Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma X Bonilla, L Parmentier, B King, F Bezrukov, G Kaya, V Zoete, ... Nature genetics 48 (4), 398-406, 2016 | 450 | 2016 |
APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication VB Seplyarskiy, RA Soldatov, KY Popadin, SE Antonarakis, GA Bazykin, ... Genome research 26 (2), 174-182, 2016 | 187 | 2016 |
Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence JM Goldmann, VB Seplyarskiy, WSW Wong, T Vilboux, PB Neerincx, ... Nature genetics 50 (4), 487-492, 2018 | 83 | 2018 |
Population sequencing data reveal a compendium of mutational processes in the human germ line VB Seplyarskiy, RA Soldatov, E Koch, RJ McGinty, JM Goldmann, ... Science 373 (6558), 1030-1035, 2021 | 53 | 2021 |
Gene age predicts the strength of purifying selection acting on gene expression variation in humans KY Popadin, M Gutierrez-Arcelus, T Lappalainen, A Buil, J Steinberg, ... The American Journal of Human Genetics 95 (6), 660-674, 2014 | 45 | 2014 |
Human mismatch repair system balances mutation rates between strands by removing more mismatches from the lagging strand MA Andrianova, GA Bazykin, SI Nikolaev, VB Seplyarskiy Genome research 27 (8), 1336-1343, 2017 | 44 | 2017 |
Heterogeneity of the Transition/Transversion Ratio in Drosophila and Hominidae Genomes VB Seplyarskiy, P Kharchenko, AS Kondrashov, GA Bazykin Molecular biology and evolution 29 (8), 1943-1955, 2012 | 41 | 2012 |
Extraordinary genetic diversity in a wood decay mushroom MA Baranova, MD Logacheva, AA Penin, VB Seplyarskiy, YY Safonova, ... Molecular biology and evolution 32 (10), 2775-2783, 2015 | 40 | 2015 |
Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations VB Seplyarskiy, EE Akkuratov, N Akkuratova, MA Andrianova, SI Nikolaev, ... Nature genetics 51 (1), 36-41, 2019 | 38 | 2019 |
Evolution of local mutation rate and its determinants NV Terekhanova, VB Seplyarskiy, RA Soldatov, GA Bazykin Molecular biology and evolution 34 (5), 1100-1109, 2017 | 36 | 2017 |
The origin of human mutation in light of genomic data VB Seplyarskiy, S Sunyaev Nature Reviews Genetics 22 (10), 672-686, 2021 | 34 | 2021 |
Prevalence of Multinucleotide Replacements in Evolution of Primates and Drosophila NV Terekhanova, GA Bazykin, A Neverov, AS Kondrashov, ... Molecular biology and evolution 30 (6), 1315-1325, 2013 | 29 | 2013 |
APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context VB Seplyarskiy, MA Andrianova, GA Bazykin Genome research 27 (2), 175-184, 2017 | 24 | 2017 |
Polymerase ζ activity is linked to replication timing in humans: evidence from mutational signatures VB Seplyarskiy, GA Bazykin, RA Soldatov Molecular Biology and Evolution 32 (12), 3158-3172, 2015 | 21 | 2015 |
Crossing-over in a hypervariable species preferentially occurs in regions of high local similarity VB Seplyarskiy, MD Logacheva, AA Penin, MA Baranova, EV Leushkin, ... Molecular biology and evolution 31 (11), 3016-3025, 2014 | 18 | 2014 |
Human genome meeting 2016: houston, TX, USA. 28 February-2 March 2016 AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ... Human genomics 10, 1-40, 2016 | 17 | 2016 |
Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain … MA Andrianova, GK Chetan, MK Sibin, T Mckee, D Merkler, ... The Journal of pathology 243 (3), 331-341, 2017 | 16 | 2017 |
A mutation rate model at the basepair resolution identifies the mutagenic effect of Polymerase III transcription V Seplyarskiy, EM Koch, DJ Lee, JS Lichtman, HH Luan, SR Sunyaev Nature Genetics 55 (12), 2235-2242, 2023 | 9 | 2023 |
Extended family with germline pathogenic variant in polymerase delta provides strong evidence for recessive effect of proofreading inactivation MA Andrianova, VB Seplyarskiy, M Terradas, AB Sánchez-Heras, P Mur, ... bioRxiv, 2022.07. 20.500591, 2022 | 4 | 2022 |
Enrichment of somatic mutations in schizophrenia brain targets prenatally active transcription factor bindings sites EA Maury, A Jones, V Seplyarskiy, C Rosenbluh, T Bae, Y Wang, ... bioRxiv, 2022.02. 23.481681, 2022 | 4 | 2022 |