About: Tom H Karlsen

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0002-8289-9931)

Attributes	Values
rdf:type	Item
description	연구원 (ko) araştırmacı (tr) wetenschapper (nl) дослідник (uk) norsk forsker (nb) investigador noruegu (ast) باحث (معرف أورسيد 0000-0002-8289-9931) (ar) researcher (ORCID 0000-0002-8289-9931) (en)
rdfs:label	Tom H Karlsen (en) Tom H Karlsen (nl) Tom H Karlsen (sl) Tom Hemming Karlsen (nb)
skos:prefLabel	Tom H Karlsen (en) Tom H Karlsen (nl) Tom H Karlsen (sl) Tom Hemming Karlsen (nb)
name	Tom H Karlsen (en) Tom H Karlsen (nl) Tom H Karlsen (sl) Tom Hemming Karlsen (nb)
given name	wds:Q93051413-83C95252-155F-4D05-8D88-01D9DA534150
given name	Tom
instance of	wds:Q93051413-BA32BC80-E49A-4C1E-B4AB-989D607A016D
instance of	Homo sapiens
CRIStin ID	wds:Q93051413-62fac097-4202-f92a-0e3d-966a883e2878
CRIStin ID	16715
skos:altLabel	Tom Karlsen (en)
occupation	wds:Q93051413-BB491596-FA85-4714-A6A7-87D4C165B7F3
sex or gender	wds:Q93051413-64669da0-412c-97f5-c28b-9531b00998a0
country of citizenship	wds:Q93051413-2a3c107a-487b-b90a-45b8-713bc733eebf
family name	wds:Q93051413-A84E36D5-EACB-40A7-BFA2-52AADC82E72D
occupation	researcher
sex or gender	male
country of citizenship	Norway
family name	Karlsen
ORCID iD	wds:Q93051413-B9BE1BB6-B78B-4937-912E-772835A43BAC
ORCID iD	https://orcid.org/0000-0002-8289-9931
ORCID iD	0000-0002-8289-9931
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q93051413
is author of	Characterization of animal models for primary sclerosing cholangitis (PSC). Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility Prevalence of Sclerosing Cholangitis Detected by Magnetic Resonance Cholangiography in Patients With Long-term Inflammatory Bowel Disease Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Genome-wide association analysis in primary sclerosing cholangitis Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9 Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Urine proteomic analysis differentiates cholangiocarcinoma from primary sclerosing cholangitis and other benign biliary disorders. Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis Update on primary sclerosing cholangitis SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels The genetics of complex cholestatic disorders The utility of genome-wide association studies in hepatology Update on primary sclerosing cholangitis Primary sclerosing cholangitis Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota. Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis Novel insights into autoimmune liver diseases provided by genome-wide association studies Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci Characterization of Intestinal Microbiota in Ulcerative Colitis Patients with and without Primary Sclerosing Cholangitis The biliary epithelium presents antigens to and activates natural killer T cells Association Between HLA Haplotypes and Increased Serum Levels of IgG4 in Patients With Primary Sclerosing Cholangitis The gut microbial profile in patients with primary sclerosing cholangitis is distinct from patients with ulcerative colitis without biliary disease and healthy controls Enhanced liver fibrosis score predicts transplant-free survival in primary sclerosing cholangitis. 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 Imputation of KIR Types from SNP Variation Data Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region Genome-wide association studies--a summary for the clinical gastroenterologist Novel target genes and a valid biomarker panel identified for cholangiocarcinoma No association between the TUCAN (CARD8) Cys10Stop mutation and inflammatory bowel disease in a large retrospective German and a clinically well-characterized Norwegian sample. Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis Genetics of cholestatic liver disease in 2010. Liver transplantation in the Nordic countries - An intention to treat and post-transplant analysis from The Nordic Liver Transplant Registry 1982-2013. Differences in long-term survival among liver transplant recipients and the general population: a population-based Nordic study. Liver transplantation for cholangiocarcinoma: Selection is essential for acceptable results Immunosuppression after liver transplantation for primary sclerosing cholangitis influences activity of inflammatory bowel disease. A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis Genetics of liver disease: From pathophysiology to clinical practice Deciphering the genetic predisposition to primary sclerosing cholangitis Rare variants at 16p11.2 are associated with common variable immunodeficiency In vitro evaluation of new surface coatings for extracorporeal circulation Surrogate endpoints for clinical trials in primary sclerosing cholangitis: Review and results from an International PSC Study Group consensus process Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. Phenotyping and auto-antibody production by liver-infiltrating B cells in primary sclerosing cholangitis and primary biliary cholangitis. High-throughput T-cell receptor sequencing across chronic liver diseases reveals distinct disease-associated repertoires. Primary sclerosing cholangitis is associated with extended HLA-DR3 and HLA-DR6 haplotypes

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