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Georgia L. Wiesner

Georgia L. Wiesner, M.D., M.S.

Director, Clinical and Translational Hereditary Cancer Program
Ingram Professor of Cancer Research
Professor of Medicine
Cancer Geneticist

Profile

Dr. Georgia L. Wiesner is an Ingram Professor of Cancer Research, Professor of Medicine in the Division of Genetic Medicine and the Director of the new Clinical and Translational Hereditary Cancer Program for the Vanderbilt-Ingram Cancer Center. As one of the few physicians in the country with dual certification in Internal Medicine and Medical Genetics, Dr.
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Dr. Georgia L. Wiesner is an Ingram Professor of Cancer Research, Professor of Medicine in the Division of Genetic Medicine and the Director of the new Clinical and Translational Hereditary Cancer Program for the Vanderbilt-Ingram Cancer Center. As one of the few physicians in the country with dual certification in Internal Medicine and Medical Genetics, Dr. Wiesner has devoted her career to understanding the factors that cause cancer susceptibility. Since joining the Vanderbilt faculty in 2012, she has established a comprehensive Hereditary Cancer Clinic and research program for patients and family members who are prone to develop cancer.

Dr. Wiesner has a long-standing research interest in hereditary cancer susceptibility mainly focused on colon cancer and is also studying how genetic tests are used in clinical medicine as well as various ethical, legal and social aspects of genomic medicine. She established the Hereditary Cancer Registry in 2015 that collects clinical information, genetic testing and research testing on patients and their family members. In the future, the registry will also develop a new cancer risk prediction program that will exploit efforts in electronic family history taking and related strategies in precision medicine. This approach will help to identify Vanderbilt patients at higher cancer risk, so that these patients can be informed about the appropriate screening and other treatment options. In addition, Dr. Wiesner has established VICC as a research site along with Dana Farber in a pilot multi-centered study of lung cancer.

Dr. Wiesner is a current member of the Genetic/Familial High Risk Assessment, Breast & Ovarian Panel of the National Comprehensive Cancer Network (NCCN).This committee provides expert opinion in formulating guidelines for care of patient and families with heritable cancer syndromes. Her previous service includes the Editor-in-Chief of the Cancer Genetics PDQ Editorial Board at the National Cancer Institute from 2001 to 2005, and the Board of Directors for the American Society of Human Genetics, a past- President of the Board of Directors of the American Board of Medical Genetics and past-Chair of the Residency Review Committee for Medical Genetics (ACGME).

Prior to establishing her research programs at Vanderbilt, Dr. Wiesner served in several leadership capacities at Case-Western Reserve University (CWRU) and University Hospitals of Cleveland. She was the Director of the Center for Human Genetics from 2000 to 2008, Medical Director of the Clinical Cancer Genetics program from 1995 to 2012, and founded the first specialized clinic for delivery of genetic services to patients and families with hereditary cancer susceptibility in Northeastern Ohio.

Education
  • M.D., University of Minnesota, Minneapolis, Minnesota (1985)
  • M.S., University of Minnesota, Minneapolis, Minnesota (1981)
  • Internal Medicine Residency, University of Minnesota Medical Center (1988)
  • Chief Internal Medicine Resident, University of Minnesota Medical Center (1989)
  • Medical Genetics Fellowship, University of Minnesota Medical Center (1992)
 
Publications
  • Daly MB, Pilarski R, Axilbund JE, Berry M, Buys SS, Crawford B, Farmer M, Friedman S, Garber JE, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Rana H, Reiser G, Robson ME, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wick MJ, Wiesner GL, Dwyer M, Kumar R, Darlow S. Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015. J Natl Compr Canc Netw. 2016 Feb; 14(2): 153-62. PMID: 26850485, PII: 14/2/153, ISSN: 1540-1413.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/26850485.
