 8. PMID 20678250 DOI: 10.1186/2040-2392-1-8 |
0.606 |
|
| 2010 |
Conde L, Halperin E, Akers NK, Brown KM, Smedby KE, Rothman N, Nieters A, Slager SL, Brooks-Wilson A, Agana L, Riby J, Liu J, Adami HO, Darabi H, Hjalgrim H, ... ... Camp NJ, et al. Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Nature Genetics. 42: 661-4. PMID 20639881 DOI: 10.1038/Ng.626 |
0.413 |
|
| 2010 |
Christensen GB, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, Eeles R, Easton D, ... ... Camp NJ, et al. Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses. The Prostate. 70: 735-44. PMID 20333727 DOI: 10.1002/Pros.21106 |
0.444 |
|
| 2010 |
Slager SL, Goldin LR, Strom SS, Lanasa MC, Spector LG, Rassenti L, Leis JF, Camp NJ, Kay NE, Vachon CM, Glenn M, Weinberg JB, Rabe KG, Cunningham JM, Achenbach SJ, et al. Genetic susceptibility variants for chronic lymphocytic leukemia. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 1098-102. PMID 20332261 DOI: 10.1158/1055-9965.Epi-09-1217 |
0.409 |
|
| 2010 |
Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Santangelo S, Stewart SE, Scharf J, et al. Linkage analysis of Tourette syndrome in a large Utah pedigree American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 656-662. PMID 19777563 DOI: 10.1002/Ajmg.B.31035 |
0.375 |
|
| 2010 |
Christensen GB, Knight S, Camp NJ. The sumLINK statistic for genetic linkage analysis in the presence of heterogeneity. Genetic Epidemiology. 33: 628-36. PMID 19217022 DOI: 10.1002/Gepi.20414 |
0.448 |
|
| 2010 |
Rigas S, Parry M, Reed M, Camp N, Cox A. Assessing the functional role of caspase-8 gene variants in breast cancer Breast Cancer Research. 12: 24. DOI: 10.1186/Bcr2521 |
0.356 |
|
| 2010 |
Felipe RLV, Curtin K, Camp N, Prchal JT. Genetic Investigation by Shared Genomic Segment and Linkage Study of a Unique Family with Primary Familial and Congenital Polycythemia Blood. 116: 4783-4783. DOI: 10.1182/Blood.V116.21.4783.4783 |
0.479 |
|
| 2010 |
Slager S, Rabe K, Achenbach S, Vachon C, Goldin L, Strom S, Lanasa MC, Spector LG, Rassenti LZ, Leis J, Camp N, Glenn M, Kay NE, Cunningham JM, Hanson CA, et al. Investigation of CLL-Susceptibility Loci with Monoclonal B-Cell Lymphocytosis (MBL) Risk and Confirmation of Recently Reported CLL-Susceptibility Loci Blood. 116: 2443-2443. DOI: 10.1182/Blood.V116.21.2443.2443 |
0.449 |
|
| 2010 |
Abo RP, Parry M, Rigas SH, Cox A, Camp NJ. Abstract 2844: Association of genetic variants in TNFRSF10B and breast cancer Cancer Research. 70: 2844-2844. DOI: 10.1158/1538-7445.Am10-2844 |
0.754 |
|
| 2010 |
Parry M, Elliott G, Abo R, Camp NJ, Neal DE, Donovan JL, Hamdy FC, Cox A. Abstract 2843: Caspase-8 gene SNPs in prostate cancer susceptibility: a replication study Cancer Research. 70: 2843-2843. DOI: 10.1158/1538-7445.Am10-2843 |
0.716 |
|
| 2009 |
Piccolo SR, Abo RP, Allen-Brady K, Camp NJ, Knight S, Anderson JL, Horne BD. Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study. Bmc Proceedings. 3: S46. PMID 20018038 DOI: 10.1186/1753-6561-3-S7-S46 |
0.774 |
|
| 2009 |
