Lista de obras - Halit Ongen - Dominio Público Uruguay

A complete tool set for molecular QTL discovery and analysis

artículo científico publicado en 2017

Alternative Splicing QTLs in European and African Populations

artículo científico publicado en 2015

Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome

artículo científico publicado en 2013

Characterising cis-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues

artículo científico publicado en 2017

Comprehensive evaluation of coding region point mutations in microsatellite‐unstable colorectal cancer

artículo científico publicado en 2018

Contribution of allelic imbalance to colorectal cancer

scientific article published in Nature Communications

Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation

artículo científico publicado en 2013

Corrigendum: Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

artículo científico publicado en 2017

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Estimating the causal tissues for complex traits and diseases

artículo científico publicado en 2017

Fast and efficient QTL mapper for thousands of molecular phenotypes.

artículo científico publicado en 2015

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

artículo científico publicado en 2011

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.

artículo científico publicado en 2016

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

MethCORR modelling of methylomes from formalin-fixed paraffin-embedded tissue enables characterization and prognostication of colorectal cancer

artículo científico publicado en 2020

Molecular-Subtype-Specific Biomarkers Improve Prediction of Prognosis in Colorectal Cancer

artículo científico

Non-CpG island promoter hypomethylation and miR-149 regulate the expression of SRPX2 in colorectal cancer

artículo científico publicado en 2012

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

artículo científico publicado en 2013

Publisher Correction: MethCORR modelling of methylomes from formalin-fixed paraffin-embedded tissue enables characterization and prognostication of colorectal cancer

scientific article published on 03 June 2020

Putative cis-regulatory drivers in colorectal cancer

artículo científico publicado en 2014

SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism

artículo científico publicado en 2016

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

artículo científico publicado en 2007

The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases

artículo científico publicado en 2016

The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression

artículo científico publicado en 2017

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

artículo científico publicado en 2015

Transcriptome and genome sequencing uncovers functional variation in humans

artículo científico publicado en 2013

Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

article

Lista de obras de Halit Ongen

A complete tool set for molecular QTL discovery and analysis

Alternative Splicing QTLs in European and African Populations

Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome

Characterising cis-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues

Comprehensive evaluation of coding region point mutations in microsatellite‐unstable colorectal cancer

Contribution of allelic imbalance to colorectal cancer

Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Corrigendum: Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Estimating the causal tissues for complex traits and diseases

Fast and efficient QTL mapper for thousands of molecular phenotypes.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

MethCORR modelling of methylomes from formalin-fixed paraffin-embedded tissue enables characterization and prognostication of colorectal cancer

Molecular-Subtype-Specific Biomarkers Improve Prediction of Prognosis in Colorectal Cancer

Non-CpG island promoter hypomethylation and miR-149 regulate the expression of SRPX2 in colorectal cancer

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Publisher Correction: MethCORR modelling of methylomes from formalin-fixed paraffin-embedded tissue enables characterization and prognostication of colorectal cancer

Putative cis-regulatory drivers in colorectal cancer

SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases

The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

Transcriptome and genome sequencing uncovers functional variation in humans

Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation