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Lista de obras de Grant W. Montgomery

"No thanks, it keeps me awake": the genetics of coffee-attributed sleep disturbance

artículo científico publicado en 2007

4th Pediatric Allergy and Asthma Meeting (PAAM)

artículo científico publicado en 2016

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

artículo científico publicado en 2011

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

article published in 2005

A Deletion Mutation in GDF9 in Sisters with Spontaneous DZ Twins

article by Grant W. Montgomery et al published 1 December 2004 in CrossRef Listing of Deleted DOIs

A Genome Scan for Epidermal Skin Pattern in Adolescent Twins Reveals Suggestive Linkage on 12p13.31

A Genome-Wide Analysis of Liberal and Conservative Political Attitudes

article

A Msp I restriction fragment length polymorphism at the ovine locus for glucagon ⬇️

artículo científico publicado el 1 de enero de 1991

A PstI restriction fragment length polymorphism at the ovine locus for poly-ubiquitin

scientific article published on 01 January 1991

A PvuII polymorphism at the ovine corticotrophin releasing hormone (CRH) locus

scientific article published on 01 January 1992

A PvuII restriction fragment length polymorphism at the ovine uncoupling protein locus

artículo científico publicado el 1 de enero de 1992

A Report of Dizygous Monochorionic Twins

artículo científico publicado en 2003

A TaqI polymorphism at the ovine alpha-inhibin locus

artículo científico publicado el 1 de enero de 1991

A case of true hermaphroditism reveals an unusual mechanism of twinning

artículo científico publicado en 2006

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

scientific article published on 31 May 2019

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2011

A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

artículo científico publicado en 2013

A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

artículo científico publicado en 2012

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

artículo científico publicado en 2004

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

artículo científico publicado en 2010

A genome-wide association study for reading and language abilities in two population cohorts.

artículo científico publicado en 2013

A genome-wide association study identifies five loci influencing facial morphology in Europeans

artículo científico publicado en 2012

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

artículo científico publicado en 2008

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 alcohol-dependence symptom counts in extended pedigrees identifies C15orf53

artículo científico publicado en 2012

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 early menopause and the combined impact of identified variants

artículo científico publicado en 2013

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

artículo científico publicado en 2012

A genome-wide association study of self-rated health

artículo científico publicado en 2010

A genome-wide association study of sleep habits and insomnia

artículo científico publicado en 2013

A genome-wide association study to identify genetic markers associated with endometrial cancer grade

artículo científico publicado en 2012

A genome-wide linkage scan for age at menarche in three populations of European descent

artículo científico publicado en 2008

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.

artículo científico publicado en 2012

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions

article published in 2006

A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

artículo científico publicado en 2011

A genome-wide study on the perception of the odorants androstenone and galaxolide

artículo científico publicado en 2012

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

artículo científico publicado en 2010

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.

artículo científico publicado en 2005

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

artículo científico publicado en 2007

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 association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A linkage study of academic skills defined by the Queensland core skills test

artículo científico publicado en 2005

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

artículo científico publicado en 2010

A major quantitative trait locus for CD4–CD8 ratio is located on chromosome 11

article

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

artículo científico publicado en 2012

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

artículo científico publicado en 2014

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

artículo científico publicado en 2012

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

artículo científico publicado en 2013

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

artículo científico publicado en 2011

A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence

artículo científico publicado en 2016

A possible smoking susceptibility locus on chromosome 11p12: evidence from sex-limitation linkage analyses in a sample of Australian twin families

artículo científico publicado en 2005

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

scientific journal article

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 SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color

artículo científico publicado en 2008

A study of the TNF/LTA/LTB locus and susceptibility to severe malaria in highland papuan children and adults

artículo científico publicado en 2010

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

artículo científico publicado en 2007

A twin study of breastfeeding with a preliminary genome-wide association scan

artículo científico publicado en 2014

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

AB028. Identifying the functional role of VEZT gene for endometriosis risk

artículo científico publicado en 2015

ADH single nucleotide polymorphism associations with alcohol metabolism in vivo

scientific article published on 04 February 2009

ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

artículo científico publicado en 2013

ATG16L1 T300A Shows Strong Associations With Disease Subgroups in a Large Australian IBD Population: Further Support for Significant Disease Heterogeneity

article

Abnormal prefrontal activation directly related to pre-synaptic striatal dopamine dysfunction in people at clinical high risk for psychosis

artículo científico publicado en 2009

Abstract 20: POT1 mutations predispose to familial melanoma

Abstract 3266: Expression quantitative trait locus analysis of triple negative breast cancer

artículo científico publicado en 2014

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

Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures

artículo científico publicado en 2009

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

artículo científico publicado en 2015

Age-related susceptibility to severe malaria associated with galectin-2 in highland Papuans

artículo científico publicado en 2010

Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.

