Lista de obras - Allan F McRae - Dominio Público Uruguay

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A Localized Negative Genetic Correlation Constrains Microevolution of Coat Color in Wild Sheep

artículo científico publicado en 2008

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

artículo científico publicado en 2009

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

artículo científico publicado en 2013

A genome-wide 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 simple linear regression method for quantitative trait loci linkage analysis with censored observations

artículo científico publicado en 2006

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

artículo científico publicado en 2010

An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort

article

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

artículo científico publicado en 2020

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

artículo científico publicado en 2010

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

artículo científico publicado en 2017

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Association study of common mitochondrial variants and cognitive ability

artículo científico publicado en 2009

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

scientific article published on 09 October 2020

Bayesian reassessment of the epigenetic architecture of complex traits

artículo científico publicado en 2020

Bone density in sheep: genetic variation and quantitative trait loci localisation.

artículo científico publicado en 2003

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

artículo científico publicado en 2020

Childhood intelligence attenuates the association between biological ageing and health outcomes in later life

scientific article published on 28 November 2019

Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder

artículo científico publicado en 2011

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

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

artículo científico publicado en 2009

Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep

article

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

Correction: GWAS on family history of Alzheimer's disease.

artículo científico publicado en 2019

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

artículo científico publicado en 2017

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

article published in 2018

DNA methylation profiles in monozygotic and dizygotic twins.

artículo científico publicado en 2009

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

artículo científico publicado en 2016

DNA methylation-based measures of biological age: meta-analysis predicting time to death

artículo científico publicado en 2016

Development of a linkage map and mapping of phenotypic polymorphisms in a free-living population of Soay sheep (Ovis aries)

artículo científico publicado en 2006

Divergence between human populations estimated from linkage disequilibrium

artículo científico publicado en 2008

Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies

artículo científico publicado en 2017

Epigenetic Signatures of Cigarette Smoking

artículo científico publicado en 2016

Epigenetic prediction of complex traits and death

article by Daniel L McCartney et al published 27 September 2018 in Genome Biology

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With <i>KLF9</i> and <i>DOT1L</i>

artículo científico publicado en 2021

Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

scientific article published on 06 December 2019

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

article

Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait

scientific article published on 30 April 2019

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

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 of epigenetic aging rates in blood reveals a critical role for TERT.

artículo científico publicado en 2018

GWAS on family history of Alzheimer's disease

artículo científico publicado en 2018

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

artículo científico publicado en 2011

Genetic influences on life span and its relationship to personality: a 16-year follow-up study of a sample of aging twins

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Genome-wide average DNA methylation is determined in utero

artículo científico publicado en 2018

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

artículo científico publicado en 2021

Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank

scientific article published on 14 August 2019

Geographical structure and differential natural selection among North European populations

scientific article published on 05 March 2009

Horn type and horn length genes map to the same chromosomal region in Soay sheep

artículo científico publicado en 2009

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

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

artículo científico publicado en 2018

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

scientific article published on 23 August 2019

Meta-analysis of epigenome-wide association studies of cognitive abilities

artículo científico publicado en 2018

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

artículo científico publicado en 2021

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

artículo científico publicado el 17 de febrero de 2013

Power and SNP tagging in whole mitochondrial genome association studies

artículo científico publicado en 2008

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

scientific article published on 28 April 2020

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

retracted scholarly article

Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines.

artículo científico

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture

scientific article published on 23 September 2020

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

artículo científico

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

artículo científico publicado en 2012

The epigenetic clock and telomere length are independently associated with chronological age and mortality

artículo científico publicado en 2016

The epigenetic clock and telomere length are independently associated with chronological age and mortality

artículo científico publicado en 2017

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

Trajectories of inflammatory biomarkers over the eighth decade and their associations with immune cell profiles and epigenetic ageing

article by Anna J Stevenson et al published 20 December 2018 in Clinical epigenetics

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

artículo científico publicado en 2008

Lista de obras de Allan F McRae

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

A Localized Negative Genetic Correlation Constrains Microevolution of Coat Color in Wild Sheep

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

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

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

A simple linear regression method for quantitative trait loci linkage analysis with censored observations

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

An epigenetic score for BMI based on DNA methylation correlates with poor physical health and major disease in the Lothian Birth Cohort

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

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

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Association study of common mitochondrial variants and cognitive ability

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

Bayesian reassessment of the epigenetic architecture of complex traits

Bone density in sheep: genetic variation and quantitative trait loci localisation.

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

Childhood intelligence attenuates the association between biological ageing and health outcomes in later life

Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

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

Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Correction: GWAS on family history of Alzheimer's disease.

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

DNA methylation profiles in monozygotic and dizygotic twins.

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

DNA methylation-based measures of biological age: meta-analysis predicting time to death

Development of a linkage map and mapping of phenotypic polymorphisms in a free-living population of Soay sheep (Ovis aries)

Divergence between human populations estimated from linkage disequilibrium

Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies

Epigenetic Signatures of Cigarette Smoking

Epigenetic prediction of complex traits and death

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With <i>KLF9</i> and <i>DOT1L</i>

Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

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

Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait

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

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

GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

GWAS on family history of Alzheimer's disease

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

Genetic influences on life span and its relationship to personality: a 16-year follow-up study of a sample of aging twins

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

Genome-wide average DNA methylation is determined in utero

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

Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank

Geographical structure and differential natural selection among North European populations

Horn type and horn length genes map to the same chromosomal region in Soay sheep

Identification of 55,000 Replicated DNA Methylation QTL

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

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

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

Meta-analysis of epigenome-wide association studies of cognitive abilities

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

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

Power and SNP tagging in whole mitochondrial genome association studies

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

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

Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines.

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture

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

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

The epigenetic clock and telomere length are independently associated with chronological age and mortality

The epigenetic clock and telomere length are independently associated with chronological age and mortality

The transcriptional landscape of age in human peripheral blood

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

Trajectories of inflammatory biomarkers over the eighth decade and their associations with immune cell profiles and epigenetic ageing

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