Yoshiko Hashii

Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia

Masafumi Seki, Shunsuke Kimura, Tomoya Isobe et al. · Nature Genetics · 2017 · 133 citations

Medicine, Molecular Genetics, Oncology +15

Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia

Tetsuya Niihori, Meri Ouchi‐Uchiyama, Yoji Sasahara et al. · The American Journal of Human Genetics · 2015 · 127 citations · Full text

Medicine, Molecular Genetics, Radiology +7

Identification of Severe Combined Immunodeficiency by T-Cell Receptor Excision Circles Quantification Using Neonatal Guthrie Cards

Yoichi Morinishi, Kohsuke Imai, Noriko Nakagawa et al. · The Journal of Pediatrics · 2009 · 120 citations

Life Sciences, Immunology, Pediatrics +12

Characterization of pediatric Philadelphia-negative B-cell precursor acute lymphoblastic leukemia with kinase fusions in Japan

Toshihiko Imamura, Nobutaka Kiyokawa, Motohiro Kato et al. · Blood Cancer Journal · 2016 · 68 citations · Full text

Medicine, Hematology, Oncology +17

<i><scp>IKZF</scp>1</i> deletion is associated with a poor outcome in pediatric B‐cell precursor acute lymphoblastic leukemia in Japan

Daisuke Asai, Toshihiko Imamura, Souichi Suenobu et al. · Cancer Medicine · 2013 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17