artículo científico publicado en 2011

Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

scientific article published on June 2012

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

artículo científico publicado en 2016

An ApaI polymorphism at the ovine tissue inhibitor of metalloproteinase locus (TIMP)

scientific article published on 01 August 1994

An Extremes of Phenotype Approach Confirms Significant Genetic Heterogeneity in Patients with Ulcerative Colitis

artículo científico publicado en 2022

An Xba RFLP at the ovine basic fibroblast growth factor locus (FGFB)

artículo científico publicado en 1993

An autosomal genetic linkage map of the sheep genome

artículo científico publicado en 1995

An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project

artículo científico publicado en 2008

An interaction between season of calving and nutrition on the resumption of ovarian cycles in post-partum beef cattle

scientific article published on 01 January 1985

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

artículo científico publicado en 2018

Analysis of DNA methylation associates the cystine-glutamate antiporter SLC7A11 with risk of Parkinson's disease

artículo científico publicado en 2020

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

artículo científico publicado en 2006

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

Analysis of the 5q31 33 locus shows an association between single nucleotide polymorphism variants in the IL-5 gene and symptomatic infection with the human blood fluke, Schistosoma japonicum

scientific article published on December 2007

Anxiety and comorbid measures associated with PLXNA2.

artículo científico publicado en 2007

Applying polygenic risk scores to postpartum depression

artículo científico publicado en 2014

Assessment of PALB2 as a candidate melanoma susceptibility gene

artículo científico publicado en 2014

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

artículo científico publicado en 2017

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects

artículo científico publicado en 2013

Association and interaction analyses of eight genes under asthma linkage peaks

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 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 polymorphisms in the progesterone receptor gene and endometriosis

artículo científico publicado en 2005

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 mapping

artículo científico

Association of Helicobacter pylori infection with reduced risk for esophageal cancer is independent of environmental and genetic modifiers

artículo científico publicado en 2010

Association of OPRD1 polymorphisms with heroin dependence in a large case-control series

artículo científico publicado en 2012

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

artículo científico publicado en 2016

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

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

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

artículo científico publicado en 2013

Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults.

artículo científico publicado en 2009

Association of current and former smoking with body mass index: A study of smoking discordant twin pairs from 21 twin cohorts

artículo científico publicado en 2018

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

artículo científico publicado en 2011

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

artículo científico publicado en 2015

Association of the gastric alcohol dehydrogenase gene ADH7 with variation in alcohol metabolism

artículo científico publicado en 2007

Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression

artículo científico publicado en 2008

Association study of candidate variants of COMT with neuroticism, anxiety and depression

artículo científico publicado en 2008

Association study of common mitochondrial variants and cognitive ability

artículo científico publicado en 2009

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

artículo científico publicado en 2009

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Assumption-free Estimation of Heritability from Genome-wide Identity-by-descent Sharing between Fullsibs

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

artículo científico publicado en 2006

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

scientific article published on 01 May 2019

Autosomal genetic control of human gene expression does not differ across the sexes

artículo científico publicado en 2016

Autosomal linkage analysis for cannabis use behaviors in Australian adults

artículo científico publicado en 2008

BRAF polymorphisms and risk of melanocytic neoplasia

artículo científico publicado en 2005

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

artículo científico publicado en 2016

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

artículo científico publicado en 2010

Blood gene expression studies in migraine: Potential and caveats

artículo científico publicado en 2016

Body composition, smoking, and spontaneous dizygotic twinning

artículo científico publicado en 2008

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene

artículo científico publicado en 2012

Butyrylcholinesterase: association with the metabolic syndrome and identification of 2 gene loci affecting activity

artículo científico publicado en 2006

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 identify genes for alcohol consumption in samples ascertained for heterogeneous purposes?

artículo científico publicado en 2009

Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression

artículo científico publicado en 2012

Characterization and linkage mapping of ten sheep microsatellite markers derived from a sheep x hamster cell hybrid.

artículo científico publicado en 1996

Characterization of the methylation patterns of MS4A2 in atopic cases and controls

artículo científico publicado en 2009

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

artículo científico publicado en 2013

Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs

artículo científico publicado en 2006

Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1

artículo científico publicado en 2015

Cognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphisms

artículo científico publicado en 2011

Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci

artículo científico publicado en 2007

Combined genome scans for body stature in 6602 European twins: evidence for common Caucasian loci

Common Genetic Variants Influence Whorls in Fingerprint Patterns

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion.

artículo científico publicado en 2012

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 breast cancer susceptibility loci are associated with triple-negative breast cancer

artículo científico publicado en 2011

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

artículo científico publicado en 2012

Common genetic influences underlie comorbidity of migraine and endometriosis

artículo científico publicado en 2009

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

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 polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

artículo científico publicado en 2015

Common sequence variants on 20q11.22 confer melanoma susceptibility

artículo científico publicado en 2008

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

Comparative linkage mapping of genes on sheep chromosome 3 provides evidence of chromosomal rearrangements in the evolution of the Bovidae

article

Complex genetics of female fertility

article

Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation

artículo científico publicado en 2019

Comprehensive analysis of tagging sequence variants inDTNBP1shows no association with schizophrenia or with its composite neurocognitive endophenotypes

article

Concentrations of FSH are elevated in new-born ewe lambs carrying the Booroola F gene but not in lambs from a prolific Romney strain.

artículo científico publicado en 1989

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

artículo científico publicado en 2012

Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data

artículo científico publicado en 2013

Consistently replicating locus linked to migraine on 10q22-q23

artículo científico publicado en 2008

Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression

artículo científico publicado en 2017

Contribution of genetic variation to transgenerational inheritance of DNA methylation

artículo científico publicado en 2014

Correction: Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Correction: Pathway Analysis of Smoking Quantity in Multiple GWAS Identifies Cholinergic and Sensory Pathways.

