☰

Shiro Ogawa, Ph.D. - Publications

Affiliations: 
2004 University of British Columbia, Vancouver, Vancouver, BC, Canada 
Area:
Electronics and Electrical Engineering
Tree Info Similar researchers PubMed Report error

213 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Murakami K, Yamaguchi Y, Kida Y, Morikawa Y, Ujiie H, Sugahara H, Nannya Y, Ogawa S, Kanakura Y. Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations. Internal Medicine (Tokyo, Japan). PMID 34053991 DOI: 10.2169/internalmedicine.7571-21  0.316
2021 Ochi Y, Ogawa S. Chromatin-Spliceosome Mutations in Acute Myeloid Leukemia. Cancers. 13. PMID 33799787 DOI: 10.3390/cancers13061232  0.337
2021 Fujishima N, Kohmaru J, Koyota S, Kuba K, Saga T, Omokawa A, Moritoki Y, Ueki S, Ishida F, Nakao S, Matsuda A, Ohta A, Tohyama K, Yamasaki H, Usuki K, ... ... Ogawa S, et al. Clonal hematopoiesis in adult pure red cell aplasia. Scientific Reports. 11: 2253. PMID 33500526 DOI: 10.1038/s41598-021-81890-5  0.325
2020 Todisco G, Creignou M, Gallì A, Guglielmelli P, Rumi E, Roncador M, Rizzo E, Nannya Y, Pietra D, Elena C, Bono E, Molteni E, Rosti V, Catricalá S, Sarchi M, ... ... Ogawa S, et al. Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2-mutated neoplasms. Leukemia. 35: 2371-2381. PMID 33349666 DOI: 10.1038/s41375-020-01106-z  0.33
2020 Ueno H, Yoshida K, Shiozawa Y, Nannya Y, Iijima-Yamashita Y, Kiyokawa N, Shiraishi Y, Chiba K, Tanaka H, Isobe T, Seki M, Kimura S, Makishima H, Nakagawa MM, Kakiuchi N, ... ... Ogawa S, et al. Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. Blood Advances. 4: 5165-5173. PMID 33095873 DOI: 10.1182/bloodadvances.2019001307  0.34
2020 Bernard E, Nannya Y, Hasserjian RP, Devlin SM, Tuechler H, Medina-Martinez JS, Yoshizato T, Shiozawa Y, Saiki R, Malcovati L, Levine MF, Arango JE, Zhou Y, Solé F, Cargo CA, ... ... Ogawa S, et al. Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes. Nature Medicine. PMID 32747829 DOI: 10.1038/S41591-020-1008-Z  0.312
2020 Imataki O, Ishida T, Kubo H, Uemura M, Nanya Y, Kawakami K, Ogawa S, Kadowaki N. A Case of Tyrosine Kinase Inhibitor-Resistant Chronic Myeloid Leukemia, Chronic Phase with ASXL1 Mutation. Case Reports in Oncology. 13: 449-455. PMID 32399015 DOI: 10.1159/000506452  0.332
2020 Malcovati L, Stevenson K, Papaemmanuil E, Neuberg D, Bejar R, Boultwood J, Bowen DT, Campbell PJ, Ebert BL, Fenaux P, Haferlach T, Heuser M, Jansen JH, Komrokji RS, Maciejewski JP, ... ... Ogawa S, et al. SF3B1-mutant myelodysplastic syndrome as a distinct disease subtype - A Proposal of the International Working Group for the Prognosis of Myelodysplastic Syndromes (IWG-PM). Blood. PMID 32347921 DOI: 10.1182/Blood.2020004850  0.307
2020 Ochi Y, Kon A, Sakata T, Nakagawa MM, Nakazawa N, Kakuta M, Kataoka K, Koseki H, Nakayama M, Morishita D, Tsuruyama T, Saiki R, Yoda A, Okuda R, Yoshizato T, ... ... Ogawa S, et al. Combined Cohesin-Runx1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes. Cancer Discovery. PMID 32249213 DOI: 10.1158/2159-8290.Cd-19-0982  0.307
2020 Secardin L, Limia CEG, di Stefano A, Bonamino MH, Saliba J, Kataoka K, Rehen SK, Raslova H, Marty C, Ogawa S, Vainchenker W, Monte-Mor BDCR, Plo I. TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells. Stem Cell Research. 44: 101755. PMID 32193150 DOI: 10.1016/J.Scr.2020.101755  0.303
2020 Ogawa S. Genetic basis of myelodysplastic syndromes. Proceedings of the Japan Academy. Series B, Physical and Biological Sciences. 96: 107-121. PMID 32161209 DOI: 10.2183/pjab.96.009  0.309
2020 Mylonas E, Yoshida K, Frick M, Hoyer K, Christen F, Kaeda J, Obenaus M, Noerenberg D, Hennch C, Chan W, Ochi Y, Shiraishi Y, Shiozawa Y, Zenz T, Oakes CC, ... ... Ogawa S, et al. Single-cell analysis based dissection of clonality in myelofibrosis. Nature Communications. 11: 73. PMID 31911629 DOI: 10.1038/s41467-019-13892-x  0.315
2020 Inagaki R, Nakagawa MM, Nannya Y, Xingxing Q, Zhao L, Takeda J, Yoda A, Kon A, Tsurumi H, Makishima H, Ogawa S. Analysis of Clonal Evolution of AML Using Simultaneous Single-Cell DNA/RNA Analysis Blood. 136: 1-1. DOI: 10.1182/blood-2020-143320  0.334
2020 Nakagawa MM, Inagaki R, Kuroda Y, Nannya Y, Zhao L, Ochi Y, Takeda J, Xingxing Q, Yoda A, Kon A, Kakiuchi N, Makishima H, Matsuda S, Ogawa S. Distinct Pathogenesis of Clonal Hematopoiesis Revealed By Single Cell RNA Sequencing Integrated with Highly Sensitive Genotyping Method Blood. 136: 34-34. DOI: 10.1182/blood-2020-142157  0.307
2020 Ochi Y, Yoshida K, Huang Y, Kuo M, Sasaki K, Hosoya N, Hiramoto N, Bera R, Nannya Y, Shiozawa Y, Takeda J, Watatani Y, Makishima H, Shiraishi Y, Chiba K, ... ... Ogawa S, et al. Prognostic Relevance of Genetic Abnormalities in Blastic Transformation of Chronic Myeloid Leukemia Blood. 136: 3-4. DOI: 10.1182/BLOOD-2020-140629  0.309
2020 Makishima H, Nannya Y, Takeda J, Momozawa Y, Saiki R, Yoshizato T, Atsuta Y, Iijima-Yamashita Y, Yoshida K, Shiraishi Y, Nagata Y, Shiozawa Y, Onizuka M, Chiba K, Tanaka H, ... ... Ogawa S, et al. Clinical Impacts of Germline DDX41 Mutations on Myeloid Neoplasms Blood. 136: 38-40. DOI: 10.1182/blood-2020-140174  0.329
2020 Matsuo H, Yoshida K, Nakatani K, Harata Y, Higashitani M, Ito Y, Kamikubo Y, Shiozawa Y, Shiraishi Y, Chiba K, Tanaka H, Okada A, Nannya Y, Takeda J, Ueno H, ... ... Ogawa S, et al. KRAS mutations Frequently Coexist with High-Risk MLL Fusions and Are Independent Adverse Prognostic Factors in MLL-Rearranged Acute Myeloid Leukemia Blood. 136: 28-29. DOI: 10.1182/blood-2020-134648  0.312
2019 Nagata Y, Makishima H, Kerr CM, Przychodzen BP, Aly M, Goyal A, Awada H, Asad MF, Kuzmanovic T, Suzuki H, Yoshizato T, Yoshida K, Chiba K, Tanaka H, Shiraishi Y, ... ... Ogawa S, et al. Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes. Nature Communications. 10: 5386. PMID 31772163 DOI: 10.1038/s41467-019-13001-y  0.32
2019 Madan V, Li J, Zhou S, Teoh WW, Han L, Meggendorfer M, Malcovati L, Cazzola M, Ogawa S, Haferlach T, Yang H, Koeffler HP. Distinct and convergent consequences of splice factor mutations in myelodysplastic syndromes. American Journal of Hematology. PMID 31680297 DOI: 10.1002/Ajh.25673  0.304
2019 Kimura S, Hasegawa D, Yoshimoto Y, Seki M, Daida A, Sekiguchi M, Hirabayashi S, Hosoya Y, Kobayashi M, Miyano S, Ogawa S, Takita J, Manabe A. Duplication of F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma. Oncology Letters. 17: 3323-3329. PMID 30867766 DOI: 10.3892/ol.2019.9985  0.347
2019 Mori M, Hira A, Yoshida K, Muramatsu H, Okuno Y, Shiraishi Y, Anmae M, Yasuda J, Tadaka S, Kinoshita K, Osumi T, Noguchi Y, Adachi S, Kobayashi R, Kawabata H, ... ... Ogawa S, et al. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients. Haematologica. PMID 30792206 DOI: 10.3324/Haematol.2018.207241  0.321
2019 Polprasert C, Takeuchi Y, Kakiuchi N, Yoshida K, Assanasen T, Sitthi W, Bunworasate U, Pirunsarn A, Wudhikarn K, Lawasut P, Uaprasert N, Kongkiatkamon S, Moonla C, Sanada M, Akita N, ... ... Ogawa S, et al. Frequent germline mutations of in sporadic subcutaneous panniculitis-like T-cell lymphoma. Blood Advances. 3: 588-595. PMID 30792187 DOI: 10.1182/Bloodadvances.2018028340  0.356
2019 Ogawa S. Genetics of MDS. Blood. 133: 1049-1059. PMID 30670442 DOI: 10.1182/blood-2018-10-844621  0.335
2019 Haase D, Stevenson KE, Neuberg D, Maciejewski JP, Nazha A, Sekeres MA, Ebert BL, Garcia-Manero G, Haferlach C, Haferlach T, Kern W, Ogawa S, Nagata Y, Yoshida K, Graubert TA, et al. TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups. Leukemia. PMID 30635634 DOI: 10.1038/S41375-018-0351-2  0.315
2019 Christen F, Hoyer K, Yoshida K, Hou HA, Waldhueter N, Heuser M, Hills RK, Chan W, Hablesreiter R, Blau O, Ochi Y, Klement P, Chou WC, Blau IW, Tang JL, ... ... Ogawa S, et al. Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients. Blood. PMID 30610028 DOI: 10.1182/blood-2018-05-852822  0.353
2019 Okuda R, Makishima H, Nannya Y, Ochi Y, Yoshizato T, Nagata Y, Yoshida K, Sanada M, Takeda J, Saiki R, Shiraishi Y, Miyano S, Kern W, Baer C, Nadarajah N, ... ... Ogawa S, et al. Distinct, Ethnic, Clinical, and Genetic Characteristics of Myelodysplastic Syndromes with Der(1;7) Blood. 134: 5392-5392. DOI: 10.1182/blood-2019-129943  0.314
2019 Takeda J, Yoshida K, Nannya Y, Shih L, Kon A, Yoda A, Ochi Y, Shiozawa Y, Yoshizato T, Kerr CM, Shiraishi Y, Chiba K, Nagata Y, Hangaishi A, Kitano T, ... ... Ogawa S, et al. Novel Molecular Pathogenesis and Therapeutic Target in Acute Erythroid Leukemia Blood. 134: 914-914. DOI: 10.1182/BLOOD-2019-129940  0.333
