Hiroyuki Morino

3.2k citations

78 papers · 1.2k indexed · h-index 20

Neurology top 2%
- Amyotrophic Lateral Sclerosis Research 17
- Parkinson's Disease Mechanisms and Treatments 16
- Neurological diseases and metabolism 10
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 22
Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 17
- Parkinson's Disease Mechanisms and Treatments 16
- Neurological diseases and metabolism 10
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 5
Molecular Biology
- Mitochondrial Function and Pathology 18
Physiology
- Alzheimer's disease research and treatments 10
Genetics
- Neurogenetic and Muscular Disorders Research 6

Co-authors: Hideshi Kawakami Hirofumi Maruyama Yuishin Izumi Masaya Oda Shigenobu Nakamura Ryosuke Miyamoto Fukashi Udaka Ryuji Kaji
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Neurology (4 papers)Movement Disorders (4 papers)Journal of the Neurological Sciences (4 papers)
Partner nations: Japan United States United Kingdom

In The Last Decade

Hiroyuki Morino

73 papers receiving 1.2k citations

Peers

Countries citing papers authored by Hiroyuki Morino

Since Specialization

Citations

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

Fields of papers citing papers by Hiroyuki Morino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Hiroyuki Morino, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hiroyuki Morino Line = papers co-authored together Hiroyuki Morino links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The long-term effects of heated tobacco product exposure on the central nervous system in a mouse model of prodromal Alzheimer's disease Scientific Reports ·Y. Wang,Yu Yamazaki,Elisabeti Fátima Teixeira Barbosa,Abhishek Kumar Biswal,刘春伟,孙振田,Masahiro Nakamori,Hiroyuki Morino,Tetsuya Takahashi,Hirofumi Maruyama	2024	4
2	An autopsy case of type A FTLD‐TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequently Neuropathology ·Soledad Kassai,Adriana Eloisa Ayala Medina,Evelyn Daugherty,Akitoshi Takeda,Takahito Yoshizaki,Joji Kawabe,A. Petit,Hiroyuki Morino,守大内田,Tomoyasu Matsubara,Hiroyuki Hatsuta,Masato Hasegawa,Shigeo Murayama,Yoshiaki Itoh	2024	1
3	Clinical and Pathological Features of FTDP ‐17 with MAPT p.K298_H299insQ Mutation Movement Disorders Clinical Practice ·Hiroyuki Morino,Takashi Kurashige,Yukiko Matsuda,Maiko Ono,Naruhiko Sahara,Tomohiro Miyasaka,Yoshiyuki Soeda,Hitoshi Shimada,Yu Yamazaki,Tetsuya Takahashi,Yuishin Izumi,Hidefumi Ito,Hirofumi Maruyama,守大内田,Koji Arihiro,Tetsuya Suhara,Akihiko Takashima,Hideshi Kawakami	2024	2
4	Pulmonary Arterial Hypertension in Neurofibromatosis Type 1: A Case with a Novel <i>NF1</i> Gene Mutation Internal Medicine ·Shusuke Yagi,Ce Wang,修司奥野,Ryosuke Miyamoto,Hiroyuki Morino,沈穎,Yoshiaki Kubo,Takayuki Ise,Głowińska‐Olszewska Barbara,A. E. Bremner,Kenya Kusunose,Koji Yamaguchi,Hirotsugu Yamada,Takeshi Soeki,Tetsuzo Wakatsuki,Daiju Fukuda,Masataka Sata	2024	0
5	Th17 and effector CD8 T cells relate to disease progression in amyotrophic lateral sclerosis: a case control study Journal of Neuroinflammation ·I. V. Il'in,Koji Fujita,Yuumi Okuzono,Dnyaneshwar Warude,Gou Li-na,V. F. Li,Naoko Matsui,Hiroyuki Morino,Yusuke Kikukawa,Yuishin Izumi	2024	2
6	‘Raisin bread sign’ feature of pontine autosomal dominant microangiopathy and leukoencephalopathy Brain Communications ·Fatiha Meraza,Takashi Kurashige,Tomohiko Ohshita,Kodai Kume,Niels Kærgaard,Tomohisa Nezu,Shiro Aoki,Kazuhide Ochi,Hiroyuki Morino,Eiichi Nomura,Hiroshi Yamashita,Mayumi Kaneko,Hirofumi Maruyama,Hideshi Kawakami	2023	2
7	Gastrointestinal cancer occurs as extramuscular manifestation in FSHD1 patients Journal of Human Genetics ·Takashi Kurashige,Hiroyuki Morino,TS Jung,Evgeniya V. Utyaganova,Danielle Heberle Viegas,Takao Hinoi,Ichizo Nishino,Tsuyoshi Torii,Hirofumi Maruyama	2022	1
8	Socio-economic impact on epilepsy outside of the nation-wide COVID-19 pandemic area Epilepsy & Behavior ·Shuichiro Neshige,Shiro Aoki,Juan Fernando de Laiglesia yGonzález de Peredo,Hiroyuki Morino,Koji Iida,Hirofumi Maruyama	2021	10
9	Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging Neurology Genetics ·Fatiha Meraza,Tomohisa Nezu,熊谷千津,孙振田,Stanislav Koshutin,Takashi Kurashige,Hiroki Ueno,Tetsuya Takahashi,Hiroyuki Morino,Jun Sone,Yasushi Iwasaki,Gen Sobue,Hirofumi Maruyama	2021	12