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2018

DIFFUSION IMAGING PROTOCOL EFFECTS ON GENETIC ASSOCIATIONS.

artículo científico publicado en 2012

DISCOVERY OF GENES THAT AFFECT HUMAN BRAIN CONNECTIVITY: A GENOME-WIDE ANALYSIS OF THE CONNECTOME.

artículo científico publicado en 2012

DNA methylation age of blood predicts all-cause mortality in later life

artículo científico publicado en 2015

DNA methylation profiles in monozygotic and dizygotic twins.

artículo científico publicado en 2009

DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

artículo científico publicado en 2014

Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis In Montpellier, France

artículo científico publicado en 2013

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

artículo científico publicado en 2014

Determination of genetic relationships among five indigenous Chinese goat breeds with six microsatellite markers

article

Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts

artículo científico publicado en 2017

Digital quantification of human eye color highlights genetic association of three new loci

artículo científico publicado en 2010

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.

artículo científico publicado en 2011

Discovery of genetic risk factors for disease

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

Dizygotic twinning

artículo científico publicado en 2007

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes

artículo científico publicado en 2003

Dizygotic twinning is not linked to variation at the alpha-inhibin locus on human chromosome 2

artículo científico publicado en 2000

Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample

artículo científico publicado en 2010

Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

artículo científico publicado en 2017

Does the sex of one's co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts

artículo científico publicado en 2017

Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

artículo científico publicado en 2010

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation

artículo científico publicado en 2010

Education in Twins and Their Parents Across Birth Cohorts Over 100 years: An Individual-Level Pooled Analysis of 42-Twin Cohorts

artículo científico publicado en 2017

Educational attainment: a genome wide association study in 9538 Australians

artículo científico publicado en 2011

Effect of the BDNF V166M polymorphism on working memory in healthy adolescents

artículo científico publicado en 2006

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

artículo científico publicado en 2008

Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans

article

Effects of scrotal heating on sperm surface protein PH-20 expression in sheep

artículo científico publicado en 2004

Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

article by Patrick F. Sullivan et al published 1 August 2006 in CrossRef Listing of Deleted DOIs

Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

article by Patrick F. Sullivan et al published August 2006 in Twin Research and Human Genetics

Endometrial vezatin and its association with endometriosis risk

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Epidermal growth factor gene (EGF) polymorphism and risk of melanocytic neoplasia

artículo científico publicado en 2004

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

article

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

article

Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scholarly article published in Nature Genetics

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

artículo científico publicado en 2016

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

article

Erratum: Meta-analysis of genome-wide association studies of anxiety disorders

article

Erratum: Testing replication of a 5-SNP set for general cognitive ability in six population samples

scholarly article published in European Journal of Human Genetics

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Estimation of the Rate of SNP Genotyping Errors From DNA Extracted From Different Tissues

article published in 2005

European and Polynesian admixture in the Norfolk Island population.

artículo científico publicado en 2009

Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan

artículo científico publicado en 2005

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

artículo científico publicado en 2010

Evidence for mitochondrial genetic control of autosomal gene expression

artículo científico publicado en 2016

Evidence for the involvement of the RSG2 gene in risk for anxiety and related phenotypes in an elderly population not selected for this trait

article

Evidence of CNIH3 involvement in opioid dependence.

artículo científico publicado en 2015

Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein

artículo científico publicado en 2012

Evidence of genetic effects on blood lead concentration

artículo científico publicado en 2007

Evidence of inbreeding depression on human height

artículo científico publicado en 2012

Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences

artículo científico publicado en 2016

Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls

artículo científico publicado en 2012

Exhaustive Search of the SNP-SNP Interactome Identifies Epistatic Effects on Brain Volume in Two Cohorts

artículo científico publicado en 2013

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

Familial twinning and fertility in Dutch mothers of twins

article by Chantal Hoekstra et al published 15 December 2008 in American Journal of Medical Genetics

Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents.

artículo científico publicado en 2009

Feeding patterns in pigs: The effects of amino acid deficiency ⬇️

artículo científico publicado el 1 de junio de 1978

Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study

artículo científico

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

artículo científico publicado en 2015

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

Follistatin (FST), growth hormone receptor (GHR) and prolactin receptor (PRLR) genes map to the same region of sheep chromosome 16

article

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

artículo científico publicado en 2012

Functional evaluation of genetic variants associated with endometriosis near GREB1.