2019 Nannya Y, Tobiasson M, Bernard E, Sato S, Creignou M, Takeda J, Zhao L, Shiraishi Y, Chiba K, Tanaka H, Tsurumi H, Kasahara S, Taguchi M, Takaori AK, Ohyashiki K, ... ... Ogawa S, et al. Molecular Characteristics That Predict Response to Azacitidine Therapy Blood. 134: 4246-4246. DOI: 10.1182/blood-2019-129420  0.325
2019 Nagata Y, Makishima H, Kerr CM, Patel BJ, Awada H, Adema V, Visconte V, Mukherjee S, Laframboise T, Nazha A, Radivoyevitch T, Sekeres MA, Ogawa S, Maciejewski JP. Mutational Type and Configuration of an Individual Gene May Differentially Impact the Clinical and Phenotypic Features Blood. 134: 2992-2992. DOI: 10.1182/blood-2019-128893  0.342
2019 Svidnicki MCCM, Campos PDM, Ferreira Filho MA, Fujiura CAL, Yoshizato T, Makishima H, Ogawa S, Olalla Saad ST. Mutations in Triple-Negative Patients with Myeloproliferative Neoplasms Blood. 134: 5395-5395. DOI: 10.1182/blood-2019-128764  0.355
2019 Kaburagi T, Yamato G, Shiba N, Yoshida K, Hara Y, Shiraishi Y, Ohki K, Sotomatsu M, Arakawa H, Matsuo H, Shimada A, Taki T, Kiyokawa N, Tomizawa D, Horibe K, ... ... Ogawa S, et al. Recurrent Gene Mutations in Pediatric Patients with AML By Targeted Sequencing ―the Jccg Study, JPLSG AML-05― Blood. 134: 2697-2697. DOI: 10.1182/blood-2019-126545  0.336
2019 Inagaki R, Nakagawa MM, Nannya Y, Xingxing Q, Zhao L, Takeda J, Yoda A, Kon A, Tsurumi H, Makishima H, Ogawa S. Analysis of Mechanisms Underlying Clonal Evolution of AML By a New Single-Cell Sequencing Platform Blood. 134: 542-542. DOI: 10.1182/blood-2019-126444  0.338
2019 Hara Y, Taki T, Yamato G, Yoshida K, Shiozawa Y, Shiba N, Kaburagi T, Shiraishi Y, Ohki K, Kawamura M, Sotomatsu M, Arakawa H, Matsuo H, Shimada A, Toki T, ... ... Ogawa S, et al. Clinical Features of Pediatric Acute Myeloid Leukemia with TP53 and CDKN2A/2B copy Number Alterations Blood. 134: 2727-2727. DOI: 10.1182/blood-2019-126263  0.303
2019 Matsuo H, Yoshida K, Nakatani K, Kamikubo Y, Tomizawa D, Taga T, Kiyokawa N, Ogawa S, Meggendorfer M, Haferlach C, Adachi S. Coexistence and Prognostic Significance of EVI1 Expression and Driver Mutations in KMT2A-Rearranged Acute Myeloid Leukemia Blood. 134: 1409-1409. DOI: 10.1182/blood-2019-124652  0.314
2019 Mylonas E, Yoshida K, Frick M, Hoyer K, Christen F, Kaeda J, Obenaus M, Nörenberg D, Hennch C, Chan W, Ochi Y, Shiraishi Y, Shiozawa Y, Zenz T, Oakes CC, ... ... Ogawa S, et al. Single-Cell Analysis Based Dissection of Clonality in Myelofibrosis Blood. 134: 469-469. DOI: 10.1182/blood-2019-123367  0.355
2019 Motomura M, Inoue Y, Nagata Y, Yoshizato T, Baer C, Momozawa Y, Nadarajah N, Nannya Y, Yoshida K, Haferlach C, Kern W, Atsuta Y, Iijima-Yamashita Y, Shiraishi Y, Onizuka M, ... ... Ogawa S, et al. PPM1D and DNMT3A Mutations in Myelodysplasia and Clonal Hematopoiesis Blood. 134: 1709-1709. DOI: 10.1182/blood-2019-122032  0.337
2018 Matsuo H, Yoshida K, Fukumura K, Nakatani K, Noguchi Y, Takasaki S, Noura M, Shiozawa Y, Shiraishi Y, Chiba K, Tanaka H, Okada A, Nannya Y, Takeda J, Ueno H, ... ... Ogawa S, et al. Recurrent mutations in -rearranged acute myeloid leukemia. Blood Advances. 2: 2879-2889. PMID 30381403 DOI: 10.1182/bloodadvances.2018019398  0.354
2018 Yabe M, Koike T, Ohtsubo K, Imai E, Morimoto T, Takakura H, Koh K, Yoshida K, Ogawa S, Ito E, Okuno Y, Muramatsu H, Kojima S, Matsuo K, Mori M, et al. Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia. Annals of Hematology. PMID 30368588 DOI: 10.1007/s00277-018-3517-0  0.319
2018 Kudo K, Ueno H, Sato T, Kubo K, Kanezaki R, Kobayashi A, Kamio T, Sasaki S, Terui K, Kurose A, Yoshida K, Shiozawa Y, Toki T, Ogawa S, Ito E. Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation. Genes, Chromosomes & Cancer. PMID 30350464 DOI: 10.1002/gcc.22676  0.304
2018 Kawashima N, Akashi A, Nagata Y, Kihara R, Ishikawa Y, Asou N, Ohtake S, Miyawaki S, Sakura T, Ozawa Y, Usui N, Kanamori H, Ito Y, Imai K, Suehiro Y, ... ... Ogawa S, et al. Clinical significance of ASXL2 and ZBTB7A mutations and C-terminally truncated RUNX1-RUNX1T1 expression in AML patients with t(8;21) enrolled in the JALSG AML201 study. Annals of Hematology. PMID 30251205 DOI: 10.1007/s00277-018-3492-5  0.335
2018 Kotani S, Yoda A, Kon A, Kataoka K, Ochi Y, Shiozawa Y, Hirsch C, Takeda J, Ueno H, Yoshizato T, Yoshida K, Nakagawa MM, Nannya Y, Kakiuchi N, Yamauchi T, ... ... Ogawa S, et al. Molecular pathogenesis of disease progression in MLL-rearranged AML. Leukemia. PMID 30209403 DOI: 10.1038/s41375-018-0253-3  0.32
2018 Shiozawa Y, Malcovati L, Gallì A, Sato-Otsubo A, Kataoka K, Sato Y, Watatani Y, Suzuki H, Yoshizato T, Yoshida K, Sanada M, Makishima H, Shiraishi Y, Chiba K, Hellström-Lindberg E, ... ... Ogawa S, et al. Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia. Nature Communications. 9: 3649. PMID 30194306 DOI: 10.1038/s41467-018-06063-x  0.301
2018 Shah UA, Chung EY, Giricz O, Pradhan K, Kataoka K, Gordon-Mitchell S, Bhagat TD, Mai Y, Wei Y, Ishida E, Choudhary GS, Joseph A, Rice R, Gitego N, Parrish C, ... ... Ogawa S, et al. North American ATLL has a distinct mutational and transcriptional profile and responds to epigenetic therapies. Blood. PMID 30104217 DOI: 10.1182/Blood-2018-01-824607  0.344
2018 Hamada M, Doisaki S, Okuno Y, Muramatsu H, Hama A, Kawashima N, Narita A, Nishio N, Yoshida K, Kanno H, Manabe A, Taga T, Takahashi Y, Miyano S, Ogawa S, et al. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia. International Journal of Hematology. PMID 29936674 DOI: 10.1007/s12185-018-2482-7  0.307
2018 Imi T, Katagiri T, Hosomichi K, Zaimoku Y, Hoang Nguyen V, Nakagawa N, Tajima A, Yoshizato T, Ogawa S, Nakao S. Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia. Blood Advances. 2: 1000-1012. PMID 29720492 DOI: 10.1182/bloodadvances.2017013953  0.309
2018 Arends CM, Galan-Sousa J, Hoyer K, Chan W, Jäger M, Yoshida K, Seemann R, Noerenberg D, Waldhueter N, Fleischer-Notter H, Christen F, Schmitt CA, Dörken B, Pelzer U, Sinn M, ... ... Ogawa S, et al. Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis. Leukemia. PMID 29491455 DOI: 10.1038/s41375-018-0047-7  0.328
2018 Murakami N, Okuno Y, Yoshida K, Shiraishi Y, Nagae G, Suzuki K, Narita A, Sakaguchi H, Kawashima N, Wang X, Xu Y, Chiba K, Tanaka H, Hama A, Sanada M, ... ... Ogawa S, et al. Integrated molecular profiling of juvenile myelomonocytic leukemia. Blood. PMID 29437595 DOI: 10.1182/blood-2017-07-798157  0.322
2018 Berger G, Kroeze LI, Koorenhof-Scheele TN, de Graaf AO, Yoshida K, Ueno H, Shiraishi Y, Miyano S, van den Berg E, Schepers H, van der Reijden BA, Ogawa S, Vellenga E, Jansen JH. Early detection and evolution of pre-leukemic clones in therapy-related myeloid neoplasms following autologous SCT. Blood. PMID 29311096 DOI: 10.1182/blood-2017-09-805879  0.339
2018 Kamijo R, Itonaga H, Kihara R, Nagata Y, Hata T, Asou N, Ohtake S, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Naoe T, Kiyoi H, Miyazaki Y. Distinct gene alterations with a high percentage of myeloperoxidase-positive leukemic blasts in de novo acute myeloid leukemia. Leukemia Research. 65: 34-41. PMID 29306105 DOI: 10.1016/j.leukres.2017.12.006  0.314
2018 Goyal A, Mirzaev I, Asad MFB, Awada H, Hirsch CM, Makishima H, Yoshida K, Przychodzen BP, Nazha A, Mukherjee S, Sekeres MA, Ogawa S, Radivoyevitch T, Scott J, Maciejewski JP, et al. Genotype-Resultant Morphology of Myelodysplastic Syndromes (MDS) Blood. 132: 1824-1824. DOI: 10.1182/Blood-2018-99-119345  0.341
2018 Nagata Y, Makishima H, Yoshizato T, Suzuki H, Hirsch CM, Goyal A, Awada H, Asad MFB, Kuzmanovic T, Przychodzen BP, Yoshida K, Chiba K, Tanaka H, Shiraishi Y, Miyano S, ... ... Ogawa S, et al. Invariant Patterns of Clonal Succession Determines Specific Phenotypic and Clinical Features of Myelodysplastic Syndromes (MDS) Blood. 132: 104-104. DOI: 10.1182/BLOOD-2018-99-118861  0.335
2018 Nagata Y, Makishima H, Hirsch CM, Awada H, Goyal A, Kuzmanovic T, Przychodzen BP, Yoshizato T, Yoshida K, Chiba K, Tanaka H, Shiraishi Y, Miyano S, Mukherjee S, Radivoyevitch T, ... ... Ogawa S, et al. Distinct Features of Chip-Derived and De Novo MDS Blood. 132: 2572-2572. DOI: 10.1182/BLOOD-2018-99-117763  0.329
2018 Kon A, Nannya Y, Nakagawa M, Kataoka K, Sanada M, Nakayama M, Koseki H, Ogawa S. Biological Characterization of the U2af1 S34F Mutation in the Pathogenesis of Myelodysplasia Blood. 132: 3080-3080. DOI: 10.1182/BLOOD-2018-99-117453  0.302
2018 Labuhn M, Perkins K, Papaemmanuil E, Garnett C, Matzk S, Amstislavskiy V, Metzner M, Kennedy A, Scheer C, Yoshida K, Schwarzer A, Crispino JD, Taub JW, Weiss MJ, Ito E, ... Ogawa S, et al. Modelling the Progression of a Preleukemic Stage to Overt Leukemia in Children with Down Syndrome Blood. 132: 543-543. DOI: 10.1182/Blood-2018-99-116661  0.346
