Keitaro Yamada

483 citations

31 papers · 347 indexed · h-index 11

Co-authors: Toshiyuki Fukao Keiko Yanagihara Naomi Kondo Toshiyuki Mano Yasuhisa Toribe N Mutoh Hirotomo Saitsu Yasuhiro Suzuki
Topics: Metabolism and Genetic Disorders (6 papers)RNA modifications and cancer (4 papers)Epilepsy research and treatment (4 papers)
Cited by: Clinical Biochemistry Molecular Biology Hematology
Journals: Human Mutation The Journal of Biochemistry Epilepsy & Behavior
Partner nations: Japan United States Netherlands

In The Last Decade

Keitaro Yamada

29 papers receiving 339 citations

Peers

Countries citing papers authored by Keitaro Yamada

Since Specialization

Citations

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

Fields of papers citing papers by Keitaro Yamada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keitaro Yamada

This figure shows the co-authorship network connecting the top 25 collaborators of Keitaro Yamada. A scholar is included among the top collaborators of Keitaro Yamada 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 Keitaro Yamada. Keitaro Yamada 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	A Novel Constitutively Active c . 98 G > C , p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization 2023 ·Human Mutation ·(unknown),(unknown),Keitaro Yamada,(unknown),Mitsuko Nakashima,Shima Eda,Tohru Matsuki,Masashi Nishikawa,Koh‐ichi Nagata,Yasushi Enokido,Hirotomo Saitsu,Atsuo Nakayama	0
2	Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review 2021 ·Journal of Human Genetics ·Kazuki Watanabe,Mitsuko Nakashima,Satoko Kumada,(unknown),Mikako Enokizono,Keitaro Yamada,Mitsuhiro Kato,Hirotomo Saitsu	16
3	Effectiveness of lacosamide in children and young adults previously treated with other sodium channel blockers 2021 ·Epilepsy & Behavior ·Takeshi Suzuki,Jun Natsume,(unknown),(unknown),Hiroyuki Yamamoto,(unknown),(unknown),Tetsuo Kubota,Takeshi Tsuji,Toru Kato,Keitaro Yamada,Koichi Maruyama,Akihisa Okumura,Yoshiyuki Takahashi,Hiroyuki Kidokoro	2
4	Current status of surviving patients with arginase 1 deficiency in Japan 2021 ·Molecular Genetics and Metabolism Reports ·Jun Kido,Shirou Matsumoto,Eiko Takeshita,Chiemi Hayakawa,Keitaro Yamada,Jiro Kagawa,Yoko Nakajima,Tetsuya Ito,Hiroyuki Iijima,Fumio Endo,Kimitoshi Nakamura	6
5	Is hiragana decoding impaired in children with periventricular leukomalacia? 2018 ·Brain and Development ·N. Kurahashi,(unknown),(unknown),(unknown),(unknown),(unknown),Takeshi Suzuki,(unknown),Keitaro Yamada,Kosaburo Aso,Koichi Maruyama,Miho Nakamura	3
6	PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder 2017 ·Journal of Human Genetics ·Takeshi Mizuguchi,Mitsuko Nakashima,Mitsuhiro Kato,Keitaro Yamada,Tohru Okanishi,Nina Ekhilevitch,Hanna Mandel,Ayelet Eran,(unknown),Yukio Sawaishi,Hirotaka Motoi,Masaaki Shiina,Kazuhiro Ogata,Satoko Miyatake,Noriko Miyake,Hirotomo Saitsu,Naomichi Matsumoto	53
7	Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations 2017 ·Brain and Development ·N. Kurahashi,Noriko Miyake,Seiji Mizuno,Eriko Koshimizu,Hirokazu Kurahashi,Keitaro Yamada,Jun Natsume,Yusuke Aoki,Miho Nakamura,(unknown),(unknown),(unknown),Naomichi Matsumoto,Koichi Maruyama	16
8	Arts syndrome with a novel missense mutation in the PRPS1 gene: A case report 2016 ·Brain and Development ·Koichi Maruyama,(unknown),N. Kurahashi,(unknown),Keitaro Yamada,Akihiro Hashiguchi,Hiroshi Takashima,Rosa J. Torres,Kosaburo Aso	9
9	The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy 2016 ·Brain and Development ·(unknown),Jun Natsume,Hiroyuki Kidokoro,Naoko Ishihara,Hiroyuki Yamamoto,Yoshiteru Azuma,Yuji Ito,N. Kurahashi,Takeshi Tsuji,Motomasa Suzuki,Kazuya Itomi,Keitaro Yamada,Hirokazu Kurahashi,Shinpei Abe,Akihisa Okumura,Koichi Maruyama,Tamiko Negoro,Kazuyoshi Watanabe,Seiji Kojima	6
