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

Lubbe, Steven J.; Escott-Price, Valentina; Gibbs, J. Raphael; Nalls, Mike A.; Bras, Jose; Price, T. Ryan; Nicolas, Aude; Jansen, Iris E.; Mok, Kin Y.; Pittman, Alan M.; Tomkins, James E.; Lewis, Patrick A.; Noyce, Alastair J.; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R.; Levine, Adam P.; Brice, Alexis; Gasser, Thomas; Hardy, John; Heutink, Peter; Wood, NicholasW.; Singleton, Andrew B.; Williams, Nigel M.; Morris, Huw R. (2016)
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia

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

Blauwendraat, Cornelis; Francescatto, Margherita; Gibbs, J. Raphael; Jansen, Iris E.; Simon-Sanchez, Javier; Hernandez, Dena G.; Dillman, Allissa A.; Singleton, Andrew B.; Cookson, Mark R.; Rizzu, Patrizia; Heutink, Peter (2016)
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

Jansen, Iris E.; Ye, Hui; Heetveld, Sasja; Lechler, Marie C.; Michels, Helen; Seinstra, Renee I.; Lubbe, Steven J.; Drouet, Valerie; Lesage, Suzanne; Majounie, Elisa; Gibbs, J. Raphael; Nalls, Mike A.; Ryten, Mina; Botia, Juan A.; Vandrovcova, Jana; Simon-Sanchez, Javier; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Blauwendraat, Cornelis; Chouhan, Amit K.; Li, Yarong; Yogi, Puja; Amin, Najaf; van Duijn, Cornelia M.; Morris, Huw R.; Brice, Alexis; Singleton, Andrew B.; David, Della C.; Nollen, Ellen A.; Jain, Shushant; Shulman, Joshua M.; Heutink, Peter (2017)
EIF4G1 mutations do not cause Parkinson's disease

Nichols, Noah; Bras, Jose M.; Hernandez, Dena G.; Jansen, Iris E.; Lesage, Suzanne; Lubbe, Steven; Singleton, Andrew B. (2015)
Establishing the role of rare coding variants in known Parkinson's disease risk loci

Jansen, Iris E.; Gibbs, J. Raphael; Nalls, Mike A.; Price, T. Ryan; Lubbe, Steven; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Williams, Nigel M.; Brice, Alexis; Hardy, John; Wood, Nicholas W.; Morris, Huw R.; Gasser, Thomas; Singleton, Andrew B.; Heutink, Peter; Sharma, Manu (2017)
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

Robak, Laurie A.; Jansen, Iris E.; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Jankovic, Joseph; Heutink, Peter; Shulman, Joshua M. (2017)
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

Witoelar, Aree; Jansen, Iris E.; Wang, Yunpeng; Desikan, Rahul S.; Gibbs, J. Raphael; Blauwendraat, Cornelis; Thompson, Wesley K.; Hernandez, Dena G.; Djurovic, Srdjan; Schork, Andrew J.; Bettella, Francesco; Ellinghaus, David; Franke, Andre; Lie, Benedicte A.; McEvoy, Linda K.; Karlsen, Tomh.; Lesage, Suzanne; Morris, Huw R.; Brice, Alexis; Wood, Nicholas W.; Heutink, Peter; Hardy, John; Singleton, Andrew B.; Dale, Anders M.; Gasser, Thomas; Andreassen, Ole A.; 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; Mok, Kin Y.; Jansen, Iris; Sharma, Manu; Tesson, Christelle; Mangone, Graziella; Lesage, Suzanne; Bras, Jose M.; Shulman, Joshua M.; Sheerin, Una-Marie; Diez-Fairen, Monica; Pastor, Pau; Jose Marti, Maria; Ezquerra, Mario; Tolosa, Eduardo; Correia-Guedes, Leonor; Ferreira, Joaquim; Amin, Najaf; van Duijn, Cornelia M.; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Nalls, Michael; Simon-Sanchez, 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 E.; Schulte, Claudia; Simon-Sanchez, Javier; Metzger, Florian G.; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis (2016)
Prediction of cognition in Parkinson's disease with a clinical-genetic score: a longitudinal analysis of nine cohorts

Liu, Ganqiang; Locascio, Joseph J.; Corvol, Jean-Christophe; Boot, Brendon; Liao, Zhixiang; Page, Kara; Franco, Daly; Burke, Kyle; Jansen, Iris E.; Trisini-Lipsanopoulos, Ana; Winder-Rhodes, Sophie; Tanner, Caroline M.; Lang, Anthony E.; Eberly, Shirley; Elbaz, Alexis; Brice, Alexis; Mangone, Graziella; Ravina, Bernard; Shoulson, Ira; Cormier-Dequaire, Florence; Heutink, Peter; van Hilten, Jacobus J.; Barker, Roger A.; Williams-Gray, Caroline H.; Marinus, Johan; Scherzer, Clemens R. (2017)
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

Liu, Ganqiang; Boot, Brendon; Locascio, Joseph J.; Jansen, Iris E.; Winder-Rhodes, Sophie; Eberly, Shirley; Elbaz, Alexis; Brice, Alexis; Ravina, Bernard; van Hilten, Jacobus J.; Cormier-Dequaire, Florence; Corvol, Jean-Christophe; Barker, Roger A.; Heutink, Peter; Marinus, Johan; Williams-Gray, Caroline H.; Scherzer, Clemens R. (2016)
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

Blauwendraat, Cornelis; Wilke, Carlo; Simon-Sanchez, Javier; Jansen, Iris E.; Reifschneider, Anika; Capell, Anja; Haass, Christian; 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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