Lista de obras -

A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression

artículo científico publicado en 2018

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics

artículo científico publicado en 2018

A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cell

artículo científico publicado en 2014

A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study

artículo científico publicado en 2020

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

artículo científico publicado en 2017

Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

scientific article published on 01 July 2019

DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility

scientific article published on 04 July 2019

Determining Risk of Colorectal Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors

artículo científico publicado en 2018

Discovery of common and rare genetic risk variants for colorectal cancer

artículo científico publicado en 2018

Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data

artículo científico publicado en 2017

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

artículo científico publicado en 2012

Familial aggregation of pure tone hearing thresholds in an aging European population

artículo científico publicado en 2013

GRM7 variants confer susceptibility to age-related hearing impairment

artículo científico publicado en 2008

Genetic mechanisms of immune evasion in colorectal cancer

artículo científico publicado en 2018

Genetic predictors of severe skin toxicity in stage III colon cancer patients treated with cetuximab: NCCTG N0147 (Alliance)

scientific article published on 17 November 2020

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

article

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

artículo científico publicado en 2008

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

artículo científico publicado en 2015

Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians

scientific article published on 11 December 2019

Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

artículo científico publicado en 2018

Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival

artículo científico publicado en 2020

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

artículo científico publicado en 2015

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

artículo científico publicado en 2019

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

artículo científico publicado en 2008

Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis

artículo científico publicado en 2020

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

artículo científico publicado en 2007

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

artículo científico publicado en 2016

Lista de obras de

A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics

A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cell

A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility

Determining Risk of Colorectal Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors

Discovery of common and rare genetic risk variants for colorectal cancer

Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Familial aggregation of pure tone hearing thresholds in an aging European population

GRM7 variants confer susceptibility to age-related hearing impairment

Genetic mechanisms of immune evasion in colorectal cancer

Genetic predictors of severe skin toxicity in stage III colon cancer patients treated with cetuximab: NCCTG N0147 (Alliance)

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians

Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Shared heritability and functional enrichment across six solid cancers

Shared heritability and functional enrichment across six solid cancers

The genetic architecture of type 2 diabetes

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension