T
Tatyana Krasnov
Researcher at Rabin Medical Center
Publications - 14
Citations - 522
Tatyana Krasnov is an academic researcher from Rabin Medical Center. The author has contributed to research in topics: Congenital Neutropenia & Medicine. The author has an hindex of 7, co-authored 9 publications receiving 471 citations. Previous affiliations of Tatyana Krasnov include Tel Aviv University.
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Journal ArticleDOI
CATSPER2, a human autosomal nonsyndromic male infertility gene
Nili Avidan,Hannah Tamary,Orly Dgany,Orly Dgany,Daniel Cattan,Alexandre Pariente,Michel Thulliez,N. Borot,Lucien Moati,Alain Barthelme,Lea Shalmon,Lea Shalmon,Tatyana Krasnov,Tatyana Krasnov,Edna Ben-Asher,Tsvyia Olender,Miriam Khen,Issac Yaniv,Rina Zaizov,Hanna Shalev,Jean Delaunay,Marc Fellous,Doron Lancet,Jacques S. Beckmann +23 more
TL;DR: To the best of the knowledge, the involvement of CATSPER2 in asthenoteratozoospermia is the first description of a human autosomal gene defect associated with nonsyndromic male infertility.
Journal ArticleDOI
Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1
Orly Dgany,Orly Dgany,Nili Avidan,Jean Delaunay,Tatyana Krasnov,Tatyana Krasnov,Lea Shalmon,Lea Shalmon,Hanna Shalev,Tal Eidelitz-Markus,Joseph Kapelushnik,Daniel Cattan,Alexandre Pariente,Michel Tulliez,Aurore Crétien,Pierre-Olivier Schischmanoff,Achille Iolascon,Eithan Fibach,Ariel Koren,Jochen Rössler,Martine Le Merrer,I Yaniv,Rina Zaizov,Edna Ben-Asher,Tsvyia Olender,Doron Lancet,Jacques S. Beckmann,Hannah Tamary,Hannah Tamary +28 more
TL;DR: These findings, and the cellular phenotype, suggest that codanin-1 may be involved in nuclear envelope integrity, conceivably related to microtubule attachments, as well as underlies normal erythropoiesis.
Journal ArticleDOI
High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis.
Hannah Tamary,Shraga Aviner,Enrique Freud,Hagit Miskin,Tatyana Krasnov,Michael Schwarz,Isaac Yaniv +6 more
TL;DR: Early cholelithiasis was detected in children and young adults with HS and the authors recommend early annual biliary ultrasonography in HS children, starting at about 4 years of age.
Journal ArticleDOI
Clinical and molecular variability in congenital dyserythropoietic anaemia type I
Hannah Tamary,Orly Dgany,Alexis Proust,Tatyana Krasnov,Nili Avidan,Tal Eidelitz-Markus,Gil Tchernia,David Geneviève,Valérie Cormier-Daire,Brigitte Bader-Meunier,Corinne Ferrero-Vacher,Martine Munzer,Ralph A. Gruppo,Eithan Fibach,Osnat Konen,Isaac Yaniv,Jean Delaunay +16 more
TL;DR: No correlation could be established between the expected levels of codanin‐1 or the nature of the mutation and the severity of the clinical manifestations in most patients studied, but six novel mutations in the CDAN1 gene were identified and five single nucleotide polymorphisms previously unreported in the literature or the SNP database were identified.
Journal ArticleDOI
A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I.
TL;DR: The results confirm the authors' previous findings and add neonatal manifestations not previously described, particularly hyperbilirubinemia and thrombocytopenia, to early diagnosis of CDA type I.