Kenjiro Kosaki

10.1k citations

363 papers · 5.2k indexed · h-index 35

Molecular Biology top 2%
Genetics top 1%
Surgery top 5%
Pediatrics, Perinatology and Child Health top 2%
Pulmonary and Respiratory Medicine top 5%

Co-authors: Rika Kosaki Toshiki Takenouchi Brett Casey Chiharu Torii Tomoko Uehara Nobuhiko Okamoto Takao Takahashi Hisato Suzuki
Topics: Genomic variations and chromosomal abnormalities (55 papers)Genomics and Rare Diseases (36 papers)Genetics and Neurodevelopmental Disorders (33 papers)
Cited by: Genetics Developmental Biology
Journals: Proceedings of the National Academy of Sciences Nature CommunicationsSHILAP Revista de lepidopterología
Partner nations: Japan United States Netherlands

In The Last Decade

Kenjiro Kosaki

342 papers receiving 5.0k citations

Peers

Countries citing papers authored by Kenjiro Kosaki

Since Specialization

Citations

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

Fields of papers citing papers by Kenjiro Kosaki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kenjiro Kosaki

This figure shows the co-authorship network connecting the top 25 collaborators of Kenjiro Kosaki. A scholar is included among the top collaborators of Kenjiro Kosaki 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 Kenjiro Kosaki. Kenjiro Kosaki 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	Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases 2024 ·Orphanet Journal of Rare Diseases ·Clara D.M. van Karnebeek,Anne O’Donnell‐Luria,Gareth Baynam,Anaı̈s Baudot,Tudor Groza,Judith Jans,Timo Lassmann,(unknown),Stephen B. Montgomery,(unknown),Stefaan Sansen,Ruty Mehrian‐Shai,Charles A. Steward,Kenjiro Kosaki,(unknown),Bekim Sadiković	7
2	A novel missense variant of <i>FGD1</i> disrupts critical cysteine residues of the FYVE domain in Japanese siblings with Aarskog–Scott syndrome 2024 ·Clinical Pediatric Endocrinology ·Ikuko Takahashi,Atsuko Noguchi,(unknown),Yoko Sato,Hisato Suzuki,Mamiko Yamada,Kenjiro Kosaki,Tsutomu Takahashi	0
3	Molecular basis of carotid body tumor and associated clinical features in Japan identified by genomic, immunohistochemical, and clinical analyses 2023 ·Clinical Genetics ·(unknown),Hideki Mutai,(unknown),(unknown),Shin Saito,(unknown),(unknown),(unknown),(unknown),(unknown),Kenjiro Kosaki,Hiroyuki Ozawa,Tatsuo Matsunaga	3
4	miR-514a promotes neuronal development in human iPSC-derived neurons 2023 ·Frontiers in Cell and Developmental Biology ·(unknown),Satoru Takahashi,Keiichiro Suzuki,Kenjiro Kosaki,Keita Tsujimura	0
5	Pro108Ser mutation of SARS-CoV-2 3CLpro reduces the enzyme activity and ameliorates the clinical severity of COVID-19 2022 ·Scientific Reports ·(unknown),Yasuaki Kabe,Susumu Uchiyama,Yuka W. Iwasaki,Hirotsugu Ishizu,Yoshifumi Uwamino,Toshiki Takenouchi,Shunsuke Uno,Makoto Ishii,Takahiro Maruno,Masanori Noda,Mitsuru Murata,Naoki Hasegawa,Hideyuki Saya,Yuko Kitagawa,Koichi Fukunaga,Masayuki Amagai,Haruhiko Siomi,Makoto Suematsu,Kenjiro Kosaki,(unknown)	18
6	De novo non-synonymous CTR9 variants are associated with motor delay and macrocephaly: human genetic and zebrafish experimental evidence 2022 ·Human Molecular Genetics ·Hisato Suzuki,Kana Aoki,Kenji Kurosawa,Kazuo Imagawa,Tatsuyuki Ohto,Mamiko Yamada,Toshiki Takenouchi,Kenjiro Kosaki,Tohru Ishitani	1
7	Familial hemophagocytic lymphohistiocytosis syndrome due to lysinuric protein intolerance: a patient with a novel compound heterozygous pathogenic variant in SLC7A7 2022 ·International Journal of Hematology ·(unknown),Kenichi Sakamoto,(unknown),Takashi Taga,Kenjiro Kosaki,Yoshihiro Maruo	4
8	Four pedigrees with aminoacyl-tRNA synthetase abnormalities 2021 ·Neurological Sciences ·Nobuhiko Okamoto,Fuyuki Miya,Tatsuhiko Tsunoda,Yonehiro Kanemura,Shinji Saitoh,Mitsuhiro Kato,Kumiko Yanagi,Tadashi Kaname,Kenjiro Kosaki	10
9	Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants 2021 ·Human Genome Variation ·Takenori Tozawa,Akira Nishimura,(unknown),(unknown),(unknown),Takeshi Yoshida,Naoko Nakagawa,Takahito Wada,Shinji Kosugi,Tomoko Uehara,Toshiki Takenouchi,Kenjiro Kosaki,Tomohiro Chiyonobu	4
