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Gray, David E.

HudsonAlpha Institute for Biotechnology

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7Paper Count
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Published Papers 7
Publication Date
Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
err2023-06-21
err3
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errLemke, Amy A.; Thompson, Michelle L.; Gimpel, Emily C.; McNamara, Katelyn C.; Rich, Carla A.; Finnila, Candice R.; Cochran, Meagan E.; Lawlor, James M. J.; East, Kelly M.; Bowling, Kevin M.; Latner, Donald R.; Hiatt, Susan M.; Amaral, Michelle D.; Kelley, Whitley V.; Greve, Veronica; Gray, David E.; Felker, Stephanie A.; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly E.; Hendon, Laura G.; Janani, Hillary M.; Johnston, Marla; Merin, Lee Ann; Deans, Sarah L.; Tuura, Carly; Hughes, Trent; Williams, Heather; Laborde, Kelly; Neu, Matthew B.; Patrick-Esteve, Jessica; Hurst, Anna C. E.; Kirmse, Brian M.; Savich, Renate; Spedale, Steven B.; Knight, Sara J.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.; Brothers, Kyle B.
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Genome sequencing as a first-line diagnostic test for hospitalized infants
err2022-04-01
err29
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errBowling, Kevin M.; Thompson, Michelle L.; Finnila, Candice R.; Hiatt, Susan M.; Latner, Donald R.; Amaral, Michelle D.; Lawlor, James M. J.; East, Kelly M.; Cochran, Meagan E.; Greve, Veronica; Kelley, Whitley, V; Gray, David E.; Felker, Stephanie A.; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly E.; Hendon, Laura G.; Janani, Hillary M.; Johnston, Marla; Merin, Lee Ann; Deans, Sarah L.; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew B.; Patrick-Esteve, Jessica; Hurst, Anna C. E.; Kandasamy, Jegen; Carlo, Wally; Brothers, Kyle B.; Kirmse, Brian M.; Savich, Renate; Superneau, Duane; Spedale, Steven B.; Knight, Sara J.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.
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Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders
err2021-04-01
err33
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errHiatt, Susan M.; Lawlor, James M. J.; Handley, Lori H.; Ramaker, Ryne C.; Rogers, Brianne B.; Partridge, E. Christopher; Boston, Lori Beth; Williams, Melissa; Plott, Christopher B.; Jenkins, Jerry; Gray, David E.; Holt, James M.; Bowling, Kevin M.; Bebin, E. Martina; Grimwood, Jane; Schmutz, Jeremy; Cooper, Gregory M.
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Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls
err2021-02-01
err8
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errBowling, Kevin M.; Thompson, Michelle L.; Gray, David E.; Lawlor, James M. J.; Williams, Kelly; East, Kelly M.; Kelley, Whitley V.; Moss, Irene P.; Absher, Devin M.; Partridge, E. Christopher; Hurst, Anna C. E.; Edberg, Jeffrey C.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.
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Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder
err2019-04-01
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errHiatt, Susan M.; Thompson, Michelle L.; Prokop, Jeremy W.; Lawlor, James M. J.; Gray, David E.; Bebin, E. Martina; Rinne, Tuula; Kempers, Marlies; Pfundt, Rolph; van Bon, Bregje W.; Mignot, Cyril; Nava, Caroline; Depienne, Christel; Kalsner, Louisa; Rauch, Anita; Joset, Pascal; Bachmann-Gagescu, Ruxandra; Wentzensen, Ingrid M.; McWalter, Kirsty; Cooper, Gregory M.
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Genomic sequencing identifies secondary findings in a cohort of parent study participants
err2018-12-01
err24
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errThompson, Michelle L.; Finnila, Candice R.; Bowling, Kevin M.; Brothers, Kyle B.; Neu, Matthew B.; Amaral, Michelle D.; Hiatt, Susan M.; East, Kelly M.; Gray, David E.; Lawlor, James M. J.; Kelley, Whitley V.; Lose, Edward J.; Rich, Carla A.; Simmons, Shirley; Levy, Shawn E.; Myers, Richard M.; Barsh, Gregory S.; Bebin, E. Martina; Cooper, Gregory M.
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Genomic diagnosis for children with intellectual disability and/or developmental delay
err2017-05-30
err191
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errBowling, Kevin M.; Thompson, Michelle L.; Amaral, Michelle D.; Finnila, Candice R.; Hiatt, Susan M.; Engel, Krysta L.; Cochran, J. Nicholas; Brothers, Kyle B.; East, Kelly M.; Gray, David E.; Kelley, Whitley V.; Lamb, Neil E.; Lose, Edward J.; Rich, Carla A.; Simmons, Shirley; Whittle, Jana S.; Weaver, Benjamin T.; Nesmith, Amy S.; Myers, Richard M.; Barsh, Gregory S.; Bebin, E. Martina; Cooper, Gregory M.
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