2018 Nakagawa MM, Inagaki R, Nannya Y, Zhao L, Kuroda Y, Takeda J, Qi X, Yoda A, Kon A, Tsurumi H, Makishima H, Matsuda S, Ogawa S. Analysis of Clonal Evolution/Heterogeneity of MDS By Simultaneous Detection of Both Mutation and Gene Expression By Single Cell Sequencing Blood. 132: 1800-1800. DOI: 10.1182/BLOOD-2018-99-116448  0.331
2018 Ueno H, Yoshida K, Shiozawa Y, Nannya Y, Iijima-Yamashita Y, Kiyokawa N, Shiraishi Y, Chiba K, Tanaka H, Isobe T, Seki M, Kimura S, Makishima H, Kakiuchi N, Kataoka K, ... ... Ogawa S, et al. The Prognostic Value of TP53 Mutations Depends on Clinical Backgrounds in Pediatric Patients with Acute Lymphoblastic Leukemia Blood. 132: 4077-4077. DOI: 10.1182/BLOOD-2018-99-115617  0.335
2018 Kaburagi T, Yamato G, Shiba N, Yoshida K, Hara Y, Shiraishi Y, Ohki K, Sotomatsu M, Arakawa H, Matsuo H, Shimada A, Kiyokawa N, Tomizawa D, Taga T, Horibe K, ... ... Ogawa S, et al. Comprehensive Analysis of 343 Genes Using Targeted Sequencing Panel By Next-Generation Sequencer in 77 Pediatric AML Patients with Normal and Complex Karyotypes: Jccg Study, JPLSG AML-05 Blood. 132: 1530-1530. DOI: 10.1182/BLOOD-2018-99-114632  0.349
2018 Ochi Y, Yoshida K, Huang Y, Kuo M, Shiozawa Y, Nannya Y, Shiraishi Y, Okada A, Chiba K, Tanaka H, Miyano S, Takaori-Kondo A, Shih L, Ogawa S. Molecular Profiling of Blastic Transformation in Chronic Myeloid Leukemia Blood. 132: 1725-1725. DOI: 10.1182/BLOOD-2018-99-114512  0.352
2018 Mori T, Ono Y, Maruoka H, Shimomura Y, Hiramoto N, Yoshioka S, Takeda J, Nannya Y, Ogawa S, Ishikawa T. High Resolution Melt Analysis for Rapid and Cost-Effective Screening of TP53 Mutations in Patients with Myeloid Malignancies Blood. 132: 1485-1485. DOI: 10.1182/blood-2018-99-112031  0.346
2018 Matsuo H, Yoshida K, Fukumura K, Nakatani K, Noguchi Y, Takasaki S, Noura M, Shiozawa Y, Shiraishi Y, Chiba K, Tanaka H, Okada A, Nannya Y, Takeda J, Ueno H, ... ... Ogawa S, et al. Recurrent Genomic Aberrations of D-Type Cyclins Are Therapeutic Targets of CDK4/6 Inhibitors in t(8;21) and MLL-Rearranged Acute Myeloid Leukemia Blood. 132: 2797-2797. DOI: 10.1182/BLOOD-2018-99-111073  0.362
2018 Mori M, Hira A, Yoshida K, Muramatsu H, Okuno Y, Anmae M, Tamura K, Yasuda J, Osumi T, Noguchi Y, Adachi S, Kawabata H, Takaori-Kondo A, Kojima S, Ogawa S, et al. Characterization of Pathogenic Variants and Clinical Phenotypes in 117 Japanese Fanconi Anemia Patients Blood. 132: 3860-3860. DOI: 10.1182/BLOOD-2018-99-110362  0.305
2017 Nagata Y, Ogawa S. A novel prognostic model incorporating genetic profiling for myelodysplastic syndromes. [Rinsho Ketsueki] the Japanese Journal of Clinical Hematology. 58: 776-786. PMID 28781274 DOI: 10.11406/rinketsu.58.776  0.318
2017 Hirabayashi S, Seki M, Hasegawa D, Kato M, Hyakuna N, Shuo T, Kimura S, Yoshida K, Kataoka K, Fujii Y, Shiraishi Y, Chiba K, Tanaka H, Kiyokawa N, Miyano S, ... Ogawa S, et al. Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia. Pediatric Blood & Cancer. PMID 28544751 DOI: 10.1002/pbc.26647  0.321
2017 Sekinaka Y, Mitsuiki N, Imai K, Yabe M, Yabe H, Mitsui-Sekinaka K, Honma K, Takagi M, Arai A, Yoshida K, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, ... ... Ogawa S, et al. Common Variable Immunodeficiency Caused by FANC Mutations. Journal of Clinical Immunology. PMID 28493158 DOI: 10.1007/s10875-017-0396-4  0.333
2017 Togasaki E, Takeda J, Yoshida K, Shiozawa Y, Takeuchi M, Oshima M, Saraya A, Iwama A, Yokote K, Sakaida E, Hirase C, Takeshita A, Imai K, Okumura H, Morishita Y, ... ... Ogawa S, et al. Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia. Blood Cancer Journal. 7: e559. PMID 28452984 DOI: 10.1038/bcj.2017.36  0.351
2017 Yip BH, Steeples V, Repapi E, Armstrong RN, Llorian M, Roy S, Shaw J, Dolatshad H, Taylor S, Verma A, Bartenstein M, Vyas P, Cross NCP, Malcovati L, Cazzola M, ... ... Ogawa S, et al. The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes. The Journal of Clinical Investigation. PMID 28436936 DOI: 10.1172/JCI91363  0.315
2017 Malcovati L, Gallì A, Travaglino E, Ambaglio I, Rizzo E, Molteni E, Elena C, Ferretti VV, Catricalà S, Bono E, Todisco G, Bianchessi A, Rumi E, Zibellini S, Pietra D, ... ... Ogawa S, et al. Clinical significance of somatic mutation in unexplained blood cytopenia. Blood. 129: 3371-3378. PMID 28424163 DOI: 10.1182/blood-2017-01-763425  0.324
2017 Yoshizato T, Nannya Y, Atsuta Y, Shiozawa Y, Iijima-Yamashita Y, Yoshida K, Shiraishi Y, Suzuki H, Nagata Y, Sato Y, Kakiuchi N, Matsuo K, Onizuka M, Kataoka K, Chiba K, ... ... Ogawa S, et al. Impact of genetic alterations in stem-cell transplantation for myelodysplasia and secondary acute myeloid leukemia. Blood. PMID 28223278 DOI: 10.1182/blood-2016-12-754796  0.312
2017 Nguyen TB, Sakata-Yanagimoto M, Asabe Y, Matsubara D, Kano J, Yoshida K, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Izutsu K, Nakamura N, Takeuchi K, Miyoshi H, Ohshima K, ... ... Ogawa S, et al. Identification of cell-type-specific mutations in nodal T-cell lymphomas. Blood Cancer Journal. 7: e516. PMID 28157189 DOI: 10.1038/bcj.2016.122  0.311
2017 Makishima H, Ogawa S. Gene mutations in myelodysplastic syndromes. [Rinsho Ketsueki] the Japanese Journal of Clinical Hematology. 57: 2543-2553. PMID 28090024 DOI: 10.11406/rinketsu.57.2543  0.319
2017 Yamato G, Shiba N, Yoshida K, Shiraishi Y, Hara Y, Ohki K, Okubo J, Okuno H, Chiba K, Tanaka H, Kinoshita A, Moritake H, Kiyokawa N, Tomizawa D, Park MJ, ... ... Ogawa S, et al. ASXL2 Mutations are Frequently Found in Pediatric AML Patients with t(8;21)/RUNX1-RUNX1T1 and Associated with a Better Prognosis. Genes, Chromosomes & Cancer. PMID 28063196 DOI: 10.1002/gcc.22443  0.327
2017 Frick M, Arends CM, Galan-Sousa J, Hoyer K, Chan W, Jäger M, Yoshida K, Seemann R, Nörenberg D, Waldhüter N, Fleischer-Notter H, Christen F, Schmitt CA, Dorken B, Pelzer U, ... ... Ogawa S, et al. Clonal Hematopoiesis: Cell of Origin, Lineage Repartition and Dynamic Evolution during Chemotherapy Blood. 130: 632-632. DOI: 10.1182/BLOOD.V130.SUPPL_1.632.632  0.343
2017 Ding L, Sun Q, Tan K, Chien W, Mayakonda A, Lin D, Loh X, Xiao J, Meggendorfer M, Alpermann T, Garg M, Lim S, Madan V, Hattori N, Nagata Y, ... ... Ogawa S, et al. Abstract 2450: Mutational profiling of MLL-PTD acute myeloid leukemia Cancer Research. 77: 2450-2450. DOI: 10.1158/1538-7445.Am2017-2450  0.338
2016 Makishima H, Yoshizato T, Yoshida K, Sekeres MA, Radivoyevitch T, Suzuki H, Przychodzen B, Nagata Y, Meggendorfer M, Sanada M, Okuno Y, Hirsch C, Kuzmanovic T, Sato Y, Sato-Otsubo A, ... ... Ogawa S, et al. Dynamics of clonal evolution in myelodysplastic syndromes. Nature Genetics. PMID 27992414 DOI: 10.1038/ng.3742  0.316
2016 Ding L, Sun QY, Tan KT, Chien W, Thippeswamy AM, Eng Juh AY, Kawamata N, Nagata Y, Xiao JF, Loh XY, Lin DC, Garg M, Lim SL, Liu LZ, Madan V, ... ... Ogawa S, et al. Mutational landscape of pediatric acute lymphoblastic leukemia. Cancer Research. PMID 27872090 DOI: 10.1158/0008-5472.CAN-16-1303  0.327
2016 Shiba N, Yoshida K, Shiraishi Y, Okuno Y, Yamato G, Hara Y, Nagata Y, Chiba K, Tanaka H, Terui K, Kato M, Park MJ, Ohki K, Shimada A, Takita J, ... ... Ogawa S, et al. Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia. British Journal of Haematology. PMID 27470916 DOI: 10.1111/bjh.14247  0.336
2016 Sun QY, Ding LW, Tan KT, Chien W, Mayakonda A, Lin DC, Loh XY, Xiao JF, Meggendorfer M, Alpermann T, Garg M, Lim SL, Madan V, Hattori N, Nagata Y, ... ... Ogawa S, et al. Ordering of mutations in acute myeloid leukemia with partial tandem duplication of MLL (MLL-PTD). Leukemia. PMID 27389053 DOI: 10.1038/leu.2016.160  0.341
2016 Niemöller C, Renz N, Bleul S, Blagitko-Dorfs N, Greil C, Yoshida K, Pfeifer D, Follo M, Duyster J, Claus R, Ogawa S, Lübbert M, Becker H. Single cell genotyping of exome sequencing-identified mutations to characterize the clonal composition and evolution of inv(16) AML in a CBL mutated clonal hematopoiesis. Leukemia Research. 47: 41-46. PMID 27244256 DOI: 10.1016/j.leukres.2016.05.008  0.333
2016 Madan V, Shyamsunder P, Han L, Mayakonda A, Nagata Y, Sundaresan J, Kanojia D, Yoshida K, Ganesan S, Hattori N, Fulton N, Tan KT, Alpermann T, Kuo MC, Rostami S, ... ... Ogawa S, et al. Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia. Leukemia. PMID 27063598 DOI: 10.1038/leu.2016.69  0.354
2016 Sawada G, Niida A, Uchi R, Hirata H, Shimamura T, Suzuki Y, Shiraishi Y, Chiba K, Imoto S, Takahashi Y, Iwaya T, Sudo T, Hayashi T, Takai H, Kawasaki Y, ... ... Ogawa S, et al. Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population. Gastroenterology. PMID 26873401 DOI: 10.1053/J.Gastro.2016.01.035  0.325
