Tanya Krasnov

Petah Tiqwa, M 49202, Israel

Last Updated: 09/26/2026

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Found 22 publications

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

Journal: Genes

Published: August 22, 2025

Erratum to: Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Erratum to: Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Journal: Haematologica

Published: January 01, 2025

A Variable Clinical Presentation of Hemoglobin City of Hope.

A Variable Clinical Presentation of Hemoglobin City of Hope.

Journal: Clinical genetics

Published: September 27, 2024

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Journal: Pediatric blood & cancer

Published: June 16, 2024

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Journal: European journal of haematology

Published: December 19, 2023

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Journal: British journal of haematology

Published: August 28, 2023

Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis.

Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis.

Journal: Platelets

Published: February 08, 2022

Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.

Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.

Journal: Haematologica

Published: September 30, 2021

Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.

Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.

Journal: British journal of haematology

Published: September 25, 2020

Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Journal: Haematologica

Published: March 27, 2019

Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent.

Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent.

Journal: Acta haematologica

Published: March 08, 2019

Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).

Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).

Journal: Human molecular genetics

Published: June 22, 2018

Showing 1-12 of 22

Last Updated: 09/26/2026