Kyoko Takano

1.8k citations

55 papers · 875 indexed · h-index 16

Co-authors: Mutsuo Sekiguchi Charles E. Schwartz Shawn Witham Emil Alexov Yusaku Nakabeppu Shinji Saitoh Hitoshi Osaka Noriko Aida
Topics: RNA regulation and disease (8 papers)Metabolism and Genetic Disorders (7 papers)Genetic Syndromes and Imprinting (6 papers)
Cited by: Genetics Clinical Biochemistry Molecular Biology
Journals: Journal of Molecular Biology The Journal of Clinical Endocrinology & Metabolism Annals of Neurology
Partner nations: Japan United States Australia

In The Last Decade

Kyoko Takano

53 papers receiving 860 citations

Peers

Countries citing papers authored by Kyoko Takano

Since Specialization

Citations

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

Fields of papers citing papers by Kyoko Takano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kyoko Takano

This figure shows the co-authorship network connecting the top 25 collaborators of Kyoko Takano. A scholar is included among the top collaborators of Kyoko Takano 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 Kyoko Takano. Kyoko Takano 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 nationwide survey of Schaaf-Yang syndrome in Japan 2022 ·Journal of Human Genetics ·Yutaka Negishi,Kenji Kurosawa,Kyoko Takano,Keiko Matsubara,Takeshi Nishiyama,Shinji Saitoh	2
2	Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency 2021 ·Thyroid ·Hideyuki Iwayama,Hiroki Kakita,(unknown),(unknown),Kyoko Takano,Masahiro Kikuchi,Yasuko Fujisawa,Hitoshi Osaka,Yasumasa Yamada,Akihisa Okumura,Khemraj Hirani,Roy E. Weiss,Samuel Refetoff	14
3	High-amplitude fast activity in EEG: An early diagnostic marker in children with beta-propeller protein-associated neurodegeneration (BPAN) 2020 ·Clinical Neurophysiology ·Hiroyuki Kidokoro,Hiroyuki Yamamoto,Tetsuo Kubota,Mitsuo Motobayashi,(unknown),Tomohiko Nakata,Kyoko Takano,Naoko Shiba,(unknown),Masaharu Tanaka,(unknown),(unknown),(unknown),Takeshi Suzuki,Kazuhiro Muramatsu,Jun Natsume	5
4	A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature 2019 ·Molecular Case Studies ·Aritoshi Iida,Kyoko Takano,Eri Takeshita,(unknown),Shinichi Hirabayashi,Yuji Inaba,Shunichi Kosugi,Yoichiro Kamatani,Yukihide Momozawa,Michiaki Kubo,Eiji Nakagawa,Ken Inoue,Yu-ichi Goto	8
5	Aggregate formation analysis of GFAPR416W found in one case of Alexander disease 2018 ·Brain and Development ·(unknown),(unknown),Eriko F. Jimbo,Hiroko Shimbo,Kyoko Takano,Mizue Iai,Sumimasa Yamashita,Tomohide Goto,Noriko Aida,(unknown),Takanori Yamagata,Hitoshi Osaka	1
6	A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8 2017 ·Human Genome Variation ·Tsuneaki Yoshinaga,Katsuya Nakamura,(unknown),Tomomi Yamaguchi,Kyoko Takano,Keiko Wakui,Tomoki Kosho,Kunihiro Yoshida,Yoshimitsu Fukushima,Yoshiki Sekijima	12
7	Immediate suppression of seizure clusters by corticosteroids in PCDH19 female epilepsy 2015 ·Seizure ·Norimichi Higurashi,Yukitoshi Takahashi,(unknown),Yuji Sugawara,Hiroshi Sakuma,(unknown),Takahito Inoue,(unknown),(unknown),Masaharu Ohfu,Kazuya Itomi,Kyoko Takano,(unknown),Shinichi Hirose	44
8	A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy 2014 ·Brain and Development ·Kyoko Takano,(unknown),Mutsumi Sato,(unknown),(unknown),(unknown),Mizue Iai,Sumimasa Yamashita,(unknown),Noriko Aida,Yoshinori Tsurusaki,Hirotomo Saitsu,Naomichi Matsumoto,Hitoshi Osaka	6
