Concepedia

Author

Mark A. Durham

Neurological Research Institute

Also Known As

Mark A Durham, Mark A. Durham, Mark Durham

25

Publications

433

Citations

12

H-Index

22

Concepts

All Affiliations

Neurological Research InstituteUniversity of MichiganBaylor College of MedicineTexas Children's HospitalHoward Hughes Medical Institute
MA

About

Mark A. Durham is an author at Neurological Research Institute specializing in medicine, pathogenesis, and autoimmune disease.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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91

2

Health Sciences

1

1

66

3

Cell Biology

1

1

66

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Cellular Physiology

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1

66

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Medical Laboratory Science

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25

Mark A. Durham

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12

Publications

406

Citations

12

H-Index

YearCitations

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,

Human Molecular Genetics

2013

66

Soundscapes reveal disturbance impacts: biophonic response to wildfire in the Sonoran Desert Sky Islands

Amandine Gasc, Benjamin L. Gottesman, Dante Francomano,

Landscape Ecology

2018

61

Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome

Laura A. Lavery, Kerstin Ure, Ying‐Wooi Wan,

eLife

2020

57

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,

Developmental Dynamics

2014

45

Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders

Jian Zhou, Hamdan Hamdan, Hari Krishna Yalamanchili,

Proceedings of the National Academy of Sciences

2022

42

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,

Neuron

2022

27

Enhanced neutrophil chemiluminescence in familial mediterranean fever

Peter A. Anton, Stephan R. Targan, Steven R. Vigna,

Journal of Clinical Immunology

1988

25

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,

Neuron

2024

21

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,

Developmental Cell

2024

19

Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder

Jirair K. Bedoyan, Valerie M. Schaibley, Weiping Peng,

Journal of Medical Genetics

2012

17

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