Masakazu Kohda

2.5k citations

36 papers · 725 indexed · h-index 14

Co-authors: Yasushi Okazaki Akira Ohtake Kei Murayama Yoshihito Kishita Takuya Awata Takuya Fushimi Masaru Shimura Motonobu Katoh
Topics: Mitochondrial Function and Pathology (17 papers)Metabolism and Genetic Disorders (13 papers)ATP Synthase and ATPases Research (8 papers)
Cited by: Clinical Biochemistry Ophthalmology Molecular Biology
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Scientific Reports
Partner nations: Japan United States China

In The Last Decade

Masakazu Kohda

33 papers receiving 719 citations

Peers

Countries citing papers authored by Masakazu Kohda

Since Specialization

Citations

This map shows the geographic impact of Masakazu Kohda'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 Masakazu Kohda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Masakazu Kohda more than expected).

Fields of papers citing papers by Masakazu Kohda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Masakazu Kohda. 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 Masakazu Kohda. The network helps show where Masakazu Kohda may publish in the future.

Co-authorship network of co-authors of Masakazu Kohda

This figure shows the co-authorship network connecting the top 25 collaborators of Masakazu Kohda. A scholar is included among the top collaborators of Masakazu Kohda 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 Masakazu Kohda. Masakazu Kohda is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	SNP associations in the L-citrulline metabolic pathway and vascular aging in the Japanese population 2025 ·PLoS ONE ·(unknown),(unknown),Sachiko Ishida,Masakazu Kohda,Takayuki Yazawa,Masahiko Morita	0
2	A Japanese patient with neonatal biotin-responsive basal ganglia disease 2022 ·Human Genome Variation ·Mizuki Kobayashi,Yuichi Suzuki,(unknown),Ayako Matsunaga,Masakazu Kohda,Yasushi Okazaki,Kei Murayama,Takanori Yamagata,Hitoshi Osaka	2
3	Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan 2021 ·Scientific Reports ·(unknown),Masaru Shimura,Taro Yamazaki,Hiroko Harashima,Takuya Fushimi,Tomoko Tsuruoka,(unknown),Keiko Ichimoto,Ayako Matsunaga,(unknown),Yukiko Yatsuka,Yoshihito Kishita,Masakazu Kohda,Akira Namba,Yoshimasa Kamei,Yasushi Okazaki,Shinji Kosugi,Akira Ohtake,Kei Murayama	1
4	A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome 2021 ·Scientific Reports ·Yoshihito Kishita,Kaori Ishikawa,Kazuto Nakada,Jun‐Ichi Hayashi,Takuya Fushimi,Masaru Shimura,Masakazu Kohda,Akira Ohtake,Kei Murayama,Yasushi Okazaki	12
5	Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL 2020 ·Genes ·Nurun Nahar Borna,Yoshihito Kishita,Norio Sakai,Yusuke Hamada,Koji Kamagata,Masakazu Kohda,Akira Ohtake,Kei Murayama,Yasushi Okazaki	8
6	Mitochondrial complex deficiency by novel compound heterozygous TMEM 70 variants and correlation with developmental delay, undescended testicle, and left ventricular noncompaction in a Japanese patient: A case report 2019 ·SHILAP Revista de lepidopterología ·Keiichi Hirono,Fukiko Ichida,(unknown),Minako Ogawa‐Tominaga,Takuya Fushimi,René G. Feichtinger,Johannes A. Mayr,Masakazu Kohda,Yoshihito Kishita,Yasushi Okazaki,Akira Ohtake,Kei Murayama	13
7	Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background 2019 ·International Journal of Cardiology ·(unknown),Yoshihito Kishita,Masakazu Kohda,Yosuke Mizuno,Takuya Fushimi,Ayako Matsunaga,Yukiko Yatsuka,Tomoko Hirata,Hiroko Harashima,Atsuhito Takeda,Akihiro Nakaya,Yasushi Sakata,Shigetoyo Kogaki,Akira Ohtake,Kei Murayama,Yasushi Okazaki	33
8	Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome 2019 ·Neurogenetics ·Nurun Nahar Borna,Yoshihito Kishita,Masakazu Kohda,Sze Chern Lim,Masaru Shimura,Yibo Wu,Kaoru Mogushi,Yukiko Yatsuka,Hiroko Harashima,(unknown),Takuya Fushimi,Keiko Ichimoto,Kei Murayama,Akira Ohtake,Yasushi Okazaki	44
9	Characteristics of MUTYH variants in Japanese colorectal polyposis patients 2018 ·International Journal of Clinical Oncology ·(unknown),Tatsuro Yamaguchi,Hidetaka Eguchi,(unknown),Masakazu Kohda,Koichi Koizumi,Shinichiro Horiguchi,Yasushi Okazaki,Hideyuki Ishida	6
10	Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation 2018 ·Brain and Development ·Akihiko Miyauchi,Hitoshi Osaka,Masako Nagashima,(unknown),Yukifumi Monden,Masakazu Kohda,Yoshihito Kishita,Yasushi Okazaki,Kei Murayama,Akira Ohtake,Takanori Yamagata	13
