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), 1193-1201, 2011 | 951 | 2011 |
Human disease-associated genetic variation impacts large intergenic non-coding RNA expression V Kumar, HJ Westra, J Karjalainen, DV Zhernakova, T Esko, B Hrdlickova, ... PLoS genetics 9 (1), e1003201, 2013 | 348 | 2013 |
Genetic variation in the non-coding genome: Involvement of micro-RNAs and long non-coding RNAs in disease B Hrdlickova, RC de Almeida, Z Borek, S Withoff Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1842 (10 …, 2014 | 298 | 2014 |
The influence of a short-term gluten-free diet on the human gut microbiome MJ Bonder, EF Tigchelaar, X Cai, G Trynka, MC Cenit, B Hrdlickova, ... Genome medicine 8, 1-11, 2016 | 275 | 2016 |
Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity B Hrdlickova, V Kumar, K Kanduri, DV Zhernakova, S Tripathi, ... Genome medicine 6, 1-14, 2014 | 119 | 2014 |
Genome-wide analysis of STAT3-mediated transcription during early human Th17 cell differentiation SK Tripathi, Z Chen, A Larjo, K Kanduri, K Nousiainen, T Äijo, ... Cell reports 19 (9), 1888-1901, 2017 | 116 | 2017 |
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations A Márquez, M Kerick, A Zhernakova, J Gutierrez-Achury, WM Chen, ... Genome medicine 10, 1-13, 2018 | 87 | 2018 |
Systematic annotation of celiac disease loci refines pathological pathways and suggests a genetic explanation for increased interferon-gamma levels V Kumar, J Gutierrez-Achury, K Kanduri, R Almeida, B Hrdlickova, ... Human molecular genetics 24 (2), 397-409, 2015 | 86 | 2015 |
Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing M Harakalova, M Mokry, B Hrdlickova, I Renkens, K Duran, H Van Roekel, ... Nature protocols 6 (12), 1870-1886, 2011 | 79 | 2011 |
Matrix metalloproteinase 8 (MMP8) gene polymorphisms in chronic periodontitis LI Holla, B Hrdlickova, J Vokurka, A Fassmann Archives of Oral Biology 57 (2), 188-196, 2012 | 51 | 2012 |
Association of Toll‐like receptor 9 haplotypes with chronic periodontitis in Czech population LI Holla, J Vokurka, B Hrdlickova, P Augustin, A Fassmann Journal of clinical periodontology 37 (2), 152-159, 2010 | 39 | 2010 |
Fibroblast growth factor 2 protein stability provides decreased dependence on heparin for induction of FGFR signaling and alters ERK signaling dynamics Z Koledova, J Sumbal, A Rabata, G de La Bourdonnaye, R Chaloupkova, ... Frontiers in Cell and Developmental Biology 7, 331, 2019 | 37 | 2019 |
Wellcome Trust Case Control Consortium (WTCCC) G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ... Thelma BK, Cukrowska B, Urcelay E, Bilbao JR, Mearin ML, Barisani D, Barrett …, 2011 | 37 | 2011 |
Relationship between the 17q21 locus and adult asthma in a Czech population B Hrdlickova, LI Holla Human immunology 72 (10), 921-925, 2011 | 30 | 2011 |
Interferon-γ+ 874A/T polymorphism in relation to generalized chronic periodontitis and the presence of periodontopathic bacteria LI Holla, B Hrdlickova, P Linhartová, A Fassmann archives of oral biology 56 (2), 153-158, 2011 | 28 | 2011 |
A locus at 7p14. 3 predisposes to refractory celiac disease progression from celiac disease B Hrdlickova, CJ Mulder, G Malamut, B Meresse, M Platteel, Y Kamatani, ... European journal of gastroenterology & hepatology 30 (8), 828-837, 2018 | 27 | 2018 |
Celiac disease: moving from genetic associations to causal variants B Hrdlickova, HJ Westra, L Franke, C Wijmenga Clinical genetics 80 (3), 203-313, 2011 | 26 | 2011 |
Haplotypes of the IL-1 gene cluster are associated with gastroesophageal reflux disease and Barrett’s esophagus LI Holla, PB Linhartova, B Hrdlickova, F Marek, J Dolina, V Rihak, Z Kala Human immunology 74 (9), 1161-1169, 2013 | 21 | 2013 |
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) PreventCD Study Group. Wellcome Trust Case Control Consortium (WTCCC) Dense genotyping identifies and localizes … G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ... Nat. Genet 43, 1193-1201, 2011 | 20 | 2011 |
Haplotype analysis of the interleukin-18 gene in Czech patients with allergic disorders VA Izakovicova Holla L, Hrdlickova B, Schuller M Hum Immunol 71 (6), 592-7, 2010 | 20 | 2010 |