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Author/Creator Williams, Nigel M

1. Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk. Issue 1 (15th January 2021)

Authors:
Lubbe, Steven J; Bustos, Bernabe I; Hu, Jing; Krainc, Dimitri; Joseph, Theresita; Hehir, Jason; Tan, Manuela; Zhang, Weijia; Escott-Price, Valentina; Williams, Nigel M; Blauwendraat, Cornelis; Singleton, Andrew B; Morris, Huw R
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 1(2021)
Page Start:
78
Record Type:
Journal Article
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2. CSF-resident CD4+ T-cells display a distinct gene expression profile with relevance to immune surveillance and multiple sclerosis. Issue 3 (13th July 2021)

Authors:
Hrastelj, James; Andrews, Robert; Loveless, Samantha; Morgan, Joanne; Bishop, Stefan Mark; Bray, Nicholas J; Williams, Nigel M; Robertson, Neil P
Journal:
Brain communications
Issue:
Volume 3:Issue 3(2021)
Page Start:
Record Type:
Journal Article
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3. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Issue 6 (May 2016)

Authors:
Mok, Kin Y; Sheerin, Una; Simón-Sánchez, Javier; Salaka, Afnan; Chester, Lucy; Escott-Price, Valentina; Mantripragada, Kiran; Doherty, Karen M; Noyce, Alastair J; Mencacci, Niccolo E; Lubbe, Steven J; Williams-Gray, Caroline H; Barker, Roger A; van Dijk, Karin D; Berendse, Henk W; Heutink, Peter;...
Journal:
Lancet neurology
Issue:
Volume 15:Issue 6(2016:May)
Page Start:
585
Record Type:
Journal Article
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4. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. Issue 10 (October 2015)

Authors:
Nalls, Mike A; McLean, Cory Y; Rick, Jacqueline; Eberly, Shirley; Hutten, Samantha J; Gwinn, Katrina; Sutherland, Margaret; Martinez, Maria; Heutink, Peter; Williams, Nigel M; Hardy, John; Gasser, Thomas; Brice, Alexis; Price, T Ryan; Nicolas, Aude; Keller, Margaux F; Molony, Cliona; Gibbs, J Rap...
Journal:
Lancet neurology
Issue:
Volume 14:Issue 10(2015:Oct.)
Page Start:
1002
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