Zobrazeno 1 - 4
of 4
pro vyhledávání: '"James M. J. Lawlor"'
Autor:
Alexandra “Xan” C. H. Nowakowski PhD, MPH, Gabriella “Ella” Balasa BS, Miriam F. Figueira PhD, Francis “Tré” J. LaRosa BS, James M. J. Lawlor MS
Publikováno v:
Inquiry: The Journal of Health Care Organization, Provision, and Financing, Vol 59 (2022)
Care for many progressive chronic diseases continues to improve, allowing patients to survive and thrive for longer periods of time 1 . People living with such conditions may now find themselves able to achieve long-term goals in education and career
Externí odkaz:
https://doaj.org/article/f8932cb2ab6b4049924431117c982f51
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
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
Autor:
Michelle L. Thompson, Candice R. Finnila, Kevin M. Bowling, Kyle B. Brothers, Matthew B. Neu, Michelle D. Amaral, Susan M. Hiatt, Kelly M. East, David E. Gray, James M. J. Lawlor, Whitley V. Kelley, Edward J. Lose, Carla A. Rich, Shirley Simmons, Shawn E. Levy, Richard M. Myers, Gregory S. Barsh, E. Martina Bebin, Gregory M. Cooper
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
PURPOSEClinically relevant secondary variants were identified in parents enrolled with a child with developmental delay and intellectual disability.METHODSExome/genome sequencing and analysis of 789 ‘unaffected’ parents was performed.RESULTSPatho