artículo científico publicado en 2015

Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerström Test for Nicotine Dependence

artículo científico publicado en 2009

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

artículo científico publicado en 2011

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

article

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

artículo científico publicado en 2013

GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association

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

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

Gamma-aminobutyric acid receptor genes and nicotine dependence: evidence for association from a case-control study

artículo científico publicado en 2008

Gender Diagnosticity and Androgen Receptor Gene CAG Repeat Sequence

article

Gene network effects on brain microstructure and intellectual performance identified in 472 twins

artículo científico publicado en 2012

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Generation of immortalized human endometrial stromal cell lines with different endometriosis risk genotypes

artículo científico publicado en 2019

Genes controlling ovulation rate in sheep

artículo científico publicado en 2001

Genes encoding the alpha and beta chains of follicle-stimulating hormone are not sites for the Booroola (FecB) mutation in sheep

artículo científico publicado el 1 de agosto de 1992

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Biomarkers for Endometriosis

Genetic Clustering on the Hippocampal Surface for Genome-Wide Association Studies

article by Derrek P Hibar et al published 2013 in Lecture Notes in Computer Science

Genetic Risk Factors for Endometriosis

Genetic and environmental effects on body mass index from infancy to the onset of adulthood: an individual-based pooled analysis of 45 twin cohorts participating in the COllaborative project of Development of Anthropometrical measures in Twins (CODA

artículo científico publicado en 2016

Genetic and environmental exposures constrain epigenetic drift over the human life course

artículo científico publicado en 2014

Genetic and environmental influences on adult human height across birth cohorts from 1886 to 1994.

scientific article published on 14 December 2016

Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

artículo científico publicado en 2016

Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

artículo científico publicado en 2020

Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries

artículo científico publicado en 2009

Genetic and nongenetic variation revealed for the principal components of human gene expression

scientific article published on 11 September 2013

Genetic architecture of circulating lipid levels

artículo científico publicado en 2011

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

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

artículo científico publicado en 2016

Genetic basis of a cognitive complexity metric

artículo científico publicado en 2015

Genetic burden associated with varying degrees of disease severity in endometriosis

artículo científico publicado en 2015

Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

artículo científico publicado en 2011

Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood

artículo científico publicado en 2017

Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

artículo científico publicado en 2007

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

artículo científico publicado en 2017

Genetic effects on toxic and essential elements in humans: arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

artículo científico publicado en 2010

Genetic evidence of assortative mating in humans

scholarly article

Genetic linkage analysis between protein polymorphisms and the FecB major gene in sheep

artículo científico publicado el 1 de enero de 1992

Genetic linkage findings for DSM-IV nicotine withdrawal in two populations

artículo científico publicado en 2009

Genetic linkage of proteolipid protein (PLP)and thyroxine-binding globulin (TBG) on the ovine X chromosome

artículo científico publicado en 1994

Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples

artículo científico publicado en 2007

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

artículo científico publicado en 2016

Genetic loci for retinal arteriolar microcirculation

artículo científico publicado en 2013

Genetic mapping of the endothelin receptor type A gene on sheep Chromosome 17

article

Genetic mapping of the laminin gamma 2 gene on sheep Chromosome 12

article

Genetic mapping of the ovine homologue of the mouse Hacl1 gene to sheep chromosome 1

article

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

artículo científico publicado en 2018

Genetic predisposition to schizophrenia associated with increased use of cannabis

artículo científico publicado en 2014

Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome

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 susceptibility in IBD: overlap between ulcerative colitis and Crohn's disease

artículo científico publicado en 2013

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits

artículo científico publicado en 2011

Genetic variants associated with disordered eating

scientific journal article

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

artículo científico publicado en 2016

Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits

scientific journal article

Genetic variants in RBFOX3 are associated with sleep latency

artículo científico publicado en 2016

Genetic variants near PDGFRA are associated with corneal curvature in Australians

artículo científico publicado en 2012

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

Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins

artículo científico publicado en 2011

Genetics of Dizygotic Twinning: A Feasibility Study for a Biobank

article

Genetics of dizygotic twinning: a feasibility study for a biobank

artículo científico publicado en 2004

Genetics of endometriosis

artículo científico publicado en 2015

Genetics of endometriosis: State of the art on genetic risk factors for endometriosis

article

Genetics of serum dehydroepiandrosterone sulfate and its relationship to insulin in a population-based cohort of twin subjects

artículo científico publicado en 2002

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up

artículo científico publicado en 2015

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome Scale Epigenetic Profiling Reveals Five Distinct Subtypes of Colorectal Cancer

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

artículo científico publicado en 2007

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 Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

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

scientific article published on 27 February 2020

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

artículo científico publicado en 2011

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 analysis of formalin-fixed paraffin embedded colorectal cancer tissue

artículo científico publicado en 2014

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

artículo científico publicado en 2018

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Genome-wide association analysis identifies 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 coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

artículo científico publicado en 2011

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

artículo científico publicado en 2019

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

artículo científico publicado en 2013

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

artículo científico publicado en 2013

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 meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

article

Genome-wide association meta-analysis of age at first cannabis use

artículo científico publicado en 2018

Genome-wide association reveals dopamine-related genetic effects on caudate volume

scholarly article by J L Stein et al published 25 August 2011 in Molecular Psychiatry

