Associated Papers
Limited availability of variant-specific germ line data creates challenges in the interpretation of myeloid NGS panels.
Winer AJ et al.
Blood Vessels, Thrombosis & Hemostasis, 2026
Inherited Predispositions to Myeloid Neoplasms: Pathogenesis and Clinical Implications.
Liu YC et al.
Annual Review of Pathology, 2025
Genetic predisposition to myelodysplastic syndrome: Genetic counseling and transplant implications.
Liu Y et al.
Seminars in Hematology, 2024
Ankrd26 is a retinoic acid-responsive plasma membrane-binding and -shaping protein critical for proper cell differentiation.
Englisch AS et al.
Cell Reports, 2024
DDX41 mutations in patients with non-myeloid hematologic neoplasms.
Jelloul FZ et al.
American Journal of Hematology, 2023
Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26.
Homan CC et al.
Blood, 2023
ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms.
Sullivan MJ et al.
Current Hematologic Malignancy Reports, 2022
Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.
Gilad O et al.
Haematologica, 2022
Molecular Pathogenesis in Myeloid Neoplasms with Germline Predisposition.
Gao J et al.
Life (basel, Switzerland), 2021
5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia.
Marconi C et al.
Journal of Hematology & Oncology, 2017
Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.
Cardoso SR et al.
Leukemia, 2016
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.
Foley SB et al.
Ebiomedicine, 2015
26023681 (PubMed )
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