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Gary Bellus

As seen in: The American Journal of Human Genetics, medRxiv
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Articles by Gary Bellus

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

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By Eric Anderson, Stephan Holger Drukewitz, Sukhleen Kour, Deepa Rajan, Karen Stals, Deirdre Donnelly, Tiong Y. Tan, Zornitza Stark, Pia Zacher, Nicolas Chatron, Séverine Drunat, Yoann Vial, Xenia Latypova, Jonathan Levy, Alain Verloes, Jennefer N. Carter, Devon E. Bonner, Suma P. Shankar, Jonathan Bernstein, Julie Cohen, Anne M. Comi, Deanna Alexis Carere, Lisa Dyer, Sureni V. Mullegama, Pedro A. Sanchez-Lara, Katheryn Grand, Hyung-Goo Kim, Afif Ben-Mahmoud, Sidney M. Gospe, Gary Bellus, Renske Oegema, Anita Rauch, Ivan Ivanovski, Frédéric Tran Mau-Them, Aurore Garde, Rachel A. Rabin, John Pappas, Annette E. Bley, Timo Wagner, Eva L. Decker, Carsten Bergmann Verified, Henri Margot, Johannes R. Lemke, Rami Abou Jamra, Julia Hentschel, Heather C Mefford, Amit Singh, Udai Bhan Pandey, Konrad Platzer, Anuradha V. Chimata, Senta Schönnagel, John F. Mantovani, Pauline Monin, Rebecca S. Belles, Klaske D. Lichtenbelt, Janna Bredow, Louis Domenach
| The American Journal of Human Genetics Verified
Keywords KDM2A neurodevelopmental disorder epigenetic machinery Introduction The epigenetic machinery encompasses proteins that function as writers, erasers, readers, and remodelers of epigenetic marks on DNA and histones. The eraser KDM2A removes mono- and di-methylation from histone 3 at lysine 36 (H3K36).
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Phenotypic Findings Associated with Variation in Elastin

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By Anne Justice, Melissa Kelly, Joshua Green, Gary Bellus
| medRxiv
Dr. Kozel is funded through her role as a member of the Division of Intramural Research for NHLBI. None of the authors have any interests to declare. Dr. Kozel is funded through her role as a member of the Division of Intramural Research for NHLBI. None of the authors have any interests to declare. Funding for this study was through a cooperative agreement from the National Heart, Lung, and Blood Institute (NHLBI) of the United States National Institutes of Health 1U01HL146188- 01A1, Marc S.
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