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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene by Thomas V. Fernandez, Zsanett P. Williams, Tina Kline, Shreenath Rajendran, Farhan Augustine, Nicole Wright, Catherine A. W. Sullivan, Emily Olfson, Sarah B. Abdallah, Wenzhong Liu, Ellen J. Hoffman, Abha R. Gupta, Harvey S. Singer
Published 2023-01-01
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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. by Thomas V Fernandez, Zsanett P Williams, Tina Kline, Shreenath Rajendran, Farhan Augustine, Nicole Wright, Catherine A W Sullivan, Emily Olfson, Sarah B Abdallah, Wenzhong Liu, Ellen J Hoffman, Abha R Gupta, Harvey S Singer
Published 2023-01-01
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No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti... by John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Thomas V Fernandez, Michael T Murtha, Samuel Anyanwu, Gordon T Ober, Melanie J Raubeson, Nicholas M DiLullo, Natalie Villa, Zainabdul Waqar, Catherine Sullivan, Luis Gonzalez, A Jeremy Willsey, So-Yeon Choe, Benjamin M Neale, Mark J Daly, Matthew W State
Published 2015-01-01
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Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD by Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, Tourette International Collaborative Genetics (TIC Genetics), Vanessa H. Bal, Kate Langley, Joanna Martin, Pieter J. Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A. Heiman, Jay A. Tischfield, Thomas V. Fernandez, Michael J. Owen, Michael C. O’Donovan, Anita Thapar, Matthew W. State, A. Jeremy Willsey
Published 2023-12-01
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