Profile

Michael Hammer

Research Scientist, Ecology and Evolutionary Biology | Research Scientist, Neurology | Member of the Graduate Faculty | Research Scientist, BIO5 Institute

Collaboration(34)

Page 1 of 7

Grants(9)

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Publications(123)

Recent

Leukocyte differential gene expression prognostic value for high versus low seizure frequency in temporal lobe epilepsy

2024

Sex differences in physiological response to increased neuronal excitability in a knockin mouse model of pediatric epilepsy

2024

Clinical severity is correlated with age at seizure onset and biophysical properties of recurrent gain of function variants associated with SCN8A-related epilepsy

2023

Eye movement defects in KO zebrafish reveals as a causative gene for an X-linked intellectual disability

2023

Greater female than male resilience to mortality and morbidity in the Scn8a mouse model of pediatric epilepsy

2023

A sporadic case of severe peripheral neuropathy expands the phenotypic range of TUBB2A mutations.

2023

The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Treatment of a Rare Pediatric Neurodevelopmental Syndrome

2023

text-decoration:none; Distinguishing Loss- and Gain-of-Function SCN8A Variants Using a Random Forest Classification Model Trained on Clinical Features

2023

Teaching case: hemiplegic migraine due to dominant ATP1A2 mutation

2023

SCN8A Related Epilepsy and/or Neurodevelopmental Disorders

2023

Profile

Michael Hammer

Collaboration(34)

Helena Morrison

Nirav Merchant

Denise Roe

Baldassarre Stea

Todd Vanderah

Grants(9)

Publications(123)

Leukocyte differential gene expression prognostic value for high versus low seizure frequency in temporal lobe epilepsy

Sex differences in physiological response to increased neuronal excitability in a knockin mouse model of pediatric epilepsy

Clinical severity is correlated with age at seizure onset and biophysical properties of recurrent gain of function variants associated with SCN8A-related epilepsy

Eye movement defects in KO zebrafish reveals as a causative gene for an X-linked intellectual disability

Greater female than male resilience to mortality and morbidity in the Scn8a mouse model of pediatric epilepsy

A sporadic case of severe peripheral neuropathy expands the phenotypic range of TUBB2A mutations.

The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Treatment of a Rare Pediatric Neurodevelopmental Syndrome

text-decoration:none; Distinguishing Loss- and Gain-of-Function SCN8A Variants Using a Random Forest Classification Model Trained on Clinical Features

Teaching case: hemiplegic migraine due to dominant ATP1A2 mutation

SCN8A Related Epilepsy and/or Neurodevelopmental Disorders