Manabu Funayama

7.7k total citations · 1 hit paper
76 papers, 3.8k citations indexed

About

Manabu Funayama is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Manabu Funayama has authored 76 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Neurology, 26 papers in Molecular Biology and 23 papers in Neurology. Recurrent topics in Manabu Funayama's work include Parkinson's Disease Mechanisms and Treatments (53 papers), Neurological diseases and metabolism (23 papers) and Neurological disorders and treatments (15 papers). Manabu Funayama is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (53 papers), Neurological diseases and metabolism (23 papers) and Neurological disorders and treatments (15 papers). Manabu Funayama collaborates with scholars based in Japan, United States and Canada. Manabu Funayama's co-authors include Nobutaka Hattori, Fumiya Obata, Kazuko Hasegawa, Hisayuki Kowa, Shoji Tsuji, Hiroyuki Tomiyama, Hiroyo Yoshino, Masaaki Saito, Kenya Nishioka and Yuanzhe Li and has published in prestigious journals such as Nature Communications, Neurology and Annals of Neurology.

In The Last Decade

Manabu Funayama

72 papers receiving 3.7k 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.

PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria

2012 415 citations Manabu Funayama, Kahori Shiba‐Fukushima et al. profile →

Peers

Countries citing papers authored by Manabu Funayama

Since Specialization

Citations

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

Fields of papers citing papers by Manabu Funayama

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manabu Funayama

This figure shows the co-authorship network connecting the top 25 collaborators of Manabu Funayama. A scholar is included among the top collaborators of Manabu Funayama 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 Manabu Funayama. Manabu Funayama 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	Motor and Cognitive Outcome After Subthalamic Nucleus Deep Brain Stimulation in Patients with Parkinson's Disease Harboring GBA1 Variant 2025 ·Movement Disorders Clinical Practice ·(unknown), Genko Oyama, Mai Shimizu, Haruka Takeshige‐Amano, Takashi Ogawa, Wataru Sako, Noriko Nishikawa, Taku Hatano, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Masanobu Ito, Hirokazu Iwamuro, Atsushi Umemura, (unknown)	1
2	Identification of DAGLB variants in Japanese early-onset Parkinson’s disease 2025 ·Journal of Neural Transmission ·Yue Luo, Manabu Funayama, (unknown), Yuanzhe Li, Hiroyo Yoshino, Satoshi Yamashita, Akira Mori, Ryoichi Nakamura, Yoshio Hashizume, Mari Yoshida, Yuichi Riku, (unknown), Nobutaka Hattori	0
3	The Utility of Long‐Read Sequencing in Diagnosing Early Onset Parkinson's Disease 2024 ·Annals of Neurology ·Kensuke Daida, Hiroyo Yoshino, Laksh Malik, (unknown), (unknown), (unknown), Kimberly Paquette, Yuanzhe Li, Kenya Nishioka, (unknown), Makito Hirano, Kenta Takahashi, Mikhail Kolmogorov, Kimberley J. Billingsley, Manabu Funayama, Cornelis Blauwendraat, Nobutaka Hattori	2
4	Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes 2023 ·Stem Cell Research ·Kei‐ichi Ishikawa, (unknown), Manabu Funayama, Nobutaka Hattori, Wado Akamatsu	0
5	Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease 2023 ·Movement Disorders ·Kensuke Daida, Manabu Funayama, Kimberley J. Billingsley, Laksh Malik, (unknown), Hampton L. Leonard, Mary B. Makarious, Hirotaka Iwaki, Jinhui Ding, J. Raphael Gibbs, (unknown), Hiroyo Yoshino, Kotaro Ogaki, Genko Oyama, Kenya Nishioka, Risa Nonaka, Wado Akamatsu, Cornelis Blauwendraat, Nobutaka Hattori	15
6	Molecular genetics of Parkinson’s disease: Contributions and global trends 2022 ·Journal of Human Genetics ·Manabu Funayama, Kenya Nishioka, Yuanzhe Li, Nobutaka Hattori	100
