Lista de obras -

A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain

artículo científico publicado en 2015

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

artículo científico publicado en 2011

Common DNA markers can account for more than half of the genetic influence on cognitive abilities

artículo científico publicado en 2013

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

artículo científico publicado en 2012

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

artículo científico publicado en 2012

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

artículo científico publicado en 2012

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

artículo científico publicado en 2013

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

artículo científico publicado en 2010

Comparison of methods to account for relatedness in genome-wide association studies with family-based data

artículo científico publicado en 2014

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

artículo científico publicado en 2015

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

artículo científico publicado en 2010

Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke

artículo científico publicado en 2015

Genetic comorbidities in Parkinson's disease

artículo científico publicado en 2013

Genetic loci for retinal arteriolar microcirculation

artículo científico publicado en 2013

Genetic overlap between diagnostic subtypes of ischemic stroke

artículo científico publicado en 2015

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

artículo científico publicado en 2014

Genome-wide association and functional follow-up reveals new loci for kidney function

artículo científico publicado en 2012

Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis ⬇️

artículo científico publicado en 2016

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

artículo científico publicado en 2013

Genome-wide estimates of inbreeding in unrelated individuals and their association with cognitive ability

artículo científico publicado en 2013

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

artículo científico publicado en 2012

Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis

artículo científico publicado en 2014

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci ⬇️

artículo científico publicado el 9 de junio de 2013

Implication of a rare deletion at distal 16p11.2 in schizophrenia

artículo científico publicado en 2013

Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis

artículo científico publicado en 2013

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

artículo científico publicado en 2012

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

artículo científico publicado en 2011

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

artículo científico publicado en 2013

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

artículo científico publicado en 2014

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

artículo científico publicado en 2014

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

artículo científico publicado en 2013

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset

artículo científico publicado en 2014

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

artículo científico publicado en 2016

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

artículo científico publicado en 2014

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis

artículo científico publicado en 2013

The role of toll-like receptor variants in acute anterior uveitis

artículo científico publicado en 2011

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

artículo científico publicado en 2012

Using phenotypic heterogeneity to increase the power of genome-wide association studies: application to age at onset of ischaemic stroke subphenotypes

artículo científico publicado en 2013

Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway

artículo científico publicado en 2014

Lista de obras de

A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

Common DNA markers can account for more than half of the genetic influence on cognitive abilities

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Comparison of methods to account for relatedness in genome-wide association studies with family-based data

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke

Genetic comorbidities in Parkinson's disease

Genetic loci for retinal arteriolar microcirculation

Genetic overlap between diagnostic subtypes of ischemic stroke

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

Genome-wide association and functional follow-up reveals new loci for kidney function

Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis ⬇️

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

Genome-wide estimates of inbreeding in unrelated individuals and their association with cognitive ability

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci ⬇️

Implication of a rare deletion at distal 16p11.2 in schizophrenia

Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis

The role of toll-like receptor variants in acute anterior uveitis

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

Using phenotypic heterogeneity to increase the power of genome-wide association studies: application to age at onset of ischaemic stroke subphenotypes

Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway