Miriam H. Meisler

Biochemistry, Genetics and Molecular Biology · University of Michigan

Established · publishing since 1966

Ion channel regulation and function Neuroscience and Neuropharmacology Research Epilepsy research and treatment Genetics and Neurodevelopmental Disorders Pancreatic function and diabetes

Publications

303

Citations

21,049

Est. group size

Recurring co-author estimate

Active years

Publishing since 1966

In context

Among 1,668 established Biochemistry, Genetics and Molecular Biology PIs within our index

Citations: 21,049cohort median 3,422

Publications / year (recent): 2.8cohort median 4.8

Typically publishes in teams of ~12 · 18% small-team papers (≤3 authors) · across 9 venues

Publication cadence

Publications per year over the last 10 years — averaging 2.8/year recently

Collaborators per year

Distinct co-authors at University of Michigan each year — a rough indication of whether the group around this researcher has been growing or contracting. An estimate from co-authorship, not a roster: collaborators are not necessarily lab members, and recent years can be under-counted while indexing catches up.

Recent publications

Base Editing Rescue of Seizures and SUDEP in SCN8A Developmental Epileptic Encephalopathy
bioRxiv (Cold Spring Harbor Laboratory) · 2025
Sodium Channelopathies in Human and Animal Models of Epilepsy and Neurodevelopmental Disorders
2024
Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice
Frontiers in Molecular Neuroscience · 2022
SCN8A encephalopathy: Mechanisms and models
Epilepsia · 2019
Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders
European Journal of Paediatric Neurology · 2019
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies
The American Journal of Human Genetics · 2018
Mapt deletion fails to rescue premature lethality in two models of sodium channel epilepsy
Annals of Clinical and Translational Neurology · 2018
Aberrant Sodium Channel Currents and Hyperexcitability of Medial Entorhinal Cortex Neurons in a Mouse Model of SCN8A Encephalopathy
Journal of Neuroscience · 2017
Neuropathology of childhood‐onset basal ganglia degeneration caused by mutation of VAC14
Annals of Clinical and Translational Neurology · 2017
Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy
Bone · 2017
SCN8A mutation in a child presenting with seizures and developmental delays
Molecular Case Studies · 2016

Publishes in

Epilepsia×7
Annals of Neurology×3
Neurobiology of Disease×3
Nature reviews. Neuroscience×2
The American Journal of Human Genetics×2

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This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.

Last updated Jul 25, 2026.

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