Katrina Gwinn
Katrina Gwinn
Medical Reviewer, FDA
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Cited by
Cited by
α-Synuclein locus triplication causes Parkinson's disease
AB Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, ...
science 302 (5646), 841-841, 2003
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308-1312, 2009
How common are the “common” neurologic disorders?
D Hirtz, DJ Thurman, K Gwinn-Hardy, M Mohamed, AR Chaudhuri, ...
Neurology 68 (5), 326-337, 2007
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
J Lewis, E McGowan, J Rockwood, H Melrose, P Nacharaju, ...
Nature genetics 25 (4), 402-405, 2000
Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications
M Farrer, J Kachergus, L Forno, S Lincoln, DS Wang, M Hulihan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers
CF Lippa, JE Duda, M Grossman, HI Hurtig, D Aarsland, BF Boeve, ...
Neurology 68 (11), 812-819, 2007
Lewy bodies and parkinsonism in families with parkin mutations
M Farrer, P Chan, R Chen, L Tan, S Lincoln, D Hernandez, L Forno, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
Diagnostic criteria for psychosis in Parkinson's disease: report of an NINDS, NIMH work group
B Ravina, K Marder, HH Fernandez, JH Friedman, W McDonald, ...
Movement Disorders 22 (8), 1061-1068, 2007
Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
MJ Devine, M Ryten, P Vodicka, AJ Thomson, T Burdon, H Houlden, ...
Nature communications 2 (1), 440, 2011
Genetic classification of primary neurodegenerative disease
J Hardy, K Gwinn-Hardy
Science 282 (5391), 1075-1079, 1998
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
MK Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, ...
Neurology 63 (12), 2280-2287, 2004
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
HC Fung, S Scholz, M Matarin, J Simón-Sánchez, D Hernandez, A Britton, ...
The Lancet Neurology 5 (11), 911-916, 2006
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
R Crook, A Verkkoniemi, J Perez-Tur, N Mehta, M Baker, H Houlden, ...
Nature medicine 4 (4), 452-455, 1998
α-Synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication
DW Miller, SM Hague, J Clarimon, M Baptista, K Gwinn-Hardy, ...
Neurology 62 (10), 1835-1838, 2004
Genetics of Parkinson's disease and parkinsonism
J Hardy, H Cai, MR Cookson, K Gwinn‐Hardy, A Singleton
Annals of neurology 60 (4), 389-398, 2006
Genomic investigation of α‐synuclein multiplication and parkinsonism
OA Ross, AT Braithwaite, LM Skipper, J Kachergus, MM Hulihan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
The role of radiotracer imaging in Parkinson disease
B Ravina, D Eidelberg, JE Ahlskog, RL Albin, DJ Brooks, M Carbon, ...
Neurology 64 (2), 208-215, 2005
A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor
M Farrer, K Gwinn-Hardy, M Muenter, FW DeVrieze, R Crook, J Perez-Tur, ...
Human molecular genetics 8 (1), 81-85, 1999
Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation
S Hague, E Rogaeva, D Hernandez, C Gulick, A Singleton, M Hanson, ...
Annals of neurology 54 (2), 271-274, 2003
Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans
J Van De Leemput, J Chandran, MA Knight, LA Holtzclaw, S Scholz, ...
PLoS genetics 3 (6), e108, 2007
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