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Publications by Eibhlin Conneally
Targeted Next-Generation Sequencing of Familial Platelet Disorder With Predisposition to Acute Myeloid Leukaemia
British Journal of Haematology
Hematology
An Acquired NRAS Mutation Contributes to Neutrophilic Progression in a Patient With Primary Myelofibrosis
British Journal of Haematology
Hematology
Related publications
RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)
Seminars in Hematology
Hematology
Targeted Next Generation Sequencing of PDGFRB Rearranged Myeloid Neoplasms With Monocytosis
American Journal of Hematology
Hematology
Identifying Leukemia-Specific Neoepitopes From Next-Generation Sequencing Data to Develop Targeted Immunotherapy for Pediatric Acute Myeloid Leukemiaig
Biology of Blood and Marrow Transplantation
Transplantation
Hematology
Targeted Therapy According to Next Generation Sequencing-Based Panel Sequencing
Fukushima Journal of Medical Sciences
Medicine
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
Inter-Laboratory Evaluation of a Next-Generation Sequencing Panel for Acute Myeloid Leukemia
Molecular Diagnosis and Therapy
Medicine
Molecular Medicine
Genetics
Pharmacology
Measurable Residual Disease (MRD) Detection by Next Generation Sequencing (NGS) in Acute Lymphoblastic LEUKAEMIA (ALL)
Pathology
Forensic Medicine
Pathology
Clinical Utility of Next-Generation Sequencing-Based Minimal Residual Disease in Paediatric B-Cell Acute Lymphoblastic Leukaemia
British Journal of Haematology
Hematology
Targeted Sequencing of Cancer-Associated Genes in Hepatocellular Carcinoma Using Next Generation Sequencing
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
