Masakazu Kohda

2.5k citations

36 papers · 725 indexed · h-index 14

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 13
Ophthalmology top 5%
Molecular Biology
- Mitochondrial Function and Pathology 17
- ATP Synthase and ATPases Research 8
- RNA modifications and cancer 4
Genetics
- Genomics and Rare Diseases 4
Cancer Research
- Cancer Genomics and Diagnostics 3
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 4
Artificial Intelligence
- Speech Recognition and Synthesis 3

Co-authors: Yasushi Okazaki Akira Ohtake Kei Murayama Yoshihito Kishita Takuya Awata Takuya Fushimi Masaru Shimura Motonobu Katoh
Cited by: Clinical Biochemistry Ophthalmology Molecular Biology
Journals: SHILAP Revista de lepidopterología (1 paper)PLoS ONE (3 papers)Scientific Reports (2 papers)
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

The 25 scholars most cited alongside Masakazu Kohda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Masakazu Kohda Line = papers co-authored together Masakazu Kohda links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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

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