2016 Nguyen TQ, Saitoh M, Trinh HT, Doan NM, Mizuno Y, Seki M, Sato Y, Ogawa S, Mizuguchi M. Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis-van Creveld syndrome. Congenital Anomalies. PMID 26748586 DOI: 10.1111/cga.12155  0.307
2016 Nagata Y, Makishima H, Radivoyevitch T, Hirsch CM, Przychodzen BP, Kuzmanovic T, Li S, Yoshida K, Yoshizato T, Adema V, Negoro E, Clemente MJ, Hosono N, Shiraishi Y, Chiba K, ... ... Ogawa S, et al. Landscape of Subclonal Mutations in Myelodysplastic Syndromes (MDS) Allows for a Novel Hierarchy of Clonal Advantage By Combining Germline and Somatic Mutations Blood. 128: 957-957. DOI: 10.1182/BLOOD.V128.22.957.957  0.326
2016 Ueno H, Yoshida K, Yamashita Y, Shiozawa Y, Ishida T, Tsukamoto H, Shiraishi Y, Tanaka H, Chiba K, Deguchi T, Sato A, Hashii Y, Tokimasa S, Hara J, Kosaka Y, ... ... Ogawa S, et al. Landscape of Driver Mutations and Their Clinical Impacts in Pediatric Acute Lymphoblastic Leukemia Blood. 128: 912-912. DOI: 10.1182/BLOOD.V128.22.912.912  0.351
2016 Sun Q, Ding L, Tan K, Chien W, Mayakonda A, Yeoh AEJ, Kawamata N, Nagata Y, Jin-Fen X, Loh X, Lin D, Garg M, Jiang Y, Xu L, Lim S, ... ... Ogawa S, et al. Mutational Landscape of Pediatric Acute Lymphoblastic Leukemia Blood. 128: 452-452. DOI: 10.1182/BLOOD.V128.22.452.452  0.318
2016 Nagao Y, Mimura N, Takeda J, Oshima M, Yoshida K, Shiozawa Y, Aoyama K, Saraya A, Koide S, Shiraishi Y, Chiba K, Tanaka H, Kawajiri-Manako C, Hasegawa N, Sakai S, ... ... Ogawa S, et al. Distinctive Genetic Features of Plasma Cells in POEMS Syndrome Blood. 128: 4404-4404. DOI: 10.1182/BLOOD.V128.22.4404.4404  0.331
2016 Makishima H, Yoshizato T, Yoshida K, Sekeres MA, Radivoyevitch T, Suzuki H, Przychodzen BP, Nagata Y, Meggendorfer M, Sanada M, Okuno Y, Hirsch CM, Kuzmanovic T, Shiozawa Y, Sato Y, ... ... Ogawa S, et al. the Impact of Clonal Dynamics on Prognosis and Outcome in Myelodysplastic Syndromes Blood. 128: 4287-4287. DOI: 10.1182/BLOOD.V128.22.4287.4287  0.318
2016 Yoshida K, Shiraishi Y, Chiba K, Okuno Y, Nakamoto-Matsubara R, Koriyama S, Yoshizato T, Shiozawa Y, Kataoka K, Ueno H, Takeda J, Tanaka H, Hayano A, Homma J, Fukai J, ... ... Ogawa S, et al. Whole-Genome Sequencing of Primary Central Nervous System Lymphoma and Diffuse Large B-Cell Lymphoma Blood. 128: 4112-4112. DOI: 10.1182/BLOOD.V128.22.4112.4112  0.321
2016 Isobe T, Yoshida K, Kobayashi C, Shiraishi Y, Chiba K, Tanaka H, Fukuda S, Yamamoto S, Tatsuno K, Aoki Y, Miyamura T, Tsutsumi S, Kiyokawa N, Ishihara T, Tomizawa D, ... ... Ogawa S, et al. Genome-Wide Mutational Landscape of Infant Acute Lymphoblastic Leukemia Blood. 128: 4070-4070. DOI: 10.1182/BLOOD.V128.22.4070.4070  0.317
2016 Takeda J, Chiba K, Shiraishi Y, Yoshizato T, Shiozawa Y, Nagata Y, Hangaishi A, Ishiyama K, Kataoka K, Sanada M, Tanaka H, Usuki K, Miyawaki S, Miyano S, Ganser A, ... Ogawa S, et al. Genetic Profile of Acute Erythroid Leukemia Blood. 128: 40-40. DOI: 10.1182/BLOOD.V128.22.40.40  0.352
2016 Murakami N, Muramatsu H, Okuno Y, Sakaguchi H, Yoshida K, Ueno T, Shiraishi Y, Chiba K, Tanaka H, Kojima D, Sekiya Y, Suzuki K, Kawashima N, Narita A, Nishio N, ... ... Ogawa S, et al. Comprehensive Genetic Analysis in Cases of Juvenile Myelomonocytic Leukemia for Prognostic Estimation Blood. 128: 3159-3159. DOI: 10.1182/blood.v128.22.3159.3159  0.301
2016 Malcovati L, Gallì A, Travaglino E, Ambaglio I, Rizzo E, Molteni E, Elena C, Catricalà S, Bono E, Bianchessi A, Todisco G, Rumi E, Ferretti VV, Papaemmanuil E, Ogawa S, et al. Predictive Value of Mutation Analysis in the Diagnostic Approach to Patients with Unexplained Cytopenia Blood. 128: 298-298. DOI: 10.1182/BLOOD.V128.22.298.298  0.324
2016 Watatani Y, Sato Y, Nishida K, Miyoshi H, Shiraishi Y, Chiba K, Hiroko T, Ueno H, Kakiuchi N, Shiozawa Y, Yoshizato T, Yoshida K, Sanada M, Miyano S, Ohshima K, ... ... Ogawa S, et al. Molecular Heterogeneity in Peripheral T-Cell Lymphoma Not Otherwise Specified Revealed By Comprehensive Mutational Profiling Blood. 128: 2927-2927. DOI: 10.1182/BLOOD.V128.22.2927.2927  0.331
2016 Shiba N, Yoshida K, Shiraishi Y, Yuichi S, Hara Y, Yamato G, Kaburagi T, Sanada M, Ohki K, Park M, Tomizawa D, Chiba K, Tanaka H, Sotomatsu M, Arakawa H, ... ... Ogawa S, et al. Transcriptome Analysis Revealed the Entire Genetic Understanding of Pediatric Acute Myeloid Leukemia with a Normal Karyotype Blood. 128: 2850-2850. DOI: 10.1182/blood.v128.22.2850.2850  0.345
2016 Ogawa S. Clonal hematopoiesis in acquired aplastic anemia Blood. 128: 337-347. DOI: 10.1182/blood-2016-01-636381  0.322
2015 Nagata Y, Kontani K, Enami T, Kataoka K, Ishii R, Totoki Y, Kataoka TR, Hirata M, Aoki K, Nakano K, Kitanaka A, Sakata-Yanagimoto M, Egami S, Shiraishi Y, Chiba K, ... ... Ogawa S, et al. Variegated RHOA mutations in adult T-cell leukemia/lymphoma. Blood. PMID 26574607 DOI: 10.1182/blood-2015-06-644948  0.318
2015 Garg M, Nagata Y, Kanojia D, M T A, Yoshida K, Keloth SH, Jiang ZZ, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ding LW, Alpermann T, Sun QY, ... ... Ogawa S, et al. Profiling of somatic mutations of acute myeloid leukemia, FLT3-ITD subgroup at diagnosis and relapse. Blood. PMID 26438511 DOI: 10.1182/Blood-2015-05-646240  0.348
2015 Okuno Y, Hoshino A, Muramatsu H, Kawashima N, Wang X, Yoshida K, Wada T, Gunji M, Toma T, Kato T, Shiraishi Y, Iwata A, Hori T, Kitoh T, Chiba K, ... ... Ogawa S, et al. Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism. Journal of Clinical Immunology. PMID 26407811 DOI: 10.1007/s10875-015-0202-0  0.319
2015 Huang D, Nagata Y, Grossmann V, Radivoyevitch T, Okuno Y, Nagae G, Hosono N, Schnittger S, Sanada M, Przychodzen B, Kon A, Polprasert C, Shen W, Clemente MJ, Phillips JG, ... ... Ogawa S, et al. BRCC3 mutations in myeloid neoplasms. Haematologica. PMID 26001790 DOI: 10.3324/Haematol.2014.111989  0.347
2015 Polprasert C, Schulze I, Sekeres MA, Makishima H, Przychodzen B, Hosono N, Singh J, Padgett RA, Gu X, Phillips JG, Clemente M, Parker Y, Lindner D, Dienes B, Jankowsky E, ... ... Ogawa S, et al. Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms. Cancer Cell. 27: 658-70. PMID 25920683 DOI: 10.1016/J.Ccell.2015.03.017  0.304
2015 Shiota M, Yang X, Kubokawa M, Morishima T, Tanaka K, Mikami M, Yoshida K, Kikuchi M, Izawa K, Nishikomori R, Okuno Y, Wang X, Sakaguchi H, Muramatsu H, Kojima S, ... ... Ogawa S, et al. Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases. Journal of Clinical Immunology. 35: 454-8. PMID 25896945 DOI: 10.1007/s10875-015-0163-3  0.316
2015 Molenaar RJ, Thota S, Nagata Y, Patel B, Clemente M, Hirsh C, Viny AD, Hosano N, Bleeker FE, Meggendorfer M, Alpermann T, Shiraishi Y, Chiba K, Tanaka H, van Noorden CJ, ... ... Ogawa S, et al. Clinical and biological implications of ancestral and non-ancestral IDH1 and IDH2 mutations in myeloid neoplasms. Leukemia. PMID 25836588 DOI: 10.1038/leu.2015.91  0.3
2015 Kawashima-Goto S, Imamura T, Seki M, Kato M, Yoshida K, Sugimoto A, Kaneda D, Fujiki A, Miyachi M, Nakatani T, Osone S, Ishida H, Taki T, Takita J, Shiraishi Y, ... ... Ogawa S, et al. Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient. International Journal of Hematology. 101: 411-6. PMID 25430085 DOI: 10.1007/s12185-014-1711-y  0.363
2015 Wang R, Yoshida K, Toki T, Sawada T, Uechi T, Okuno Y, Sato-Otsubo A, Kudo K, Kamimaki I, Kanezaki R, Shiraishi Y, Chiba K, Tanaka H, Terui K, Sato T, ... ... Ogawa S, et al. Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia. British Journal of Haematology. 168: 854-64. PMID 25424902 DOI: 10.1111/bjh.13229  0.333
2015 Dumitriu B, Feng X, Townsley DM, Ueda Y, Yoshizato T, Calado RT, Yang Y, Wakabayashi Y, Kajigaya S, Ogawa S, Zhu J, Young NS. Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemia. Blood. 125: 706-9. PMID 25406353 DOI: 10.1182/blood-2014-10-607572  0.348
2015 Kurtovic-Kozaric A, Przychodzen B, Singh J, Konarska MM, Clemente MJ, Otrock ZK, Nakashima M, Hsi ED, Yoshida K, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Boultwood J, et al. PRPF8 defects cause missplicing in myeloid malignancies. Leukemia. 29: 126-36. PMID 24781015 DOI: 10.1038/Leu.2014.144  0.312
2015 Suzuki H, Aoki K, Chiba K, Sato Y, Shiozawa Y, Shiraishi Y, Shimamura T, Niida A, Motomura K, Ohka F, Nakamura H, Mizoguchi M, Abe T, Muragaki Y, Watanabe R, ... ... Ogawa S, et al. The landscape and clonal architecture in lower grade glioma. Journal of Clinical Oncology. 33: 2008-2008. DOI: 10.1200/Jco.2015.33.15_Suppl.2008  0.321
2015 Ogura H, Ohga S, Aoki T, Utsugisawa T, Takahashi H, Iwai A, Watanabe K, Okuno Y, Yoshida K, Miyano S, Ogawa S, Kojima S, Kanno H. COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants Blood. 126: 934-934. DOI: 10.1182/BLOOD.V126.23.934.934  0.305
