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Lista de obras de Stuart Macgregor

A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families

artículo científico publicado en 2011

A Novel Approach for Pathway Analysis of GWAS Data Highlights Role of BMP Signaling and Muscle Cell Differentiation in Colorectal Cancer Susceptibility

artículo científico publicado en 2017

A Novel Approach for Pathway Analysis of GWAS Data Highlights Role of BMP Signaling and Muscle Cell Differentiation in Colorectal Cancer Susceptibility - Erratum

artículo científico publicado en 2017

A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.

artículo científico publicado en 2017

A common variant near TGFBR3 is associated with primary open angle glaucoma.

artículo científico publicado en 2015

A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42

artículo científico publicado en 2004

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.

artículo científico publicado en 2013

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

artículo científico publicado en 2012

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

artículo científico publicado en 2010

A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus

scientific journal article

A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations

artículo científico publicado en 2010

A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

artículo científico publicado en 2011

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 single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease

artículo científico publicado en 2006

A variant in FTO shows association with melanoma risk not due to BMI

artículo científico publicado en 2013

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

artículo científico publicado en 2010

ABCA transporter gene expression and poor outcome in epithelial ovarian cancer

artículo científico publicado en 2014

ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas

scientific article published on August 2013

ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure

artículo científico publicado en 2015

Abstract 4487: An INDEL variant confers melanoma risk through PARP1 expression regulation

Abstract 5493: Genome-wide study of carboplatin and paclitaxel disposition in ovarian cancer patients

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

Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma

artículo científico publicado en 2015

Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci

artículo científico publicado en 2017

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

artículo científico publicado en 2018

Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates

artículo científico publicado en 2006

Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study

artículo científico publicado en 2015

Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

scholarly article by Anne E. Cust published in June 2018

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study.

artículo científico publicado en 2017

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

artículo científico publicado en 2020

Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration.

artículo científico publicado en 2016

Association Between Population Density and Genetic Risk for Schizophrenia

Association between coffee consumption and overall risk of being diagnosed with or dying from cancer among >300 000 UK Biobank participants in a large-scale Mendelian randomization study

artículo científico publicado en 2019

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

artículo científico publicado en 2014

Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk

artículo científico publicado en 2013

Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the alcohol challenge twin study

artículo científico publicado en 2012

Association between putative functional variants in the PSMB9 gene and risk of melanoma--re-analysis of published melanoma genome-wide association studies

scientific article published on 27 March 2013

Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy

artículo científico publicado en 2016

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus

artículo científico publicado en 2011

Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study

artículo científico publicado en 2016

Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults

artículo científico publicado en 2014

Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis

artículo científico publicado en 2009

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

artículo científico

Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability

artículo científico publicado en 2019

Author Correction: Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

scientific article published on 04 December 2019

Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

scientific article published on 11 March 2020

Author Response: Stronger Association of CDKN2B-AS1 Variants in Female Normal-Tension Glaucoma Patients in a Japanese Population.

artículo científico publicado en 2016

Bias, precision and heritability of self-reported and clinically measured height in Australian twins

artículo científico publicado en 2006

Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1).

artículo científico publicado en 2005

Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population

artículo científico publicado en 2009

Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes

article

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

artículo científico publicado en 2015

Combined analysis of keratinocyte cancers identifies novel genome-wide loci

artículo científico publicado en 2019

Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma

scientific article published in 2018

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

artículo científico publicado en 2012

Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

artículo científico publicado en 2010

Common sequence variants on 20q11.22 confer melanoma susceptibility

artículo científico publicado en 2008

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

artículo científico publicado en 2014

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

artículo científico publicado en 2010

Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma

artículo científico publicado en 2017

Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia

artículo científico publicado en 2006

Copy number variation at chromosome 5q21.2 is associated with intraocular pressure

artículo científico publicado en 2013

Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo.

artículo científico publicado en 2010

Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction

artículo científico publicado en 2005

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

artículo científico publicado en 2018

Does polygenic risk influence associations between sun exposure and melanoma?: a prospective cohort analysis

artículo científico publicado en 2019

Effect of increased body mass index on risk of diagnosis or death from cancer

scientific article published on 08 February 2019

Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the alcohol challenge twin study

artículo científico publicado en 2008

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

article

European and Polynesian admixture in the Norfolk Island population.