  • Schneider JL, Davis J, Kauffman TL, Reiss JA, McGinley C, Arnold K, Zepp J, Gilmore M, Muessig KR, Syngal S, Acheson L, Wiesner GL, Peterson SK, Goddard KA. Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators. Genet. Med [print-electronic]. 2016 Feb; 18(2): 152-61. PMID: 25880440, PMCID: PMC4608844, PII: gim201543, DOI: 10.1038/gim.2015.43, ISSN: 1530-0366.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/25880440.
  • Hunter JE, Zepp JM, Gilmore MJ, Davis JV, Esterberg EJ, Muessig KR, Peterson SK, Syngal S, Acheson LS, Wiesner GL, Reiss JA, Goddard KA. Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers. Cancer [print-electronic]. 2015 Sep 9/15/2015; 121(18): 3281-9. PMID: 26036338, PMCID: PMC4560979, DOI: 10.1002/cncr.29470, ISSN: 1097-0142.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/26036338.
  • Hampel H, Bennett RL, Buchanan A, Pearlman R, Wiesner GL, . A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. Genet. Med [print-electronic]. 2015 Jan; 17(1): 70-87. PMID: 25394175, PII: gim2014147, DOI: 10.1038/gim.2014.147.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/25394175.
  • Daly MB, Pilarski R, Axilbund JE, Buys SS, Crawford B, Friedman S, Garber JE, Horton C, Kaklamani V, Klein C, Kohlmann W, Kurian A, Litton J, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Pasche B, Reiser G, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wiesner GL, Dwyer MA, Kumar R, . Genetic/familial high-risk assessment: breast and ovarian, version 1.2014. J Natl Compr Canc Netw. 2014 Sep; 12(9): 1326-38. PMID: 25190698, PII: 12/9/1326.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/25190698.
  • Hall MJ, Forman AD, Pilarski R, Wiesner G, Giri VN. Gene panel testing for inherited cancer risk. J Natl Compr Canc Netw. 2014 Sep; 12(9): 1339-46. PMID: 25190699, PII: 12/9/1339, ISSN: 1540-1413.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/25190699.
  • Guda K, Fink SP, Milne GL, Molyneaux N, Ravi L, Lewis SM, Dannenberg AJ, Montgomery CG, Zhang S, Willis J, Wiesner GL, Markowitz SD. Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance. Cancer Prev Res (Phila) [print-electronic]. 2014 Aug; 7(8): 805-12. PMID: 24838973, PMCID: PMC4125515, PII: 1940-6207.CAPR-14-0108, DOI: 10.1158/1940-6207.CAPR-14-0108, ISSN: 1940-6215.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/24838973.
  • Dressler LG, Smolek S, Ponsaran R, Markey JM, Starks H, Gerson N, Lewis S, Press N, Juengst E, Wiesner GL, . IRB perspectives on the return of individual results from genomic research. Genet. Med [print-electronic]. 2012 Feb; 14(2): 215-22. PMID: 22241094, PMCID: PMC3493147, PII: gim201110, DOI: 10.1038/gim.2011.10, ISSN: 1530-0366.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/22241094.
  • Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Snapinn KW, Griffin MQ, Wiesner GL, Burke W, . Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis. Genet. Med [print-electronic]. 2012 Feb; 14(2): 236-42. PMID: 22241102, PMCID: PMC3448270, PII: gim201157, DOI: 10.1038/gim.2011.57, ISSN: 1530-0366.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/22241102.
  • Gray-McGuire C, Guda K, Adrianto I, Lin CP, Natale L, Potter JD, Newcomb P, Poole EM, Ulrich CM, Lindor N, Goode EL, Fridley BL, Jenkins R, Le Marchand L, Casey G, Haile R, Hopper J, Jenkins M, Young J, Buchanan D, Gallinger S, Adams M, Lewis S, Willis J, Elston R, Markowitz SD, Wiesner GL. Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. Cancer Res [print-electronic]. 2010 Jul 7/1/2010; 70(13): 5409-18. PMID: 20551049, PMCID: PMC2896448, PII: 0008-5472.CAN-10-0188, DOI: 10.1158/0008-5472.CAN-10-0188, ISSN: 1538-7445.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/20551049.
