Cleo van Diemen
Cleo van Diemen
Dept of Genetics, University Medical Center Groningen
Verified email at umcg.nl - Homepage
TitleCited byYear
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ...
Nature genetics 43 (12), 1193, 2011
6122011
Detecting shared pathogenesis from the shared genetics of immune-related diseases
A Zhernakova, CC Van Diemen, C Wijmenga
Nature Reviews Genetics 10 (1), 43, 2009
5032009
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP
A Zhernakova, EM Festen, L Franke, G Trynka, CC van Diemen, ...
The American Journal of Human Genetics 82 (5), 1202-1210, 2008
2302008
A disintegrin and metalloprotease 33 polymorphisms and lung function decline in the general population
CC Van Diemen, DS Postma, JM Vonk, M Bruinenberg, JP Schouten, ...
American journal of respiratory and critical care medicine 172 (3), 329-333, 2005
2262005
Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease
J Romanos, CC Van Diemen, IM Nolte, G Trynka, A Zhernakova, J Fu, ...
Gastroenterology 137 (3), 834-840. e3, 2009
1522009
Common and different genetic background for rheumatoid arthritis and coeliac disease
MJH Coenen, G Trynka, S Heskamp, B Franke, CC van Diemen, ...
Human molecular genetics 18 (21), 4195-4203, 2009
1292009
Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness
GH Koppelman, DA Meyers, TD Howard, SL Zheng, GA Hawkins, ...
American journal of respiratory and critical care medicine 180 (10), 929-935, 2009
1272009
Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans
SP Smeekens, A Ng, V Kumar, MD Johnson, TS Plantinga, C Van Diemen, ...
Nature communications 4, 1342, 2013
1072013
Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease
K Fransen, MC Visschedijk, S van Sommeren, JY Fu, L Franke, ...
Human molecular genetics 19 (17), 3482-3488, 2010
1072010
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants
J Romanos, A Rosén, V Kumar, G Trynka, L Franke, A Szperl, ...
Gut 63 (3), 415-422, 2014
952014
Lung function loss, smoking, vitamin C intake, and polymorphisms of the glutamate-cysteine ligase genes
M Siedlinski, DS Postma, CC van Diemen, A Blokstra, HA Smit, ...
American journal of respiratory and critical care medicine 178 (1), 13-19, 2008
922008
A disintegrin and metalloprotease 33 and chronic obstructive pulmonary disease pathophysiology
MME Gosman, HM Boezen, CC van Diemen, JB Snoeck-Stroband, ...
Thorax 62 (3), 242-247, 2007
862007
Restricted IgA repertoire in both B-1 and B-2 cell-derived gut plasmablasts
M Stoel, HQ Jiang, CC van Diemen, JCAM Bun, PM Dammers, ...
The Journal of Immunology 174 (2), 1046-1054, 2005
812005
Decorin and TGF-β 1 polymorphisms and development of COPD in a general population
CC van Diemen, DS Postma, JM Vonk, M Bruinenberg, IM Nolte, ...
Respiratory research 7 (1), 89, 2006
702006
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease
M Stoffels, A Szperl, A Simon, MG Netea, TS Plantinga, M van Deuren, ...
Annals of the rheumatic diseases 73 (2), 455-461, 2014
652014
Genetic analysis in a Dutch study sample identifies more ulcerative colitis susceptibility loci and shows their additive role in disease risk
EAM Festen, PCF Stokkers, CC Van Diemen, AA Van Bodegraven, ...
The American journal of gastroenterology 105 (2), 395, 2010
552010
Superoxide dismutases, lung function and bronchial responsiveness in a general population
M Siedlinski, CC van Diemen, DS Postma, JM Vonk, HM Boezen
European Respiratory Journal 33 (5), 986-992, 2009
462009
DNA methylation in childhood asthma: an epigenome-wide meta-analysis
CJ Xu, C Söderhäll, M Bustamante, N Baïz, O Gruzieva, U Gehring, ...
The lancet Respiratory medicine 6 (5), 379-388, 2018
452018
Genetic variation in TIMP1 but not MMPs predict excess FEV 1 decline in two general population-based cohorts
CC van Diemen, DS Postma, M Siedlinski, A Blokstra, HA Smit, ...
Respiratory research 12 (1), 57, 2011
432011
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
KA Hunt, DJ Smyth, T Balschun, M Ban, V Mistry, T Ahmad, V Anand, ...
Nature genetics 44 (1), 3, 2012
422012
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