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List of works by David A Hinds

A common allele on chromosome 9 associated with coronary heart disease

scientific article

A full genome search in multiple sclerosis

article

A genetic variant near olfactory receptor genes influences cilantro preference

article

A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins

scientific article published in February 2003

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

scientific article

A genomewide association study of skin pigmentation in a South Asian population

scientific article

A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping

scientific article published on June 2007

A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping

scientific article

A lattice model for protein structure prediction at low resolution ⬇️

scientific article published on April 1, 1992

A multi-stage genome-wide association study of uterine fibroids in African Americans

scientific article

A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk.

scientific article

A second generation human haplotype map of over 3.1 million SNPs

scientific article

A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus

scientific article published in July 1998

A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

scientific article published on 29 July 2007

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism

scientific article published in October 1999

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

scientific article published on 30 June 2020

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on osteoporosis in humans and mice

scientific article published on 31 December 2018

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

article

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

scientific article

Assessment of clinical validity of a breast cancer risk model combining genetic and clinical information

scientific article

Assessment of the genetic basis of rosacea by genome-wide association study

scientific article published on 19 February 2015

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 studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

scientific article published on 14 January 2019

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

scientific article published on 01 May 2019

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

scientific article published on 01 September 2018

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

scientific article published in November 2001

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

scientific article

Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus

scientific article published on 23 December 2015

Common deletions and SNPs are in linkage disequilibrium in the human genome

scientific article published on 04 December 2005

Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana

scientific article

Comparison of family history and SNPs for predicting risk of complex disease

scientific article

Comprehensive whole-genome and candidate gene analysis for response to statin therapy in the Treating to New Targets (TNT) cohort

scientific article published on 12 February 2009

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

scientific article published on November 2016

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

scientific article published on 17 December 2015

Detection and interpretation of shared genetic influences on 42 human traits

scientific article published on 16 May 2016

Economic evaluation of using a genetic test to direct breast cancer chemoprevention in white women with a previous breast biopsy.

scientific article published in April 2014

Efficient replication of over 180 genetic associations with self-reported medical data

scientific article (publication date: 2011)

Eleven loci with new reproducible genetic associations with allergic disease risk

scientific article published on 18 April 2018

Erratum to: A multi-stage genome-wide association study of uterine fibroids in African Americans

scientific article published on 4 October 2017

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

article

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

scientific article published in October 2016

Erratum: Detection and interpretation of shared genetic influences on 42 human traits

article

Escape from crossover interference increases with maternal age.

scientific article

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism

scientific article published in June 1999

Fine-scale recombination patterns differ between chimpanzees and humans

scientific article

From structure to sequence and back again

scientific article published in April 1996

GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person

scientific article published on 2 February 2016

GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci

scientific article

Gene expression imputation identifies candidate genes and susceptibility loci associated with cutaneous squamous cell carcinoma

scientific article published in Nature Communications

Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling

scientific article published on 20 August 2016

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

scientific article published on 6 September 2017

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

scientific article

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 association and differential expression of PITX2 with acute appendicitis

scientific article

Genetic variants associated with breast size also influence breast cancer risk

scientific article (publication date: 30 June 2012)

Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

scientific article

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

scientific article published on 18 April 2016

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

scientific article published on 24 June 2011

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

scientific article published on 12 March 2012

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.

scientific article

Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways

scientific article

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

scientific article published on 05 December 2016

Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways

scientific article published on 25 February 2019

Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia

scientific article

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

scientific article published on 26 April 2018

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

scientific article published in Nature Communications

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

scientific article published on 14 January 2019

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

scientific article

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis

Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus

scientific article

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

scientific article

Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

scholarly article by Johannes Waage et al published August 2018 in Nature Genetics

Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections

scientific article published on 19 September 2017

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

scientific article published on 24 October 2019

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

scientific article published on 16 April 2018

Genome-wide association studies of antidepressant class response and treatment-resistant depression

scientific article published on 26 October 2020

Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma

scientific article published on 19 August 2016

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

scientific article published on 28 September 2020

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

scientific article published on 11 May 2016

Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.

scientific article published on 18 July 2016

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles

scientific article

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

scientific article

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

scientific article published on 04 February 2019

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.: Supplementary Information

Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

scientific article

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates

scientific article published on March 2003

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

scientific article published on 23 September 2016

Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

scientific article

Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.

scientific article published on August 2016

Identification of genetic loci shared between schizophrenia and the Big Five personality traits

scientific article published on 22 May 2017

Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality

scientific article

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis

scientific article

Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants

scientific article

Matching strategies for genetic association studies in structured populations

scientific article

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

scientific article

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

scientific article

Modeling prior information of common genetic variants improves gene discovery for neuroticism

scientific article published on 30 August 2017

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

scientific article published on 19 October 2015

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

scientific article published on 21 November 2017

Novel associations for hypothyroidism include known autoimmune risk loci

scientific article (publication date: 2012)

Phenome-wide association studies across large population cohorts support drug target validation

scientific article published in Nature Communications

Phenome-wide association study using research participants' self-reported data provides insight into the Th17 and IL-17 pathway

scientific article published in November 2017

Pooled versus individual genotyping in a breast cancer genome-wide association study

scientific article

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

scientific article published on 01 July 2019

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

scientific article

Replicability and robustness of genome-wide-association studies for behavioral traits

scientific article

Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence

scientific article

Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome

scientific article

Shared genetic aetiology of puberty timing between sexes and with health-related outcomes

scientific article

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

scientific article published on 30 October 2017

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

scientific article published on 7 February 2017

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

scientific article

Social and non-social autism symptoms and trait domains are genetically dissociable

scientific article published on 03 September 2019

The biology of genomes: sequence gives way to function

scientific article

Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma

scientific article

Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.

scientific article

Variant in PNPLA3 is associated with alcoholic liver disease

scientific article published on 29 November 2009

Variation in the FGFR2 gene and the effect of a low-fat dietary pattern on invasive breast cancer

scientific article

Variation in the FGFR2 gene and the effects of postmenopausal hormone therapy on invasive breast cancer

scientific article published on 27 October 2009

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

scientific article published on 12 July 2018

Whole-genome patterns of common DNA variation in three human populations

scientific article

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

scientific article

minimac2: faster genotype imputation

scientific article

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