C. Gokhale

Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplification

D. Evans, S. Huson, R. Ramsden, 2007, Journal of Medical Genetics.

Screening of potential novel candidate genes in schwannomatosis patients

A. Wallace, R. Charlton, C. Gokhale, 2022, Human mutation.

Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1-related schwannomatosis

D. Evans, S. Rutherford, A. Wallace, 2017, Neurology.

What are the implications in individuals with unilateral vestibular schwannoma and other neurogenic tumors?

D. Evans, S. Huson, R. Ramsden, 2008, Journal of neurosurgery.

Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?

S. Huson, R. Ramsden, A. Wallace, 2007, Clinical genetics.

Prenatal Detection of PIK3CA-related Overgrowth Spectrum in Cultured Amniocytes Using Long-range PCR and Next-generation Sequencing

M. Kilby, E. Quinlan-Jones, C. Bell, 2016, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes

E. Harkness, E. Miles, A. Wallace, 2016, Human mutation.

Bilateral vestibular schwannomas in older patients: NF2 or chance?

D. Evans, S. Huson, R. Ramsden, 2015, Journal of Medical Genetics.

including MLPA presentation and sensitive mutation analysis uni/bilaterality of vestibular schwannoma at Mosaicism in NF2 an update of risk based on

R. Ramsden, C. Gokhale, G. Evans, 2007 .