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Lista de obras de Caroline Hayward

3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.

artículo científico publicado en 2006

50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

article

52 Genetic Loci Influencing Myocardial Mass

artículo científico publicado en 2016

A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

artículo científico publicado en 2016

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila

artículo científico publicado en 2011

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

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

artículo científico publicado en 2011

A general approach for haplotype phasing across the full spectrum of relatedness

artículo científico publicado en 2014

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition

artículo científico publicado en 2007

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

artículo científico publicado en 2015

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

artículo científico publicado en 2015

A meta-analysis of genome-wide association studies of epigenetic age acceleration

A meta-analysis of genome-wide association studies of epigenetic age acceleration

artículo científico publicado en 2019

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

artículo científico publicado en 2010

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly

article

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A strategy to incorporate prior knowledge into correlation network cutoff selection

scientific article published on 14 October 2020

A validation of the diathesis-stress model for depression in Generation Scotland

article

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

artículo científico publicado en 2016

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

scientific article published on 29 July 2019

Apolipoprotein E is not related to memory abilities at 70 years of age.

artículo científico publicado en 2008

Apolipoprotein e gene variability and cognitive functions at age 79: a follow-up of the Scottish mental survey of 1932.

artículo científico publicado en 2004

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

artículo científico publicado en 2019

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

artículo científico publicado en 2011

Association of Medication with the Human Plasma N-Glycome

artículo científico publicado en 2012

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Association of existing and new candidate genes for anxiety, depression and personality traits in older people

artículo científico publicado en 2010

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

artículo científico publicado en 2014

Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study

artículo científico publicado en 2014

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Associations of ‘Relative corticosterone deficiency’ with genetic variation in CYP17A1 and metabolic syndrome features

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

artículo científico

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

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome

artículo científico publicado en 2010

Biochemical characterisation of the C1QTNF5 gene associated with late-onset retinal degeneration. A genetic model of age-related macular degeneration

artículo científico publicado en 2006

Biological, clinical and population relevance of 95 loci for blood lipids

artículo científico publicado en 2010

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

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

artículo científico publicado en 2020

Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates

artículo científico publicado en 2011

Cognitive ability at age 11 and 70 years, information processing speed, and APOE variation: the Lothian Birth Cohort 1936 study

artículo científico publicado en 2009

Cognitive change and the APOE epsilon 4 allele

artículo científico publicado en 2002

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common genetic variants associate with serum phosphorus concentration

artículo científico publicado en 2010

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

artículo científico publicado en 2014

Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study.

artículo científico publicado en 2014

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

artículo científico publicado en 2018

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

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

artículo científico publicado en 2010

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

artículo científico publicado en 2010

Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine

artículo científico publicado en 2016

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis

artículo científico publicado en 2014

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

scientific article published on 24 October 2008

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

artículo científico publicado en 2010

Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological research

artículo científico publicado en 2014

Complement C3 variant and the risk of age-related macular degeneration

artículo científico publicado en 2007

Complement factor D in age-related macular degeneration

artículo científico publicado en 2011

Complement factor h autoantibodies and age-related macular degeneration.

artículo científico publicado en 2010

Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease

artículo científico publicado en 2010

Copy number variation across European populations

artículo científico publicado en 2011

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

artículo científico publicado en 2015

CovidLife: a resource to understand mental health, well-being and behaviour during the COVID-19 pandemic in the UK

artículo científico publicado en 2021

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

artículo científico publicado en 2018

Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults

artículo científico publicado en 2015

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

scientific article published on 19 December 2013

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Dietary Factors Associated with Plasma Thyroid Peroxidase and Thyroglobulin Antibodies

artículo científico publicado en 2017

Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course

artículo científico publicado en 2015

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

artículo científico publicado en 2012

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

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

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.

artículo científico publicado en 2006

Disentangling the genetics of lean mass

article

Does inbreeding affect N-glycosylation of human plasma proteins?

artículo científico publicado en 2011

Effect of Smoking on Blood Pressure and Resting Heart Rate: A Mendelian Randomization Meta-Analysis in the CARTA Consortium

artículo científico publicado en 2015

Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits

article

Electronic health record and genome-wide genetic data in Generation Scotland participants.

artículo científico publicado en 2017

Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycome

artículo científico publicado en 2012

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

article

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

article

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

artículo científico publicado en 2017

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches.

artículo científico publicado en 2006

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

artículo científico publicado en 2017

Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies

artículo científico publicado en 2011

Evidence of inbreeding depression on human height

artículo científico publicado en 2012

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Exome-wide association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

