Tatsuya Kishino

6.1k total citations · 1 hit paper
64 papers, 3.3k citations indexed

About

Tatsuya Kishino is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tatsuya Kishino has authored 64 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 46 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tatsuya Kishino's work include Genetic Syndromes and Imprinting (26 papers), Epigenetics and DNA Methylation (20 papers) and Genomic variations and chromosomal abnormalities (15 papers). Tatsuya Kishino is often cited by papers focused on Genetic Syndromes and Imprinting (26 papers), Epigenetics and DNA Methylation (20 papers) and Genomic variations and chromosomal abnormalities (15 papers). Tatsuya Kishino collaborates with scholars based in Japan, United States and Thailand. Tatsuya Kishino's co-authors include Joseph Wagstaff, Marc Lalande, Norio Niikawa, Tohru Ohta, Naomichi Matsumoto, Shun’ichiro Taniguchi, Eiko Hidaka, Junji Sagara, Tsutomu Katsuyama and Tsukasa Higuchi and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Molecular and Cellular Biology.

In The Last Decade

Tatsuya Kishino

63 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

UBE3A/E6-AP mutations cause Angelman syndrome

1997 969 citations Tatsuya Kishino, Joseph Wagstaff et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Tatsuya Kishino Japan	27	2.4k	1.9k	572	318	234	64	3.3k
Andreas Tzschach Germany	30	2.1k 0.9×	1.8k 0.9×	255 0.4×	201 0.6×	266 1.1×	104	3.3k
Marlène Rio France	33	2.2k 0.9×	1.7k 0.9×	263 0.5×	225 0.7×	207 0.9×	112	3.5k
Ian A. Glass United States	36	2.9k 1.2×	2.1k 1.1×	1.1k 2.0×	199 0.6×	259 1.1×	122	4.4k
Samantha J.L. Knight United Kingdom	38	3.0k 1.2×	4.0k 2.1×	657 1.1×	230 0.7×	189 0.8×	89	5.8k
Joan Overhauser United States	31	1.9k 0.8×	1.9k 1.0×	480 0.8×	180 0.6×	96 0.4×	86	3.4k
Célia Bádenas Spain	33	2.2k 0.9×	1.4k 0.7×	400 0.7×	229 0.7×	374 1.6×	139	3.9k
Heather E. McDermid Canada	29	2.1k 0.9×	2.0k 1.0×	294 0.5×	95 0.3×	119 0.5×	64	3.3k
Stefan J. White Netherlands	31	1.9k 0.8×	1.3k 0.7×	301 0.5×	294 0.9×	91 0.4×	76	3.3k
Christiane Zweier Germany	30	2.3k 0.9×	1.9k 1.0×	193 0.3×	726 2.3×	162 0.7×	82	4.0k
Cédric Le Caignec France	29	1.7k 0.7×	1.5k 0.8×	770 1.3×	107 0.3×	107 0.5×	76	3.1k

Countries citing papers authored by Tatsuya Kishino

Since Specialization

Citations

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

Fields of papers citing papers by Tatsuya Kishino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tatsuya Kishino

This figure shows the co-authorship network connecting the top 25 collaborators of Tatsuya Kishino. A scholar is included among the top collaborators of Tatsuya Kishino 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 Tatsuya Kishino. Tatsuya Kishino 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

Watanabe, Kaori, Tatsuya Kishino, Akira Kinoshita, et al.. (2023). Proline-rich transmembrane protein 2 knock-in mice present dopamine-dependent motor deficits. The Journal of Biochemistry. 174(6). 561–570. 1 indexed citations

Kishino, Tatsuya, et al.. (2018). Application of droplet digital PCR in the analysis of genome integration and organization of the transgene in BAC transgenic mice. Scientific Reports. 8(1). 6638–6638. 4 indexed citations

Kishino, Tatsuya, et al.. (2014). Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos. Gene. 553(1). 63–68. 5 indexed citations

