Yu-ichi Goto
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Explore the profile of Yu-ichi Goto including associated specialties, affiliations and a list of published articles.
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Articles
212
Citations
4005
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Recent Articles
1.
Funaguma S, Iida A, Saito Y, Tanboon J, De Los Reyes F, Sonehara K, et al.
Nat Commun
. 2025 Feb;
16(1):1318.
PMID: 39920152
Transposon-like human element 1B (THE1B) originates from ancient retroviral sequences integrated into the primate genome approximately 50 million years ago, now accounting for at least 27,233 copies in the human...
2.
Abe-Hatano C, Inoue K, Takeshita E, Kawai Y, Tokunaga K, Goto Y
J Med Genet
. 2024 Oct;
61(12):1119-1122.
PMID: 39467646
Pathogenic variants of WD repeat domain 45 () cause neurodegeneration with brain iron accumulation 5 (NBIA5), which is characterised by progressive neurological regression and brain iron accumulation in adulthood. Early...
3.
Iijima K, Fujii H, Suzuki F, Murayama K, Goto Y, Saito Y, et al.
Front Neurol
. 2024 Jul;
15:1419104.
PMID: 39081340
Introduction: Low-grade epilepsy-associated tumors are the second most common histopathological diagnoses in cases of drug-resistant focal epilepsy. However, the connection between neuroimaging features and genetic alterations in these tumors is...
4.
Enokida T, Yoshida N, Tatsumi M, Hidese S, Goto Y, Hoshino M, et al.
Heliyon
. 2024 May;
10(10):e30695.
PMID: 38770306
Schizophrenia is a syndrome with multiple etiologies, one of which is the potential for an autoimmune disease of the brain such as N-methyl-d-aspartate receptor (NMDAR) encephalitis, which can induce psychosis...
5.
Shirakawa Y, Li H, Inoue Y, Izumi H, Kaga Y, Goto Y, et al.
IBRO Neurosci Rep
. 2024 Jan;
16:67-77.
PMID: 38229888
The homozygous () mouse, which shows hearing impairment, also exhibits anxiety accompanied by a reduction in cortical parvalbumin (PV)-positive GABAergic interneurons. Recently, a mutation in splicing factor Ser/Arg repetitive matrix...
6.
Kawai Y, Watanabe Y, Omae Y, Miyahara R, Khor S, Noiri E, et al.
PLoS Genet
. 2023 Dec;
19(12):e1010625.
PMID: 38060463
The Japanese archipelago is a terminal location for human migration, and the contemporary Japanese people represent a unique population whose genomic diversity has been shaped by multiple migrations from Eurasia....
7.
Aoki Y, Dai H, Furuta F, Akamatsu T, Oshima T, Takahashi N, et al.
Cell Commun Signal
. 2023 Jun;
21(1):126.
PMID: 37268943
Background: Microglial cells play an important role in the immune system in the brain. Activated microglial cells are not only injurious but also neuroprotective. We confirmed marked lectin-like oxidized low-density...
8.
Akahoshi K, Nakagawa E, Goto Y, Inoue K
BMC Med Genomics
. 2023 Mar;
16(1):43.
PMID: 36879246
Background: X-linked methyl-CpG-binding protein 2 (MECP2) duplication syndrome is prevalent in approximately 1% of X-linked intellectual disabilities. Accumulating evidence has suggested that MECP2 is the causative gene of MECP2 duplication...
9.
Dai H, Kitami Y, Goto Y, Itoh M
Int J Mol Sci
. 2022 Nov;
23(22).
PMID: 36430502
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the gene that encodes methyl CpG-binding protein 2 (MECP2) and is characterized by the loss of acquired motor...
10.
Omae Y, Goto Y, Tokunaga K
Hum Genome Var
. 2022 Nov;
9(1):38.
PMID: 36333292
There are six national centers (6NCs) for advanced and specialized medicine in Japan that conduct basic and clinical research on major diseases that have a substantial impact on national health....