Genome-wide association studies and genetic architecture of common human diseases

artículo científico publicado en 2011

Genome-wide association studies and human disease: from trickle to flood

artículo científico publicado en 2009

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.

artículo científico publicado en 2012

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

artículo científico publicado en 2013

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

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

artículo científico publicado en 2016

Genome-wide association study identifies a common variant associated with risk of endometrial cancer

artículo científico publicado en 2011

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 a novel locus for cannabis dependence

artículo científico publicado en 2017

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study identifies loci affecting blood copper, selenium and zinc

artículo científico publicado en 2013

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

artículo científico publicado en 2011

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

artículo científico publicado en 2018

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 identifies three loci associated with melanoma risk

scientific article published on 05 July 2009

Genome-wide association study identifies three new melanoma susceptibility loci

artículo científico publicado en 2011

Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

artículo científico publicado en 2011

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

artículo científico publicado en 2009

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

artículo científico publicado en 2023

Genome-wide association study of a quantitative disordered gambling trait

artículo científico publicado en 2012

Genome-wide association study of blood lead shows multiple associations near ALAD

artículo científico publicado en 2015

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

artículo científico

Genome-wide association study of height and body mass index in Australian twin families

artículo científico publicado en 2010

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits

artículo científico publicado en 2013

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

scientific article published on 27 July 2018

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

artículo científico publicado en 2016

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 more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

article

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

artículo científico publicado en 2018

Genome-wide association study of working memory brain activation

artículo científico publicado en 2016

Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample

scientific article published on 11 June 2013

Genome-wide association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Genome-wide autozygosity is associated with lower general cognitive ability

artículo científico publicado en 2015

Genome-wide average DNA methylation is determined in utero

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 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 linkage scan for loci influencing plasma triglycerides

article

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 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

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 identifies six novel loci associated with habitual coffee consumption

artículo científico publicado en 2014

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

artículo científico publicado en 2010

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures

artículo científico publicado en 2016

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

artículo científico publicado en 2005

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

artículo científico publicado en 2013

Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

artículo científico publicado en 2018

Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms

artículo científico publicado en 2017

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 scans of red cell indices suggest linkage on chromosome 6q23.

scientific article published on September 2006

Genomewide significant linkage to migrainous headache on chromosome 5q21.

artículo científico publicado en 2005

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

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 and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

Genomic inflation factors under polygenic inheritance

artículo científico publicado en 2011

Geographical structure and differential natural selection among North European populations

scientific article published on 05 March 2009

Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study

artículo científico publicado en 2013

H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence

artículo científico publicado en 2010

HLA and genomewide allele sharing in dizygotic twins

artículo científico publicado en 2006

Hemani et al. reply

artículo científico publicado en 2014

Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

artículo científico publicado en 2014

High intake of folate from food sources is associated with reduced risk of esophageal cancer in an Australian population.

artículo científico publicado en 2010

High prevalence of sessile serrated adenomas with BRAF mutations: a prospective study of patients undergoing colonoscopy.

artículo científico publicado en 2006

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

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells.

artículo científico publicado en 2001

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins.

artículo científico publicado en 2014

Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning geneFecB

article

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

artículo científico publicado en 2010

IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers

artículo científico publicado en 2001

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

artículo científico publicado en 2010

Identification of 55,000 Replicated DNA Methylation QTL

artículo científico publicado en 2018

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 a candidate gene for astigmatism

scientific journal article

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

artículo científico publicado en 2014

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Identification of nine new susceptibility loci for endometrial cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms.

artículo científico publicado en 2011

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood.

artículo científico publicado en 2018

Identifying the biological basis of GWAS hits for endometriosis.

artículo científico publicado en 2015

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

artículo científico publicado en 2015

Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia

artículo científico publicado en 2012

Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins

artículo científico publicado en 2011

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

scientific article published on 23 August 2019

Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations

artículo científico publicado en 2015

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

artículo científico publicado en 2012

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

artículo científico publicado en 2016

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

Influence of suckling frequency and bromocryptine treatment on the resumption of ovarian cycles in post-partum beef cattle

artículo científico publicado en 1982

Insights into Assessing the Genetics of Endometriosis

artículo científico publicado en 2012

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

artículo científico publicado en 2016

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

artículo científico publicado en 2018

Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes

artículo científico publicado en 2011

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

artículo científico publicado en 2004

International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents

artículo científico publicado en 2016

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

Investigating the relationship between iron and depression

artículo científico

Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer

artículo científico publicado en 2012

Isocitrate dehydrogenase 1 R132C mutation occurs exclusively in microsatellite stable colorectal cancers with the CpG island methylator phenotype

artículo científico publicado en 2014

KCNN4 gene variant is associated with ileal Crohn's Disease in the Australian and New Zealand population

artículo científico publicado en 2010

KRAS variation and risk of endometriosis

artículo científico publicado en 2006

LPAR1 and ITGA4 regulate peripheral blood monocyte counts

Large Autosomal Copy-Number Differences within Unselected Monozygotic Twin Pairs are Rare

