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Julie A. Douglas, Ph.D. - Publications

Affiliations: 
2001 University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Biostatistics Biology, Genetics
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32 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
2018 Chen H, Douglas J, Gordon W, Thompson D, Couch F, Fasching P, Hall P, Hopper J, Maskarenic G, Pollan M, Stone J, Tamimi R, Lindstroem S. Abstract 224: Evidence for a shared genetic basis between breast cancer and mammographic density phenotypes Epidemiology. DOI: 10.1158/1538-7445.Am2018-224  0.306
2015 Lindström S, Thompson DJ, Paterson AD, Li J, Gierach GL, Scott C, Stone J, Douglas JA, Dos-Santos-Silva I, Fernandez-Navarro P, Verghase J, Smith P, Brown J, Luben R, Wareham NJ, et al. Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Nature Communications. 6: 8358. PMID 26349435 DOI: 10.1038/Ncomms9358  0.316
2015 Stone J, Thompson DJ, Dos Santos Silva I, Scott C, Tamimi RM, Lindstrom S, Kraft P, Hazra A, Li J, Eriksson L, Czene K, Hall P, Jensen M, Cunningham J, Olson JE, ... ... Douglas JA, et al. Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures. Cancer Research. 75: 2457-67. PMID 25862352 DOI: 10.1158/0008-5472.Can-14-2012  0.325
2014 Lindström S, Thompson DJ, Paterson AD, Li J, Gierach GL, Scott C, Stone J, Douglas JA, dos-Santos-Silva I, Fernandez-Navarro P, Verghase J, Smith P, Brown J, Luben R, Wareham NJ, et al. Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Nature Communications. 5: 5303. PMID 25342443 DOI: 10.1038/Ncomms6303  0.334
2014 Johnson AM, Zuhlke KA, Plotts C, McDonnell SK, Middha S, Riska SM, Schaid DJ, Thibodeau SN, Douglas JA, Cooney KA. Mutational landscape of candidate genes in familial prostate cancer. The Prostate. 74: 1371-8. PMID 25111073 DOI: 10.1002/Pros.22849  0.379
2013 Shah KP, Douglas JA. A method to prioritize quantitative traits and individuals for sequencing in family-based studies. Plos One. 8: e62545. PMID 23626830 DOI: 10.1371/Journal.Pone.0062545  0.354
2011 Montasser ME, Douglas JA, Roy-Gagnon MH, Van Hout CV, Weir MR, Vogel R, Parsa A, Steinle NI, Snitker S, Brereton NH, Chang YP, Shuldiner AR, Mitchell BD. Determinants of blood pressure response to low-salt intake in a healthy adult population. Journal of Clinical Hypertension (Greenwich, Conn.). 13: 795-800. PMID 22051423 DOI: 10.1111/J.1751-7176.2011.00523.X  0.631
2010 Iniesta MD, Gorin MA, Chien LC, Thomas SM, Milliron KJ, Douglas JA, Merajver SD. Absence of CHEK2*1100delC mutation in families with hereditary breast cancer in North America. Cancer Genetics and Cytogenetics. 202: 136-40. PMID 20875877 DOI: 10.1016/J.Cancergencyto.2010.07.124  0.323
2010 Van Hout CV, Levin AM, Rampersaud E, Shen H, O'Connell JR, Mitchell BD, Shuldiner AR, Douglas JA. Extent and distribution of linkage disequilibrium in the Old Order Amish. Genetic Epidemiology. 34: 146-50. PMID 19697356 DOI: 10.1002/Gepi.20444  0.673
2009 Gorin MA, Iniesta MD, Douglas JA, Milliron KJ, Merajver SD. Absence of the CHEK2*1100delC mutation in non-BRCA1/2 families with multiple cancer types in a high-risk clinic population of Caucasian ancestry. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 11040. PMID 27963982 DOI: 10.1200/Jco.2009.27.15_Suppl.11040  0.325
2009 Ray AM, Zuhlke KA, Johnson GR, Levin AM, Douglas JA, Lange EM, Cooney KA. Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families. British Journal of Cancer. 101: 2043-7. PMID 19935797 DOI: 10.1038/Sj.Bjc.6605433  0.371
2009 Ray AM, Zuhlke KA, Levin AM, Douglas JA, Cooney KA, Petros JA. Sequence variation in the mitochondrial gene cytochrome c oxidase subunit I and prostate cancer in African American men. The Prostate. 69: 956-60. PMID 19267350 DOI: 10.1002/Pros.20943  0.328
2008 Douglas JA, Roy-Gagnon MH, Zhou C, Mitchell BD, Shuldiner AR, Chan HP, Helvie MA. Mammographic breast density--evidence for genetic correlations with established breast cancer risk factors. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 3509-16. PMID 19029399 DOI: 10.1158/1055-9965.Epi-08-0480  0.31
2008 Levin AM, Machiela MJ, Zuhlke KA, Ray AM, Cooney KA, Douglas JA. Chromosome 17q12 variants contribute to risk of early-onset prostate cancer. Cancer Research. 68: 6492-5. PMID 18701471 DOI: 10.1158/0008-5472.Can-08-0348  0.38
