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Author/Creator Farrer, Matthew

1. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Issue 11 (2nd November 2012)

Authors:
Sharma, Manu; Ioannidis, John P A; Aasly, Jan O; Annesi, Grazia; Brice, Alexis; Bertram, Lars; Bozi, Maria; Barcikowska, Maria; Crosiers, David; Clarke, Carl E; Facheris, Maurizio F; Farrer, Matthew; Garraux, Gaetan; Gispert, Suzana; Auburger, Georg; Vilariño-Güell, Carles; Hadjigeorgiou, Georgio...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 11(2012)
Page Start:
721
Record Type:
Journal Article
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2. A scan without evidence is not evidence of absence: Scans without evidence of dopaminergic deficit in a symptomatic leucine‐rich repeat kinase 2 mutation carrier. Issue 3 (21st December 2015)

Authors:
Wile, Daryl J.; Dinelle, Katie; Vafai, Nasim; McKenzie, Jessamyn; Tsui, Joseph K.; Schaffer, Paul; Ding, Yu‐Shin; Farrer, Matthew; Sossi, Vesna; Stoessl, A. Jon
Journal:
Movement disorders
Issue:
Volume 31:Issue 3(2016)
Page Start:
405
Record Type:
Journal Article
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4. Assess the documentation of cognitive tests and biomarkers in electronic health records via natural language processing for Alzheimer's disease and related dementias. (February 2023)

Authors:
Chen, Zhaoyi; Zhang, Hansi; Yang, Xi; Wu, Songzi; He, Xing; Xu, Jie; Guo, Jingchuan; Prosperi, Mattia; Wang, Fei; Xu, Hua; Chen, Yong; Hu, Hui; DeKosky, Steven T; Farrer, Matthew; Guo, Yi; Wu, Yonghui; Bian, Jiang
Journal:
International journal of medical informatics
Issue:
Volume 170(2023)
Page Start:
Record Type:
Journal Article
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7. Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studies. Issue 5 (May 2017)

Authors:
Wile, Daryl J; Agarwal, Pankaj A; Schulzer, Michael; Mak, Edwin; Dinelle, Katherine; Shahinfard, Elham; Vafai, Nasim; Hasegawa, Kazuko; Zhang, Jing; McKenzie, Jessamyn; Neilson, Nicole; Strongosky, Audrey; Uitti, Ryan J; Guttman, Mark; Zabetian, Cyrus P; Ding, Yu-Shin; Adam, Mike; Aasly, Jan; Wsz...
Journal:
Lancet neurology
Issue:
Volume 16:Issue 5(2017:May)
Page Start:
351
Record Type:
Journal Article
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8. SETD1B-associated neurodevelopmental disorder. Issue 3 (16th June 2020)

Authors:
Roston, Alexandra; Evans, Dan; Gill, Harinder; McKinnon, Margaret; Isidor, Bertrand; Cogné, Benjamin; Mwenifumbo, Jill; van Karnebeek, Clara; An, Jianghong; Jones, Steven J M; Farrer, Matthew; Demos, Michelle; Connolly, Mary; Gibson, William T
Other Names:
author non-byline.; Adam Shelin author non-byline.; Dragojlovic Nick author non-byline.; Souich Christèle du author non-byline.; Elliott Alison M author non-byline.; Lehman Anna author non-byline.; Lynd Larry author non-byline.; Mwenifumbo Jill author non-byline.; Nelson Tanya N author non-bylin...
Journal:
Journal of medical genetics
Issue:
Volume 58:Issue 3(2021)
Page Start:
196
Record Type:
Journal Article
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9. The commercial genetic testing landscape for Parkinson's disease. (November 2021)

Authors:
Cook, Lola; Schulze, Jeanine; Verbrugge, Jennifer; Beck, James C.; Marder, Karen S.; Saunders-Pullman, Rachel; Klein, Christine; Naito, Anna; Alcalay, Roy N.; Brice, Alexis; Kumeh, Amasi; West, Andrew B.; Singleton, Andrew; Naito, Anna; Schüle, Birgitt; Fiske, Brian; Gabbert, Carolin; Klein, Chri...
Journal:
Parkinsonism & related disorders
Issue:
Volume 92(2021)
Page Start:
107
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