Yamada, Takahiro, Mitsuko Nakashima, Hisanori Minakami, et al.. (2010). A type of familial cleft of the soft palate maps to 2p24.2–p24.1 or 2p21–p12. Journal of Human Genetics. 55(2). 124–126. 4 indexed citations

Yoshiura, Koh-ichiro, Tatsuro Kondoh, Hirofumi Ohashi, et al.. (2009). Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome. Journal of Human Genetics. 54(5). 304–309. 27 indexed citations

Mapendano, Christophe K., Tatsuya Kishino, Shinji Kondo, et al.. (2006). Expression of the Snurf–Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain. Journal of Human Genetics. 51(3). 236–243. 18 indexed citations

Shimokawa, Osamu, Noriko Miyake, Nadiya Sosonkina, et al.. (2005). Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 136A(1). 49–51. 52 indexed citations

Watanabe, Akira, Yoko Nakano, Sadanori Akita, et al.. (2005). PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses. Journal of Human Genetics. 51(1). 38–46. 54 indexed citations

Shimokawa, Osamu, Kenji Kurosawa, Naoki Harada, et al.. (2004). Molecular characterization of inv dup del(8p): Analysis of five cases. American Journal of Medical Genetics Part A. 128A(2). 133–137. 61 indexed citations

10.

Miyake, Noriko, Naoki Harada, Osamu Shimokawa, et al.. (2004). On the reported 8p22‐p23.1 duplication in Kabuki make‐up syndrome (KMS) and its absence in patients with typical KMS. American Journal of Medical Genetics Part A. 128A(2). 170–172. 24 indexed citations

11.

Yamada, Takahiro, Kohzoh Mitsuya, Tomohiko Kayashima, et al.. (2003). Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32. Genomics. 83(3). 402–412. 16 indexed citations

12.

Kayashima, Tomohiko, Kentaro Yamasaki, Keiichiro Joh, et al.. (2003). Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting. Genomics. 81(6). 644–647. 15 indexed citations

13.

Sugawara, Hirotake, Naoki Harada, Naomichi Matsumoto, et al.. (2002). A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet. Journal of Human Genetics. 47(3). 136–139. 26 indexed citations

14.

Kantaputra, Piranit Nik, Kentaro Yamasaki, Takafumi Ishida, Tatsuya Kishino, & Norio Niikawa. (2002). A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai family. American Journal of Medical Genetics. 111(3). 301–306. 5 indexed citations

15.

Komatsu, Kazuki, N. Nakamura, Mohsen Ghadami, et al.. (2002). Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family. Journal of Human Genetics. 47(8). 395–399. 23 indexed citations

16.

Yamada, Koki, Pornprot Limprasert, Takashi Kitaoka, et al.. (2001). Two Thai families with Norrie disease (ND): Association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier. American Journal of Medical Genetics. 100(1). 52–55. 19 indexed citations

17.

Malzac, Perrine, Hayley Webber, A. Moncla, et al.. (1998). Mutation Analysis of UBE3A in Angelman Syndrome Patients. The American Journal of Human Genetics. 62(6). 1353–1360. 121 indexed citations

18.

Saijo, Masafumi, Yoshihisa Sakai, Tatsuya Kishino, et al.. (1995). Molecular Cloning of a Human Protein That Binds to the Retinoblastoma Protein and Chromosomal Mapping. Genomics. 27(3). 511–519. 33 indexed citations

19.

Kobayashi, Toshihide, Tatsuya Kishino, Naomichi Matsumoto, et al.. (1995). Isolation of microdissection clones from rat Chromosome 10. Mammalian Genome. 6(3). 216–218. 7 indexed citations

20.

Tamura, Toshiya, Tohru Ohta, Hidenobu Soejima, et al.. (1993). Mapping of the bone morphogenetic protein 1 gene (BMP1) to 8p21: removal of BMP1 from candidacy for the bone disorder in Langer-Giedion syndrome. Cytogenetic and Genome Research. 64(3-4). 208–209. 6 indexed citations

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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