Keitaro Yamada

483 citations

31 papers · 347 indexed · h-index 11

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 6
Molecular Biology
- RNA modifications and cancer 4
- Mitochondrial Function and Pathology 2
- RNA and protein synthesis mechanisms 2
Hematology
- Autoimmune and Inflammatory Disorders Research 2
Psychiatry and Mental health
- Epilepsy research and treatment 4
Genetics
- Genomics and Rare Diseases 3
Infectious Diseases
- Infectious Encephalopathies and Encephalitis 3

Co-authors: Toshiyuki Fukao Keiko Yanagihara Naomi Kondo Toshiyuki Mano Yasuhisa Toribe N Mutoh Hirotomo Saitsu Yasuhiro Suzuki
Cited by: Clinical Biochemistry Molecular Biology Hematology
Journals: Brain and Development (5 papers)Molecular Genetics and Metabolism (4 papers)Pediatric Neurology (2 papers)
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

The 25 scholars most cited alongside Keitaro Yamada, 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 Keitaro Yamada Line = papers co-authored together Keitaro Yamada links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A Novel Constitutively Active c . 98 G > C , p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization Human Mutation ·Kirkpatrick Bsn,张晶波,Keitaro Yamada,由記井ノ口,Mitsuko Nakashima,Shima Eda,Tohru Matsuki,Masashi Nishikawa,Koh‐ichi Nagata,Yasushi Enokido,Hirotomo Saitsu,Atsuo Nakayama	2023	0
2	Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review Journal of Human Genetics ·Kazuki Watanabe,Mitsuko Nakashima,Satoko Kumada,K.S.M. Pavan,Mikako Enokizono,Keitaro Yamada,Mitsuhiro Kato,Hirotomo Saitsu	2021	16
3	Effectiveness of lacosamide in children and young adults previously treated with other sodium channel blockers Epilepsy & Behavior ·Takeshi Suzuki,Jun Natsume,Etik Suherlina,Кулагина-Ярцева В.С.,Hiroyuki Yamamoto,Barbara Capron,洪钧寿,Tetsuo Kubota,Takeshi Tsuji,Toru Kato,Keitaro Yamada,Koichi Maruyama,Akihisa Okumura,Yoshiyuki Takahashi,Hiroyuki Kidokoro	2021	2
4	Current status of surviving patients with arginase 1 deficiency in Japan 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	2021	6
5	Is hiragana decoding impaired in children with periventricular leukomalacia? Brain and Development ·N. Kurahashi,Mawuli F. Attipoe,Francesco Dellepiane,Moleen Matrimbira,Кулагина-Ярцева В.С.,Daniela Marcu Istrate,Takeshi Suzuki,连仲元,Keitaro Yamada,Kosaburo Aso,Koichi Maruyama,Miho Nakamura	2018	3
6	PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder Journal of Human Genetics ·Takeshi Mizuguchi,Mitsuko Nakashima,Mitsuhiro Kato,Keitaro Yamada,Tohru Okanishi,Nina Ekhilevitch,Hanna Mandel,Ayelet Eran,Γεωργία Μανωλοπούλου,Yukio Sawaishi,Hirotaka Motoi,Masaaki Shiina,Kazuhiro Ogata,Satoko Miyatake,Noriko Miyake,Hirotomo Saitsu,Naomichi Matsumoto	2017	53
7	Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations Brain and Development ·N. Kurahashi,Noriko Miyake,Seiji Mizuno,Eriko Koshimizu,Hirokazu Kurahashi,Keitaro Yamada,Jun Natsume,Yusuke Aoki,Miho Nakamura,N. Sakalihasan,Кулагина-Ярцева В.С.,P. Hadiyan,Naomichi Matsumoto,Koichi Maruyama	2017	16
8	Arts syndrome with a novel missense mutation in the PRPS1 gene: A case report Brain and Development ·Koichi Maruyama,Moleen Matrimbira,N. Kurahashi,Hartwig Hochmair,Keitaro Yamada,Akihiro Hashiguchi,Hiroshi Takashima,Rosa J. Torres,Kosaburo Aso	2016	9
