about
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseCommon variants at five new loci associated with early-onset inflammatory bowel diseaseDeep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociUlcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association studyGenome-wide association identifies multiple ulcerative colitis susceptibility lociAssociation of DLG5 R30Q variant with inflammatory bowel diseaseIdiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locusGenetic variation in myosin IXB is associated with ulcerative colitisMeta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesMeta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47RS-SNP: a random-set method for genome-wide association studiesInvestigation of multiple susceptibility loci for inflammatory bowel disease in an Italian cohort of patients.Variants at the 3p21 locus influence susceptibility and phenotype both in adults and early-onset patients with inflammatory bowel disease.Associations between genetic polymorphisms in IL-33, IL1R1 and risk for inflammatory bowel disease.New biologics in the management of Crohn's disease: focus on certolizumab pegol.Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.HLA-DRB1 alleles may influence disease phenotype in patients with inflammatory bowel disease: a critical reappraisal with review of the literature.Crohn's Disease Localization Displays Different Predisposing Genetic VariantsGenetic sharing and heritability of paediatric age of onset autoimmune diseases.MAST3: a novel IBD risk factor that modulates TLR4 signaling.Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studiesReplication of interleukin 23 receptor and autophagy-related 16-like 1 association in adult- and pediatric-onset inflammatory bowel disease in Italy.Enteropathic spondyloarthropathy: a common genetic background with inflammatory bowel disease?Genetics and ulcerative colitis: what are the clinical implications?Erythrocyte-mediated delivery of dexamethasone in patients with mild-to-moderate ulcerative colitis, refractory to mesalamine: a randomized, controlled study.Genome-wide expression profiling identifies an impairment of negative feedback signals in the Crohn's disease-associated NOD2 variant L1007fsinsC.Do pancreatic cancer and chronic pancreatitis share the same genetic risk factors? A PANcreatic Disease ReseArch (PANDoRA) consortium investigation.The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans.Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance.Metabolomic profile in pancreatic cancer patients: a consensus-based approach to identify highly discriminating metabolites.IL-1beta-511 and IL-1RN*2 polymorphisms in inflammatory bowel disease: An Italian population study and meta-analysis of European studies.The expression of leucine-rich repeat gene family members in colorectal cancer.Erythrocytes-mediated delivery of dexamethasone 21-phosphate in steroid-dependent ulcerative colitis: a randomized, double-blind Sham-controlled study.Association study of a polymorphism in clock gene PERIOD3 and risk of inflammatory bowel disease.High resolution melting (HRM) analysis for the detection of ER22/23EK, BclI, and N363S polymorphisms of the glucocorticoid receptor gene.Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.Association of genetic profiles to Crohn's disease by linear combinations of single nucleotide polymorphisms.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Anna Latiano
@ast
Anna Latiano
@en
Anna Latiano
@es
Anna Latiano
@nl
Anna Latiano
@sl
type
label
Anna Latiano
@ast
Anna Latiano
@en
Anna Latiano
@es
Anna Latiano
@nl
Anna Latiano
@sl
prefLabel
Anna Latiano
@ast
Anna Latiano
@en
Anna Latiano
@es
Anna Latiano
@nl
Anna Latiano
@sl
P1053
R-1965-2016
P106
P1153
6602508103
P21
P31
P3829
P496
0000-0003-3719-2061