Ken Saida

958 total citations
37 papers, 275 citations indexed

About

Ken Saida is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Ken Saida has authored 37 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Hematology. Recurrent topics in Ken Saida's work include Renal Diseases and Glomerulopathies (6 papers), Genetic Syndromes and Imprinting (5 papers) and Platelet Disorders and Treatments (4 papers). Ken Saida is often cited by papers focused on Renal Diseases and Glomerulopathies (6 papers), Genetic Syndromes and Imprinting (5 papers) and Platelet Disorders and Treatments (4 papers). Ken Saida collaborates with scholars based in Japan, United States and Brazil. Ken Saida's co-authors include Masao Ogura, Koichi Kamei, Mai Sato, Naomichi Matsumoto, Shuichi Ito, Masaki Takahashi, H. Machida, Takeshi Mizuguchi, Shuichi Ito and Atsushi Fujita and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Ken Saida

36 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ken Saida Japan 10 114 92 61 48 36 37 275
Tahir Naeem Khan Pakistan 11 118 1.0× 59 0.6× 69 1.1× 30 0.6× 47 1.3× 32 308
Margherita Baldassarri Italy 10 120 1.1× 91 1.0× 24 0.4× 15 0.3× 17 0.5× 21 281
Korbinian M. Riedhammer Germany 10 134 1.2× 47 0.5× 59 1.0× 31 0.6× 14 0.4× 26 231
Pallavi Khattar United States 8 78 0.7× 15 0.2× 33 0.5× 25 0.5× 27 0.8× 18 260
Pauline Krug France 8 53 0.5× 35 0.4× 21 0.3× 42 0.9× 23 0.6× 17 235
Francesca Giacopelli Italy 12 182 1.6× 133 1.4× 68 1.1× 18 0.4× 21 0.6× 21 415
Patricia L. Brazee United States 9 131 1.1× 35 0.4× 38 0.6× 58 1.2× 10 0.3× 13 320
Mohammed El‐Khateeb Jordan 9 249 2.2× 17 0.2× 67 1.1× 136 2.8× 27 0.8× 15 351
Ronak Lakhia United States 11 272 2.4× 197 2.1× 38 0.6× 27 0.6× 14 0.4× 15 448
Linus A. Völker Germany 10 126 1.1× 46 0.5× 125 2.0× 60 1.3× 41 1.1× 26 274

Countries citing papers authored by Ken Saida

Since Specialization
Citations

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

Fields of papers citing papers by Ken Saida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ken Saida

This figure shows the co-authorship network connecting the top 25 collaborators of Ken Saida. A scholar is included among the top collaborators of Ken Saida 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 Ken Saida. Ken Saida 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.
Oliveira, Zilda Najjar Prado de, Maria Cecília Rivitti Machado, Rachel Sayuri Honjo, et al.. (2024). Advantages of whole-exome sequencing over immunomapping in 67 Brazilian patients with epidermolysis bullosa. Anais Brasileiros de Dermatologia. 99(3). 350–356. 1 indexed citations
2.
Okazaki, Tetsuya, Tatsuya Kawaguchi, Kaori Adachi, et al.. (2022). Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion. Human Genome Variation. 9(1). 14–14. 3 indexed citations
3.
Hamanaka, Kohei, Keita Miyoshi, Jiahui Sun, et al.. (2022). Amelioration of a neurodevelopmental disorder by carbamazepine in a case having a gain-of-function GRIA3 variant. Human Genetics. 141(2). 283–293. 2 indexed citations
4.
Saida, Ken, Masayuki Sasaki, Eriko Koshimizu, et al.. (2021). Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clinical Genetics. 100(6). 722–730. 18 indexed citations
5.
Itai, Toshiyuki, Satoko Miyatake, Naomi Tsuchida, et al.. (2021). Novel CLTC variants cause new brain and kidney phenotypes. Journal of Human Genetics. 67(1). 1–7. 6 indexed citations
6.
Saida, Ken, Tokiko Fukuda, Daryl A. Scott, et al.. (2021). OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation. Frontiers in Cell and Developmental Biology. 9. 631428–631428. 6 indexed citations
7.
Hirano, Makito, Wataru Satake, Nobuko Moriyama, et al.. (2020). Bardet–Biedl syndrome and related disorders in Japan. Journal of Human Genetics. 65(10). 847–853. 10 indexed citations
8.
Okamoto, Tomoko, Ken Saida, Yuji Saitoh, et al.. (2020). Neuronal intranuclear inclusion disease presenting with an MELAS-like episode in chronic polyneuropathy. Neurology Genetics. 6(6). e531–e531. 25 indexed citations
9.
Ishimori, Shingo, Koichi Kamei, Takashi Ando, et al.. (2020). Influenza virus vaccination in children with nephrotic syndrome: insignificant risk of relapse. Clinical and Experimental Nephrology. 24(11). 1069–1076. 9 indexed citations
10.
Saida, Ken, Koichi Kamei, Naoya Morisada, et al.. (2019). A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease. CEN Case Reports. 9(1). 19–23. 7 indexed citations
11.
Saida, Ken, Chong Ae Kim, José Ricardo Magliocco Ceroni, et al.. (2019). Hemorrhagic stroke and renovascular hypertension with Grange syndrome arising from a novel pathogenic variant in YY1AP1. Journal of Human Genetics. 64(9). 885–890. 9 indexed citations
12.
Saida, Ken, Tsuyoshi Fukuda, Kana Mizuno, et al.. (2019). Pharmacokinetics and Pharmacodynamics Estimation of Eculizumab in a 2-Year-Old Girl With Atypical Hemolytic Uremic Syndrome: A Case Report With 4-Year Follow-Up. Frontiers in Pediatrics. 7. 519–519. 3 indexed citations
13.
Saida, Ken, Atsushi Fujita, Kohei Hamanaka, et al.. (2018). SOFT syndrome in a patient from Chile. American Journal of Medical Genetics Part A. 179(3). 338–340. 10 indexed citations
14.
Saida, Ken, Koichi Kamei, Masao Ogura, et al.. (2018). Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report. Transplantation Proceedings. 50(10). 3925–3927. 4 indexed citations
15.
Hirano, Makito, Wataru Satake, Kenji Ihara, et al.. (2015). The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan. PLoS ONE. 10(9). e0136317–e0136317. 17 indexed citations
16.
Ito, Naoko, Hiroshi Hataya, Ken Saida, et al.. (2015). Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan. Clinical and Experimental Nephrology. 20(2). 265–272. 20 indexed citations
17.
Saida, Ken, et al.. (2014). Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants. European Journal of Pediatrics. 174(4). 551–555. 10 indexed citations
18.
Saida, Ken, Tomohiko Nakamura, Takehiko Hiroma, Kiyohiro Takigiku, & Satoshi Yasukochi. (2013). Preoperative left ventricular internal dimension in end-diastole as earlier identification of early patent ductus arteriosus operation and postoperative intensive care in very low birth weight infants. Early Human Development. 89(10). 821–823. 5 indexed citations
19.
Saida, Ken, Yuji Kamijo, Yoshihiko Hidaka, et al.. (2013). A case of adult Dent disease in Japan with advanced chronic kidney disease. CEN Case Reports. 3(2). 132–138. 1 indexed citations
20.

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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