Hannah Tamary - Concepedia

Author

Hannah Tamary

Schneider Children's Medical Center ORCID

Also Known As

Cynthia Stapornwongkul, H Tamary, H. TAMARY, H. Tamary, Hannah Tamary, Hannah Tamary,, Joanne Yacobovitch, Monika Szemkus, Tamary Hannah, Tamary, H

220

Publications

6.9K

Citations

H-Index

141

Concepts

All Affiliations

Schneider Children's Medical Center Tel Aviv University Rabin Medical Center Soroka Medical Center Sheba Medical Center

About

Hannah Tamary is an author at Schneider Children's Medical Center specializing in medicine, hematology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	49	3.5K
2	Health Sciences	10	10	538
3	Public Health	9	9	496
4	Allergy	2	2	77
5	Natural Sciences	1	1	19

Hannah Tamary

111

Publications

6.1K

Citations

H-Index

Page 1

	Year	Citations
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, Cell Is MutatedLymphoid NeoplasiaHematological MalignancyGranulocyteMedicine	2003	916
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, The Lancet Haematology Pulmonary EmbolismThrombosisVenous ThrombosisAcute Venous ThromboembolismHematology	2019	294
CATSPER2, a human autosomal nonsyndromic male infertility gene Nili Avidan, Hannah Tamary, Orly Dgany, European Journal of Human Genetics InfertilityAndrologyFertilityGeneticsMale Infertility	2003	206
Recommendations regarding splenectomy in hereditary hemolytic anemias Achille Iolascon, Immacolata Andolfo, Wilma Barcellini, Haematologica AnemiaImmunohematologyLaboratory HematologyExpert OpinionThalassemia Syndromes	2017	206
A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia Lionel Arnaud, Carole Saison, Virginie Helias, The American Journal of Human Genetics Transcriptional RegulationDevelopmental BiologyGenetic DisorderGeneticsInherited Metabolic Disease	2010	196
Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome Anna Marrone, Amanda J. Walne, Hannah Tamary, Blood Bone Marrow FailureMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2007	173
Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1 Orly Dgany, Nili Avidan, J. Delaunay, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseHematology	2002	166
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations Julian Thalhammer, Gerhard Kindle, Alexandra Nieters, Journal of Allergy and Clinical Immunology VaccinationPrimary ImmunodeficiencyMaternal ImmunizationInborn ErrorsAutoimmune Disease	2021	161
Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I Hannah Tamary, Hanna Shalev, Galit Perez‐Avraham, Blood	2008	139
How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel Philip S. Rosenberg, Hannah Tamary, Blanche P. Alter American Journal of Medical Genetics Part A	2011	132

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