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NGS-based multi-gene panel testing in hematological malignancies: germline variants and related issues

Rinshō ketsueki, 2022, Vol.63 (4), p.308

Nannya, Yasuhito

2022

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Utility of voriconazole therapeutic drug monitoring: a meta-analysis

Journal of antimicrobial chemotherapy, 2016-07, Vol.71 (7), p.1786-1799

2016

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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis

Nature medicine, 2021-07, Vol.27 (7), p.1239-1249

2021

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Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome

Nature cell biology, 2022-03, Vol.24 (3), p.299

2022

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Hematological effects on peri-transplant use of linezolid in adults undergoing single-unit cord blood transplantation

Annals of hematology, 2021-11, Vol.100 (11), p.2867-2869

2021

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Genetic deletion and pharmacologic inhibition of E3 ubiquitin ligase HOIP impairs the propagation of myeloid leukemia

Leukemia, 2023-01, Vol.37 (1), p.122-133

2023

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Low urinary sodium-to-potassium ratio in the early phase following single-unit cord blood transplantation is a predictive factor for poor non-relapse mortality in adults

Scientific reports, 2024-01, Vol.14 (1), p.1413-1413, Article 1413

2024

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Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice

Blood, 2018-02, Vol.131 (6), p.621-635

2018

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Clonal hematopoiesis in adult pure red cell aplasia

Scientific reports, 2021-01, Vol.11 (1), p.2253-2253, Article 2253

2021

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Novel DDX41 variants in Thai patients with myeloid neoplasms

International journal of hematology, 2020-02, Vol.111 (2), p.241-246

2020

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A germline HLTF mutation in familial MDS induces DNA damage accumulation through impaired PCNA polyubiquitination

Leukemia, 2019-07, Vol.33 (7), p.1773-1782

2019

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Complete Bone Marrow Necrosis with Charcot-Leyden Crystals Caused by Myeloid Neoplasm with Mutated NPM1 and TET2

Internal Medicine, 2022/11/01, Vol.61(21), pp.3265-3269

2022

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Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations

Internal Medicine, 2021/12/01, Vol.60(23), pp.3785-3788

2021

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

Cancer research (Chicago, Ill.), 2005-07, Vol.65 (14), p.6071-6079

2005

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Factors associated with clonal hematopoiesis and interaction with marrow environment

Journal of bone and mineral metabolism, 2023-05, Vol.41 (3), p.380-387

Nannya, Yasuhito

2023

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An eltrombopag‐induced remission of bone‐marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly

British journal of haematology, 2022-09, Vol.198 (5), p.e75-e77

2022

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Anti-spike protein antibody titer at the time of breakthrough infection of SARS-CoV-2 omicron

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2022-07, Vol.28 (7), p.1015-1017

2022

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Germline RUNX1 translocation in familial platelet disorder with propensity to myeloid malignancies

Annals of hematology, 2022, Vol.101 (1), p.237-239

2022

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Identification of an asymptomatic Shwachman–Bodian–Diamond syndrome mutation in a patient with acute myeloid leukemia

International journal of hematology, 2022-03, Vol.115 (3), p.428-434

2022

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Development of Philadelphia chromosome-negative acute myeloid leukemia with IDH2 and NPM1 mutations in a patient with chronic myeloid leukemia who showed a major molecular response to tyrosine kinase inhibitor therapy

International journal of hematology, 2021-06, Vol.113 (6), p.936-940

2021

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Gain‐of‐function mutations and copy number increases of Notch2 in diffuse large B‐cell lymphoma

Cancer science, 2009-05, Vol.100 (5), p.920-926

2009

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Case report: Immune pressure on hematopoietic stem cells can drastically expand glycosylphosphatidylinositol-deficient clones in paroxysmal nocturnal hemoglobinuria

Frontiers in immunology, 2024-01, Vol.14, p.1329403

2024

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Recurrent CDC25C mutations drive malignant transformation in FPD/AML

Nature communications, 2014-08, Vol.5 (1), p.4770-4770, Article 4770

2014

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NGS-based multi-gene panel testing in hematological malignancies: germline variants and related issues

Utility of voriconazole therapeutic drug monitoring: a meta-analysis

Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis

Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome

Hematological effects on peri-transplant use of linezolid in adults undergoing single-unit cord blood transplantation

Genetic deletion and pharmacologic inhibition of E3 ubiquitin ligase HOIP impairs the propagation of myeloid leukemia

Frequent genetic alterations in immune checkpoint–related genes in intravascular large B-cell lymphoma

Low urinary sodium-to-potassium ratio in the early phase following single-unit cord blood transplantation is a predictive factor for poor non-relapse mortality in adults

Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice

Clonal hematopoiesis in adult pure red cell aplasia

Novel DDX41 variants in Thai patients with myeloid neoplasms

A germline HLTF mutation in familial MDS induces DNA damage accumulation through impaired PCNA polyubiquitination

Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms

Complete Bone Marrow Necrosis with Charcot-Leyden Crystals Caused by Myeloid Neoplasm with Mutated NPM1 and TET2

Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

Factors associated with clonal hematopoiesis and interaction with marrow environment

An eltrombopag‐induced remission of bone‐marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly

Anti-spike protein antibody titer at the time of breakthrough infection of SARS-CoV-2 omicron

Germline RUNX1 translocation in familial platelet disorder with propensity to myeloid malignancies

Identification of an asymptomatic Shwachman–Bodian–Diamond syndrome mutation in a patient with acute myeloid leukemia

Development of Philadelphia chromosome-negative acute myeloid leukemia with IDH2 and NPM1 mutations in a patient with chronic myeloid leukemia who showed a major molecular response to tyrosine kinase inhibitor therapy

Gain‐of‐function mutations and copy number increases of Notch2 in diffuse large B‐cell lymphoma

Case report: Immune pressure on hematopoietic stem cells can drastically expand glycosylphosphatidylinositol-deficient clones in paroxysmal nocturnal hemoglobinuria

Recurrent CDC25C mutations drive malignant transformation in FPD/AML

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