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Keys for community dialogue: Preparing ethnically mixed cities in Israel for addressing conflictual overlap of cultural holidays

Conflict resolution quarterly, 2022, Vol.40 (1), p.45-59

Shemer, Orna

2022

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Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

British journal of haematology, 2020-09, Vol.190 (6), p.909-915

2020

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Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE‐related immune thrombocytopenia

Pediatric blood & cancer, 2024-05, Vol.71 (5), p.e30911-n/a

2024

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Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series

Pediatric blood & cancer, 2022-10, Vol.69 (10), p.e29902-n/a

2022

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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, 2021-05, Vol.193 (3), p.570-580

2021

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Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene

Pediatric blood & cancer, 2020-06, Vol.67 (6), p.e28237-n/a

2020

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

British journal of haematology, 2024-03, Vol.204 (3), p.1067-1071

2024

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Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome

Pediatric blood & cancer, 2021-10, Vol.68 (10), p.e29138-n/a

2021

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Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

European journal of haematology, 2024-08, Vol.113 (2), p.146-162

2024

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Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias

European journal of haematology, 2018-09, Vol.101 (3), p.297-304

2018

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Essential thrombocythemia A retrospective case series

Pediatric blood & cancer, 2020-05, Vol.67 (5), p.e28183-n/a

2020

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Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (20), p.5241-5246

2018

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Evaluating platelet function disorders in children with bleeding tendency - A single center study

Platelets (Edinburgh), 2017-10, Vol.28 (7), p.676-681

2017

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Keys for community dialogue: Preparing ethnically mixed cities in I srael for addressing conflictual overlap of cultural holidays

Conflict resolution quarterly, 2022-09, Vol.40 (1), p.45-59

Shemer, Orna

2022

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

Haematologica (Roma), 2020-07, Vol.105 (7), p.1825-1834

2020

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

Haematologica (Roma), 2022-09, Vol.107 (9), p.2081-2095

2022

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Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Cell stem cell, 2016-01, Vol.18 (1), p.73-78

2016

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Community Agency as Infrastructure for Cultural Responsiveness: Learning from the Success of a Socially Excluded Community of Mountain Jews

Journal of international migration and integration, 2024-03, Vol.25 (1), p.443-463

2024

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

Platelets (Edinburgh), 2022-05, Vol.33 (4), p.645-648

2022

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Cdan1 Is Essential for Primitive Erythropoiesis

Frontiers in physiology, 2021-06, Vol.12, p.685242-685242

2021

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Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear

Blood, 2018-06, Vol.131 (24), p.2737-2737

2018

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Is less more? Intravenous immunoglobulin for pediatric immune thrombocytopenia

Therapeutic advances in hematology, 2024, Vol.15, p.20406207241279202

2024

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The outsider within: The agentic practices of Family Group Conference coordinators in the context of families with children at risk

Child & family social work, 2024-05, Vol.29 (2), p.560-570

2024

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Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias

Molecular diagnosis & therapy, 2020-08, Vol.24 (4), p.397-407

2020

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Bringing in the third wheel: A pilot study on the triadic encounter of social workers, immigrants, and community interpreters in Israel

International journal of intercultural relations, 2022-01, Vol.86, p.64-73

2022

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Keys for community dialogue: Preparing ethnically mixed cities in Israel for addressing conflictual overlap of cultural holidays

Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE‐related immune thrombocytopenia

Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series

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

Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene

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

Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias

Essential thrombocythemia A retrospective case series

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

Evaluating platelet function disorders in children with bleeding tendency - A single center study

Keys for community dialogue: Preparing ethnically mixed cities in I srael for addressing conflictual overlap of cultural holidays

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

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

Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Community Agency as Infrastructure for Cultural Responsiveness: Learning from the Success of a Socially Excluded Community of Mountain Jews

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

Cdan1 Is Essential for Primitive Erythropoiesis

Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear

Is less more? Intravenous immunoglobulin for pediatric immune thrombocytopenia

The outsider within: The agentic practices of Family Group Conference coordinators in the context of families with children at risk

Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias

Bringing in the third wheel: A pilot study on the triadic encounter of social workers, immigrants, and community interpreters in Israel

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