Knight S, Abo RP, Wong J, Thomas A, Camp NJ. Pedigree association: assigning individual weights to pedigree members for genetic association analysis. Bmc Proceedings. 3: S121. PMID 20017987 DOI: 10.1186/1753-6561-3-S7-S121 |
0.673 |
|
| 2009 |
Curtin K, Lin WY, George R, Katory M, Shorto J, Cannon-Albright LA, Smith G, Bishop DT, Cox A, Camp NJ. Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 2476-84. PMID 19690184 DOI: 10.1158/1055-9965.Epi-09-0187 |
0.452 |
|
| 2009 |
Cao TM, Lazzeroni LC, Tsai S, Pang WW, Kao A, Camp NJ, Thomas A, Shizuru JA. Identification of a major susceptibility locus for lethal graft-versus-host disease in MHC-matched mice. Journal of Immunology (Baltimore, Md. : 1950). 183: 462-9. PMID 19525392 DOI: 10.4049/Jimmunol.0900454 |
0.352 |
|
| 2009 |
Allen-Brady K, Farnham JM, Camp NJ, Karlins E, Ostrander EA, Cannon-Albright LA. No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. Bmc Research Notes. 2: 94. PMID 19476645 DOI: 10.1186/1756-0500-2-94 |
0.643 |
|
| 2009 |
Gaudet MM, Milne RL, Cox A, Camp NJ, Goode EL, Humphreys MK, Dunning AM, Morrison J, Giles GG, Severi G, Baglietto L, English DR, Couch FJ, Olson JE, Wang X, et al. Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 1610-6. PMID 19423537 DOI: 10.1158/1055-9965.Epi-08-0745 |
0.696 |
|
| 2009 |
Camp NJ, Farnham JM, Wong J, Christensen GB, Thomas A, Cannon-Albright LA. Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 1290-4. PMID 19336566 DOI: 10.1158/1055-9965.Epi-08-0327 |
0.45 |
|
| 2009 |
Shephard ND, Abo R, Rigas SH, Frank B, Lin WY, Brock IW, Shippen A, Balasubramanian SP, Reed MW, Bartram CR, Meindl A, Schmutzler RK, Engel C, Burwinkel B, Cannon-Albright LA, ... ... Camp NJ, et al. A breast cancer risk haplotype in the caspase-8 gene. Cancer Research. 69: 2724-8. PMID 19318553 DOI: 10.1158/0008-5472.Can-08-4266 |
0.8 |
|
| 2009 |
Curtin K, Lin WY, George R, Katory M, Shorto J, Cannon-Albright LA, Bishop DT, Cox A, Camp NJ. Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 616-21. PMID 19155440 DOI: 10.1158/1055-9965.Epi-08-0690 |
0.433 |
|
| 2009 |
Curtin K, Iles MM, Camp NJ. Identifying rarer genetic variants for common complex diseases: Diseased versus neutral discovery panels Annals of Human Genetics. 73: 54-60. PMID 19132978 DOI: 10.1111/J.1469-1809.2008.00483.X |
0.437 |
|
| 2009 |
Teerlink CC, Camp NJ, Bansal A, Crapo R, Hughes D, Kort E, Rowe K, Cannon-Albright LA. Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource. European Journal of Human Genetics : Ejhg. 17: 636-43. PMID 19092775 DOI: 10.1038/Ejhg.2008.236 |
0.361 |
|
| 2009 |
Lanasa MC, Allgood SD, Slager SL, Camp NJ, Kay NE, Spector LG, Rassenti LZ, Hanson CA, Gockerman JP, Goodman BK, Strom SS, Call TG, Cerhan JR, Leis J, Marti G, et al. Family-Associated Monoclonal B Lymphocytosis Shows Differences From CLL That Suggest An Indolent Biology. Blood. 114: 1241-1241. DOI: 10.1182/Blood.V114.22.1241.1241 |
0.319 |
|
| 2009 |
Goldin LR, Lanasa MC, Slager SL, Strom SS, Camp NJ, Cerhan JR, Spector LG, Leis JF, Morrison VA, Rassenti LZ, Rabe K, Fontaine L, Allgood SD, Abbasi F, Kay NE, et al. Monoclonal B-Cell Lymphocytosis Is Commonly Observed Among Unaffected Members of High Risk CLL Families. Blood. 114: 1232-1232. DOI: 10.1182/Blood.V114.22.1232.1232 |
