Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Debra Lochner Doyle"'
Autor:
Steven M. Harrison, Debra Lochner Doyle, Elaine Lyon, Kandamurugu Manickam, Kristin G. Monaghan, Sonja A. Rasmussen, Michael S. Watson, Michael F. Murray, Maren T. Scheuner, Monica A. Giovanni, Glenn E. Palomaki
Publikováno v:
Genetics in Medicine. 23:989-995
Autor:
Deborah Cragun, Kee Chan, Georgia Hurst, David A. Chambers, Laura Senier, Juan L. Rodriguez, Debra Lochner Doyle, Mindy Clyne
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
To assess the implementation of evidence-based genomic medicine and its population-level impact on health outcomes and to promote public health genetics interventions, in 2015 the Roundtable on Genomics and Precision Health of the National Academies
Autor:
Sura Alwan, Angus John Clarke, Kenneth H. Astrin, Marina Bartsakoulia, Deepika D’Cunha Burkardt, Constantina Chalikiopoulou, Joshua L. Deignan, Robert J. Desnick, Shweta U. Dhar, Debra Lochner Doyle, Malcolm A. Ferguson-Smith, Jan M. Friedman, John M. Graham Jr., Daniel Graziano, Wayne W. Grody, Rachel Irving, Kenneth L. Jones, Marilyn C. Jones, Theodora Katsila, Muin J. Khoury, Matthew J. McGinniss, Molly A. McGinniss, John B. Moeschler, Angeliki Panagiotara, George P. Patrinos, Maren T. Scheuner, Edward H. Schuchman, Amita Sehgal, Efthymios Skoufas, Nancy B. Spinner, Massimo Trucco, Evangelia-Eirini Tsermpini, Marc S. Williams, Shirley L. Zhang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbb62a0f26475f610ec661df0838a173
https://doi.org/10.1016/b978-0-12-812536-6.01002-6
https://doi.org/10.1016/b978-0-12-812536-6.01002-6
Autor:
Muin J. Khoury, Debra Lochner Doyle
This chapter reviews the emergence and progress in the field of public health genetics/genomics. Firmly rooted in two fields with a rich and disparate history (medical genetics and public health), public health genomics has taken shape only in the pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adef854ab2da72990c330da00290a97b
https://doi.org/10.1016/b978-0-12-812536-6.00014-6
https://doi.org/10.1016/b978-0-12-812536-6.00014-6
Autor:
Matthew R.G. Taylor, Robert J. Ostrander, Debra Lochner Doyle, Alisha Keehn, Celia Kaye, Joann Bodurtha, Susanna Ginsburg, Mathew J. Edick, Michele A. Lloyd-Puryear, Megan Lyon
Publikováno v:
Genetics in Medicine
Purpose To outline structures for regional genetic services support centers that improve access to clinical genetic services. Methods A workgroup (WG) and advisory committee (AC) (1) conducted a comprehensive review of existing models for delivering
Autor:
Angela R. Bradbury, Stephanie M. Fullerton, Debra G.B. Leonard, Theodore G. Ganiats, George Isham, Kimberly A. Kaphingst, Catherine Wicklund, James P. Evans, Marissa Levine, Catharine Wang, Ellen Matloff, Leonard W. Ortmann, Debra Lochner Doyle, Nazneen Aziz, Michael F. Murray, Misha Angrist, Kristen Young, Muin J. Khoury, Wendy R. Uhlmann, W. David Dotson, Joan Scott, Sun Hee Rim, Sara Imhof, Jill Hagenkord, Ann G. Zauber, Bruce R. Korf
Publikováno v:
NAM Perspectives.
Autor:
Megan Lyon, Susanna Ginsburg, Celia Kaye, Joann Bodurtha, Debra Lochner Doyle, Robert J. Ostrander, Mathew J. Edick, Matthew R.G. Taylor, Michele A. Lloyd-Puryear, Alisha Keehn
Publikováno v:
Genetics in Medicine. 22:241
Publikováno v:
Journal of early hearing detection and intervention. 3(1)
This study assessed whether children with oral clefts are appropriately classified as at-risk for hearing loss at the time of newborn hearing screening and describes their screening and diagnostic results.Birth certificates were used to identify chil
Autor:
David L. Veenstra, Debra Lochner Doyle, Gregory F. Guzauskas, Jacquie Stock, Sylvia Mann Au, Louis P. Garrison
Publikováno v:
Genetics in Medicine. 15:84-87
Genetic services policymakers and insurers often make coverage decisions in the absence of complete evidence of clinical utility and under budget constraints. We evaluated genetic services stakeholder opinions on the potential usefulness of decision-
Publikováno v:
Journal of Genetic Counseling. 17:424-433
In 1995, the Pedigree Standardization Task Force (PSTF) of the National Society of Genetic Counselors (NSGC) proposed a system of pedigree nomenclature. Recently, the PSTF (now called the Pedigree Standardization Work Group or PSWG) sought evidence t