H
Hannah Tamary
Researcher at Tel Aviv University
Publications - 154
Citations - 5146
Hannah Tamary is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Congenital dyserythropoietic anemia type I & Anemia. The author has an hindex of 34, co-authored 145 publications receiving 4487 citations. Previous affiliations of Hannah Tamary include Yale University & Rabin Medical Center.
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Journal ArticleDOI
Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
Jérôme Feldmann,Isabelle Callebaut,Graça Raposo,Stéphanie Certain,Delphine Bacq,Cécile Dumont,Nathalie Lambert,Marie Ouachée-Chardin,Gaëlle Chédeville,Hannah Tamary,Véronique Minard-Colin,Etienne Vilmer,Stéphane Blanche,Françoise Le Deist,Alain Fischer,Geneviève de Saint Basile +15 more
TL;DR: In this article, the locus of a perforin (+) FHL subtype (FHL3), observed in 10 patients, was mapped to 17q25. This region contains hMunc13-4, a member of the Munc13 family of proteins involved in vesicle priming.
Journal ArticleDOI
A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia
Lionel Arnaud,Carole Saison,Virginie Helias,Nicole Lucien,Dominique Steschenko,Marie-Catherine Giarratana,Claude Préhu,Bernard Foliguet,Lory Montout,Alexandre G. de Brevern,Alain Francina,Pierre Ripoche,Odile Fenneteau,Lydie Da Costa,T. Peyrard,Gail Coghlan,Niels Ove Illum,Henrik Birgens,Hannah Tamary,Achille Iolascon,Jean Delaunay,Gil Tchernia,Jean-Pierre Cartron +22 more
TL;DR: The study of this disease-causing mutation in KLF1 provides further insights into the roles of this transcription factor during erythropoiesis in humans.
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
Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.
Anna Marrone,Amanda J. Walne,Hannah Tamary,Yuka Masunari,Michael Kirwan,Richard Beswick,Tom Vulliamy,Inderjeet Dokal +7 more
TL;DR: It is demonstrated that homozygous TERT mutations, resulting in a pure but severe telomerase deficiency, produce a phenotype of classical AR-DC and its severe variant, the HH syndrome.
Journal ArticleDOI
Rivaroxaban compared with standard anticoagulants for the treatment of acute venous thromboembolism in children: a randomised, controlled, phase 3 trial
Christoph Male,Anthonie W. A. Lensing,Joseph S. Palumbo,Joseph S. Palumbo,Riten Kumar,Ildar Nurmeev,Kerry Hege,Damien Bonnet,Philip Connor,Helene L. Hooimeijer,Marcela Torres,Anthony K.C. Chan,Gili Kenet,Susanne Holzhauer,Amparo Santamaría,Pascal Amedro,Elizabeth Chalmers,Paolo Simioni,Rukhmi Bhat,Donald L. Yee,Olga Lvova,Jan Beyer-Westendorf,Tina T. Biss,Ida Martinelli,Paola Saracco,Marjolein Peters,Krisztián Kállay,Cynthia Gauger,M. Patricia Massicotte,Guy Young,Akos F. Pap,Madhurima Majumder,William T. Smith,Jürgen F. Heubach,Scott D. Berkowitz,Kirstin Thelen,Dagmar Kubitza,Mark Crowther,Martin H. Prins,Paul Monagle,Angelo Claudio Molinari,Ulrike Nowak Göttl,Juan Chain,Jeremy D. Robertson,Katharina Thom,Werner Streif,Rudolf Schwarz,Klaus Schmitt,Gernot Grangl,An Van Damme,Philip Maes,Veerle Labarque,Antonio Petrilli,Sandra Loggeto,Estela Azeka,Leonardo R. Brandão,Doan Le,Christine Sabapathy,Paola Giordano,Runhui Wu,Jie Ding,Wenyan Huang,Jianhua Mao,Päivi Lähteenmäki,Stephane Decramer,Toralf Bernig,Martin Chada,Godfrey Chan,Krisztian Kally,Beatrice Nolan,Shoshana Revel-Vilk,Hannah Tamary,Carina Levin,Daniela Tormene,Maria Abbattista,Andrea Artoni,Takanari Ikeyama,Ryo Inuzuka,Satoshi Yasukochi,Michelle Morales Soto,Karina A Solis Labastida,Monique H Suijker,Marike Bartels,Rienk Y Tamminga,C. Heleen van Ommen,D. Maroeska Te Loo,Rui Anjos,Lyudmila Zubarovskaya,Natalia Popova,Elena Samochatova,Margarita Belogurova,Pavel Svirin,Tatiana Shutova,Vladimir Lebedev,Olga Barbarash,Pei L Koh,Joyce C Mei,Ludmila Podracka,Rubén Berrueco,Maria F Fernandez,Tony Frisk,Sebastian Grunt,Johannes Rischewski,Manuela Albisetti-Pedroni,Ali Antmen,Hüseyin Tokgöz,Zeynep Karakas,Jayashree Motwani,Michael D. Williams,John D. Grainger,Jeanette Payne,Mike Richards,Susan Baird,Neha Bhatnagar,Angela Aramburo,Shelley Crary,Tung Wynn,Shannon Carpenter,Sanjay Ahuja,Neil A. Goldenberg,Gary M. Woods,Kamar Godder,Ajovi Scott-Emuakpor,Gavin Roach,Leslie Raffini,Nirmish Shah,Sanjay J. Shah,Courtney D. Thornburg,Ayesha Zia,Roger Berkow +129 more
TL;DR: Treatment with rivaroxaban resulted in a similarly low recurrence risk and reduced thrombotic burden without increased bleeding, as compared with standard anticoagulants in children with acute venous thromboembolism.