Manabu Funayama
Overview
Explore the profile of Manabu Funayama including associated specialties, affiliations and a list of published articles.
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Articles
101
Citations
2592
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Recent Articles
1.
Okuzumi A, Hatano T, Matsumoto G, Nojiri S, Ueno S, Imamichi-Tatano Y, et al.
Nat Med
. 2025 Jan;
31(2):698.
PMID: 39856337
No abstract available.
2.
Daida K, Yoshino H, Malik L, Baker B, Ishiguro M, Genner R, et al.
Ann Neurol
. 2024 Dec;
97(4):753-765.
PMID: 39699073
Objective: Variants in PRKN and PINK1 are the leading cause of early-onset autosomal recessive Parkinson's disease, yet many cases remain genetically unresolved. We previously identified a 7 megabases complex structural...
3.
Ishiguro M, Funayama M, Hatano T, Nishida H, Wada Y, Noda K, et al.
Heliyon
. 2024 Aug;
10(15):e35271.
PMID: 39170205
Background: Biallelic variants in , which encodes protein-nucleic acid deglycase DJ-1, can cause early-onset Parkinson's disease (PD). Although many patients with variants have been identified from European and Middle Eastern...
4.
Ikeda A, Meng H, Taniguchi D, Mio M, Funayama M, Nishioka K, et al.
PNAS Nexus
. 2024 Aug;
3(8):pgae319.
PMID: 39131911
CHCHD2 and CHCHD10, linked to Parkinson's disease and amyotrophic lateral sclerosis-frontotemporal dementia (ALS), respectively, are mitochondrial intermembrane proteins that form a heterodimer. This study aimed to investigate the impact of...
5.
Daida K, Yoshino H, Malik L, Baker B, Ishiguro M, Genner R, et al.
medRxiv
. 2024 Aug;
PMID: 39108517
Background: Mutations within the genes and are the leading cause of early onset autosomal recessive Parkinson's disease (PD). However, the genetic cause of most early-onset PD (EOPD) cases still remains...
6.
Tezuka T, Ishiguro M, Taniguchi D, Osogaguchi E, Shiba-Fukushima K, Ogata J, et al.
Neurobiol Dis
. 2024 Jun;
199:106571.
PMID: 38901781
Leucine-rich repeat kinase 2 (LRRK2) is the most common gene responsible for familial Parkinson's disease (PD). The gene product of LRRK2 contains multiple protein domains, including armadillo repeat, ankyrin repeat,...
7.
Hattori N, Funayama M, Imai Y, Hatano T
J Neural Transm (Vienna)
. 2024 Mar;
131(6):709-719.
PMID: 38478097
Twenty-five years have passed since the causative gene for familial Parkinson's disease (PD), Parkin (now PRKN), was identified in 1998; PRKN is the most common causative gene in young-onset PD....
8.
Ong S, Funayama M, Mangyoku Y, Kawai H, Yoshino H, Li Y, et al.
Mov Disord
. 2023 Dec;
39(3):626-627.
PMID: 38146173
No abstract available.
9.
Ishikawa K, Shiga T, Funayama M, Hattori N, Akamatsu W
Stem Cell Res
. 2023 Dec;
74:103271.
PMID: 38100917
Appropriate control induced pluripotent stem cells (iPSCs) are essential for studying iPSCs derived from patients with Parkinson's disease (PD). In this study, we established an iPSC line from a healthy...
10.
Ishikawa K, Shiga T, Funayama M, Hattori N, Akamatsu W
Stem Cell Res
. 2023 Dec;
74:103270.
PMID: 38100911
The appropriate control of induced pluripotent stem cells (iPSCs) is essential for studying iPSCs derived from patients with Parkinson's disease (PD). Here, we established an iPSC line from a healthy...