about
The DNA sequence of the human X chromosomeGeneration of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysisGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisAn ENU-induced mutation of miR-96 associated with progressive hearing loss in miceGenome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A regionWhole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array dataLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesGenome-wide association analysis identifies 13 new risk loci for schizophreniaGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityA genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.The zebrafish reference genome sequence and its relationship to the human genomeHigh-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.A novel CpG island set identifies tissue-specific methylation at developmental gene loci.Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus.Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competitionComplex exon-intron marking by histone modifications is not determined solely by nucleosome distribution.Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.The correlation between reading and mathematics ability at age twelve has a substantial genetic component.Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.Genome-wide association study identifies five new breast cancer susceptibility lociGenetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.Genome-wide screening for genetic alterations in esophageal cancer by aCGH identifies 11q13 amplification oncogenes associated with nodal metastasisTranscription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function.Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociCommon variants near ATM are associated with glycemic response to metformin in type 2 diabetesAccurate and reliable high-throughput detection of copy number variation in the human genome.Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeresCommon variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.Large-scale association analysis identifies new risk loci for coronary artery diseasePolymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan ChildrenA comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH.Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays.Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Cordelia Langford
@ast
Cordelia Langford
@en
Cordelia Langford
@es
Cordelia Langford
@nl
Cordelia Langford
@sl
type
label
Cordelia Langford
@ast
Cordelia Langford
@en
Cordelia Langford
@es
Cordelia Langford
@nl
Cordelia Langford
@sl
prefLabel
Cordelia Langford
@ast
Cordelia Langford
@en
Cordelia Langford
@es
Cordelia Langford
@nl
Cordelia Langford
@sl