K Imaizumi

1.2k total citations
27 papers, 885 citations indexed

About

K Imaizumi is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, K Imaizumi has authored 27 papers receiving a total of 885 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in K Imaizumi's work include Genomic variations and chromosomal abnormalities (4 papers), Viral gastroenteritis research and epidemiology (3 papers) and Connective tissue disorders research (3 papers). K Imaizumi is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Viral gastroenteritis research and epidemiology (3 papers) and Connective tissue disorders research (3 papers). K Imaizumi collaborates with scholars based in Japan, United Kingdom and United States. K Imaizumi's co-authors include Yoshikazu Kuroki, Mitsuo Masuno, Nathaniel H. Robin, Erich Roessler, Luisa Nanni, Diana W. Bianchi, Mary Ella Pierpont, Kenneth Lyons Jones, Miguel Del Campo and Kathryn A. Steinhaus and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

K Imaizumi

27 papers receiving 863 citations

Peers

K Imaizumi

MB

GENET

SURGE

DB

PPCH

Alicia Delicado Spain

Diana García‐Cruz Mexico

K. Fried Israel

Donna L. Daentl United States

B. Rafael Elejalde United States

Kosuke Izumi United States

A. David France

Saghira Malik Sharif United Kingdom

Lakshmi Mehta United States

M D Crawfurd United Kingdom

Alicia Delicado Spain

K Imaizumi

340 ×0.6

MB

459 ×1.1

GENET

129 ×0.9

SURGE

37 ×0.4

DB

201 ×2.3

PPCH

Citations per year, relative to K Imaizumi K Imaizumi (= 1×) peers Alicia Delicado

Countries citing papers authored by K Imaizumi

Since Specialization

Citations

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

Fields of papers citing papers by K Imaizumi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Imaizumi

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

1.

Ito, Taichi, et al.. (2024). AIbZIP/CREB3L4 Promotes Cell Proliferation via the SKP2-p27 Axis in Luminal Androgen Receptor Subtype Triple-Negative Breast Cancer. Molecular Cancer Research. 22(4). 373–385. 4 indexed citations

2.

Hino, Shin‐ichiro, Shinichi Kondo, Hiroshi Sekiya, et al.. (2007). Molecular mechanisms responsible for aberrant splicing of SERCA1 in myotonic dystrophy type 1. Human Molecular Genetics. 16(23). 2834–2843. 81 indexed citations

3.

Kimura, Junko, Kazuya Tachibana, K Imaizumi, Kenji Kurosawa, & Yoshikazu Kuroki. (2003). Longitudinal growth and height velocity of Japanese children with Down's syndrome. Acta Paediatrica. 92(9). 1039–1042. 10 indexed citations

4.

Kimura, Junko, Kazuya Tachibana, K Imaizumi, Kenji Kurosawa, & Yoshikazu Kuroki. (2003). Longitudinal growth and height velocity of Japanese children with Down's syndrome. Acta Paediatrica. 92(9). 1039–1042. 23 indexed citations

5.

Ohyama, Makiko, Michiko Yamanaka, K Imaizumi, et al.. (2000). Umbilical Cord Ulcer: a Serious in Utero Complication of Intestinal Atresia. Placenta. 21(4). 432–435. 22 indexed citations

6.

Nanni, Luisa, Jeffrey E. Ming, Maureen Bocian, et al.. (1999). The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly. Human Molecular Genetics. 8(13). 2479–2488. 274 indexed citations

7.

Adachi, Masanori, Katsuro Tachibana, Mitsuo Masuno, et al.. (1998). Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion. European Journal of Pediatrics. 157(1). 34–38. 45 indexed citations

8.

Nishimura, Gen, Takeshi Okada, Katsuro Tachibana, et al.. (1997). Osteopathia striata, short stature, and characteristic facies: a previously unknown skeletal dysplasia. European Journal of Pediatrics. 156(8). 631–635. 4 indexed citations

9.

Masuno, Mitsuo, K Imaizumi, Yoshihisa Fukushima, et al.. (1997). Median cleft of upper lip and pedunculated skin masses associated with de novo reciprocal translocation 46,X,t(X;16)(q28;q11.2).. Journal of Medical Genetics. 34(11). 952–954. 21 indexed citations

10.

Fukuda, Seiji, Nobuyuki Shimozawa, Yasuyuki Suzuki, et al.. (1996). Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.. PubMed. 59(6). 1210–20. 82 indexed citations

11.

Masuno, Mitsuo, et al.. (1995). Osteodysplastic primordial dwarfism. Clinical Dysmorphology. 4(1). 57???62–57???62. 4 indexed citations

12.

Tanaka, Yukichi, Yuka Sasaki, Kazuya Tachibana, et al.. (1994). Gonadal mixed germ cell tumor combined with a large hemangiomatous lesion in a patient with Turner's syndrome and 45,X/46,X, +mar karyotype.. PubMed. 118(11). 1135–8. 11 indexed citations

13.

Kuromaru, Ryuichi, K Imaizumi, Yasukazu Nakamura, et al.. (1992). Monozygotic Twins with Discordant Sex. Acta geneticae medicae et gemellologiae twin research. 41(4). 301–310. 20 indexed citations

14.

Imaizumi, K, Tadashi Kajii, & Norio Niikawa. (1981). 13S+. Giant satellites or de novo rearrangement?. Human Genetics. 59(3). 266–8. 1 indexed citations

15.

Fujiwara, Tooru, et al.. (1973). Sexual maturation of laboratory-bred male cynomolgus monkeys (Macaca fascicularis).. PubMed. 22 Suppl(0). 403–9. 7 indexed citations

16.

KATSUBE, Yasuji, Toshikatsu Hagiwara, Hiroshi Miyakawa, T Muto, & K Imaizumi. (1969). Studies on toxoplasmosis. 2. Distribution of Toxoplasma in the organs of cat and dog cases of latent infection occurring naturally.. PubMed. 22(5). 319–26. 2 indexed citations

17.

Goto, Shin G., et al.. (1969). Aging and Location of Acid Ribonuclease in Liver of Various Animals. Journal of Gerontology. 24(3). 305–308. 14 indexed citations

18.

TAKASAKA, MASAO, et al.. (1969). Shigellosis in cynomolgus monkeys (Macaca irus). VII. Experimental production of dysentery with a relatively small dose of Shigella flexneri 2a in ascorbic acid deficient monkeys.. PubMed. 22(3). 149–62. 8 indexed citations

19.

TAKASAKA, MASAO, et al.. (1968). Shigellosis in cynomolgus monkeys (Macaca irua). VI. The inoculation with various doses of Shigella flexneri 2a into cecal lumen.. PubMed. 21(4). 275–81. 8 indexed citations

20.

TAKASAKA, MASAO, et al.. (1967). Shigellosis in cynomolgus monkeys (Macaca irus). V. Resistance acquired by the repetition of experimental oral infection with Shigella flexneri 2A and fluctuation of serum agglutinin titer.. PubMed. 20(4). 341–8. 7 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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