Shino Shimada

1.1k citations

36 papers · 545 indexed · h-index 15

Co-authors: Toshiyuki Yamamoto Keiko Shimojima Nobuhiko Okamoto Makiko Ōsawa Noriko Sangu Midori Sugawara Masami Togawa Yoshihiro Maegaki
Topics: Genomic variations and chromosomal abnormalities (15 papers)Genetics and Neurodevelopmental Disorders (10 papers)RNA regulation and disease (7 papers)
Cited by: Genetics Clinical Biochemistry Molecular Biology
Journals: Gene Journal of the Neurological Sciences Molecular Genetics and Metabolism
Partner nations: Japan United States France

In The Last Decade

Shino Shimada

33 papers receiving 476 citations

Peers

Countries citing papers authored by Shino Shimada

Since Specialization

Citations

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

Fields of papers citing papers by Shino Shimada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shino Shimada

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Neurodevelopmental milestone acquisition following early hemispherotomy in Sturge-Weber syndrome 2025 ·Seizure ·Yasushi Iimura,Hiroharu Suzuki,Takumi Mitsuhashi,(unknown),(unknown),(unknown),(unknown),Mitsuru Ikeno,(unknown),(unknown),Shino Shimada,T. Akiba,Shimpei Matsuda,Hidenori Sugano,Akihide Kondo	0
2	A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication 2024 ·Human Genome Variation ·T. Akiba,Shino Shimada,Katsumi Imai,Satoru Takahashi	0
3	A case report of hydrocephalus due to diffuse villous hyperplasia of the choroid plexus: surgical treatment by combination a flexible videoscope with a rigid endoscope 2023 ·Child s Nervous System ·(unknown),(unknown),Shinpei Matsuda,Shino Shimada,(unknown),Yasuaki Nakao,Takuji Yamamoto	0
4	Functional analysis of a de novo variant in the neurodevelopment and generalized epilepsy disease gene NBEA 2021 ·Molecular Genetics and Metabolism ·Thomas Boulin,Omar A. Itani,Sonia El Mouridi,(unknown),Marie Gendrel,Ellen F. Macnamara,Ariane Soldatos,Jennifer L. Murphy,Mark Gorman,(unknown),Shino Shimada,(unknown),Gary A. Silverman,Dustin Baldridge,May Christine V. Malicdan,Tim Schedl,Stephen C. Pak	7
5	Mutations in GET4 disrupt the transmembrane domain recognition complex pathway 2020 ·Journal of Inherited Metabolic Disease ·Mitali A. Tambe,Bobby G. Ng,Shino Shimada,Lynne A. Wolfe,David R. Adams,(unknown),William A. Gahl,Michael J. Bamshad,Deborah A. Nickerson,May Christine V. Malicdan,Hudson H. Freeze	5
6	An episode of acute encephalopathy with biphasic seizures and late reduced diffusion followed by hemiplegia and intractable epilepsy observed in a patient with a novel frameshift mutation in HNRNPU 2018 ·Brain and Development ·Shino Shimada,Hirokazu Oguni,(unknown),(unknown),Susumu Ito,(unknown),Tomoyuki Nakazawa,(unknown),Jun‐ichi Takanashi,Satoru Nagata,Toshiyuki Yamamoto	13
7	The first Japanese case of leukodystrophy with ovarian failure arising from novel compound heterozygous AARS2 mutations 2016 ·Journal of Human Genetics ·(unknown),(unknown),Yoshinori Tsurusaki,Shino Shimada,Keiko Shimojima,Megumi Asada‐Utsugi,(unknown),Norihito Uemura,Hirofumi Yamashita,Kengo Uemura,Ryōsuke Takahashi,Naomichi Matsumoto,Toshiyuki Yamamoto	27
8	Novel compound heterozygous LIAS mutations cause glycine encephalopathy 2015 ·Journal of Human Genetics ·Yoshinori Tsurusaki,Ryuta Tanaka,Shino Shimada,Keiko Shimojima,Masaaki Shiina,Mitsuko Nakashima,Hirotomo Saitsu,Noriko Miyake,Kazuhiro Ogata,Toshiyuki Yamamoto,Naomichi Matsumoto	16
9	Leukoencephalopathy associated with 11q24 deletion involving the gene encoding hepatic and glial cell adhesion molecule in two patients 2015 ·European Journal of Medical Genetics ·Toshiyuki Yamamoto,Shino Shimada,Keiko Shimojima,Noriko Sangu,Shinsuke Ninomiya,Masaya Kubota	8