0.358 |
|
| 2008 |
Anderson JL, Horne BD, Kolek MJ, Muhlestein JB, Mower CP, Park JJ, May HT, Camp NJ, Carlquist JF. Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility. American Heart Journal. 156: 1155-1162.e2. PMID 19033013 DOI: 10.1016/J.Ahj.2008.07.006 |
0.514 |
|
| 2008 |
Piccolo SR, Camp N, Frey LJ. Polygenic model for predicting breast cancer risk via genome-wide polymorphisms Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 1094. PMID 18999159 |
0.335 |
|
| 2008 |
Abo R, Knight S, Wong J, Cox A, Camp NJ. hapConstructor: automatic construction and testing of haplotypes in a Monte Carlo framework. Bioinformatics (Oxford, England). 24: 2105-7. PMID 18653522 DOI: 10.1093/Bioinformatics/Btn359 |
0.717 |
|
| 2008 |
Rausch T, Thomas A, Camp NJ, Cannon-Albright LA, Facelli JC. A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease. Computers in Biology and Medicine. 38: 826-36. PMID 18547558 DOI: 10.1016/J.Compbiomed.2008.04.011 |
0.397 |
|
| 2008 |
Gibbs D, Yang Z, Constantine R, Ma X, Camp NJ, Yang X, Chen H, Jorgenson A, Hau V, Dewan A, Zeng J, Harmon J, Buehler J, Brand JM, Hoh J, et al. Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration. Vision Research. 48: 685-9. PMID 18207215 DOI: 10.1016/J.Visres.2007.10.022 |
0.468 |
|
| 2008 |
Thomas A, Camp NJ, Farnham JM, Allen-brady K, Cannon-albright LA. Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays Annals of Human Genetics. 72: 279-287. PMID 18093282 DOI: 10.1111/J.1469-1809.2007.00406.X |
0.714 |
|
| 2008 |
Shephard N, Brock I, Camp N, Canon-Albright L, Frank B, Burwinkel B, Cox A. Multicentre study of CASP8 polymorphisms in breast cancer Breast Cancer Research. 10: 51. DOI: 10.1186/Bcr1935 |
0.499 |
|
| 2007 |
Christensen GB, Cannon-Albright LA, Thomas A, Camp NJ. Extracting disease risk profiles from expression data for linkage analysis: application to prostate cancer. Bmc Proceedings. 1: S82. PMID 18466585 DOI: 10.1186/1753-6561-1-S1-S82 |
0.447 |
|
| 2007 |
Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A. Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. Bmc Proceedings. 1: S160. PMID 18466506 DOI: 10.1186/1753-6561-1-S1-S160 |
0.738 |
|
| 2007 |
Curtin K, Wong J, Allen-Brady K, Camp NJ. Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1. Bmc Proceedings. 1: S12. PMID 18466461 DOI: 10.1186/1753-6561-1-S1-S12 |
0.721 |
|
| 2007 |
Curtin K, Wong J, Allen-Brady K, Camp NJ. PedGenie: meta genetic association testing in mixed family and case-control designs. Bmc Bioinformatics. 8: 448. PMID 18005446 DOI: 10.1186/1471-2105-8-448 |
0.676 |
|
| 2007 |
Horne BD, Camp NJ, Carlquist JF, Muhlestein JB, Kolek MJ, Nicholas ZP, Anderson JL. Multiple-polymorphism associations of 7 matrix metalloproteinase and tissue inhibitor metalloproteinase genes with myocardial infarction and angiographic coronary artery disease. American Heart Journal. 154: 751-8. PMID 17893005 DOI: 10.1016/J.Ahj.2007.06.030 |
0.51 |
|
| 2007 |
Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA. Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. The Prostate. 67: 1456-64. PMID 17654497 DOI: 10.1002/Pros.20631 |
