Katrina Gwinn-Hardy

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

Wen-Lang Lin, John Hardy, Peter Davies, 2000, Nature Genetics.

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.

Sonja W. Scholz, John Hardy, Mar Matarin, 2007, Human molecular genetics.

Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications

Matthew J. Farrer, Dennis W. Dickson, Zbigniew K. Wszolek, 2004 .

Familial Lewy Body Diseases

A. Singleton, K. Gwinn‐Hardy, Katrina Gwinn-Hardy, 2002, Journal of geriatric psychiatry and neurology.

Mutation at the SCA17 locus is not a common cause of parkinsonism.

John Hardy, Bernard Ravina, Melissa Hanson, 2003, Parkinsonism & related disorders.

Parkinson's disease and dementia with Lewy bodies: a difference in dose?

A. Singleton, K. Gwinn‐Hardy, Katrina Gwinn-Hardy, 2004, The Lancet.

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

Paola Giunti, Sonja W. Scholz, Elsdon Storey, 2007, PLoS genetics.

Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation

Vincenzo Bonifati, John Hardy, Peter Heutink, 2003, Annals of neurology.