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Lista de obras de Martin D Tobin

A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos.

artículo científico publicado en 2018

A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample

artículo científico publicado en 2011

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

artículo científico publicado en 2010

APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema

artículo científico publicado en 2013

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

artículo científico publicado en 2015

Adjusting for bias and unmeasured confounding in Mendelian randomization studies with binary responses

artículo científico publicado en 2008

Age at menarche and lung function: a Mendelian randomization study.

artículo científico publicado en 2017

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

artículo científico publicado en 2015

Allelic variant of NOS1AP effects on cardiac alternans of repolarization during exercise testing

artículo científico publicado en 2011

An integrated approach to the meta-analysis of genetic association studies using Mendelian randomization

artículo científico publicado en 2004

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

artículo científico publicado en 2016

Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population

artículo científico publicado en 2005

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

artículo científico publicado en 2007

Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

scientific article published on 01 June 2019

Bed occupancy rates and hospital-acquired Clostridium difficile infection: a cohort study

artículo científico publicado en 2013

Blood eosinophil count and airway epithelial transcriptome relationships in COPD versus asthma

artículo científico publicado en 2019

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

Body mass index, asthma, and genetic variation ⬇️

artículo científico publicado el 1 de abril de 2013

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels

artículo científico publicado en 2013

Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED)

artículo científico publicado en 2019

Commentary: development of Mendelian randomization: from hypothesis test to 'Mendelian deconfounding'

scientific article published on 01 February 2004

Common Variation in the WNK1 Gene and Blood Pressure in Childhood

article

Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease

artículo científico publicado en 2014

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

artículo científico publicado en 2009

Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population

artículo científico publicado en 2008

Common variants near TERC are associated with mean telomere length

artículo científico publicado en 2010

Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

artículo científico publicado en 2014

Coronary Artery Disease-Associated Locus on Chromosome 9p21 and Early Markers of Atherosclerosis

artículo científico publicado en 2008

Covariance components models for longitudinal family data

artículo científico publicado en 2005

DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).

artículo científico publicado en 2014

Determinants of day-night difference in blood pressure, a comparison with determinants of daytime and night-time blood pressure

artículo científico publicado en 2016

Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

artículo científico publicado en 2015

Discovery of novel heart rate-associated loci using the Exome Chip

artículo científico publicado en 2017

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

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

Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function

artículo científico publicado en 2011

Epigenome-wide association study of lung function level and its change

artículo científico publicado en 2019

Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.

artículo científico publicado en 2017

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

artículo científico publicado en 2018

Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.

artículo científico publicado en 2016

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.

artículo científico publicado en 2018

Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy

artículo científico publicado en 2011

GSTCD and INTS12 regulation and expression in the human lung

artículo científico publicado en 2013

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations

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

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

artículo científico publicado en 2019

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

artículo científico publicado en 2017

Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline

artículo científico publicado en 2017

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.

artículo científico publicado en 2017

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

artículo científico publicado en 2017

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

artículo científico publicado en 2017

Genome-wide association analysis identifies six new loci associated with forced vital capacity

artículo científico publicado en 2014

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

artículo científico publicado en 2011

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

artículo científico publicado en 2012

Genome-wide association studies in lung disease

artículo científico publicado en 2011

Genome-wide association study identifies 74 loci associated with educational attainment

artículo científico publicado en 2016

Genome-wide association study identifies five loci associated with lung function

artículo científico publicado en 2010

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

artículo científico publicado en 2008

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

artículo científico publicado en 2007

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 copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity

artículo científico publicado en 2016

Genome-wide association study to identify genetic determinants of severe asthma.

artículo científico publicado en 2012

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function

artículo científico publicado en 2012

Genomewide association analysis of coronary artery disease

artículo científico publicado en 2007

Genomic copy number variation, human health, and disease

artículo científico publicado en 2009

Haplotype estimation for biobank-scale data sets

artículo científico publicado en 2016

Heritability of early repolarization: a population-based study

artículo científico publicado en 2011

High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report

artículo científico publicado en 2019

Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function.

artículo científico publicado en 2018

Identification of seven loci affecting mean telomere length and their association with disease

artículo científico publicado en 2013

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

artículo científico publicado en 2018

Identifying potential causal effects of age at menarche: a Mendelian randomization phenome-wide association study

artículo científico publicado en 2020

Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip

artículo científico publicado en 2012

Integrative pathway genomics of lung function and airflow obstruction

artículo científico publicado en 2015

International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents

artículo científico publicado en 2016

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

artículo científico publicado en 2017

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

artículo científico publicado en 2017

Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function ⬇️

artículo científico publicado en 2014

Leukotriene B4production in healthy subjects carrying variants of the arachidonate 5-lipoxygenase-activating protein gene associated with a risk of myocardial infarction

article

Longitudinal data analysis in pedigree studies

artículo científico publicado en 2003

Mendelian randomisation and causal inference in observational epidemiology

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Meta-analysis of Mendelian randomization studies incorporating all three genotypes

artículo científico publicado en 2008

Meta-analysis of exome array data identifies six novel genetic loci for lung function

scientific article published on 12 January 2018

Meta-analysis of exome array data identifies six novel genetic loci for lung function

Meta-analysis of genetic studies using Mendelian randomization--a multivariate approach

artículo científico publicado en 2005

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

artículo científico publicado en 2019

Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study

artículo científico publicado en 2018

Molecular mechanisms underlying variations in lung function: a systems genetics analysis

artículo científico publicado en 2015

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

artículo científico publicado en 2019

New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

scholarly article published 12 June 2018

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

artículo científico publicado en 2015

Opportunities and challenges in the genetics of COPD 2010: an International COPD Genetics Conference report

artículo científico publicado en 2011

Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study

artículo científico publicado en 2013

Pharmacogenetic interactions and their potential effects on genetic analyses of blood pressure.

artículo científico publicado en 2010

Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia

artículo científico publicado en 2017

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

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

scientific article published on 31 July 2013

Seeking consent to tissue banking: a survey of health professionals in childhood cancer

article

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

artículo científico publicado en 2015

South Asian ethnicity and risk of childhood accidents: an ecological study at enumeration district level in Leicester.

artículo científico publicado en 2002

Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls

artículo científico publicado en 2017

Teaching and learning about human sexuality in undergraduate medical education

artículo científico publicado en 2002

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

artículo científico publicado en 2016

The impact of low-frequency and rare variants on lipid levels

artículo científico publicado en 2015

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

artículo científico publicado en 2008

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

artículo científico publicado en 2013

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci ⬇️

artículo científico publicado en 2009

The vitamin D binding protein axis modifies disease severity in lymphangioleiomyomatosis

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Tumour necrosis factor gene complex polymorphisms in chronic obstructive pulmonary disease

artículo científico publicado en 2007

Understanding the impact of pre-analytic variation in haematological and clinical chemistry analytes on the power of association studies

artículo científico publicado en 2014

Use of FEV1 as a measure of lung health in the UK BiLEVE study - Authors' reply

artículo científico publicado en 2015

Variants associated with expression have sex-differential effects on lung function

artículo científico publicado en 2020

What can genetics tell us about the cause of fixed airflow obstruction?

artículo científico publicado en 2012

Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction.

artículo científico publicado en 2014

Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

scientific article published on 14 October 2020

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

artículo científico publicado en 2017

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