0.686 |
|
| 2007 |
Zintzaras E, Kitsios G, Kent D, Camp NJ, Atwood L, Hopkins PN, Hunt SC. Genome-wide scans meta-analysis for pulse pressure. Hypertension. 50: 557-64. PMID 17635856 DOI: 10.1161/Hypertensionaha.107.090316 |
0.343 |
|
| 2007 |
Horne BD, Camp NJ, Anderson JL, Mower CP, Clarke JL, Kolek MJ, Carlquist JF. Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease. Journal of the American College of Cardiology. 49: 2053-60. PMID 17512363 DOI: 10.1016/J.Jacc.2007.02.039 |
0.542 |
|
| 2007 |
Camp NJ, Cannon-Albright LA, Farnham JM, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, et al. Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics. Human Molecular Genetics. 16: 1271-8. PMID 17478474 DOI: 10.1093/Hmg/Ddm075 |
0.413 |
|
| 2007 |
Christensen GB, Camp NJ, Farnham JM, Cannon-Albright LA. Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees Prostate. 67: 605-613. PMID 17299800 DOI: 10.1002/Pros.20554 |
0.42 |
|
| 2006 |
Yang Z, Camp NJ, Sun H, Tong Z, Gibbs D, Cameron DJ, Chen H, Zhao Y, Pearson E, Li X, Chien J, Dewan A, Harmon J, Bernstein PS, Shridhar V, et al. A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science (New York, N.Y.). 314: 992-3. PMID 17053109 DOI: 10.1126/Science.1133811 |
0.443 |
|
| 2006 |
Camp NJ, Farnham JM, Cannon-Albright LA. Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees. Cancer Research. 66: 10205-12. PMID 17047086 DOI: 10.1158/0008-5472.Can-06-1233 |
0.409 |
|
| 2006 |
Horne BD, Camp NJ, Muhlestein JB, Cannon-Albright LA. Identification of excess clustering of coronary heart diseases among extended pedigrees in a genealogical population database. American Heart Journal. 152: 305-11. PMID 16875915 DOI: 10.1016/J.Ahj.2005.12.028 |
0.457 |
|
| 2006 |
Allen-Brady K, Cannon-Albright LA, Neuhausen SL, Camp NJ. A role for XRCC4 in age at diagnosis and breast cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 1306-10. PMID 16835328 DOI: 10.1158/1055-9965.Epi-05-0959 |
0.694 |
|
| 2006 |
Horne BD, Carlquist JF, Cannon-Albright LA, Muhlestein JB, McKinney JT, Kolek MJ, Clarke JL, Anderson JL, Camp NJ. High-resolution characterization of linkage disequilibrium structure and selection of tagging single nucleotide polymorphisms: application to the cholesteryl ester transfer protein gene. Annals of Human Genetics. 70: 524-34. PMID 16759183 DOI: 10.1111/J.1469-1809.2005.00244.X |
0.598 |
|
| 2006 |
Allen-Brady K, Wong J, Camp NJ. PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. Bmc Bioinformatics. 7: 209. PMID 16620382 DOI: 10.1186/1471-2105-7-209 |
0.713 |
|
| 2006 |
Thomas A, Camp NJ. Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting. Bioinformatics (Oxford, England). 22: 771-2. PMID 16410318 DOI: 10.1093/Bioinformatics/Btk049 |
0.302 |
|
| 2005 |
Coon H, Matsunami N, Stevens J, Miller J, Pingree C, Camp NJ, Thomas A, Krasny L, Lainhart J, Leppert MF, McMahon W. Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree. Human Heredity. 60: 220-6. PMID 16391490 DOI: 10.1159/000090546 |
0.361 |
|
| 2005 |
