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Gregory M. Cooper

alabama

75H-index
358Paper Count
4.5WCitation Count
Published Papers 139
Publication Date
Biallelic FGF4 Variants Linked to Thoracic Dystrophy and Respiratory Insufficiency
err2025-04-22
err0
errOAAI
errLaura M. Watts; Esther Kinning; Donald R. Latner; Marla Johnston; Jessica Patrick-Esteve; Gregory M. Cooper; Stephen R. F. Twigg; Alistair T. Pagnamenta; Jenny C. Taylor
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Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselors
err2024-09-01
err1
PREAI
errColeman, Tanner F.; Pugh, Jada; Kelley, Whitley, V; East, Kelly M.; Greve, Veronica; Finnila, Candice R.; Henson, Ava; Korf, Bruce R.; Barsh, Gregory S.; Cooper, Gregory M.; Cochran, Meagan E.
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Allele-specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs
err2024-08-16
err0
PREAI
errAnderson, Ashlyn G.; Moyers, Belle A.; Loupe, Jacob M.; Rodriguez-Nunez, Ivan; Felker, Stephanie A.; Lawlor, James M. J.; Bunney, William E.; Bunney, Blynn G.; Cartagena, Preston M.; Sequeira, Adolfo; Watson, Stanley J.; Akil, Huda; Mendenhall, Eric M.; Cooper, Gregory M.; Myers, Richard M.
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Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing
err2023-08-01
err4
errOAAI
errFelker, Stephanie A.; Lawlor, James M. J.; Hiatt, Susan M.; Thompson, Michelle L.; Latner, Donald R.; Finnila, Candice R.; Bowling, Kevin M.; Bonnstetter, Zachary T.; Bonini, Katherine E.; Kelly, Nicole R.; V. Kelley, Whitley; Hurst, Anna C. E.; Rashid, Salman; Kelly, Melissa A.; Nakouzi, Ghunwa; Hendon, Laura G.; Bebin, E. Martina; Kenny, Eimear E.; Cooper, Gregory M.
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Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
err2023-06-21
err3
errOAAI
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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Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
err2023-02-01
err7
errOAAI
errHiatt, Susan M.; Trajkova, Slavica; Sebastiano, Matteo Rossi; Partridge, E. Christopher; Abidi, Fatima E.; Anderson, Ashlyn; Ansar, Muhammad; Antonarakis, Stylianos E.; Azadi, Azadeh; Bachmann-Gagescu, Ruxandra; Bartuli, Andrea; Benech, Caroline; Berkowitz, Jennifer L.; Betti, Michael J.; Brusco, Alfredo; Cannon, Ashley; Caron, Giulia; Chen, Yanmin; Cochran, Meagan E.; Coleman, Tanner F.; Crenshaw, Molly M.; Cuisset, Laurence; Curry, Cynthia J.; Darvish, Hossein; Demirdas, Serwet; Descartes, Maria; Douglas, Jessica; Dyment, David A.; Elloumi, Houda Zghal; Ermondi, Giuseppe; Faoucher, Marie; Farrow, Emily G.; Felker, Stephanie A.; Fisher, Heather; Hurst, Anna C. E.; Joset, Pascal; Kelly, Melissa A.; Kmoch, Stanislav; Leadem, Benjamin R.; Lyons, Michael J.; Macchiaiolo, Marina; Magner, Martin; Mandrile, Giorgia; Mattioli, Francesca; McEown, Megan; Meadows, Sarah K.; Medne, Livija; Meeks, Naomi J. L.; Montgomery, Sarah; Napier, Melanie P.; Natowicz, Marvin; Newberry, Kimberly M.; Niceta, Marcello; Noskova, Lenka; Nowak, Catherine B.; Noyes, Amanda G.; Osmond, Matthew; Prijoles, Eloise J.; Pugh, Jada; Pullano, Verdiana; Quelin, Chloe; Rahimi-Aliabadi, Simin; Rauch, Anita; Redon, Sylvia; Reymond, Alexandre; Schwager, Caitlin R.; Sellars, Elizabeth A.; Scheuerle, Angela E.; Shukarova-Angelovska, Elena; Skraban, Cara; Stolerman, Elliot; Sullivan, Bonnie R.; Tartaglia, Marco; Thiffault, Isabelle; Uguen, Kevin; Umana, Luis A.; Bever, Yolande van; Crabben, Saskia N. van der; Slegtenhorst, Marjon A. van; Waisfisz, Quinten; Washington, Camerun; Rodan, Lance H.; Myers, Richard M.; Cooper, Gregory M.
