Zobrazeno 1 - 10
of 361
pro vyhledávání: '"Michael S Watson"'
Autor:
Kent, Alastair
Publikováno v:
Journal of Medical Ethics, 2000 Dec 01. 26(6), 482-482.
Externí odkaz:
https://www.jstor.org/stable/27718614
Publikováno v:
International Journal of Neonatal Screening, Vol 8, Iss 3, p 41 (2022)
Progress in newborn screening (NBS) has been driven for 60 years by developments in science and technology, growing consumer advocacy, the actions of providers involved in the care of rare disease patients, and by federal and State government funding
Externí odkaz:
https://doaj.org/article/effae7a4000a43fc8f581638bb840b54
Autor:
Alastair Kent
Publikováno v:
Journal of Medical Ethics. 26:482-482
This volume represents the conclusions of a multidisciplinary task force established by the US National Institutes of Health and Department of Energy working groups on the ethics, legal and social implications of human genome research. It ranges acro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::337fc4484d39e74119aed334d1d6a41b
https://doi.org/10.1136/jme.26.6.482
https://doi.org/10.1136/jme.26.6.482
Autor:
Patricia A. Deverka, Mary A. Majumder, Angela G. Villanueva, Margaret Anderson, Annette C. Bakker, Jessica Bardill, Eric Boerwinkle, Tania Bubela, Barbara J. Evans, Nanibaa’ A. Garrison, Richard A. Gibbs, Robert Gentleman, David Glazer, Melissa M. Goldstein, Hank Greely, Crane Harris, Bartha M. Knoppers, Barbara A. Koenig, Isaac S. Kohane, Salvatore La Rosa, John Mattison, Christopher J. O’Donnell, Arti K. Rai, Heidi L. Rehm, Laura L. Rodriguez, Robert Shelton, Tania Simoncelli, Sharon F. Terry, Michael S. Watson, John Wilbanks, Robert Cook-Deegan, Amy L. McGuire
Publikováno v:
Genome Medicine, Vol 9, Iss 1, Pp 1-5 (2017)
Abstract National and international public–private partnerships, consortia, and government initiatives are underway to collect and share genomic, personal, and healthcare data on a massive scale. Ideally, these efforts will contribute to the creati
Externí odkaz:
https://doaj.org/article/43ff14be39e04396b9359b9b20c8caf0
Autor:
Clement B. Sledge
Publikováno v:
New England Journal of Medicine. 326:208-208
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a20ac9690236bc884f0c7647c21ab8ae
https://doi.org/10.1056/nejm199201163260321
https://doi.org/10.1056/nejm199201163260321
Autor:
Wendy K. Chung, Jonathan S. Berg, Jeffrey R. Botkin, Steven E. Brenner, Jeffrey P. Brosco, Kyle B. Brothers, Robert J. Currier, Amy Gaviglio, Walter E. Kowtoniuk, Colleen Olson, Michele Lloyd‐Puryear, Annamarie Saarinen, Mustafa Sahin, Yufeng Shen, Elliott H. Sherr, Michael S. Watson, Zhanzhi Hu
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics, vol 190, iss 2
In the US, newborn screening (NBS) is a unique health program that supports health equity and screens virtually every baby after birth, and has brought timely treatments to babies since the 1960's. With the decreasing cost of sequencing and the impro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690504d36cf726a7c15b830403d24819
https://doi.org/10.1002/ajmg.c.31988
https://doi.org/10.1002/ajmg.c.31988
Autor:
Deborah I. Ritter, Sameek Roychowdhury, Angshumoy Roy, Shruti Rao, Melissa J. Landrum, Dmitriy Sonkin, Mamatha Shekar, Caleb F. Davis, Reece K. Hart, Christine Micheel, Meredith Weaver, Eliezer M. Van Allen, Donald W. Parsons, Howard L. McLeod, Michael S. Watson, Sharon E. Plon, Shashikant Kulkarni, Subha Madhavan, on behalf of the ClinGen Somatic Cancer Working Group
Publikováno v:
Genome Medicine, Vol 8, Iss 1, Pp 1-9 (2016)
Abstract Background To truly achieve personalized medicine in oncology, it is critical to catalog and curate cancer sequence variants for their clinical relevance. The Somatic Working Group (WG) of the Clinical Genome Resource (ClinGen), in cooperati
Externí odkaz:
https://doaj.org/article/6ef4b9fea20b4dbbbfc2a9f4940e7437