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The origin of human mutation in light of genomic data

Nature reviews. Genetics, 2021-10, Vol.22 (10), p.672

2021

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Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma

Nature genetics, 2016-04, Vol.48 (4), p.398-406

2016

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APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication

Genome research, 2016-02, Vol.26 (2), p.174

2016

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Extraordinary Genetic Diversity in a Wood Decay Mushroom

Molecular biology and evolution, 2015-10, Vol.32 (10), p.2775-2783

2015

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Gene Age Predicts the Strength of Purifying Selection Acting on Gene Expression Variation in Humans

American journal of human genetics, 2014-12, Vol.95 (6), p.660-674

2014

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Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Nature genetics, 2018-04, Vol.50 (4), p.487-492

2018

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APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context

Genome research, 2017-02, Vol.27 (2), p.175

2017

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Evolution of Local Mutation Rate and Its Determinants

Molecular biology and evolution, 2017-05, Vol.34 (5), p.1100-1109

2017

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Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations

Nature genetics, 2019-01, Vol.51 (1), p.36-41

2019

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Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells

European journal of human genetics : EJHG, 2024-04, Vol.32 (7), p.837-845

2024

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Population sequencing data reveal a compendium of mutational processes in the human germ line

Science (American Association for the Advancement of Science), 2021-08, Vol.373 (6558), p.1030-1035

2021

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Polymerase ζ Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures

Molecular biology and evolution, 2015-12, Vol.32 (12), p.3158-3172

2015

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Publisher Correction: Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Nature genetics, 2021-08, Vol.53 (8), p.1270-1270

2021

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Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours

The Journal of pathology, 2017-11, Vol.243 (3), p.331-341

2017

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Prevalence of multinucleotide replacements in evolution of primates and Drosophila

Molecular biology and evolution, 2013-06, Vol.30 (6), p.1315-1325

2013

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Heterogeneity of the transition/transversion ratio in Drosophila and Hominidae genomes

Molecular biology and evolution, 2012-08, Vol.29 (8), p.1943-1955

2012

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Germline De Novo Mutation Clusters Arise During Oocyte Aging in Genomic Regions With High Double-Strand-Break Incidence

Obstetrical & gynecological survey, 2018-09, Vol.73 (9), p.531-532

2018

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Crossing-over in a hypervariable species preferentially occurs in regions of high local similarity

Molecular biology and evolution, 2014-11, Vol.31 (11), p.3016-3025

2014

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Prevalence of Multinucleotide Replacements in Evolution of Primates and Drosophila

Molecular biology and evolution, 2013-06, Vol.30 (6), p.1315-1325

2013

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Polymerase [Zeta] Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures

Molecular biology and evolution, 2015-12, Vol.32 (12), p.3158

2015

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Population sequencing data reveal a compendium of mutational processes in human germline

Science (American Association for the Advancement of Science), 2021-08, Vol.373 (6558), p.1030-1035

2021

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The origin of human mutation in light of genomic data

Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma

APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication

Extraordinary Genetic Diversity in a Wood Decay Mushroom

Gene Age Predicts the Strength of Purifying Selection Acting on Gene Expression Variation in Humans

Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context

Evolution of Local Mutation Rate and Its Determinants

Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations

Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells

Population sequencing data reveal a compendium of mutational processes in the human germ line

Polymerase ζ Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures

Publisher Correction: Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours

Prevalence of multinucleotide replacements in evolution of primates and Drosophila

Heterogeneity of the transition/transversion ratio in Drosophila and Hominidae genomes

Germline De Novo Mutation Clusters Arise During Oocyte Aging in Genomic Regions With High Double-Strand-Break Incidence

Crossing-over in a hypervariable species preferentially occurs in regions of high local similarity

Prevalence of Multinucleotide Replacements in Evolution of Primates and Drosophila

Polymerase [Zeta] Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures

Population sequencing data reveal a compendium of mutational processes in human germline

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