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions

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

artículo científico publicado en 2015

Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

artículo científico publicado en 2005

Linkage analysis of a model quantitative trait in humans: finger ridge count shows significant multivariate linkage to 5q14.1.

artículo científico publicado en 2007

Linkage analysis of alcohol dependence symptoms in the community

artículo científico publicado en 2009

Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins

article

Linkage and Association Analysis of Spectrophotometrically Quantified Hair Color in Australian Adolescents: the Effect of OCA2 and HERC2

article

Linkage and association analyses of longitudinally measured lipid phenotypes in adolescence

artículo científico publicado en 2008

Linkage and association analysis of radiation damage repair genes XRCC3 and XRCC5 with nevus density in adolescent twins

artículo científico publicado en 2003

Linkage mapping of genes encoding bone morphogenetic proteins 1, 4 and 5 in Sheep

article

Linkage mapping of wool keratin and keratin-associated protein genes in sheep

article

Linkage of LHB and MAG to GPI on sheep Chromosome 14

artículo científico publicado en 1995

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

artículo científico publicado en 2011

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

artículo científico publicado en 2009

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

Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding

artículo científico publicado en 2012

Major quantitative trait locus for eosinophil count is located on chromosome 2q

artículo científico publicado en 2004

Mapping the Horns (Ho) locus in sheep: a further locus controlling horn development in domestic animals

artículo científico publicado en 1996

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake

artículo científico publicado en 2008

Meta-Analysis of Genome-Wide Association Studies of Anxiety Disorders

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

artículo científico publicado en 2012

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

artículo científico publicado en 2012

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 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scientific journal article

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

artículo científico publicado en 2017

Meta-analysis identifies seven susceptibility loci involved in the atopic march

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

artículo científico publicado en 2015

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

artículo científico publicado en 2015

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

artículo científico publicado en 2021

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

artículo científico publicado en 2011

Meta-analysis of genome-wide association studies for personality.

artículo científico publicado en 2010

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Meta-analysis of genome-wide association studies of anxiety disorders.

artículo científico publicado en 2016

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

Metabolic and biochemical effects of low-to-moderate alcohol consumption

artículo científico publicado en 2012

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

scientific article published on 12 August 2019

Microsatellite stable colorectal cancers stratified by the BRAF V600E mutation show distinct patterns of chromosomal instability

artículo científico publicado en 2014

Mining the human phenome using allelic scores that index biological intermediates

artículo científico publicado en 2013

Mode of conception of twin pregnancies: willingness to reply to survey items and comparison of survey data to hospital records

artículo científico publicado en 2008

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

artículo científico publicado en 2014

Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis

artículo científico publicado en 2015

Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

artículo científico publicado en 2013

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

artículo científico publicado en 2009

Multicohort analysis of the maternal age effect on recombination

artículo científico publicado en 2015

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

artículo científico publicado en 2011

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

artículo científico publicado en 2010

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

artículo científico publicado en 2009

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

artículo científico publicado en 2020

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q

article

Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner

artículo científico publicado en 2000

Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning

artículo científico publicado en 2001

NRAS and BRAF Mutations in Cutaneous Melanoma and the Association with MC1R Genotype: Findings from Spanish and Austrian Populations

article

Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses

artículo científico publicado en 2012

New Lessons about Endometriosis - Somatic Mutations and Disease Heterogeneity

artículo científico publicado en 2017

New gene functions in megakaryopoiesis and platelet formation

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

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

No Association Between General Cognitive Ability and Rare Copy Number Variation ⬇️

artículo científico publicado el 17 de febrero de 2013

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

artículo científico publicado en 2017

No association of candidate genes with cannabis use in a large sample of Australian twin families

artículo científico publicado en 2011

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

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan

artículo científico publicado en 2009

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Novel genes identified in a high-density genome wide association study for nicotine dependence

scientific journal article

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

artículo científico publicado en 2014

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

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

artículo científico publicado en 2018

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

Novel variants in growth differentiation factor 9 in mothers of dizygotic twins

artículo científico publicado en 2006

Obesity gene NEGR1 associated with white matter integrity in healthy young adults

artículo científico publicado en 2014

Oncogenic PIK3CA mutations in colorectal cancers and polyps

artículo científico publicado en 2011

Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females

artículo científico publicado en 2005

PARP1polymorphisms play opposing roles in melanoma occurrence and survival

POLE mutations in families predisposed to cutaneous melanoma

artículo científico publicado en 2015

POT1 loss-of-function variants predispose to familial melanoma

artículo científico publicado en 2014

PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals

artículo científico publicado en 2013

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways

artículo científico publicado en 2012

Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method

artículo científico

Physiology and Molecular Genetics of Mutations that Increase Ovulation Rate in Sheep ⬇️

