Yo-ichi Nabeshima

11.1k total citations · 1 hit paper
47 papers, 8.6k citations indexed

About

Yo-ichi Nabeshima is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Yo-ichi Nabeshima has authored 47 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Cell Biology and 7 papers in Genetics. Recurrent topics in Yo-ichi Nabeshima's work include Parathyroid Disorders and Treatments (5 papers), Pluripotent Stem Cells Research (5 papers) and Genetic Syndromes and Imprinting (4 papers). Yo-ichi Nabeshima is often cited by papers focused on Parathyroid Disorders and Treatments (5 papers), Pluripotent Stem Cells Research (5 papers) and Genetic Syndromes and Imprinting (4 papers). Yo-ichi Nabeshima collaborates with scholars based in Japan, United States and South Korea. Yo-ichi Nabeshima's co-authors include Makoto Kuro‐o, Ryozo Nagai, Akihiro Iida, Yutaka Matsumura, Hiroki Aizawa, Takako Shiraki-Iida, Yoshio Ohyama, Masahiko Kurabayashi, Tatsuo Suga and Tadashi Kaname and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Yo-ichi Nabeshima

47 papers receiving 8.5k 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.

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

1997 3.0k citations Makoto Kuro‐o, Yutaka Matsumura et al. Nature profile →

Peers

Yo-ichi Nabeshima

NEPHR

GENET

SURGE

Yo‐ichi Nabeshima Japan

Marcy C. Speer United States

Brian Harding United Kingdom

Chyuan‐Sheng Lin United States

Nicholas J. Laping United States

Settara C. Chandrasekharappa United States

Nine V.A.M. Knoers Netherlands

Detlef Böckenhauer United Kingdom

Hugo H. Marti Germany

Stephen J. Marx United States

Yo‐ichi Nabeshima Japan

Yo-ichi Nabeshima

4.8k ×1.2

3.1k ×1.1

NEPHR

3.1k ×1.4

GENET

782 ×0.8

SURGE

944 ×1.0

Citations per year, relative to Yo-ichi Nabeshima Yo-ichi Nabeshima (= 1×) peers Yo‐ichi Nabeshima

Countries citing papers authored by Yo-ichi Nabeshima

Since Specialization

Citations

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

Fields of papers citing papers by Yo-ichi Nabeshima

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yo-ichi Nabeshima. 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 Yo-ichi Nabeshima. The network helps show where Yo-ichi Nabeshima may publish in the future.

Co-authorship network of co-authors of Yo-ichi Nabeshima

This figure shows the co-authorship network connecting the top 25 collaborators of Yo-ichi Nabeshima. A scholar is included among the top collaborators of Yo-ichi Nabeshima 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 Yo-ichi Nabeshima. Yo-ichi Nabeshima 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

Hattori, Kouya, et al.. (2024). Nicotinamide phosphoribosyl transferase in mammary gland epithelial cells is required for nicotinamide mononucleotide production in mouse milk. Biochemical and Biophysical Research Communications. 728. 150346–150346. 1 indexed citations

Shikanai, Mima, et al.. (2018). Caveolin-1 Promotes Early Neuronal Maturation via Caveolae-Independent Trafficking of N-Cadherin and L1. iScience. 7. 53–67. 32 indexed citations

Fujiyama, Tomoyuki, Satoshi Miyashita, Yousuke Tsuneoka, et al.. (2018). Forebrain Ptf1a Is Required for Sexual Differentiation of the Brain. Cell Reports. 24(1). 79–94. 20 indexed citations

Shin, Eun‐Joo, Yoon Hee Chung, Ji Hoon Jeong, et al.. (2015). Melatonin Attenuates Memory Impairment Induced by Klotho Gene Deficiency Via Interactive Signaling Between MT2 Receptor, ERK, and Nrf2-Related Antioxidant Potential. The International Journal of Neuropsychopharmacology. 18(6). 65 indexed citations

Shin, Eun‐Joo, Sun Seek Min, Yoon Hee Chung, et al.. (2013). Inactivation of JAK2/STAT3 Signaling Axis and Downregulation of M1 mAChR Cause Cognitive Impairment in klotho Mutant Mice, a Genetic Model of Aging. Neuropsychopharmacology. 38(8). 1426–1437. 59 indexed citations

