J
Jennie M. Blackwell
Researcher at University of Western Australia
Publications - 1
Citations - 223
Jennie M. Blackwell is an academic researcher from University of Western Australia. The author has contributed to research in topics: Genome-wide association study & Single-nucleotide polymorphism. The author has an hindex of 1, co-authored 1 publications receiving 211 citations. Previous affiliations of Jennie M. Blackwell include University of Cambridge.
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Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Chris C. A. Spencer,Vincent Plagnol,Amy Strange,Michelle Gardner,Coro Paisán-Ruiz,Gavin Band,Roger A. Barker,Céline Bellenguez,Kailash P. Bhatia,Hannah Blackburn,Jennie M. Blackwell,Jennie M. Blackwell,Elvira Bramon,Martin A. Brown,Matthew A. Brown,David J. Burn,Juan-Pablo Casas,Juan-Pablo Casas,Patrick F. Chinnery,Carl E Clarke,Aiden Corvin,Nicholas John Craddock,Panos Deloukas,Sarah Edkins,J.M. Evans,Colin Freeman,Emma Gray,John Hardy,Gavin Hudson,Sarah E. Hunt,Janusz Jankowski,Cordelia Langford,Andrew J. Lees,Hugh S. Markus,Christopher G. Mathew,Mark I. McCarthy,Karen E. Morrison,Colin N. A. Palmer,J. P. Pearson,Leena Peltonen,Matti Pirinen,Robert Plomin,Simon C. Potter,Anna Rautanen,Stephen Sawcer,Zhan Su,Richard C. Trembath,Ananth C. Viswanathan,Ananth C. Viswanathan,Nigel W. Williams,Huw R. Morris,Peter Donnelly,Nicholas W. Wood +52 more
TL;DR: A genome-wide association study in 1705 Parkinson's disease UK patients and 5175 UK controls, the largest sample size so far for a PD GWAS, found weak but consistent evidence of association for common variants located in three previously published associated regions.