Andreas Puschmann

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2014
Mark Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
Theuns, J. ; Verstraeten, A. ; Sleegers, K. ; Wauters, E. ; Gijselinck, I. ; Smolders, S. ; Crosiers, D. ; Corsmit, E. ; Elinck, E. and Sharma, M. , et al. (2014) In Neurology 83(21). p.13-1906
- Contribution to journal › Article
Mark Genotype-Phenotype Correlations in Parkinson Disease
Puschmann, Andreas ^LU and Wszolek, Zbigniew K (2014) p.259-285
- Chapter in Book/Report/Conference proceeding › Book chapter
Mark Neuroacanthocytosis - Clinical variability (a report on six cases)
Dulski, J. ; Soltan, W. ; Schinwelski, M. ; Sitek, E. J. ; Rudzinska, Monika ; Wójcik-Pedziwiatr, M. ; Wictor, L. ^LU ; Schön, F. ; Puschmann, A. ^LU and Klempir, J. , et al. (2014) Eighteenth International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 29(Suppl 1). p.194-194
- Contribution to journal › Published meeting abstract
Mark Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
Heckman, Michael G. ; Elbaz, Alexis ; Soto-Ortolaza, Alexandra I. ; Serie, Daniel J ; Aasly, Jan O. ; Annesi, Grazia ; Auburger, Georg ; Bacon, Justin A. ; Boczarska-Jedynak, Magdalena and Bozi, Maria , et al. (2014) In Neurobiology of Aging 35(1). p.5-266
- Contribution to journal › Article
2013
Mark GWAS risk factors in Parkinson's disease : LRRK2 coding variation and genetic interaction with PARK16
Soto-Ortolaza, A. I. ; Heckman, M. G. ; Labbe, C. ; Serie, D. J. ; Puschmann, Andreas ^LU ; Rayaprolu, S. ; Strongosky, A. ; Boczarska-Jedynak, M. ; Opala, G. and Krygowska-Wajs, A. , et al. (2013) In American Journal of Neurodegenerative Disease 2(4). p.99-287
- Contribution to journal › Article
Mark Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
Vemula, Satya R ; Puschmann, Andreas ^LU ; Xiao, Jianfeng ; Rudzinska, Monika ; Frei, Karen P ; Truong, Daniel D ; Wszolek, Zbigniew K and LeDoux, Mark S (2013) In Human Molecular Genetics 22(12). p.2510-2519
- Contribution to journal › Article
Mark Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
Lindquist, SG ; Duno, M ; Batbayli, M ; Puschmann, Andreas ^LU ; Braendgaard, H ; Mardosiene, S ; Svenstrup, K ; Pinborg, LH ; Vestergaard, K and Hjermind, LE , et al. (2013) In Clinical Genetics 83(3). p.279-283
- Contribution to journal › Article
Mark Monogenic Parkinson's disease and parkinsonism: Clinical phenotypes and frequencies of known mutations.
Puschmann, Andreas ^LU (2013) In Parkinsonism & Related Disorders 19(4). p.407-415
- Contribution to journal › Scientific review
Mark Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
Heckman, Michael G. ; Soto-Ortolaza, Alexandra I. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria ; Brice, Alexis and Brighina, Laura , et al. (2013) In Movement Disorders 28(12). p.1740-1744
- Contribution to journal › Article
Mark Olfactory Dysfunction.
Puschmann, Andreas ^LU and Wszolek, Zbigniew K. (2013) p.335-348
- Chapter in Book/Report/Conference proceeding › Book chapter

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