Yoshida, Shosei, Mamiko Sukeno, Toshinori Nakagawa, et al.. (2006). The first round of mouse spermatogenesis is a distinctive program that lacks the self-renewing spermatogonia stage. Development. 133(8). 1495–1505. 289 indexed citations

Nishimura, Takashi, Tomoya Yamaguchi, Katsuhiro Kato, et al.. (2005). PAR-6–PAR-3 mediates Cdc42-induced Rac activation through the Rac GEFs STEF/Tiam1. Nature Cell Biology. 7(3). 270–277. 308 indexed citations

Komatsu, Kouji, Tomohiro Kurisaki, Aki Masuda, et al.. (2003). Essential roles of Meltrin β (ADAM19) in heart development. Developmental Biology. 267(1). 14–28. 76 indexed citations

Matsuo, Naoki, Mami Terao, Yo-ichi Nabeshima, & Mikio Hoshino. (2003). Roles of STEF/Tiam1, guanine nucleotide exchange factors for Rac1, in regulation of growth cone morphology. Molecular and Cellular Neuroscience. 24(1). 69–81. 44 indexed citations

10.

Yahata, Kensei, Kiyoshi Mori, Masashi Mukoyama, et al.. (2003). Regulation of stanniocalcin 1 and 2 expression in the kidney by klotho gene. Biochemical and Biophysical Research Communications. 310(1). 128–134. 27 indexed citations

11.

Nakagoshi, Hideki, et al.. (2002). Refinement of wingless Expression by a Wingless- and Notch-Responsive Homeodomain Protein, Defective Proventriculus. Developmental Biology. 249(1). 44–56. 23 indexed citations

12.

Mizuguchi, Rumiko, Michiya Sugimori, Hirohide Takebayashi, et al.. (2001). Combinatorial Roles of Olig2 and Neurogenin2 in the Coordinated Induction of Pan-Neuronal and Subtype-Specific Properties of Motoneurons. Neuron. 31(5). 757–771. 345 indexed citations

13.

Wakimoto, Koji, Makoto Kuro‐o, Noriyuki Yanaka, et al.. (2001). Expression of Na+/Ca2+ exchanger (NCX1) gene in the developmental mouse embryo and adult mouse brain. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 130(2). 191–198. 12 indexed citations

14.

Mori, Kiyoshi, Kensei Yahata, Masashi Mukoyama, et al.. (2000). Disruption of klotho Gene Causes an Abnormal Energy Homeostasis in Mice. Biochemical and Biophysical Research Communications. 278(3). 665–670. 53 indexed citations

15.

Wakimoto, Koji, Makoto Kuro‐o, Noriyuki Yanaka, et al.. (2000). Isolation and Characterization of Na⁺/Ca²⁺Exchanger Gene and Splicing Isoforrns in Mice. DNA sequence. 11(1-2). 75–81. 2 indexed citations

16.

Yahata, Kensei, Kiyoshi Mori, Hiroshi Arai, et al.. (2000). Molecular cloning and expression of a novel klotho-related protein. Journal of Molecular Medicine. 78(7). 389–394. 47 indexed citations

17.

Kurisaki, Tomohiro, Aki Masuda, Noriko Osumi, Yo-ichi Nabeshima, & Atsuko Fujisawa‐Sehara. (1998). Spatially- and temporally-restricted expression of meltrin α (ADAM12) and β (ADAM19) in mouse embryo. Mechanisms of Development. 73(2). 211–215. 87 indexed citations

18.

Nakagoshi, Hideki, Minako Hoshi, Yo-ichi Nabeshima, & Fumio Matsuzaki. (1998). A novel homeobox gene mediates the Dpp signal to establish functional specificity within target cells. Genes & Development. 12(17). 2724–2734. 54 indexed citations

19.

Ohyama, Yoshio, Masahiko Kurabayashi, Hiroaki Masuda, et al.. (1998). Molecular Cloning of RatklothocDNA: Markedly Decreased Expression ofklothoby Acute Inflammatory Stress. Biochemical and Biophysical Research Communications. 251(3). 920–925. 132 indexed citations

20.

Nakagoshi, Hideki, et al.. (1995). Asymmetric segregation of the homeodomain protein Prospero duringDrosophila development. Nature. 377(6550). 627–630. 281 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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