Lista de obras - Adam Auton - Dominio Público Uruguay

A Pedigree-Based Map of Recombination in the Domestic Dog Genome

artículo científico publicado en 2016

A common sequence motif associated with recombination hot spots and genome instability in humans

A fine-scale chimpanzee genetic map from population sequencing

artículo científico publicado en 2012

A global reference for human genetic variation

artículo científico publicado en 2015

A map of human genome variation from population-scale sequencing ⬇️

artículo científico publicado el 28 de octubre de 2010

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

A simple genetic architecture underlies morphological variation in dogs

artículo científico publicado en 2010

Age-related somatic mutations in the cancer genome

artículo científico publicado en 2015

An integrated map of genetic variation from 1,092 human genomes

artículo científico publicado en 2012

An integrated map of structural variation in 2,504 human genomes

artículo científico publicado en 2015

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

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

Australin: a chromosomal passenger protein required specifically for Drosophila melanogaster male meiosis

artículo científico publicado en 2008

Author Correction: Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

scientific article published on 26 March 2020

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

artículo científico publicado en 2020

Bayesian refinement of association signals for 14 loci in 3 common diseases

artículo científico publicado en 2012

Biased Gene Conversion and Its Impact on Genome Evolution

article

Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder

artículo científico publicado en 2014

Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population

artículo científico publicado en 2019

Classic selective sweeps were rare in recent human evolution

artículo científico publicado en 2011

Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations

artículo científico publicado en 2010

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Complex population structure in African village dogs and its implications for inferring dog domestication history

artículo científico publicado en 2009

Correction: Inferring Human Colonization History Using a Copying Model.

artículo científico publicado en 2008

Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq

artículo científico publicado en 2018

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes.

artículo científico publicado en 2013

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

artículo científico publicado en 2013

Erratum: Genes mirror geography within Europe

scientific article published in Nature

Escape from crossover interference increases with maternal age.

artículo científico publicado en 2015

Estimating recombination rates from genetic variation in humans

artículo científico

Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes

artículo científico publicado en 2017

False Negatives Are a Significant Feature of Next Generation Sequencing Callsets

Genes mirror geography within Europe

artículo científico publicado en 2008

Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population

artículo científico publicado en 2015

Genetic predisposition to mosaic Y chromosome loss in blood

scientific article published on 20 November 2019

Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

Genetic recombination is targeted towards gene promoter regions in dogs.

artículo científico publicado en 2013

Genome studies must account for history-Response

artículo científico publicado en 2019

Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication

artículo científico publicado en 2010

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

artículo científico publicado en 2019

Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

scientific article published on 28 February 2020

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 of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

scientific article published on 28 August 2019

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

artículo científico publicado en 2007

Genome-wide patterns of genetic variation in worldwide Arabidopsis thaliana accessions from the RegMap panel

artículo científico publicado en 2012

Genome-wide patterns of population structure and admixture in West Africans and African Americans

artículo científico publicado en 2010

Global distribution of genomic diversity underscores rich complex history of continental human populations

artículo científico publicado en 2009

Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

artículo científico publicado en 2014

Inferring human colonization history using a copying model

artículo científico publicado en 2008

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

artículo científico publicado en 2019

Mobile elements drive recombination hotspots in the core genome of Staphylococcus aureus.

artículo científico publicado en 2014

Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder

artículo científico publicado en 2014

Multiple instances of ancient balancing selection shared between humans and chimpanzees

artículo científico publicado en 2013

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

artículo científico publicado en 2012

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

artículo científico publicado en 2016

Recombination rate estimation in the presence of hotspots

artículo científico publicado en 2007

Refined genetic maps reveal sexual dimorphism in human meiotic recombination at multiple scales

artículo científico publicado en 2017

The estimation of recombination rates from population genetic data ⬇️

doctoral thesis by Adam Auton

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24 ⬇️

artículo científico publicado el 25 de enero de 2012

Tracking genes and finding mutations: finding genes for complex traits in the domestic dog (Canis familiaris).

artículo científico publicado en 2010

Lista de obras de Adam Auton

A Pedigree-Based Map of Recombination in the Domestic Dog Genome

A common sequence motif associated with recombination hot spots and genome instability in humans

A fine-scale chimpanzee genetic map from population sequencing

A global reference for human genetic variation

A map of human genome variation from population-scale sequencing ⬇️

A second generation human haplotype map of over 3.1 million SNPs

A simple genetic architecture underlies morphological variation in dogs

Age-related somatic mutations in the cancer genome

An integrated map of genetic variation from 1,092 human genomes

An integrated map of structural variation in 2,504 human genomes

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

Australin: a chromosomal passenger protein required specifically for Drosophila melanogaster male meiosis

Author Correction: Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

Bayesian refinement of association signals for 14 loci in 3 common diseases

Biased Gene Conversion and Its Impact on Genome Evolution

Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder

Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population

Classic selective sweeps were rare in recent human evolution

Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Complex population structure in African village dogs and its implications for inferring dog domestication history

Correction: Inferring Human Colonization History Using a Copying Model.

Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

Erratum: Genes mirror geography within Europe

Escape from crossover interference increases with maternal age.

Estimating recombination rates from genetic variation in humans

Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes

False Negatives Are a Significant Feature of Next Generation Sequencing Callsets

Genes mirror geography within Europe

Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population

Genetic predisposition to mosaic Y chromosome loss in blood

Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

Genetic recombination is targeted towards gene promoter regions in dogs.

Genome studies must account for history-Response

Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication

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

Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

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

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

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

Genome-wide patterns of genetic variation in worldwide Arabidopsis thaliana accessions from the RegMap panel

Genome-wide patterns of population structure and admixture in West Africans and African Americans

Global distribution of genomic diversity underscores rich complex history of continental human populations

Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

Inferring human colonization history using a copying model

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

Mobile elements drive recombination hotspots in the core genome of Staphylococcus aureus.

Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder

Multiple instances of ancient balancing selection shared between humans and chimpanzees

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

Recombination rate estimation in the presence of hotspots

Refined genetic maps reveal sexual dimorphism in human meiotic recombination at multiple scales

The estimation of recombination rates from population genetic data ⬇️

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24 ⬇️

Tracking genes and finding mutations: finding genes for complex traits in the domestic dog (Canis familiaris).