  • , Hudson TJ, Anderson W, Artez A, Barker AD, Bell C, Bernabé RR, Bhan MK, Calvo F, Eerola I, Gerhard DS, Guttmacher A, Guyer M, Hemsley FM, Jennings JL, Kerr D, Klatt P, Kolar P, Kusada J, Lane DP, Laplace F, Youyong L, Nettekoven G, Ozenberger B, Peterson J, Rao TS, Remacle J, Schafer AJ, Shibata T, Stratton MR, Vockley JG, Watanabe K, Yang H, Yuen MM, Knoppers BM, Bobrow M, Cambon-Thomsen A, Dressler LG, Dyke SO, Joly Y, Kato K, Kennedy KL, Nicolás P, Parker MJ, Rial-Sebbag E, Romeo-Casabona CM, Shaw KM, Wallace S, Wiesner GL, Zeps N, Lichter P, Biankin AV, Chabannon C, Chin L, Clément B, de Alava E, Degos F, Ferguson ML, Geary P, Hayes DN, Hudson TJ, Johns AL, Kasprzyk A, Nakagawa H, Penny R, Piris MA, Sarin R, Scarpa A, Shibata T, van de Vijver M, Futreal PA, Aburatani H, Bayés M, Botwell DD, Campbell PJ, Estivill X, Gerhard DS, Grimmond SM, Gut I, Hirst M, López-Otín C, Majumder P, Marra M, McPherson JD, Nakagawa H, Ning Z, Puente XS, Ruan Y, Shibata T, Stratton MR, Stunnenberg HG, Swerdlow H, Velculescu VE, Wilson RK, Xue HH, Yang L, Spellman PT, Bader GD, Boutros PC, Campbell PJ, Flicek P, Getz G, Guigó R, Guo G, Haussler D, Heath S, Hubbard TJ, Jiang T, Jones SM, Li Q, López-Bigas N, Luo R, Muthuswamy L, Ouellette BF, Pearson JV, Puente XS, Quesada V, Raphael BJ, Sander C, Shibata T, Speed TP, Stein LD, Stuart JM, Teague JW, Totoki Y, Tsunoda T, Valencia A, Wheeler DA, Wu H, Zhao S, Zhou G, Stein LD, Guigó R, Hubbard TJ, Joly Y, Jones SM, Kasprzyk A, Lathrop M, López-Bigas N, Ouellette BF, Spellman PT, Teague JW, Thomas G, Valencia A, Yoshida T, Kennedy KL, Axton M, Dyke SO, Futreal PA, Gerhard DS, Gunter C, Guyer M, Hudson TJ, McPherson JD, Miller LJ, Ozenberger B, Shaw KM, Kasprzyk A, Stein LD, Zhang J, Haider SA, Wang J, Yung CK, Cros A, Liang Y, Gnaneshan S, Guberman J, Hsu J, Bobrow M, Chalmers DR, Hasel KW, Joly Y, Kaan TS, Kennedy KL, Knoppers BM, Lowrance WW, Masui T, Nicolás P, Rial-Sebbag E, Rodriguez LL, Vergely C, Yoshida T, Grimmond SM, Biankin AV, Bowtell DD, Cloonan N, deFazio A, Eshleman JR, Etemadmoghadam D, Gardiner BB, Kench JG, Scarpa A, Sutherland RL, Tempero MA, Waddell NJ, Wilson PJ, McPherson JD, Gallinger S, Tsao MS, Shaw PA, Petersen GM, Mukhopadhyay D, Chin L, DePinho RA, Thayer S, Muthuswamy L, Shazand K, Beck T, Sam M, Timms L, Ballin V, Lu Y, Ji J, Zhang X, Chen F, Hu X, Zhou G, Yang Q, Tian G, Zhang L, Xing X, Li X, Zhu Z, Yu Y, Yu J, Yang H, Lathrop M, Tost J, Brennan P, Holcatova I, Zaridze D, Brazma A, Egevard L, Prokhortchouk E, Banks RE, Uhlén M, Cambon-Thomsen A, Viksna J, Ponten F, Skryabin