10	FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report BMC Neurology ·Stanislav Koshutin,Tomohiko Ohshita,Takashi Kurashige,Hiroyuki Morino,Kodai Kume,Hiroshi Yamashita,Gen Sobue,Yasushi Iwasaki,Jun Sone,Hideshi Kawakami,Hirofumi Maruyama	2021	21
11	Knockdown of optineurin controls C2C12 myoblast differentiation via regulating myogenin and MyoD expressions Differentiation ·Ken-Ichi Ishikawa,D. McLaren,Yoshito Nagano,孙振田,Juan Fernando de Laiglesia yGonzález de Peredo,Takashi Kurashige,Tetsuya Takahashi,Hiroyuki Morino,Hideshi Kawakami,Masayasu Matsumoto,Hirofumi Maruyama	2021	2
12	Optineurin defects cause TDP43-pathology with autophagic vacuolar formation Neurobiology of Disease ·Takashi Kurashige,Masahito Kuramochi,Ryosuke Ohsawa,Yui Yamashita,Go Shioi,Hiroyuki Morino,Masaki Kamada,Takashi Ayaki,Hidefumi Ito,Yusuke Sotomaru,Hirofumi Maruyama,Hideshi Kawakami	2020	19
13	Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia Journal of Human Genetics ·Бровко Кирилл Анатольевич,Kodai Kume,Yukiko Matsuda,Takashi Kurashige,Susan Barleben,Ryosuke Ohsawa,Hiroyuki Morino,Д Т Батов,Satoshi Kaneko,Toshihiko Suenaga,Akira Kakizuka,Hideshi Kawakami	2020	9
14	Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease Neurology ·Yuishin Izumi,Ryosuke Miyamoto,Hiroyuki Morino,Akio Yoshizawa,Kazuto Nishinaka,Fukashi Udaka,Masakuni Kameyama,Hirofumi Maruyama,Hideshi Kawakami	2013	47
15	Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case series SHILAP Revista de lepidopterología ·Hiroki Ueno,Keitaro Kobatake,Masayasu Matsumoto,Hiroyuki Morino,Hirofumi Maruyama,Hideshi Kawakami	2011	7
16	The UCHL1 S18Y polymorphism and Parkinson’s disease in a Japanese population Parkinsonism & Related Disorders ·Katherine W. Snapinn,Eric B. Larson,Hideshi Kawakami,Hiroshi Ujike,Amy R. Borenstein,Yuishin Izumi,Ryuji Kaji,Hirofumi Maruyama,Ignácio F. Mata,Hiroyuki Morino,Masaya Oda,Debby W. Tsuang,Dora Yearout,Karen L. Edwards,Cyrus P. Zabetian	2011	5
17	The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia Journal of the Neurological Sciences ·Eiji Tanaka,Hirofumi Maruyama,Hiroyuki Morino,Akshyat Shah,Hideshi Kawakami	2007	8
18	Possible Reduced Penetrance of Expansion of 44 to 47 CAG/CAA Repeats in the TATA-Binding Protein Gene in Spinocerebellar Ataxia Type 17 Archives of Neurology ·Masaya Oda,Hirofumi Maruyama,Osamu Komure,Hiroyuki Morino,H. S. W.,Yuishin Izumi,Tohru Imamura,Minoru Yasuda,Jian Guo Li,Montaño Forero,Masayasu Matsumoto,Hideshi Kawakami	2004	44
19	SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6 The American Journal of Human Genetics ·Yuishin Izumi,Hirofumi Maruyama,Masaya Oda,Hiroyuki Morino,Lúcia de Souza Lima Safi,Hidefumi Ito,Iwao Sasaki,Hiroyasu Tanaka,Osamu Komure,Fukashi Udaka,Shigenobu Nakamura,Hideshi Kawakami	2003	49
20	Dinucleotide repeat polymorphism in interferon‐γ gene is not associated with sporadic Alzheimer's disease American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Masaya Oda,Hirofumi Maruyama,Yuishin Izumi,Hiroyuki Morino,Tsuyoshi Torii,Shigenobu Nakamura,Hideshi Kawakami	2003	2

About Hiroyuki Morino

Hiroyuki Morino is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 78 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (22 papers), Mitochondrial Function and Pathology (18 papers), Amyotrophic Lateral Sclerosis Research (17 papers), Parkinson's Disease Mechanisms and Treatments (16 papers), Neurological diseases and metabolism (10 papers), Alzheimer's disease research and treatments (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Metabolism and Genetic Disorders (5 papers). The work is most often cited by research in Neurology (494 citations), Cellular and Molecular Neuroscience (564 citations) and Neurology (216 citations). Hiroyuki Morino has collaborated with scholars based in Japan, United States and United Kingdom. Frequent co-authors include Hideshi Kawakami, Hirofumi Maruyama, Yuishin Izumi, Masaya Oda, Shigenobu Nakamura, Ryosuke Miyamoto, Fukashi Udaka, Ryuji Kaji, Yukiko Matsuda and Ryosuke Ohsawa. Their work appears in journals such as Neurology, Movement Disorders, Journal of the Neurological Sciences, BMC Neurology and Neuropathology.

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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