Suivre
Vladimir Seplyarskiy
Vladimir Seplyarskiy
Harvard Medical School
Adresse e-mail validée de bwh.harvard.edu
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Année
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
4452016
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
1872016
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
832018
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
522021
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
452014
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
442017
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
412012
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
402015
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
372019
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
362017
The origin of human mutation in light of genomic data
VB Seplyarskiy, S Sunyaev
Nature Reviews Genetics 22 (10), 672-686, 2021
312021
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
292013
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
242017
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
212015
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
182014
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
172016
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
152017
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
92023
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
42022
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
42022
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