2015 Bejar R, Papaemmanuil E, Haferlach T, Garcia-Manero G, Maciejewski JP, Sekeres MA, Walter MJ, Graubert TA, Cazzola M, Malcovati L, Ogawa S, Fenaux P, Hellstrom-Lindberg E, Kern W, Boultwood J, et al. Somatic Mutations in MDS Patients Are Associated with Clinical Features and Predict Prognosis Independent of the IPSS-R: Analysis of Combined Datasets from the International Working Group for Prognosis in MDS-Molecular Committee Blood. 126: 907-907. DOI: 10.1182/Blood.V126.23.907.907  0.301
2015 Makishima H, Yoshida K, LaFramboise T, Yoshizato T, Ruffalo M, Sekeres MA, Przychodzen B, Suzuki H, Sanada M, Nagata Y, Okuno Y, Sato Y, Sato-Otsubo A, Clemente MJ, Hosono N, ... ... Ogawa S, et al. Serial Sequencing in Myelodysplastic Syndromes Reveals Dynamic Changes in Clonal Architecture and Allows for a New Prognostic Assessment of Mutations Detected in Cross-Sectional Testing Blood. 126: 709-709. DOI: 10.1182/BLOOD.V126.23.709.709  0.331
2015 Niemöller C, Bleul S, Blagitko-Dorfs N, Greil C, Yoshida K, Claus R, Pfeifer D, Ogawa S, Lübbert M, Becker H. Single Cell Genotyping of Inv(16) AML in CBL Mutated Clonal Hematopoiesis Characterizes Clonal Architecture and Evolution of Exome Sequencing-Identified Mutations in the Protein Tyrosine Phosphatase Ptprt and Other Genes Blood. 126: 3834-3834. DOI: 10.1182/BLOOD.V126.23.3834.3834  0.335
2015 Narita A, Okuno Y, Muramatsu H, Yoshida K, Shiraishi Y, Sekiya Y, Chiba K, Tanaka H, Wang X, Kawashima N, Nishio N, Doisaki S, Hama A, Takahashi Y, Sakaguchi H, ... ... Ogawa S, et al. Genetic Background of Idiopathic Bone Marrow Failure Syndromes in Children Blood. 126: 3610-3610. DOI: 10.1182/BLOOD.V126.23.3610.3610  0.334
2015 Watatani Y, Nagata Y, Grossmann V, Okuno Y, Yoshizato T, Shiozawa Y, Nagae G, Yoshida K, Kataoka K, Schnittger S, Sanada M, Kon A, Shiraishi Y, Chiba K, Tanaka H, ... ... Ogawa S, et al. Two Novel Distinct Subtypes of Myeloid Neoplasms Molecularly Associated with Histone H3K36 Methylations Blood. 126: 2841-2841. DOI: 10.1182/BLOOD.V126.23.2841.2841  0.342
2015 Yoshida K, Nakamoto-Matsubara R, Chiba K, Okuno Y, Kakiuchi N, Shiraishi Y, Sato Y, Suzuki H, Yoshizato T, Shiozawa Y, Kataoka K, Ueno H, Takeda J, Nagata Y, Tanaka H, ... ... Ogawa S, et al. Genetic Basis of Primary Central Nervous System Lymphoma Blood. 126: 2687-2687. DOI: 10.1182/BLOOD.V126.23.2687.2687  0.349
2015 Shiba N, Yoshida K, Shiraishi Y, Hara Y, Yamato G, Kaburaki T, Sanada M, Oki K, Tomizawa D, Sotomatsu M, Arakawa H, Horibe K, PARK M, Taga T, Adachi S, ... ... Ogawa S, et al. Detection of Novel Pathogenic Gene Rearrangements in Pediatric Acute Myeloid Leukemia By RNA Sequencing Blood. 126: 2575-2575. DOI: 10.1182/BLOOD.V126.23.2575.2575  0.334
2015 Negoro E, Hosono N, Shen W, Yoshizato T, Patel BJ, Hirsh C, Przychodzen B, Clemente MJ, Mahfouz RZ, Wodnar-Filipowicz A, Makishima H, Ogawa S, Sekeres MA, Maciejewski JP. Myelodysplastic Syndrome (MDS)-Determining Clonal Events at Presentation of Aplastic Anemia (AA) Blood. 126: 1652-1652. DOI: 10.1182/BLOOD.V126.23.1652.1652  0.336
2015 Nakamoto-Matsubara R, Sakata-Yanagimoto M, Nguyen T, Furuta J, Ito T, Komeno T, Ogawa S, Chiba S. G17V Rhoa Mutation in Circulating DNA Is a Useful Marker for Diagnosis of AITL and AITL-Related Lymphoma Blood. 126: 1447-1447. DOI: 10.1182/BLOOD.V126.23.1447.1447  0.335
2015 Yamashita Y, Sanada M, Yoshida K, Ueno H, Tanaka H, Shiraishi Y, Chiba K, Imamura T, Miyano S, Kato K, Kojima S, Ogawa S, Horibe K. Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia Blood. 126: 1425-1425. DOI: 10.1182/BLOOD.V126.23.1425.1425  0.338
2015 Shiozawa Y, Malcovati L, Sato-Otsubo A, Gallì A, Yoshida K, Yoshizato T, Sato Y, Kataoka K, Sanada M, Makishima H, Shiraishi Y, Chiba K, Miyano S, Lindberg EH, Ogawa S, et al. Different Mutant Splicing Factors Cause Distinct Missplicing Events and Give Rise to Different Clinical Phenotypes in Myelodysplastic Syndromes Blood. 126: 139-139. DOI: 10.1182/BLOOD.V126.23.139.139  0.347
2015 Katagiri T, Tominaga R, Kataoka K, Maeda A, Gomyo H, Mizuno I, Murayama T, Ogawa S, Nakao S. A Cure for Paroxysmal Nocturnal Hemoglobinuria Using Molecular Targeted Therapy Specific to a Driver Mutation Blood. 126: 1215-1215. DOI: 10.1182/BLOOD.V126.23.1215.1215  0.307
2015 Kataoka K, Nagata Y, Kitanaka A, Shiraishi Y, Yasunaga J, Totoki Y, Chiba K, Sato-Otsubo A, Kotani S, Sanada M, Tanaka H, Suzuki H, Sato Y, Shiozawa Y, Yoshizato T, ... ... Ogawa S, et al. Frequent Activating Somatic Alterations in T-Cell Receptor / NF-κb Signaling in Adult T-Cell Leukemia/Lymphoma Blood. 126: 113-113. DOI: 10.1182/blood.v126.23.113.113  0.328
2015 Takagi M, Imai K, Piao J, Yamashita M, Hoshino A, Okano T, Kanegane H, Muramatsu H, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Yoshida K, Ueno H, ... Ogawa S, et al. Whole-Exome Analysis of Autoimmune Lymphoproliferative Syndrome-like Diseases Blood. 126: 1022-1022. DOI: 10.1182/BLOOD.V126.23.1022.1022  0.339
2014 Shen W, Clemente MJ, Hosono N, Yoshida K, Przychodzen B, Yoshizato T, Shiraishi Y, Miyano S, Ogawa S, Maciejewski JP, Makishima H. Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. The Journal of Clinical Investigation. 124: 4529-38. PMID 25244093 DOI: 10.1172/JCI74747  0.344
2014 Damm F, Mylonas E, Cosson A, Yoshida K, Della Valle V, Mouly E, Diop M, Scourzic L, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Kikushige Y, Davi F, Lambert J, ... ... Ogawa S, et al. Acquired initiating mutations in early hematopoietic cells of CLL patients. Cancer Discovery. 4: 1088-101. PMID 24920063 DOI: 10.1158/2159-8290.CD-14-0104  0.336
2014 Seki M, Yoshida K, Shiraishi Y, Shimamura T, Sato Y, Nishimura R, Okuno Y, Chiba K, Tanaka H, Kato K, Kato M, Hanada R, Nomura Y, Park MJ, Ishida T, ... ... Ogawa S, et al. Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma. Cancer Research. 74: 2742-9. PMID 24675358 DOI: 10.1158/0008-5472.CAN-13-2470  0.304
2014 Becker H, Yoshida K, Blagitko-Dorfs N, Claus R, Pantic M, Abdelkarim M, Niemöller C, Greil C, Hackanson B, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Döhner K, Schnittger S, ... ... Ogawa S, et al. Tracing the development of acute myeloid leukemia in CBL syndrome. Blood. 123: 1883-6. PMID 24493670 DOI: 10.1182/blood-2013-10-533844  0.325
2014 Kihara R, Nagata Y, Kiyoi H, Kato T, Yamamoto E, Suzuki K, Chen F, Asou N, Ohtake S, Miyawaki S, Miyazaki Y, Sakura T, Ozawa Y, Usui N, Kanamori H, ... ... Ogawa S, et al. Comprehensive analysis of genetic alterations and their prognostic impacts in adult acute myeloid leukemia patients. Leukemia. 28: 1586-95. PMID 24487413 DOI: 10.1038/leu.2014.55  0.337
2014 Sakata-Yanagimoto M, Enami T, Yoshida K, Shiraishi Y, Ishii R, Miyake Y, Muto H, Tsuyama N, Sato-Otsubo A, Okuno Y, Sakata S, Kamada Y, Nakamoto-Matsubara R, Tran NB, Izutsu K, ... ... Ogawa S, et al. Somatic RHOA mutation in angioimmunoblastic T cell lymphoma. Nature Genetics. 46: 171-5. PMID 24413737 DOI: 10.1038/ng.2872  0.333
2014 Haferlach T, Nagata Y, Grossmann V, Okuno Y, Bacher U, Nagae G, Schnittger S, Sanada M, Kon A, Alpermann T, Yoshida K, Roller A, Nadarajah N, Shiraishi Y, Shiozawa Y, ... ... Ogawa S, et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia. 28: 241-7. PMID 24220272 DOI: 10.1182/Blood.V122.21.521.521  0.3
2014 Lin TL, Nagata Y, Kao HW, Sanada M, Okuno Y, Huang CF, Liang DC, Kuo MC, Lai CL, Lee EH, Shih YS, Tanaka H, Shiraishi Y, Chiba K, Lin TH, ... ... Ogawa S, et al. Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations. Haematologica. 99: 28-36. PMID 23996483 DOI: 10.3324/haematol.2013.091249  0.309
2014 Young NS, Dumitriu B, Ogawa S. Acquired Aplastic Anemia: New Genetics, New Genomics Blood. 124: SCI-21-SCI-21. DOI: 10.1182/BLOOD.V124.21.SCI-21.SCI-21  0.359
2014 Shiozawa Y, Sato-Otsubo S, Gallì A, Yoshida K, Yoshizato T, Sato Y, Kataoka K, Sanada M, Shiraishi Y, Chiba K, Miyano S, Malcovati L, Cazzola M, Ogawa S. Comprehensive Analysis of Aberrant RNA Splicing in Myelodysplastic Syndromes Blood. 124: 826-826. DOI: 10.1182/BLOOD.V124.21.826.826  0.326
2014 Makishima H, Yoshida K, LaFramboise T, Przychodzen BP, Ruffalo M, Gómez-Seguí I, Shiraishi Y, Sanada M, Nagata Y, Sato Y, Sato-Otsubo A, Chiba K, Tanaka H, Nakamaki T, Hofmann W, ... ... Ogawa S, et al. In Analogy to AML, MDS Can be Sub-Classified By Ancestral Mutations Blood. 124: 823-823. DOI: 10.1182/BLOOD.V124.21.823.823  0.33
2014 Kataoka K, Nagata Y, Kitanaka A, Totoki Y, Yasunaga J, Kotani S, Sato-Otsubo A, Sanada M, Shiraishi Y, Shimamura T, Chiba K, Tanaka H, Suzuki H, Sato Y, Shiozawa Y, ... ... Ogawa S, et al. Landscape of Genetic Alterations in Adult T-Cell Leukemia/Lymphoma Blood. 124: 75-75. DOI: 10.1182/BLOOD.V124.21.75.75  0.357
