Hidehito Inagaki

3.3k total citations
98 papers, 2.1k citations indexed

About

Hidehito Inagaki is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Hidehito Inagaki has authored 98 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 43 papers in Genetics and 23 papers in Plant Science. Recurrent topics in Hidehito Inagaki's work include Genomic variations and chromosomal abnormalities (27 papers), Chromosomal and Genetic Variations (21 papers) and Prenatal Screening and Diagnostics (20 papers). Hidehito Inagaki is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Chromosomal and Genetic Variations (21 papers) and Prenatal Screening and Diagnostics (20 papers). Hidehito Inagaki collaborates with scholars based in Japan, United States and Poland. Hidehito Inagaki's co-authors include Hiroki Kurahashi, Tamae Ohye, Hiroshi Kogo, Takema Kato, Beverly S. Emanuel, Makiko Tsutsumi, Kazuhiro Furukawa, Yasuo Hotta, Hiroshi Ichinose and Akihiko Koga and has published in prestigious journals such as Science, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Hidehito Inagaki

97 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hidehito Inagaki Japan	25	1.4k	713	392	289	202	98	2.1k
Takuro Horii Japan	26	2.3k 1.6×	628 0.9×	135 0.3×	117 0.4×	185 0.9×	68	2.6k
K. John McLaughlin United States	29	2.8k 2.0×	937 1.3×	281 0.7×	200 0.7×	804 4.0×	58	3.6k
Ramaiah Nagaraja United States	20	1.1k 0.8×	609 0.9×	211 0.5×	83 0.3×	134 0.7×	44	1.5k
Ordan J. Lehmann Canada	29	1.5k 1.0×	685 1.0×	71 0.2×	134 0.5×	225 1.1×	56	2.6k
Petko M. Petkov United States	28	1.8k 1.3×	934 1.3×	550 1.4×	72 0.2×	84 0.4×	50	2.8k
Yoshihiro Jinno Japan	26	1.6k 1.1×	921 1.3×	296 0.8×	422 1.5×	58 0.3×	76	2.4k
Félix Recillas‐Targa Mexico	31	3.1k 2.2×	898 1.3×	387 1.0×	106 0.4×	65 0.3×	106	3.7k
Sandrine Caburet France	23	1.3k 0.9×	686 1.0×	229 0.6×	98 0.3×	462 2.3×	39	1.9k
Susan A. Ledbetter United States	18	1.4k 1.0×	1.1k 1.6×	464 1.2×	201 0.7×	18 0.1×	28	2.0k
Judith Singer–Sam United States	24	1.5k 1.1×	918 1.3×	126 0.3×	152 0.5×	84 0.4×	38	1.9k

Countries citing papers authored by Hidehito Inagaki

Since Specialization

Citations

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

Fields of papers citing papers by Hidehito Inagaki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hidehito Inagaki

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

Inagaki, Hidehito, Hiroshi Hirata, Masaki Ito, et al.. (2025). Fine-tuning of heading time by earliness per se effect due to multi-allelic variants in VRN-B3 locus of hexaploid wheat. Planta. 261(5). 97–97.

Inagaki, Hidehito, Tatsuya Nakano, Yoshiharu Nakaoka, et al.. (2024). Comparative Analysis of Two NGS-Based Platforms for Product-of-Conception Karyotyping. Genes. 15(8). 1100–1100. 1 indexed citations

Seki, Atsuhito, Takashi Kuroiwa, Atsushi Maeda, et al.. (2023). A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome. JSES International. 7(4). 714–718. 1 indexed citations

Mariya, Tasuku, Takema Kato, Hidehito Inagaki, et al.. (2022). Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes. Journal of Human Genetics. 67(6). 363–368. 9 indexed citations

Nishizawa, Haruki, Hidehito Inagaki, Keisuke Hitachi, et al.. (2022). Characterization of the MG828507 lncRNA Located Upstream of the FLT1 Gene as an Etiology for Pre-Eclampsia. Journal of Clinical Medicine. 11(15). 4603–4603. 1 indexed citations

Inagaki, Hidehito, et al.. (2022). Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant. Human Molecular Genetics. 32(8). 1301–1312. 8 indexed citations

Kawamura, Rie, Takema Kato, Fumihiko Suzuki, et al.. (2020). A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia. Journal of Human Genetics. 65(8). 705–709. 13 indexed citations

Tsukamoto, Kentaro, Naoaki Shinzawa, Akito Kawai, et al.. (2020). The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis. Nature Communications. 11(1). 3571–3571. 23 indexed citations

Suzuki, Fumihiko, Takema Kato, Rie Kawamura, et al.. (2019). Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome. Case Reports in Obstetrics and Gynecology. 2019. 1–5. 2 indexed citations

10.

Katagiri, Satoshi, Takaaki Hayashi, Katsuhiro Hosono, et al.. (2018). Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy. Scientific Reports. 8(1). 11507–11507. 8 indexed citations

11.

Ibara, Satoshi, et al.. (2018). Lethal persistent pulmonary hypertension of the newborn in Bohring–Opitz syndrome. American Journal of Medical Genetics Part A. 176(5). 1245–1248. 5 indexed citations

12.

Ishihara, Naoko, et al.. (2018). A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant. Brain and Development. 41(3). 285–291. 10 indexed citations

13.

Inagaki, Hidehito, Takema Kato, Makiko Tsutsumi, et al.. (2016). Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements. Frontiers in Genetics. 7. 125–125. 19 indexed citations

14.

Nishizawa, Haruki, et al.. (2016). Mutation analysis of the JUNO gene in female infertility of unknown etiology. SHILAP Revista de lepidopterología. 3 indexed citations

15.

Ohye, Tamae, Hidehito Inagaki, Masaru Ihira, et al.. (2014). Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6. Scientific Reports. 4(1). 4559–4559. 22 indexed citations

16.

Inagaki, Hidehito, Qinyu Hao, Masaru Sakamoto, et al.. (2013). Identification of an enhancer region for immune activation in the human GTP cyclohydrolase I gene. Biochemical and Biophysical Research Communications. 442(1-2). 72–78. 2 indexed citations

17.

Kurahashi, Hiroki, et al.. (2011). Molecular basis of maternal age‐related increase in oocyte aneuploidy. Congenital Anomalies. 52(1). 8–15. 30 indexed citations

18.

Ohye, Tamae, Hidehito Inagaki, Hiroshi Kogo, et al.. (2010). Paternal origin of the de novo constitutional t(11;22)(q23;q11). European Journal of Human Genetics. 18(7). 783–787. 38 indexed citations

19.

Kurahashi, Hiroki, Hidehito Inagaki, Tamae Ohye, et al.. (2006). Chromosomal Translocations Mediated by Palindromic DNA. Cell Cycle. 5(12). 1297–1303. 29 indexed citations

20.

Ashley, Terry, Hidehito Inagaki, Allen D. Seftel, et al.. (2006). Meiotic Recombination and Spatial Proximity in the Etiology of the Recurrent t(11;22). The American Journal of Human Genetics. 79(3). 524–538. 41 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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