Mitsuko Nakashima

11.1k total citations
191 papers, 4.4k citations indexed

About

Mitsuko Nakashima is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Mitsuko Nakashima has authored 191 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 113 papers in Molecular Biology, 88 papers in Genetics and 19 papers in Physiology. Recurrent topics in Mitsuko Nakashima's work include Genetics and Neurodevelopmental Disorders (49 papers), Genomics and Rare Diseases (36 papers) and Genomic variations and chromosomal abnormalities (24 papers). Mitsuko Nakashima is often cited by papers focused on Genetics and Neurodevelopmental Disorders (49 papers), Genomics and Rare Diseases (36 papers) and Genomic variations and chromosomal abnormalities (24 papers). Mitsuko Nakashima collaborates with scholars based in Japan, United States and Malaysia. Mitsuko Nakashima's co-authors include Hirotomo Saitsu, Naomichi Matsumoto, Noriko Miyake, Yoshinori Tsurusaki, Mitsuhiro Kato, Edward R. Canda, Satoko Miyatake, Nobuhiko Okamoto, Masaaki Shiina and Kazuhiro Ogata and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Mitsuko Nakashima

182 papers receiving 4.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitsuko Nakashima Japan 39 2.5k 1.6k 404 370 332 191 4.4k
Helger G. Yntema Netherlands 35 2.7k 1.1× 2.6k 1.6× 372 0.9× 399 1.1× 218 0.7× 100 4.9k
Arif B. Ekici Germany 42 2.6k 1.0× 1.6k 1.0× 384 1.0× 313 0.8× 311 0.9× 195 5.1k
A. Micheil Innes Canada 33 2.0k 0.8× 1.1k 0.7× 353 0.9× 325 0.9× 348 1.0× 113 3.5k
Dorit Lev Israel 39 2.0k 0.8× 1.0k 0.6× 642 1.6× 319 0.9× 164 0.5× 188 4.9k
Hossein Najmabadi Iran 41 3.5k 1.4× 1.7k 1.1× 426 1.1× 494 1.3× 386 1.2× 292 6.5k
Alessandra Renieri Italy 46 4.1k 1.6× 4.2k 2.6× 420 1.0× 515 1.4× 301 0.9× 246 8.2k
Dalil Hamroun France 24 2.1k 0.8× 976 0.6× 361 0.9× 230 0.6× 278 0.8× 60 3.5k
Fernando Kok Brazil 31 2.1k 0.8× 1.1k 0.7× 544 1.3× 432 1.2× 559 1.7× 177 3.9k
Lihadh Al‐Gazali United Arab Emirates 35 3.2k 1.3× 1.8k 1.1× 707 1.8× 587 1.6× 941 2.8× 116 5.5k
Richard J. Leventer Australia 37 1.8k 0.7× 1.4k 0.9× 670 1.7× 362 1.0× 258 0.8× 142 4.8k

Countries citing papers authored by Mitsuko Nakashima

Since Specialization
Citations

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

Fields of papers citing papers by Mitsuko Nakashima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuko Nakashima

This figure shows the co-authorship network connecting the top 25 collaborators of Mitsuko Nakashima. A scholar is included among the top collaborators of Mitsuko Nakashima 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 Mitsuko Nakashima. Mitsuko Nakashima 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
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Kato, Mitsuhiro, Akihiko Ishiyama, Tomohiro Kumada, et al.. (2024). Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield. Journal of Human Genetics. 69(12). 629–637. 2 indexed citations
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Watanabe, Kazuki, Kazuo Kubota, Mitsuko Nakashima, & Hirotomo Saitsu. (2023). A case of infantile spasms with three possibly pathogenic de novo missense variants in NF1 and GABBR1. Human Genome Variation. 10(1). 30–30.
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Kato, Mitsuhiro, et al.. (2023). Novel compound heterozygous ATP1A2 variants in a patient with fetal akinesia/hypokinesia sequence. American Journal of Medical Genetics Part A. 194(3). e63453–e63453. 1 indexed citations
7.
Monden, Yukifumi, Yasuyuki Nozaki, Kazuki Watanabe, et al.. (2022). A TUBB4A Met363Thr variant in pediatric hypomyelination without atrophy of the basal ganglia. Human Genome Variation. 9(1). 19–19.
8.
Watanabe, Kazuki, Mitsuko Nakashima, Tomoyasu Bunai, et al.. (2022). Cognitive Impairment in a Complex Family With AAGGG and ACAGG Repeat Expansions in RFC1 Detected by ExpansionHunter Denovo. Neurology Genetics. 8(3). e682–e682. 6 indexed citations
9.
Fukumura, Shinobu, et al.. (2022). Two novel heterozygous variants in ATP1A3 cause movement disorders. Human Genome Variation. 9(1). 7–7.
10.
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
11.
Watanabe, Kazuki, Mitsuko Nakashima, Satoko Kumada, et al.. (2021). Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review. Journal of Human Genetics. 66(12). 1193–1197. 16 indexed citations
12.
Takahashi, Yukitoshi, Tokito Yamaguchi, Asako Horino, et al.. (2019). Quinidine therapy and therapeutic drug monitoring in four patients with KCNT1 mutations. Epileptic Disorders. 21(1). 48–54. 31 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.
Sekiguchi, Futoshi, Maryam Sedghi, Mansoor Salehi, et al.. (2018). A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features. Journal of Human Genetics. 63(4). 487–491. 10 indexed citations
15.
Uchiyama, Yuri, Shinji Kunishima, Masaaki Shiina, et al.. (2018). A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia. Clinical Genetics. 94(6). 548–553. 20 indexed citations
16.
Tsuchida, Naomi, Keisuke Hamada, Masaaki Shiina, et al.. (2018). GRIN2D variants in three cases of developmental and epileptic encephalopathy. Clinical Genetics. 94(6). 538–547. 16 indexed citations
17.
Yoshida, Michiko, Mitsuko Nakashima, Tohru Okanishi, et al.. (2017). Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum. Clinical Genetics. 93(2). 368–373. 26 indexed citations
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Tsuchida, Naomi, Mitsuko Nakashima, Akihiko Miyauchi, et al.. (2017). Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy. Clinical Genetics. 93(2). 266–274. 23 indexed citations
19.
Tsurusaki, Yoshinori, Nobuhiko Okamoto, Hirofumi Ohashi, et al.. (2013). Coffin–Siris syndrome is a SWI/SNF complex disorder. Clinical Genetics. 85(6). 548–554. 103 indexed citations
20.
Nakashima, Mitsuko. (2002). A qualitative inquiry into the psychosocial and spiritual well-being of older adults at the end of life. UMI Dissertation Services eBooks. 4 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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