2014 Bejar R, Papaemmanuil E, Haferlach T, Garcia-Manero G, Maciejewski JP, Sekeres MA, Walter MJ, Graubert TA, Cazzola M, Malcovati L, Campbell PJ, Ogawa S, Boultwood J, Bowen D, Tauro S, et al. TP53 Mutation Status Divides MDS Patients with Complex Karyotypes into Distinct Prognostic Risk Groups: Analysis of Combined Datasets from the International Working Group for MDS-Molecular Prognosis Committee Blood. 124: 532-532. DOI: 10.1182/Blood.V124.21.532.532  0.33
2014 Okuno Y, Narita A, Muramatsu H, Yoshida K, Hama A, Wang X, Xu Y, Kawashima N, Sakaguchi H, Doisaki S, Takahashi Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, ... Ogawa S, et al. Whole-Exome Sequencing Reveals a Paucity of Somatic Gene Mutations in Aplastic Anemia and Refractory Cytopenia of Childhood Blood. 124: 4388-4388. DOI: 10.1182/BLOOD.V124.21.4388.4388  0.346
2014 Dienes B, Przychodzen BP, Clemente M, Shen W, Polprasert C, Hosono N, Miyano S, Shiraishi Y, Yoshida K, Ogawa S, Sekeres MA, Saunthararajah Y, Maciejewski JP, Makishima H. Impact and Function of Somatic PHF6 Mutations in Myeloid Neoplasms Blood. 124: 3581-3581. DOI: 10.1182/BLOOD.V124.21.3581.3581  0.373
2014 Seki M, Yoshida K, Yuichi S, Chiba K, Tanaka H, Kato M, Hanada R, Miyano S, Hayashi Y, Ogawa S, Takita J. Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia Blood. 124: 3527-3527. DOI: 10.1182/BLOOD.V124.21.3527.3527  0.326
2014 Nguyen TB, Sakata-Yanagimoto M, Asabe Y, Yoshida K, Muto H, Nakamoto-Matsubara R, Izutsu K, Nakamura N, Takeuchi K, Ogawa S, Chiba S. Identification of Cell-Type-Specific Mutations in Angioimmunoblastic T-Cell Lymphoma Blood. 124: 3025-3025. DOI: 10.1182/blood.v124.21.3025.3025  0.336
2014 Yoshizato T, Dumitriu B, Hosokawa K, Makishima H, Yoshida K, Sato A, Okuno Y, Kataoka K, Chiba K, Tanaka H, Shiraishi Y, Nagata Y, Suzuki H, Sato Y, Shiozawa Y, ... ... Ogawa S, et al. Chronological Analysis of Clonal Evolution in Acquired Aplastic Anemia Blood. 124: 253-253. DOI: 10.1182/BLOOD.V124.21.253.253  0.37
2014 Nagata Y, Enami T, Kontani K, Kataoka K, Sakata-Yanagimoto M, Kitanaka A, Sato A, Shiraishi Y, Chiba K, Tanaka H, Shiozawa Y, Yoshizato T, Kon A, Yoshida K, Sanada M, ... ... Ogawa S, et al. Novel Biological Effects and Distinct Patterns of Rhoa Mutations in Adult T-Cell Leukemia/Lymphoma and Angioimmunoblastic T Cell Lymphoma Blood. 124: 2215-2215. DOI: 10.1182/BLOOD.V124.21.2215.2215  0.321
2014 Thota S, Makishima H, Przychodzen BP, Viny AD, Patel BJ, Radivoyevitch T, Sekeres MA, Carraway HE, Haferlach T, Ogawa S, Maciejewski JP. The Impact of Clonal Architecture of IDH1 and IDH2 Mutant Cases on the Biology of Myeloid Malignancies Blood. 124: 1897-1897. DOI: 10.1182/BLOOD.V124.21.1897.1897  0.329
2014 Patel BJ, Huang D, Thota S, Przychodzen BP, Sakaguchi H, Kojima S, Ogawa S, Sekeres MA, Makishima H, Maciejewski JP. Chronic Myelomonocytic Leukemia (CMML) Can be Categorized By Ancestral Mutational Events Blood. 124: 1893-1893. DOI: 10.1182/BLOOD.V124.21.1893.1893  0.322
2014 Yamaguchi H, Sakaguchi H, Yoshida K, Yabe M, Yabe H, Okuno Y, Muramatsu H, Yui S, Inokuchi K, Ito E, Ogawa S, Kojima S. The Clinical and Genetic Features of Dyskeratosis Congenita, Cryptic Dyskeratosis Congenita, and Hoyeraal-Hreidarsson Syndrome in Japan Blood. 124: 1608-1608. DOI: 10.1182/BLOOD.V124.21.1608.1608  0.317
2014 Polprasert C, Schulze I, Sekeres MA, Makishima H, Przychodzen BP, Hosono N, Singh J, Padgett RA, Gu X, Jankowsky E, Clemente M, Dienes B, Mukherjee S, Krug U, Klein H, ... ... Ogawa S, et al. DDX41 Is a Tumor Suppressor Gene Associated with Inherited and Acquired Mutations Blood. 124: 125-125. DOI: 10.1182/Blood.V124.21.125.125  0.347
2014 Ahn J, Kim H, Kim Y, Lee I, Kim NY, Minden MD, Jung CW, Jang J, Kim H, Moon JH, Sohn SK, Won J, Kim S, Kim N, Yoshida K, ... Ogawa S, et al. An Adverse Prognostic Effect of Homozygous TET2 Mutational Status on the Relapse Risk of Acute Myeloid Leukemia Patients of Normal Karyotype Blood. 124: 1052-1052. DOI: 10.1182/blood.v124.21.1052.1052  0.32
2014 Yamato G, Shiba N, Yoshida K, Ohki K, Park M, Hara Y, Tomizawa D, Sotomatsu M, Taga T, Adachi S, Tawa A, Horibe K, Arakawa H, Ogawa S, Hayashi Y. Clinical Features of Patients with ASXL1 and ASXL2 Mutations in Pediatric Acute Myeloid Leukemia Blood. 124: 1024-1024. DOI: 10.1182/BLOOD.V124.21.1024.1024  0.335
2014 Suzuki H, Aoki K, Ohka F, Motomura K, Fujii M, Sanada M, Nakamura H, Mizoguchi M, Abe T, Muragaki Y, Wakabayashi T, Ogawa S, Natsume A. GE-34 * THE MUTATIONAL LANDSCAPE AND TEMPORAL AND SPATIAL CLONAL EVOLUTION TO PROGRESSION IN 351 LOW-GRADE GLIOMAS Neuro-Oncology. 16: v103-v104. DOI: 10.1093/Neuonc/Nou256.33  0.329
2014 Meng X, Lin D, Nagata Y, Sato Y, Goh BC, Lee SC, Yu FG, Ogawa S, Loh KS, Koeffler HP. O1-18-3Exome Sequencing And Snp Array Reveal Epigenome Modifier Defects In Nasopharyngeal Carcinoma Annals of Oncology. 25. DOI: 10.1093/Annonc/Mdu435.42  0.313
2013 Muto T, Sashida G, Oshima M, Wendt GR, Mochizuki-Kashio M, Nagata Y, Sanada M, Miyagi S, Saraya A, Kamio A, Nagae G, Nakaseko C, Yokote K, Shimoda K, Koseki H, ... ... Ogawa S, et al. Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders. The Journal of Experimental Medicine. 210: 2627-39. PMID 24218139 DOI: 10.1084/jem.20131144  0.322
2013 Yoshida K, Toki T, Okuno Y, Kanezaki R, Shiraishi Y, Sato-Otsubo A, Sanada M, Park MJ, Terui K, Suzuki H, Kon A, Nagata Y, Sato Y, Wang R, Shiba N, ... ... Ogawa S, et al. The landscape of somatic mutations in Down syndrome-related myeloid disorders. Nature Genetics. 45: 1293-9. PMID 24056718 DOI: 10.1038/ng.2759  0.309
2013 Damm F, Chesnais V, Nagata Y, Yoshida K, Scourzic L, Okuno Y, Itzykson R, Sanada M, Shiraishi Y, Gelsi-Boyer V, Renneville A, Miyano S, Mori H, Shih LY, Park S, ... ... Ogawa S, et al. BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders. Blood. 122: 3169-77. PMID 24047651 DOI: 10.1182/blood-2012-11-469619  0.34
2013 Kon A, Shih LY, Minamino M, Sanada M, Shiraishi Y, Nagata Y, Yoshida K, Okuno Y, Bando M, Nakato R, Ishikawa S, Sato-Otsubo A, Nagae G, Nishimoto A, Haferlach C, ... ... Ogawa S, et al. Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. Nature Genetics. 45: 1232-7. PMID 23955599 DOI: 10.1038/Ng.2731  0.311
2013 Makishima H, Yoshida K, Nguyen N, Przychodzen B, Sanada M, Okuno Y, Ng KP, Gudmundsson KO, Vishwakarma BA, Jerez A, Gomez-Segui I, Takahashi M, Shiraishi Y, Nagata Y, Guinta K, ... ... Ogawa S, et al. Somatic SETBP1 mutations in myeloid malignancies. Nature Genetics. 45: 942-6. PMID 23832012 DOI: 10.1038/ng.2696  0.344
2013 Sakaguchi H, Okuno Y, Muramatsu H, Yoshida K, Shiraishi Y, Takahashi M, Kon A, Sanada M, Chiba K, Tanaka H, Makishima H, Wang X, Xu Y, Doisaki S, Hama A, ... ... Ogawa S, et al. Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia. Nature Genetics. 45: 937-41. PMID 23832011 DOI: 10.1038/ng.2698  0.327
2013 Saida S, Watanabe K, Sato-Otsubo A, Terui K, Yoshida K, Okuno Y, Toki T, Wang R, Shiraishi Y, Miyano S, Kato I, Morishima T, Fujino H, Umeda K, Hiramatsu H, ... ... Ogawa S, et al. Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome. Blood. 121: 4377-87. PMID 23482930 DOI: 10.1182/blood-2012-12-474387  0.317
2013 Shiba N, Yoshida K, Nagata Y, Kon A, Okuno Y, Shiraishi Y, Kato M, Park M, Ohki K, Takita J, Kanazawa T, Kudo K, Ito E, Sanada M, Tomizawa D, ... ... Ogawa S, et al. Whole-Exome Resequencing Identifies Somatic Mutations Of BCOR and BCORL1 Transcriptional Corepressor Genes and Major Cohesin Complex Component Genes In Pediatric Acute Myeloid Leukemia Blood. 122: 834-834. DOI: 10.1182/BLOOD.V122.21.834.834  0.348
2013 Sakata-Yanagimoto M, Enami T, Yoshida K, Shiraishi Y, Ishii R, Miyake Y, Muto H, Tsuyama N, Okuno Y, Sakata S, Kamada Y, Nakamoto-Matsubara R, Nguyen T, Izutsu K, Ohta Y, ... ... Ogawa S, et al. Somatic G17V Rhoa Mutation Specifies Angioimmunoblastic T-Cell Lymphoma Blood. 122: 815-815. DOI: 10.1182/BLOOD.V122.21.815.815  0.334
2013 Shen W, Przychodzen BP, Clemente MJ, Dienes B, Yoshisato T, Sanada M, Yoshida K, Ogawa S, Maciejewski JP, Makishima H. The Presence Of Leukemogenic Mutational Events In Paroxysmal Nocturnal Hemoglobinuria Suggests That Clonal Architecture Of Bone Marrow Failure Is Similar To Myelodysplastic Syndrome Blood. 122: 804-804. DOI: 10.1182/BLOOD.V122.21.804.804  0.349
2013 Makishima H, LaFramboise T, Przychodzen BP, Yoshida K, Ruffalo M, Gómez-Seguí I, Husseinzadeh HD, Shiraishi Y, Sanada M, Nagata Y, Sato Y, Sato-Otsubo A, Chiba K, Tanaka H, Nakamaki T, ... ... Ogawa S, et al. Clinical “MUTATOME” Of Myelodysplastic Syndrome; Comparison To Primary Acute Myelogenous Leukemia Blood. 122: 518-518. DOI: 10.1182/BLOOD.V122.21.518.518  0.318
