Daisuke Ieda

416 total citations
16 papers, 164 citations indexed

About

Daisuke Ieda is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daisuke Ieda has authored 16 papers receiving a total of 164 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daisuke Ieda's work include Genetic Syndromes and Imprinting (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and RNA regulation and disease (4 papers). Daisuke Ieda is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and RNA regulation and disease (4 papers). Daisuke Ieda collaborates with scholars based in Japan. Daisuke Ieda's co-authors include Shinji Saitoh, Ikumi Hori, Ayako Hattori, Yutaka Negishi, Kei Ohashi, Y. Nakamura, Hirotomo Saitsu, Mitsuko Nakashima, Takuya Hiraide and Kazuhiko Nakabayashi and has published in prestigious journals such as PLoS ONE, Journal of Medical Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Daisuke Ieda

15 papers receiving 164 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daisuke Ieda Japan	8	103	101	16	16	12	16	164
Alfonso Caro‐Llopis Spain	7	102 1.0×	132 1.3×	16 1.0×	23 1.4×	10 0.8×	14	190
Monika Weisz Hubshman Israel	6	79 0.8×	108 1.1×	11 0.7×	13 0.8×	7 0.6×	7	165
Benjamin Kamien Australia	9	124 1.2×	128 1.3×	42 2.6×	11 0.7×	9 0.8×	19	228
Jessica Sebastian United States	6	64 0.6×	92 0.9×	21 1.3×	6 0.4×	11 0.9×	11	146
Haley Streff United States	9	100 1.0×	93 0.9×	8 0.5×	10 0.6×	8 0.7×	24	188
Dominik S. Westphal Germany	7	82 0.8×	51 0.5×	19 1.2×	7 0.4×	9 0.8×	29	159
Yoko Hiraki Japan	10	97 0.9×	131 1.3×	22 1.4×	6 0.4×	6 0.5×	17	219
Dana Marafi United States	8	88 0.9×	70 0.7×	6 0.4×	13 0.8×	9 0.8×	24	171
Yannis Duffourd France	10	115 1.1×	132 1.3×	24 1.5×	5 0.3×	12 1.0×	25	221
Fabio Sirchia Italy	9	103 1.0×	108 1.1×	33 2.1×	4 0.3×	10 0.8×	35	208

Countries citing papers authored by Daisuke Ieda

Since Specialization

Citations

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

Fields of papers citing papers by Daisuke Ieda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daisuke Ieda

This figure shows the co-authorship network connecting the top 25 collaborators of Daisuke Ieda. A scholar is included among the top collaborators of Daisuke Ieda 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 Daisuke Ieda. Daisuke Ieda is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Hori, Ikumi, et al.. (2024). A nationwide survey of Vici syndrome in Japan. Brain and Development. 46(10). 309–312.

Fujimoto, Masanori, Y. Nakamura, Kana Hosoki, et al.. (2024). Genotype-phenotype correlation over time in Angelman syndrome: Researching 134 patients. Human Genetics and Genomics Advances. 5(4). 100342–100342. 3 indexed citations

Fujimoto, Masanori, Y. Nakamura, Daisuke Ieda, et al.. (2022). Angelman syndrome with mosaic paternal uniparental disomy suggestive of mitotic nondisjunction. Journal of Human Genetics. 68(2). 87–90. 1 indexed citations

Hori, Ikumi, Daisuke Ieda, Y. Nakamura, et al.. (2021). Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variant. Brain and Development. 43(4). 590–595. 1 indexed citations

Ieda, Daisuke, Fuyuki Miya, Masami Asai, et al.. (2021). Hemorrhagic shock and encephalopathy syndrome in a patient with a de novo heterozygous variant in KIF1A. Brain and Development. 44(3). 249–253. 2 indexed citations

Ieda, Daisuke, Yutaka Negishi, Tomomi Miyamoto, et al.. (2020). Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes. PLoS ONE. 15(8). e0237814–e0237814. 7 indexed citations

Negishi, Yutaka, Daisuke Ieda, Ikumi Hori, et al.. (2019). Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy. Orphanet Journal of Rare Diseases. 14(1). 277–277. 21 indexed citations

Nakamura, Y., Yusuke Okuno, Hideki Muramatsu, et al.. (2019). A novel CUL4B splice site variant in a young male exhibiting less pronounced features. Human Genome Variation. 6(1). 43–43. 4 indexed citations

Ieda, Daisuke, Ikumi Hori, Y. Nakamura, et al.. (2019). A novel splicing mutation in SLC9A6 in a boy with Christianson syndrome. Human Genome Variation. 6(1). 15–15. 7 indexed citations

10.

Hiraide, Takuya, Ayako Hattori, Daisuke Ieda, et al.. (2019). De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences. Epilepsia Open. 4(3). 476–481. 26 indexed citations

11.

Ieda, Daisuke, Ikumi Hori, Y. Nakamura, et al.. (2018). A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia. Brain and Development. 40(6). 489–492. 12 indexed citations

12.

Kato, Kohji, Seiji Mizuno, Shinobu Fukumura, et al.. (2018). Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhood. Brain and Development. 40(8). 678–684. 16 indexed citations

13.

Kato, Koji, Fuyuki Miya, Ikumi Hori, et al.. (2017). A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate. Journal of Human Genetics. 62(9). 861–863. 18 indexed citations

14.

Nakamura, Y., Yusuke Okuno, Hideki Muramatsu, et al.. (2017). Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum. Brain and Development. 40(2). 134–139. 20 indexed citations

15.

Nakamura, Y., Ayako Hattori, Mitsuko Nakashima, et al.. (2017). A de novo p.Arg756Cys mutation in ATP1A3 causes a distinct phenotype with prolonged weakness and encephalopathy triggered by fever. Brain and Development. 40(3). 222–225. 7 indexed citations

16.

Hori, Ikumi, Rie Kawamura, Kazuhiko Nakabayashi, et al.. (2017). CTCF deletion syndrome: clinical features and epigenetic delineation. Journal of Medical Genetics. 54(12). 836–842. 19 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.

Explore authors with similar magnitude of impact