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Hrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, William S Stevenson, Neil V Morgan & David J Rabbolini. (2022) Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases. Platelets 33:8, pages 1107-1112.
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Ibrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, Kate Downes, Kathleen Freson, Joanne Mason, Paula Page, Kim Reay, Bethan Myers & Neil V Morgan. (2022) A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder. Platelets 33:2, pages 320-323.
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Verónica Palma-Barqueros, José María Bastida, María José López Andreo, Ana Zámora-Cánovas, Carlo Zaninetti, Juan Francisco Ruiz-Pividal, Natalia Bohdan, José Padilla, Raúl Teruel-Montoya, Ana Marín-Quilez, Nuria Revilla, Ana Sánchez-Fuentes, Agustín Rodriguez-Alen, Rocío Benito, Vicente Vicente, Teodoro Iturbe, Andreas Greinacher, María Luisa Lozano & José Rivera. (2023) Platelet transcriptome analysis in patients with germline RUNX1 mutations. Journal of Thrombosis and Haemostasis 21:5, pages 1352-1365.
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Juehua Gao, Yihua Chen & Madina Sukhanova. (2021) Molecular Pathogenesis in Myeloid Neoplasms with Germline Predisposition. Life 12:1, pages 46.
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Svetlana Korinfskaya, Sreeja Parameswaran, Matthew T. Weirauch & Artem Barski. (2021) Runx Transcription Factors in T Cells—What Is Beyond Thymic Development?. Frontiers in Immunology 12.
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Verónica Palma-Barqueros, Nuria Revilla, Ana Sánchez, Ana Zamora Cánovas, Agustín Rodriguez-Alén, Ana Marín-Quílez, José Ramón González-Porras, Vicente Vicente, María Luisa Lozano, José María Bastida & José Rivera. (2021) Inherited Platelet Disorders: An Updated Overview. International Journal of Molecular Sciences 22:9, pages 4521.
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Nabin Karki, Natasha Savage & Abdullah Kutlar. (2021) Novel Germline RUNX1 Mutation Associated with Familial Thrombocytopenia as well as B-Acute Lymphoblastic Leukemia: A Case Report and Review of the Literature. Case Reports in Oncology 14:1, pages 439-445.
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Loredana Bury, Emanuela Falcinelli & Paolo Gresele. (2021) Learning the Ropes of Platelet Count Regulation: Inherited Thrombocytopenias. Journal of Clinical Medicine 10:3, pages 533.
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Laura Simon, Jean-François Spinella, Chi-Yuan Yao, Vincent-Philippe Lavallée, Isabel Boivin, Geneviève Boucher, Eric Audemard, Marie-Eve Bordeleau, Sébastien Lemieux, Josée Hébert & Guy Sauvageau. (2020)
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Catherine Tang, David J. Rabbolini, Marie‐Christine Morel‐Kopp, David E. Connor, Philip Crispin, Christopher M. Ward & William S. Stevenson. (2020) The clinical heterogeneity of RUNX1 associated familial platelet disorder with predisposition to myeloid malignancy – A case series and review of the literature. Research and Practice in Thrombosis and Haemostasis 4:1, pages 106-110.
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Ibrahim Almazni, Rachel Stapley & Neil V. Morgan. (2019) Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding. Frontiers in Cardiovascular Medicine 6.
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Thomas Menter, Pontus Lundberg, Friedel Wenzel, Jan Dirks, Paula Fernandez, Dorothea Friess, Stefan Dirnhofer & Alexandar Tzankov. (2019) <b><i>RUNX1</i></b> Mutations Can Lead to Aberrant Expression of CD79a and PAX5 in Acute Myelogenous Leukemias: A Potential Diagnostic Pitfall. Pathobiology 86:2-3, pages 162-166.
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