Andreas Puschmann

Author PubWeight™ 17.46^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	VPS35 mutations in Parkinson disease.	Am J Hum Genet	2011	4.16
2	Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.	Lancet Neurol	2011	3.36
3	Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.	Hum Mol Genet	2013	1.79
4	Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.	Ann Neurol	2011	1.40
5	Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new cases.	Parkinsonism Relat Disord	2012	1.12
6	GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.	Am J Neurodegener Dis	2013	1.03
7	Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.	PLoS One	2012	0.88
8	Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia.	BMC Neurol	2012	0.85
9	Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.	Mov Disord	2013	0.79
10	Unverricht-Lundborg disease-a misnomer?	Mov Disord	2009	0.78
11	Alpha-synuclein repeat variants and survival in Parkinson's disease.	Mov Disord	2014	0.77
12	LRRK2 variation and Parkinson's disease in African Americans.	Mov Disord	2010	0.75