10	Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease 2015 ·Brain and Development ·Shino Shimada,Keiko Shimojima,Noriko Sangu,Ai Hoshino,Yasuo Hachiya,Tatsuyuki Ohto,(unknown),(unknown),(unknown),Saori Kinjo,Yoshinori Tsurusaki,Naomichi Matsumoto,Masafumi Morimoto,Toshiyuki Yamamoto	7
11	An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities 2014 ·Journal of Human Genetics ·Toshiyuki Yamamoto,Anna Wilsdon,Shelagh Joss,Bertrand Isidor,Anna Erlandsson,Mohnish Suri,Noriko Sangu,Shino Shimada,Keiko Shimojima,Cédric Le Caignec,Lena Samuelsson,M Stefanova	38
12	Clinical impacts of genomic copy number gains at Xq28 2014 ·Human Genome Variation ·Toshiyuki Yamamoto,Keiko Shimojima,Shino Shimada,Kenji Yokochi,(unknown),Keiko Yanagihara,Katsumi Imai,Nobuhiko Okamoto	29
13	MLC1 mutations in Japanese patients with megalencephalic leukoencephalopathy with subcortical cysts 2014 ·Human Genome Variation ·Shino Shimada,Keiko Shimojima,Teruaki Masuda,(unknown),(unknown),Hiroko Tsukamoto,(unknown),Akira Oka,Toshiyuki Yamamoto	4
14	Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4 2013 ·American Journal of Medical Genetics Part A ·Toshiyuki Yamamoto,Masami Togawa,Shino Shimada,Noriko Sangu,Keiko Shimojima,Nobuhiko Okamoto	25
15	De novo triplication of 11q12.3 in a patient with developmental delay and distinctive facial features 2013 ·Molecular Cytogenetics ·Toshiyuki Yamamoto,Mari Matsuo,Shino Shimada,Noriko Sangu,Keiko Shimojima,(unknown),Kayoko Saito	3
16	Novel compound heterozygous mutations of POLR3A revealed by whole-exome sequencing in a patient with hypomyelination 2013 ·Brain and Development ·Keiko Shimojima,Shino Shimada,Akiko Tamasaki,Shinjiro Akaboshi,Yuta Komoike,Akira Saito,Toru Furukawa,Toshiyuki Yamamoto	19
17	Microdeletions of 3p21.31 characterized by developmental delay, distinctive features, elevated serum creatine kinase levels, and white matter involvement 2013 ·American Journal of Medical Genetics Part A ·(unknown),Norio Sakai,Shino Shimada,(unknown),Keiko Ishigaki,Yusuke Hamada,(unknown),(unknown),Koji Tominaga,Keiko Shimojima,Keiichi Ozono,Makiko Ōsawa,Toshiyuki Yamamoto	22
18	An unmasked mutation of EIF2B2 due to submicroscopic deletion of 14q24.3 in a patient with vanishing white matter disease 2012 ·American Journal of Medical Genetics Part A ·Shino Shimada,Kazushi Miya,(unknown),Yuki Watanabe,Tomohiro Kumada,Midori Sugawara,Keiko Shimojima,Toshiyuki Yamamoto	10
19	A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features 2012 ·Gene ·Kazushi Miya,Keiko Shimojima,Midori Sugawara,Shino Shimada,(unknown),(unknown),(unknown),Hirokazu Kanegane,Toshio Miyawaki,Toshiyuki Yamamoto	14
20	MECP2 duplication syndrome in both genders 2012 ·Brain and Development ·Shino Shimada,Nobuhiko Okamoto,Masahiro Ito,Yasuhiro Arai,Ken Momosaki,Masami Togawa,Yoshihiro Maegaki,Midori Sugawara,Keiko Shimojima,Makiko Ōsawa,Toshiyuki Yamamoto	39

About Shino Shimada

Shino Shimada is a scholar working on Genetics, Aging and Clinical Biochemistry, having authored 36 papers that have together received 545 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (10 papers) and RNA regulation and disease (7 papers). The work is most often cited by research in Genetics (318 citations), Clinical Biochemistry (33 citations) and Molecular Biology (315 citations). Shino Shimada has collaborated with scholars based in Japan, United States and France. Frequent co-authors include Toshiyuki Yamamoto, Keiko Shimojima, Nobuhiko Okamoto, Makiko Ōsawa, Noriko Sangu, Midori Sugawara, Masami Togawa, Yoshihiro Maegaki, Atsushi Ishii and Masako Sakauchi. Their work appears in journals such as Gene, Journal of the Neurological Sciences and Molecular Genetics and Metabolism.

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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