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Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing
err2022-11-21
err8
errOAAI
errBowling, Kevin M.; Thompson, Michelle L.; Kelly, Melissa A.; Scollon, Sarah; Slavotinek, Anne M.; Powell, Bradford C.; Kirmse, Brian M.; Hendon, Laura G.; Brothers, Kyle B.; Korf, Bruce R.; Cooper, Gregory M.; Greally, John M.; Hurst, Anna C. E.
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Short-Term Administration of HIV Protease Inhibitor Saquinavir Improves Skull Bone Healing with Enhanced Osteoclastogenesis
err2022-09-19
err1
errOAAI
errLiu, Haixia; Shen, Yun; Zhao, Bingkun; Poon, Enoch H.; Qi, Shengcai; Ker, Dai Fei Elmer; Billiar, Timothy R.; Cooper, Gregory M.; Xu, Yuanzhi; Wang, Dan
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Genome sequencing as a first-line diagnostic test for hospitalized infants
err2022-04-01
err29
errOAAI
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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Parental impact of genome sequencing during the neonatal period
err2022-03-01
err0
errOAAI
errBrothers, Kyle; Rich, Carla; Gimpel, Emily; East, Kelly; Cochran, Meagan; Greve, Veronica; Kelley, Whitley V.; Jackson, Kelly; Hendon, Laura; Luedecke, Amanda; Janani, Hillary; Meddaugh, Hannah; Latner, Donald; Bowling, Kevin; Thompson, Michelle; Finnila, Candice; Hiatt, Susan; Amaral, Michelle; Lawlor, James; Gray, David; Felker, Stephanie; Cannon, Ashley; Johnston, Marla; Merin, Lee Ann; Deans, Sarah; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew; Patrick-Esteve, Jessica; Hurst, Anna; Kandasamy, Jegen; Carlo, Waldemar; Kirmse, Brian; Savich, Renate; Superneau, Duane; Spedale, Steven; Knight, Sara; Barsh, Gregory; Korf, Bruce; Cooper, Gregory
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Integration of genomics into primary care via the Alabama Genomic Health Initiative
err2022-03-01
err0
errOAAI
errKorf, Bruce; Absher, Devin; Asif, Irfan; Bateman, Lori; Barsh, Gregory; Bowling, Kevin; Cooper, Gregory; Davis, Brittney; East, Kelly; Finnila, Candice; Goff, Blake; Kelly, Melissa; Kelley, Whitley; Latner, Donald; Lawlor, James; Limdi, Nita; May, Thomas; Might, Matthew; Moss, Irene; Nakano, Mariko; Osborne, Tiffany; Sodeke, Stephen; Stout, Adriana; Thompson, Michelle
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Comparing error rates in disclosure of genome sequencing results between non-genetics providers and genetic counselors
err2022-03-01
err1
errOAAI
errCochran, Meagan; East, Kelly; Kelley, Whitley V.; Greve, Veronica; Henson, Ava; Finnila, Candice; Danila, Maria; Savich, Renate; Brothers, Kyle; Spedale, Steven; Patrick-Esteve, Jessica; Sims, Brian; Carlo, Waldemar; Barsh, Gregory; Korf, Bruce; Cooper, Gregory
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The clinical significance of poisoned splicing variants in early-onset neurodevelopmental disorders
err2022-03-01
err0
errOAAI
errFelker, Stephanie; Lawlor, James; Latner, Donald; Thompson, Michelle; Bowling, Kevin; Hiatt, Susan; Finnila, Candice; Cooper, Gregory
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Expansion of long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders and multiple congenital anomalies
err2022-03-01
err0
errOAAI
errHiatt, Susan; Lawlor, James; Handley, Lori; Bonnstetter, Zachary; Jenkins, Jerry; Lovell, John; Holt, James; Finnila, Candice; Thompson, Michelle; Latner, Donald; Partridge, Christopher; Plott, Christopher; Boston, Lori Beth; Williams, Melissa; Bowling, Kevin; Grimwood, Jane; Schmutz, Jeremy; Cooper, Gregory
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Long-read genome sequencing secondary processing pipelines provide variant call accuracy that exceeds current clinical standards for short-read genome sequencing
err2022-03-01
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errOAAI
errHolt, James; Handley, Lori; Lawlor, James; Hiatt, Susan; Cooper, Gregory; Grimwood, Jane; Nakouzi, Ghunwa
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SouthSeq: Genome sequencing for a diverse population of hospitalized infants
err2022-03-01
err0
errOAAI
errLatner, Donald; Bowling, Kevin; Thompson, Michelle; Finnila, Candice; Hiatt, Susan; Amaral, Michelle; Lawlor, James; East, Kelly; Cochran, Meagan; Greve, Veronica; Kelley, Whitley V.; Gray, David; Felker, Stephanie; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly; Hendon, Laura; Janani, Hillary; Johnston, Marla; Merin, Lee Ann; Deans, Sarah; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew; Patrick-Esteve, Jessica; Hurst, Anna; Kandasamy, Jegen; Carlo, Waldemar; Brothers, Kyle; Kirmse, Brian; Savich, Renate; Superneau, Duane; Spedale, Steven; Knight, Sara; Barsh, Gregory; Korf, Bruce; Cooper, Gregory
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Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
err2021-05-01
err20
errOAAI
errVoisin, Norine; Schnur, Rhonda E.; Douzgou, Sofia; Hiatt, Susan M.; Rustad, Cecilie F.; Brown, Natasha J.; Earl, Dawn L.; Keren, Boris; Levchenko, Olga; Geuer, Sinje; Verheyen, Sarah; Johnson, Diana; Zarate, Yuri A.; Hancarova, Miroslava; Amor, David J.; Bebin, E. Martina; Blatterer, Jasmin; Brusco, Alfredo; Cappuccio, Gerarda; Charrow, Joel; Chatron, Nicolas; Cooper, Gregory M.; Courtin, Thomas; Dadali, Elena; Delafontaine, Julien; Del Giudice, Ennio; Doco, Martine; Douglas, Ganka; Eisenkolbl, Astrid; Funari, Tara; Giannuzzi, Giuliana; Gruber-Sedlmayr, Ursula; Guex, Nicolas; Heron, Delphine; Holla, Oystein L.; Hurst, Anna C. E.; Juusola, Jane; Kronn, David; Lavrov, Alexander; Lee, Crystle; Lorrain, Severine; Merckoll, Else; Mikhaleva, Anna; Norman, Jennifer; Pradervand, Sylvain; Prchalova, Darina; Rhodes, Lindsay; Sanders, Victoria R.; Sedlacek, Zdenek; Seebacher, Heidelis A.; Sellars, Elizabeth A.; Sirchia, Fabio; Takenouchi, Toshiki; Tanaka, Akemi J.; Taska-Tench, Heidi; Tonne, Elin; Tveten, Kristian; Vitiello, Giuseppina; Vlckova, Marketa; Uehara, Tomoko; Nava, Caroline; Yalcin, Binnaz; Kosaki, Kenjiro; Donnai, Dian; Mundlos, Stefan; Brunetti-Pierri, Nicola; Chung, Wendy K.; Reymond, Alexandre
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Genome-wide strand asymmetry in massively parallel reporter activity favors genic strands
err2021-04-20
err2
errOAAI
errRoberts, Brian S.; Partridge, E. Christopher; Moyers, Bryan A.; Agarwal, Vikram; Newberry, Kimberly M.; Martin, Beth K.; Shendure, Jay; Myers, Richard M.; Cooper, Gregory M.
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A state-based approach to genomics for rare disease and population screening
err2021-04-01
err22
errOAAI
errEast, Kelly M.; Kelley, Whitley V.; Cannon, Ashley; Cochran, Meagan E.; Moss, Irene P.; May, Thomas; Nakano-Okuno, Mariko; Sodeke, Stephen O.; Edberg, Jeffrey C.; Cimino, James J.; Fouad, Mona; Curry, William A.; Hurst, Anna C. E.; Bowling, Kevin M.; Thompson, Michelle L.; Bebin, E. Martina; Johnson, Robert D.; Acemgil, Aras; Acemgil, Aras; Crossman, David K.; Finnila, Candice R.; Gray, David E.; Greve, Veronica; Hardy, Sharonda; Hiatt, Susan M.; Latner, Donald R.; Lawlor, James M. J.; Miskell, Edrika L.; Narmore, Whitney; Schach, Julie H.; Cooper, Gregory M.; Might, Matthew; Barsh, Gregory S.; Korf, Bruce R.
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Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders
err2021-04-01
err33
errOAAI
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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