Paper Details

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Paper Title

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

Paper Journal Title

Hum Mutat

Paper Citation Count

87

Paper Publication Year

2018

Bio Mention

Mesh Descriptor

Author Name	Affiliation
Deborah I Ritter	Texas Children's Hospital, Baylor College of Medicine
Stephanie M Fullerton	University of Washington
Stephanie M Fullerton	University of Washington
Lucia A Hindorff	National Human Genome Research Institute (NHGRI)
Lucia A Hindorff	National Human Genome Research Institute (NHGRI)
Barbara A Koenig	University of California san francisco
Erin M Ramos	National Human Genome Research Institute (NHGRI)
Mathew W Wright	Stanford University
James Zou	Stanford University
Vence L Bonham	National Human Genome Research Institute (NHGRI)
Sharon E Plon	Texas Children's Hospital, Baylor College of Medicine
Carlos D Bustamante	Stanford University
Carlos D Bustamante	Stanford University

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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