artículo científico publicado el 1 de mayo de 1992

Polymorphism at the ovine major histocompatibility complex class II loci

artículo científico publicado en 1996

Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma

artículo científico publicado en 2011

Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma

artículo científico publicado en 2009

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

scientific article published on 23 July 2008

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

artículo científico publicado en 2016

Population genetic differentiation of height and body mass index across Europe

artículo científico publicado en 2015

Power and SNP tagging in whole mitochondrial genome association studies

artículo científico publicado en 2008

Predicting white matter integrity from multiple common genetic variants

artículo científico publicado en 2012

Prevalence of Germline BAP1, CDKN2A, and CDK4 Mutations in an Australian Population-Based Sample of Cutaneous Melanoma Cases

artículo científico publicado en 2015

Priorities for endometriosis research: recommendations from an international consensus workshop.

artículo científico publicado en 2009

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

QTLs identified for P3 amplitude in a non-clinical sample: importance of neurodevelopmental and neurotransmitter genes

artículo científico publicado en 2007

Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye Study.

artículo científico publicado en 2009

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

RETRACTED ARTICLE: Detection and replication of epistasis influencing transcription in humans

retracted scholarly article

Rapid inexpensive genome-wide association using pooled whole blood

artículo científico publicado en 2009

Rapid screening of 4000 individuals for germ-line variations in the BRAF gene

artículo científico publicado en 2006

Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language

artículo científico publicado en 2008

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

artículo científico publicado en 2011

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

artículo científico publicado en 2012

Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults

scientific article published on 30 May 2013

Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G x E) interaction

artículo científico publicado en 2008

Research Priorities for Endometriosis

artículo científico publicado en 2016

Restriction fragment length polymorphisms at the ovine locus for the alpha-subunit of pituitary glycoprotein hormones

artículo científico publicado en 1991

Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season.

artículo científico publicado en 2013

Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis

artículo científico publicado en 2011

S1169 KCNN4 Gene Variant Is Associated with Ileal Crohn's Disease

article

SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample

artículo científico publicado en 2011

Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study

artículo científico publicado en 2013

Seasonal differences in ovarian activity in cows

scientific article published on 01 August 1984

Seasonal effects on gene expression

artículo científico publicado en 2015

Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder

artículo científico publicado en 2015

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

artículo científico publicado en 2010

Sequence variants in three loci influence monocyte counts and erythrocyte volume

artículo científico publicado en 2009

Serum Inhibin A and B Concentrations During the Menstrual Cycle in Mothers of Spontaneous Dizygotic Twins

artículo científico publicado en 2003

Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure

artículo científico publicado en 2014

Seventy-five genetic loci influencing the human red blood cell

artículo científico publicado en 2012

Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families

artículo científico publicado en 2005

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

artículo científico publicado en 2013

Shared genetic control of expression and methylation in peripheral blood

artículo científico publicado en 2016

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

artículo científico publicado en 2020

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Sharing a Placenta is Associated With a Greater Similarity in DNA Methylation in Monochorionic Versus Dichorionic Twin Pars in Blood at Age 14.

artículo científico publicado en 2015

Sheep linkage mapping: RFLP markers for comparative mapping studies ⬇️

artículo científico publicado el 1 de agosto de 1995

Sheep linkage mapping: nineteen linkage groups derived from the analysis of paternal half-sib families

artículo científico publicado en 1994

Sheep linkage mapping: restriction fragment length polymorphism detection with heterologous cDNA probes

artículo científico publicado el 1 de enero de 1992

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

artículo científico publicado en 2017

Should Genetics Now Be Considered the Pre-eminent Etiologic Factor in Endometriosis?

artículo científico publicado en 2019

Signatures of negative selection in the genetic architecture of human complex traits

artículo científico publicado en 2018

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

article

Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers

artículo científico publicado en 2008

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

artículo científico publicado en 2012

Smoking behaviour modifiesIL23r-associated disease risk in patients with Crohn's disease

Some aspects of thecal and granulosa cell function during follicular development in the bovine ovary

scientific article published on 01 September 1984

Spectrophotometric methods for quantifying pigmentation in human hair-influence of MC1R genotype and environment

artículo científico publicado en 2008

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

artículo científico publicado en 2018

Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression

scientific article published on April 2009

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

artículo científico publicado en 2008

Systematic identification of trans eQTLs as putative drivers of known disease associations

artículo científico publicado en 2013

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

artículo científico publicado en 2019

Testing Two Evolutionary Theories of Human Aging with DNA Methylation Data.

artículo científico

Testing replication of a 5-SNP set for general cognitive ability in six population samples

article

Testing the role of circadian genes in conferring risk for psychiatric disorders

artículo científico publicado en 2014

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

artículo científico publicado en 2010

The Anorexia Nervosa Genetics Initiative: Overview and Methods

article

The Anorexia Nervosa: Genetics Initiative (ANGI): Australia and New Zealand join forces.

