Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Donald R. Latner"'
Autor:
Nita A Limdi, Devin Absher, Irf Asif, Lori Bateman, Greg Barsh, Kevin M. Bowling, Gregory M. Cooper, Brittney H. Davis, Kelly M. East, Candice R. Finnila, Blake Goff, Susan Hiatt, Melissa Kelly, Whitley V. Kelley, Bruce R. Korf, Donald R. Latner, James Lawlor, Thomas May, Matt Might, Irene P. Moss, Mariko Nakano-Okuno, Tiffany Osborne, Stephen Sodeke, Adriana Stout, Michelle L. Thompson
Publikováno v:
Journal of Clinical and Translational Science, Vol 7, Pp 100-101 (2023)
OBJECTIVES/GOALS: Supported by the State of Alabama, the Alabama Genomic Health Initiative (AGHI) is aimed at preventing and treating common conditions with a genetic basis. This joint UAB Medicine-HudsonAlpha Institute for Biotechnology effort provi
Externí odkaz:
https://doaj.org/article/837b5bfa60884410b37c71dec2ad6f9f
Autor:
Rita Czakó Stinnett, Andrew S. Beck, Elena N. Lopareva, Rebecca J. McNall, Donald R. Latner, Carole J. Hickman, Paul A. Rota, Bettina Bankamp
Publikováno v:
mSphere, Vol 5, Iss 6 (2020)
ABSTRACT Between 2015 and 2017, routine molecular surveillance in the United States detected multiple mumps viruses (MuVs) with mutations in the small hydrophobic (SH) gene compared to a reference virus of the same genotype. These mutations include a
Externí odkaz:
https://doaj.org/article/78d8d502d69d41fe8f55f93131f94d32
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:
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
Autor:
Stephanie A Felker, James MJ Lawlor, Susan M Hiatt, Michelle L Thompson, Donald R Latner, Candice R Finnila, Kevin M Bowling, Zachary T Bonnstetter, Katherine E Bonini, Nicole R Kelly, Whitley V Kelley, Anna CE Hurst, Melissa A Kelly, Ghunwa Nakouzi, Laura G Hendon, E Martina Bebin, Eimear E Kenny, Gregory M Cooper
PurposeNeurodevelopmental disorders (NDDs) often result from rare genetic variation, but genomic testing yield for NDDs remains around 50%, suggesting some clinically relevant rare variants may be missed by standard analyses. Here we analyze “poiso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d216d5994ea7884fe8a6e070dedbfec
https://doi.org/10.1101/2023.01.12.523654
https://doi.org/10.1101/2023.01.12.523654
Autor:
Sun B. Sowers, Kiana Anthony, Sara Mercader, Heather Colley, Stephen N. Crooke, Paul A. Rota, Donald R. Latner, Carole J. Hickman
Publikováno v:
J Clin Microbiol
Laboratory confirmation of infection is an essential component of measles surveillance. Detection of measles-specific IgM in serum by enzyme-linked immunosorbent assay (ELISA) is the most common method used to confirm measles infection. ELISA formats
Autor:
Sun B. Sowers, Kiana Anthony, Sara Mercader, Heather Colley, Stephen N. Crooke, Paul A. Rota, Donald R. Latner, Carole J. Hickman
Laboratory confirmation of infection is an essential component of measles surveillance. Detection of measles specific IgM in serum by enzyme linked immunosorbent assay (ELISA) is the most used method for confirming measles infection. ELISA formats va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e000a256fe642aa24a06857759d1e857
https://doi.org/10.1101/2022.09.02.22279538
https://doi.org/10.1101/2022.09.02.22279538
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
PurposeSouthSeq, a translational research study to perform genome sequencing (GS) for infants with symptoms suggestive of a genetic disorder, was conducted in NICUs in the Southeastern US. Recruitment targeted racial/ethnic minorities and rural, medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94497677121ed14a19dbae2b2378b755
https://doi.org/10.1101/2021.08.31.21262633
https://doi.org/10.1101/2021.08.31.21262633
Autor:
Paul A. Rota, Donald R. Latner, Carole J. Hickman, Elena N. Lopareva, Bettina Bankamp, Rita Czakó Stinnett, Rebecca J. McNall, Andrew S. Beck
Publikováno v:
mSphere
mSphere, Vol 5, Iss 6 (2020)
mSphere, Vol 5, Iss 6 (2020)
Mumps virus (MuV) outbreaks occur in the United States despite high coverage with measles, mumps, rubella (MMR) vaccine. Routine genotyping of laboratory-confirmed mumps cases has been practiced in the United States since 2006 to enhance mumps survei
Autor:
Kelly M. East, Whitley V. Kelley, Ashley Cannon, Meagan E. Cochran, Irene P. Moss, Thomas May, Mariko Nakano-Okuno, Stephen O. Sodeke, Jeffrey C. Edberg, James J. Cimino, Mona Fouad, William A. Curry, Anna C.E. Hurst, Kevin M. Bowling, Michelle L. Thompson, E. Martina Bebin, Robert D. Johnson, Aras Acemgil, David K. Crossman, Candice R. Finnila, David E. Gray, Veronica Greve, Sharonda Hardy, Susan M. Hiatt, Donald R. Latner, James M.J. Lawlor, Edrika L. Miskell, Whitney Narmore, Julie H. Schach, Gregory M. Cooper, Matthew Might, Gregory S. Barsh, Bruce R. Korf
Publikováno v:
Genet Med
PURPOSE: The Alabama Genomic Health Initiative (AGHI) is a state-funded effort to provide genomic testing. AGHI engages two distinct cohorts across the state of Alabama. One cohort includes children and adults with undiagnosed rare disease; a second