D-Index & Metrics Best Publications
Genetics
Japan
2023
Medicine
Japan
2023

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 106 Citations 44,708 987 World Ranking 3803 National Ranking 80
Genetics D-index 105 Citations 43,182 932 World Ranking 392 National Ranking 10

Research.com Recognitions

Awards & Achievements

2023 - Research.com Medicine in Japan Leader Award

2023 - Research.com Genetics in Japan Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Cancer
  • Mutation

Seishi Ogawa mainly investigates Immunology, Genetics, Cancer research, Leukemia and Mutation. His research in Immunology intersects with topics in Hematopoietic stem cell transplantation, Haematopoiesis, Stem cell and Transplantation. Seishi Ogawa interconnects Somatic cell, Loss of heterozygosity, Lymphoma, Tumor suppressor gene and Epigenetics in the investigation of issues within Cancer research.

His Leukemia research incorporates themes from Myeloid, Germline mutation, Myeloid leukemia and Pancytopenia. His studies deal with areas such as Molecular biology, Internal medicine and NPM1 as well as Mutation. His Gene study combines topics in areas such as Cancer and Epithelium.

His most cited work include:

  • Frequent pathway mutations of splicing machinery in myelodysplasia (1387 citations)
  • Landscape of genetic lesions in 944 patients with myelodysplastic syndromes (791 citations)
  • Oncogenic mutations of ALK kinase in neuroblastoma. (686 citations)

What are the main themes of his work throughout his whole career to date?

Seishi Ogawa mainly focuses on Cancer research, Genetics, Internal medicine, Mutation and Leukemia. Seishi Ogawa studies Myeloid leukemia, a branch of Cancer research. The concepts of his Internal medicine study are interwoven with issues in Gastroenterology and Oncology.

His Mutation research incorporates elements of Somatic cell and Somatic evolution in cancer. Myelodysplastic syndromes is closely connected to Myeloid in his research, which is encompassed under the umbrella topic of Leukemia. The various areas that Seishi Ogawa examines in his Immunology study include Haematopoiesis and Allele.

He most often published in these fields:

  • Cancer research (36.12%)
  • Genetics (28.79%)
  • Internal medicine (20.60%)

What were the highlights of his more recent work (between 2017-2021)?

  • Cancer research (36.12%)
  • Internal medicine (20.60%)
  • Mutation (20.23%)

In recent papers he was focusing on the following fields of study:

Seishi Ogawa spends much of his time researching Cancer research, Internal medicine, Mutation, Oncology and Gene. His Cancer research study incorporates themes from Cancer, Leukemia and Haematopoiesis. His Haematopoiesis research is multidisciplinary, incorporating elements of Progenitor cell, Human leukocyte antigen and Immunology.

His research combines Gene mutation and Internal medicine. In his study, Transcription factor is strongly linked to Cell biology, which falls under the umbrella field of Mutation. Gene is a subfield of Genetics that Seishi Ogawa explores.

Between 2017 and 2021, his most popular works were:

  • Age-related remodelling of oesophageal epithelia by mutated cancer drivers (192 citations)
  • Age-related remodelling of oesophageal epithelia by mutated cancer drivers (192 citations)
  • Prognostic relevance of genetic alterations in diffuse lower-grade gliomas. (84 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Cancer
  • Mutation

His primary scientific interests are in Cancer research, Mutation, Gene, Internal medicine and Myeloid. His Cancer research research includes themes of Exome sequencing, Carcinogenesis, Cancer, Transcriptome and Lymphoma. His Mutation research is multidisciplinary, incorporating perspectives in Somatic cell, Immune system, Somatic evolution in cancer, Biopsy and Cell biology.

His Gene study introduces a deeper knowledge of Genetics. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Oncology, Gene mutation and NPM1. His Myeloid study combines topics from a wide range of disciplines, such as Haematopoiesis, Myeloid leukemia, Exome, Leukemia and Transplantation.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Frequent pathway mutations of splicing machinery in myelodysplasia

Kenichi Yoshida;Masashi Sanada;Yuichi Shiraishi;Daniel Nowak.
Nature (2011)

2061 Citations

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

T Haferlach;Y Nagata;V Grossmann;Y Okuno.
Leukemia (2014)

1370 Citations

Autologous Induced Stem-Cell–Derived Retinal Cells for Macular Degeneration

Michiko Mandai;Akira Watanabe;Yasuo Kurimoto;Yasuhiko Hirami.
The New England Journal of Medicine (2017)

1176 Citations

Oncogenic mutations of ALK kinase in neuroblastoma.

Yuyan Chen;Junko Takita;Young Lim Choi;Motohiro Kato.
Nature (2008)

978 Citations

Control of carrier density by self-assembled monolayers in organic field-effect transistors

S. Kobayashi;T. Nishikawa;T. Nishikawa;T. Takenobu;S. Mori.
Nature Materials (2004)

977 Citations

Integrated molecular analysis of clear-cell renal cell carcinoma.

Yusuke Sato;Tetsuichi Yoshizato;Yuichi Shiraishi;Shigekatsu Maekawa.
Nature Genetics (2013)

957 Citations

KIF5B-RET fusions in lung adenocarcinoma.

Takashi Kohno;Hitoshi Ichikawa;Yasushi Totoki;Kazuki Yasuda.
Nature Medicine (2012)

884 Citations

A Robust Algorithm for Copy Number Detection Using High-Density Oligonucleotide Single Nucleotide Polymorphism Genotyping Arrays

Yasuhito Nannya;Masashi Sanada;Kumi Nakazaki;Noriko Hosoya.
Cancer Research (2005)

803 Citations

A novel signaling molecule, p130, forms stable complexes in vivo with v-Crk and v-Src in a tyrosine phosphorylation-dependent manner.

R Sakai;A Iwamatsu;N Hirano;S Ogawa.
The EMBO Journal (1994)

793 Citations

Mutational landscape and clonal architecture in grade II and III gliomas

Hiromichi Suzuki;Kosuke Aoki;Kenichi Chiba;Yusuke Sato.
Nature Genetics (2015)

717 Citations

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