Cannon-Albright LA, Farnham JM, Thomas A, Camp NJ. Identification and study of Utah pseudo-isolate populations - Prospects for gene identification American Journal of Medical Genetics. 137: 269-275. PMID 16096997 DOI: 10.1002/Ajmg.A.30893 |
0.303 |
|
| 2005 |
Allen-Brady K, Camp NJ. Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes. Bmc Cancer. 5: 99. PMID 16091150 DOI: 10.1186/1471-2407-5-99 |
0.713 |
|
| 2005 |
Camp NJ, Farnham JM, Cannon Albright LA. Genomic search for prostate cancer predisposition loci in Utah pedigrees. The Prostate. 65: 365-74. PMID 16037989 DOI: 10.1002/Pros.20287 |
0.42 |
|
| 2005 |
Xu J, Dimitrov L, Chang BL, Adams TS, Turner AR, Meyers DA, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Bishop T, ... ... Camp NJ, et al. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. American Journal of Human Genetics. 77: 219-29. PMID 15988677 DOI: 10.1086/432377 |
0.419 |
|
| 2005 |
Allen-Brady K, Camp NJ, Ward JH, Cannon-Albright LA. Lobular breast cancer: excess familiality observed in the Utah Population Database. International Journal of Cancer. 117: 655-61. PMID 15929077 DOI: 10.1002/Ijc.21236 |
0.685 |
|
| 2005 |
Berthelemy-Okazaki N, Zhao Y, Yang Z, Camp NJ, Farnham J, Parker D, Tsuruda J, Macdonald J, Zhang K, Cannon-Albright LA. Examination of ELN as a candidate gene in the Utah intracranial aneurysm pedigrees. Stroke; a Journal of Cerebral Circulation. 36: 1283-4. PMID 15890991 DOI: 10.1161/01.Str.0000166198.05439.F8 |
0.402 |
|
| 2005 |
Camp NJ, Lowry MR, Richards RL, Plenk AM, Carter C, Hensel CH, Abkevich V, Skolnick MH, Shattuck D, Rowe KG, Hughes DC, Cannon-Albright LA. Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 85-93. PMID 15806581 DOI: 10.1002/Ajmg.B.30177 |
0.324 |
|
| 2005 |
Camp NJ, Cannon-Albright LA. Dissecting the genetic etiology of major depressive disorder using linkage analysis. Trends in Molecular Medicine. 11: 138-44. PMID 15760772 DOI: 10.1016/J.Molmed.2005.01.002 |
0.347 |
|
| 2005 |
Albright LA, Schwab A, Camp NJ, Farnham JS, Thomas A. Population-based risk assessment for other cancers in relatives of hereditary prostate cancer (HPC) cases. The Prostate. 64: 347-55. PMID 15754348 DOI: 10.1002/Pros.20248 |
0.337 |
|
| 2005 |
Horne BD, Anderson JL, Carlquist JF, Muhlestein JB, Renlund DG, Bair TL, Pearson RR, Camp NJ. Generating genetic risk scores from intermediate phenotypes for use in association studies of clinically significant endpoints. Annals of Human Genetics. 69: 176-86. PMID 15720299 DOI: 10.1046/J.1529-8817.2005.00155.X |
0.603 |
|
| 2005 |
Camp NJ, Swensen J, Horne BD, Farnham JM, Thomas A, Cannon-Albright LA, Tavtigian SV. Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer. Genetic Epidemiology. 28: 232-43. PMID 15593091 DOI: 10.1002/Gepi.20054 |
0.625 |
|
| 2005 |
Farnham JM, Camp NJ, Swensen J, Tavtigian SV, Albright LA. Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees. Human Genetics. 116: 179-85. PMID 15592687 DOI: 10.1007/S00439-004-1220-9 |
0.403 |
|
| 2005 |
Horne BD, Anderson JL, Carlquist JF, Muhlestein JB, Renlund DG, Bair TL, Pearson RR, Camp NJ. Generating Genetic Risk Scores from Intermediate Phenotypes for Use in Association Studies of Clinically Significant Endpoints: Genetic Risk Scores & Clinical Endpoints Annals of Human Genetics. 69: 176-186. DOI: 10.1046/J.1469-1809.2005.00155.X |
