V
Vladislav S Baranov
Researcher at Saint Petersburg State University
Publications - 143
Citations - 2219
Vladislav S Baranov is an academic researcher from Saint Petersburg State University. The author has contributed to research in topics: Population & SMA*. The author has an hindex of 19, co-authored 138 publications receiving 1968 citations. Previous affiliations of Vladislav S Baranov include Russian Academy & Kirov Military Medical Academy.
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Journal ArticleDOI
Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes
J. Claiborne Stephens,David Reich,David Goldstein,Hyoung Doo Shin,Michael W. Smith,Mary Carrington,Cheryl A. Winkler,Gavin A. Huttley,Rando Allikmets,Lynn M. Schriml,Bernard Gerrard,Michael Malasky,Maria D. Ramos,Susanne Morlot,Maria Tzetis,Carole Oddoux,Francesco S. di Giovine,Georgios Nasioulas,David Chandler,Michael Aseev,Matthew Hanson,Luba Kalaydjieva,Damjan Glavač,Paolo Gasparini,Emmanuel Kanavakis,Mireille Claustres,Marios Kambouris,Harry Ostrer,Gordon W. Duff,Vladislav S Baranov,Hiljar Sibul,Andres Metspalu,David Goldman,Nicholas G. Martin,David L. Duffy,Jörg Schmidtke,Xavier Estivill,Stephen J. O'Brien,Michael Dean +38 more
TL;DR: The geographic cline of CCR5-Delta32 frequencies and its recent emergence are consistent with a historic strong selective event, driving its frequency upward in ancestral Caucasian populations.
Journal ArticleDOI
Possible involvement of arylamine N-acetyltransferase 2, glutathione S-transferases M1 and T1 genes in the development of endometriosis
H. Baranova,Michel Canis,T. Ivaschenko,E. Albuisson,R. Bothorishvilli,Vladislav S Baranov,P. Malet,Maurice-Antoine Bruhat +7 more
TL;DR: The involvement of both NAT2 and GSTM1 detoxification system genes in the pathogenesis of endometriosis and the possible impact of NAT2 gene polymorphism in the development of different forms of this disease are suggested.
Journal ArticleDOI
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
Thilo Dörk,Milan Macek,F. Mekus,Burkhard Tümmler,J. Tzountzouris,Teresa Casals,Alice Krebsová,Monika Koudova,I. Sakmaryová,V. Vavrova,D. Zemková,E. Ginter,N.V. Petrova,T. Ivaschenko,Vladislav S Baranov,M. Witt,A. Pogorzelski,Jerzy Bal,C. Zékanowsky,K. Wagner,Manfred Stuhrmann,I. Bauer,Hans H. Seydewitz,Thomas Neumann,S. Jakubiczka,C. Kraus,B. Thamm,M. Nechiporenko,L. A. Livshits,N. Mosse,G. Tsukerman,Ludevit Kadasi,M. Ravnik-Glavač,Damjan Glavač,Radovan Komel,Katja Vouk,Vaidutis Kučinskas,Astrida Krumina,M. Teder,S. Kocheva,Georgi D. Efremov,Tuncer Onay,Betul Kirdar,G. Malone,Martin Schwarz,Z. Zhou,K.J. Friedman,Soukeyna Carles,Mireille Claustres,D. Bozon,C. Verlingue,Claude Férec,Maria Tzetis,Emmanuel Kanavakis,Harry Cuppens,Cristina Bombieri,Pier Franco Pignatti,Federica Sangiuolo,Albena Jordanova,Jelena Kusic,Dragica Radojkovic,Jadranka Sertić,Darko Richter,A. Stavljenić Rukavina,E. Bjorck,Birgitta Strandvik,H. Cardoso,M. Montgomery,B. Nakielna,D. Hughes,Xavier Estivill,Isabel Aznarez,E. Tullis,L.-C. Tsui,Julian Zielenski +74 more
TL;DR: It is concluded that the 21-kb deletion of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is a frequent and severe CF mutation in populations of Eastern- and Western-Slavic descent.
Journal ArticleDOI
Glutathione S-transferase M1 gene polymorphism and susceptibility to endometriosis in a French population
H. Baranova,R. Bothorishvilli,Michel Canis,E. Albuisson,S Perriot,E. Glowaczower,Maurice-Antoine Bruhat,Vladislav S Baranov,P. Malet +8 more
TL;DR: The unusually high frequency of homozygotes for the GSTM 1 gene deletion among patients with endometriosis suggests a possible contribution of environmental toxins in the pathogenesis of this disease due to the absence or low activity of GSTM1 enzyme.
Journal ArticleDOI
Proportion of the GSTM1 0/0 genotype in some Slavic populations and its correlation with cystic fibrosis and some multifactorial diseases.
Vladislav S Baranov,T. Ivaschenko,B. Bakay,M. V. Aseev,R. Belotserkovskaya,H. Baranova,Paul Malet,J. Perriot,P. Mouraire,V. N. Baskakov,G. A. Savitskyi,S. M. Gorbushin,S. I. Deyneka,E. Michnin,A. Barchuck,V. Vakharlovsky,G. Pavlov,V. I. Shilko,T. Guembitzkaya,L. Kovaleva +19 more
TL;DR: The notion that GSTM1 deletion should be considered as a convenient genetic marker for the early detection of groups at higher risk of many diseases caused by environmental and genetic factors, where manifestation depends on the lack of detoxification, is supported.