Keiji Inohaya

1.6k total citations
35 papers, 1.2k citations indexed

About

Keiji Inohaya is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Keiji Inohaya has authored 35 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 9 papers in Cell Biology and 7 papers in Genetics. Recurrent topics in Keiji Inohaya's work include Developmental Biology and Gene Regulation (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Zebrafish Biomedical Research Applications (7 papers). Keiji Inohaya is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Zebrafish Biomedical Research Applications (7 papers). Keiji Inohaya collaborates with scholars based in Japan, United States and Germany. Keiji Inohaya's co-authors include Akira Kudō, Yoshiro Takano, Shigeki Yasumasu, Ichiro Iuchi, Kenjiro Yamagami, Kazuo Araki, Masato Kinoshita, Norio Yoshizaki, Mari Kawaguchi and Kaori Sano and has published in prestigious journals such as Nature Communications, Development and The Journal of Comparative Neurology.

In The Last Decade

Keiji Inohaya

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keiji Inohaya Japan 20 703 265 248 144 134 35 1.2k
Tatsuo S. Hamazaki Japan 24 581 0.8× 295 1.1× 188 0.8× 427 3.0× 87 0.6× 36 1.5k
Manuel Marí‐Beffa Spain 21 666 0.9× 202 0.8× 334 1.3× 69 0.5× 75 0.6× 41 1.2k
Janine A. Danks Australia 28 1.2k 1.6× 253 1.0× 109 0.4× 88 0.6× 138 1.0× 75 2.3k
Naoyuki Wada Japan 21 1.0k 1.4× 308 1.2× 285 1.1× 40 0.3× 80 0.6× 47 1.5k
Danica Živković Netherlands 19 1.3k 1.8× 472 1.8× 336 1.4× 165 1.1× 27 0.2× 36 1.8k
Neil I. Bower Australia 29 1.2k 1.7× 449 1.7× 434 1.8× 69 0.5× 77 0.6× 46 2.4k
Marie‐Andrée Akimenko Canada 22 1.9k 2.7× 476 1.8× 708 2.9× 124 0.9× 189 1.4× 38 2.5k
Tomasz Furmanek Norway 22 651 0.9× 473 1.8× 140 0.6× 217 1.5× 263 2.0× 55 1.5k
Violette Thermes France 12 515 0.7× 214 0.8× 185 0.7× 47 0.3× 48 0.4× 21 873
Pamela C. Yelick United States 26 1.5k 2.1× 585 2.2× 409 1.6× 29 0.2× 165 1.2× 54 2.3k

Countries citing papers authored by Keiji Inohaya

Since Specialization
Citations

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

Fields of papers citing papers by Keiji Inohaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keiji Inohaya

