Publications by authors named "Mark A Durham"

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Functional divergence of Capicua isoforms explains differential tissue vulnerability in neurological disease.
Hamin Lee, Esmeralda Villavicencio Gonzalez, Elias M Rivera, Mark A Durham, Ronald Richman

bioRxiv· November 2025

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Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis.
Sameer S Bajikar, Jian Zhou, Ryan O'Hara, Harini P Tirumala, Mark A Durham

Neuron· February 2025

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A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain.
Jessica C Butts, Sih-Rong Wu, Mark A Durham, Ryan S Dhindsa, Jean-Pierre Revelli

Dev Cell· August 2024

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drives the heterogeneity of the pontine nuclei neurons and promotes their differentiation.
Sih-Rong Wu, Jessica C Butts, Matthew S Caudill, Jean-Pierre Revelli, Ryan S Dhindsa, Mark A Durham

Sci Adv· June 2023

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Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1.
Stephanie L Coffin, Mark A Durham, Larissa Nitschke, Eder Xhako, Amanda M Brown

Neuron· March 2023

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Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1.
Stephanie L Coffin, Mark A Durham, Larissa Nitschke, Eder Xhako, Amanda M Brown

Neuron· February 2023

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MeCP2 regulates , a dosage-sensitive gene critical for neurological function.
Sameer S Bajikar, Ashley G Anderson, Jian Zhou, Mark A Durham, Alexander J Trostle

Elife· February 2023

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Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disorders.
Jian Zhou, Hamdan Hamdan, Hari Krishna Yalamanchili, Kaifang Pang, Amy E Pohodich, Mark A Durham

Proc Natl Acad Sci U S A· January 2022

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Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome.
Laura A Lavery, Kerstin Ure, Ying-Wooi Wan, Chongyuan Luo, Alexander J Trostle, Mark A Durham

Elife· March 2020

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The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.
Ethan D Sperry, Elizabeth A Hurd, Mark A Durham, Elyse N Reamer, Adam B Stein

Dev Dyn· September 2014

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Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletion.
Andrea H Seeley, Mark A Durham, Mark A Micale, Jeffrey Wesolowski, Bradley R Foerster

Am J Med Genet A· August 2014

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CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.
Joseph A Micucci, Wanda S Layman, Elizabeth A Hurd, Ethan D Sperry, Sophia F Frank, Mark A Durham

Hum Mol Genet· January 2014

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