Browsing Universitätsbibliographie by Author "Jansen, Iris Elisabeth"

Now showing items 1-13 of 13

Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

Jansen, Iris Elisabeth; Sharma, Manu; Gasser, Thomas; Heutink, Peter (2016)
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia

Wilke, Carlo; Deuschle, Christian; Hobert, Markus Alexander; Jansen, Iris Elisabeth; Heutink, Peter; Gasser, Thomas; Maetzler, Walter; Blauwendraat, Cornelis; Metzger, Florian G.; Synofzik, Matthis (2017)
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe

Blauwendraat, Cornelis; Francescatto, Margherita; Jansen, Iris Elisabeth; Simón-Sánchez, Javier; Rizzu, Patrizia; Heutink, Peter (2016)
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

Jansen, Iris Elisabeth; Heetveld, Sasja; Lechler, Marie; Simón-Sánchez, Javier; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Blauwendraat, Cornelis; David, Della C.; Jain, Shushant; Heutink, Peter (2017)
EIF4G1 mutations do not cause Parkinson's disease

Jansen, Iris Elisabeth (2015)
Establishing the role of rare coding variants in known Parkinson's disease risk loci

Jansen, Iris Elisabeth; Gasser, Thomas; Heutink, Peter; Sharma, Manu (2017)
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

Jansen, Iris Elisabeth; Heutink, Peter (2017)
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

Jansen, Iris Elisabeth; Blauwendraat, Cornelis; Heutink, Peter; Gasser, Thomas; Sharma, Manu (2017)
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population

Giri, Anamika; Sharma, Manu; Jansen, Iris Elisabeth; Simón-Sánchez, Javier (2017)
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants

Blauwendraat, Cornelis; Wilke, Carlo; Jansen, Iris Elisabeth; Schulte, Claudia; Simón-Sánchez, Javier; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Metzger, Florian G.; Synofzik, Matthis (2016)
Prediction of cognition in Parkinson's disease with a clinical-genetic score: a longitudinal analysis of nine cohorts

Jansen, Iris Elisabeth; Heutink, Peter (2017)
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

Jansen, Iris Elisabeth; Heutink, Peter (2016)
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

Blauwendraat, Cornelis; Wilke, Carlo; Simón-Sánchez, Javier; Jansen, Iris Elisabeth; Castillo-Lizardo, Melissa; Biskup, Saskia; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis (2018)

Now showing items 1-13 of 13

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