Marie Morimoto

1.7k total citations
10 papers, 183 citations indexed

About

Marie Morimoto is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Marie Morimoto has authored 10 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Immunology. Recurrent topics in Marie Morimoto's work include Neurogenetic and Muscular Disorders Research (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Autoimmune and Inflammatory Disorders Research (3 papers). Marie Morimoto is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Autoimmune and Inflammatory Disorders Research (3 papers). Marie Morimoto collaborates with scholars based in United States, Canada and Serbia. Marie Morimoto's co-authors include Cornelius F. Boerkoel, May Christine V. Malicdan, William A. Gahl, Zoraida Diaz-Perez, Charles E. Schwartz, Yi Zhu, Hongbo Wang, Camilo Toro, R. Grace Zhai and Elena‐Raluca Nicoli and has published in prestigious journals such as Nature Communications, Journal of the Neurological Sciences and Journal of Medical Genetics.

In The Last Decade

Marie Morimoto

9 papers receiving 182 citations

Peers

Marie Morimoto

MB

IMMUN

GENET

CB

EPIDE

Libo Yao China

Antonia Piazzesi Germany

Diane Gleeson United Kingdom

Behzad M. Toosi Canada

Michael Schutzbier Austria

Maureen V. Akinyi Finland

Alejandro Correa-Sáez Spain

Elena Repnikova United States

Christine Ott Germany

Hiroyuki Hozumi Japan

Libo Yao China

Marie Morimoto

160 ×1.3

MB

40 ×1.7

IMMUN

39 ×1.7

GENET

21 ×1.1

CB

22 ×1.2

EPIDE

Citations per year, relative to Marie Morimoto Marie Morimoto (= 1×) peers Libo Yao

Countries citing papers authored by Marie Morimoto

Since Specialization

Citations

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

Fields of papers citing papers by Marie Morimoto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Morimoto

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

All Works

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10 of 10 papers shown

1.

Laššuthová, Petra, et al.. (2025). Biallelic variants in the RFC4 gene cause a rapidly progressive congenital myopathy with severe hypotonia and axial weakness. Neuromuscular Disorders. 51. 105366–105366.

2.

Morimoto, Marie, Elena‐Raluca Nicoli, Joseph C. Roney, et al.. (2023). Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literature. Journal of Medical Genetics. 61(3). 212–223. 8 indexed citations

3.

Morimoto, Marie, Elena‐Raluca Nicoli, Joshi Stephen, et al.. (2023). cDNA sequencing increases the molecular diagnostic yield in Chediak-Higashi syndrome. Frontiers in Genetics. 14. 2 indexed citations

4.

Sharma, Prashant, Elena‐Raluca Nicoli, Marie Morimoto, et al.. (2019). Chediak-Higashi syndrome: A review of the past, present, and future. Drug Discovery Today Disease Models. 31. 31–36. 25 indexed citations

5.

Li, Chong, Jennifer M. Brazill, Yi Zhu, et al.. (2017). Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome. Nature Communications. 8(1). 1257–1257. 65 indexed citations

6.

Kasai, Takashi, Ikuko Mizuta, Makoto Suematsu, et al.. (2017). Early-onset Parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: Do PGK-1 mutations contribute to vulnerability to Parkinsonism?. Journal of the Neurological Sciences. 381. 358–358. 2 indexed citations

7.

Morimoto, Marie, Kunho Choi, Cornelius F. Boerkoel, & Kyoung Sang Cho. (2016). Chromatin changes inSMARCAL1deficiency: A hypothesis for the gene expression alterations of Schimke immuno-osseous dysplasia. Nucleus. 7(6). 560–571. 7 indexed citations

8.

Morimoto, Marie, Zhongxin Yu, Andrew K. Gormley, et al.. (2015). Transcriptional and posttranscriptional mechanisms contribute to the dysregulation of elastogenesis in Schimke immuno-osseous dysplasia. Pediatric Research. 78(6). 609–617. 5 indexed citations

9.

Morimoto, Marie & Cornelius F. Boerkoel. (2013). The Role of Nuclear Bodies in Gene Expression and Disease. Biology. 2(3). 976–1033. 63 indexed citations

10.

Morimoto, Marie, Christèle du Souich, Joanne Trinh, et al.. (2011). Expression profile of NSDHL in human peripheral tissues. Journal of Molecular Histology. 43(1). 95–106. 6 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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