CHCHD2 and Parkinson's disease

The Lancet Neurology

Volumn 14, Issue 7, 2015, Pages 678-679

  Jansen, Iris E ^a,b   Bras, Jose M ^c   Lesage, Suzanne ^d,e   Schulte, Claudia ^b,f   Gibbs, J Raphael ^g   Nalls, Mike A ^g   Brice, Alexis ^d,e   Wood, Nicholas W ^c   Morris, Huw ^h   Hardy, John A ⁱ   Singleton, Andrew B ^g   Gasser, Thomas ^b,f   Heutink, Peter ^a,b,f   Sharma, Manu ^f,j  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^b GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d SORBONNE UNIVERSITÉ   (France)

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^f UNIVERSITY OF TÜBINGEN   (Germany)

^g NATIONAL INSTITUTE ON AGING   (United States)

^h NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

ⁱ UNIVERSITY COLLEGE LONDON   (United Kingdom)

^j UNIVERSITY OF TÜBINGEN   (Germany)

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Author keywords

[No Author keywords available]

Indexed keywords

CHCHD2 GENE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; LETTER; MOLECULAR PATHOLOGY; NEUROPATHOLOGY; NONHUMAN; PARKINSON DISEASE; PRIORITY JOURNAL; DNA SEQUENCE; FEMALE; GENETIC LINKAGE; GENETICS; MALE; MISSENSE MUTATION; PARKINSONISM; PROCEDURES;

MITOCHONDRIAL PROTEIN; TRANSCRIPTION FACTOR;

FEMALE; GENETIC LINKAGE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MITOCHONDRIAL PROTEINS; MUTATION, MISSENSE; PARKINSONIAN DISORDERS; SEQUENCE ANALYSIS, DNA; TRANSCRIPTION FACTORS;

EID: 84930512273     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(15)00094-0     Document Type: Letter

References (4)

1. Trinh J, Farrer M Advances in the genetics of Parkinson disease. Nat Rev Neurol 2013, 9:445-454.
2. Funayama M, Ohe K, Amo T, et al. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Lancet Neurol 2015, 14:274-282.
3. Satake W, Nakabayashi Y, Mizuta I, et al. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009, 41:1303-1307.
4. Nalls MA, Pankratz N, Lill CM, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat Genet 2014, 46:989-993.