Hirofumi Kodera

2.1k total citations
12 papers, 381 citations indexed

About

Hirofumi Kodera is a scholar working on Molecular Biology, Immunology and Allergy and Cell Biology. According to data from OpenAlex, Hirofumi Kodera has authored 12 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Immunology and Allergy and 2 papers in Cell Biology. Recurrent topics in Hirofumi Kodera's work include Cell Adhesion Molecules Research (3 papers), DNA Repair Mechanisms (2 papers) and RNA regulation and disease (2 papers). Hirofumi Kodera is often cited by papers focused on Cell Adhesion Molecules Research (3 papers), DNA Repair Mechanisms (2 papers) and RNA regulation and disease (2 papers). Hirofumi Kodera collaborates with scholars based in Japan, Poland and India. Hirofumi Kodera's co-authors include Hirotomo Saitsu, Naomichi Matsumoto, Yoshinori Tsurusaki, Noriko Miyake, Mitsuko Nakashima, Kengo Sakaguchi, Ryo Takeuchi, Yukinobu Uchiyama, Hitoshi Osaka and Isao Yuasa and has published in prestigious journals such as Nature Communications, Biochemical and Biophysical Research Communications and Epilepsia.

In The Last Decade

Hirofumi Kodera

12 papers receiving 373 citations

Peers

Countries citing papers authored by Hirofumi Kodera

Since Specialization

Citations

This map shows the geographic impact of Hirofumi Kodera's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hirofumi Kodera with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hirofumi Kodera more than expected).

Fields of papers citing papers by Hirofumi Kodera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hirofumi Kodera. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hirofumi Kodera. The network helps show where Hirofumi Kodera may publish in the future.

Co-authorship network of co-authors of Hirofumi Kodera

This figure shows the co-authorship network connecting the top 25 collaborators of Hirofumi Kodera. A scholar is included among the top collaborators of Hirofumi Kodera based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hirofumi Kodera. Hirofumi Kodera is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	COL4A1 and COL4A2 Mutations Analyses with Perinatal Arterial ?schemic Stroke 2020 ·(unknown), Kürşat Bora Çarman, Çoşkun Yarar, Hirofumi Kodera, Hirotomo Saitsu, Naomichi Matsumoto	1
2	Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infection 2016 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Robert Śmigiel, (unknown), (unknown), Hirofumi Kodera, Marek Sąsiadek, Naomichi Matsumoto, Maria Sąsiadek, Hirotomo Saitsu	10
3	Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy 2014 ·Journal of Human Genetics ·Hirofumi Kodera, Hitoshi Osaka, Mizue Iai, Noriko Aida, Akio Yamashita, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto	24
4	De novo SOX11 mutations cause Coffin–Siris syndrome 2014 ·Nature Communications ·Yoshinori Tsurusaki, Eriko Koshimizu, Hirofumi Ohashi, Shubha R. Phadke, Ikuyo Kou, Masaaki Shiina, Toshifumi Suzuki, Nobuhiko Okamoto, Shintaro Imamura, Michiaki Yamashita, Satoshi Watanabe, Koh-ichiro Yoshiura, Hirofumi Kodera, Satoko Miyatake, Mitsuko Nakashima, Hirotomo Saitsu, Kazuhiro Ogata, Shiro Ikegawa, Noriko Miyake, Naomichi Matsumoto	93
5	Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation 2014 ·Clinical Genetics ·Hirofumi Kodera, N Ando, Isao Yuasa, Yoshinao Wada, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Shinji Saitoh, Naomichi Matsumoto, Hirotomo Saitsu	49
6	PIGO mutations in intractable epilepsy and severe developmental delay with mild elevation of alkaline phosphatase levels 2014 ·Epilepsia ·Kazuyuki Nakamura, Hitoshi Osaka, Yoshiko Murakami, (unknown), Kiyomi Nishiyama, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Taroh Kinoshita, Naomichi Matsumoto, Hirotomo Saitsu	36
7	Whole‐exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies 2013 ·American Journal of Medical Genetics Part A ·Yukiko Kondo, Eriko Koshimizu, André Mégarbané, Haruka Hamanoue, Ippei Okada, Kiyomi Nishiyama, Hirofumi Kodera, Satoko Miyatake, Yoshinori Tsurusaki, Mitsuko Nakashima, Hiroshi Doi, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto	15
8	Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage? 2013 ·Child s Nervous System ·Mehmet Serdar Kütük, (unknown), Hirofumi Kodera, Naomichi Matsumoto, Hirotomo Saitsu, Selim Doğanay, Mehmet Canpolat, Mehmet Dolanbay, Ekrem Ünal, Munis Dündar	9
9	De Novo Mutations inSLC35A2Encoding a UDP-Galactose Transporter Cause Early-Onset Epileptic Encephalopathy 2013 ·Human Mutation ·Hirofumi Kodera, Kazuyuki Nakamura, Hitoshi Osaka, Yoshihiro Maegaki, Kazuhiro Haginoya, Shuji Mizumoto, Mitsuhiro Kato, Nobuhiko Okamoto, Mizue Iai, Yukiko Kondo, Kiyomi Nishiyama, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Kiyoshi Hayasaka, Kazuyuki Sugahara, Isao Yuasa, Yoshinao Wada, Naomichi Matsumoto, Hirotomo Saitsu	85
10	Characterization of marine X-family DNA polymerases and comparative analysis of base excision repair proteins 2011 ·Biochemical and Biophysical Research Communications ·Hirofumi Kodera, Ryo Takeuchi, Yukinobu Uchiyama, Yoichi Takakusagi, Kazuki Iwabata, (unknown), Naoto Hanzawa, Fumio Sugawara, Kengo Sakaguchi	4
11	Distribution and roles of X-family DNA polymerases in eukaryotes 2008 ·Biochimie ·Yukinobu Uchiyama, Ryo Takeuchi, Hirofumi Kodera, Kengo Sakaguchi	52
12	[Evolution and functions of X-family DNA polymerases in eukaryotes]. 2008 ·PubMed ·Yukinobu Uchiyama, Ryo Takeuchi, Hirofumi Kodera, Kengo Sakaguchi	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact