The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics-Reference-Cited by-同舟云学术

The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics

Published:2018-10-11 Issue:11 Volume:39 Page:1713-1720
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Popejoy Alice B.¹^ORCID,Ritter Deborah I.²,Crooks Kristy³⁴,Currey Erin⁵,Fullerton Stephanie M.⁶,Hindorff Lucia A.⁵,Koenig Barbara⁷,Ramos Erin M.⁵,Sorokin Elena P.¹,Wand Hannah¹,Wright Mathew W.¹^ORCID,Zou James¹,Gignoux Christopher R.⁴,Bonham Vence L.⁸,Plon Sharon E.²,Bustamante Carlos D.¹,

Affiliation:

1. Department of Biomedical Data ScienceStanford University Standford California

2. Department of PediatricsTexas Children's HospitalBaylor College of Medicine Houston Texas

3. Department of PathologyUniversity of ColoradoAnschutz Medical Campus Aurora Colorado

4. Department of MedicineDivision of Bioinformatics and Personalized MedicineUniversity of Colorado Anschutz Medical Campus Aurora Colorado

5. Division of Genomics and SocietyNational Human Genome Research Institute (NHGRI) Bethesda Maryland

6. Department of Bioethics & HumanitiesUniversity of Washington Seattle Washington

7. Department of Anthropology, History, and Social MedicineUniversity of California San Francisco

8. Social and Behavioral Research BranchNational Human Genome Research Institute (NHGRI) Bethesda Maryland

Funder

National Human Genome Research Institute

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23644

Reference40 articles.

1. Leveraging local ancestry to detect gene-gene interactions in genome-wide data

2. Will Precision Medicine Move Us beyond Race?

3. Primary Care Physicians' Collection, Comfort, and Use of Race and Ethnicity in Clinical Practice in the United States

4. The Importance of Race and Ethnic Background in Biomedical Research and Clinical Practice

5. Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk

Cited by 99 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Artificial intelligence, ChatGPT, and other large language models for social determinants of health: Current state and future directions;Cell Reports Medicine;2024-01

2. The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants;Blood;2023-12-14

3. Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers;AJOB Empirical Bioethics;2023-11-14

4. Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing;JAMA Network Open;2023-10-25

5. Frequency of Variants in Mendelian Alzheimer’s Disease Genes within the Alzheimer’s Disease Sequencing Project (ADSP);2023-10-25