Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures.

Autor: Popejoy AB; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Center for Biomedical Ethics, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: apopejoy@stanford.edu., Crooks KR; Department of Pathology, University of Colorado, Aurora, CO 80045, USA., Fullerton SM; Department of Bioethics & Humanities, University of Washington School of Medicine, Seattle, WA 98195, USA., Hindorff LA; Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Hooker GW; Concert Genetics, Nashville, TN 37204, USA., Koenig BA; Program in Bioethics, University of California San Francisco Laurel Heights, San Francisco, CA 94118, USA., Pino N; Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Ramos EM; Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Ritter DI; Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX 77030, USA., Wand H; Department of Pathology, Stanford University, Stanford, CA 94305, USA; Department of Cardiology, Stanford Healthcare, Stanford, CA 94305, USA., Wright MW; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA 94305, USA., Yudell M; Department of Community Health and Prevention, Dornsife School of Public Health, Drexel University, Philadelphia, PA 19104, USA., Zou JY; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA 94305, USA., Plon SE; Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX 77030, USA., Bustamante CD; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA 94305, USA., Ormond KE; Stanford Center for Biomedical Ethics, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Genetics, Stanford University, Stanford, CA 94305, USA.

Publikováno v: American journal of human genetics [Am J Hum Genet] 2020 Jul 02; Vol. 107 (1), pp. 72-82. Date of Electronic Publication: 2020 Jun 06.

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

Autor: Popejoy AB; Department of Biomedical Data Science, Stanford University, Standford, California., Ritter DI; Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas., Crooks K; Department of Pathology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado.; Department of Medicine, Division of Bioinformatics and Personalized Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado., Currey E; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland., Fullerton SM; Department of Bioethics & Humanities, University of Washington, Seattle, Washington., Hindorff LA; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland., Koenig B; Department of Anthropology, History, and Social Medicine, University of California, San Francisco., Ramos EM; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland., Sorokin EP; Department of Biomedical Data Science, Stanford University, Standford, California., Wand H; Department of Biomedical Data Science, Stanford University, Standford, California., Wright MW; Department of Biomedical Data Science, Stanford University, Standford, California., Zou J; Department of Biomedical Data Science, Stanford University, Standford, California., Gignoux CR; Department of Medicine, Division of Bioinformatics and Personalized Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado., Bonham VL; Social and Behavioral Research Branch, National Human Genome Research Institute (NHGRI), Bethesda, Maryland., Plon SE; Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas., Bustamante CD; Department of Biomedical Data Science, Stanford University, Standford, California.

Publikováno v: Human mutation [Hum Mutat] 2018 Nov; Vol. 39 (11), pp. 1713-1720.

Impact of structural racism on inclusion and diversity in precision oncology: A scoping and critical review of the literature.

Autor: Geneviève, Lester D.¹ lester.genevieve@unibas.ch, Elger, Bernice S.^1,2, Wangmo, Tenzin¹

Publikováno v: Cambridge Prisms: Precision Medicine. 2023, Vol. 1, p1-17. 17p.

Abandoning the word Caucasian.

Autor: Tschirgi, Matthew L., Liaquat, Khalida, Mahey Kumar, Meenakshi, Wilson, Kate L.

Publikováno v: Journal of Genetic Counseling; Oct2023, Vol. 32 Issue 5, p930-936, 7p

Towards the multileveled and processual conceptualisation of racialised individuals in biomedical research.

Autor: Malinowska, Joanna Karolina, Żuradzki, Tomasz

Publikováno v: Synthese; Jan2023, Vol. 201 Issue 1, p1-36, 36p