Mitrovič, Mitja
Mitja Mitrovič
VIAF ID: 350154441719035460006 ( Personal )
Permalink: http://viaf.org/viaf/350154441719035460006
Preferred Forms
- 100 0 _ ‡a Mitja Mitrovič
- 100 1 _ ‡a Mitrovič, Mitja
4xx's: Alternate Name Forms (6)
Works
Title | Sources |
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AKT isoforms modulate Th1-like Treg generation and function in human autoimmune disease | |
Analiza talilnih krivulj visoke ločljivosti za hitro gensko tipizacijo polimorfizmov SNP gena NOD2/CARD15 | |
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci | |
Asociacijska analiza nekaterih kandidatnih genov izbranih z orodji bioinformatike pri bolnikih s kronično vnetno črevesno boleznijo : diplomska naloga | |
Bioinformatic approaches for candidate gene selection in patients with inflammatory bowel diseases | |
Birth characteristics and risk of febrile seizures | |
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis | |
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease | |
Fine-mapping inflammatory bowel disease loci to single-variant resolution | |
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | |
Genetic variants associated with autoimmunity drive NFkB signaling and responses to inflammatory stimuli | |
Genetski dejavniki tveganja in farmakogenomika kompleksnih bolezni prebavil : zaključno poročilo o rezultatih raziskovalnega projekta | |
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease | |
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 | |
High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients | |
Host-microbe interactions have shaped the genetic architecture of inflammatorybowel disease | |
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes | |
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes a genetic association study | |
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population | |
The intermediate filament protein, vimentin, is a regulator of NOD2 activity | |
Limited evidence for parent-of-origin effects in inflammatory bowel disease associated loci | |
Low-frequency and rare-coding variation contributes to multiple sclerosis risk | |
Machine learning algorithms based on genotype data predict subgroup of refractory Crohn's disease patients requiring biological therapy | |
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility | |
Obdelava podatkov genske tipizacije polimorfizmov pridobljenih z uporabo DNK mikromrež Processing of genotype data obtained with DNA microarrays | |
Quality control of data obtained with DNA microarrays : the immunochip project | |
The quest for genetic risk factors for Crohn's disease in the post-GWAS era | |
Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity |