Tetsuya Kibe

650 total citations
23 papers, 484 citations indexed

About

Tetsuya Kibe is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Tetsuya Kibe has authored 23 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 7 papers in Genetics. Recurrent topics in Tetsuya Kibe's work include Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Blood properties and coagulation (2 papers). Tetsuya Kibe is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Blood properties and coagulation (2 papers). Tetsuya Kibe collaborates with scholars based in Japan, Germany and United States. Tetsuya Kibe's co-authors include Brian J. Poindexter, Roger J. Bick, Gretchen J. Darlington, Kazumi Ishimura‐Oka, Heinz Linhart, Francesco J. DeMayo, Yoshiro Wada, Kenji Yokochi, Tatsuya Ishikawa and Kiyoshi Kidouchi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genomics and Advances in experimental medicine and biology.

In The Last Decade

Tetsuya Kibe

23 papers receiving 474 citations

Peers

Countries citing papers authored by Tetsuya Kibe

Since Specialization

Citations

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

Fields of papers citing papers by Tetsuya Kibe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuya Kibe

This figure shows the co-authorship network connecting the top 25 collaborators of Tetsuya Kibe. A scholar is included among the top collaborators of Tetsuya Kibe 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 Tetsuya Kibe. Tetsuya Kibe 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	Ask-Upmark kidney in a girl with neurofibromatosis type 1 2020 ·CEN Case Reports ·(unknown), Tetsuya Kibe, (unknown), Midori Awazu	1
2	Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis 2017 ·Blood Coagulation & Fibrinolysis ·Satoru Yoshida, Tetsuya Kibe, (unknown), Shinichiro Koizumi, Kenji Nara, Koji Amano, Nobuo Okumura	5
3	Predominant Corticospinal Tract Involvement in a Late Infant with Krabbe Disease 2016 ·PubMed ·(unknown), Tetsuya Kibe, (unknown), Norio Sakai, Kenji Yokochi	7
4	Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state 2015 ·Brain and Development ·(unknown), Ichizo Nishino, (unknown), Takao Togawa, (unknown), (unknown), Tetsuya Kibe, Norihisa Koyama, Kenji Yokochi	9
5	[Cervical myelopathy associated with os odontoideum after botulinum toxin treatment in a patient with cerebral palsy]. 2014 ·PubMed ·(unknown), Tetsuya Kibe, Kenji Yokochi	1
6	Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia 2012 ·Brain and Development ·Tetsuya Kibe, (unknown), Kenji Yokochi, Nobuo Okumura	2
7	Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale 2010 ·American Journal of Medical Genetics Part A ·Tetsuya Kibe, Yuka Mori, Tohru Okanishi, Keiko Shimojima, Kenji Yokochi, Toshiyuki Yamamoto	14
8	Delayed gyration with pontocerebellar hypoplasia type 1 2009 ·Brain and Development ·Tohru Okanishi, Yuka Mori, (unknown), Satoru Kobayashi, Hideyuki Nakashima, Tetsuya Kibe, Kenji Yokochi, Hajime Togari, Ikuya Nonaka	1
9	A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease 2008 ·Brain and Development ·Tetsuya Kibe, (unknown), Kenji Yokochi, Akiko Iwaki	6
10	Refractory epilepsy accompanying acute encephalitis with multifocal cortical lesions: Possible autoimmune etiology 2007 ·Brain and Development ·Tohru Okanishi, Yuka Mori, Tetsuya Kibe, Yukitoshi Takahashi, Yoshiaki Saito, Yoshihiro Maegaki, Kenji Yokochi	16
11	C/EBPα is required for differentiation of white, but not brown, adipose tissue 2001 ·Proceedings of the National Academy of Sciences ·Heinz Linhart, Kazumi Ishimura‐Oka, Francesco J. DeMayo, Tetsuya Kibe, (unknown), Brian J. Poindexter, Roger J. Bick, Gretchen J. Darlington	268
12	Diffuse central nervous system lupus involving white matter, basal ganglia, thalami and brainstem 1999 ·Brain and Development ·(unknown), Tetsuya Kibe, Shinji Fujimoto, Tatsuya Ishikawa, (unknown), (unknown), Yoshiro Wada	21
13	Serial MRI findings of benign poliomyelitis 1996 ·Brain and Development ·Tetsuya Kibe, Shinji Fujimoto, Tatsuya Ishikawa, (unknown), Yoshiro Wada, Tatsuo Banno, (unknown)	4
14	Deletion of small nuclear ribonucleoprotein polypeptide N (SNRPN) in Prader-Willi syndrome detected by fluorescence in situ hybridization: Two sibs with the typical phenotype without a cytogenetic deletion in chromosome 15q 1996 ·American Journal of Medical Genetics ·Tatsuya Ishikawa, Tetsuya Kibe, Yoshiro Wada	12
15	Glycosylation and Placental Transport of Immunoglobulin G. 1996 ·Journal of Clinical Biochemistry and Nutrition ·Tetsuya Kibe, Shinji Fujimoto, (unknown), Hajime Togari, Yoshiro Wada, Setsuo Okada, Hiroaki Nakagawa, Yoshinori Tsukamoto, Noriko Takahashi	41
16	ヒト染色体領域8q23.3‐q24.11と2q33‐qterの微小解剖 DNAライブラリーの構築とそのクローンの分離 1992 ·Genomics ·Takeshi Hirota, Kazuhiro Tsukamoto, Han‐Xiang Deng, (unknown), Tohru Ohta, (unknown), Tetsuya Kibe, (unknown), Norio Niikawa	1
17	Microdissection of human chromosomal regions 8q23.3–q24.11 and 2q33-qter: Construction of DNA libraries and isolation of their clones 1992 ·Genomics ·(unknown), Kazuhiro Tsukamoto, Han‐Xiang Deng, Koh-ichiro Yoshiura, Tohru Ohta, Takaya Tohma, Tetsuya Kibe, Naoki Harada, Yoshihiro Jinno, Norio Niikawa	20
18	Isolation of 2 novel RFLP markers and their localization at 2q35 by microdissection and subsequent enzymatic amplification 1992 ·The Japanese Journal of Human Genetics ·Tetsuya Kibe, Kazuhiro Tsukamoto, (unknown), Koh-ichiro Yoshiura, Tohru Ohta, Takaya Tohma, Toshiya Tamura, Yoshihiro Jinno, Norio Niikawa	1
19	Automated Quantitative Analysis for Orotidine and Uridine/Thymine in Urine by High-Performance Liquid Chromatography with Column Switching 1991 ·Advances in experimental medicine and biology ·Kiyoshi Kidouchi, Chié Nakamura, Toshiyuki Katoh, Tetsuya Kibe, Satoru Ohba, Yoshiro Wada	3
20	Automated determination of orotic acid, uracil and pseudouridine in urine by high-performance liquid chromatography with column switching 1991 ·Journal of Chromatography B Biomedical Sciences and Applications ·Satoru Ohba, Kiyoshi Kidouchi, Toshiyuki Katoh, Tetsuya Kibe, Masanori Kobayashi, Yoshiro Wada	29

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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