10	Predictive value of EEG findings at control of epileptic spasms for seizure relapse in patients with West syndrome 2014 ·Seizure ·Keitaro Yamada,Yasuhisa Toribe,(unknown),(unknown),(unknown),Yukiko Mogami,Keiko Yanagihara,Toshiyuki Mano,Yasuhiro Suzuki	24
11	Thalamic Lesions in Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion 2014 ·Pediatric Neurology ·N. Kurahashi,Takeshi Tsuji,Toru Kato,(unknown),(unknown),Keitaro Yamada,Hirokazu Kurahashi,Koichi Maruyama,(unknown),Tetsuo Kubota,Shinji Saitoh,Jun Natsume,Akihisa Okumura	2
12	MRI Findings and Steroid Therapy for Neuralgic Amyotrophy in Children 2011 ·Pediatric Neurology ·Keitaro Yamada,Toshiyuki Mano,Yasuhisa Toribe,Keiko Yanagihara,Yasuhiro Suzuki	4
13	Diagnostic accuracy of blood and CSF lactate in identifying children with mitochondrial diseases affecting the central nervous system 2011 ·Brain and Development ·Keitaro Yamada,Yasuhisa Toribe,Keiko Yanagihara,Toshiyuki Mano,(unknown),Yasuhiro Suzuki	32
14	Prolonged Elevation of Serum Neuron-Specific Enolase in Children After Clinical Diagnosis of Brain Death 2011 ·Journal of Child Neurology ·Yasuhiro Suzuki,Yukiko Mogami,(unknown),Keitaro Yamada,Keiko Yanagihara,(unknown),Toshiyuki Mano	7
15	Comparison of biochemical markers in cerebrospinal fluid and serum between endovascular therapy and surgery for patients with subarachnoid hemorrhage; neuron-specific enolase, S-100B protein, basic fibroblast growth factor, and vascular endothelial growth factor. 2009 ·Myong Hwa Yamamoto,Mitsuhito Mase,Marcello Di Nisio,(unknown),Keitaro Yamada	1
16	Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): Identification of a Km mutant and an analysis of the mutational sites in the structure 2007 ·Molecular Genetics and Metabolism ·(unknown),Toshiyuki Fukao,Antti M. Haapalainen,(unknown),Keitaro Yamada,Franco Lilliu,Shoji Yano,Peter N. Robinson,Michael K. Gibson,Ronald J. A. Wanders,Grant A. Mitchell,Rik K. Wierenga,Naomi Kondo	16
17	Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human Succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene 2006 ·Molecular Genetics and Metabolism ·Keitaro Yamada,Toshiyuki Fukao,(unknown),(unknown),Jos P.N. Ruiter,Ronald J. A. Wanders,Naomi Kondo	18
18	Identification of Alu-mediated, large deletion-spanning exons 2–4 in a patient with mitochondrial acetoacetyl-CoA thiolase deficiency 2006 ·Molecular Genetics and Metabolism ·(unknown),Toshiyuki Fukao,(unknown),Keitaro Yamada,K. Michael Gibson,Naomi Kondo	26
19	A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency 2006 ·Molecular Genetics and Metabolism ·Toshiyuki Fukao,(unknown),Marie-Odile Rolland,M. T. Zabot,Andreas Schulze,Keitaro Yamada,Naomi Kondo	18
20	Two Distinct Upstream Regions Are Involved in Expression of the Catalase Gene in Schizosaccharomyces pombe in Response to Oxidative Stress 1998 ·The Journal of Biochemistry ·(unknown),Keitaro Yamada,N Mutoh	17

About Keitaro Yamada

Keitaro Yamada is a scholar working on Clinical Biochemistry, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health, having authored 31 papers that have together received 347 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (6 papers), RNA modifications and cancer (4 papers) and Epilepsy research and treatment (4 papers). The work is most often cited by research in Clinical Biochemistry (85 citations), Molecular Biology (189 citations) and Hematology (28 citations). Keitaro Yamada has collaborated with scholars based in Japan, United States and Netherlands. Frequent co-authors include Toshiyuki Fukao, Keiko Yanagihara, Naomi Kondo, Toshiyuki Mano, Yasuhisa Toribe, N Mutoh, Hirotomo Saitsu, Yasuhiro Suzuki, Mitsuko Nakashima and Naomichi Matsumoto. Their work appears in journals such as Human Mutation, The Journal of Biochemistry and Epilepsy & Behavior.

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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