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Lista de obras de David Evans

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

artículo científico publicado en 2016

A Genome-Wide Scan for Eysenckian Personality Dimensions in Adolescent Twin Sibships: Psychoticism, Extraversion, Neuroticism, and Lie

artículo científico publicado en 2008

A Note on Including Phenotypic Information from Monozygotic Twins in Variance Components Qtl Linkage Analysis

artículo científico publicado en 2003

A Note on the Power to Detect Transmission Distortion in Parent-Child Trios via the Transmission Disequilibrium Test

article

A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations

artículo científico publicado en 2005

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

artículo científico publicado en 2011

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

artículo científico publicado en 2004

A genome-wide approach to children's aggressive behavior: The EAGLE consortium

artículo científico publicado en 2015

A genome-wide association meta-analysis identifies new childhood obesity loci

artículo científico publicado en 2012

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

artículo científico publicado en 2016

A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

artículo científico publicado en 2013

A genome-wide association study for reading and language abilities in two population cohorts.

artículo científico publicado en 2013

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

artículo científico publicado en 2010

A genome-wide association study of body mass index across early life and childhood

artículo científico publicado en 2015

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

artículo científico publicado en 2009

A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom

article

A major quantitative trait locus for CD4–CD8 ratio is located on chromosome 11

article

A novel common variant in DCST2 is associated with length in early life and height in adulthood

artículo científico publicado en 2014

A population-based study of genetic variation and psychotic experiences in adolescents

artículo científico publicado en 2013

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

A simulation study concerning the effect of varying the residual phenotypic correlation on the power of bivariate quantitative trait loci linkage analysis

artículo científico publicado en 2004

A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure

artículo científico publicado en 2010

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

scientific article published on 03 January 2017

Adult height variants affect birth length and growth rate in children

artículo científico publicado en 2011

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2018

Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2).

artículo científico publicado en 2014

Antibody response to common human viruses is shaped by genetic factors

artículo científico publicado en 2018

Applying polygenic risk scores to postpartum depression

artículo científico publicado en 2014

Are obesity risk genes associated with binge eating in adolescence?

artículo científico publicado en 2015

Are serum concentrations of vitamin B-12 causally related to cardiometabolic risk factors and disease? A Mendelian randomization study

artículo científico publicado en 2018

Assessing the Role of DNA Methylation-Derived Neutrophil-to-Lymphocyte Ratio in Rheumatoid Arthritis

article

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study

scientific article published in the British Medical Journal

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

artículo científico publicado en 2017

Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs

artículo científico publicado en 2011

Association and interaction analyses of eight genes under asthma linkage peaks

article

Association of Forced Vital Capacity with the Developmental Gene NCOR2.

artículo científico publicado en 2016

Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children ⬇️

artículo científico publicado en 2011

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

artículo científico publicado en 2007

Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs

artículo científico publicado en 2013

Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier

artículo científico publicado en 2011

Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control study

artículo científico publicado en 2014

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2019

Authors' response to Hartwig and Davies

artículo científico publicado en 2016

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

artículo científico publicado en 2020

Back to school to protect against coronary heart disease?

artículo científico publicado en 2017

Biometrical genetics

artículo científico publicado en 2002

Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

artículo científico publicado en 2017

Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies

artículo científico publicado en 2019

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

artículo científico publicado en 2016

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

artículo científico publicado en 2013

Circulating Selenium and Prostate Cancer Risk: A Mendelian Randomization Analysis

Cis and trans effects of human genomic variants on gene expression.

artículo científico publicado en 2014

Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals

artículo científico publicado en 2009

Collider scope: when selection bias can substantially influence observed associations.

artículo científico publicado en 2017

Common Genetic Variants Influence Whorls in Fingerprint Patterns

artículo científico publicado en 2015

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

artículo científico publicado en 2013

Common variants in the region around Osterix are associated with bone mineral density and growth in childhood

artículo científico publicado en 2009

Common variants near MC4R are associated with fat mass, weight and risk of obesity

artículo científico publicado en 2008

Common variation contributes to the genetic architecture of social communication traits.

artículo científico publicado en 2013

Common variation near ROBO2 is associated with expressive vocabulary in infancy.

artículo científico publicado en 2014

Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature

artículo científico publicado en 2013

Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

artículo científico publicado en 2014

Correction to: The Augmented Classical Twin Design: Incorporating Genome-Wide Identity by Descent Sharing Into Twin Studies in Order to Model Violations of the Equal Environments Assumption

artículo científico publicado en 2021

Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES).

artículo científico publicado en 2015

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

artículo científico publicado en 2020

Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals

artículo científico publicado en 2017

Do the genetic or environmental determinants of anxiety and depression change with age? A longitudinal study of Australian twins

artículo científico publicado en 2004

Does bone resorption stimulate periosteal expansion? A cross-sectional analysis of β-C-telopeptides of type I collagen (CTX), genetic markers of the RANKL pathway, and periosteal circumference as measured by pQCT.

artículo científico publicado en 2014

ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients

artículo científico publicado en 2015

Effects of BMI, fat mass, and lean mass on asthma in childhood: a Mendelian randomization study

artículo científico publicado en 2014

Elucidating the genetics of craniofacial shape

article

Elucidating the role of maternal environmental exposures on offspring health and disease using two-sample Mendelian randomization

article

Epigenome-wide Association of DNA Methylation in Whole Blood With Bone Mineral Density

artículo científico publicado en 2017

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

artículo científico publicado en 2016

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

article

Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

artículo científico publicado en 2017

Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes.