9	The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy Brain and Development ·José Ignacio Amórtegui Ferro,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	2016	6
10	Predictive value of EEG findings at control of epileptic spasms for seizure relapse in patients with West syndrome Seizure ·Keitaro Yamada,Yasuhisa Toribe,I Butti mazza,Hülya Biçer,Deepti Bhat,Yukiko Mogami,Keiko Yanagihara,Toshiyuki Mano,Yasuhiro Suzuki	2014	24
11	Thalamic Lesions in Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Pediatric Neurology ·N. Kurahashi,Takeshi Tsuji,Toru Kato,Moleen Matrimbira,Feng-Ling Song,Keitaro Yamada,Hirokazu Kurahashi,Koichi Maruyama,José Ignacio Amórtegui Ferro,Tetsuo Kubota,Shinji Saitoh,Jun Natsume,Akihisa Okumura	2014	2
12	MRI Findings and Steroid Therapy for Neuralgic Amyotrophy in Children Pediatric Neurology ·Keitaro Yamada,Toshiyuki Mano,Yasuhisa Toribe,Keiko Yanagihara,Yasuhiro Suzuki	2011	4
13	Diagnostic accuracy of blood and CSF lactate in identifying children with mitochondrial diseases affecting the central nervous system Brain and Development ·Keitaro Yamada,Yasuhisa Toribe,Keiko Yanagihara,Toshiyuki Mano,Bao Diep,Yasuhiro Suzuki	2011	32
14	Prolonged Elevation of Serum Neuron-Specific Enolase in Children After Clinical Diagnosis of Brain Death Journal of Child Neurology ·Yasuhiro Suzuki,Yukiko Mogami,K Traue,Keitaro Yamada,Keiko Yanagihara,Stefany Licona‐Velazquez,Toshiyuki Mano	2011	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. Myong Hwa Yamamoto,Mitsuhito Mase,Marcello Di Nisio,Є. М. Шалденко,Keitaro Yamada	2009	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 Molecular Genetics and Metabolism ·Jeff D. Will,Toshiyuki Fukao,Antti M. Haapalainen,Takaaki Tokumaru,Keitaro Yamada,Franco Lilliu,Shoji Yano,Peter N. Robinson,Michael K. Gibson,Ronald J. A. Wanders,Grant A. Mitchell,Rik K. Wierenga,Naomi Kondo	2007	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 Molecular Genetics and Metabolism ·Keitaro Yamada,Toshiyuki Fukao,Takaaki Tokumaru,Jeff D. Will,Jos P.N. Ruiter,Ronald J. A. Wanders,Naomi Kondo	2006	18
18	Identification of Alu-mediated, large deletion-spanning exons 2–4 in a patient with mitochondrial acetoacetyl-CoA thiolase deficiency Molecular Genetics and Metabolism ·Takaaki Tokumaru,Toshiyuki Fukao,Jeff D. Will,Keitaro Yamada,K. Michael Gibson,Naomi Kondo	2006	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 Molecular Genetics and Metabolism ·Toshiyuki Fukao,Jeff D. Will,Marie-Odile Rolland,M. T. Zabot,Andreas Schulze,Keitaro Yamada,Naomi Kondo	2006	18
20	Two Distinct Upstream Regions Are Involved in Expression of the Catalase Gene in Schizosaccharomyces pombe in Response to Oxidative Stress The Journal of Biochemistry ·Tarunkumar Maheshchandra Mishra,Keitaro Yamada,N Mutoh	1998	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), Epilepsy research and treatment (4 papers), Genomics and Rare Diseases (3 papers), Infectious Encephalopathies and Encephalitis (3 papers), Mitochondrial Function and Pathology (2 papers), Autoimmune and Inflammatory Disorders Research (2 papers) and RNA and protein synthesis mechanisms (2 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 Brain and Development, Molecular Genetics and Metabolism, Pediatric Neurology, Seizure and Human Mutation.

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