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Considerations for policymakers for improving health care through telegenetics: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

Autor: Heather E, Williams, Lila, Aiyar, Mary Beth, Dinulos, David, Flannery, Michelle L, McClure, Michele A, Lloyd-Puryear, Kunal, Sanghavi, Tracy L, Trotter, David, Viskochil

Publikováno v: Genetics in Medicine. 24:2211-2219

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::034bba2ce52d0fee7607e20789a88223
https://doi.org/10.1016/j.gim.2022.07.017

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Commentary from the Minority Genetic Professionals Network on the AGCPD Taskforce analysis of select criteria and performance on the ABGC certification examination by Myers et al. (2021)

Autor: Sylvia Mann, Lila Aiyar, Michelle Takemoto, Liann Jimmons

Publikováno v: Journal of Genetic Counseling. 31:324-325

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2b109dc4c8347083431c8b09e29c43f0
https://doi.org/10.1002/jgc4.1561

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Introduction: The state of minority and health disparities in research and practice in genetic counseling and genomic medicine

Autor: Vivian Ota Wang, Lila Aiyar, Nadine Channaoui

Publikováno v: Journal of genetic counselingReferences. 29(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c340535fa64fe1bc636efd8a8b8783
https://pubmed.ncbi.nlm.nih.gov/32250031

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Prenatal presentation in a patient with Baraitser-Winter cerebrofrontofacial syndrome and a novel ACTB variant

Autor: Tammy Stumbaugh, Bruce Chen, Lila Aiyar, Robert Wallerstein, Helen L Lau, Greigh I. Hirata

Publikováno v: Clinical Dysmorphology. 28:162-164

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c798f054ba285823a5a1af8cc3e7961
https://doi.org/10.1097/mcd.0000000000000266

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Risk estimates for complex disorders: comparing personal genome testing and family history

Autor: Robin Z. Hayeems, Shoshana J. Wodak, Annie Dupuis, Lila Aiyar, Lea Velsher, David Chitayat, Shuye Pu, Cheryl Shuman, Jill Davies

Publikováno v: Genetics in Medicine. 16:231-237

Personal genome testing allows the identification of single-nucleotide polymorphisms associated with an increased risk for common complex disorders. An area of concern in the use of personal genome testing is how risk estimates generated differ from

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0276acf82a660cb90a2f979345b889e
https://doi.org/10.1038/gim.2013.115

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