Matthew J. Farrer And NotFloride

List of bibliographic references

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
000166	Fatma Nabli [Tunisie] ; Samia Ben Sassi ; Rim Amouri ; John E. Duda ; Matthew J. Farrer ; Fayçal Hentati	Motor phenotype of LRRK2-associated Parkinson's disease: a Tunisian longitudinal study.
000225	Emil K. Gustavsson [Norvège] ; Ilaria Guella ; Joanne Trinh ; Chelsea Szu-Tu ; Alex Rajput ; Ali H. Rajput ; John C. Steele ; Martin Mckeown ; Beom S. Jeon ; Jan O. Aasly ; Matthew J. Farrer	Genetic variability of the retromer cargo recognition complex in parkinsonism.
000238	Maria Skaalum Petersen ; Sara Bech ; Ekaterina Nosova ; Jan Aasly ; Matthew J. Farrer	Familial aggregation of Parkinson's disease in the Faroe Islands.
000279	Emil K. Gustavsson [Norvège] ; Joanne Trinh ; Ilaria Guella ; Carles Vilari O-Güell ; Silke Appel-Cresswell ; A Jon Stoessl ; Joseph K. Tsui ; Martin Mckeown ; Alex Rajput ; Ali H. Rajput ; Jan O. Aasly ; Matthew J. Farrer	DNAJC13 genetic variants in parkinsonism.
000638	Silke Appel-Cresswell [Canada] ; Ali H. Rajput ; Vesna Sossi ; Christina Thompson ; Vanessa Silva ; Jessamyn Mckenzie ; Katherine Dinelle ; Siobhan E. Mccormick ; Carles Vilari O-Güell ; A Jon Stoessl ; Dennis W. Dickson ; Chris A. Robinson ; Matthew J. Farrer ; Alex Rajput	Clinical, positron emission tomography, and pathological studies of DNAJC13 p.N855S Parkinsonism.
000684	Eiichi Araki [Japon] ; Yoshio Tsuboi ; Justus Daechsel ; Austen Milnerwood ; Carles Vilarino-Guell ; Naoki Fujii ; Takayasu Mishima ; Takayuki Oka ; Hideo Hara ; Jiro Fukae ; Matthew J. Farrer	A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy.
000738	Andrew B. Singleton [États-Unis] ; Matthew J. Farrer [Canada] ; Vincenzo Bonifati [Pays-Bas]	The genetics of Parkinson’s disease: progress and therapeutic implications
000B09	Silke Appel-Cresswell [Canada] ; Carles Vilarino-Guell ; Mary Encarnacion ; Holly Sherman ; Irene Yu ; Brinda Shah ; David Weir ; Christina Thompson ; Chelsea Szu-Tu ; Joanne Trinh ; Jan O. Aasly ; Alex Rajput ; Ali H. Rajput ; A. Jon Stoessl ; Matthew J. Farrer	Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.
002075	Carles Vilari O-Güell [États-Unis] ; Owen A. Ross [États-Unis] ; Alexandra I. Soto [États-Unis] ; Matthew J. Farrer [États-Unis] ; Kristoffer Haugarvoll [États-Unis, Norvège] ; Jan O. Aasly [Norvège] ; Ryan J. Uitti [États-Unis] ; Zbigniew K. Wszolek [États-Unis]	Reported mutations in GIGYF2 are not a common cause of Parkinson's disease

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