D-Index & Metrics Best Publications

Hideyuki Ogawa

Osaka University
Japan

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 Citations Publications World Ranking National Ranking

Molecular Biology D-index 46 Citations 10,874 82 World Ranking 1880 National Ranking 160

Overview

What is he best known for?

The fields of study he is best known for:

Gene
DNA
Amino acid

The scientist’s investigation covers issues in Molecular biology, DNA repair, Homologous recombination, Mutant and Cell biology. His Molecular biology study combines topics in areas such as Genetic recombination, Meiosis, Mitosis, DNA and RAD51. His research investigates the connection between DNA repair and topics such as MRX complex that intersect with issues in Mre11 complex.

His Homologous recombination research is included under the broader classification of Genetics. His work deals with themes such as MRE11 Homologue Protein and Endodeoxyribonucleases, which intersect with Genetics. His research in Mutant intersects with topics in Gene conversion and Rad50.

His most cited work include:

Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein (1071 citations)
Rad51‐deficient vertebrate cells accumulate chromosomal breaks prior to cell death (719 citations)
Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recA (451 citations)

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

Hideyuki Ogawa focuses on Molecular biology, DNA, Genetics, Gene and Escherichia coli. His Molecular biology study incorporates themes from Nucleic acid sequence, Biochemistry, Mutant, DNA repair and Repressor lexA. His DNA repair study integrates concerns from other disciplines, such as MRX complex, Lambda phage, DNA replication and Cell biology.

His MRX complex research includes themes of Mre11 complex, Mitosis and A-DNA. His study in DNA is interdisciplinary in nature, drawing from both Bacteriophage, Replication protein A, Bacteria, Repressor and In vitro recombination. His studies deal with areas such as Genetic recombination and Saccharomyces cerevisiae as well as Homologous recombination.

He most often published in these fields:

Molecular biology (59.52%)
DNA (38.10%)
Genetics (35.71%)

What were the highlights of his more recent work (between 1992-2018)?

Homologous recombination (28.57%)
Genetics (35.71%)
Molecular biology (59.52%)

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

His main research concerns Homologous recombination, Genetics, Molecular biology, RAD51 and Meiosis. His Homologous recombination research is multidisciplinary, incorporating elements of Genetic recombination, Saccharomyces cerevisiae, Binding domain and Protein folding. His work carried out in the field of Molecular biology brings together such families of science as Mitosis, Mutant, DNA, DNA repair and Escherichia coli.

Hideyuki Ogawa has researched Mitosis in several fields, including Cell culture, Transgene and A-DNA. The concepts of his DNA repair study are interwoven with issues in MRX complex, Rad50 and Cell biology. His RAD51 study is concerned with the larger field of Gene.

Between 1992 and 2018, his most popular works were:

Rad51‐deficient vertebrate cells accumulate chromosomal breaks prior to cell death (719 citations)
Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recA (451 citations)
A DNA damage response pathway controlled by Tel1 and the Mre11 complex. (342 citations)

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

Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein

Akira Shinohara;Hideyuki Ogawa;Tomoko Ogawa.
Cell (1992)

1496 Citations

Rad51‐deficient vertebrate cells accumulate chromosomal breaks prior to cell death

Eiichiro Sonoda;Masao S. Sasaki;Jean Marie Buerstedde;Olga Bezzubova.
The EMBO Journal (1998)

957 Citations

Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recA

Akira Shinohara;Hideyuki Ogawa;Yoichi Matsuda;Noriko Ushio.
Nature Genetics (1993)

641 Citations

Complex Formation and Functional Versatility of Mre11 of Budding Yeast in Recombination

Takehiko Usui;Tsutomu Ohta;Hiroyuki Oshiumi;Hiroyuki Oshiumi;Jun-ichi Tomizawa.
Cell (1998)

483 Citations

A DNA damage response pathway controlled by Tel1 and the Mre11 complex.

Takehiko Usui;Takehiko Usui;Hideyuki Ogawa;Hideyuki Ogawa;John H.J Petrini.
Molecular Cell (2001)

458 Citations

Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.

K Johzuka;H Ogawa.
Genetics (1995)

383 Citations

Organization of the recA gene of Escherichia coli

Toshihiro Horii;Tomoko Ogawa;Hideyuki Ogawa.
Proceedings of the National Academy of Sciences of the United States of America (1980)

353 Citations

Studies on radiation-sensitive mutants of E. coli. I. Mutants defective in the repair synthesis.

Hideyuki Ogawa;Kazunori Shimada;Jun-ichi Tomizawa.
Molecular Genetics and Genomics (1968)

305 Citations

An essential gene, ESR1, is required for mitotic cell growth, DNA repair and meiotic recombination in Saccharomyces cerevisiae.

Ryuichi Kato;Hideyuki Ogawa.
Nucleic Acids Research (1994)

302 Citations

A Novel mre11 Mutation Impairs Processing of Double-Strand Breaks of DNA during Both Mitosis and Meiosis

Hideo Tsubouchi;Hideyuki Ogawa.
Molecular and Cellular Biology (1998)