Mami Yamasaki

3.4k total citations
83 papers, 2.2k citations indexed

About

Mami Yamasaki is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Mami Yamasaki has authored 83 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 24 papers in Pediatrics, Perinatology and Child Health and 17 papers in Surgery. Recurrent topics in Mami Yamasaki's work include Fetal and Pediatric Neurological Disorders (21 papers), Neurogenesis and neuroplasticity mechanisms (14 papers) and Pluripotent Stem Cells Research (13 papers). Mami Yamasaki is often cited by papers focused on Fetal and Pediatric Neurological Disorders (21 papers), Neurogenesis and neuroplasticity mechanisms (14 papers) and Pluripotent Stem Cells Research (13 papers). Mami Yamasaki collaborates with scholars based in Japan, United States and Canada. Mami Yamasaki's co-authors include Yonehiro Kanemura, Hideyuki Okano, Vance Lemmon, Hideki Mori, Tomoko Shofuda, P. Thompson, Satoshi Kobayashi, Nobuhiko Okamoto, Hiroyuki Kamiguchi and Atsuyo Yamamoto and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annual Review of Neuroscience.

In The Last Decade

Mami Yamasaki

80 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mami Yamasaki Japan 25 1.0k 662 568 360 346 83 2.2k
Gisela Barbany Sweden 21 1.2k 1.2× 1.0k 1.6× 435 0.8× 557 1.5× 169 0.5× 64 3.4k
Susan Kenwrick United Kingdom 24 1.6k 1.6× 851 1.3× 302 0.5× 263 0.7× 770 2.2× 48 2.9k
Hui Z. Sheng China 21 2.6k 2.5× 797 1.2× 449 0.8× 155 0.4× 744 2.2× 39 3.6k
Rebecca A. Ihrie United States 25 1.5k 1.4× 476 0.7× 1.0k 1.8× 470 1.3× 239 0.7× 54 2.7k
Shigemi Hayashi United States 11 3.2k 3.1× 460 0.7× 625 1.1× 184 0.5× 832 2.4× 12 4.1k
Verónica Palma Chile 24 1.4k 1.4× 249 0.4× 285 0.5× 275 0.8× 318 0.9× 64 2.1k
Eva Sonnenberg-Riethmacher Germany 14 1.1k 1.1× 663 1.0× 302 0.5× 103 0.3× 253 0.7× 17 2.2k
Stefan Liebau Germany 32 1.9k 1.9× 785 1.2× 404 0.7× 553 1.5× 215 0.6× 83 3.1k
Michael J. Shamblott United States 27 2.1k 2.1× 260 0.4× 272 0.5× 402 1.1× 584 1.7× 50 3.4k
Massimo Signore United Kingdom 24 1.8k 1.7× 362 0.5× 185 0.3× 183 0.5× 460 1.3× 30 2.5k

Countries citing papers authored by Mami Yamasaki

Since Specialization
Citations

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

Fields of papers citing papers by Mami Yamasaki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mami Yamasaki

This figure shows the co-authorship network connecting the top 25 collaborators of Mami Yamasaki. A scholar is included among the top collaborators of Mami Yamasaki 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 Mami Yamasaki. Mami Yamasaki 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.
Maeda, Keisuke, et al.. (2019). EP17.29: Prenatal diagnosis of aplasia cutis congenita and congenital defect of scalp and skull. Ultrasound in Obstetrics and Gynecology. 54(S1). 341–341. 1 indexed citations
2.
Hori, Ikumi, Fuyuki Miya, Yutaka Negishi, et al.. (2018). A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome. Journal of Human Genetics. 63(9). 957–963. 10 indexed citations
3.
Shigemizu, Daichi, Fuyuki Miya, Shintaro Akiyama, et al.. (2018). IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis. Scientific Reports. 8(1). 5608–5608. 20 indexed citations
4.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2017). Novel MCA/ID syndrome with ASH1L mutation. American Journal of Medical Genetics Part A. 173(6). 1644–1648. 29 indexed citations
5.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2017). A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology. American Journal of Medical Genetics Part A. 173(10). 2690–2696. 7 indexed citations
6.
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
7.
Hamada, Nanako, Yutaka Negishi, Makoto Mizuno, et al.. (2016). Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability. Journal of Neurochemistry. 140(1). 82–95. 13 indexed citations
8.
Shofuda, Tomoko, Mitsuhiro Kato, Ritsuko K. Pooh, et al.. (2016). In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations. Molecular Brain. 9(1). 70–70. 16 indexed citations
9.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2014). KIF1A mutation in a patient with progressive neurodegeneration. Journal of Human Genetics. 59(11). 639–641. 42 indexed citations
10.
Shofuda, Tomoko, Daisuke Kanematsu, Atsuyo Yamamoto, et al.. (2013). Feeder-Free Generation and Long-Term Culture of Human Induced Pluripotent Stem Cells Using Pericellular Matrix of Decidua Derived Mesenchymal Cells. PLoS ONE. 8(1). e55226–e55226. 18 indexed citations
11.
Ishihara, Masahiro, et al.. (2013). “No-No” Type Bobble-Head Doll Syndrome in an Infant With an Arachnoid Cyst of the Posterior Fossa: A Case Report. Pediatric Neurology. 49(6). 474–476. 7 indexed citations
12.
Takenouchi, Toshiki, et al.. (2012). Hydrocephalus with Hirschsprung disease: Severe end of X‐linked hydrocephalus spectrum. American Journal of Medical Genetics Part A. 158A(4). 812–815. 8 indexed citations
13.
Moritake, Kouzo, Hidemasa Nagai, Takeshi Miyazaki, et al.. (2007). Analysis of a Nationwide Survey on Treatment and Outcomes of Congenital Hydrocephalus in Japan. Neurologia medico-chirurgica. 47(10). 453–461. 14 indexed citations
14.
Mori, Hideki, Kazuaki Ninomiya, Masahiro Kino‐oka, et al.. (2006). Effect of neurosphere size on the growth rate of human neural stem/progenitor cells. Journal of Neuroscience Research. 84(8). 1682–1691. 107 indexed citations
15.
Kanemura, Yonehiro, Hideki Mori, Mohammed Omedul Islam, et al.. (2005). In Vitro Screening of Exogenous Factors for Human Neural Stem/Progenitor Cell Proliferation Using Measurement of Total ATP Content in Viable Cells. Cell Transplantation. 14(9). 673–682. 12 indexed citations
16.
Islam, Mohammed Omedul, Yonehiro Kanemura, Hideki Mori, et al.. (2005). Characterization of ABC transporter ABCB1 expressed in human neural stem/progenitor cells. FEBS Letters. 579(17). 3473–3480. 42 indexed citations
17.
Ishibashi, Satoru, Masanori Sakaguchi, Toshihiko Kuroiwa, et al.. (2004). Human neural stem/progenitor cells, expanded in long‐term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils. Journal of Neuroscience Research. 78(2). 215–223. 140 indexed citations
18.
Kanemura, Yonehiro, Mami Yamasaki, Hirokazu Fujikawa, et al.. (2001). Musashi1, an evolutionarily conserved neural RNA-binding protein, is a versatile marker of human glioma cells in determining their cellular origin, malignancy, and proliferative activity. Differentiation. 68(2-3). 141–152. 117 indexed citations
19.
Otsuki, Hideo, et al.. (2001). Intraoperative ultrasound arteriography with the “Coded Harmonic Angio” technique. Journal of neurosurgery. 94(6). 992–995. 14 indexed citations
20.
Kanemura, Yonehiro, Shoju Hiraga, Takanori Ohnishi, et al.. (1999). Isolation and expression analysis of a novel human homologue of the Drosophila glial cells missing (gcm) gene. FEBS Letters. 442(2-3). 151–156. 48 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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