Xinan Wang

发表

Paroxysmal nocturnal hemoglobinuria and telomere length predicts response to immunosuppressive therapy in pediatric aplastic anemia

Y. Okuno, E. Ito, H. Moritake, 2015, Haematologica.

Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Journal of Clinical Immunology.

Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia.

Y. Hayashi, H. Kawaguchi, Yoko Furukawa-Hibi, 2012, Blood.

Clinical course of juvenile myelomonocytic leukemia in the blast crisis phase treated by acute myeloid leukemia-oriented chemotherapy and allogeneic hematopoietic stem cell transplantation

S. Kojima, H. Muramatsu, H. Sakaguchi, 2014, International Journal of Hematology.

Serial investigation of PTPN11 mutation in nonhematopoietic tissues in a patient with juvenile myelomonocytic leukemia who was treated with unrelated cord blood transplantation

T. Imamura, H. Hosoi, S. Kojima, 2015, International Journal of Hematology.

Germline Mutation of CBL Is Associated With Moyamoya Disease in a Child With Juvenile Myelomonocytic Leukemia and Noonan Syndrome‐Like Disorder

S. Kojima, H. Muramatsu, Y. Chinen, 2015, Pediatric blood & cancer.

Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2012, British journal of haematology.

Aldehyde dehydrogenase‐2 polymorphism contributes to the progression of bone marrow failure in children with idiopathic aplastic anaemia

S. Kojima, H. Muramatsu, Yoshiyuki Takahashi, 2015, British journal of haematology.

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Nature Genetics.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Integrated molecular profiling of juvenile myelomonocytic leukemia.

H. Aburatani, S. Miyano, Y. Shiraishi, 2018, Blood.

MEF2D-BCL9 Fusion Gene Is Associated With High-Risk Acute B-Cell Precursor Lymphoblastic Leukemia in Adolescents.

Y. Okuno, S. Kojima, Kyogo Suzuki, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia

E. Ito, H. Moritake, S. Ohga, 2014, Haematologica.

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

S. Miyano, Y. Shiraishi, K. Chiba, 2016, International Journal of Hematology.

Clinical utility of next‐generation sequencing‐based minimal residual disease in paediatric B‐cell acute lymphoblastic leukaemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2017, British journal of haematology.

Markedly High Plasma Thrombopoietin (TPO) Level is a Predictor of Poor Response to Immunosuppressive Therapy in Children With Acquired Severe Aplastic Anemia

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric blood & cancer.

Correlation of rabbit antithymocyte globulin serum levels and clinical outcomes in children who received hematopoietic stem cell transplantation from an alternative donor

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric transplantation.

A Cytokine‐Based Diagnostic Program in Pediatric Aplastic Anemia and Hypocellular Refractory Cytopenia of Childhood

Y. Okuno, S. Kojima, H. Muramatsu, 2016, Pediatric blood & cancer.

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Haematologica.

Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

S. Miyano, Y. Shiraishi, K. Chiba, 2015, Journal of Clinical Immunology.

Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Genetics in Medicine.

Clinical Utility of Next-Generation Sequencing-Based Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia

Y. Okuno, S. Kojima, Kyogo Suzuki, 2015 .

JAK2, MPL, and CALR mutations in children with essential thrombocythemia

Y. Okuno, T. Imamura, S. Ohga, 2016, International Journal of Hematology.

Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, PloS one.

Germline Mutation of CBL Is Associated With Moyamoya Disease in a Child With Juvenile Myelomonocytic Leukemia and Noonan Syndrome‐Like Disorder

S. Kojima, H. Muramatsu, Y. Chinen, 2015, Pediatric blood & cancer.

Application of extensively targeted next-generation sequencing for the diagnosis of primary immunodeficiencies.

Y. Okuno, S. Kojima, H. Muramatsu, 2016, The Journal of allergy and clinical immunology.