Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma
Bonilla, Ximena, Parmentier, Laurent, King, Bryan, Bezrukov, Fedor, Kaya, Gürkan, Zoete, Vincent, Seplyarskiy, Vladimir B, Sharpe, Hayley J, McKee, Thomas, Letourneau, Audrey, Ribaux, Pascale G, Popadin, Konstantin, Basset-Seguin, Nicole, Chaabene, Rouaa Ben, Santoni, Federico A, Andrianova, Maria A, Guipponi, Michel, Garieri, Marco, Verdan, Carole, Grosdemange, Kerstin, Sumara, Olga, Eilers, Martin, Aifantis, Iannis, Michielin, Olivier, de Sauvage, Frederic J, Antonarakis, Stylianos E, Nikolaev, Sergey I
Published in Nature genetics (01.04.2016)
Published in Nature genetics (01.04.2016)
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Five latent factors underlie response to immunotherapy
Usset, Joseph, Rosendahl Huber, Axel, Andrianova, Maria A., Batlle, Eduard, Carles, Joan, Cuppen, Edwin, Elez, Elena, Felip, Enriqueta, Gómez-Rey, Marina, Lo Giacco, Deborah, Martinez-Jimenez, Francisco, Muñoz-Couselo, Eva, Siu, Lillian L., Tabernero, Josep, Vivancos, Ana, Muiños, Ferran, Gonzalez-Perez, Abel, Lopez-Bigas, Nuria
Published in Nature genetics (12.09.2024)
Published in Nature genetics (12.09.2024)
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APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context
Seplyarskiy, Vladimir B, Andrianova, Maria A, Bazykin, Georgii A
Published in Genome research (01.02.2017)
Published in Genome research (01.02.2017)
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Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells
Andrianova, Maria A, Seplyarskiy, Vladimir B, Terradas, Mariona, Sánchez-Heras, Ana Beatriz, Mur, Pilar, Soto, José Luis, Aiza, Gemma, Borràs, Emma, Kondrashov, Fyodor A, Kondrashov, Alexey S, Bazykin, Georgii A, Valle, Laura
Published in European journal of human genetics : EJHG (01.07.2024)
Published in European journal of human genetics : EJHG (01.07.2024)
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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
Andrianova, Maria A, Chetan, Ghati Kasturirangan, Sibin, Madathan Kandi, Mckee, Thomas, Merkler, Doron, Narasinga, Rao KVL, Ribaux, Pascale, Blouin, Jean‐Louis, Makrythanasis, Periklis, Seplyarskiy, Vladimir B, Antonarakis, Stylianos E, Nikolaev, Sergey I
Published in The Journal of pathology (01.11.2017)
Published in The Journal of pathology (01.11.2017)
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Provider risks connected with uncertainty in the legal nature of online games’ terms of use
Andrianova, Maria A., Vlasenko, Ellina V.
Published in T͡S︡ifrovoe pravo (Moscow, Russia) (03.11.2020)
Published in T͡S︡ifrovoe pravo (Moscow, Russia) (03.11.2020)
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Are Nonsense Alleles of Drosophila melanogaster Genes under Any Selection?
Potapova, Nadezhda A, Andrianova, Maria A, Bazykin, Georgii A, Kondrashov, Alexey S
Published in Genome biology and evolution (01.04.2018)
Published in Genome biology and evolution (01.04.2018)
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Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations
Seplyarskiy, Vladimir B., Akkuratov, Evgeny E., Akkuratova, Natalia, Andrianova, Maria A., Nikolaev, Sergey I., Bazykin, Georgii A., Adameyko, Igor, Sunyaev, Shamil R.
Published in Nature genetics (01.01.2019)
Published in Nature genetics (01.01.2019)
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Journal Article
Error-prone bypass of DNA lesions during lagging strand replication is a common source of germline and cancer mutations
Seplyarskiy, Vladimir, Akkuratov, Evgeny E, Akkuratova, Natalia V, Andrianova, Maria A, Nikolaev, Sergey I, Bazykin, Georgii A, Adameyko, Igor, Sunyaev, Shamil R
Published in bioRxiv (26.05.2018)
Published in bioRxiv (26.05.2018)
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