Lista de obras -

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

artículo científico publicado en 2016

Allele-specific repression of lymphotoxin-alpha by activated B cell factor-1

artículo científico publicado en 2004

Applying Genomics in Heart Transplantation.

artículo científico publicado en 2018

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

artículo científico publicado en 2014

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

artículo científico publicado en 2011

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

artículo científico publicado en 2010

Candidate gene association resource (CARe): design, methods, and proof of concept

artículo científico publicado en 2010

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

artículo científico publicado en 2011

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

artículo científico publicado en 2010

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

artículo científico publicado en 2008

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

artículo científico publicado en 2015

Copy number variations in alternative splicing gene networks impact lifespan

artículo científico publicado en 2013

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

artículo científico publicado en 2016

Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect

artículo científico publicado en 2014

Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol

artículo científico publicado en 2011

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

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

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

artículo científico publicado en 2016

Examination of genetic variants influencing lipid traits in pediatric populations.

artículo científico publicado en 2012

Fatty-acid binding protein 4 gene polymorphisms and plasma levels in children with obstructive sleep apnea

artículo científico publicado en 2011

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

artículo científico publicado en 2013

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

artículo científico publicado en 2012

Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing

artículo científico publicado en 2017

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

artículo científico publicado en 2015

Genetic variance in nitric oxide synthase and endothelin genes among children with and without endothelial dysfunction

artículo científico publicado en 2013

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

artículo científico publicado en 2016

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia

artículo científico publicado en 2013

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

artículo científico publicado en 2013

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

artículo científico publicado en 2013

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

scientific journal article

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

artículo científico publicado en 2011

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

artículo científico publicado en 2011

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

artículo científico publicado en 2014

Identification of common genetic variation that modulates alternative splicing

artículo científico publicado en 2007

Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry

artículo científico publicado en 2011

Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)

artículo científico publicado en 2015

Implications of inter-population linkage disequilibrium patterns on the approach to a disease association study in the human MHC class III.

artículo científico publicado en 2006

In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading

artículo científico publicado en 2003

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.

artículo científico publicado en 2014

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

artículo científico publicado en 2014

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

artículo científico publicado en 2015

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Mendelian randomization of blood lipids for coronary heart disease

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

artículo científico publicado en 2015

Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia

artículo científico publicado en 2015

Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels

artículo científico publicado en 2014

Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts

artículo científico publicado en 2012

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

Pharmacogenomics in kidney transplant recipients and potential for integration into practice

artículo científico publicado en 2020

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

scientific article published on 14 January 2020

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

scientific article published on 31 July 2013

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

artículo científico publicado en 2016

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

artículo científico publicado en 2012

The landscape of recombination in African Americans

artículo científico publicado en 2011

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

artículo científico publicado en 2010

Trans-ethnic meta-analysis of white blood cell phenotypes

artículo científico publicado en 2014

Whole-genome sequencing in an autism multiplex family

artículo científico publicado en 2013

Lista de obras de

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

Allele-specific repression of lymphotoxin-alpha by activated B cell factor-1

Applying Genomics in Heart Transplantation.

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Candidate gene association resource (CARe): design, methods, and proof of concept

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Copy number variations in alternative splicing gene networks impact lifespan

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect

Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

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

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Examination of genetic variants influencing lipid traits in pediatric populations.

Fatty-acid binding protein 4 gene polymorphisms and plasma levels in children with obstructive sleep apnea

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

Genetic variance in nitric oxide synthase and endothelin genes among children with and without endothelial dysfunction

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

Identification of common genetic variation that modulates alternative splicing

Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry

Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)

Implications of inter-population linkage disequilibrium patterns on the approach to a disease association study in the human MHC class III.

In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Mendelian randomization of blood lipids for coronary heart disease

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

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia

Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels

Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Pharmacogenomics in kidney transplant recipients and potential for integration into practice

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

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

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

The landscape of recombination in African Americans

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

Trans-ethnic meta-analysis of white blood cell phenotypes

Whole-genome sequencing in an autism multiplex family