Journal Article (15)
1.
Journal Article
48 (3), pp. 391 - 398 (2012)
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS. Neurobiology of Disease 2.
Journal Article
49 (11), pp. 721 - 726 (2012)
A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics (London) 3.
Journal Article
33 (9), pp. 1366 - 1372 (2012)
Developing the "next generation" of genetic association databases for complex diseases. Human Mutation 4.
Journal Article
49 (9), pp. 558 - 562 (2012)
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Journal of Medical Genetics (London) 5.
Journal Article
33 (9), pp. 1311 - 1314 (2012)
Databases for neurogenetics: Introduction, overview, and challenges. Human Mutation 6.
Journal Article
79 (7), pp. 659 - 667 (2012)
Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 7.
Journal Article
14 (7), pp. 663 - 669 (2012)
Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining. GENETICS IN MEDICINE 8.
Journal Article
83 (6), pp. 705 - 713 (2012)
[The genetic profile of multiple sclerosis: risk genes and the "dark matter"]. Der Nervenarzt 9.
Journal Article
78 (16), pp. 1250 - 1257 (2012)
Role of common and rare APP DNA sequence variants in Alzheimer disease. Neurology 10.
Journal Article
8 (3), p. e1002548 (2012)
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database. PLoS Genetics 11.
Journal Article
33 (1), pp. 201 e9 - 18 (2012)
Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD. Neurobiology of Aging 12.
Journal Article
33 (1), pp. 201.e9 - 201.e18 (2012)
Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD. Neurobiology of Aging 13.
Journal Article
13 (1), pp. 83 - 6 (2012)
Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample. Neurogenetics 14.
Journal Article
73 (1), pp. 35 - 46 (2012)
On the Meta-Analysis of Genome-Wide Association Studies: A Robust and Efficient Approach to Combine Population and Family-Based Studies. Human Heredity 15.
Journal Article
73 (1), pp. 35 - 46 (2012)
On the Meta-Analysis of Genome-Wide Association Studies: A Robust and Efficient Approach to Combine population and Family-Based Studies. Human Heredity Book Chapter (1)
16.
Book Chapter
107, pp. 79 - 100. Elsevier (2012)
The Genetics of Alzheimer's Disease. In: Progress in Molecular Biology and Translational Science: Molecular Biology of Neurodegenerative Diseases, Vol. Conference Paper (1)
17.
Conference Paper
78, (2012)
Comprehensive Research Synopsis and Systematic Meta-Analyses in ALS Genetics: The ALSGene Database (P01.095). Neurology Poster (1)
18.
Poster
Assessment and Genetic Associations of the 2d:4d Finger-Length Ratio within the Berlin Aging Study Ii (Base-Ii). GSA Sixty-Fifth Annual Scientific Meeting: Charting New Frontiers in Aging, San Diego, CA (2012)