artículo científico publicado en 2009

Evaluating a Causal Relationship between Complement Factor I Protein Level and Advanced Age-Related Macular Degeneration Using Mendelian Randomization

artículo científico publicado en 2022

Evaluating the Association Between Keratoconus and the Corneal Thickness Genes in an Independent Australian Population

article

Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies

artículo científico publicado en 2010

Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"

artículo científico publicado en 2010

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

artículo científico publicado en 2019

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

scientific article published on 01 September 2019

False Disease Region Identification From Identity-By-Descent Haplotype Sharing in the Presence of Phenocopies

article published in 2006

Familiality of postpartum depression in unipolar disorder: results of a family study

artículo científico publicado en 2006

Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.

artículo científico publicado en 2018

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

artículo científico publicado en 2010

From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes

artículo científico publicado en 2012

Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers

artículo científico publicado en 2011

GAIA: an easy-to-use web-based application for interaction analysis of case-control data

artículo científico publicado en 2006

GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development

artículo científico publicado en 2011

GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia

artículo científico publicado en 2018

GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration

artículo científico publicado en 2016

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

scientific article published on 16 September 2019

Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma

artículo científico publicado en 2016

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 and environmental factors in conjunctival UV autofluorescence

artículo científico publicado en 2015

Genetic burden associated with varying degrees of disease severity in endometriosis

artículo científico publicado en 2015

Genetic loci for retinal arteriolar microcirculation

artículo científico publicado en 2013

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

artículo científico publicado en 2018

Genetic variants near PDGFRA are associated with corneal curvature in Australians

artículo científico publicado en 2012

Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images

Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK.

artículo científico publicado en 2006

Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study

artículo científico publicado en 2017

Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.

artículo científico publicado en 2003

Genome partitioning of genetic variation for height from 11,214 sibling pairs

artículo científico publicado en 2007

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

artículo científico publicado en 2003

Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging

artículo científico publicado en 2017

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

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect

artículo científico publicado en 2018

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

artículo científico publicado en 2015

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

artículo científico publicado en 2016

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

artículo científico publicado en 2010

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 highlights light-induced signaling as a driver for refractive error

artículo científico publicado en 2018

Genome-wide association meta-analysis identifies new endometriosis risk loci

artículo científico publicado en 2012

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 in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis

artículo científico publicado en 2016

Genome-wide association study for ovarian cancer susceptibility using pooled DNA.

artículo científico publicado en 2012

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 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 loci predisposing to cutaneous melanoma

artículo científico publicado en 2011

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

artículo científico publicado en 2018

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

article

Genome-wide association study identifies three new melanoma susceptibility loci

artículo científico publicado en 2011

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

scientific article published on 27 July 2018

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 paclitaxel and carboplatin disposition in women with epithelial ovarian cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

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

artículo científico publicado en 2015

Genome-wide meta-analysis identifies novel loci associated with age-related macular degeneration

artículo científico publicado en 2020

Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.

artículo científico publicado en 2018

Germline genetic contributions to risk for esophageal adenocarcinoma, Barrett's esophagus, and gastroesophageal reflux

artículo científico publicado en 2013

Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer

artículo científico publicado en 2016

Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma

artículo científico publicado en 2016

Haplotype reference consortium panel: Practical implications of imputations with large reference panels

artículo científico publicado en 2017

Height and overall cancer risk and mortality: evidence from a Mendelian randomisation study on 310,000 UK Biobank participants.

artículo científico publicado en 2018

Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting

artículo científico publicado en 2022

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

artículo científico publicado en 2008

Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian Cancer

publication published on 23 June 2021

Identification of a candidate gene for astigmatism

scientific journal article

Identification of a genetic variant associated with treatment outcome in ovarian cancer: the potential role of cholesterol metabolism as a determinant of response to chemotherapy

Identification of a melanoma susceptibility locus and somatic mutation in TET2.