10	The Inhibitor of Apoptosis Protein Livin Confers Resistance to Fas-Mediated Immune Cytotoxicity in Refractory Lymphoma 2020 ·Cancer Research ·Eiji Sugihara,(unknown),Satoru Osuka,Takatsune Shimizu,Sayaka Ueno,Shogo Okazaki,Tomonori Yaguchi,Yutaka Kawakami,Kenjiro Kosaki,Taka-Aki Sato,Shinichiro Okamoto,Hideyuki Saya	10
11	Clonal Expansion of Second-Hit Cells with Somatic Recombinations or C>T Transitions Form Porokeratosis in MVD or MVK Mutant Heterozygotes 2019 ·Journal of Investigative Dermatology ·Akiharu Kubo,Takashi Sasaki,Hisato Suzuki,Aiko Shiohama,(unknown),Showbu Sato,Harumi Fujita,(unknown),Noriko Umegaki‐Arao,Tomoko Kawai,Kazuhiko Nakabayashi,Kenichiro Hata,Daisuke Yamada,Yoichi Matsubara,Kenjiro Kosaki,Masayuki Amagai	33
12	A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome 2018 ·Journal of Human Genetics ·Ikumi Hori,Fuyuki Miya,Yutaka Negishi,Ayako Hattori,N Ando,Keith A. Boroevich,Nobuhiko Okamoto,Mitsuhiro Kato,Tatsuhiko Tsunoda,Mami Yamasaki,Yonehiro Kanemura,Kenjiro Kosaki,Shinji Saitoh	10
13	Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese 2018 ·Nature Communications ·Yukinori Okada,Yukihide Momozawa,Saori Sakaue,Masahiro Kanai,Kazuyoshi Ishigaki,Masato Akiyama,Toshihiro Kishikawa,Yasumichi Arai,Takashi Sasaki,Kenjiro Kosaki,Makoto Suematsu,Koichi Matsuda,Kazuhiko Yamamoto,Michiaki Kubo,Nobuyoshi Hirose,Yoichiro Kamatani	84
14	Novel MCA/ID syndrome with ASH1L mutation 2017 ·American Journal of Medical Genetics Part A ·Nobuhiko Okamoto,Fuyuki Miya,Tatsuhiko Tsunoda,Mitsuhiro Kato,Shinji Saitoh,Mami Yamasaki,Yonehiro Kanemura,Kenjiro Kosaki	29
15	In utero exposure to dioxin causes neocortical dysgenesis through the actions of p27 ^Kip1 2010 ·Proceedings of the National Academy of Sciences ·Takayuki Mitsuhashi,Junzo Yonemoto,Hirohito Sone,Yasuhiro Kosuge,Kenjiro Kosaki,Takao Takahashi	22
16	Screening for Alagille Syndrome Mutations in the JAG1 and NOTCH2 Genes Using Denaturing High-Performance Liquid Chromatography 2007 ·Genetic Testing ·(unknown),Chiharu Torii,Rika Kosaki,Kenji Kurosawa,Hiroshi Yoshihashi,Koji Muroya,Nobuhiko Okamoto,Yoriko Watanabe,Tomoki Kosho,(unknown),Osamu Matsuda,(unknown),Kosuke Izumi,Takao Takahashi,Kenjiro Kosaki	7
17	Multiplex PCR/Liquid Chromatography Assay for Screening of Subtelomeric Rearrangements 2007 ·Genetic Testing ·Toru Udaka,Issei Imoto,Yoshinori Aizu,Chiharu Torii,Kosuke Izumi,Rika Kosaki,Takao Takahashi,Shin Hayashi,Johji Inazawa,Kenjiro Kosaki	3
18	Screening for Partial Deletions in the CREBBP Gene in Rubinstein–Taybi Syndrome Patients Using Multiplex PCR/Liquid Chromatography 2006 ·Genetic Testing ·Toru Udaka,Kenji Kurosawa,Kosuke Izumi,Shinobu Yoshida,Masato Tsukahara,Nobuhiko Okamoto,Chiharu Torii,Rika Kosaki,Mitsuo Masuno,(unknown),Takao Takahashi,Kenjiro Kosaki	12
19	Screening for CHARGE Syndrome Mutations in the CHD7 Gene Using Denaturing High-Performance Liquid Chromatography 2006 ·Genetic Testing ·Michihiko Aramaki,Toru Udaka,Chiharu Torii,(unknown),Rika Kosaki,Takao Takahashi,Kenjiro Kosaki	12
20	Comprehensive Screening of the Thiopurine Methyltransferase Polymorphisms by Denaturing High-Performance Liquid Chromatography 2005 ·Genetic Testing ·Toru Udaka,Chiharu Torii,Daisuke Takahashi,Tetsuya Mori,Michihiko Aramaki,Rika Kosaki,Yusuke Tanigawara,Takao Takahashi,Kenjiro Kosaki	7

About Kenjiro Kosaki

Kenjiro Kosaki is a scholar working on Genetics, Developmental Biology and Genetics, having authored 363 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (55 papers), Genomics and Rare Diseases (36 papers) and Genetics and Neurodevelopmental Disorders (33 papers). The work is most often cited by research in Genetics (1.8k citations), Genetics (464 citations) and Developmental Biology (91 citations). Kenjiro Kosaki has collaborated with scholars based in Japan, United States and Netherlands. Frequent co-authors include Rika Kosaki, Toshiki Takenouchi, Brett Casey, Chiharu Torii, Tomoko Uehara, Nobuhiko Okamoto, Takao Takahashi, Hisato Suzuki, Takao Takahashi and Tsutomu Ogata. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

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