Takuya Hiraide

671 total citations
34 papers, 441 citations indexed

About

Takuya Hiraide is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Takuya Hiraide has authored 34 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Takuya Hiraide's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Takuya Hiraide is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Takuya Hiraide collaborates with scholars based in Japan and Malaysia. Takuya Hiraide's co-authors include Hirotomo Saitsu, Mitsuko Nakashima, Tsutomu Ogata, Naomichi Matsumoto, Tokiko Fukuda, Hitoshi Osaka, Masayuki Sasaki, Tadashi Kaname, Chihiro Ohba and Mitsuhiro Kato and has published in prestigious journals such as Human Genetics, Journal of Neurology and Frontiers in Neurology.

In The Last Decade

Takuya Hiraide

33 papers receiving 440 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takuya Hiraide Japan 12 271 185 82 56 26 34 441
Danielle Gleason United States 7 319 1.2× 156 0.8× 71 0.9× 79 1.4× 43 1.7× 7 487
Sébastien Moutton France 12 212 0.8× 211 1.1× 64 0.8× 45 0.8× 33 1.3× 17 367
Eleonora Di Gregorio Italy 17 389 1.4× 170 0.9× 134 1.6× 54 1.0× 28 1.1× 32 569
Tatjana Bierhals Germany 13 271 1.0× 201 1.1× 51 0.6× 42 0.8× 55 2.1× 26 446
Antonio Vitobello France 13 446 1.6× 212 1.1× 79 1.0× 48 0.9× 22 0.8× 36 595
Emily Tuttle United States 7 211 0.8× 113 0.6× 42 0.5× 62 1.1× 19 0.7× 10 314
Jane Juusola United States 13 218 0.8× 192 1.0× 34 0.4× 28 0.5× 33 1.3× 22 390
Shino Shimada Japan 15 315 1.2× 318 1.7× 68 0.8× 23 0.4× 62 2.4× 36 545
Kathryn Friend Australia 12 375 1.4× 320 1.7× 68 0.8× 30 0.5× 57 2.2× 16 521
Ivan Litvinenko Bulgaria 9 155 0.6× 68 0.4× 87 1.1× 67 1.2× 19 0.7× 21 282

Countries citing papers authored by Takuya Hiraide

Since Specialization
Citations

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

Fields of papers citing papers by Takuya Hiraide

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takuya Hiraide

This figure shows the co-authorship network connecting the top 25 collaborators of Takuya Hiraide. A scholar is included among the top collaborators of Takuya Hiraide 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 Takuya Hiraide. Takuya Hiraide 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.
Hikoya, Akiko, et al.. (2025). Vitamin A Deficiency in Children With Autism Spectrum Disorder. Cureus. 17(1). e77129–e77129. 1 indexed citations
2.
Hiraide, Takuya, Yusuke Ito, Hiroshi Uchida, et al.. (2024). Case Report: Novel compound heterozygous TPRKB variants cause Galloway-Mowat syndrome. Frontiers in Pediatrics. 12. 1360867–1360867. 1 indexed citations
3.
Hiraide, Takuya, Kazuki Watanabe, Kimiyoshi Sakaguchi, et al.. (2023). RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing. Journal of Human Genetics. 69(2). 91–99. 7 indexed citations
4.
Hiraide, Takuya, et al.. (2023). A deep intronic TCTN2 variant activating a cryptic exon predicted by SpliceRover in a patient with Joubert syndrome. Journal of Human Genetics. 68(7). 499–505. 6 indexed citations
5.
Hiraide, Takuya, Yohei Masunaga, Akira Honda, et al.. (2022). Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata. Journal of Human Genetics. 67(5). 303–306. 3 indexed citations
6.
Hiraide, Takuya, Yohei Masunaga, Hidetaka Yamada, et al.. (2021). Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole‐exome sequencing. Clinical Genetics. 100(1). 40–50. 27 indexed citations
7.
Matsushita, Hiroko, Takuya Hiraide, Katsumi Hayakawa, et al.. (2021). Compound heterozygous ADAMTS9 variants in Joubert syndrome-related disorders without renal manifestation. Brain and Development. 44(2). 161–165. 5 indexed citations
8.
Hiraide, Takuya, Taihei Tanaka, Yohei Masunaga, et al.. (2021). Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant. Journal of Human Genetics. 66(12). 1185–1187. 4 indexed citations
9.
Hiraide, Takuya, Shinobu Fukumura, Akiyo Yamamoto, Mitsuko Nakashima, & Hirotomo Saitsu. (2020). Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have incomplete penetrance. Brain and Development. 43(3). 470–474. 4 indexed citations
10.
Sasaki, Masayuki, Takuya Hiraide, Eri Takeshita, et al.. (2020). A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis. Brain and Development. 42(6). 462–467. 6 indexed citations
11.
Hiraide, Takuya, Mitsuko Nakashima, Takahiro Ikeda, et al.. (2020). Identification of a deep intronic POLR3A variant causing inclusion of a pseudoexon derived from an Alu element in Pol III-related leukodystrophy. Journal of Human Genetics. 65(10). 921–925. 17 indexed citations
12.
Hamano, Shin‐ichiro, Kenjiro Kikuchi, Reiko Koichihara, et al.. (2020). A recurrent TMEM106B mutation in hypomyelinating leukodystrophy: A rapid diagnostic assay. Brain and Development. 42(8). 603–606. 9 indexed citations
13.
Nakashima, Mitsuko, Takuya Hiraide, Kenji Kurosawa, et al.. (2019). A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination. Molecular Genetics & Genomic Medicine. 7(8). e814–e814. 16 indexed citations
14.
Hiraide, Takuya, et al.. (2019). Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases. Brain and Development. 41(5). 474–479. 6 indexed citations
15.
Nakashima, Mitsuko, Jun Tohyama, Eiji Nakagawa, et al.. (2019). Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures. Journal of Human Genetics. 64(4). 313–322. 51 indexed citations
16.
Okanishi, Tohru, Yoshifumi Arai, Mitsuyo Nishimura, et al.. (2019). Three Cases of Hemiconvulsion-Hemiplegia-Epilepsy Syndrome With Focal Cortical Dysplasia Type IIId. Frontiers in Neurology. 10. 1233–1233. 6 indexed citations
17.
Hiraide, Takuya, et al.. (2019). A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly. Journal of Human Genetics. 64(11). 1127–1132. 15 indexed citations
18.
19.
Sasaki, Masayuki, Chihiro Ohba, Mizue Iai, et al.. (2015). Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 gene. Journal of Neurology. 262(5). 1278–1284. 50 indexed citations
20.
Ohba, Chihiro, Kazuhiro Haginoya, Hitoshi Osaka, et al.. (2015). De novo KIF1A mutations cause intellectual deficit, cerebellar atrophy, lower limb spasticity and visual disturbance. Journal of Human Genetics. 60(12). 739–742. 39 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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