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

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

artículo científico publicado en 2017

Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations

scientific article published on 12 November 2003

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

Face covering adherence is positively associated with better mental health and wellbeing: a longitudinal analysis of the CovidLife surveys

artículo científico publicado en 2021

Factors associated with sharing e-mail information and mental health survey participation in large population cohorts

artículo científico publicado en 2019

Feasibility and ethics of using data from the Scottish newborn blood spot archive for research

artículo científico publicado en 2022

Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies

artículo científico publicado en 1997

Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

artículo científico publicado en 2015

Fructose-1,6-Bisphosphatase: Genetic and Physical Mapping to Human Chromosome 9q22.3 and Evaluation in Non-Insulin-Dependent Diabetes Mellitus

artículo científico publicado en 1995

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

artículo científico publicado en 2013

Gel electrophoresis of amniotic fluid acetylcholinesterase as an aid to the prenatal diagnosis of fetal defects

artículo científico publicado en 1980

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

article

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

General Framework for Meta-Analysis of Haplotype Association Tests

artículo científico publicado en 2016

Genes predict village of origin in rural Europe

artículo científico publicado en 2010

Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease

artículo científico publicado en 2016

Genetic Stratification to Identify Risk Groups for Alzheimer's Disease

artículo científico publicado en 2017

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 and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis

artículo científico publicado en 2016

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

artículo científico publicado en 2018

Genetic and environmental risk for chronic pain and the contribution of risk variants for psychiatric disorders. Results from Generation Scotland: Scottish Family Health Study and UK Biobank

article

Genetic and shared couple environmental contributions to smoking and alcohol use in the UK population

artículo científico publicado en 2019

Genetic architecture of circulating lipid levels

artículo científico publicado en 2011

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression

artículo científico publicado en 2020

Genetic comparison of a Croatian isolate and CEPH European founders

artículo científico publicado en 2010

Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life

article

Genetic determinants of circulating sphingolipid concentrations in European populations

scientific article published on 02 October 2009

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

artículo científico publicado en 2014

Genetic evidence of assortative mating in humans

article

Genetic influences on oxidative stress and their association with normal cognitive ageing

artículo científico publicado en 2005

Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

artículo científico publicado en 2013

Genetic mechanisms of critical illness in Covid-19

scientific article published on 11 December 2020

Genetic predictors of fibrin D-dimer levels in healthy adults

artículo científico publicado en 2011

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Genetic variants in RBFOX3 are associated with sleep latency

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Genetic variants linked to education predict longevity

artículo científico publicado en 2016

Genetic variation in complement regulators and susceptibility to age-related macular degeneration

artículo científico publicado en 2011

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

artículo científico publicado en 2011

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 of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

artículo científico publicado en 2015

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 Meta-Analyses Of Stratified Depression In Generation Scotland And UK Biobank

article

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

artículo científico publicado en 2016

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income

artículo científico publicado en 2019

Genome-wide analysis of epistasis in body mass index using multiple human populations

artículo científico publicado en 2012

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 analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

artículo científico publicado en 2013

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

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

artículo científico publicado en 2011

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

artículo científico publicado en 2020

Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population

artículo científico publicado en 2019

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

artículo científico publicado en 2018

Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

artículo científico publicado en 2020

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

artículo científico publicado en 2015

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

artículo científico publicado en 2016

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

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 genetic risk underlying primary rhegmatogenous retinal detachment

artículo científico publicado en 2013

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations

artículo científico publicado en 2012

Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

artículo científico publicado en 2018

Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3

artículo científico publicado en 2012

Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112,117)

article

Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117).

artículo científico publicado en 2017

Genome-wide association study of anthropometric traits in Korcula Island, Croatia

artículo científico publicado en 2009

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP

article

Genome-wide association study of biochemical traits in Korcula Island, Croatia

artículo científico publicado en 2009

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 common variants associated with brachial circumference: a meta-analysis of 14 cohorts

artículo científico publicado en 2012

Genome-wide association uncovers shared genetic effects among personality traits and mood states

artículo científico publicado en 2012

Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

article

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

artículo científico publicado en 2017

Genome-wide linkage analysis of serum creatinine in three isolated European populations.

artículo científico publicado en 2009

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-analyses of stratified depression in Generation Scotland and UK Biobank.

artículo científico publicado en 2018

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

artículo científico publicado en 2017

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

scientific journal article

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

artículo científico publicado en 2014

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

artículo científico publicado en 2021

Genome-wide methylation data improves dissection of the effect of smoking on body mass index

artículo científico publicado en 2020

Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

artículo científico publicado en 2016

Genomic analysis of family data reveals additional genetic effects on intelligence and personality

article

Genomic analysis of family data reveals additional genetic effects on intelligence and personality.