K, Stratton MR, Futreal PA, Birney E, Borg A, Børresen-Dale AL, Caldas C, Foekens JA, Martin S, Reis-Filho JS, Richardson AL, Sotiriou C, Stunnenberg HG, Thoms G, van de Vijver M, van't Veer L, Calvo F, Birnbaum D, Blanche H, Boucher P, Boyault S, Chabannon C, Gut I, Masson-Jacquemier JD, Lathrop M, Pauporté I, Pivot X, Vincent-Salomon A, Tabone E, Theillet C, Thomas G, Tost J, Treilleux I, Calvo F, Bioulac-Sage P, Clément B, Decaens T, Degos F, Franco D, Gut I, Gut M, Heath S, Lathrop M, Samuel D, Thomas G, Zucman-Rossi J, Lichter P, Eils R, Brors B, Korbel JO, Korshunov A, Landgraf P, Lehrach H, Pfister S, Radlwimmer B, Reifenberger G, Taylor MD, von Kalle C, Majumder PP, Sarin R, Rao TS, Bhan MK, Scarpa A, Pederzoli P, Lawlor RA, Delledonne M, Bardelli A, Biankin AV, Grimmond SM, Gress T, Klimstra D, Zamboni G, Shibata T, Nakamura Y, Nakagawa H, Kusada J, Tsunoda T, Miyano S, Aburatani H, Kato K, Fujimoto A, Yoshida T, Campo E, López-Otín C, Estivill X, Guigó R, de Sanjosé S, Piris MA, Montserrat E, González-Díaz M, Puente XS, Jares P, Valencia A, Himmelbauer H, Quesada V, Bea S, Stratton MR, Futreal PA, Campbell PJ, Vincent-Salomon A, Richardson AL, Reis-Filho JS, van de Vijver M, Thomas G, Masson-Jacquemier JD, Aparicio S, Borg A, Børresen-Dale AL, Caldas C, Foekens JA, Stunnenberg HG, van't Veer L, Easton DF, Spellman PT, Martin S, Barker AD, Chin L, Collins FS, Compton CC, Ferguson ML, Gerhard DS, Getz G, Gunter C, Guttmacher A, Guyer M, Hayes DN, Lander ES, Ozenberger B, Penny R, Peterson J, Sander C, Shaw KM, Speed TP, Spellman PT, Vockley JG, Wheeler DA, Wilson RK, Hudson TJ, Chin L, Knoppers BM, Lander ES, Lichter P, Stein LD, Stratton MR, Anderson W, Barker AD, Bell C, Bobrow M, Burke W, Collins FS, Compton CC, DePinho RA, Easton DF, Futreal PA, Gerhard DS, Green AR, Guyer M, Hamilton SR, Hubbard TJ, Kallioniemi OP, Kennedy KL, Ley TJ, Liu ET, Lu Y, Majumder P, Marra M, Ozenberger B, Peterson J, Schafer AJ, Spellman PT, Stunnenberg HG, Wainwright BJ, Wilson RK, Yang H. International network of cancer genome projects. Nature. 2010 Apr 4/15/2010; 464(7291): 993-8. PMID: 20393554, PMCID: PMC2902243, PII: nature08987, DOI: 10.1038/nature08987, ISSN: 1476-4687.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/20393554.
  • Lemke AA, Trinidad SB, Edwards KL, Starks H, Wiesner GL, . Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection. J Empir Res Hum Res Ethics. 2010 Mar; 5(1): 83-91. PMID: 20235866, PMCID: PMC2902178, DOI: 10.1525/jer.2010.5.1.83, ISSN: 1556-2646.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/20235866.
