Mark W. Kellett
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 18 publications
Prevalence and natural history of schwannomas in neurofibromatosis type 2 (NF2): the influence of pathogenic variants.
Journal: European journal of human genetics : EJHG
Published: February 08, 2021
Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 22, 2019
Identifying the deficiencies of current diagnostic criteria for neurofibromatosis 2 using databases of 2777 individuals with molecular testing.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 21, 2018
Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene.
Journal: The Laryngoscope
Published: April 10, 2018
Schwannomatosis: a genetic and epidemiological study.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: March 31, 2018
Spinal ependymomas in NF2: a surgical disease?
Journal: Journal of neuro-oncology
Published: May 28, 2017
High-Grade Glioma is not a Feature of Neurofibromatosis Type 2 in the Unirradiated Patient.
Journal: Neurosurgery
Published: May 01, 2017
Gingival overgrowth: Part 2: management strategies.
Journal: British dental journal
Published: October 31, 2016
Gingival overgrowth: Part 1: aetiology and clinical diagnosis.
Journal: British dental journal
Published: October 31, 2016
"Reverse Hoover's sign" demonstrated by neurophysiology in a patient with functional dystonia.
Journal: Parkinsonism & related disorders
Published: January 18, 2016
Novel PTEN mutation with leukoencephalopathy, basal ganglia calcification and action tremor.
Journal: Parkinsonism & related disorders
Published: December 19, 2015
Last Updated: 09/26/2026