artículo científico publicado en 2018

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

artículo científico publicado en 2020

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

artículo científico publicado en 2015

Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation

artículo científico publicado en 2010

Glycans are a novel biomarker of chronological and biological ages

artículo científico publicado en 2013

Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases

artículo científico publicado en 2020

HLA-DR and pre-eclampsia in Edinburgh

artículo científico publicado en 1990

Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank

artículo científico publicado en 2017

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways

artículo científico publicado en 2011

Heavier smoking may lead to a relative increase in waist circumference: evidence for a causal relationship from a Mendelian randomisation meta-analysis. The CARTA consortium

artículo científico publicado en 2015

Heritabilities of ocular biometrical traits in two croatian isolates with extended pedigrees

artículo científico publicado en 2009

Heritability Analysis Suggests Comparable Genetic Component of Mechanical Pain Threshold and Tolerance: Table 1

artículo científico publicado en 2012

High prevalence of glaucoma in Veli Brgud, Croatia, is caused by a dominantly inherited T377M mutation in the MYOC gene

article

High-Performance Mixed Models Based Genome-Wide Association Analysis with omicABEL software

artículo científico publicado en 2014

Historic exposure to plague and present-day frequency of CCR5del32 in two isolated island communities of Dalmatia, Croatia.

artículo científico publicado en 2006

Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics

artículo científico publicado en 2009

Homozygous loss-of-function variants in European cosmopolitan and isolate populations

artículo científico publicado en 2015

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of SATB2 as the cleft palate gene on 2q32-q33.

artículo científico publicado en 2003

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

artículo científico publicado en 2013

Identification of novel differentially methylated sites with potential as clinical predictors of impaired respiratory function and COPD

artículo científico publicado en 2019

Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis

artículo científico publicado en 2014

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

artículo científico publicado en 2017

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design

artículo científico publicado en 2005

Individual multi-locus heterozygosity is associated with lower morning plasma cortisol concentrations

artículo científico publicado en 2013

Inference of identity by descent in population isolates and optimal sequencing studies

scientific article published on 30 January 2013

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

artículo científico publicado en 2012

Integrative pathway genomics of lung function and airflow obstruction

artículo científico publicado en 2015

Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort

artículo científico publicado el 2 de agosto de 2016

Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances

artículo científico publicado en 2022

Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium

artículo científico publicado en 2014

Is experimentally induced pain associated with socioeconomic status? Do poor people hurt more?

artículo científico publicado en 2014

KLOTHO genotype and cognitive ability in childhood and old age in the same individuals

artículo científico publicado en 2005

Lack of association between polymorphisms in angiotensin-converting-enzyme and methylenetetrahydrofolate reductase genes and normal cognitive ageing in humans

artículo científico publicado en 2003

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

artículo científico publicado en 2017

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

artículo científico publicado en 2012

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Leprosy epidemics during history increased protective allele frequency of PARK2/PACRG genes in the population of the Mljet Island, Croatia.

artículo científico publicado en 2011

Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

artículo científico publicado en 2009

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

artículo científico publicado en 2020

Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies

artículo científico publicado en 2013

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping

artículo científico publicado en 2012

Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.

artículo científico publicado en 2013

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

scientific article published in Nature Communications

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene

artículo científico publicado en 1997

Marfan Database (third edition): new mutations and new routines for the software

artículo científico publicado en 1998

Mediterranean diet in the southern Croatia - does it still exist?

artículo científico publicado en 2016

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

artículo científico publicado en 2012

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

artículo científico publicado en 2010

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

artículo científico publicado en 2016

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 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 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 from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

artículo científico publicado en 2011

Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

artículo científico publicado en 2011

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

artículo científico publicado en 2013

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

artículo científico publicado en 2019

Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels

artículo científico publicado en 2010

Modulation of genetic associations with serum urate levels by body-mass-index in humans

artículo científico publicado en 2015

Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland

scientific article published on 27 March 2020

Molecular genetic contributions to socioeconomic status and intelligence.

artículo científico publicado en 2014

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

artículo científico publicado en 2019

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multi-trait genome-wide association study identifies new loci associated with optic disc parameters

scientific article published on 27 November 2019

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation

artículo científico publicado en 2017

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

artículo científico publicado en 2003

Mutation screening of all 65 exons of the fibrillin-1 gene in 60 patients with Marfan syndrome: Report of 12 novel mutations

artículo científico publicado en 1997

Mutations in HNF1A result in marked alterations of plasma glycan profile

artículo científico publicado en 2012

Mutations in SOX2 cause anophthalmia

artículo científico publicado en 2003

Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

artículo científico publicado en 2017

New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals

artículo científico publicado en 2017

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

scientific article published on 29 July 2019

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

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

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.