11	A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy 2017 ·Journal of Human Genetics ·Nurun Nahar Borna,Yoshihito Kishita,Kaori Ishikawa,Kazuto Nakada,Jun‐Ichi Hayashi,Yoshimi Tokuzawa,Masakazu Kohda,Hiromi Nyuzuki,(unknown),(unknown),Atsuhito Takeda,Kei Murayama,Akira Ohtake,Yasushi Okazaki	5
12	Barth Syndrome: Different Approaches to Diagnosis 2017 ·The Journal of Pediatrics ·(unknown),Yoshihito Kishita,Masakazu Kohda,Yukiko Yatsuka,Tomoko Hirata,Yosuke Mizuno,Hiroko Harashima,Keiichi Hirono,Fukiko Ichida,Atsuko Noguchi,Masayuki Yoshida,(unknown),Ritsuo Nishiuchi,Atsuhito Takeda,Akihiro Nakaya,Yasushi Sakata,Kei Murayama,Akira Ohtake,Yasushi Okazaki	12
13	HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families 2016 ·Journal of Human Genetics ·Atsuko Imai,Masakazu Kohda,Akihiro Nakaya,Yasushi Sakata,Kei Murayama,Akira Ohtake,Mark Lathrop,Yasushi Okazaki,Jürg Ott	9
14	Identification of a Japanese Lynch syndrome patient with large deletion in the 3′ region of theEPCAMgene 2015 ·Japanese Journal of Clinical Oncology ·Hidetaka Eguchi,Kensuke Kumamoto,Okihide Suzuki,Masakazu Kohda,(unknown),Yasushi Okazaki,Hideyuki Ishida	7
15	Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report 2014 ·Brain and Development ·(unknown),Yoshihiro Maegaki,Kei Murayama,Taro Yamazaki,Masakazu Kohda,Akira Ohtake,Hiroyasu Iwasa,Yukiko Yatsuka,Yasushi Okazaki,(unknown),Ikuo Nagata,Mitsuo Toyoshima,Yoshiaki Saito,Masayuki Itoh,Ichizo Nishino,Kousaku Ohno	11
16	Diagnosis and molecular basis of mitochondrial respiratory chain disorders: Exome sequencing for disease gene identification 2014 ·Biochimica et Biophysica Acta (BBA) - General Subjects ·Akira Ohtake,Kei Murayama,Masayuki Mori,Hiroko Harashima,Taro Yamazaki,Shunsuke Tamaru,Yukiko Yamashita,Yoshihito Kishita,Yutaka Nakachi,Masakazu Kohda,Yoshimi Tokuzawa,Yosuke Mizuno,Yohsuke Moriyama,Hiroyuki Kato,Yasushi Okazaki	43
17	A Genome-Wide Association Study for Diabetic Retinopathy in a Japanese Population: Potential Association with a Long Intergenic Non-Coding RNA 2014 ·PLoS ONE ·Takuya Awata,(unknown),Susumu Kurihara,(unknown),Yumi Miyashita,Shigehiro Katayama,Keisuke Mori,Shin Yoneya,Masakazu Kohda,Yasushi Okazaki,Taro Maruyama,Akira Shimada,Kazuki Yasuda,Nao Nishida,Katsushi Tokunaga,Asako Koike	67
18	Homozygosity Mapping on Homozygosity Haplotype Analysis to Detect Recessive Disease-Causing Genes from a Small Number of Unrelated, Outbred Patients 2011 ·PLoS ONE ·Koichi Hagiwara,Hiroyuki Morino,(unknown),Tomoaki Tanaka,Hitoshi Miyazawa,Tomoko Suzuki,Masakazu Kohda,Yasushi Okazaki,Kuniaki Seyama,Hideshi Kawakami	6
19	A quantitatively-modeled homozygosity mapping algorithm, qHomozygosityMapping, utilizing whole genome single nucleotide polymorphism genotyping data 2010 ·BMC Bioinformatics ·Huqun,(unknown),Hiroyuki Morino,Hiroshi Miyazawa,Tomoaki Tanaka,Tomoko Suzuki,Masakazu Kohda,Hideshi Kawakami,Yasushi Okazaki,Kuniaki Seyama,Koichi Hagiwara	9
20	Homozygosity Haplotype Allows a Genomewide Search for the Autosomal Segments Shared among Patients 2007 ·The American Journal of Human Genetics ·Hitoshi Miyazawa,Masaaki Kato,Takuya Awata,Masakazu Kohda,Hiroyasu Iwasa,Nobuyuki Koyama,Tomoaki Tanaka,Huqun,Shunei Kyo,Yasushi Okazaki,Koichi Hagiwara	45

About Masakazu Kohda

Masakazu Kohda is a scholar working on Clinical Biochemistry, Cancer Research and Molecular Biology, having authored 36 papers that have together received 725 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (17 papers), Metabolism and Genetic Disorders (13 papers) and ATP Synthase and ATPases Research (8 papers). The work is most often cited by research in Clinical Biochemistry (206 citations), Ophthalmology (90 citations) and Molecular Biology (515 citations). Masakazu Kohda has collaborated with scholars based in Japan, United States and China. Frequent co-authors include Yasushi Okazaki, Akira Ohtake, Kei Murayama, Yoshihito Kishita, Takuya Awata, Takuya Fushimi, Masaru Shimura, Motonobu Katoh, Shin Yoneya and Tamiko Takemura. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

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.

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