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Items: 17


Genetics and cardiovascular disease: a policy statement from the American Heart Association.

Ashley EA, Hershberger RE, Caleshu C, Ellinor PT, Garcia JG, Herrington DM, Ho CY, Johnson JA, Kittner SJ, Macrae CA, Mudd-Martin G, Rader DJ, Roden DM, Scholes D, Sellke FW, Towbin JA, Van Eyk J, Worrall BB; American Heart Association Advocacy Coordinating Committee.

Circulation. 2012 Jul 3;126(1):142-57. doi: 10.1161/CIR.0b013e31825b07f8. Epub 2012 May 29. No abstract available.


Ethical issues of predictive genetic testing for diabetes.

Haga SB.

J Diabetes Sci Technol. 2009 Jul 1;3(4):781-8. Review.


Civilian and military genetics: nondiscrimination policy in a post-GINA world.

Baruch S, Hudson K.

Am J Hum Genet. 2008 Oct;83(4):435-44. doi: 10.1016/j.ajhg.2008.09.003.


Fear of health insurance loss among individuals at risk for Huntington disease.

Oster E, Dorsey ER, Bausch J, Shinaman A, Kayson E, Oakes D, Shoulson I, Quaid K; Huntington Study Group PHAROS Investigators.

Am J Med Genet A. 2008 Aug 15;146A(16):2070-7. doi: 10.1002/ajmg.a.32422.


Access to health insurance: experiences and attitudes of those with genetic versus non-genetic medical conditions.

Kass NE, Medley AM, Natowicz MR, Hull SC, Faden RR, Plantinga L, Gostin LO.

Am J Med Genet A. 2007 Apr 1;143A(7):707-17.


Racial differences in beliefs about genetic screening among patients at inner-city neighborhood health centers.

Zimmerman RK, Tabbarah M, Nowalk MP, Raymund M, Jewell IK, Wilson SA, Ricci EM.

J Natl Med Assoc. 2006 Mar;98(3):370-7.


Development and validation of tools to assess genetic discrimination and genetically based racism.

Parrott RL, Silk KJ, Dillow MR, Krieger JL, Harris TM, Condit CM.

J Natl Med Assoc. 2005 Jul;97(7):980-90.


Direct-to-consumer sales of genetic services on the Internet.

Gollust SE, Wilfond BS, Hull SC.

Genet Med. 2003 Jul-Aug;5(4):332-7.


Why should primary care physicians know about the genetics of dementia?

Pinsky LE, Burke W, Bird TD.

West J Med. 2001 Dec;175(6):412-6. Review. No abstract available.


The role of community review in evaluating the risks of human genetic variation research.

Foster MW, Sharp RR, Freeman WL, Chino M, Bernsten D, Carter TH.

Am J Hum Genet. 1999 Jun;64(6):1719-27.


Should we genetically test everyone for haemochromatosis?

Allen K, Williamson R.

J Med Ethics. 1999 Apr;25(2):209-14.


Genetics and the British insurance industry.

Cook ED.

J Med Ethics. 1999 Apr;25(2):157-62.


Genetic testing and public policy.

Holtzman NA, Shapiro D.

BMJ. 1998 Mar 14;316(7134):852-6. Review. No abstract available.


Questioning the need for anonymous genetic counseling and testing.

Uhlmann WR, Ginsburg D, Gelehrter TD, Nicholson J, Petty EM.

Am J Hum Genet. 1996 Oct;59(4):968-70. No abstract available.


Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.

FitzGerald MG, Harkin DP, Silva-Arrieta S, MacDonald DJ, Lucchina LC, Unsal H, O'Neill E, Koh J, Finkelstein DM, Isselbacher KJ, Sober AJ, Haber DA.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8541-5.

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