Atsushi Ieshima

1.2k total citations
29 papers, 393 citations indexed

About

Atsushi Ieshima is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Atsushi Ieshima has authored 29 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Atsushi Ieshima's work include Fetal and Pediatric Neurological Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (4 papers). Atsushi Ieshima is often cited by papers focused on Fetal and Pediatric Neurological Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (4 papers). Atsushi Ieshima collaborates with scholars based in Japan, Italy and Canada. Atsushi Ieshima's co-authors include Sachio Takashima, Laurence E. Becker, Haruomi Nakamura, Kenzo Takeshita, Yoshikazu Kuroki, Yoshifumi Yamamoto, Ichiro Matsui, Kyosuke Takeshita, Kazuhiro Hashimoto and Hideo Shigematsu and has published in prestigious journals such as Human Genetics, American Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Atsushi Ieshima

28 papers receiving 388 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Atsushi Ieshima Japan 11 205 153 77 66 49 29 393
Aideen O’Doherty Ireland 7 215 1.0× 249 1.6× 172 2.2× 35 0.5× 35 0.7× 9 477
Tamar Schwartz Israel 11 136 0.7× 273 1.8× 118 1.5× 103 1.6× 25 0.5× 18 481
B Delobel France 11 313 1.5× 170 1.1× 61 0.8× 117 1.8× 19 0.4× 18 451
Julie Lauzon Canada 10 228 1.1× 196 1.3× 55 0.7× 126 1.9× 12 0.2× 23 430
Leslie A. Phillips United States 10 313 1.5× 463 3.0× 57 0.7× 40 0.6× 28 0.6× 11 752
Yann Grattau France 5 100 0.5× 112 0.7× 139 1.8× 51 0.8× 51 1.0× 5 323
LaDonna Immken United States 13 339 1.7× 372 2.4× 25 0.3× 112 1.7× 15 0.3× 21 689
Filomena Tiziana Papa Italy 14 257 1.3× 182 1.2× 33 0.4× 41 0.6× 16 0.3× 26 412
Luciano Calzari Italy 14 230 1.1× 338 2.2× 78 1.0× 166 2.5× 36 0.7× 38 519
M. G. Daker United Kingdom 13 333 1.6× 225 1.5× 37 0.5× 82 1.2× 13 0.3× 28 538

Countries citing papers authored by Atsushi Ieshima

Since Specialization
Citations

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

Fields of papers citing papers by Atsushi Ieshima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Atsushi Ieshima

This figure shows the co-authorship network connecting the top 25 collaborators of Atsushi Ieshima. A scholar is included among the top collaborators of Atsushi Ieshima 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 Atsushi Ieshima. Atsushi Ieshima 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.
Sugiura, Hiroshi, et al.. (2012). Magnetic resonance imaging in neonates with total asphyxia. Brain and Development. 35(1). 53–60. 4 indexed citations
2.
Ieshima, Atsushi, et al.. (2007). Martsolf syndrome in Japanese siblings. American Journal of Medical Genetics Part A. 143A(9). 973–978. 7 indexed citations
3.
Ohto, Tatsuyuki, Nobuaki Iwasaki, Norio Ohkoshi, et al.. (2005). A pediatric case of critical illness polyneuropathy: clinical and pathological findings. Brain and Development. 27(7). 535–538. 4 indexed citations
4.
Ieshima, Atsushi, et al.. (2003). [Epilepsy in patients with cerebral palsy--analysis of frequency and clinical prognosis].. PubMed. 35(6). 478–83. 3 indexed citations
5.
Ieshima, Atsushi. (2001). [Hair-nail ectodermal dysplasia].. PubMed. 777–8. 4 indexed citations
6.
Akaboshi, Shinjiro, Masaki Yoshimura, Toshiro Hara, et al.. (2000). A Case of Høyeraal-Hreidarsson Syndrome: Delayed Myelination and Hypoplasia of Corpus Callosum are Other Important Signs. Neuropediatrics. 31(3). 141–144. 15 indexed citations
7.
Itoh, Masayuki, et al.. (1995). Neuroleptic malignant syndrome in striatonigral degeneration. Pediatric Neurology. 13(3). 255–256. 1 indexed citations
8.
Hashimoto, Kazuhiro, et al.. (1994). Juvenile variant of Schimke immunoosseous dysplasia. American Journal of Medical Genetics. 49(3). 266–269. 25 indexed citations
9.
Takashima, Sachio, Atsushi Ieshima, Haruomi Nakamura, & Laurence E. Becker. (1989). Dendrites, dementia and the down syndrome. Brain and Development. 11(2). 131–133. 107 indexed citations
10.
Inagaki, Masatoshi, Yukio Ando, Takashi Mito, et al.. (1987). Comparison of brain imaging and neuropathology in cases of trisomy 18 and 13. Neuroradiology. 29(5). 474–479. 15 indexed citations
11.
Ieshima, Atsushi, Tatsuya Koeda, & Masumi Inagaki. (1986). Peculiar face, deafness, cleft palate, male pseudohermaphroditism, and growth and psychomotor retardation; a new autosomal recessive syndrome?. Clinical Genetics. 30(2). 136–141. 6 indexed citations
12.
Ieshima, Atsushi, et al.. (1985). Distal 15q trisomy with Dandy-Walker malformation in a female infant. The Japanese Journal of Human Genetics. 30(3). 227–232. 6 indexed citations
13.
Shigematsu, Hideo, et al.. (1985). Neuropathological and Golgi study on a case of thanatophotoric dysplasia. Brain and Development. 7(6). 628–632. 16 indexed citations
14.
Nishimura, Masaharu, et al.. (1985). [A case of Down syndrome with moyamoya disease].. PubMed. 17(1). 71–5. 4 indexed citations
15.
Ieshima, Atsushi, et al.. (1985). Clinicopathological study in a female infant with 46,XX,i(18q) showing mixed features of both trisomy 18 and monosomy 18p. The Japanese Journal of Human Genetics. 30(3). 219–226. 9 indexed citations
16.
Ieshima, Atsushi, Kousaku Ohno, & Kenzo Takeshita. (1984). Sister Chromatid Exchanges, Chromosome Aberration and Lymphocyte Proliferative Kinetics in Non‐treated and MNNG‐treated Lymphocytes from Patients with Tuberous Sclerosis. Congenital Anomalies. 24(4). 293–298. 1 indexed citations
17.
Ieshima, Atsushi, et al.. (1984). A female infant with pure duplication 12q24.2→qter. The Japanese Journal of Human Genetics. 29(3). 391–397. 9 indexed citations
18.
Ieshima, Atsushi, et al.. (1984). A morphometric CT study of Down's syndrome showing small posterior fossa and calcification of basal ganglia. Neuroradiology. 26(6). 493–498. 49 indexed citations
19.
Kuroki, Yoshikazu, Ichiro Matsui, Yoshifumi Yamamoto, & Atsushi Ieshima. (1980). The ?happy puppet? syndrome in two siblings. Human Genetics. 56(2). 227–229. 29 indexed citations
20.
Ieshima, Atsushi, Nobuaki Ogasawara, Yoshifumi Yamamoto, & Yoshikazu Kuroki. (1980). A case of r(21) with stigmata of atypical Down syndrome. Human Genetics. 55(1). 65–69. 16 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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