Joseph Gonzalez-Heydrich

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 7

Top Topics

Congenital Heart Disease

Top Venues

Journal of medical Internet research

Proceedings of the National Academy of Sciences of the United States of America

European journal of human genetics : EJHG

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

Publications

Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Ange-Line Bruel, Antonio Vitobello, Isabelle Thiffault, Linda Manwaring, Marcia Willing, Pankaj B Agrawal, Carolina Alvarez, Thomas M Kitzler, Catherine A Brownstein, Casie A Genetti, Joseph Gonzalez-Heydrich, Parul Jayakar, Jacob W Zyskind, Zehua Zhu, Clemence Vachet, Gena R Wilson, Brianna Pruniski, Anne-Marie Goyette, Yannis Duffourd, Christel Thauvin-Robinet, Christophe Philippe, Laurence Faivre
ITSN1: a novel candidate gene involved in autosomal dominant neurodevelopmental disorder spectrum. European journal of human genetics : EJHG (2021)
Jianqiao Li, Margaret A Hojlo, Sampath Chennuri, Nitin Gujral, Heather L Paterson, Kent A Shefchek, Casie A Genetti, Emily L Cohn, Kara C Sewalk, Emily A Garvey, Elizabeth D Buttermore, Nickesha C Anderson, Alan H Beggs, Pankaj B Agrawal, John S Brownstein, Melissa A Haendel, Ingrid A Holm, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study. Journal of medical Internet research 23 (3) (2021)
Richard Scott Smith, Marta Florio, Shyam K Akula, Jennifer E Neil, Yidi Wang, R Sean Hill, Melissa Goldman, Christopher D Mullally, Nora Reed, Luis Bello-Espinosa, Laura Flores-Sarnat, Fabiola Paoli Monteiro, Erasmo Barbante Casella, Filippo Pinto E Vairo, Eva Morava, Anthony J Barkovich, Joseph Gonzalez-Heydrich, Catherine A Brownstein, Steven A McCarroll, Christopher A Walsh
Early role for a Na+,K+-ATPase (ATP1A3) in brain development. Proceedings of the National Academy of Sciences of the United States of America 118 (25) (2021)