This figure shows the co-authorship network connecting the top 25 collaborators of Keiji Inohaya. A scholar is included among the top collaborators of Keiji Inohaya 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 Keiji Inohaya. Keiji Inohaya 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.
Inohaya, Keiji, et al.. (2017). The sp7 gene is required for maturation of osteoblast-lineage cells in medaka (Oryzias latipes) vertebral column development. Developmental Biology. 431(2). 252–262. 15 indexed citations
2.
Ishikawa, Yuji, Keiji Inohaya, Naoyuki Yamamoto, et al.. (2015). The Parapineal Is Incorporated into the Habenula during Ontogenesis in the Medaka Fish. Brain Behavior and Evolution. 85(4). 257–270. 9 indexed citations
3.
Chatani, Masahiro, et al.. (2015). Osteoblast and osteoclast behaviors in the turnover of attachment bones during medaka tooth replacement. Developmental Biology. 409(2). 370–381. 15 indexed citations
4.
Shimada, Atsuko, Toru Kawanishi, Takuya Kaneko, et al.. (2013). Trunk exoskeleton in teleosts is mesodermal in origin. Nature Communications. 4(1). 1639–1639. 81 indexed citations
5.
Inohaya, Keiji, et al.. (2010). sec24d encoding a component of COPII is essential for vertebra formation, revealed by the analysis of the medaka mutant, vbi. Developmental Biology. 342(1). 85–95. 44 indexed citations
6.
Inohaya, Keiji, et al.. (2010). Bef medaka mutant reveals the essential role of c-myb in both primitive and definitive hematopoiesis. Developmental Biology. 345(2). 133–143. 17 indexed citations
7.
Takashima, Shigeo, Takahiro Kage, Takako Yasuda, et al.. (2008). Phenotypic analyses of a medaka mutant reveal the importance of bilaterally synchronized expression of isthmic fgf8 for bilaterally symmetric formation of the optic tectum. genesis. 46(10). 537–545. 1 indexed citations
8.
Sano, Kaori, Keiji Inohaya, Mari Kawaguchi, et al.. (2008). Purification and characterization of zebrafish hatching enzyme – an evolutionary aspect of the mechanism of egg envelope digestion. FEBS Journal. 275(23). 5934–5946. 101 indexed citations
9.
Chandra, Abhishek, Zhi Yang, Xuchao Xue, et al.. (2007). The Medaka FoxP2, a Homologue of Human Language Gene FOXP2, has a Diverged Structure and Function. The Journal of Biochemistry. 143(3). 407–416. 11 indexed citations
10.
Inohaya, Keiji, Yoshiro Takano, & Akira Kudō. (2007). The teleost intervertebral region acts as a growth center of the centrum: In vivo visualization of osteoblasts and their progenitors in transgenic fish. Developmental Dynamics. 236(11). 3031–3046. 97 indexed citations
11.
Nakatani, Yuki, Naofumi Takamatsu, Hiroshi Hori, et al.. (2006). Medaka unextended-fin mutants suggest a role for Hoxb8a in cell migration and osteoblast differentiation during appendage formation. Developmental Biology. 293(2). 426–438. 13 indexed citations
12.
Nakatani, Yuki, et al.. (2004). Large-scale analysis of the genes involved in fin regeneration and blastema formation in the medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 861–872. 58 indexed citations
13.
Kudo, Hisaaki, Norio Amizuka, Kazuo Araki, Keiji Inohaya, & Akira Kudō. (2004). Zebrafish periostin is required for the adhesion of muscle fiber bundles to the myoseptum and for the differentiation of muscle fibers. Developmental Biology. 267(2). 473–487. 54 indexed citations
14.
Kudo, Hisaaki, Keiji Inohaya, Hayato Yokoi, et al.. (2004). A mutation in the gene for δ-aminolevulinic acid dehydratase (ALAD) causes hypochromic anemia in the medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 747–752. 18 indexed citations
15.
Inohaya, Keiji, et al.. (2004). Twist functions in vertebral column formation in medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 883–894. 46 indexed citations
16.
Inohaya, Keiji & Akira Kudō. (2000). Temporal and spatial patterns of cbfal expression during embryonic development in the teleost, Oryzias latipes. Development Genes and Evolution. 210(11). 570–574. 28 indexed citations
17.
Inohaya, Keiji, Shigeki Yasumasu, Ikuo Yasumasu, Ichiro Iuchi, & Kenjiro Yamagami. (1999). Analysis of the origin and development of hatching gland cells by transplantation of the embryonic shield in the fish, Oryzias latipes. Development Growth & Differentiation. 41(5). 557–566. 36 indexed citations
18.
Inohaya, Keiji, Shigeki Yasumasu, Kazuo Araki, et al.. (1997). Species‐dependent migration of fish hatching gland cells that commonly express astacin‐like proteases in common. Development Growth & Differentiation. 39(2). 191–197. 73 indexed citations
19.
Yasumasu, Shigeki, Hiraku Shimada, Keiji Inohaya, et al.. (1996). Different Exon–Intron Organizations of the Genes for Two Astacin‐Like Proteases, High Choriolytic Enzyme (Choriolysin H) and Low Choriolytic Enzyme (Choriolysin L), the Constituents of the Fish Hatching Enzyme. European Journal of Biochemistry. 237(3). 752–758. 19 indexed citations
20.
Inohaya, Keiji, et al.. (1995). Temporal and Spatial Patterns of Gene Expression for the Hatching Enzyme in the Teleost Embryo, Oryzias latipes. Developmental Biology. 171(2). 374–385. 77 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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