Zobrazeno 1 - 10
of 52
pro vyhledávání: '"David E Gray"'
Autor:
Susan M. Hiatt, James M.J. Lawlor, Lori H. Handley, Ryne C. Ramaker, Brianne B. Rogers, E. Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher B. Plott, Jerry Jenkins, David E. Gray, James M. Holt, Kevin M. Bowling, E. Martina Bebin, Jane Grimwood, Jeremy Schmutz, Gregory M. Cooper
Publikováno v:
HGG Advances, Vol 2, Iss 2, Pp 100023- (2021)
Summary: Exome and genome sequencing have proven to be effective tools for the diagnosis of neurodevelopmental disorders (NDDs), but large fractions of NDDs cannot be attributed to currently detectable genetic variation. This is likely, at least in p
Externí odkaz:
https://doaj.org/article/9e89b02fe99e4ca599239301f8118f70
Autor:
Kevin M. Bowling, Michelle L. Thompson, Michelle D. Amaral, Candice R. Finnila, Susan M. Hiatt, Krysta L. Engel, J. Nicholas Cochran, Kyle B. Brothers, Kelly M. East, David E. Gray, Whitley V. Kelley, Neil E. Lamb, Edward J. Lose, Carla A. Rich, Shirley Simmons, Jana S. Whittle, Benjamin T. Weaver, Amy S. Nesmith, Richard M. Myers, Gregory S. Barsh, E. Martina Bebin, Gregory M. Cooper
Publikováno v:
Genome Medicine, Vol 9, Iss 1, Pp 1-11 (2017)
Abstract Background Developmental disabilities have diverse genetic causes that must be identified to facilitate precise diagnoses. We describe genomic data from 371 affected individuals, 309 of which were sequenced as proband-parent trios. Methods W
Externí odkaz:
https://doaj.org/article/895f744bb3324791b83b71e276793d82
Autor:
Brothers, Amy A. Lemke, Michelle L. Thompson, Emily C. Gimpel, Katelyn C. McNamara, Carla A. Rich, Candice R. Finnila, Meagan E. Cochran, James M. J. Lawlor, Kelly M. East, Kevin M. Bowling, Donald R. Latner, Susan M. Hiatt, Michelle D. Amaral, Whitley V. Kelley, Veronica Greve, David E. Gray, Stephanie A. Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Trent Hughes, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C. E. Hurst, Brian M. Kirmse, Renate Savich, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper, Kyle B.
Publikováno v:
Journal of Personalized Medicine; Volume 13; Issue 7; Pages: 1026
Background: It is critical to understand the wide-ranging clinical and non-clinical effects of genome sequencing (GS) for parents in the NICU context. We assessed parents’ experiences with GS as a first-line diagnostic tool for infants with suspect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::657740f79eb9a508fdaea4a4ed6566e0
Autor:
Steven Tam, David E Gray
Publikováno v:
Journal of Small Business and Enterprise Development, 2016, Vol. 23, Issue 3, pp. 671-690.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/JSBED-07-2015-0099
Autor:
Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Donald R. Latner, Michelle D. Amaral, James M.J. Lawlor, Kelly M. East, Meagan E. Cochran, Veronica Greve, Whitley V. Kelley, David E. Gray, Stephanie A. Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C.E. Hurst, Jegen Kandasamy, Wally Carlo, Kyle B. Brothers, Brian M. Kirmse, Renate Savich, Duane Superneau, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper
Publikováno v:
Genet Med
PURPOSE: SouthSeq is a translational research study that performed genome sequencing (GS) for infants with symptoms suggestive of a genetic disorder. Recruitment targeted racial/ethnic minorities and rural, medically underserved areas in the Southeas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fd5d2980df75b4164bcfcdf944c97a7
https://doi.org/10.1016/j.gim.2021.11.020
https://doi.org/10.1016/j.gim.2021.11.020
Autor:
Steven Tam, David E Gray
Publikováno v:
European Journal of Training and Development, 2016, Vol. 40, Issue 1, pp. 2-20.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/EJTD-07-2015-0052
Publikováno v:
European Journal of Training and Development, 2014, Vol. 38, Issue 1/2, pp. 136-149.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/EJTD-07-2013-0073
Autor:
Janet Elizabeth Childerhose, Carla Rich, Kelly M. East, Whitley V. Kelley, Shirley Simmons, Candice R. Finnila, Kevin Bowling, Michelle Amaral, Susan M. Hiatt, Michelle Thompson, David E. Gray, James M. J. Lawlor, Richard M. Myers, Gregory S. Barsh, Edward J. Lose, Martina E. Bebin, Greg M. Cooper, Kyle Bertram Brothers
Publikováno v:
AJOB Empir Bioeth
BACKGROUND: The desire of parents to obtain a genetic diagnosis for their child with intellectual disability and associated symptoms has long been framed as a diagnostic odyssey, an arduous and sometimes perilous journey focused on the goal of identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03408315ddb9d6a3dc8a45e8476ca8dd
https://doi.org/10.1080/23294515.2021.1907475
https://doi.org/10.1080/23294515.2021.1907475
Autor:
Kelly M. East, Whitley V. Kelley, James M.J. Lawlor, Kelly Williams, Irene P. Moss, Gregory S. Barsh, Michelle L. Thompson, Devin Absher, Jeffrey C. Edberg, Gregory M. Cooper, Kevin M. Bowling, E. Christopher Partridge, David E. Gray, Bruce R. Korf, Anna C.E. Hurst
Publikováno v:
Genetics in Medicine. 23:280-288
Purpose To evaluate the effectiveness and specificity of population-based genomic screening in Alabama. Methods The Alabama Genomic Health Initiative (AGHI) has enrolled and evaluated 5369 participants for the presence of pathogenic/likely pathogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e46dc66c8cb2d6841a54bfb564b3f2f
https://doi.org/10.1038/s41436-020-00976-z
https://doi.org/10.1038/s41436-020-00976-z