0.542 |
|
| 2004 |
Horne BD, Camp NJ, Muhlestein JB, Cannon-Albright LA. Evidence for a heritable component in death resulting from aortic and mitral valve diseases. Circulation. 110: 3143-8. PMID 15520309 DOI: 10.1161/01.Cir.0000147189.85636.C3 |
0.467 |
|
| 2004 |
Hasstedt SJ, Camp NJ, Hopkins PN, Coon H, McKinney JT, Cawthon RM, Hunt SC. Model-fitting and linkage analysis of sodium-lithium countertransport. European Journal of Human Genetics : Ejhg. 12: 1055-61. PMID 15383825 DOI: 10.1038/Sj.Ejhg.5201262 |
0.401 |
|
| 2004 |
Hunt SC, Coon H, Hasstedt SJ, Cawthon RM, Camp NJ, Wu LL, Hopkins PN. Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. American Journal of Hypertension. 17: 511-5. PMID 15177524 DOI: 10.1016/J.Amjhyper.2004.02.019 |
0.323 |
|
| 2004 |
Thomas A, Camp NJ. Graphical modeling of the joint distribution of alleles at associated loci. American Journal of Human Genetics. 74: 1088-101. PMID 15114533 DOI: 10.1086/421249 |
0.41 |
|
| 2004 |
Horne BD, Camp NJ. Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation. Genetic Epidemiology. 26: 11-21. PMID 14691953 DOI: 10.1002/Gepi.10292 |
0.59 |
|
| 2004 |
Farnham JM, Camp NJ, Neuhausen SL, Tsuruda J, Parker D, MacDonald J, Cannon-Albright LA. Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm. Human Genetics. 114: 250-5. PMID 14605871 DOI: 10.1007/S00439-003-1044-Z |
0.399 |
|
| 2003 |
Horne BD, Malhotra A, Camp NJ. Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study. Bmc Genetics. 4: S93. PMID 14975161 DOI: 10.1186/1471-2156-4-S1-S93 |
0.521 |
|
| 2003 |
Allen-Brady K, Farnham JM, Weiler J, Camp NJ. A cautionary note on the appropriateness of using a linkage resource for an association study. Bmc Genetics. 4: S89. PMID 14975157 DOI: 10.1186/1471-2156-4-S1-S89 |
0.69 |
|
| 2003 |
Goldin LR, Camp NJ, Keen KJ, Martin LJ, Moslehi R, Ghosh S, North KE, Wyszynski DF, Blacker D. Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13. Genetic Epidemiology. 25: S78-89. PMID 14635173 DOI: 10.1002/Gepi.10288 |
0.389 |
|
| 2003 |
Abkevich V, Camp NJ, Hensel CH, Neff CD, Russell DL, Hughes DC, Plenk AM, Lowry MR, Richards RL, Carter C, Frech GC, Stone S, Rowe K, Chau CA, Cortado K, et al. Predisposition locus for major depression at chromosome 12q22-12q23.2. American Journal of Human Genetics. 73: 1271-81. PMID 14606042 DOI: 10.1086/379978 |
0.343 |
|
| 2003 |
Cannon Albright LA, Camp NJ, Farnham JM, MacDonald J, Abtin K, Rowe KG. A genealogical assessment of heritable predisposition to aneurysms. Journal of Neurosurgery. 99: 637-43. PMID 14567597 DOI: 10.3171/Jns.2003.99.4.0637 |
0.31 |
|
| 2003 |
Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC. Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees. Hypertension. 42: 322-8. PMID 12874090 DOI: 10.1161/01.Hyp.0000084874.85653.46 |
0.307 |
|
| 2002 |
Fujiwara H, Emi M, Nagai H, Nishimura T, Konishi N, Kubota Y, Ichikawa T, Takahashi S, Shuin T, Habuchi T, Ogawa O, Inoue K, Skolnick MH, Swensen J, Camp NJ, et al. Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series. Journal of Human Genetics. 47: 641-8. PMID 12522685 DOI: 10.1007/S100380200099 |