2013 Muto T, Sashida G, Oshima M, Wendt GR, Mochizuki-Kashio M, Sanada M, Miyagi S, Saraya A, Nakaseko C, Yokote K, Shimoda K, Koseki H, Suzuki Y, Sugano S, Ogawa S, et al. Concurrent Loss Of Ezh2 and Tet2 Cooperates In The Pathogenesis Of Myelodysplastic Disorders, Blood. 122: 480-480. DOI: 10.1182/BLOOD.V122.21.480.480  0.322
2013 Hosono N, Makishima H, Przychodzen B, Singh J, Padgett RA, Sekeres MA, Jerez A, Yoshida K, Shiraishi Y, Miyano S, Sanada M, Ogawa S, Maciejewski JP. Spliceosomal Gene LUC7L2 Mutation Causes Missplicing and Alteration Of Gene Expression In Myeloid Neoplasms Blood. 122: 470-470. DOI: 10.1182/Blood.V122.21.470.470  0.326
2013 Seki M, Yoshida K, Sato Y, Shiraishi Y, Chiba K, Tanaka H, Kato M, Hiwatari M, Koh K, Hanada R, Sanada M, Miyano S, Oka A, Hayashi Y, Ogawa S, et al. Genetic Landscapes Of Childhood T-Cell Acute Lymphoblastic Leukemia Blood. 122: 3786-3786. DOI: 10.1182/BLOOD.V122.21.3786.3786  0.335
2013 Narita A, Muramatsu H, Yoshida K, Okuno Y, Hama A, Wang X, Xu Y, Kawashima N, Sakaguchi H, Doisaki S, Takahashi Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, ... Ogawa S, et al. Whole Exome Sequencing Shows a Paucity Of Somatic Gene Mutations In Pediatric Idiopathic Bone Marrow Failure Syndrome Blood. 122: 3708-3708. DOI: 10.1182/blood.v122.21.3708.3708  0.339
2013 Kurtovic Kozaric A, Makishima H, Przychodzen BP, Singh J, Konarska MM, Otrock ZK, Nakashima M, Hsi ED, Yoshida K, Ogawa S, Maciejewski JP. PRPF8 Defects Cause Missplicing In Myeloid Malignancies Blood. 122: 2838-2838. DOI: 10.1182/BLOOD.V122.21.2838.2838  0.342
2013 McMahon S, Przychodzen BP, Makishima H, LaFramboise T, Yoshida K, Shiraishi Y, Sanada M, Nagata Y, Sato Y, Chiba K, Tanaka H, Miyano S, Sato-Otsubo A, Ogawa S, Maciejewski JP. Whole Exome Analysis Of Germline Alterations Associated With Myelodysplastic Syndrome Blood. 122: 2800-2800. DOI: 10.1182/BLOOD.V122.21.2800.2800  0.321
2013 Polprasert C, Makishima H, Przychodzen BP, Hosono N, Shen W, Huang D, Shiraishi Y, Miyano S, Yoshida K, Ogawa S, Maciejewski JP. Whole Exome Sequencing Detecting Kinesin Family Gene Defects In Myeloid Neoplasm Blood. 122: 2762-2762. DOI: 10.1182/BLOOD.V122.21.2762.2762  0.325
2013 Huang D, Makishima H, Du Y, Hosono N, Shen W, Polprasert C, Sekeres MA, Przychodzen B, Padgett RA, Singh J, Guinta KM, Clemente MJ, Dienes B, Afable M, Husseinzadeh HD, ... ... Ogawa S, et al. Molecular Defects In BRCC3 Complex, a Novel Pathogenic Pathway In MDS Blood. 122: 264-264. DOI: 10.1182/Blood.V122.21.264.264  0.338
2013 Shen W, Przychodzen BP, Polprasert C, Hosono N, Dienes B, Miyano S, Shiraishi Y, Yoshida K, Ogawa S, Saunthararajah Y, Maciejewski JP, Makishima H. Somatic PHF6 Mutations In Myeloid Malignancies Blood. 122: 2514-2514. DOI: 10.1182/BLOOD.V122.21.2514.2514  0.354
2013 Yoshizato T, Dumitriu B, Hosokawa K, Makishima H, Yoshida K, Okuno Y, Chiba K, Tanaka H, Shiraishi Y, Nagata Y, Katagiri T, Kon A, Clemente MJ, Sanada M, Miyano S, ... ... Ogawa S, et al. Spectrum Of Genetic Alterations In Acquired Aplastic Anemia Blood. 122: 2464-2464. DOI: 10.1182/BLOOD.V122.21.2464.2464  0.364
2013 Nagata Y, Kitanaka A, Sanada M, Sato A, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Yoshizato T, Kon A, Yoshida K, Ishiyama K, Miyawaki S, Miyano S, Shimoda K, ... Ogawa S, et al. Molecular Characterization Of Adult T-Cell Leukemia/Lymphoma Blood. 122: 1766-1766. DOI: 10.1182/BLOOD.V122.21.1766.1766  0.352
2013 Muramatsu H, Sakaguchi H, Wang X, Yoshida K, Okuno Y, Sanada M, Xu Y, Doisaki S, Narita A, Kawashima N, Hama A, Takahashi Y, Yoshida N, Shiraishi Y, Chiba K, ... ... Ogawa S, et al. Clinical and Genetic Characterization Of Patients With C-CBL Mutated Juvenile Myelomonocytic Leukemia By Whole-Exome/Deep Sequencing Blood. 122: 1565-1565. DOI: 10.1182/blood.v122.21.1565.1565  0.311
2013 Muramatsu H, Sakaguchi H, Wang X, Yoshida K, Okuno Y, Sanada M, Xu Y, Doisaki S, Narita A, Kawashima N, Hama A, Takahashi Y, Yoshida N, Shiraishi Y, Chiba K, ... ... Ogawa S, et al. Clinical and Genetic Characterization Of Patients With C-CBL Mutated Juvenile Myelomonocytic Leukemia By Whole-Exome/Deep Sequencing Blood. 122: 1564-1564. DOI: 10.1182/BLOOD.V122.21.1564.1564  0.311
2013 Yoshida K, Shiba N, Shiraishi Y, Shimada A, Terui K, Kato M, Okuno Y, Nagata Y, Kon A, Yoshizato T, Matsunawa M, Chiba K, Tanaka H, Sanada M, Miyano S, ... ... Ogawa S, et al. Whole Exome Sequencing Reveals Clonal Evolution Pattern and Driver Mutations Of Relapsed Pediatric AML Blood. 122: 1410-1410. DOI: 10.1182/BLOOD.V122.21.1410.1410  0.337
2013 Hosono N, Ramdzan ZM, Pal R, Makishima H, Przychodzen BP, Sekeres MA, Yoshida K, Shiraishi Y, Miyano S, Ogawa S, Nepveu A, Maciejewski JP. Somatic Mutations and Loss-Of-Heterozygosity Impair The DNA Repair Functions Of CUX1 in Myelodysplastic Syndromes (MDS) Blood. 122: 1246-1246. DOI: 10.1182/Blood.V122.21.1246.1246  0.324
2013 Kon A, Shih L, Minamino M, Sanada M, Shiraishi Y, Nagata Y, Yoshida K, Okuno Y, Bando M, Ishikawa S, Sato-Otsubo A, Nagae G, Nishimoto A, Haferlach C, Nowak D, ... ... Ogawa S, et al. Abstract 4602: Recurrent pathway mutations of multiple components of cohesin complex in myeloid neoplasms. Cancer Research. 73: 4602-4602. DOI: 10.1158/1538-7445.Am2013-4602  0.335
2012 Ogawa S. Splicing factor mutations in myelodysplasia. International Journal of Hematology. 96: 438-42. PMID 23054646 DOI: 10.1007/s12185-012-1182-y  0.317
2012 Meggendorfer M, Roller A, Haferlach T, Eder C, Dicker F, Grossmann V, Kohlmann A, Alpermann T, Yoshida K, Ogawa S, Koeffler HP, Kern W, Haferlach C, Schnittger S. SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML). Blood. 120: 3080-8. PMID 22919025 DOI: 10.1182/Blood-2012-01-404863  0.311
2012 Iwakawa R, Okayama H, Kohno T, Sato-Otsubo A, Ogawa S, Yokota J. Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinoma. Genes, Chromosomes & Cancer. 51: 462-72. PMID 22302706 DOI: 10.1002/gcc.21933  0.31
2012 Ogawa S. Pathway Mutations in the Splicing Machinery in Myeloid Neoplasms Blood. 120: SCI-14-SCI-14. DOI: 10.1182/BLOOD.V120.21.SCI-14.SCI-14  0.327
2012 Ito E, Yoshida K, Okuno Y, Sato-Otsubo A, Toki T, Miyano S, Shiraishi Y, Chiba K, Terui K, Wang R, Sato T, Iribe Y, Ohga S, Kuramitsu M, Hamaguchi I, ... ... Ogawa S, et al. Identification of Two New DBA Genes, RPS27 and RPL27, by Whole-Exome Sequencing in Diamond-Blackfan Anemia Patients Blood. 120: 984-984. DOI: 10.1182/BLOOD.V120.21.984.984  0.33
2012 Kon A, Shih L, Minamino M, Sanada M, Shiraishi Y, Nagata Y, Yoshida K, Okuno Y, Bando M, Ishikawa S, Sato-Otsubo A, Nagae G, Haferlach C, Nowak D, Sato Y, ... ... Ogawa S, et al. Recurrent Mutations of Multiple Components of Cohesin Complex in Myeloid Neoplasms Blood. 120: 782-782. DOI: 10.1182/Blood.V120.21.782.782  0.356
2012 Góomez-Seguíi I, Makishima H, Jerez A, Yoshida K, Przychodzen BP, Miyano S, Shiraishi Y, Husseinzadeh HD, Evans EP, Guinta KM, Hosono N, McDevitt MA, Moliterno AR, Sekeres MA, Ogawa S, et al. Novel Recurrent Mutations in the Ras-Like GTP-Binding Gene Rit1 in Myeloid Malignancies Blood. 120: 558-558. DOI: 10.1182/BLOOD.V120.21.558.558  0.356
2012 Yoshida K, Toki T, Park M, Okuno Y, Shiraishi Y, Sanada M, Kon A, Nagata Y, Sato-Otsubo A, Sato Y, Wang R, Terui K, Kanezaki R, Shiba N, Chiba K, ... ... Ogawa S, et al. Genetic Basis of Myeloid Proliferation Related to Down Syndrome Blood. 120: 535-535. DOI: 10.1182/blood.V120.21.535.535  0.34
2012 Rouphail B, Yoshida K, Husseinzadeh HD, Evans EP, Miyano S, Nagata Y, Shiraishi Y, Chiba K, Sanada M, Przychodzen BP, Gomez-Segui I, Guinta KM, Afable MG, Saunthararajah Y, Sekeres MA, ... ... Ogawa S, et al. Molecular Diversity Detected by Whole Exome Sequencing in Chronic Myelomonocytic Leukemia Blood. 120: 310-310. DOI: 10.1182/BLOOD.V120.21.310.310  0.352
2012 Nagata Y, Sato A, Kon A, Okuno Y, Chiba K, Tanaka H, Shiraishi Y, Yoshida K, Sanada M, Utsunomiya A, Yamaguchi K, Oshima K, Miyawaki S, Kitanaka A, Miyano S, ... ... Ogawa S, et al. TET2 Mutations Revealed by Whole Genome Sequencing in Adult T-Cell Leukemia. Blood. 120: 2697-2697. DOI: 10.1182/BLOOD.V120.21.2697.2697  0.348
2012 Makishima H, Yoshida K, Clemente MJ, Sanada M, Nagata Y, Afable MG, Jerez A, Chiba K, Shiraishi Y, Miyano S, Ogawa S, Maciejewski JP. Karyotypic and Genetic Abnormalities Associated with Clonal Evolution in Paroxysmal Nocturnal Hemoglobinuria. Blood. 120: 2371-2371. DOI: 10.1182/BLOOD.V120.21.2371.2371  0.367
