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Gabriele Mayr
Gabriele Mayr
Max Planck Institute for Informatics, Saarbrücken
Verified email at mpi-inf.mpg.de - Homepage
Title
Cited by
Cited by
Year
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, ...
Nature genetics 39 (2), 207-211, 2007
21432007
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility
A Franke, T Balschun, TH Karlsen, J Sventoraityte, S Nikolaus, G Mayr, ...
Nature genetics 40 (11), 1319-1323, 2008
7002008
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
E Ellinghaus, D Ellinghaus, PE Stuart, RP Nair, S Debrus, JV Raelson, ...
Nature genetics 42 (11), 991-995, 2010
3912010
Structure–function analysis of the NB-ARC domain of plant disease resistance proteins
G Van Ooijen, G Mayr, MMA Kasiem, M Albrecht, BJC Cornelissen, ...
Journal of experimental botany 59 (6), 1383-1397, 2008
3832008
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
3752013
Variants in a Novel Epidermal Collagen Gene (COL29A1) Are Associated with Atopic Dermatitis
C Söderhäll, I Marenholz, T Kerscher, F Rüschendorf, J Esparza-Gordillo, ...
PLoS biology 5 (9), e242, 2007
2662007
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)
A Franke, T Balschun, C Sina, D Ellinghaus, R Häsler, G Mayr, M Albrecht, ...
Nature genetics 42 (4), 292-294, 2010
2212010
Systematic association mapping identifies NELL1 as a novel IBD disease gene
A Franke, J Hampe, P Rosenstiel, C Becker, F Wagner, R Häsler, ...
PloS one 2 (8), e691, 2007
1622007
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies
D Ellinghaus, H Zhang, S Zeissig, S Lipinski, A Till, T Jiang, B Stade, ...
Gastroenterology 145 (2), 339-347, 2013
1572013
XIAP variants in male Crohn's disease
Y Zeissig, BS Petersen, S Milutinovic, E Bosse, G Mayr, K Peuker, ...
Gut 64 (1), 66-76, 2015
1502015
Comparative analysis of protein structure alignments
G Mayr, FS Domingues, P Lackner
BMC Structural Biology 7 (1), 1-15, 2007
1122007
Molecular basis of telaprevir resistance due to V36 and T54 mutations in the NS3-4A protease of the hepatitis C virus
C Welsch, FS Domingues, S Susser, I Antes, C Hartmann, G Mayr, ...
Genome biology 9 (1), 1-18, 2008
972008
Intragenic allele pyramiding combines different specificities of wheat Pm3 resistance alleles
S Brunner, S Hurni, P Streckeisen, G Mayr, M Albrecht, N Yahiaoui, ...
The Plant Journal 64 (3), 433-445, 2010
792010
Transcomplementation, but not physical association of the CC-NB-ARC and LRR domains of tomato R protein Mi-1.2 is altered by mutations in the ARC2 subdomain
G Van Ooijen, G Mayr, M Albrecht, BJC Cornelissen, FLW Takken
Molecular plant 1 (3), 401-410, 2008
642008
A Novel Intron Element Operates Posttranscriptionally To Regulate Human N-mycExpression
LE Sivak, G Pont-Kingdon, K Le, G Mayr, KF Tai, BT Stevens, WL Carroll
Molecular and cellular biology 19 (1), 155-163, 1999
361999
Targeted resequencing and functional testing identifies low-frequency missense variants in the gene encoding GARP as significant contributors to atopic dermatitis risk
J Manz, E Rodríguez, A ElSharawy, EM Oesau, BS Petersen, H Baurecht, ...
Journal of Investigative Dermatology 136 (12), 2380-2386, 2016
342016
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression
S Mucha, H Baurecht, N Novak, E Rodríguez, S Bej, G Mayr, H Emmert, ...
Journal of Allergy and Clinical Immunology 145 (4), 1208-1218, 2020
312020
Autophagy receptor CALCOCO2/NDP52 takes center stage in Crohn disease
A Till, S Lipinski, D Ellinghaus, G Mayr, S Subramani, P Rosenstiel, ...
Autophagy 9 (8), 1256-1257, 2013
292013
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2
S Lipinski, BS Petersen, M Barann, A Piecyk, F Tran, G Mayr, M Jentzsch, ...
Molecular Case Studies 5 (1), a002428, 2019
152019
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
T Zheng, D Ellinghaus, S Juzenas, F Cossais, G Burmeister, G Mayr, ...
Gut 70 (8), 1538-1549, 2021
112021
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