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

artículo científico publicado en 2010

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

artículo científico publicado en 2018

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

artículo científico publicado en 2013

Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability

artículo científico publicado en 2010

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

artículo científico publicado en 2013

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

artículo científico publicado en 2016

Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

artículo científico publicado en 2013

Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis

artículo científico publicado en 2015

Genetic evidence of assortative mating in humans

article

Genetic influences on trajectories of systolic blood pressure across childhood and adolescence

artículo científico publicado en 2013

Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis

artículo científico publicado en 2012

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

artículo científico publicado en 2016

Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence

artículo científico publicado en 2015

Genetic variants in the vitamin d receptor are associated with advanced prostate cancer at diagnosis: findings from the prostate testing for cancer and treatment study and a systematic review

artículo científico publicado en 2009

Genetic variation associated with differential educational attainment in adults has anticipated associations with school performance in children

artículo científico publicado en 2014

Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies

scientific journal article

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants

artículo científico publicado en 2005

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin

artículo científico publicado en 2014

Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition

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 11 risk variants associated with the asthma with hay fever phenotype

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 and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

artículo científico publicado en 2013

Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone

artículo científico publicado en 2010

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.

artículo científico publicado en 2018

Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus

artículo científico publicado en 2014

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

artículo científico publicado en 2014

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

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 four loci associated with eruption of permanent teeth

artículo científico publicado en 2011

Genome-wide association study identifies loci affecting blood copper, selenium and zinc

artículo científico publicado en 2013

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.

artículo científico publicado en 2018

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 ankylosing spondylitis identifies non-MHC susceptibility loci

artículo científico publicado en 2010

Genome-wide association study of blood lead shows multiple associations near ALAD

artículo científico publicado en 2015

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 of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

artículo científico publicado en 2018

Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3

artículo científico publicado en 2014

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

artículo científico publicado en 2018

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

artículo científico publicado en 2013

Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position

artículo científico publicado en 2012

Genome-wide association study reveals multiple loci associated with primary tooth development during infancy

artículo científico publicado en 2010

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

artículo científico publicado en 2012

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

artículo científico publicado en 2011

Genome-wide association: a promising start to a long race

artículo científico publicado en 2006

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

artículo científico publicado en 2013

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

artículo científico publicado en 2012

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

artículo científico publicado en 2011

Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort

artículo científico publicado en 2012

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

artículo científico publicado en 2005

Genome-wide screening for DNA variants associated with reading and language traits

artículo científico publicado en 2014

Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

artículo científico publicado en 2018

Genomewide scans of red cell indices suggest linkage on chromosome 6q23.

scientific article published on September 2006

Genomic influences on alcohol problems in a population-based sample of young adults

artículo científico publicado en 2015

Genotype prediction using a dense map of SNPs

artículo científico publicado en 2004

Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

artículo científico publicado en 2004

HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics

artículo científico publicado en 2016

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

artículo científico publicado en 2009

Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium

artículo científico publicado en 2016

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

artículo científico publicado en 2014

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

artículo científico publicado en 2017

Identification of atopic dermatitis subgroups in children from 2 longitudinal birth cohorts

artículo científico publicado en 2017

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

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

artículo científico publicado en 2013

Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies

Incorporating Known Genetic Variants Does Not Improve the Accuracy of PSA Testing to Identify High Risk Prostate Cancer on Biopsy

artículo científico publicado en 2015

Integrative pathway genomics of lung function and airflow obstruction

artículo científico publicado en 2015

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

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

artículo científico publicado en 2016

Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes

artículo científico publicado en 2019

Investigating a Potential Causal Relationship Between Maternal Blood Pressure During Pregnancy and Future Offspring Cardiometabolic Health

artículo científico publicado en 2022

Investigating a possible causal relationship between maternal serum urate concentrations and offspring birthweight: a Mendelian randomization study

artículo científico publicado en 2022

Investigating the genetic association between ERAP1 and ankylosing spondylitis

artículo científico publicado en 2009

Is there a higher genetic load of susceptibility loci in familial ankylosing spondylitis?

artículo científico publicado en 2012

Joint developmental trajectories of internalizing and externalizing disorders between childhood and adolescence

artículo científico publicado en 2016

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.

