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Lista de obras de Dale R Nyholt

A Comparison of DNA Pools Constructed Following Whole Genome Amplification for Two-Stage SNP Genotyping Designs

article published in 2005

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

artículo científico publicado en 2016

A Report of Dizygous Monochorionic Twins

artículo científico publicado en 2003

A case of true hermaphroditism reveals an unusual mechanism of twinning

artículo científico publicado en 2006

A continuum of genetic liability for minor and major depression.

artículo científico publicado en 2017

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

artículo científico publicado en 2010

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility

artículo científico publicado en 2012

A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality

artículo científico publicado en 2010

A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor

artículo científico publicado en 2012

A genome-wide association study of sleep habits and insomnia

artículo científico publicado en 2013

A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine

artículo científico publicado en 2008

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.

artículo científico publicado en 2005

A high-density association screen of 155 ion transport genes for involvement with common migraine

artículo científico publicado en 2008

A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer’s disease and gastrointestinal tract disorders

artículo científico publicado en 2022

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications

scientific journal article

A reanalysis of 409 European-Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity.

artículo científico publicado en 2008

A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies

artículo científico publicado en 2010

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

artículo científico publicado en 2004

A typical migraine susceptibility region localizes to chromosome 1q31

artículo científico publicado en 2002

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

A versatile gene-based test for genome-wide association studies

artículo científico publicado en 2010

Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

artículo científico publicado en 2016

Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry

artículo científico publicado en 2017

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

article

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

artículo científico publicado en 2017

Association Study of the Dystrobrevin-Binding Gene With Schizophrenia in Australian and Indian Samples

article

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

artículo científico publicado en 2010

Association between endometriosis and the interleukin 1A (IL1A) locus

artículo científico publicado en 2014

Association mapping

artículo científico

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 a low density lipoprotein receptor microsatellite variant with obesity

artículo científico publicado en 1997

Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples.

artículo científico publicado en 2006

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Bayesian latent trait modeling of migraine symptom data

artículo científico publicado en 2009

Beyond Endometriosis Genome-Wide Association Study: From Genomics to Phenomics to the Patient

artículo científico publicado en 2016

Blood gene expression studies in migraine: Potential and caveats

artículo científico publicado en 2016

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

artículo científico publicado en 2017

CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

artículo científico publicado en 2015

Can we predict those at higher risk for migraine?

artículo científico publicado en 2016

Co-occurrence and symptomatology of fatigue and depression

artículo científico publicado en 2016

Cohort Profile: Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium).

artículo científico

Common SNPs explain a large proportion of the heritability for human height

artículo científico publicado en 2010

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis

artículo científico publicado en 2008

Common genetic influences underlie comorbidity of migraine and endometriosis

artículo científico publicado en 2009

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

artículo científico publicado en 2009

Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis

artículo científico publicado en 2014

Common variants in the trichohyalin gene are associated with straight hair in Europeans

artículo científico publicado en 2009

Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk

artículo científico publicado en 2008

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

artículo científico publicado en 2014

Consistently replicating locus linked to migraine on 10q22-q23

artículo científico publicado en 2008

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

artículo científico publicado en 2015

Cross-Trait Genetic Analyses Indicate Pleiotropy and Complex Causal Relationships between Headache and Thyroid Function Traits

artículo científico publicado en 2022

DCAF4, a novel gene associated with leucocyte telomere length

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Educational attainment: a genome wide association study in 9538 Australians

artículo científico publicado en 2011

Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.

artículo científico publicado en 2016

Enrichment of SNPs in Functional Categories Reveals Genes Affecting Complex Traits.

artículo científico publicado en 2016

Erratum: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

article

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

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

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

artículo científico publicado en 2012

Evaluation of Nyholt’s Procedure for Multiple Testing Correction – Author’s Reply

scientific article published on 05 August 2005

Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis.

artículo científico publicado en 2010

Exclusion of angiotensinogen gene in molecular basis of human hypertension: Sibpair linkage and association analyses in Australian Anglo-Caucasians

article

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

Familial Aggregation of Migraine and Depression: Insights From a Large Australian Twin Sample

artículo científico publicado en 2016

Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.