9	A Three-Year-Old Boy With Glucose Transporter Type 1 Deficiency Syndrome Presenting With Episodic Ataxia 2013 ·Pediatric Neurology ·(unknown),Hiroko Shimbo,Kyoko Takano,Takahito Wada,Hitoshi Osaka	19
10	Idiopathic Cranial Polyneuropathy With Unilateral IX and X and Contralateral XI Nerve Palsy in a 4-Year-Old Boy 2012 ·Pediatric Neurology ·(unknown),(unknown),Kyoko Takano,(unknown),Hitoshi Osaka	3
11	Two percent of patients suspected of having Angelman syndrome have TCF4 mutations 2010 ·Clinical Genetics ·Kyoko Takano,Michael J. Lyons,C. D. Moyes,Julie R. Jones,CE Schwartz	40
12	A loss‐of‐function mutation in the FTSJ1 gene causes nonsyndromic X‐linked mental retardation in a japanese family 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Kyoko Takano,Eiji Nakagawa,Ken Inoue,Fumiaki Kamada,Shigeo Kure,Yu‐ichi Goto	36
13	Investigations of the Quality of Hospital Electric Power Supply and the Tolerance of Medical Electric Devices to Voltage Dips 2007 ·Journal of Medical Systems ·Eisuke Hanada,(unknown),Kyoko Takano,(unknown)	8
14	Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I 2003 ·Pediatric Neurology ·Kyoko Takano,(unknown),(unknown),Akira Sudo,Kimiaki Uetake,Shinji Saitoh	11
15	A Practical Procedure to Prevent Electromagnetic Interference with Electronic Medical Equipment 2002 ·Journal of Medical Systems ·Eisuke Hanada,Kyoko Takano,(unknown),Kouji Matsumura,Yoshiaki Watanabe,Yoshiaki Nose	9
16	Germline mosaicism of a novel mutation in lysosome‐associated membrane protein‐2 deficiency (Danon disease) 2002 ·Annals of Neurology ·Maki Takahashi,Ayaka Yamamoto,Kyoko Takano,Akira Sudo,Takahito Wada,Yu‐ichi Goto,Ichizo Nishino,Shinji Saitoh	25
17	Possible Electromagnetic Interference with Electronic Medical Equipment by Radio Waves Coming from Outside the Hospital 2001 ·Journal of Medical Systems ·Eisuke Hanada,Kenji Kodama,Kyoko Takano,Yoshiaki Watanabe,Yoshiaki Nose	15
18	Characterization of phe B gene encoding catechol 2,3-dioxygenase 1994 ·Letters in Applied Microbiology ·Tatsuji Nishihara,Takahiko Yamada,Kyoko Takano,Shin‐Ichi Osada,J Nishikawa,Masayoshi Imagawa	1
19	Roles of two types of O6-methylguanine-DNA methyltransferases in DNA repair 1991 ·Mutation Research/DNA Repair ·Kyoko Takano,(unknown),Mutsuo Sekiguchi	40
20	Functional sites of the Ada regulatory protein of Escherichia coli 1988 ·Journal of Molecular Biology ·Kyoko Takano,Yusaku Nakabeppu,Mutsuo Sekiguchi	49

About Kyoko Takano

Kyoko Takano is a scholar working on Clinical Biochemistry, Neurology and Medical Laboratory Technology, having authored 55 papers that have together received 875 indexed citations. Recurring topics across this work include RNA regulation and disease (8 papers), Metabolism and Genetic Disorders (7 papers) and Genetic Syndromes and Imprinting (6 papers). The work is most often cited by research in Genetics (310 citations), Clinical Biochemistry (69 citations) and Molecular Biology (541 citations). Kyoko Takano has collaborated with scholars based in Japan, United States and Australia. Frequent co-authors include Mutsuo Sekiguchi, Charles E. Schwartz, Shawn Witham, Emil Alexov, Yusaku Nakabeppu, Shinji Saitoh, Hitoshi Osaka, Noriko Aida, Takahito Wada and Akira Sudo. Their work appears in journals such as Journal of Molecular Biology, The Journal of Clinical Endocrinology & Metabolism and Annals of Neurology.

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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