Takako Takano

1.2k total citations
49 papers, 925 citations indexed

About

Takako Takano is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Takako Takano has authored 49 papers receiving a total of 925 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 21 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Takako Takano's work include Genomic variations and chromosomal abnormalities (9 papers), Virus-based gene therapy research (5 papers) and Lysosomal Storage Disorders Research (4 papers). Takako Takano is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Virus-based gene therapy research (5 papers) and Lysosomal Storage Disorders Research (4 papers). Takako Takano collaborates with scholars based in Japan, United States and Poland. Takako Takano's co-authors include Yasuko Yamanouchi, Harry Holthöfer, Hugh R. Brady, Marie Hébert, Keisaku Yamane, Shinsuke Kataoka, Yôsuke Ishii, Kenji Kimura, Tomohiro Tamura and Takuji Shirasawa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and The Journal of Immunology.

In The Last Decade

Takako Takano

47 papers receiving 880 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takako Takano Japan 18 379 207 145 139 135 49 925
Roland Günther United States 24 582 1.5× 396 1.9× 140 1.0× 300 2.2× 216 1.6× 56 1.6k
Maria Morini Italy 17 218 0.6× 103 0.5× 52 0.4× 195 1.4× 52 0.4× 73 957
Yasuko Ishikawa Japan 18 621 1.6× 93 0.4× 69 0.5× 74 0.5× 34 0.3× 62 1.1k
Ming‐Qing Gao China 21 539 1.4× 154 0.7× 28 0.2× 144 1.0× 165 1.2× 41 1.1k
U. Weyer Germany 13 443 1.2× 149 0.7× 57 0.4× 217 1.6× 284 2.1× 19 894
Matthew R. Evans United Kingdom 16 326 0.9× 124 0.6× 83 0.6× 55 0.4× 106 0.8× 33 996
Evan B. Janovitz United States 19 317 0.8× 137 0.7× 23 0.2× 66 0.5× 74 0.5× 40 981
Jacques Mathieu France 9 375 1.0× 132 0.6× 65 0.4× 129 0.9× 59 0.4× 9 688
Katsumi Hanada Japan 20 363 1.0× 85 0.4× 24 0.2× 190 1.4× 67 0.5× 67 1.2k
Adelina Gama Portugal 20 413 1.1× 150 0.7× 47 0.3× 106 0.8× 75 0.6× 56 1.3k

Countries citing papers authored by Takako Takano

Since Specialization
Citations

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

Fields of papers citing papers by Takako Takano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takako Takano

