Suchergebnisse - "Harris, Clare"

PubPharm (11)

1

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

enthalten in: American journal of human genetics | 2016

von Lesage, S. | Drouet, V. | Majounie, E. | +141

CommentIn: Mov Disord. 2016 Sep;31(9):1340. - PMID 27213732

2

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

enthalten in: Neurobiology of aging | 2015

von Nalls, M. | Bras, J. | Hernandez, D. | +133

3

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

enthalten in: Nature genetics | 2014

von Nalls, M. | Pankratz, N. | Lill, C. | +156

4

Susceptibility loci for pigmentation and melanoma in relation to Parkinson's disease

enthalten in: Neurobiology of aging | 2014

von Dong, J. | Gao, J. | Nalls, M. | +106

5

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

enthalten in: Proceedings of the National Academy of Sciences of the United States of America | 2014

von Beilina, A. | Rudenko, I. | Kaganovich, A. | +120

CommentIn: Proc Natl Acad Sci U S A. 2014 Feb 18;111(7):2402-3. - PMID 24510898

6

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

enthalten in: Journal of neurology, neurosurgery, and psychiatry | 2013

von Klebe, S. | Golmard, J. | Nalls, M. | +132

7

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

enthalten in: Human molecular genetics | 2013

von Holmans, P. | Moskvina, V. | Jones, L. | +128

ErratumIn: Hum Mol Genet. 2014 Jan 15;23(2):562 Sadd, Mohamad [corrected to Saad, Mohamad]

8

Serum iron levels and the risk of Parkinson disease : a Mendelian randomization study

enthalten in: PLoS medicine | 2013

von Pichler, I. | Del Greco M, F. | Gögele, M. | +118

ErratumIn: PLoS Med. 2013 Jun;10(6). doi:10.1371/annotation/c4d81646-0c0e-4a3e-9425-b220bae2d8b6

9

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

enthalten in: Human molecular genetics | 2012

von Keller, M. | Saad, M. | Bras, J. | +129

ErratumIn: Hum Mol Genet. 2013 Apr 15;22(8):1696

10

A two-stage meta-analysis identifies several new loci for Parkinson's disease

enthalten in: PLoS genetics | 2011

von International Parkinson's Disease Genomics Consortium (IPDGC) | Wellcome Trust Case Control Consortium 2 (WTCCC2) | Plagnol, V. | +99