Elizabeth Gillanders, Ph.D. - Publications

Affiliations: 
2006 Johns Hopkins University, Baltimore, MD 
Area:
Genetics

77 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2016 Zanetti KA, Wang Z, Aldrich M, Amos CI, Blot WJ, Bowman ED, Burdette L, Cai Q, Caporaso N, Chung CC, Gillanders EM, Haiman CA, Hansen HM, Henderson BE, Kolonel LN, et al. Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung Cancer (Amsterdam, Netherlands). 98: 33-42. PMID 27393504 DOI: 10.1016/j.lungcan.2016.05.008  0.36
2016 Machiela MJ, Zhou W, Karlins E, Sampson JN, Freedman ND, Yang Q, Hicks B, Dagnall C, Hautman C, Jacobs KB, Abnet CC, Aldrich MC, Amos C, Amundadottir LT, Arslan AA, ... ... Gillanders EM, et al. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome. Nature Communications. 7: 11843. PMID 27291797 DOI: 10.1038/ncomms11843  0.36
2016 Simonds NI, Ghazarian AA, Pimentel CB, Schully SD, Ellison GL, Gillanders EM, Mechanic LE. Review of the Gene-Environment Interaction Literature in Cancer: What Do We Know? Genetic Epidemiology. PMID 27061572 DOI: 10.1002/gepi.21967  0.36
2015 Law MH, Bishop DT, Lee JE, Brossard M, Martin NG, Moses EK, Song F, Barrett JH, Kumar R, Easton DF, Pharoah PD, Swerdlow AJ, Kypreou KP, Taylor JC, Harland M, ... ... Gillanders EM, et al. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics. PMID 26237428 DOI: 10.1038/ng.3373  0.36
2015 Carrick DM, Mehaffey MG, Sachs MC, Altekruse S, Camalier C, Chuaqui R, Cozen W, Das B, Hernandez BY, Lih CJ, Lynch CF, Makhlouf H, McGregor P, McShane LM, Phillips Rohan J, ... ... Gillanders EM, et al. Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue. Plos One. 10: e0127353. PMID 26222067 DOI: 10.1371/journal.pone.0127353  0.36
2015 Peng B, Chen HS, Mechanic LE, Racine B, Clarke J, Gillanders E, Feuer EJ. Genetic data simulators and their applications: an overview. Genetic Epidemiology. 39: 2-10. PMID 25504286 DOI: 10.1002/gepi.21876  0.36
2015 Taber JM, Chang CQ, Lam TK, Gillanders EM, Hamilton JG, Schully SD. Prevalence and correlates of receiving and sharing high-penetrance cancer genetic test results: findings from the Health Information National Trends Survey. Public Health Genomics. 18: 67-77. PMID 25427996 DOI: 10.1159/000368745  0.36
2015 Chen HS, Hutter CM, Mechanic LE, Amos CI, Bafna V, Hauser ER, Hernandez RD, Li C, Liberles DA, McAllister K, Moore JH, Paltoo DN, Papanicolaou GJ, Peng B, Ritchie MD, ... ... Gillanders EM, et al. Genetic simulation tools for post-genome wide association studies of complex diseases. Genetic Epidemiology. 39: 11-9. PMID 25371374 DOI: 10.1002/gepi.21870  0.36
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, DÄ™bniak 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  0.36
2014 Bhatia G, Tandon A, Patterson N, Aldrich MC, Ambrosone CB, Amos C, Bandera EV, Berndt SI, Bernstein L, Blot WJ, Bock CH, Caporaso N, Casey G, Deming SL, Diver WR, ... ... Gillanders EM, et al. Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture. American Journal of Human Genetics. 95: 437-44. PMID 25242497 DOI: 10.1016/j.ajhg.2014.08.011  0.36
2014 Iles MM, Bishop DT, Taylor JC, Hayward NK, Brossard M, Cust AE, Dunning AM, Lee JE, Moses EK, Akslen LA, Andresen PA, Avril MF, Azizi E, Scarrà GB, ... ... Gillanders EM, et al. The effect on melanoma risk of genes previously associated with telomere length. Journal of the National Cancer Institute. 106. PMID 25231748 DOI: 10.1093/jnci/dju267  0.36
2014 Paltoo DN, Rodriguez LL, Feolo M, Gillanders E, Ramos EM, Rutter JL, Sherry S, Wang VO, Bailey A, Baker R, Caulder M, Harris EL, Langlais K, Leeds H, Luetkemeier E, et al. Data use under the NIH GWAS data sharing policy and future directions. Nature Genetics. 46: 934-8. PMID 25162809 DOI: 10.1038/ng.3062  0.36
2014 Carrick DM, Mette E, Hoyle B, Rogers SD, Gillanders EM, Schully SD, Mechanic LE. The use of biospecimens in population-based research: a review of the National Cancer Institute's Division of Cancer Control and Population Sciences grant portfolio. Biopreservation and Biobanking. 12: 240-5. PMID 25162460 DOI: 10.1089/bio.2014.0009  0.36
2014 Feigelson HS, Goddard KA, Hollombe C, Tingle SR, Gillanders EM, Mechanic LE, Nelson SA. Approaches to integrating germline and tumor genomic data in cancer research. Carcinogenesis. 35: 2157-63. PMID 25115441 DOI: 10.1093/carcin/bgu165  0.36
2014 Bethea TN, Kitahara CM, Sonderman J, Patel AV, Harvey C, Knutsen SF, Park Y, Park SY, Fraser GE, Jacobs EJ, Purdue MP, Stolzenberg-Solomon RZ, Gillanders EM, Blot WJ, Palmer JR, et al. A pooled analysis of body mass index and pancreatic cancer mortality in african americans. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 23: 2119-25. PMID 25017247 DOI: 10.1158/1055-9965.EPI-14-0422  0.36
2013 Safaeian M, Rajaraman P, Hartge P, Yeager M, Linet M, Butler MA, Ruder AM, Purdue MP, Hsing A, Beane-Freeman L, Hoppin JA, Albanes D, Weinstein SJ, Inskip PD, Brenner A, ... ... Gillanders EM, et al. Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk. Cancer Causes & Control : Ccc. 24: 1885-91. PMID 23903690 DOI: 10.1007/s10552-013-0244-7  0.36
