Publications by authors named "Gary D Clark"

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Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.
Hormos Salimi Dafsari, Celine Deneubourg, Kritarth Singh, Reza Maroofian, Zita Suprenant, Gary D Clark

Ann Neurol· November 2025

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Long-term efficacy and safety of cannabidiol in patients with tuberous sclerosis complex: 3-year results from the cannabidiol expanded access program.
Arie Weinstock, E Martina Bebin, Daniel Checketts, Gary D Clark, Jerzy P Szaflarski

Epilepsia Open· October 2024

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The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing.
Shenglan Li, Sen Zhao, Jefferson C Sinson, Aleksandar Bajic, Jill A Rosenfeld, Gary D Clark

Am J Hum Genet· May 2024

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TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system.
Shyam K Akula, Jack H Marciano, Youngshin Lim, David Exposito-Alonso, Norma K Hylton, Gary D Clark

Proc Natl Acad Sci U S A· January 2023

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Clinical Profile and Long-Term Outcome in Neonatal Cerebral Sinus Venous Thrombosis.
Isabella Herman, Cemal Karakas, Troy A Webber, Stephen F Kralik, Danielle S Takacs, Gary D Clark

Pediatr Neurol· August 2021

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The Finances of Neurology in a Major Children's Hospital.
Michael LaRose, Brian D Cordasco, Dan DiPrisco, Gary D Clark

Neurol Clin· August 2021

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Neurology in a Pandemic.
Gary D Clark, Timothy E Lotze

Neurol Clin· August 2021

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Novel Treatments and Clinical Research in Child Neurology.
Gary D Clark, Timothy E Lotze

Neurol Clin· August 2021

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Memento Akademia: Introduction and Editorial Regarding the State of Child Neurology.
Gary D Clark, James J Riviello

Neurol Clin· August 2021

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Neurocutaneous Melanocytosis and Leptomeningeal Melanoma.
Victoria Mitre, Kenneth Heym, Gary D Clark, Rajkumar Venkatramani

J Pediatr Hematol Oncol· March 2021

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Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Ash Zawerton, Cyril Mignot, Ashley Sigafoos, Patrick R Blackburn, Abdul Haseeb, Gary D Clark, Karl J Clark

Genet Med· March 2020

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Case report of prenatal bilateral cerebellar infarction: implications for social-behavioral functioning.
Sara E Whiting, Audrey M Carson, Gary D Clark, David D Schwartz

Clin Neuropsychol· July 2019

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Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes.
Orrin Devinsky, Chloe Verducci, Elizabeth A Thiele, Linda C Laux, Anup D Patel, Gary D Clark

Epilepsy Behav· September 2018

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Cockayne Syndrome Complicated by Moyamoya Vasculopathy and Stroke.
Robert C Stowe, Andres Jimenez-Gomez, Alfred Balasa, Gary D Clark

Pediatr Neurol· September 2018

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Evaluation of Safety in Exceeding Maximum Adult Doses of Commonly Used Second-Generation Antiepileptic Drugs in Pediatric Patients.
Mindl M Messinger, Sunita N Misra, Gary D Clark, Shannon M DiCarlo

J Pediatr Pharmacol Ther· January 2017

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Platelet-Activating Factor Acetylhydrolase and Brain Development.
Gary D Clark

Enzymes· November 2015

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Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria.
David R Murdock, Gary D Clark, Matthew N Bainbridge, Irene Newsham, Yuan-Qing Wu

Am J Med Genet A· September 2011

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Bilateral in utero cerebellar infarction.
Safdar A Ansari, Jill V Hunter, Lisa M Nassif, Gary D Clark, Melissa B Ramocki

J Child Neurol· July 2011

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Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2.
Melissa B Ramocki, Fernando Scaglia, Pawel Stankiewicz, John W Belmont, Jeremy Y Jones, Gary D Clark

Am J Med Genet A· July 2011

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Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1.
Guangcheng Zhang, Amir H Assadi, Mila Roceri, Gary D Clark, Gabriella D'Arcangelo

Brain Res· April 2009

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Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice.
Amir H Assadi, Guangcheng Zhang, Robert McNeil, Gary D Clark, Gabriella D'Arcangelo

Neurosci Lett· July 2008

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Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
William B Dobyns, Ghayda Mirzaa, Susan L Christian, Kristin Petras, Jessica Roseberry, Gary D Clark

Am J Med Genet A· July 2008

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Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
Jonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, Sung-Hae L Kang, Chin-to Fong, Gary D Clark

Genet Med· July 2007

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The Pafah1b complex interacts with the reelin receptor VLDLR.
Guangcheng Zhang, Amir H Assadi, Robert S McNeil, Uwe Beffert, Anthony Wynshaw-Boris, Gary D Clark

PLoS One· February 2007

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Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas.
Stephen M Maricich, Jeffrey L Neul, Timothy E Lotze, Andreea C Cazacu, Timothy M Uyeki, Gary D Clark

Pediatrics· November 2004

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