artículo científico publicado en 2014

Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus

artículo científico publicado en 2018

Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study

artículo científico publicado en 2013

Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island

artículo científico publicado en 2010

Linkage Analysis in a Large Family from Pakistan with Depression and a High Incidence of Consanguineous Marriages

scholarly article by Muhammad Ayub et al published 2008 in Human Heredity

LocusTrack: Integrated visualization of GWAS results and genomic annotation

artículo científico publicado en 2015

Longitudinal data analysis in pedigree studies

artículo científico publicado en 2003

Longitudinal variance-components analysis of the Framingham Heart Study data

artículo científico publicado en 2003

Melanoma genetics: recent findings take us beyond well-traveled pathways

artículo científico publicado en 2012

Mendelian Randomization Study for Genetically Predicted Polyunsaturated Fatty Acids Levels on Overall Cancer Risk and Mortality

artículo científico publicado en 2019

Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia

scientific article published on 30 March 2020

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

artículo científico publicado en 2014

Most common 'sporadic' cancers have a significant germline genetic component

artículo científico publicado en 2014

Most pooling variation in array-based DNA pooling is attributable to array error rather than pool construction error

artículo científico publicado en 2007

Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma

artículo científico publicado en 2021

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

scientific article published on 27 November 2019

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

artículo científico publicado en 2020

Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based Studies

article

New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances

scientific article published on 01 June 2019

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

artículo científico publicado en 2017

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

artículo científico publicado en 2013

No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study

artículo científico publicado en 2019

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

artículo científico publicado en 2018

Obesity and risk of esophageal adenocarcinoma and Barrett's esophagus: a Mendelian randomization study

artículo científico publicado en 2014

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder

artículo científico publicado en 2005

Optimal selection of markers from DNA pooling experiments

artículo científico publicado en 2009

Optimal two-stage testing for family-based genome-wide association studies

artículo científico publicado en 2008

P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?

artículo científico publicado en 2009

PARP1polymorphisms play opposing roles in melanoma occurrence and survival

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

article

Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients

artículo científico publicado en 2011

Pleiotropic analysis of cancer risk loci on esophageal adenocarcinoma risk

artículo científico publicado en 2015

Polymorphisms in Genes of Relevance for Oestrogen and Oxytocin Pathways and Risk of Barrett's Oesophagus and Oesophageal Adenocarcinoma: A Pooled Analysis from the BEACON Consortium

artículo científico publicado en 2015

Polymorphisms in genes in the androgen pathway and risk of Barrett's esophagus and esophageal adenocarcinoma

artículo científico publicado en 2015

Polyunsaturated fatty acids and risk of melanoma: A Mendelian randomisation analysis.

artículo científico publicado en 2018

Pooled genome wide association detects association upstream of FCRL3 with Graves' disease

artículo científico publicado en 2016

Potential influence of socioeconomic status on genetic correlations between alcohol consumption measures and mental health

article

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

artículo científico publicado en 2011

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

article

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

artículo científico publicado en 2019

Quantitative trait locus analysis of longitudinal quantitative trait data in complex pedigrees

artículo científico publicado en 2005

Rapid inexpensive genome-wide association using pooled whole blood

artículo científico publicado en 2009

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma.

artículo científico publicado en 2016

Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls

artículo científico publicado en 2015

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Survival outcomes in patients with multiple primary melanomas.

artículo científico publicado en 2015

Sweet Taste Perception is Associated with Body Mass Index at the Phenotypic and Genotypic Level

artículo científico publicado en 2016

Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets

artículo científico publicado en 2018

The effect on melanoma risk of genes previously associated with telomere length

artículo científico publicado en 2014

The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample

artículo científico publicado en 2008

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

artículo científico publicado en 2011

Time spent outdoors in childhood is associated with reduced risk of myopia as an adult

artículo científico publicado en 2021

Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

artículo científico publicado en 2018

Use of phenotypic covariates in association analysis by sequential addition of cases

artículo científico publicado en 2006

VEGAS2: Software for More Flexible Gene-Based Testing

artículo científico publicado en 2014

Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder

artículo científico publicado en 2006

Vitamin D and overall cancer risk and cancer mortality: a Mendelian randomization study

artículo científico publicado en 2018

Vitamin D receptor gene polymorphisms have negligible effect on human height

artículo científico publicado en 2008

WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness

artículo científico publicado en 2015

When do myopia genes have their effect? Comparison of genetic risks between children and adults

artículo científico publicado en 2016

Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma.

artículo científico publicado en 2017