Lista de obras - David A Hinds - Dominio Público Uruguay

A common allele on chromosome 9 associated with coronary heart disease

artículo científico publicado en 2007

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

artículo científico publicado en 2003

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

artículo científico publicado en 2013

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

artículo científico publicado en 2007

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

artículo científico publicado en 2007

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

artículo científico publicado en 2006

A lattice model for protein structure prediction at low resolution ⬇️

artículo científico publicado el 1 de abril de 1992

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

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

artículo científico publicado en 1998

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

artículo científico publicado en 2007

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

artículo científico publicado en 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

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

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

artículo científico publicado en 2004

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

artículo científico publicado en 2010

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

artículo científico publicado en 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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2001

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2007

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

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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

Detection and interpretation of shared genetic influences on 42 human traits

artículo científico publicado en 2016

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Eleven loci with new reproducible genetic associations with allergic disease risk.

artículo científico publicado en 2018

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

artículo científico publicado en 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

artículo científico publicado en 2016

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

article

Escape from crossover interference increases with maternal age.

artículo científico publicado en 2015

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

artículo científico publicado en 1999

Fine-scale recombination patterns differ between chimpanzees and humans

artículo científico publicado en 2005

From structure to sequence and back again.

artículo científico publicado en 1996

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

artículo científico publicado en 2017

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 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

artículo científico publicado en 2018

Genetic variants associated with breast size also influence breast cancer risk

artículo científico publicado en 2012

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

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 the MRPS30 region and postmenopausal breast cancer risk

artículo científico publicado en 2011

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

artículo científico publicado en 2012

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

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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

artículo científico publicado en 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

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 of chronotype in 697,828 individuals provides insights into circadian rhythms

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2020

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

artículo científico publicado en 2016

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 novel susceptibility loci for cutaneous squamous cell carcinoma.

artículo científico publicado en 2016

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

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

artículo científico publicado en 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

artículo científico publicado en 2008

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

artículo científico publicado en 2003

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

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Matching strategies for genetic association studies in structured populations

artículo científico publicado en 2004

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 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

artículo científico publicado en 2017

Novel associations for hypothyroidism include known autoimmune risk loci

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado en 2010

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

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

artículo científico publicado en 2004

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

artículo científico publicado en 2017

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

artículo científico publicado en 2012

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

artículo científico publicado en 2005

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

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Variant in PNPLA3 is associated with alcoholic liver disease

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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

artículo científico publicado en 2005

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

artículo científico publicado en 2015

minimac2: faster genotype imputation

artículo científico publicado en 2014

Lista de obras de David A Hinds

A common allele on chromosome 9 associated with coronary heart disease

A full genome search in multiple sclerosis

A genetic variant near olfactory receptor genes influences cilantro preference

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

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

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

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

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

A lattice model for protein structure prediction at low resolution ⬇️

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

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

A second generation human haplotype map of over 3.1 million SNPs

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

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

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

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

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on osteoporosis in humans and mice

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

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

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

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

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

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

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

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

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

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

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

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

Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana

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

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

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

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

Detection and interpretation of shared genetic influences on 42 human traits

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

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

Eleven loci with new reproducible genetic associations with allergic disease risk.

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

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

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

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

Escape from crossover interference increases with maternal age.

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

Fine-scale recombination patterns differ between chimpanzees and humans

From structure to sequence and back again.

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

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

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

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

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

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

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

Genetic association and differential expression of PITX2 with acute appendicitis

Genetic variants associated with breast size also influence breast cancer risk

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

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

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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