Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?-Reference-Cited by-同舟云学术

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Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?

Published:2022-06 Issue:6 Volume:109 Page:981-988
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Appelbaum Paul S.,Burke Wylie,Parens Erik,Zeevi David A.,Arbour Laura,Garrison Nanibaa’ A.,Bonham Vence L.,Chung Wendy K.

Funder

Genome Canada

National Institutes of Health

National Human Genome Research Institute

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. The clinical experience: Hereditary cancer testing by a 25-gene panel;Obeid;J. Clin. Oncol.,2014

2. A systematic comparison of traditional and multigene panel testing for hereditary breast and ovarian cancer genes in more than 1000 patients;Lincoln;J. Mol. Diagn.,2015

3. Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening;Frey;Gynecol. Oncol.,2015

4. Uptake, results, and outcomes of germline multiple-gene sequencing after diagnosis of breast cancer;Kurian;JAMA Oncol,2018

5. Lack of diversity in genomic databases is a barrier to translating precision medicine research into practice;Landry;Health Aff. (Millwood).,2018

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1. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing;Genetics in Medicine;2024-10

2. Alleviating misclassified germline variants in underrepresented populations: A strategy using popmax;Genetics in Medicine;2024-06

3. Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds;The American Journal of Human Genetics;2024-05

4. Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system;Cell Reports Medicine;2024-05

5. Parkinson’s Disease is Predominantly a Genetic Disease;Journal of Parkinson's Disease;2024-04-23

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