  • Slavin TP, Wiesner GL. Developmental defects and childhood cancer. Curr. Opin. Pediatr. 2009 Dec; 21(6): 717-23. PMID: 19812499, DOI: 10.1097/MOP.0b013e328332c612, ISSN: 1531-698X.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/19812499.
  • Guda K, Moinova H, He J, Jamison O, Ravi L, Natale L, Lutterbaugh J, Lawrence E, Lewis S, Willson JK, Lowe JB, Wiesner GL, Parmigiani G, Barnholtz-Sloan J, Dawson DW, Velculescu VE, Kinzler KW, Papadopoulos N, Vogelstein B, Willis J, Gerken TA, Markowitz SD. Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers. Proc. Natl. Acad. Sci. U.S.A [print-electronic]. 2009 Aug 8/4/2009; 106(31): 12921-5. PMID: 19617566, PMCID: PMC2722285, PII: 0901454106, DOI: 10.1073/pnas.0901454106, ISSN: 1091-6490.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/19617566.
  • Guda K, Natale L, Lutterbaugh J, Wiesner GL, Lewis S, Tanner SM, Tomsic J, Valle L, de la Chapelle A, Elston RC, Willis J, Markowitz SD. Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients. Cancer Res [print-electronic]. 2009 Jun 6/15/2009; 69(12): 4959-61. PMID: 19509225, PMCID: PMC2739986, PII: 0008-5472.CAN-09-0225, DOI: 10.1158/0008-5472.CAN-09-0225, ISSN: 1538-7445.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/19509225.
  • Simon C, Acheson L, Burant C, Gerson N, Schramm S, Lewis S, Wiesner G. Patient interest in recording family histories of cancer via the Internet. Genet. Med. 2008 Dec; 10(12): 895-902. PMID: 19092442, PMCID: PMC3342847, PII: 00125817-200812000-00006, DOI: 10.1097/GIM.0b013e31818de708, ISSN: 1530-0366.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/19092442.
  • Daley D, Lewis S, Platzer P, MacMillen M, Willis J, Elston RC, Markowitz SD, Wiesner GL. Identification of susceptibility genes for cancer in a genome-wide scan: results from the colon neoplasia sibling study. Am. J. Hum. Genet [print-electronic]. 2008 Mar; 82(3): 723-36. PMID: 18313025, PMCID: PMC2427227, PII: S0002-9297(08)00137-7, DOI: 10.1016/j.ajhg.2008.01.007, ISSN: 1537-6605.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/18313025.
  • Ochs-Balcom HM, Wiesner G, Elston RC. A meta-analysis of the association of N-acetyltransferase 2 gene (NAT2) variants with breast cancer. Am. J. Epidemiol [print-electronic]. 2007 Aug 8/1/2007; 166(3): 246-54. PMID: 17535831, PII: kwm066, DOI: 10.1093/aje/kwm066, ISSN: 0002-9262.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/17535831.
  • Daley D, Morgan W, Lewis S, Willis J, Elston RC, Markowitz SD, Wiesner GL. Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?. Cancer Epidemiol. Biomarkers Prev. 2007 May; 16(5): 892-4. PMID: 17507611, PII: 16/5/892, DOI: 10.1158/1055-9965.EPI-06-0965, ISSN: 1055-9965.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/17507611.
  • Nosek TM, Cohen M, Matthews A, Papp K, Wolf N, Wrenn G, Sher A, Coulter K, Martin J, Wiesner GL. A serious gaming/immersion environment to teach clinical cancer genetics. Stud Health Technol Inform. 2007; 125: 355-60. PMID: 17377303, ISSN: 0926-9630.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/17377303.
  • Acheson LS, Zyzanski SJ, Stange KC, Deptowicz A, Wiesner GL. Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer. J. Clin. Oncol [print-electronic]. 2006 Dec 12/1/2006; 24(34): 5395-402. PMID: 17088568, PII: JCO.2006.07.2462, DOI: 10.1200/JCO.2006.07.2462, ISSN: 1527-7755.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/17088568.