artículo científico publicado en 2010

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Nicastrin gene polymorphisms, cognitive ability level and cognitive ageing

artículo científico publicado en 2005

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degeneration

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

artículo científico publicado en 2010

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

artículo científico publicado en 2010

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

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 pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration

artículo científico publicado en 2017

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

artículo científico publicado en 2018

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

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

artículo científico publicado en 2013

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

artículo científico publicado en 2016

Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study

artículo científico publicado en 2018

Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort

artículo científico publicado en 2015

Polygenic risk for coronary artery disease is associated with cognitive ability in older adults

artículo científico publicado en 2016

Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

Polymorphisms in the gene encoding 11B-hydroxysteroid dehydrogenase type 1 (HSD11B1) and lifetime cognitive change

artículo científico publicado en 2005

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia

article published in 2017

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

artículo científico publicado en 2019

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

Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

artículo científico publicado en 2018

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

artículo científico publicado en 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Quantifying the increase in average human heterozygosity due to urbanisation

artículo científico publicado en 2008

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

artículo científico publicado en 2016

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

artículo científico publicado en 2015

Rare coding variants and X-linked loci associated with age at menarche

artículo científico publicado en 2015

Recent genomic heritage in Scotland

artículo científico publicado en 2015

Recurrence ofSOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

artículo científico publicado en 2015

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

artículo científico publicado en 2018

Regional variation in health is predominantly driven by lifestyle rather than genetics

artículo científico publicado en 2017

Replication of the diathesis-stress model for depression in Generation Scotland

article

Runs of Homozygosity in European Populations

artículo científico publicado en 2008

Runs of homozygosity in European populations

artículo científico publicado en 2008

RuralCovidLife: A new resource for the impact of the pandemic on rural Scotland

artículo científico publicado en 2022

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

scientific journal article

SMAD7 variant rs4939827 is associated with colorectal cancer risk in Croatian population

artículo científico publicado en 2013

SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies.

artículo científico publicado en 2011

Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

artículo científico publicado en 2011

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

artículo científico publicado en 2013

Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression

artículo científico publicado en 2016

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers

artículo científico publicado en 2014

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

artículo científico publicado en 2018

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

TeenCovidLife: a resource to understand the impact of the COVID-19 pandemic on adolescents in Scotland

artículo científico publicado en 2022

The Eysenck personality factors: Psychometric structure, reliability, heritability and phenotypic and genetic correlations with psychological distress in an isolated Croatian population

The Greeks in the West: genetic signatures of the Hellenic colonisation in southern Italy and Sicily

artículo científico publicado en 2015

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

artículo científico publicado en 2015

The Stratification Of Major Depressive Disorder Into Genetic Subgroups

scholarly article published 5 May 2017

The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis

artículo científico publicado en 2010

The Uromodulin Gene Locus Shows Evidence of Pathogen Adaptation through Human Evolution

artículo científico publicado en 2016

The association between galactosylation of immunoglobulin G and body mass index.

artículo científico publicado en 2013

The brain-derived neurotrophic factor Val66Met polymorphism is associated with age-related change in reasoning skills

artículo científico publicado en 2006

The functional COMT polymorphism, Val 158 Met, is associated with logical memory and the personality trait intellect/imagination in a cohort of healthy 79 year olds

artículo científico publicado en 2005

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

artículo científico publicado en 2016

The influence of X chromosome variants on trait neuroticism

article

The low single nucleotide polymorphism heritability of plasma and saliva cortisol levels

artículo científico

The power of genetic diversity in genome-wide association studies of lipids

The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits

artículo científico publicado en 2013

The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability

article by Riccardo E Marioni et al published 22 April 2014 in Proceedings of the Royal Society B

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Uncovering networks from genome-wide association studies via circular genomic permutation

artículo científico publicado en 2012

Understanding biological mechanisms underlying adverse birth outcomes in developing countries: protocol for a prospective cohort (AMANHI bio-banking) study

artículo científico publicado en 2017

Variability, heritability and environmental determinants of human plasma N-glycome

artículo científico publicado en 2009

Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease

article

Variation in the dysbindin gene and normal cognitive function in three independent population samples

artículo científico publicado en 2008

Variation in the uric acid transporter gene (SLC2A9) and memory performance

artículo científico publicado en 2010

Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people

artículo científico publicado en 2011

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

artículo científico publicado en 2014

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis

artículo científico publicado en 2016

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