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Epigenetic silencing of MIR203 in multiple myeloma

British journal of haematology, 2011-09, Vol.154 (5), p.569-578

2011

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NF‐E2 mutation as a novel cause for inherited thrombocytopenia

British journal of haematology, 2020-04, Vol.189 (2), p.e41-e44

2020

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Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene

Journal of pediatric hematology/oncology, 2020-10, Vol.42 (7), p.e696-e697

2020

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The significance of dyserythropoiesis

British journal of haematology, 2014-02, Vol.164 (3), p.313-313

So, Chi‐Chiu

2014

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Subtle skin involvement in nodal γδ peripheral T-cell lymphoma

Journal of dermatology, 2015-03, Vol.42 (3), p.328-330

2015

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High BCL6 expression predicts better prognosis, independent of BCL6 translocation status, translocation partner, or BCL6-deregulating mutations, in gastric lymphoma

Blood, 2006-10, Vol.108 (7), p.2373-2383

2006

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A laboratory strategy for genotyping haemoglobin H disease in the Chinese

Journal of clinical pathology, 2007-08, Vol.60 (8), p.931-934

2007

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Epigenetic inactivation of the miR-124-1 in haematological malignancies

PloS one, 2011-04, Vol.6 (4), p.e19027

2011

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Diagnostic challenges in a case of B cell lymphoma unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma

International journal of hematology, 2013-10, Vol.98 (4), p.478-482

2013

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Spontaneous resolution of refractory cytopenia of childhood with monosomy 7 in an infant without an identifiable genetic cause

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

2022

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Homoharringtonine (omacetaxine mepesuccinate) as an adjunct for FLT3-ITD acute myeloid leukemia

Science translational medicine, 2016-10, Vol.8 (359), p.359ra129

2016

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NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing

The Journal of molecular diagnostics : JMD, 2022-10, Vol.24 (10), p.1089-1099

2022

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Reference values for reticulocyte haemoglobin equivalent in healthy Chinese children under 5 years and its associations with various blood parameters

BMJ paediatrics open, 2024-08, Vol.8 (1), p.e002736

2024

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Epigenetic inactivation of the MIR34B/C in multiple myeloma

Blood, 2011-11, Vol.118 (22), p.5901-5904

2011

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A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease

Annals of hematology, 2017-06, Vol.96 (6), p.1005-1014

2017

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Diagnosis and prevention of thalassemia

Critical reviews in clinical laboratory sciences, 2013-11, Vol.50 (6), p.125-141

2013

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CD44 activation in mature B-cell malignancies by a novel recurrent IGH translocation

Blood, 2010-03, Vol.115 (12), p.2458-2461

2010

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Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms

Journal of clinical pathology, 2016-11, Vol.69 (11), p.1017-1024

2016

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Is HbA 2 level a reliable diagnostic measurement for β‐thalassemia trait in people with iron deficiency?

American journal of hematology, 2012-01, Vol.87 (1), p.114-116

2012

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Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing

Journal of clinical pathology, 2015-01, Vol.68 (1), p.69-72

2015

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Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses

Hemoglobin, 2016-01, Vol.40 (1), p.70-73

2016

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Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis

Annals of hematology, 2015-05, Vol.94 (5), p.875-877

2015

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Pure red cell aplasia associated with CD20+ myeloma: complete remission with rituximab

Annals of hematology, 2013-10, Vol.92 (10), p.1425-1426

2013

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Can morphological assessment limit the use of specific genetic testing to exclude chronic myeloid leukaemia?

British journal of haematology, 2007-05, Vol.137 (4), p.377-377

2007

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May–Hegglin anomaly

British journal of haematology, 2003-02, Vol.120 (3), p.373-373

2003

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Epigenetic silencing of MIR203 in multiple myeloma

NF‐E2 mutation as a novel cause for inherited thrombocytopenia

Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene

The significance of dyserythropoiesis

Subtle skin involvement in nodal γδ peripheral T-cell lymphoma

High BCL6 expression predicts better prognosis, independent of BCL6 translocation status, translocation partner, or BCL6-deregulating mutations, in gastric lymphoma

A laboratory strategy for genotyping haemoglobin H disease in the Chinese

Epigenetic inactivation of the miR-124-1 in haematological malignancies

Diagnostic challenges in a case of B cell lymphoma unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma

Spontaneous resolution of refractory cytopenia of childhood with monosomy 7 in an infant without an identifiable genetic cause

Homoharringtonine (omacetaxine mepesuccinate) as an adjunct for FLT3-ITD acute myeloid leukemia

NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing

Reference values for reticulocyte haemoglobin equivalent in healthy Chinese children under 5 years and its associations with various blood parameters

Epigenetic inactivation of the MIR34B/C in multiple myeloma

A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease

Diagnosis and prevention of thalassemia

CD44 activation in mature B-cell malignancies by a novel recurrent IGH translocation

Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms

Is HbA 2 level a reliable diagnostic measurement for β‐thalassemia trait in people with iron deficiency?

Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing

Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses

Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis

Pure red cell aplasia associated with CD20+ myeloma: complete remission with rituximab

Can morphological assessment limit the use of specific genetic testing to exclude chronic myeloid leukaemia?

May–Hegglin anomaly

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