2008 Beebe-Dimmer JL, Levin AM, Ray AM, Zuhlke KA, Machiela MJ, Halstead-Nussloch BA, Johnson GR, Cooney KA, Douglas JA. Chromosome 8q24 markers: risk of early-onset and familial prostate cancer. International Journal of Cancer. Journal International Du Cancer. 122: 2876-9. PMID 18360876 DOI: 10.1002/Ijc.23471  0.367
2008 Douglas JA, Sandefur CI. PedMine--a simulated annealing algorithm to identify maximally unrelated individuals in population isolates. Bioinformatics (Oxford, England). 24: 1106-8. PMID 18321883 DOI: 10.1093/Bioinformatics/Btn087  0.311
2007 Levin AM, Zuhlke KA, Ray AM, Cooney KA, Douglas JA. Sequence variation in alpha-methylacyl-CoA racemase and risk of early-onset and familial prostate cancer. The Prostate. 67: 1507-13. PMID 17683075 DOI: 10.1002/Pros.20642  0.337
2007 Douglas JA, Levin AM, Zuhlke KA, Ray AM, Johnson GR, Lange EM, Wood DP, Cooney KA. Common variation in the BRCA1 gene and prostate cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 1510-6. PMID 17585057 DOI: 10.1158/1055-9965.Epi-07-0137  0.379
2007 Levin AM, Ray AM, Zuhlke KA, Douglas JA, Cooney KA. Association between germline variation in the FHIT gene and prostate cancer in Caucasians and African Americans. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 1294-7. PMID 17548701 DOI: 10.1158/1055-9965.Epi-06-1054  0.348
2006 Amundadottir LT, Sulem P, Gudmundsson J, Helgason A, Baker A, Agnarsson BA, Sigurdsson A, Benediktsdottir KR, Cazier JB, Sainz J, Jakobsdottir M, Kostic J, Magnusdottir DN, Ghosh S, Agnarsson K, ... ... Douglas J, et al. A common variant associated with prostate cancer in European and African populations. Nature Genetics. 38: 652-8. PMID 16682969 DOI: 10.1038/Ng1808  0.361
2005 Douglas JA, Gruber SB, Meister KA, Bonner J, Watson P, Krush AJ, Lynch HT. History and molecular genetics of Lynch syndrome in family G: a century later. Jama. 294: 2195-202. PMID 16264161 DOI: 10.1001/Jama.294.17.2195  0.307
2005 Douglas JA, Zuhlke KA, Beebe-Dimmer J, Levin AM, Gruber SB, Wood DP, Cooney KA. Identifying susceptibility genes for prostate cancer--a family-based association study of polymorphisms in CYP17, CYP19, CYP11A1, and LH-beta. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 14: 2035-9. PMID 16103457 DOI: 10.1158/1055-9965.Epi-05-0170  0.345
2005 Rozek LS, Lipkin SM, Fearon ER, Hanash S, Giordano TJ, Greenson JK, Kuick R, Misek DE, Taylor JM, Douglas JA, Rennert G, Gruber SB. CDX2 polymorphisms, RNA expression, and risk of colorectal cancer. Cancer Research. 65: 5488-92. PMID 15994917 DOI: 10.1158/0008-5472.Can-04-3645  0.325
2004 Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, ... ... Douglas JA, et al. A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Diabetes. 53: 821-9. PMID 14988269 DOI: 10.2337/Diabetes.53.3.821  0.666
2002 Douglas JA, Skol AD, Boehnke M. Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. American Journal of Human Genetics. 70: 487-95. PMID 11791214 DOI: 10.1086/338919  0.665
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  0.541
2001 Douglas JA, Erdos MR, Watanabe RM, Braun A, Johnston CL, Oeth P, Mohlke KL, Valle TT, Ehnholm C, Buchanan TA, Bergman RN, Collins FS, Boehnke M, Tuomilehto J. The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences. Diabetes. 50: 886-90. PMID 11289057 DOI: 10.2337/Diabetes.50.4.886  0.5
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  0.488
2000 Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, et al. The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci. American Journal of Human Genetics. 67: 1186-200. PMID 11032784  0.59
2000 Douglas JA, Boehnke M, Lange K. A multipoint method for detecting genotyping errorsand mutations in sibling-pair linkage data American Journal of Human Genetics. 66: 1287-1297. PMID 10739757 DOI: 10.1086/302861  0.623
2000 Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, et al. The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. II. An Autosomal Genome Scan for Diabetes-Related Quantitative-Trait Loci The American Journal of Human Genetics. 67: 1186-1200. DOI: 10.1016/S0002-9297(07)62949-8  0.661
2000 Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamäki K, Chines P, Balow J, Birznieks G, Chang J, Eldridge W, ... ... Douglas JA, et al. The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. American Journal of Human Genetics. 67: 1174-1185. DOI: 10.1016/S0002-9297(07)62948-6  0.669
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