Hideki Mutai

1.9k citations

63 papers · 1.2k indexed · h-index 20

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics 40
Otorhinolaryngology top 2%
- Ear Surgery and Otitis Media 7
Neurology top 5%
- Vestibular and auditory disorders 11
Molecular Biology
- RNA regulation and disease 8
- Connexins and lens biology 8
- Mitochondrial Function and Pathology 5
- Congenital heart defects research 5
Cell Biology top 10%
Cognitive Neuroscience
- Hearing Loss and Rehabilitation 6

Co-authors: Stefan Heller Tatsuo Matsunaga Gábor Keresztes Noriko Morimoto Kazunori Namba Sawako Masuda Kimitaka Kaga Atsuko Nakano
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: Scientific Reports (7 papers)Biochemical and Biophysical Research Communications (6 papers)Orphanet Journal of Rare Diseases (4 papers)
Partner nations: Japan United States South Korea

In The Last Decade

Hideki Mutai

59 papers receiving 1.2k citations

Peers

Countries citing papers authored by Hideki Mutai

Since Specialization

Citations

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

Fields of papers citing papers by Hideki Mutai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Hideki Mutai, 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 Hideki Mutai Line = papers co-authored together Hideki Mutai links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Structural basis for pathogenic variants of GJB2 and hearing levels of patients with hearing loss BMC Research Notes ·Kazunori Namba,Hideki Mutai,Tatsuo Matsunaga,Hiroki Kaneko	2024	0
2	Molecular basis of carotid body tumor and associated clinical features in Japan identified by genomic, immunohistochemical, and clinical analyses Clinical Genetics ·de Goeje,Hideki Mutai,Kylie Tanner,H Wang,Shin Saito,Satya Omprabha,Deborah L. Hoffert,Guoxue Shangguan,Pacyna. J.M.,Fuyuki Miya,Kenjiro Kosaki,Hiroyuki Ozawa,Tatsuo Matsunaga	2023	3
3	Phenotype–genotype correlation in patients with typical and atypical branchio-oto-renal syndrome Scientific Reports ·Masatsugu Masuda,Dairaku,Kiyomitsu Nara,Hideki Mutai,Naoya Morisada,Kazumoto Iijima,Noriko Morimoto,Atsuko Nakano,Yoon Sik Eom,Yasuhide Okamoto,Sawako Masuda,温晓楠,Kaoru Ogawa,Tatsuo Matsunaga	2022	8
4	Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans PLoS Genetics ·Hideki Mutai,Koichiro Wasano,Yukihide Momozawa,Yoichiro Kamatani,Fuyuki Miya,Sawako Masuda,Noriko Morimoto,Kiyomitsu Nara,Satoe Takahashi,Tatsuhiko Tsunoda,Kazuaki Homma,Michiaki Kubo,Tatsuo Matsunaga	2020	40
5	A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10 BMC Pediatrics ·Noriomi Suzuki,Hideki Mutai,Fuyuki Miya,Tatsuhiko Tsunoda,Hiroshi Terashima,Noriko Morimoto,Tatsuo Matsunaga	2018	13
6	Gene expression dataset for whole cochlea of Macaca fascicularis Scientific Reports ·Hideki Mutai,Fuyuki Miya,Hiroaki Shibata,Yasuhiro Yasutomi,Tatsuhiko Tsunoda,Tatsuo Matsunaga	2018	5
7	Mitochondrial mutations in maternally inherited hearing loss BMC Medical Genetics ·Hideki Mutai,Ljijana Radosevic-Jelic,Kenjiro Kosaki,Kaoru Ogawa,Tatsuo Matsunaga	2017	20
8	Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss Orphanet Journal of Rare Diseases ·Nobuko Yamamoto,Hideki Mutai,Kazunori Namba,Noriko Morita,Shin Masuda,Yasuyuki Nishi,Atsuko Nakano,Sawako Masuda,Masato Fujioka,Kimitaka Kaga,Kaoru Ogawa,Tatsuo Matsunaga	2017	19
9	Molecular Impairment Mechanisms of Novel OPA1 Mutations Predicted by Molecular Modeling in Patients With Autosomal Dominant Optic Atrophy and Auditory Neuropathy Spectrum Disorder Otology & Neurotology ·Kazunori Namba,Hideki Mutai,Aistė Buitvidaitė,H. Yagi,Carlos Feria Pérez,Mohammad Akbar Hosain,Jingran Qian,Hiroki Kaneko,Tomoko Shintani,Kimitaka Kaga,Tatsuo Matsunaga	2016	9