2013 Monda KL, Chen GK, Taylor KC, Palmer C, Edwards TL, Lange LA, Ng MC, Adeyemo AA, Allison MA, Bielak LF, Chen G, Graff M, Irvin MR, Rhie SK, Li G, ... ... Gillanders EM, et al. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nature Genetics. 45: 690-6. PMID 23583978 DOI: 10.1038/ng.2608  0.36
2013 Ghazarian AA, Simonds NI, Bennett K, Pimentel CB, Ellison GL, Gillanders EM, Schully SD, Mechanic LE. A review of NCI's extramural grant portfolio: Identifying opportunities for future research in genes and environment in cancer Cancer Epidemiology Biomarkers and Prevention. 22: 501-507. PMID 23462918 DOI: 10.1158/1055-9965.EPI-13-0156  0.36
2013 Iles MM, Law MH, Stacey SN, Han J, Fang S, Pfeiffer R, Harland M, Macgregor S, Taylor JC, Aben KK, Akslen LA, Avril MF, Azizi E, Bakker B, Benediktsdottir KR, ... ... Gillanders EM, et al. A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics. 45: 428-32, 432e1. PMID 23455637 DOI: 10.1038/ng.2571  0.36
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  0.36
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  0.36
2012 Khoury MJ, Freedman AN, Gillanders EM, Harvey CE, Kaefer C, Reid BC, Rogers S, Schully SD, Seminara D, Verma M. Frontiers in cancer epidemiology: a challenge to the research community from the Epidemiology and Genomics Research Program at the National Cancer Institute. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 999-1001. PMID 22665580 DOI: 10.1158/1055-9965.EPI-12-0525  0.36
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  0.36
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  0.36
2011 Barrett JH, Iles MM, Harland M, Taylor JC, Aitken JF, Andresen PA, Akslen LA, Armstrong BK, Avril MF, Azizi E, Bakker B, Bergman W, Bianchi-Scarrà G, Bressac-de Paillerets B, Calista D, ... ... Gillanders EM, et al. Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics. 43: 1108-13. PMID 21983787 DOI: 10.1038/ng.959  0.36
2011 Khoury MJ, Clauser SB, Freedman AN, Gillanders EM, Glasgow RE, Klein WM, Schully SD. Population sciences, translational research, and the opportunities and challenges for genomics to reduce the burden of cancer in the 21st century. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 20: 2105-14. PMID 21795499 DOI: 10.1158/1055-9965.EPI-11-0481  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
2010 Schully SD, Benedicto CB, Gillanders EM, Wang SS, Khoury MJ. Translational research in cancer genetics: The road less traveled Public Health Genomics. 14: 1-8. PMID 20051673 DOI: 10.1159/000272897  0.36
2009 Bishop DT, Demenais F, Iles MM, Harland M, Taylor JC, Corda E, Randerson-Moor J, Aitken JF, Avril MF, Azizi E, Bakker B, Bianchi-Scarrà G, Bressac-de Paillerets B, Calista D, Cannon-Albright LA, ... ... Gillanders EM, et al. Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics. 41: 920-5. PMID 19578364 DOI: 10.1038/ng.411  0.36
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  0.36
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  0.36
2008 Brown KM, Macgregor S, Montgomery GW, Craig DW, Zhao ZZ, Iyadurai K, Henders AK, Homer N, Campbell MJ, Stark M, Thomas S, Schmid H, Holland EA, Gillanders EM, Duffy DL, et al. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics. 40: 838-40. PMID 18488026 DOI: 10.1038/ng.163  0.36
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  0.36
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  0.36
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  0.36
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  0.36
2007 Goldstein AM, Chan M, Harland M, Hayward NK, Demenais F, Bishop DT, Azizi E, Bergman W, Bianchi-Scarra G, Bruno W, Calista D, Albright LA, Chaudru V, Chompret A, Cuellar F, ... ... Gillanders EM, et al. Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. Journal of Medical Genetics. 44: 99-106. PMID 16905682 DOI: 10.1136/jmg.2006.043802  0.36
2006 Goldstein AM, Chan M, Harland M, Gillanders EM, Hayward NK, Avril MF, Azizi E, Bianchi-Scarra G, Bishop DT, Bressac-de Paillerets B, Bruno W, Calista D, Cannon Albright LA, Demenais F, Elder DE, et al. High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Research. 66: 9818-28. PMID 17047042 DOI: 10.1158/0008-5472.CAN-06-0494  0.36
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  0.36
2006 Rendtorff ND, Zhu M, Fagerheim T, Antal TL, Jones M, Teslovich TM, Gillanders EM, Barmada M, Teig E, Trent JM, Friderici KH, Stephan DA, Tranebjaerg L. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. European Journal of Human Genetics : Ejhg. 14: 1097-105. PMID 16773128 DOI: 10.1038/sj.ejhg.5201670  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
2002 Scacheri PC, Gillanders EM, Subramony SH, Vedanarayanan V, Crowe CA, Thakore N, Bingler M, Hoffman EP. Novel mutations in collagen VI genes: Expansion of the Bethlem myopathy phenotype Neurology. 58: 593-602. PMID 11865138  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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: 10.1038/2477  0.36
Show low-probability matches.