V. Stinton

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India

K. Bhatia, N. Wood, M. Davis, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Acquired Isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations

S. Akiki, D. McMullan, M. Griffiths, 2005, Leukemia.

DNA Profiling: A Genetic Study of Two VNTR Loci in the East Midlands

S. Mastana, V. Stinton, 1996 .

Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

N. Wood, D. Healy, M. Davis, 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

Evidence for 28 genetic disorders discovered by combining healthcare and research data

Patrick J. Short, M. Hurles, L. Vissers, 2020, Nature.

The contribution of X-linked coding variation to severe developmental disorders

M. Hurles, R. Sandford, D. Baralle, 2020, Nature Communications.

A Yorkshire family with adult‐onset cranio‐cervical primary torsion dystonia

N. Quinn, K. Bhatia, N. Wood, 2000, Movement disorders : official journal of the Movement Disorder Society.

Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA?

P. Garrard, J. Holton, M. Reilly, 2002, Journal of neurology, neurosurgery, and psychiatry.

Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996–2020: development of a national resource of patient-level genomics laboratory records

A. Antoniou, D. Eccles, C. Turnbull, 2022, Journal of Medical Genetics.