10	Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1 Auris Nasus Larynx ·Shujiro Minami,Hideki Mutai,Kazunori Namba,Hirokazu Sakamoto,Tatsuo Matsunaga	2016	10
11	A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss Biochemical and Biophysical Research Communications ·Sawako Masuda,Kazunori Namba,Hideki Mutai,Aijaz Ali Thaheem,KosinkaJiří,Hiroki Kaneko,Tatsuo Matsunaga	2014	19
12	Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study Orphanet Journal of Rare Diseases ·Hideki Mutai,Sylia Terki,Atsushi Shimizu,Chiharu Torii,Kazunori Namba,Noriko Morimoto,Jun Kudoh,Kimitaka Kaga,Kenjiro Kosaki,Tatsuo Matsunaga	2013	74
13	Moderate hearing loss associated with a novel KCNQ4 non-truncating mutation located near the N-terminus of the pore helix Biochemical and Biophysical Research Communications ·Ljijana Radosevic-Jelic,Tatsuo Matsunaga,Kazunori Namba,Hideki Mutai,Yasuhiro Inoue,Kaoru Ogawa	2013	6
14	Mitotic activity and specification of fibrocyte subtypes in the developing rat cochlear lateral wall Neuroscience ·Hideki Mutai,Reiko Nagashima,M Fujii,Tatsuo Matsunaga	2009	12
15	Expression of Pou3f3/Brn‐1 and its genomic methylation in developing auditory epithelium Developmental Neurobiology ·Hideki Mutai,Reiko Nagashima,Yoshinobu Sugitani,Tetsuo Noda,Masato Fujii,Tatsuo Matsunaga	2009	16
16	Characterization of the chicken inward rectifier K+ channel IRK1/Kir2.1 gene BMC Genomics ·Hideki Mutai,Lawrence C. Kenyon,Emily Locke,José Wilson da Silva,J. Carl Oberholtzer	2004	2
17	Absence of the RGS9·Gβ5 GTPase-activating Complex in Photoreceptors of the R9AP Knockout Mouse Journal of Biological Chemistry ·Gábor Keresztes,Kirill A. Martemyanov,Claudia M. Krispel,Hideki Mutai,A. Lath,Stéphane F. Maison,Marie E. Burns,Vadim Y. Arshavsky,Stefan Heller	2004	74
18	Vertebrate and invertebrate TRPV-like mechanoreceptors Cell Calcium ·Hideki Mutai,Stefan Heller	2003	83
19	Expression patterns of the RGS9-1 anchoring protein R9AP in the chicken and mouse suggest multiple roles in the nervous system Molecular and Cellular Neuroscience ·Gábor Keresztes,Hideki Mutai,Hiroshi Hibino,A. J. Hudspeth,Stefan Heller	2003	26
20	PAL31, a Novel Nuclear Protein, Expressed in the Developing Brain Biochemical and Biophysical Research Communications ·Hideki Mutai,Yasushi Toyoshima,Weiyong Sun,Naka Hattori,Satoshi Tanaka,Kunio Shiota	2000	33

About Hideki Mutai

Hideki Mutai is a scholar working on Sensory Systems, Otorhinolaryngology, Neurology, Molecular Biology and Developmental Biology, having authored 63 papers that have together received 1.2k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (40 papers), Vestibular and auditory disorders (11 papers), RNA regulation and disease (8 papers), Connexins and lens biology (8 papers), Ear Surgery and Otitis Media (7 papers), Hearing Loss and Rehabilitation (6 papers), Mitochondrial Function and Pathology (5 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Sensory Systems (626 citations), Otorhinolaryngology (145 citations), Neurology (195 citations), Molecular Biology (663 citations) and Cell Biology (132 citations). Hideki Mutai has collaborated with scholars based in Japan, United States and South Korea. Frequent co-authors include Stefan Heller, Tatsuo Matsunaga, Gábor Keresztes, Noriko Morimoto, Kazunori Namba, Sawako Masuda, Kimitaka Kaga, Atsuko Nakano, Kaoru Ogawa and Yukiko Arimoto. Their work appears in journals such as Scientific Reports, Biochemical and Biophysical Research Communications, Orphanet Journal of Rare Diseases, The Laryngoscope and International Journal of Pediatric Otorhinolaryngology.

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