artículo científico publicado en 2016

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Limb development genes underlie variation in human fingerprint patterns

artículo científico publicado en 2022

MHC-Dependent Mate Selection within 872 Spousal Pairs of European Ancestry from the Health and Retirement Study

artículo científico publicado en 2018

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1.

artículo científico publicado en 2015

Major quantitative trait locus for eosinophil count is located on chromosome 2q

artículo científico publicado en 2004

Maternal and fetal genetic contribution to gestational weight gain.

artículo científico publicado en 2017

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Mendelian Randomization: New Applications in the Coming Age of Hypothesis-Free Causality

artículo científico

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

artículo científico publicado en 2020

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

artículo científico publicado en 2010

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

artículo científico publicado en 2015

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

artículo científico publicado en 2015

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus

artículo científico publicado en 2012

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

artículo científico publicado en 2013

Mining the human phenome using allelic scores that index biological intermediates

artículo científico publicado en 2013

Molecular and population analysis of natural selection on the human haptoglobin duplication

artículo científico

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q

article

New gene functions in megakaryopoiesis and platelet formation

artículo científico publicado en 2011

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ⬇️

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

artículo científico publicado en 2014

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ⬇️

artículo científico publicado en 2018

OPG and RANK polymorphisms are both associated with cortical bone mineral density: findings from a metaanalysis of the Avon longitudinal study of parents and children and gothenburg osteoporosis and obesity determinants cohorts.

artículo científico publicado en 2010

Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease

artículo científico publicado en 2021

Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices

artículo científico publicado en 2017

Patterns of cis regulatory variation in diverse human populations

artículo científico publicado en 2012

Pharmacogenetics of antidepressant response: A polygenic approach

artículo científico publicado en 2017

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

artículo científico publicado en 2014

Polygenic scores predict alcohol problems in an independent sample and show moderation by the environment

artículo científico publicado en 2014

Postnatal growth and DNA methylation are associated with differential gene expression of the TACSTD2 gene and childhood fat mass

artículo científico publicado en 2011

Power calculations in genetic studies

artículo científico

Prospects and pitfalls in whole genome association studies

artículo científico publicado en 2005

Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

artículo científico publicado en 2019

Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ⬇️

artículo científico publicado en 2019

Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control

artículo científico publicado en 2009

RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro

scientific article published on 03 June 2020

Resolving the effects of maternal and offspring genotype on dyadic outcomes in genome wide complex trait analysis ("M-GCTA").

artículo científico publicado en 2014

Sequence variants in three loci influence monocyte counts and erythrocyte volume

artículo científico publicado en 2009

Seventy-five genetic loci influencing the human red blood cell

artículo científico publicado en 2012

Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD.

artículo científico publicado en 2015

Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes

artículo científico

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Systematic identification of genetic influences on methylation across the human life course

artículo científico publicado en 2016

TRAIT-SPECIFIC PATTERNS OF COMMON GENETIC FACTORS INFLUENCE SOCIAL-COMMUNICATION DIFFICULTIES AND ADHD SYMPTOMS DURING CHILD AND ADOLESCENT DEVELOPMENT

article

Teenage acne is influenced by genetic factors

scientific article published on 01 March 2005

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

artículo científico publicado en 2010

The Augmented Classical Twin Design: Incorporating Genome‐Wide Identity by Descent Sharing Into Twin Studies in Order to Model Violations of the Equal Environments Assumption

artículo científico publicado en 2021

The Boulder Workshop Question Box

scientific article published on 28 September 2020

The MR-Base platform supports systematic causal inference across the human phenome.

artículo científico publicado en 2018

The association between primary tooth emergence and anthropometric measures in young adults: findings from a large prospective cohort study.

artículo científico publicado en 2014

The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations

artículo científico publicado en 2016

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

artículo científico publicado en 2015

The genetic basis of spondyloarthritis: SPARTAN/IGAS 2009.

artículo científico publicado en 2010

The power of multivariate quantitative-trait loci linkage analysis is influenced by the correlation between variables

artículo científico publicado en 2002

To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

Two-stage two-locus models in genome-wide association

artículo científico publicado en 2006

Using Mendelian randomization to determine causal effects of maternal pregnancy (intrauterine) exposures on offspring outcomes: Sources of bias and methods for assessing them

artículo científico publicado en 2017

Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children

artículo científico publicado en 2016

Using a two-sample Mendelian randomization design to investigate a possible causal effect of maternal lipid concentrations on offspring birth weight

artículo científico publicado en 2019

Using adopted individuals to partition indirect maternal genetic effects into prenatal and postnatal effects on offspring phenotypes

artículo científico publicado en 2022

Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin d and prostate cancer risk

artículo científico publicado en 2013

Using structural equation modelling to jointly estimate maternal and fetal effects on birthweight in the UK Biobank

artículo científico publicado en 2018

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

scientific article published on 24 February 2014

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

artículo científico publicado en 2020

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

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