Pages that link to "Q67470670"
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The following pages link to Andre Franke (Q67470670):
Displaying 50 items.
- Systematic association mapping identifies NELL1 as a novel IBD disease gene (Q21090112) (← links)
- Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2 (Q21090700) (← links)
- A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe (Q21090783) (← links)
- The dynamic genome of Hydra (Q22122195) (← links)
- A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5 (Q22250941) (← links)
- Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (Q22251082) (← links)
- XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease (Q22252318) (← links)
- Meta-analysis and imputation refines the association of 15q25 with smoking quantity (Q24273244) (← links)
- Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability (Q24299949) (← links)
- Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis (Q24596087) (← links)
- Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease (Q24601772) (← links)
- Microbial exposure during early life has persistent effects on natural killer T cell function (Q24604308) (← links)
- Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants (Q24617796) (← links)
- Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci (Q24618592) (← links)
- Targeted enrichment of genomic DNA regions for next-generation sequencing (Q24618696) (← links)
- New loci associated with kidney function and chronic kidney disease (Q24630646) (← links)
- Association analyses identify six new psoriasis susceptibility loci in the Chinese population (Q24630768) (← links)
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (Q24635370) (← links)
- Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci (Q24670061) (← links)
- Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases (Q28072105) (← links)
- CEACAM1 regulates TIM-3-mediated tolerance and exhaustion (Q28115443) (← links)
- Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea (Q28119064) (← links)
- Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations (Q28250000) (← links)
- Early-onset Crohn's disease and autoimmunity associated with a variant in CTLA-4 (Q28250884) (← links)
- A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1 (Q28271903) (← links)
- Investigation of genetic susceptibility factors for human longevity - a targeted nonsynonymous SNP study (Q28291959) (← links)
- Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms (Q28385664) (← links)
- Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci (Q28393236) (← links)
- Fitness consequences of polymorphic inversions in the zebra finch genome (Q28598120) (← links)
- Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies (Q28647874) (← links)
- 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 (Q28651183) (← links)
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (Q28654771) (← links)
- Characterization of changes in serum anti-glycan antibodies in Crohn's disease--a longitudinal analysis (Q28740412) (← links)
- 4th Pediatric Allergy and Asthma Meeting (PAAM) (Q28818630) (← links)
- Genome-wide association analysis identifies three psoriasis susceptibility loci (Q28924376) (← links)
- Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci (Q28924378) (← links)
- Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (Q28943305) (← links)
- Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia (Q28943326) (← links)
- Genome-wide association study indicates two novel resistance loci for severe malaria (Q28943391) (← links)
- Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL (Q28943423) (← links)
- Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4 (Q28943462) (← links)
- Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci (Q28943478) (← links)
- Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis (Q28943511) (← links)
- 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data (Q28943529) (← links)
- Chromosome 7p11.2 (EGFR) variation influences glioma risk (Q28943530) (← links)
- Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. (Q29417109) (← links)
- Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). (Q29417124) (← links)
- Wnt signaling and Dupuytren's disease (Q29417139) (← links)
- A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 (Q29614873) (← links)
- DMBT1 functions as pattern-recognition molecule for poly-sulfated and poly-phosphorylated ligands (Q30179442) (← links)