artículo científico publicado en 1998

Familiality and Heritability of Fatigue in an Australian Twin Sample

artículo científico publicado en 2017

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

artículo científico publicado en 2014

Five endometrial cancer risk loci identified through genome-wide association analysis

artículo científico publicado en 2016

Functional evaluation of genetic variants associated with endometriosis near GREB1.

artículo científico publicado en 2015

G-Protein β3 Subunit Gene ( GNB3 ) Variant in Causation of Essential Hypertension

article

GENEHUNTER: your 'one-stop shop' for statistical genetic analysis?

artículo científico publicado en 2002

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

artículo científico publicado en 2013

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

artículo científico publicado en 2011

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

artículo científico publicado en 2016

Gene-based analyses reveal novel genetic overlap and allelic heterogeneity across five major psychiatric disorders

artículo científico publicado en 2016

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

artículo científico publicado en 2015

Genetic Basis of Male Pattern Baldness

article published in 2003

Genetic Risk Factors for Endometriosis

Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

artículo científico publicado en 2021

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2).

artículo científico publicado en 2016

Genetic and environmental influences on migraine: a twin study across six countries

artículo científico publicado en 2003

Genetic burden associated with varying degrees of disease severity in endometriosis

artículo científico publicado en 2015

Genetic case-control association studies - correcting for multiple testing ⬇️

artículo científico publicado el 19 de octubre de 2001

Genetic effects influencing risk for major depressive disorder in China and Europe

artículo científico publicado en 2017

Genetic epidemiology of migraine and depression

artículo científico publicado en 2016

Genetic evidence of assortative mating in humans

scholarly article

Genetic influences on handedness: data from 25,732 Australian and Dutch twin families

artículo científico publicado en 2009

Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis

artículo científico publicado en 2016

Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.

artículo científico publicado en 2018

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

artículo científico publicado en 2013

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

artículo científico publicado en 2015

Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets

artículo científico publicado en 2014

Genetic variation in female BMI increases with number of children born but failure to replicate association between GNbeta3 variants and increased BMI in parous females

artículo científico publicado en 2009

Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample

article

Genome-Wide Association Study Identifies a Locus at 7p15.2 Associated With Endometriosis

Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length

scientific article published on 27 February 2020

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 DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine

artículo científico publicado en 2018

Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Genome-wide association analysis identifies susceptibility loci for migraine without aura

artículo científico publicado en 2012

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

artículo científico publicado en 2019

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

scientific journal article

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 identifies new endometriosis risk loci

artículo científico publicado en 2012

Genome-wide association studies in migraine: current state and route to follow

artículo científico publicado en 2016

Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained

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 a locus at 7p15.2 associated with endometriosis

artículo científico publicado en 2011

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

scientific journal article

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

artículo científico publicado en 2015

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

article

Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

artículo científico publicado en 2010

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci

artículo científico publicado en 2014

Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis

artículo científico publicado en 2017

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands

artículo científico publicado en 2008

Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata

artículo científico publicado en 2012

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma ⬇️

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.

artículo científico publicado en 2005

Genomewide significant linkage to migrainous headache on chromosome 5q21.

artículo científico publicado en 2005

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 analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

artículo científico publicado en 2017

Genomic inflation factors under polygenic inheritance

artículo científico publicado en 2011

Glucose-Related Traits and Risk of Migraine—A Potential Mechanism and Treatment Consideration

artículo científico publicado en 2022

Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island.

artículo científico publicado en 2011

High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility

artículo científico publicado en 2016

Identification of IL6R and chromosome 11q13.5 as risk loci for asthma

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Improving the detection of pathways in genome-wide association studies by combined effects of SNPs from Linkage Disequilibrium blocks

artículo científico publicado en 2017

Independent Replication and Meta-Analysis for Endometriosis Risk Loci

artículo científico publicado en 2015

Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs

artículo científico publicado en 2013

KRAS variation and risk of endometriosis

artículo científico publicado en 2006

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

article

Letter to the Editor: Further evidence is required to confirm association between CACNA1C gene variants and bipolar affective disorder

article

Linkage and heritability analysis of migraine symptom groupings: a comparison of three different clustering methods on twin data

artículo científico publicado en 2009

Linking migraine frequency with family history of migraine

artículo científico publicado en 2018

Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations

artículo científico publicado en 2011

Low Birth Weight in MZ Twins Discordant for Birth Weight is Associated with Shorter Telomere Length and lower IQ, but not Anxiety/Depression in Later Life

artículo científico publicado en 2015

Marker selection by Akaike information criterion and Bayesian information criterion.

