Nicola J. Camp - Publications

Affiliations: 
Biomedical Informatics University of Utah, Salt Lake City, UT 
Area:
Genetics, Epidemiology, Statistics

48 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.72
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  0.52
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  0.72
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  0.52
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  0.72
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.72
2008 Camp NJ, Werner TL, Cannon-Albright LA. Familial myeloma. The New England Journal of Medicine. 359: 1734-5; author reply. PMID 18923179 DOI: 10.1056/NEJMc081677  0.52
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  0.52
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  0.52
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  0.72
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  0.72
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  0.52
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  0.72
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  0.52
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  0.52
2006 Schaid DJ, McDonnell SK, Zarfas KE, Cunningham JM, Hebbring S, Thibodeau SN, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Badzioch M, ... ... Camp NJ, et al. Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics. Human Genetics. 120: 471-85. PMID 16932970 DOI: 10.1007/s00439-006-0219-9  0.52
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  0.72
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  0.52
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  0.72
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.72
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  0.72
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  0.72
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  0.72
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  0.52
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  0.72
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