artículo científico publicado en 2015

The Association of Genetic Predisposition to Depressive Symptoms with Non-suicidal and Suicidal Self-Injuries

artículo científico publicado en 2016

The Booroola Fecundity (FecB) Gene Maps to Sheep Chromosome 6

article

The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics

artículo científico publicado en 2012

The CODATwins Project: The Cohort Description of Collaborative Project of Development of Anthropometrical Measures in Twins to Study Macro-Environmental Variation in Genetic and Environmental Effects on Anthropometric Traits

artículo científico publicado en 2015

The CODATwins Project: The Current Status and Recent Findings of COllaborative Project of Development of Anthropometrical Measures in Twins

artículo científico publicado en 2019

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The Genetic Architecture of Gene Expression in Peripheral Blood

artículo científico publicado en 2016

The Genetic Architecture of Gene Expression in Peripheral Blood

artículo científico publicado en 2017

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

artículo científico publicado en 2015

The International Endogene Study: a collection of families for genetic research in endometriosis

artículo científico publicado en 2002

The Netherlands Twin Register biobank: a resource for genetic epidemiological studies

artículo científico publicado en 2010

The anorexia nervosa genetics initiative (ANGI): Overview and methods

article

The application of AFLP fingerprinting to construct a YAC contig containing ADH2 and MTP on sheep chromosome 6.

artículo científico publicado en 1999

The duplicated gene copy of the ovine growth hormone gene contains a PvuII polymorphism in the second intron

scientific article published on 01 August 1993

The effect of X-linked dosage compensation on complex trait variation

scientific article published on 08 July 2019

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

artículo científico publicado en 2016

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

artículo científico publicado en 2014

The follicle-stimulating hormone receptor and luteinizing hormone receptor genes are closely linked in sheep and deer

artículo científico publicado en 1995

The future for genetic studies in reproduction.

artículo científico publicado en 2014

The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation

artículo científico publicado en 2012

The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

artículo científico publicado en 2011

The genetic regulation of transcription in human endometrial tissue

artículo científico publicado en 2017

The genetics of cognitive processes: candidate genes in humans and animals.

artículo científico publicado en 2001

The gonadotrophin-releasing hormone receptor maps to sheep Chromosome 6 outside of the region of the FecB locus

artículo científico publicado en 1995

The linkage map of sheep Chromosome 6 compared with orthologous regions in other species

artículo científico publicado en 1996

The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence

artículo científico publicado en 2006

The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

artículo científico publicado en 2010

The physiological effects of natural variation in growth hormone gene copy number in ram lambs.

artículo científico publicado en 1997

The renal urate transporter SLC17A1 locus: confirmation of association with gout

artículo científico publicado en 2012

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 adiposity in cardiometabolic traits: a Mendelian randomization analysis

artículo científico publicado en 2013

The role of the endocannabinoid system in aetiopathogenesis of endometriosis: A potential therapeutic target

artículo científico publicado en 2019

The search for genes contributing to endometriosis risk

artículo científico publicado en 2008

The search for the Booroola (FecB) mutation.

artículo científico publicado en 1995

The sheep gene map database (SheepBase) is now available on the World Wide Web

article

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

artículo científico publicado en 2016

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

artículo científico publicado en 2019

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

artículo científico publicado en 2018

Transferrin saturation and mortality

artículo científico publicado en 2011

Tryptophan deficiency and food intake depression in pigs

1976 doctoral thesis by Grant William Montgomery at Massey University

Tryptophan deficiency in pigs: changes in food intake and plasma levels of glucose, amino acids, insulin and growth hormone.

artículo científico publicado en 1980

Twenty-eight loci that influence serum urate levels: analysis of association with gout

artículo científico publicado en 2014

Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project

artículo científico publicado en 2016

Understanding the Pathogenesis of Endometriosis: Gene Mapping Studies

article

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

scholarly article published 19 October 2018

Use of Monozygotic Twins to Investigate the Relationship between 5HTTLPR Genotype, Depression and Stressful Life Events: An Application of Item Response Theory

article

Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6.

artículo científico publicado en 2012

Use of monozygotic twins to investigate the relationship between 5HTTLPR genotype, depression and stressful life events: an application of Item Response Theory

artículo científico publicado en 2008

Variants close to NTRK2 gene are associated with birth weight in female twins

artículo científico publicado en 2014

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

artículo científico publicado en 2007

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels

artículo científico publicado en 2008

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

artículo científico

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

artículo científico publicado en 2008

Vitamin D Pathway Gene Polymorphisms and Keratinocyte Cancers: A Nested Case-Control Study and Meta-Analysis

artículo científico publicado en 2016

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

Whole genome association scan for genetic polymorphisms influencing information processing speed

artículo científico publicado en 2010

Widespread signatures of negative selection in the genetic architecture of human complex traits

scholarly article published 3 June 2017

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

artículo científico publicado en 2008

Zygosity Differences in Height and Body Mass Index of Twins From Infancy to Old Age: A Study of the CODATwins Project

artículo científico publicado en 2015

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

artículo científico publicado en 2003

p53 mutation is common in microsatellite stable, BRAF mutant colorectal cancers

artículo científico publicado en 2011

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