  • Korf BR, Feldman G, Wiesner GL. Report of Banbury Summit meeting on training of physicians in medical genetics, October 20-22, 2004. Genet. Med. 2005 Jul; 7(6): 433-8. PMID: 16024976, PII: 00125817-200507000-00009, DOI: 10.109701.GIM.0000171324.58121.CF, ISSN: 1098-3600.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/16024976.
  • Chak A, Faulx A, Kinnard M, Brock W, Willis J, Wiesner GL, Parrado AR, Goddard KA. Identification of Barrett's esophagus in relatives by endoscopic screening. Am. J. Gastroenterol. 2004 Nov; 99(11): 2107-14. PMID: 15554988, PII: AJG40464, DOI: 10.1111/j.1572-0241.2004.40464.x, ISSN: 0002-9270.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15554988.
  • Acheson LS, Wiesner GL. Current and future applications of genetics in primary care medicine. Prim. Care. 2004 Sep; 31(3): 449-60, vii. PMID: 15331241, PII: S009545430400065X, DOI: 10.1016/j.pop.2004.05.002, ISSN: 0095-4543.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15331241.
  • Culler D, Grimes SJ, Acheson LS, Wiesner GL. Cancer genetics in primary care. Prim. Care. 2004 Sep; 31(3): 649-83, xi. PMID: 15331253, PII: S0095454304000612, DOI: 10.1016/j.pop.2004.05.001, ISSN: 0095-4543.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15331253.
  • Grimes SJ, Acheson LS, Matthews AL, Wiesner GL. Clinical consult: Marfan syndrome. Prim. Care. 2004 Sep; 31(3): 739-42, xii. PMID: 15331256, PII: S009545430400048X, DOI: 10.1016/j.pop.2004.04.005, ISSN: 0095-4543.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15331256.
  • Matthews AL, Grimes SJ, Wiesner GL, Acheson LS. Clinical consult: iron overload--hereditary hemochromatosis. Prim. Care. 2004 Sep; 31(3): 767-70, xii. PMID: 15331258, PII: S0095454304000508, DOI: 10.1016/j.pop.2004.04.007, ISSN: 0095-4543.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15331258.
  • Wiesner GL, Cassidy SB, Grimes SJ, Matthews AL, Acheson LS. Clinical consult: developmental delay/fragile X syndrome. Prim. Care. 2004 Sep; 31(3): 621-5, x. PMID: 15331251, PII: S009545430400051X, DOI: 10.1016/j.pop.2004.04.008, ISSN: 0095-4543.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/15331251.
  • Wiesner GL, Daley D, Lewis S, Ticknor C, Platzer P, Lutterbaugh J, MacMillen M, Baliner B, Willis J, Elston RC, Markowitz SD. A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2. Proc. Natl. Acad. Sci. U.S.A [print-electronic]. 2003 Oct 10/28/2003; 100(22): 12961-5. PMID: 14566058, PMCID: PMC240727, PII: 2132286100, DOI: 10.1073/pnas.2132286100, ISSN: 0027-8424.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/14566058.
  • Dugan RB, Wiesner GL, Juengst ET, O'Riordan M, Matthews AL, Robin NH. Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience. Am J Med Genet C Semin Med Genet. 2003 May 5/15/2003; 119C(1): 27-34. PMID: 12704635, DOI: 10.1002/ajmg.c.10005, ISSN: 1552-4868.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/12704635.
  • Burke W, Atkins D, Gwinn M, Guttmacher A, Haddow J, Lau J, Palomaki G, Press N, Richards CS, Wideroff L, Wiesner GL. Genetic test evaluation: information needs of clinicians, policy makers, and the public. Am. J. Epidemiol. 2002 Aug 8/15/2002; 156(4): 311-8. PMID: 12181100, ISSN: 0002-9262.
    Available from: http://www.ncbi.nlm.nih.gov/pubmed/12181100.