0.415 |
|
| 2002 |
Camp NJ, Tavtigian SV. Meta-analysis of associations of the Ser217Leu and Ala541Thr variants in ELAC2 (HPC2) and prostate cancer. American Journal of Human Genetics. 71: 1475-8. PMID 12515253 DOI: 10.1086/344516 |
0.355 |
|
| 2002 |
Camp NJ, Slattery ML. Classification tree analysis: a statistical tool to investigate risk factor interactions with an example for colon cancer (United States). Cancer Causes & Control : Ccc. 13: 813-23. PMID 12462546 DOI: 10.1023/A:1020611416907 |
0.358 |
|
| 2002 |
Ray KK, Camp NJ, Bennett CE, Francis SE, Crossman DC. Genetic variation at the interleukin-1 locus is a determinant of changes in soluble endothelial factors in patients with acute coronary syndromes. Clinical Science (London, England : 1979). 103: 303-10. PMID 12193156 DOI: 10.1042/Cs1030303 |
0.309 |
|
| 2002 |
Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ. Genome-wide linkage analysis for celiac disease in North American families. American Journal of Medical Genetics. 111: 1-9. PMID 12124726 DOI: 10.1002/Ajmg.10527 |
0.404 |
|
| 2002 |
Neuhausen SL, Weizman Z, Camp NJ, Elbedour K, Sheffield VC, Zone JJ, Carmi R. HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease. Human Immunology. 63: 502-7. PMID 12039527 DOI: 10.1016/S0198-8859(02)00395-6 |
0.381 |
|
| 2001 |
Camp NJ, Farnham JM. Correcting for multiple analyses in genomewide linkage studies Annals of Human Genetics. 65: 577-582. PMID 11851987 DOI: 10.1046/J.1469-1809.2001.6560577.X |
0.37 |
|
| 2001 |
Gutin A, Abkevich V, Camp NJ, Farnham JM, Cannon-Albright L, Thomas A. Allelic association in large pedigrees Genetic Epidemiology. 21: S571-S575. PMID 11793740 DOI: 10.1002/Gepi.2001.21.S1.S571 |
0.421 |
|
| 2001 |
Abkevich V, Camp NJ, Gutin A, Farnham JM, Cannon-Albright L, Thomas A. A robust multipoint linkage statistic (tlod) for mapping complex trait loci Genetic Epidemiology. 21: S492-S497. PMID 11793725 DOI: 10.1002/Gepi.2001.21.S1.S492 |
0.423 |
|
| 2001 |
Camp NJ, Gutin A, Abkevich V, Farnham JM, Cannon-Albright L, Thomas A. A new nonparametric linkage statistic for mapping both qualitative and quantitative trait loci Genetic Epidemiology. 21: S461-S466. PMID 11793719 DOI: 10.1002/Gepi.2001.21.S1.S461 |
0.424 |
|
| 2001 |
Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M. Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method. American Journal of Human Genetics. 69: 1278-89. PMID 11668428 DOI: 10.1086/324590 |
0.388 |
|
| 2001 |
Francis SE, Camp NJ, Burton AJ, Dewberry RM, Gunn J, Stephens-Lloyd A, Cumberland DC, Gershlick A, Crossman DC. Interleukin 1 receptor antagonist; gene polymorphism and restenosis after coronary angioplasty Heart. 86: 336-340. PMID 11514491 DOI: 10.1136/Heart.86.3.336 |
0.315 |
|
| 2001 |
Carter MJ, di Giovine FS, Jones S, Mee J, Camp NJ, Lobo AJ, Duff GW. Association of the interleukin 1 receptor antagonist gene with ulcerative colitis in Northern European Caucasians. Gut. 48: 461-7. PMID 11247888 DOI: 10.1136/Gut.48.4.461 |
0.388 |
|
| 2001 |
