Literature DB >> 17018815

Ashkenazi Jews and breast cancer: the consequences of linking ethnic identity to genetic disease.

Sherry I Brandt-Rauf1, Victoria H Raveis, Nathan F Drummond, Jill A Conte, Sheila M Rothman.   

Abstract

We explored the advantages and disadvantages of using ethnic categories in genetic research. With the discovery that certain breast cancer gene mutations appeared to be more prevalent in Ashkenazi Jews, breast cancer researchers moved their focus from high-risk families to ethnicity. The concept of Ashkenazi Jews as genetically unique, a legacy of Tay-Sachs disease research and a particular reading of history, shaped this new approach even as methodological imprecision and new genetic and historical research challenged it. Our findings cast doubt on the accuracy and desirability of linking ethnic groups to genetic disease. Such linkages exaggerate genetic differences among ethnic groups and lead to unequal access to testing and therapy.

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Year:  2006        PMID: 17018815      PMCID: PMC1751808          DOI: 10.2105/AJPH.2005.083014

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  116 in total

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6.  Early adoption of BRCA1/2 testing: who and why.

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7.  The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.

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10.  Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium.

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Review 3.  Phase changes in the BRCA policy domain.

Authors:  Stephen M Modell; Susan B King; Toby Citrin; Sharon L R Kardia
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Journal:  Clin Genet       Date:  2009-09       Impact factor: 4.438

5.  Admixture mapping: from paradigms of race and ethnicity to population history.

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6.  Survey on Addressing the Information and Support Needs of Jewish Women at Increased Risk for or Diagnosed with Breast Cancer: The Sharsheret Experience.

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7.  Genetics in an isolated population like Finland: a different basis for genomic medicine?

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8.  A scalable, aggregated genotypic-phenotypic database for human disease variation.

Authors:  Ryan Barrett; Cynthia L Neben; Anjali D Zimmer; Gilad Mishne; Wendy McKennon; Alicia Y Zhou; Jeremy Ginsberg
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9.  Race and ancestry in biomedical research: exploring the challenges.

Authors:  Timothy Caulfield; Stephanie M Fullerton; Sarah E Ali-Khan; Laura Arbour; Esteban G Burchard; Richard S Cooper; Billie-Jo Hardy; Simrat Harry; Robyn Hyde-Lay; Jonathan Kahn; Rick Kittles; Barbara A Koenig; Sandra Sj Lee; Michael Malinowski; Vardit Ravitsky; Pamela Sankar; Stephen W Scherer; Béatrice Séguin; Darren Shickle; Guilherme Suarez-Kurtz; Abdallah S Daar
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  9 in total

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