Winkelmann, Juliane
TUM Klinikum · Helmholtz Munich · Munich Cluster for Systems Neurology · Institut für Humangenetik · Technical University of Munich
11 papers on CoChatORCID 0000-0002-3074-599X
Most cited papers
- Verified
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
The International IBD Genetics Consortium (IIBDGC), Jostins, L., Ripke, S., Weersma, R. K., Duerr, R. H., McGovern, D. P., Hui, K. Y., Lee, J. C., Philip Schumm, L., Sharma, Y., et al. (2012) · Nature
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 4,722
- Verified
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Collaborative Association Study of Psoriasis (CASP), Tsoi, L. C., Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2, Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., et al. (2012) · Nature Genetics
Psoriasis: Treatment and PathogenesisGenetic Associations and Epidemiology
Cited by 1,024
- Verified
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
The UK-PSCSC Consortium, Liu, J. Z., The International IBD Genetics Consortium, The International PSC Study Group, Hov, J. R., Folseraas, T., Ellinghaus, E., Rushbrook, S. M., Doncheva, N. T., Andreassen, O. A., et al. (2013) · Nature Genetics
Liver Diseases and ImmunityGenetic Associations and Epidemiology
Cited by 391
- Verified
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Coleman, A., Santos, R. D., et al. (2017) · The Lancet Neurology
Genetic Neurodegenerative DiseasesGenetic Associations and Epidemiology
Cited by 312
- Verified
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Hammerschlag, A. R., Stringer, S., de Leeuw, C. A., Sniekers, S., Taskesen, E., Watanabe, K., Blanken, T. F., Dekker, K., te Lindert, B. H. W., Wassing, R., et al. (2017) · Nature Genetics
Sleep and related disordersGenetic Associations and Epidemiology
Cited by 289
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?Anxietas Tibiarum?: Depression and anxiety disorders in patients with restless legs syndrome
Winkelmann, J., Prager, M., Lieb, R., Pfister, H., Spiegel, B., Wittchen, H.-U., Holsboer, F., Trenkwalder, C., & Str�hle, A. (2005) · Journal of Neurology
Restless Legs Syndrome ResearchAnxiety, Depression, Psychometrics, Treatment, Cognitive Processes
Cited by 258
- Verified
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
Pottier, C., Zhou, X., Perkerson, R. B., Baker, M., Jenkins, G. D., Serie, D. J., Ghidoni, R., Benussi, L., Binetti, G., López de Munain, A., et al. (2018) · The Lancet Neurology
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 131
- Verified
Genome-wide association study in essential tremor identifies three new loci
Müller, S. H., Girard, S. L., Hopfner, F., Merner, N. D., Bourassa, C. V., Lorenz, D., Clark, L. N., Tittmann, L., Soto-Ortolaza, A. I., Klebe, S., et al. (2016) · Brain
Deep Brain Stimulation and Movement DisordersGenetic Associations and Epidemiology
Cited by 88
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The role of SCARB2 as susceptibility factor in Parkinson's disease
Hopfner, F., Schulte, E. C., Mollenhauer, B., Bereznai, B., Knauf, F., Lichtner, P., Zimprich, A., Haubenberger, D., Pirker, W., Brücke, T., et al. (2013) · Movement Disorders
Lysosomal Storage Disorders ResearchParkinson's Disease Mechanisms and Treatments
Cited by 46
- Verified
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis
Benyamin, B., Esko, T., Ried, J. S., Radhakrishnan, A., Vermeulen, S. H., Traglia, M., Gögele, M., Anderson, D., Broer, L., Podmore, C., et al. (2014) · Nature Communications
Iron Metabolism and DisordersGenetic Associations and Epidemiology
Cited by 30
- Verified
PSEA: Phenotype Set Enrichment Analysis—A New Method for Analysis of Multiple Phenotypes
Ried, J. S., Döring, A., Oexle, K., Meisinger, C., Winkelmann, J., Klopp, N., Meitinger, T., Peters, A., Suhre, K., Wichmann, H. ‐., et al. (2012) · Genetic Epidemiology
Bioinformatics and Genomic NetworksGenetic Associations and Epidemiology
Cited by 21
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