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Author Details

Chris Tyler-Smith
Wellcome Sanger Institute
1979
326
96
PMIDPaper TitleJournal TitlePublished Year
36635269HERC1 deficiency causes osteopenia through transcriptional program dysregulation during bone remodeling.Cell Death Dis2023
37612510Assembly of 43 human Y chromosomes reveals extensive complexity and variation.Nature2023
36635269HERC1 deficiency causes osteopenia through transcriptional program dysregulation during bone remodeling.Cell Death Dis2023
37500909Ghost admixture in eastern gorillas.Nat Ecol Evol2023
37612510Assembly of 43 human Y chromosomes reveals extensive complexity and variation.Nature2023
37500909Ghost admixture in eastern gorillas.Nat Ecol Evol2023
35962005Sequence analyses of Malaysian Indigenous communities reveal historical admixture between Hoabinhian hunter-gatherers and Neolithic farmers.Sci Rep2022
35962005Sequence analyses of Malaysian Indigenous communities reveal historical admixture between Hoabinhian hunter-gatherers and Neolithic farmers.Sci Rep2022
32666166A Southeast Asian origin for present-day non-African human Y chromosomes.Hum Genet2021
33740458The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects.Am J Hum Genet2021
33781384A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans.Elife2021
34352227The genomic history of the Middle East.Cell2021
33139852Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain.Eur J Hum Genet2021
32666166A Southeast Asian origin for present-day non-African human Y chromosomes.Hum Genet2021
34464968A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice.Mol Biol Evol2021
33740458The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects.Am J Hum Genet2021
33781384A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans.Elife2021
34464968A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice.Mol Biol Evol2021
34352227The genomic history of the Middle East.Cell2021
33139852Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain.Eur J Hum Genet2021
32531199Population Structure, Stratification, and Introgression of Human Structural Variation.Cell2020
32193295Insights into human genetic variation and population history from 929 diverse genomes.Science2020
32470374A Genetic History of the Near East from an aDNA Time Course Sampling Eight Points in the Past 4,000 Years.Am J Hum Genet2020
33092534Positive selection in admixed populations from Ethiopia.BMC Genet2020
32531199Population Structure, Stratification, and Introgression of Human Structural Variation.Cell2020
33092534Positive selection in admixed populations from Ethiopia.BMC Genet2020
32470374A Genetic History of the Near East from an aDNA Time Course Sampling Eight Points in the Past 4,000 Years.Am J Hum Genet2020
32193295Insights into human genetic variation and population history from 929 diverse genomes.Science2020
30581024Y Chromosome Sequences Reveal a Short Beringian Standstill, Rapid Expansion, and early Population structure of Native American Founders.Curr Biol2019
31675503Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.Cell2019
31610793Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome.Genome Biol2019
30581024Y Chromosome Sequences Reveal a Short Beringian Standstill, Rapid Expansion, and early Population structure of Native American Founders.Curr Biol2019
31116407How well do we understand the basis of classic selective sweeps in humans?FEBS Lett2019
31006515A Transient Pulse of Genetic Admixture from the Crusaders in the Near East Identified from Ancient Genome Sequences.Am J Hum Genet2019
31108506Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome.Hum Mol Genet2019
30890716Positive selection in Europeans and East-Asians at the ABCA12 gene.Sci Rep2019
31196864A Rare Deep-Rooting D0 African Y-Chromosomal Haplogroup and Its Implications for the Expansion of Modern Humans Out of Africa.Genetics2019
31675503Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.Cell2019
31610793Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome.Genome Biol2019
31196864A Rare Deep-Rooting D0 African Y-Chromosomal Haplogroup and Its Implications for the Expansion of Modern Humans Out of Africa.Genetics2019
30890716Positive selection in Europeans and East-Asians at the ABCA12 gene.Sci Rep2019
31006515A Transient Pulse of Genetic Admixture from the Crusaders in the Near East Identified from Ancient Genome Sequences.Am J Hum Genet2019
31116407How well do we understand the basis of classic selective sweeps in humans?FEBS Lett2019
31108506Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome.Hum Mol Genet2019
29343290FineMAV: prioritizing candidate genetic variants driving local adaptations in human populations.Genome Biol2018
29853687Ancient human parallel lineages within North America contributed to a coastal expansion.Science2018
29395077Response to Giem.Am J Hum Genet2018
29343290FineMAV: prioritizing candidate genetic variants driving local adaptations in human populations.Genome Biol2018
29209947Copy number variation arising from gene conversion on the human Y chromosome.Hum Genet2018
29738726Human Genetics: Busy Subway Networks in Remote Oceania?Curr Biol2018
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Collaborators

Wellcome Sanger Institute
Co-authored papers 23
Co-authored papers 18
University of Cambridge
Co-authored papers 12
Experimental Research Center, China Academy of Chinese Medical Sciences
Co-authored papers 11
Broad Institute of MIT and Harvard
Co-authored papers 11
University of Helsinki
Co-authored papers 10
4Wellcome Trust Sanger Institute
Co-authored papers 10
Co-authored papers 9
Lund University
Co-authored papers 8
Institute of Medical Genetics, Cardiff University
Co-authored papers 8
Wellcome Sanger Institute
Co-authored papers 8
Wellcome Sanger Institute
Co-authored papers 8
Co-authored papers 7
The Ohio State University
Co-authored papers 7
Department of Biology Earlham College Richmond Indiana USA.
Co-authored papers 7
The Hospital for Sick Children
Co-authored papers 7
Banaras Hindu University
Co-authored papers 7
Co-authored papers 7
Arizona State University
Co-authored papers 7
University of Utah
Co-authored papers 6
Co-authored papers 6
Big Data Institute, University of Oxford
Co-authored papers 6
University of Washington
Co-authored papers 6
University of Colorado Anschutz Medical Campus
Co-authored papers 5
Oklahoma State University
Co-authored papers 5
University of Hawaii at Hilo
Co-authored papers 5
University of Houston
Co-authored papers 5
University of Geneva
Co-authored papers 5
University of Wisconsin-Madison
Co-authored papers 5
Washington University School of Medicine
Co-authored papers 5