Tyler Mark Pierson - Cedars-Sinai Medical Center

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论文共 82 篇作者统计合作学者相似作者

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Evaluation of Corticogenesis in NuRDopathies Using Mouse and Human Cerebral Organoid Models

T. M. Pierson, G. G. Otero, S. Zhao, W. Dahlgren, K. Delgado, K. Walz, J. Young

ANNALS OF NEUROLOGY (2025): S113-S113

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Compound Heterozygous MRPS14 Variants Associated with Leigh Syndrome

Maria Gabriela Otero, Christina Freeman, Ruchi Shah,Renkui Bai, Hong Cui, Marian Castro, Zachary Myers, Eric Choy, Derek Chan, Molly Easter, Sophia Y Zhao, Madeline Babros, Ruchi Garg, Matthew Deardorff, Franklin Moser,Tyler Mark Pierson

Annals of clinical and translational neurology (2025)

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Gatad2b, Associated with the Neurodevelopmental Syndrome GAND, Plays a Critical Role in Neurodevelopment and Cortical Patterning

Clemer Abad, Maria C. Robayo,Maria del Mar Muñiz-Moreno, Maria T. Bernardi,Maria G. Otero, Christina Kosanovic,Anthony J. Griswold,Tyler Mark Pierson,Katherina Walz,Juan I. Young

Translational Psychiatry（2024）

引用2浏览0WOSNATURE引用

De Novo GRIN Variants in M3 Helix Associated with Neurological Disorders Control Channel Gating of NMDA Receptor

CELLULAR AND MOLECULAR LIFE SCIENCESno. 1 (2024)

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An Activating De Novo Variant in ARF1 Causing a Neurodevelopmental Disorder

M. Ishida, M. G. Otero, C. Freeman, P. A. Sanchez-Lara, C. M. Guardia,T. M. Pierson,J. S. Bonifacino

MOLECULAR BIOLOGY OF THE CELLno. 2 (2023): 1061-1061

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Risks and Benefits of Anesthesia for Combined Pediatric Procedures in the NIH Undiagnosed Diseases Program

Ellen F. Macnamara,Amelia Loydpierson,Yvonne L. Latour,Precilla D'Souza,Jennifer Murphy,Lynne Wolfe,Tyra Estwick,Jean M. Johnston,John Yang, Maria T. Undiagnosed Diseases Network,Maria T. Acosta,Paul R. Lee,Tyler Mark Pierson,Ariane Soldatos,Camilo Toro,Tom Markello,David R. Adams,William A. Gahl,Muhammad Yousef,Cynthia J. Tifft

Molecular Genetics and Metabolismno. 3 (2023): 107707-107707

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Expanding the Phenotype of ASXL3-related Syndrome: a Comprehensive Description of 45 Unpublished Individuals with Inherited and De Novo Pathogenic Variants in ASXL3 (vol 185A, Pg 3446, 2021)

Schaida Schirwani,Albaba J. Shadi,Deanna Alexis Carere,Maria J. Guillen Sacoto,Francisca Milan Zamora,Yue Si,Rachel Rabin,John Pappas,Deborah L. Renaud,Natalie Hauser,Evan Reid,Patricia Blanchet,Nichola Foulds,Abhijit Dixit,Richard Fisher,Ruth Armstrong,Bertrand Isidor,Benjamin Cogne,Samantha Schrier Vergano,Serwet Demirdas,Natalie Dykzeul,Julie S. Cohen,Katheryn Grand,Dayna Morel,Anne Slavotinek,Hessa F. Albassam,Swati Naik,John Dean,Nicola Ragge,Cinzia Costa,Maria Giovanna Tedesco,Rachel E. Harrison,Arjan Bouman,Emily Palen,Thomas D. Challman,Marjolein H. Willemsen,Julie Vogt,Christopher Cunniff,Katherine Bergstrom,Jagdeep S. Walia,Ange-Line Bruel,Usha Kini,Fowzan S. Alkuraya,Valerie Slegesky,Naomi Meeks,Paula Girotto,Diana Johnson,Ruth Newbury-Ecob,Charlotte W. Ockeloen,Paolo Prontera,Sally Ann Lynch,Dong Li,John M. Graham,Tyler Mark Pierson,Meena Balasubramanian

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 1 (2023): 310-310

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Functional Effects of Disease-Associated Variants Reveal That the S1–M1 Linker of the NMDA Receptor Critically Controls Channel Opening

Lingling Xie,Miranda J. McDaniel,Riley E. Perszyk,Sukhan Kim,Gerarda Cappuccio,Kevin A. Shapiro,Beatriz Muñoz-Cabello,Pedro A. Sanchez-Lara,Katheryn Grand,Jing Zhang,Kelsey A. Nocilla, Rehan Sheikh,Lluis Armengol,Roberta Romano,Tyler Mark Pierson,Hongjie Yuan,Scott J. Myers,Stephen F. Traynelis

CELLULAR AND MOLECULAR LIFE SCIENCESno. 4 (2023)

引用5浏览0WOS引用

De Novo Variants in GATAD2A in Individuals with a Neurodevelopmental Disorder: GATAD2A-related Neurodevelopmental Disorder

Elizabeth A. Werren, Alba Guxholli,Natasha Jones,Matias Wagner,Iris Hannibal,Jorge L. Granadillo,Amanda Tyndall,Amanda Moccia, Ryan Kuehl, Kristin M. Levandoski,Debra L. Day-Salvatore,Marsha Wheeler,Jessica X. Chong,Michael J. Bamshad,A. Micheil Innes,Tyler Mark Pierson,Joel P. Mackay,Stephanie L. Bielas,Donna M. Martin

Human Genetics and Genomics Advancesno. 3 (2023): 100198-100198

引用1浏览0WOS引用

Familial Bainbridge-Ropers Syndrome: Report of Familial ASXL3 Inheritance and a Milder Phenotype

Schaida Schirwani,Emily Woods,David A. Koolen,Charlotte W. Ockeloen,Sally Ann Lynch,Karl Kavanagh,John M. Graham,Katheryn Grand,Tyler Mark Pierson,Jeffrey M. Chung,Meena Balasubramanian

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2023）

引用7浏览0WOS引用

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