Lista de obras -

A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults

artículo científico publicado en 2015

A meta-analysis of genome-wide association studies identifies multiple longevity genes

scientific article published on 14 August 2019

A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions

artículo científico publicado en 2017

Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20

article

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Cerebral small vessel disease genomics and its implications across the lifespan

artículo científico publicado en 2020

Comparison of novel and existing methods for detecting differentially methylated regions

article

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

artículo científico publicado en 2019

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis

artículo científico publicado en 2016

Do changes in DNA methylation mediate or interact with SNP variation? A pharmacoepigenetic analysis

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

artículo científico publicado en 2018

Genes Involved in Interleukin-1 Receptor Type II Activities Are Associated With Asthmatic Phenotypes.

artículo científico publicado en 2016

Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits

artículo científico publicado en 2021

Genetic and environmental factors of asthma and allergy: Results of the EGEA study

artículo científico publicado en 2015

Genetic insights into biological mechanisms governing human ovarian ageing

artículo científico publicado en 2021

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women

artículo científico publicado en 2017

Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood

scientific article published on 01 October 2019

Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

artículo científico publicado en 2018

Identification of a new locus at 16q12 associated with time to asthma onset

artículo científico publicado en 2016

Impact of Genetic Determinants of HbA1c on Type 2 Diabetes Risk and Diagnosis

artículo científico publicado en 2018

Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

artículo científico publicado en 2019

Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness

artículo científico publicado en 2016

Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families

article

Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels

JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation

artículo científico publicado en 2020

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma

artículo científico publicado en 2017

New insights into the genetic etiology of Alzheimer's disease and related dementias

artículo científico publicado en 2022

PTTG1IP and MAML3, novel genomewide association study genes for severity of hyperresponsiveness in adult asthma

artículo científico publicado en 2016

Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis

artículo científico publicado en 2019

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

SigMod: an exact and efficient method to identify a strongly interconnected disease-associated module in a gene network

artículo científico publicado en 2017

The COL5A3 and MMP9 genes interact in eczema susceptibility.

artículo científico publicado en 2017

The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype

article

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

Whole genome sequence analyses of brain imaging measures in the Framingham Study

artículo científico publicado en 2017

Lista de obras de

A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults

A meta-analysis of genome-wide association studies identifies multiple longevity genes

A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions

Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Cerebral small vessel disease genomics and its implications across the lifespan

Comparison of novel and existing methods for detecting differentially methylated regions

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis

Do changes in DNA methylation mediate or interact with SNP variation? A pharmacoepigenetic analysis

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Genes Involved in Interleukin-1 Receptor Type II Activities Are Associated With Asthmatic Phenotypes.

Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits

Genetic and environmental factors of asthma and allergy: Results of the EGEA study

Genetic insights into biological mechanisms governing human ovarian ageing

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women

Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood

Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

Identification of a new locus at 16q12 associated with time to asthma onset

Impact of Genetic Determinants of HbA1c on Type 2 Diabetes Risk and Diagnosis

Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness

Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families

Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels

JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma

New insights into the genetic etiology of Alzheimer's disease and related dementias

PTTG1IP and MAML3, novel genomewide association study genes for severity of hyperresponsiveness in adult asthma

Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

SigMod: an exact and efficient method to identify a strongly interconnected disease-associated module in a gene network

The COL5A3 and MMP9 genes interact in eczema susceptibility.

The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

Whole genome sequence analyses of brain imaging measures in the Framingham Study