Gregory M Cooper (G M Cooper)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2014-2024
Publications (10 Years): 15

Top Topics

Transcription Factor

Intellectual Disability

Regulatory T Cells

Top Venues

Genome research

Nature neuroscience

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Jacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, Ivan Rodriguez-Nunez, Belle A Moyers, Katie Trausch-Lowther, Rashmi Jain, William E Bunney, Blynn G Bunney, Preston Cartagena, Adolfo Sequeira, Stanley J Watson, Huda Akil, Gregory M Cooper, Richard M Myers
Multiomic profiling of transcription factor binding and function in human brain. Nature neuroscience 27 (7) (2024)
Jacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, Ivan Rodriguez-Nunez, Belle A Moyers, Katie Trausch-Lowther, Rashmi Jain, William E Bunney, Blynn G Bunney, Preston Cartagena, Adolfo Sequeira, Stanley J Watson, Huda Akil, Gregory M Cooper, Richard M Myers
Multiomic profiling of transcription factor binding and function in human brain. Nature neuroscience (2024)
Ashlyn G Anderson, Belle A Moyers, Jacob M Loupe, Ivan Rodriguez-Nunez, Stephanie A Felker, James M J Lawlor, William E Bunney, Blynn G Bunney, Preston M Cartagena, P Adolfo Sequeira, Stanley J Watson, Huda Akil, Eric M Mendenhall, Gregory M Cooper, Richard M Myers
Allele specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs. Genome research (2024)
Ashlyn G Anderson, Belle A Moyers, Jacob M Loupe, Ivan Rodriguez-Nunez, Stephanie A Felker, James M J Lawlor, William E Bunney, Blynn G Bunney, Preston M Cartagena, P Adolfo Sequeira, Stanley J Watson, Huda Akil, Eric M Mendenhall, Gregory M Cooper, Richard M Myers
Allele specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs. Genome research (2024)
Jacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, Ivan Rodriguez-Nunez, Belle A Moyers, Katie Trausch-Lowther, Rashmi Jain, William E Bunney, Blynn G Bunney, Preston Cartagena, Adolfo Sequeira, Stanley J Watson, Huda Akil, Gregory M Cooper, Richard M Myers
Multiomic profiling of transcription factor binding and function in human brain. Nature neuroscience (2024)
Owen R Hirschi, Stephanie A Felker, Surya P Rednam, Kelly L Vallance, D Williams Parsons, Angshumoy Roy, Gregory M Cooper, Sharon E Plon
Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity. medRxiv : the preprint server for health sciences (2023)
Belle A Moyers, Jacob M Loupe, Stephanie A Felker, James M J Lawlor, Ashlyn G Anderson, Ivan Rodriguez-Nunez, William E Bunney, Blynn G Bunney, Preston M Cartagena, P Adolfo Sequeira, Stanley J Watson, Huda Akil, Eric M Mendenhall, Gregory M Cooper, Richard M Myers
Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs. bioRxiv : the preprint server for biology (2023)
Yuliya Voskobiynyk, Gopal Battu, Stephanie A Felker, Jesse Nicholas Cochran, Megan P Newton, Laura J Lambert, Robert A Kesterson, Richard M Myers, Gregory M Cooper, Erik D Roberson, Gregory S Barsh
Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy. PLoS genetics 17 (1) (2021)
Kevin M Bowling, Michelle L Thompson, David E Gray, James M J Lawlor, Kelly Williams, Kelly M East, Whitley V Kelley, Irene P Moss, Devin M Absher, E Christopher Partridge, Anna C E Hurst, Jeffrey C Edberg, Gregory S Barsh, Bruce R Korf, Gregory M Cooper
Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls. Genetics in medicine : official journal of the American College of Medical Genetics 23 (2) (2020)
Theodore G Drivas, Dong Li, Divya Nair, Joseph T Alaimo, Mariëlle Alders, Janine Altmüller, Tahsin Stefan Barakat, E Martina Bebin, Nicole L Bertsch, Patrick R Blackburn, Alyssa Blesson, Arjan M Bouman, Knut Brockmann, Perrine Brunelle, Margit Burmeister, Gregory M Cooper, Jonas Denecke, Anne Dieux-Coëslier, Holly Dubbs, Alejandro Ferrer, Danna Gal, Lauren E Bartik, Lauren B Gunderson, Linda Hasadsri, Mahim Jain, Catherine Karimov, Beth Keena, Eric W Klee, Katja Kloth, Baiba Lace, Marina Macchiaiolo, Julien L Marcadier, Jeff M Milunsky, Melanie P Napier, Xilma R Ortiz-Gonzalez, Pavel N Pichurin, Jason Pinner, Zöe Powis, Chitra Prasad, Francesca Clementina Radio, Kristen J Rasmussen, Deborah L Renaud, Eric T Rush, Carol Saunders, Duygu Selcen, Ann R Seman, Deepali N Shinde, Erica D Smith, Thomas Smol, Lot Snijders Blok, Joan M Stoler, Sha Tang, Marco Tartaglia, Michelle L Thompson, Jiddeke M van de Kamp, Jingmin Wang, Dagmar Weise, Karin Weiss, Rixa Woitschach, Bernd Wollnik, Huifang Yan, Elaine H Zackai, Giuseppe Zampino, Philippe M Campeau, Elizabeth Bhoj
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome. European journal of human genetics : EJHG 28 (10) (2020)
Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thevenon, Ange-Line Bruel, Anne-Laure Mosca-Boidron, Alice Masurel-Paulet, Alice Goldenberg, Nathalie Le Meur, Aude Charollais, Cyril Mignot, Florence Petit, Massimiliano Rossi, Julia Metreau, Valérie Layet, Daniel Amram, Odile Boute-Bénéjean, Elizabeth Bhoj, Margot A Cousin, Teresa M Kruisselbrink, Brendan C Lanpher, Eric W Klee, Elise Fiala, Dorothy K Grange, Wendy S Meschino, Susan M Hiatt, Gregory M Cooper, Hilde Olivié, Wendy E Smith, Meghan Dumas, Anna Lehman, null null, Cara Inglese, Mathilde Nizon, Renzo Guerrini, Annalisa Vetro, Eitan S Kaplan, Dolores Miramar, Julien Van Gils, Patricia Fergelot, Olaf Bodamer, Johanna C Herkert, Sander Pajusalu, Katrin Õunap, James J Filiano, Thomas Smol, Amelie Piton, Bénédicte Gérard, Sandra Chantot-Bastaraud, Thierry Bienvenu, Dong Li, Jane Juusola, Koen Devriendt, Frederic Bilan, Charlotte Poé, Martin Chevarin, Thibaud Jouan, Emilie Tisserant, Jean-Baptiste Rivière, Frédéric Tran Mau-Them, Christophe Philippe, Yannis Duffourd, William B Dobyns, Robert F Hevner, Christel Thauvin-Robinet
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature. European journal of human genetics : EJHG 28 (6) (2020)
Gregory S Barsh, Gregory M Cooper, Gregory P Copenhaver, Giorgio Sirugo, Hua Tang, Scott M Williams
Evaluating the strength of genetic results: Risks and responsibilities. PLoS genetics 15 (10) (2019)
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, Andrew A Hardigan, Jeremy W Prokop, Miroslava Hancarova, Darina Prchalova, Marketa Havlovicova, Jan Prchal, Viktor Stránecký, Dwight K C Yim, Zöe Powis, Boris Keren, Caroline Nava, Mignot Cyril, Marlène Rio, Anya Revah-Politi, Parisa Hemati, Nicholas Stong, Alejandro D Iglesias, Sharon F Suchy, Rebecca Willaert, Ingrid M Wentzensen, Patricia G Wheeler, Lauren Brick, Mariya Kozenko, Anna C E Hurst, James W Wheless, Yves Lacassie, Richard M Myers, Gregory S Barsh, Zdenek Sedlacek, Gregory M Cooper
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay. PLoS genetics 14 (11) (2018)
S M Hiatt, M D Amaral, K M Bowling, C R Finnila, M L Thompson, D E Gray, J M J Lawlor, J N Cochran, E M Bebin, K B Brothers, K M East, W V Kelley, N E Lamb, S E Levy, E J Lose, M B Neu, C A Rich, S Simmons, R M Myers, G S Barsh, Gregory M Cooper
Systematic reanalysis of genomic data improves quality of variant interpretation. Clinical genetics 94 (1) (2018)
Fumitaka Inoue, Martin Kircher, Beth K Martin, Gregory M Cooper, Daniela M Witten, Michael T McManus, Nadav Ahituv, Jay Shendure
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity. Genome research 27 (1) (2016)
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure
A general framework for estimating the relative pathogenicity of human genetic variants. Nature genetics 46 (3) (2014)