Haruo Shimazaki

4.5k total citations · 1 hit paper
73 papers, 2.9k citations indexed

About

Haruo Shimazaki is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Haruo Shimazaki has authored 73 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 24 papers in Molecular Biology and 23 papers in Neurology. Recurrent topics in Haruo Shimazaki's work include Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (14 papers) and Neurological diseases and metabolism (9 papers). Haruo Shimazaki is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (14 papers) and Neurological diseases and metabolism (9 papers). Haruo Shimazaki collaborates with scholars based in Japan, United States and Estonia. Haruo Shimazaki's co-authors include Josep Dalmau, Reiji Koide, Haiyan Wu, Alfredo Voloschin, Marc A. Dichter, Lauren Sansing, Joachim M. Baehring, Jeffrey Rossi, Myrna R. Rosenfeld and Erdem Tüzün and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

Haruo Shimazaki

70 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Paraneoplastic anti– N ‐methyl‐ D ‐aspartate receptor encephalitis associated with ovarian teratoma

2007 1.7k citations Josep Dalmau, Erdem Tüzün et al. Annals of Neurology profile →

Peers

Haruo Shimazaki

NEURO

CMN

GENET

ONCOL

Jesús Planagumà Spain

Mar Petit‐Pedrol Spain

Virginie Desestret France

Luigi Zuliani Italy

Reiji Koide Japan

Yolanda Blanco Spain

I. K. Hart United Kingdom

Luís Bataller Spain

Philippa Pettingill United Kingdom

Jaime Masjuan Spain

Jesús Planagumà Spain

Haruo Shimazaki

1.9k ×1.0

NEURO

610 ×0.7

CMN

773 ×0.9

604 ×1.0

GENET

334 ×1.0

ONCOL

Citations per year, relative to Haruo Shimazaki Haruo Shimazaki (= 1×) peers Jesús Planagumà

Countries citing papers authored by Haruo Shimazaki

Since Specialization

Citations

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

Fields of papers citing papers by Haruo Shimazaki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haruo Shimazaki

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Koh, Kishin, Haruo Shimazaki, Matsuo Ogawa, & Yoshihisa Takiyama. (2022). A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia. Human Genome Variation. 9(1). 27–27. 2 indexed citations

Koh, Kishin, Mai Tsuchiya, Hiroyuki Ishiura, et al.. (2021). Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia. Journal of Human Genetics. 67(2). 119–121. 4 indexed citations

Matsuzono, Kosuke, Tadashi Ozawa, Haruo Shimazaki, et al.. (2020). Left thalamus infarction in the thalamotuberal artery perfusion area causing subcortical diaschisis and transcortical sensory aphasia. Journal of the Neurological Sciences. 411. 116708–116708. 1 indexed citations

Matsuzono, Kosuke, Takeshi Igarashi, Tadashi Ozawa, et al.. (2020). Relapsing polychondritis coupling with cerebral amyloid deposit inducing cerebral amyloid angiopathy-related inflammation. Journal of Thrombosis and Thrombolysis. 49(4). 681–684. 2 indexed citations

Shimazaki, Haruo, Takehiko Ueyama, Naoko Adachi, et al.. (2019). Spinocerebellar ataxia type 14 caused by a nonsense mutation in the PRKCG gene. Molecular and Cellular Neuroscience. 98. 46–53. 12 indexed citations

Ozawa, Tadashi, Ryota Tanaka, Younhee Kim, et al.. (2019). Data on characteristics of reported cases of unilateral posterior reversible encephalopathy syndrome (PRES). SHILAP Revista de lepidopterología. 27. 104648–104648. 3 indexed citations

Ueno, Hideki, Kazuo Hase, Yojiro Hashiguchi, et al.. (2014). Potential Causes of Stage Migration and Their Prognostic Implications in Colon Cancer: A Nationwide Survey of Specialist Institutions in Japan. Japanese Journal of Clinical Oncology. 44(6). 547–555. 11 indexed citations

Ueno, Hideki, Eiji Shinto, Yoshiki Kajiwara, et al.. (2014). Prognostic impact of histological categorisation of epithelial–mesenchymal transition in colorectal cancer. British Journal of Cancer. 111(11). 2082–2090. 57 indexed citations

T, Oda, Osamu Hotta, Kojiro Yamamoto, et al.. (2013). Clinical and immunological implications of increase in CD208+ dendritic cells in tonsils of patients with immunoglobulin A nephropathy. Nephrology Dialysis Transplantation. 28(12). 3004–3013. 20 indexed citations

10.

Uchida, Takahiro, Oda T, Atsushi Watanabe, et al.. (2012). Idiopathic nodular glomerulosclerosis in a never-smoking, normotensive, non-obese, normal-glucose-tolerant middle-aged woman. Clinical Kidney Journal. 5(5). 445–448. 3 indexed citations

11.

Shimazaki, Haruo, Yoshihisa Takiyama, Hiroyuki Ishiura, et al.. (2012). A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55). Journal of Medical Genetics. 49(12). 777–784. 64 indexed citations

12.

Shimazaki, Haruo, Hiromi Takahashi, Hisako Endo, et al.. (2011). Immunocytochemistry of mesenteric malignant mixed müllerian tumour in peritoneal effusion cytology: case report. Cytopathology. 23(5). 334–337. 3 indexed citations

13.

Dalmau, Josep, Erdem Tüzün, Haiyan Wu, et al.. (2007). Paraneoplastic anti– N ‐methyl‐ D ‐aspartate receptor encephalitis associated with ovarian teratoma. Annals of Neurology. 61(1). 25–36. 1733 indexed citations breakdown →

14.

Kurashina, Tomoyuki, et al.. (2006). An autopsy case of fibromuscular dysplasia complicated by multiple cerebral infarctions. Nosotchu. 28(2). 318–323.

15.

Sakoe, Kumi, Haruo Shimazaki, Michito Namekawa, et al.. (2006). 16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study. Journal of the Neurological Sciences. 247(2). 180–186. 34 indexed citations

16.

Kamimura, Takeshi, Haruo Shimazaki, Mitsuya Morita, et al.. (2006). Limited Wegener's Granulomatosis Manifested by Abducens Nerve Palsy Resulting From Pachymeningitis. JCR Journal of Clinical Rheumatology. 12(5). 259–260. 7 indexed citations

17.

Osawa, Motoki, et al.. (2005). Polymerase Chain Reaction-Based Analysis Using Deaminated DNA of Dodecamer Expansions in CSTB , Associated with Unverricht-Lundborg Myoclonus Epilepsy. Genetic Testing. 9(4). 328–333. 9 indexed citations

18.

Yamamoto, Yoichi, et al.. (2005). Novel compound heterozygous mutations in sacsin-related ataxia. Journal of the Neurological Sciences. 239(1). 101–104. 15 indexed citations

19.

Namekawa, Michito, Yoshihisa Takiyama, Kumi Sakoe, et al.. (2002). A Japanese SPG4 family with a novel missense mutation of theSPG4gene: intrafamilial variability in age at onset and clinical severity. Acta Neurologica Scandinavica. 106(6). 387–391. 8 indexed citations

20.

Namekawa, Michito, Yoshihisa Takiyama, Kumi Sakoe, et al.. (2001). A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study. Journal of the Neurological Sciences. 185(1). 63–68. 17 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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