This figure shows the co-authorship network connecting the top 25 collaborators of Takako Takano. A scholar is included among the top collaborators of Takako 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 Takako Takano. Takako Takano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kawai, Tomoko, Hiroko Ogata‐Kawata, Kazuaki Nakamura, et al.. (2023). Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis. European Journal of Medical Genetics. 66(8). 104806–104806. 2 indexed citations
2.
3.
Takano, Takako, et al.. (2021). Adult acampomelic campomelic dysplasia and disorders of sex development due to a reciprocal translocation involving chromosome 17q24.3 upstream of the SOX9 gene. European Journal of Medical Genetics. 64(11). 104332–104332. 2 indexed citations
4.
Takano, Takako, et al.. (2019). Sex differences in congenital heart disease in Down syndrome: study data from medical records and questionnaires in a region of Japan. BMJ Paediatrics Open. 3(1). e000414–e000414. 5 indexed citations
5.
Ozaki, Yukinori, Koichiro Matsumoto, Masashi Takahashi, et al.. (2019). Abstract OT1-12-02: Biomarker study of patients with HER2-negative metastatic breast cancer receiving combination therapy with nivolumab, bevacizumab and paclitaxel as first-line treatment (WJOG9917BTR). Cancer Research. 79(4_Supplement). OT1–12. 2 indexed citations
6.
Takano, Takako, et al.. (2019). Tetrasomy 21 pter→q21.3 due to an extra +dic(21;21)mat in a severely psychomotor-retarded female patient without Down syndrome phenotype. European Journal of Medical Genetics. 63(4). 103824–103824.
7.
Karita, Kanae, et al.. (2008). Associations of blood selenium and serum lipid levels in Japanese premenopausal and postmenopausal women. Menopause The Journal of The North American Menopause Society. 15(1). 119–124. 34 indexed citations
8.
Karita, Kanae, et al.. (2004). Variations in Plasma Selenium Levels as a Result of the Menstrual Cycle and Pregnancy in Healthy Japanese Women. Biological Trace Element Research. 99(1-3). 83–92. 13 indexed citations
9.
Karita, Kanae, et al.. (2001). A search for calcium, magnesium and zinc levels in fingernails of 135 patients with osteogenesis imperfecta. Journal of Trace Elements in Medicine and Biology. 15(1). 36–39. 11 indexed citations
10.
Ogata, Tsutomu, Keiko Wakui, Tomoki Kosho, et al.. (2000). Structural analysis of a rare rearranged Y chromosome and its bearing on genotype–phenotype correlation. American Journal of Medical Genetics. 92(4). 256–259. 3 indexed citations
11.
Kuroyanagi, Hidehito, Jin Yan, Naohiko Seki, et al.. (1998). Human ULK1, a Novel Serine/Threonine Kinase Related to UNC-51 Kinase ofCaenorhabditis elegans:cDNA Cloning, Expression, and Chromosomal Assignment. Genomics. 51(1). 76–85. 87 indexed citations
12.
Takano, Kaoru, et al.. (1997). Pressure-Induced Apoptosis in Human Lymphoblasts. Experimental Cell Research. 235(1). 155–160. 23 indexed citations
13.
Takano, Takako, Naruhiko Sahara, Yasuko Yamanouchi, & Hiroshi Mori. (1997). Assignment of Alzheimer's presenilin-2 (PS-2) gene to 1q42.1 by fluorescence in situ hybridization. Neuroscience Letters. 221(2-3). 205–207. 3 indexed citations
14.
Hébert, Marie, Takako Takano, Harry Holthöfer, & Hugh R. Brady. (1996). Sequential morphologic events during apoptosis of human neutrophils. Modulation by lipoxygenase-derived eicosanoids. The Journal of Immunology. 157(7). 3105–3115. 147 indexed citations
15.
Takano, Takako, Yasuko Yamanouchi, Shigeo Nagafuchi, & Masao Yamada. (1996). Assignment of the Dentatorubral and Pallidoluysian Atrophy (DRPLA) Gene to 12p13.31 by Fluorescencein SituHybridization. Genomics. 32(1). 171–172. 22 indexed citations
16.
Inada, Toshiya, et al.. (1995). Dopamine D3 receptor gene polymorphism and the psychiatric symptoms seen in first-break schizophrenic patients. Psychiatric Genetics. 5(3). 113–116. 20 indexed citations
17.
Yamanouchi, Yasuko, et al.. (1994). Apolipoprotein E5 and E7 in apparently healthy Japanese males: Frequencies and relation to plasma lipid levels. The Japanese Journal of Human Genetics. 39(3). 315–325. 15 indexed citations
18.
Iida, Shūichi, Takako Takano, Kazufumi Tsubaki, Zenrō Ikezawa, & Takeshi Nishio. (1993). Evaluation of a rice [Oryza sativa] mutant as a material of hypoallergenic rice. Ikushugaku zasshi. 1 indexed citations
19.
Shimmoto, Michie, Takako Takano, Yukiko Fukuhara, et al.. (1990). Japanese-type adult galactosialidosis. A unique and common splice junction mutation causing exon skipping in the protective protein/carboxypeptidase gene.:A Unique and Common Splice Junction Mutation Causing Exon Skipping in the Protective Protein/Carboxypeptidase Gene. Proceedings of the Japan Academy Series B. 66(10). 217–222. 6 indexed citations
20.
Takano, Takako & Masakazu Hatanaka. (1974). DNA-RNA Hybrid in Cells Infected by Murine Leukemia Virus. Cold Spring Harbor Symposia on Quantitative Biology. 39(0). 1009–1014. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Roland Günther Breakdown of academic impact, for papers by Maria Morini Breakdown of academic impact, for papers by Yasuko Ishikawa Breakdown of academic impact, for papers by Ming‐Qing Gao Breakdown of academic impact, for papers by U. Weyer Breakdown of academic impact, for papers by Matthew R. Evans Breakdown of academic impact, for papers by Evan B. Janovitz Breakdown of academic impact, for papers by Jacques Mathieu Breakdown of academic impact, for papers by Katsumi Hanada Breakdown of academic impact, for papers by Adelina Gama
Rankless by CCL
2026