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Juliane Winkelmann
Juliane Winkelmann
Professor Human Genetics Technical University of Munich, Inst. of Neurogenomics Helmholtz Munich
Bestätigte E-Mail-Adresse bei tum.de - Startseite
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Zitiert von
Zitiert von
Jahr
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ...
Nature 491 (7422), 119-124, 2012
49272012
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
28662011
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
12792013
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
LC Tsoi, SL Spain, J Knight, E Ellinghaus, PE Stuart, F Capon, J Ding, ...
Nature genetics 44 (12), 1341-1348, 2012
10122012
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
A Zimprich, A Benet-Pagès, W Struhal, E Graf, SH Eck, MN Offman, ...
The American Journal of Human Genetics 89 (1), 168-175, 2011
10042011
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
J Winkelmann, B Schormair, P Lichtner, S Ripke, L Xiong, S Jalilzadeh, ...
Nature genetics 39 (8), 1000-1006, 2007
7502007
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy
P Navon Elkan, SB Pierce, R Segel, T Walsh, J Barash, S Padeh, ...
New England Journal of Medicine 370 (10), 921-931, 2014
6252014
International IBD Genetics Consortium (IIBDGC). Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ...
Nature 491 (7422), 119-124, 2012
6082012
Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome
A Zimprich, M Grabowski, F Asmus, M Naumann, D Berg, M Bertram, ...
Nature genetics 29 (1), 66-69, 2001
5662001
Narcolepsy is strongly associated with the T-cell receptor alpha locus
J Hallmayer, J Faraco, L Lin, S Hesselson, J Winkelmann, M Kawashima, ...
Nature genetics 41 (6), 708-711, 2009
5242009
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients
J Winkelmann, TC Wetter, V Collado-Seidel, T Gasser, M Dichgans, ...
Sleep 23 (5), 1-6, 2000
4792000
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
JZ Liu, JR Hov, T Folseraas, E Ellinghaus, SM Rushbrook, NT Doncheva, ...
Nature genetics 45 (6), 670-675, 2013
4152013
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
3712015
Restless legs syndrome associated with major diseases: a systematic review and new concept
C Trenkwalder, R Allen, B Högl, W Paulus, J Winkelmann
Neurology 86 (14), 1336-1343, 2016
3272016
High-density mapping of the MHC identifies a shared role for HLA-DRB1* 01: 03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis
P Goyette, G Boucher, D Mallon, E Ellinghaus, L Jostins, H Huang, ...
Nature genetics 47 (2), 172-179, 2015
3182015
“Anxietas Tibiarum” depression and anxiety disorders in patients with restless legs syndrome
J Winkelmann, M Prager, R Lieb, H Pfister, B Spiegel, HU Wittchen, ...
Journal of neurology 252, 67-71, 2005
3142005
Genome-wide association analysis of psoriatic arthritis and cutaneous psoriasis reveals differences in their genetic architecture
PE Stuart, RP Nair, LC Tsoi, T Tejasvi, S Das, HM Kang, E Ellinghaus, ...
The American Journal of Human Genetics 97 (6), 816-836, 2015
3062015
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
B Schormair, D Kemlink, D Roeske, G Eckstein, L Xiong, P Lichtner, ...
Nature genetics 40 (8), 946-948, 2008
3052008
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families
J Winkelmann, B Muller‐Myhsok, HU Wittchen, B Hock, M Prager, ...
Annals of neurology 52 (3), 297-302, 2002
3022002
Diagnostic standards for dopaminergic augmentation of restless legs syndrome: report from a World Association of Sleep Medicine–International Restless Legs Syndrome Study Group …
D García-Borreguero, RP Allen, R Kohnen, B Högl, C Trenkwalder, ...
Sleep medicine 8 (5), 520-530, 2007
2972007
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