Tanya Krasnov

Rabin Medical Center — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index349citations27works0.32yr avg
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Research Topics

Blood disorders and treatments(8), Hemoglobinopathies and Related Disorders(7), Blood groups and transfusion(6), Immunodeficiency and Autoimmune Disorders(5), Erythrocyte Function and Pathophysiology(5)

Publications27 total

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis
Genes·2025Open Access
<i>Erratum to</i>: Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population
Haematologica·2025Open Access
A Variable Clinical Presentation of Hemoglobin City of Hope
Clinical Genetics·2024Open Access
Author response for "A Variable Clinical Presentation of Hemoglobin City of Hope"
2024
Clinical and Laboratory Characteristics of Pediatric Patients With <i>ACKR1/DARC</i>‐Associated Neutropenia
Pediatric Blood & Cancer·2024Open Access
Genetic backgrounds and clinical characteristics of congenital neutropenias in <scp>Israel</scp>
European Journal Of Haematology·2024· 2 citedOpen Access
Biallelic hypomorphic variants in <i>CAD</i> cause uridine‐responsive macrocytic anaemia with elevated haemoglobin‐A2
British Journal of Haematology·2023· 1 citedOpen Access
Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children
Haematologica·2022· 22 citedOpen Access
Congenital thrombocytopenia associated with a heterozygous variant in the <i>MEIS1</i> gene encoding a transcription factor essential for megakaryopoiesis
Platelets·2022· 3 citedOpen Access
Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias
British Journal of Haematology·2020· 12 citedOpen Access
Alpha-Thalassemia Carrier due to –α&lt;sup&gt;3.7&lt;/sup&gt; Deletion: Not So Silent
Acta Haematologica·2020· 11 cited
Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population
Haematologica·2019· 41 citedOpen Access
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)
Human Molecular Genetics·2018· 53 citedOpen Access
Endoscopic findings and esophageal cancer incidence among Fanconi Anemia patients participating in an endoscopic surveillance program
Digestive and Liver Disease·2018· 15 cited
Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias
European Journal Of Haematology·2018· 40 cited
Characterization and Genotype-Phenotype Correlation of Fanconi Anemia Patients in Israel
Blood·2017
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis
European Journal Of Haematology·2017· 10 cited
Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia
Molecular Case Studies·2017· 17 citedOpen Access
Molecular diagnosis of α‐thalassemia in a multiethnic population
European Journal Of Haematology·2017· 23 cited
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis
Journal of Pediatric Hematology/Oncology·2016· 16 citedOpen Access
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Frequent Co-authors

Hannah Tamary(27), Orly Dgany(25), Joanne Yacobovich(18), Sharon Noy‐Lotan(18), Orna Steinberg‐Shemer(15), Oded Gilad(12), Tracie Goldberg(7), Carina Levin(7), Hagit Miskin(7), Amir A. Kuperman(6), Shai Izraeli(6), Ariel Koren(5), Joseph Kapelushnik(5), Dafna Brik Simon(5), Shoshana Revel‐Vilk(4), Tal Ben‐Ami(4), Hanna Shalev(3), Amos Toren(3), Ayelet Ben‐Barak(3), Ayelet Ben Barak(3)