7	Genotype-phenotype correlation of Parkinson's disease with PRKN variants 2022 ·Neurobiology of Aging ·Hiroyo Yoshino, Yuanzhe Li, Kenya Nishioka, Kensuke Daida, (unknown), Yuta Ishiguro, Daisuke Yamada, Nana Izawa, Katsunori Nishi, Noriko Nishikawa, Genko Oyama, Taku Hatano, Shinichiro Nakamura, Asako Yoritaka, Yumiko Motoi, Manabu Funayama, Nobutaka Hattori	20
8	Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p.D620N with long-term follow-up 2021 ·Parkinsonism & Related Disorders ·(unknown), Yuanzhe Li, Hiroyo Yoshino, Kensuke Daida, Yuta Ishiguro, Genko Oyama, Shinji Saiki, Manabu Funayama, Nobutaka Hattori, Kenya Nishioka	14
9	Identifying Therapeutic Agents for Amelioration of Mitochondrial Clearance Disorder in Neurons of Familial Parkinson Disease 2020 ·Stem Cell Reports ·Akihiro Yamaguchi, Kei‐ichi Ishikawa, Tsuyoshi Inoshita, Kahori Shiba‐Fukushima, Shinji Saiki, Taku Hatano, Akio Mori, Yutaka Oji, Ayami Okuzumi, Yuanzhe Li, Manabu Funayama, Yuzuru Imai, Nobutaka Hattori, Wado Akamatsu	43
10	COQ2 variants in Parkinson’s disease and multiple system atrophy 2018 ·Journal of Neural Transmission ·(unknown), Kazuaki Kanai, Yuanzhe Li, Hiroyo Yoshino, Kaoru Mogushi, (unknown), Aya Ikeda, Sumihiro Kawajiri, Yasuyuki Okuma, Kenichi Kashihara, Tatsuya Sato, Hiroshi Kondo, Manabu Funayama, Kenya Nishioka, Nobutaka Hattori	8
11	Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice 2016 ·American Journal Of Pathology ·Shigeto Sato, Masato Koike, Manabu Funayama, Junji Ezaki, Takahiro Fukuda, Takashi Ueno, Yasuo Uchiyama, Nobutaka Hattori	28
12	EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population 2014 ·Parkinsonism & Related Disorders ·Kenya Nishioka, Manabu Funayama, Carles Vilariño‐Güell, Kotaro Ogaki, (unknown), Ryogen Sasaki, Yasumasa Kokubo, Shigeki Kuzuhara, Jennifer M. Kachergus, Stephanie A. Cobb, Hirohide Takahashi, Yoshikuni Mizuno, Matthew J. Farrer, Owen A. Ross, Nobutaka Hattori	13
13	Possible involvement of iron-induced oxidative insults in neurodegeneration 2014 ·Neuroscience Letters ·Takeshi Asano, Masato Koike, (unknown), Yukiko Takeda, Tomoko Nakagawa, Taku Hatano, Satoshi Ohashi, Manabu Funayama, Kenji Yoshimi, Masato Asanuma, Shinya Toyokuni, Hideki Mochizuki, Yasuo Uchiyama, Nobutaka Hattori, Kazuhiro Iwaï	10
14	Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease 2013 ·Neurobiology of Aging ·Yuanzhe Li, Takeshi Sekine, Manabu Funayama, Lin Li, Hiroyo Yoshino, Kenya Nishioka, Hiroyuki Tomiyama, Nobutaka Hattori	60
15	VPS35 mutation in Japanese patients with typical Parkinson's disease 2012 ·Movement Disorders ·Maya Ando, Manabu Funayama, Yuanzhe Li, Kenichi Kashihara, (unknown), (unknown), Chizuko Toyoda, Katsuhiko Noguchi, Takashi Hashimoto, Naoki Nakano, Ryogen Sasaki, Yasumasa Kokubo, Shigeki Kuzuhara, Kotaro Ogaki, Chikara Yamashita, Hiroyo Yoshino, Taku Hatano, Hiroyuki Tomiyama, Nobutaka Hattori	65
16	Impaired in vivo dopamine release in parkin knockout mice 2010 ·Brain Research ·Genko Oyama, Kenji Yoshimi, (unknown), (unknown), Yong‐Ri Ren, Manabu Funayama, Yasushi Shimo, Ryōsuke Takahashi, Taizo Nakazato, Shigeru Kitazawa, Nobutaka Hattori	46
17	[Molecular genetics of PINK1]. 2007 ·PubMed ·Manabu Funayama, Nobutaka Hattori	1
18	An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family 2005 ·Annals of Neurology ·Manabu Funayama, Kazuko Hasegawa, Etsuro Ohta, Noriko Kawashima, Masaru Komiyama, Hisayuki Kowa, Shoji Tsuji, Fumiya Obata	204
19	A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2–q13.1 2002 ·Annals of Neurology ·Manabu Funayama, Kazuko Hasegawa, Hisayuki Kowa, Masaaki Saito, Shoji Tsuji, Fumiya Obata	481
20	A keratin K5 mutation (Leu 463→Pro) in a family with the Weber-Cockayne type of epidermolysis bullosa simplex 1997 ·Archives of Dermatological Research ·Kazuo Nomura, (unknown), Xianzhi Meng, Katsuto Tamai, Daisuke Sawamura, Masakiyo Hosokawa, (unknown), Manabu Funayama, Isao Hashimoto	4

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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