artículo científico publicado en 2001

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

artículo científico publicado en 2012

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 identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

artículo científico publicado en 2017

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

artículo científico publicado en 2017

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

artículo científico publicado en 2009

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

artículo científico publicado en 2011

Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect

artículo científico publicado en 2013

Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

scientific article published on 12 August 2019

Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism

article

Migraine genetics: from genome-wide association studies to translational insights

artículo científico publicado en 2016

Migraine symptomatology and major depressive disorder

artículo científico publicado en 2010

Migraine with aura and migraine without aura are not distinct entities: further evidence from a large Dutch population study

artículo científico publicado en 2006

Migrainomics - identifying brain and genetic markers of migraine

artículo científico publicado en 2017

Molecular genetic overlap between migraine and major depressive disorder

scholarly article by Yuanhao Yang et al published 11 July 2018 in European Journal of Human Genetics

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

artículo científico publicado en 2015

No Genetic Overlap Between Circulating Iron Levels and Alzheimer's Disease

artículo científico publicado en 2017

No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis

artículo científico publicado en 2012

No influence of 5-HTTLPR gene polymorphism on migraine symptomatology, comorbid depression, and chronification

artículo científico publicado en 2009

Novel hypotheses emerging from GWAS in migraine?

scientific article published on 11 January 2019

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

artículo científico publicado en 2014

On Jim Watson's APOE status: genetic information is hard to hide

artículo científico publicado en 2008

On the Probability of Dizygotic Twins Being Concordant for Two Alleles at Multiple Polymorphic Loci

scholarly article by Dale R Nyholt published 1 April 2006 in CrossRef Listing of Deleted DOIs

On the probability of dizygotic twins being concordant for two alleles at multiple polymorphic loci

artículo científico publicado en 2006

Personality, health and lifestyle in a questionnaire family study: a comparison between highly cooperative and less cooperative families

artículo científico publicado en 2007

Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis

scientific article published on 23 July 2008

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

artículo científico publicado en 2017

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

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

RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing.

artículo científico publicado en 2017

SECA: SNP effect concordance analysis using genome-wide association summary results

artículo científico publicado en 2014

Sequence variants in three loci influence monocyte counts and erythrocyte volume

artículo científico publicado en 2009

Shared Genetic Factors Underlie Migraine and Depression

artículo científico publicado en 2016

Shared Genetic Factors in the Co-Occurrence of Depression and Fatigue

artículo científico publicado en 2016

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

artículo científico publicado en 2015

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

artículo científico publicado en 2017

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts.

artículo científico publicado en 2017

Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13–15

article

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

artículo científico publicado en 2012

Strong Evidence for a Novel Schizophrenia Risk Locus on Chromosome 1p31.1 in Homogeneous Pedigrees From Tamil Nadu, India

artículo científico publicado en 2008

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis

artículo científico publicado en 2009

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

Teenage acne is influenced by genetic factors

scientific article published on 01 March 2005

Telomere length in circulating leukocytes is associated with lung function and disease.

artículo científico publicado en 2013

The future for genetic studies in reproduction.

artículo científico publicado en 2014

The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020

The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data

artículo científico publicado en 2005

The search for genes contributing to endometriosis risk

artículo científico publicado en 2008

The shared genetics of migraine and anxious depression

artículo científico publicado en 2010

Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.

artículo científico publicado en 2013

Using genomic data to make indirect (and unauthorized) estimates of disease risk.

artículo científico publicado en 2012

Variants in EMX2 and PTEN do not contribute to risk of endometriosis

artículo científico publicado en 2007

Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning

artículo científico

Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs

artículo científico publicado en 2008

Zygosity diagnosis in the absence of genotypic data: an approach using latent class analysis

artículo científico publicado en 2003

ssSNPer: identifying statistically similar SNPs to aid interpretation of genetic association studies

artículo científico publicado en 2006

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