Michael F. O'donoghue

Nottingham, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 11 publications

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Journal: Nature genetics

Published: April 23, 2026

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Journal: Nature genetics

Published: August 21, 2025

Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.

Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.

Journal: medRxiv : the preprint server for health sciences

Published: September 16, 2024

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Journal: Nature genetics

Published: September 13, 2024

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

Journal: Nature

Published: April 07, 2024

Improved survival outcomes despite older age at diagnosis: an era-by-era analysis of patients with primary central nervous system lymphoma treated at a single referral centre in the United Kingdom.

Improved survival outcomes despite older age at diagnosis: an era-by-era analysis of patients with primary central nervous system lymphoma treated at a single referral centre in the United Kingdom.

Journal: British journal of haematology

Published: May 04, 2021

Adjunctive use of the ketogenic diet in a young adult with UBE2A deficiency syndrome and super-refractory status epilepticus.

Adjunctive use of the ketogenic diet in a young adult with UBE2A deficiency syndrome and super-refractory status epilepticus.

Journal: Epilepsy & behavior reports

Published: January 04, 2021

MOG-IgG-associated demyelination: focus on atypical features, brain histopathology and concomitant autoimmunity.

MOG-IgG-associated demyelination: focus on atypical features, brain histopathology and concomitant autoimmunity.

Journal: Journal of neurology

Published: July 31, 2019

Optic ataxia and the dorsal visual steam re-visited: Impairment in bimanual haptic matching performed without vision.

Optic ataxia and the dorsal visual steam re-visited: Impairment in bimanual haptic matching performed without vision.

Journal: Cortex; a journal devoted to the study of the nervous system and behavior

Published: January 11, 2017

Relapse after treatment withdrawal of antiepileptic drugs for Juvenile Absence Epilepsy and Juvenile Myoclonic Epilepsy.

Relapse after treatment withdrawal of antiepileptic drugs for Juvenile Absence Epilepsy and Juvenile Myoclonic Epilepsy.

Journal: Seizure

Published: June 28, 2016

Stroke-like migraine attack after cranial radiation therapy: the SMART syndrome.

Stroke-like migraine attack after cranial radiation therapy: the SMART syndrome.

Journal: Practical neurology

Published: March 06, 2016

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Last Updated: 09/26/2026