Tavtigian SV, Simard J, Teng DH, Abtin V, Baumgard M, Beck A, Camp NJ, Carillo AR, Chen Y, Dayananth P, Desrochers M, Dumont M, Farnham JM, Frank D, Frye C, et al. A candidate prostate cancer susceptibility gene at chromosome 17p. Nature Genetics. 27: 172-80. PMID 11175785 DOI: 10.1038/84808 |
0.42 |
|
| 2000 |
Read RC, Camp NJ, di Giovine FS, Borrow R, Kaczmarski EB, Chaudhary AG, Fox AJ, Duff GW. An interleukin-1 genotype is associated with fatal outcome of meningococcal disease. The Journal of Infectious Diseases. 182: 1557-60. PMID 11023482 DOI: 10.1086/315889 |
0.384 |
|
| 2000 |
Camp NJ, Bansal A. A low density genome-wide search for loci involved in alcohol dependence using the transmission/disequilibrium test, sib-TDT, and two combined tests. Genetic Epidemiology. S85-90. PMID 10597417 DOI: 10.1002/Gepi.1370170715 |
0.372 |
|
| 2000 |
Cox A, Camp NJ, Cannings C, di Giovine FS, Dale M, Worthington J, John S, Ollier WE, Silman AJ, Duff GW. Combined sib-TDT and TDT provide evidence for linkage of the interleukin-1 gene cluster to erosive rheumatoid arthritis. Human Molecular Genetics. 8: 1707-13. PMID 10441334 DOI: 10.1093/Hmg/8.9.1707 |
0.361 |
|
| 1999 |
Gordon MA, Oppenheim E, Camp NJ, di Giovine FS, Duff GW, Gleeson D. Primary biliary cirrhosis shows association with genetic polymorphism of tumour necrosis factor alpha promoter region. Journal of Hepatology. 31: 242-7. PMID 10453936 DOI: 10.1016/S0168-8278(99)80220-7 |
0.42 |
|
| 1999 |
Tazi Ahnini R, Camp NJ, Cork MJ, Mee JB, Keohane SG, Duff GW, di Giovine FS. Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis. Human Molecular Genetics. 8: 1135-40. PMID 10332047 DOI: 10.1093/Hmg/8.6.1135 |
0.419 |
|
| 1999 |
Camp N, Cannings C, Sheehan N. The number of genotypic assignments on a genealogy II. Further results for linear systems Mathematical Medicine and Biology: a Journal of the Ima. 16: 213-236. DOI: 10.1093/Imammb/16.3.213 |
0.334 |
|
| 1998 |
Cox A, Camp NJ, Nicklin MJ, di Giovine FS, Duff GW. An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers. American Journal of Human Genetics. 62: 1180-8. PMID 9545388 DOI: 10.1086/301817 |
0.408 |
|
| 1998 |
Camp NJ, Bansal A. The effect of selective sampling on mapping quantitative trait loci. Genetic Epidemiology. 14: 767-72. PMID 9433575 DOI: 10.1002/(Sici)1098-2272(1997)14:6<767::Aid-Gepi34>3.0.Co;2-M |
0.35 |
|
| 1998 |
Camp NJ. Genomewide transmission/disequilibrium testing--consideration of the genotypic relative risks at disease loci. American Journal of Human Genetics. 61: 1424-30. PMID 9399906 DOI: 10.1086/301648 |
0.422 |
|
| 1998 |
Carter M, Jones S, di Giovine F, Camp N, Lobo A, Duff G. Allele 2 of the interleukin-1 receptor antagonist gene polymorphism is associated with reduced expression of interleukin-1 receptor antagonist in ulcerative colitis Gastroenterology. 114: A947. DOI: 10.1016/S0016-5085(98)83857-2 |
0.314 |
|
| 1994 |
Camp N, Cannings C, Sheehan N. The number of genotypic assignments on a genealogy. I. The method and simple examples. Ima Journal of Mathematics Applied in Medicine and Biology. 11: 95-106. PMID 8089592 DOI: 10.1093/Imammb/11.2.95 |
0.33 |
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