Lista de obras -

A robust clustering algorithm for identifying problematic samples in genome-wide association studies

artículo científico publicado en 2011

Analysis with the exome array identifies multiple new independent variants in lipid loci

artículo científico publicado en 2016

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array

artículo científico publicado en 2011

Bayesian refinement of association signals for 14 loci in 3 common diseases

artículo científico publicado en 2012

Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.

scientific article published on 05 May 2009

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Common variants near TERC are associated with mean telomere length

artículo científico publicado en 2010

Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis

artículo científico publicado en 2012

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

artículo científico publicado en 2012

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

artículo científico publicado en 2011

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

artículo científico publicado en 2018

Evidence that duplications of 22q11.2 protect against schizophrenia

artículo científico publicado en 2013

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

artículo científico publicado en 2016

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

artículo científico publicado en 2008

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

artículo científico publicado en 2009

Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis

artículo científico publicado en 2012

Genetic variants influencing circulating lipid levels and risk of coronary artery disease

artículo científico publicado en 2010

Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2.

artículo científico publicado en 2010

Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2.

artículo científico

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

artículo científico publicado en 2009

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci

artículo científico publicado en 2011

Genome-wide association study of receptive language ability of 12-year-olds

artículo científico publicado en 2014

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

artículo científico publicado en 2009

Genome-wide meta-analysis of common variant differences between men and women

artículo científico publicado en 2012

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

artículo científico publicado en 2012

Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

artículo científico publicado en 2012

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

artículo científico publicado en 2011

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

artículo científico publicado en 2011

Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach

artículo científico publicado en 2009

Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship

artículo científico publicado en 2008

LDL-cholesterol concentrations: a genome-wide association study

artículo científico publicado en 2008

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

artículo científico publicado en 2010

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

artículo científico publicado en 2007

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

artículo científico publicado en 2008

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

artículo científico publicado en 2017

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

artículo científico publicado en 2013

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

artículo científico publicado en 2009

Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study

artículo científico publicado en 2014

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

artículo científico publicado en 2011

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

artículo científico publicado en 2010

Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility

artículo científico publicado en 2008

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

scientific article published on 16 October 2012

Rheumatoid arthritis association at 6q23.

artículo científico publicado en 2007

Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.

artículo científico publicado en 2008

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

artículo científico publicado en 2007

Seven newly identified loci for autoimmune thyroid disease

artículo científico publicado en 2012

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

artículo científico publicado en 2008

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

artículo científico publicado en 2009

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

artículo científico publicado en 2010

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.

artículo científico publicado en 2015

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

artículo científico publicado en 2010

Lista de obras de

A robust clustering algorithm for identifying problematic samples in genome-wide association studies

Analysis with the exome array identifies multiple new independent variants in lipid loci

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array

Bayesian refinement of association signals for 14 loci in 3 common diseases

Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

Common variants near TERC are associated with mean telomere length

Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

Evidence that duplications of 22q11.2 protect against schizophrenia

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis

Genetic variants influencing circulating lipid levels and risk of coronary artery disease

Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2.

Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2.

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci

Genome-wide association study of receptive language ability of 12-year-olds

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

Genome-wide meta-analysis of common variant differences between men and women

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach

Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship

LDL-cholesterol concentrations: a genome-wide association study

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

Large-scale association analysis identifies new risk loci for coronary artery disease

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

Rheumatoid arthritis association at 6q23.

Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

Seven newly identified loci for autoimmune thyroid disease

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

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

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight