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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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P Epstein

Showing results (191-200 of 210) with videos related to

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Nature Neuroscience|April 13, 2021

Brain proteome-wide association study implicates novel proteins in depression pathogenesisThomas S Wingo, Yue Liu, Ekaterina S Gerasimov, et al.

American Journal of Human Genetics|October 28, 2005

Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.

Human Molecular Genetics|October 31, 2025

Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.

American Journal of Human Genetics|October 7, 2025

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022

Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.

HGG Advances|September 18, 2023

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2023

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingKimberly K Diaz Perez, Sarah W Curtis, Alba Sanchis-Juan, et al.

Fertility and Sterility|May 21, 2021

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutationCristina E Trevino, J Christopher Rounds, Krista Charen, et al.

Medrxiv : the Preprint Server for Health Sciences|April 17, 2023

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.

Nature Genetics|September 8, 2025

Multiancestry brain pQTL fine-mapping and integration with genome-wide association studies of 21 neurologic and psychiatric conditionsAliza P Wingo, Yue Liu, Selina M Vattathil, et al.

Pageof 21

Search research articles

Showing results (191-200 of 210) with videos related to

Sort By:

Pageof 21

Nature Neuroscience|April 13, 2021

Brain proteome-wide association study implicates novel proteins in depression pathogenesisThomas S Wingo, Yue Liu, Ekaterina S Gerasimov, et al.

American Journal of Human Genetics|October 28, 2005

Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cellsCharles M Krafchak, Hemant Pawar, Sayoko E Moroi, et al.

Human Molecular Genetics|October 31, 2025

Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.

American Journal of Human Genetics|October 7, 2025

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022

Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.

HGG Advances|September 18, 2023

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2023

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingKimberly K Diaz Perez, Sarah W Curtis, Alba Sanchis-Juan, et al.

Fertility and Sterility|May 21, 2021

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutationCristina E Trevino, J Christopher Rounds, Krista Charen, et al.

Medrxiv : the Preprint Server for Health Sciences|April 17, 2023

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.

Nature Genetics|September 8, 2025

Multiancestry brain pQTL fine-mapping and integration with genome-wide association studies of 21 neurologic and psychiatric conditionsAliza P Wingo, Yue Liu, Selina M Vattathil, et al.

Pageof 21