2012 Makishima H, Yoshida K, Nguyen N, Sanada M, Okuno Y, Ng KP, Przychodzen BP, Gudmundsson KO, Vishwakarma BA, Jerez A, Gomez-Segui I, Takahashi M, Shiraishi Y, Nagata Y, Guinta KM, ... ... Ogawa S, et al. Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies Blood. 120: 2-2. DOI: 10.1182/BLOOD.V120.21.2.2  0.38
2012 Hosono N, Makishima H, Jerez A, Gomez-Segui I, Przychodzen B, Sekeres MA, Miyano S, Shiraishi Y, Ogawa S, Maciejewski JP. Mutation Screening Associated with Chromosome 7 Abnormalities Using Next Generation Whole Exome Sequencing Blood. 120: 173-173. DOI: 10.1182/blood.v120.21.173.173  0.327
2012 Muramatsu H, Okuno Y, Sakaguchi H, Yoshida K, Shiraishi Y, Sanada M, Chiba K, Tanaka H, Makishima H, Wang X, Xu Y, Doisaki S, Hama A, Nakanishi K, Takahashi Y, ... ... Ogawa S, et al. Whole Exome Analysis Reveals Spectrum of Gene Mutations in Juvenile Myelomonocytic Leukemia Blood. 120: 170-170. DOI: 10.1182/BLOOD.V120.21.170.170  0.336
2012 Husseinzadeh HD, Evans EP, Yoshida K, Makishima H, Jerez A, Ruffalo M, Shiraishi Y, Miyano S, Sanada M, Chiba K, Nagata Y, Gomez-Segui I, Przychodzen BP, Wenzell C, Afable MG, ... ... Ogawa S, et al. Whole Exome Sequencing to Predict Response to Hypomethylating Agents in MDS Blood. 120: 1698-1698. DOI: 10.1182/BLOOD.V120.21.1698.1698  0.32
2012 Hosono N, Rehman H, Przychodzen B, Gomez-Segui I, Guinta KM, Yoshida K, Miyano S, Shiraishi Y, Ogawa S, Maciejewski JP, Makishima H. Various Germline Congenital Disorder Genes Are Somatically Mutated in Myeloid Malignancies Blood. 120: 1405-1405. DOI: 10.1182/BLOOD.V120.21.1405.1405  0.332
2012 Matsunawa M, Sanada M, Yamamoto R, Yoshida K, Nagata Y, Kon A, Yoshizato T, Otsu M, Nakauchi H, Ogawa S. Biological Analysis of SRSF2 Mutations in Leukemogenesis Blood. 120: 1282-1282. DOI: 10.1182/Blood.V120.21.1282.1282  0.336
2012 Shiba N, Yoshida K, Okuno Y, Shiraishi Y, Nagata Y, Ohki K, Kato M, Park M, Takita J, Kanazawa T, Kudo K, Arakawa H, Ito E, Sanada M, Miyano S, ... Ogawa S, et al. Whole Exome Sequencing Reveals Spectrum of Gene Mutations in Pediatric AML Blood. 120: 124-124. DOI: 10.1182/BLOOD.V120.21.124.124  0.352
2012 Nagata Y, Sanada M, Yoshida K, Kon A, Sato Y, Sato A, Shiraishi Y, Mori H, Miyano S, Shih L, Miyawaki S, Chiba S, Koeffler HP, Ogawa S. Abstract 5122: Integral view of copy number alteration and commonly targeted genes in MDS found a new aspect of correlation and interrelationship with mutated components of the RNA splicing machinery Cancer Research. 72: 5122-5122. DOI: 10.1158/1538-7445.Am2012-5122  0.347
2012 Kon A, Sanada M, Yoshida K, Shiraishi Y, Nagata Y, Sato Y, Sato-Otsubo A, Nagasaki M, Obara N, Sakata-Yanagimoto M, Ishiyama K, Mori H, Miyawaki S, Koeffler HP, Shih L, ... ... Ogawa S, et al. Abstract 5117: Mutations of cohesin genes in myeloid malignancy Cancer Research. 72: 5117-5117. DOI: 10.1158/1538-7445.Am2012-5117  0.357
2011 Yoshida K, Sanada M, Shiraishi Y, Nowak D, Nagata Y, Yamamoto R, Sato Y, Sato-Otsubo A, Kon A, Nagasaki M, Chalkidis G, Suzuki Y, Shiosaka M, Kawahata R, Yamaguchi T, ... ... Ogawa S, et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature. 478: 64-9. PMID 21909114 DOI: 10.1038/nature10496  0.303
2011 Yoshida K, Sanada M, Shiraishi Y, Nowak D, Nagata Y, Yamamoto R, Sato Y, Sato-Otsubo A, Kon A, Nagasaki M, Chalkidis G, Suzuki Y, Otsu M, Obara N, Sakata-Yanagimoto M, ... ... Ogawa S, et al. Frequent Pathway Mutations of Splicing Machinery in Myelodysplasia Blood. 118: 458-458. DOI: 10.1182/BLOOD.V118.21.458.458  0.337
2011 Hirabayashi S, Moetter J, Yoshida K, Heuser M, Hasle H, Fischer A, Strahm B, Schlegelberger B, Baumann I, Thol F, Stary J, Locatelli F, Zecca M, Schmugge M, Dworzak M, ... ... Ogawa S, et al. Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia Blood. 118: 2797-2797. DOI: 10.1182/BLOOD.V118.21.2797.2797  0.332
2011 Schnittger S, Meggendorfer M, Kohlmann A, Grossmann V, Yoshida K, Ogawa S, Koeffler HP, Kern W, Haferlach C, Haferlach T. SRSF2 is Mutated in 47.2% (77/163) of Chronic Myelomonocytic Leukemia (CMML) and Prognostically Favorable in Cases with Concomitant RUNX1 mutations Blood. 118: 274-274. DOI: 10.1182/Blood.V118.21.274.274  0.324
2011 Nagata Y, Sanada M, Kon A, Yoshida K, Shiraishi Y, Sato-Otsubo A, Mori H, Ishiyama K, Sakata-Yanagimoto M, Obara N, Nagasaki M, Miyawaki S, Chiba S, Miyano S, Yung SL, ... ... Ogawa S, et al. Mutational Spectrum Analysis of Interesting Correlation and Interrelationship Between RNA Splicing Pathway and Commonly Targeted Genes in Myelodysplastic Syndrome Blood. 118: 273-273. DOI: 10.1182/Blood.V118.21.273.273  0.326
2011 Kon A, Sanada M, Yoshida K, Nagata Y, Shiraishi Y, Sato Y, Sato-Otsubo A, Yamamoto R, Nagasaki M, Suzuki Y, Yamaguchi T, Otsu M, Sugano S, Chiba S, Koeffler HP, ... ... Ogawa S, et al. Functional Analysis of SRSF2 Mutations in Myelodysplastic Syndromes and Related Disorders Blood. 118: 1706-1706. DOI: 10.1182/Blood.V118.21.1706.1706  0.308
2011 Nagata Y, Sanada M, Yoshida K, Sato Y, Nakaya T, Matsubara A, Ishiyama K, Miyawaki S, Obara N, Chiba S, Shih L, Koeffler HP, Ogawa S. Abstract 4849: Profiling of multiple gene mutations in myelodysplastic syndromes using high-throughput resequenceing combined with barcode labeling Cancer Research. 71: 4849-4849. DOI: 10.1158/1538-7445.Am2011-4849  0.325
2010 Hiwatari M, Oki K, Takita J, Nishimura R, Sanada M, Okubo J, Adachi M, Sotomatsu M, Kikuchi A, Igarashi T, Hayashi Y, Ogawa S. Mutational Analysis for IDH1 and IDH2 In Pediatric Leukemia Blood. 116: 5106-5106. DOI: 10.1182/BLOOD.V116.21.5106.5106  0.341
2010 Kao H, Ogawa S, Sanada M, Liang D, Lai C, Lee E, Shih Y, Lin T, Kuo M, Huang C, Shih L. Roles of TET2 and C-CBL Mutations In the Progression of De Novo Myelodysplastic Syndrome to Acute Myeloid Leukemia Blood. 116: 4019-4019. DOI: 10.1182/BLOOD.V116.21.4019.4019  0.318
2010 Nagata Y, Sanada M, Yoshida K, Nakaya T, Matsubara A, Obara N, Ishiyama K, Miyawaki S, Takita J, Chiba S, Shih L, Koeffler HP, Ogawa S. Profiling of Multiple Gene Mutations In Myelodysplastic Syndromes Using High-Throughput Resequenceing Combined with Barcode Labeling Blood. 116: 4011-4011. DOI: 10.1182/Blood.V116.21.4011.4011  0.327
2010 Yoshida K, Sanada M, Nagata Y, Kawahata R, Kato M, Matsubara A, Takita J, Mori H, Ishiyama K, Ishikawa T, Miyawaki S, Obara N, Chiba S, Ogawa S. Whole Exome Analysis of Myelodysplastic Syndromes Using Next-Generation Resequencing Technology Blood. 116: 295-295. DOI: 10.1182/blood.v116.21.295.295  0.327
2008 Kawamata N, Ogawa S, Yamamoto G, Lehmann S, Levine RL, Pikman Y, Nannya Y, Sanada M, Miller CW, Gilliland DG, Koeffler HP. Genetic profiling of myeloproliferative disorders by single-nucleotide polymorphism oligonucleotide microarray. Experimental Hematology. 36: 1471-9. PMID 18723266 DOI: 10.1016/j.exphem.2008.06.006  0.323
2008 Masashi S, Yung SL, Suzuki T, Kato M, Sakata MY, Kumano K, Kawamata N, Takita J, Mori H, Kurokawa M, Chiba S, Omine M, Koeffler HP, Ogawa S. Genome-Wide Analysis of MDS/MPD Disclosed Frequent Homozygous C-Cbl mutations Tightly Associated with 11q-UPD Blood. 112: 855-855. DOI: 10.1182/Blood.V112.11.855.855  0.305
2007 Lee SY, Kumano K, Nakazaki K, Sanada M, Yamamoto G, Nannya Y, Suzuki R, Ota S, Ota Y, Izutsu K, Sakata-Yanagimoto M, Hangaishi A, Yagita H, Fukayama M, Seto M, ... ... Ogawa S, et al. Gain-of-Function Mutations and Copy Number Increases of Notch2 in Diffuse Large B-Cell Lymphoma. Blood. 110: 695-695. DOI: 10.1182/blood.v110.11.695.695  0.315
2007 Sanada M, Shih L, Suzuki T, Yamamoto G, Nannya Y, Sakata MY, Kato M, Kumano K, Kawamata N, Mori H, Kurokawa M, Chiba S, Omine M, Koeffler PH, Ogawa S. SNP Chip Analysis of Myelodysplastic Syndromes Disclosed High Frequency of Uniparental Disomy and a Novel Dominant Mutation as the Target of 11q UPD. Blood. 110: 119-119. DOI: 10.1182/BLOOD.V110.11.119.119  0.32
2006 Kawamata N, Ogawa S, Levine RL, Pikman Y, Nanya T, Sanada M, Miller CW, Gilliland DG, Koeffler HP. Genetic Profiling of Myeloproliferative Disorders by Single Nucleotide Polymorphism Oligonucleotide Microarray. Blood. 108: 2688-2688. DOI: 10.1182/BLOOD.V108.11.2688.2688  0.323
2003 Imai O, Kurokawa M, Izutsu K, Hangaishi A, Maki K, Ogawa S, Chiba S, Mitani K, Hirai H. Mutational analyses of the AML1 gene in patients with myelodysplastic syndrome. Leukemia & Lymphoma. 43: 617-21. PMID 12002768 DOI: 10.1080/10428190290012155  0.32
1998 Hosoya N, Hangaishi A, Ogawa S, Miyagawa K, Mitani K, Yazaki Y, Hirai H. Frameshift mutations of the hMSH6 gene in human leukemia cell lines. Japanese Journal of Cancer Research : Gann. 89: 33-9. PMID 9510473 DOI: 10.1111/j.1349-7006.1998.tb00476.x  0.308
Show low-probability matches.