Yu-ichi Goto
Overview
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
11.
Kushima I, Nakatochi M, Aleksic B, Okada T, Kimura H, Kato H, et al.
Biol Psychiatry
. 2022 Jun;
92(5):362-374.
PMID: 35667888
Background: We aimed to determine the similarities and differences in the roles of genic and regulatory copy number variations (CNVs) in bipolar disorder (BD), schizophrenia (SCZ), and autism spectrum disorder...
12.
Hashimoto K, Baba S, Nakagawa E, Sumitomo N, Takeshita E, Shimizu-Motohashi Y, et al.
Brain Dev
. 2022 May;
44(8):551-557.
PMID: 35589488
Introduction: Pathogenic truncating variants in SMC1A, which is located on chromosome Xp11.2, are known to cause infantile-onset epilepsy and severe intellectual disability in girls. Several studies have reported a correlation...
13.
Tabata K, Ishiyama A, Nakamura Y, Sasaki M, Inoue K, Goto Y
Eur J Med Genet
. 2022 Feb;
65(3):104446.
PMID: 35134569
Microdeletions encompassing the 2p14 region have been reported to cause a novel microdeletion syndrome, characterised by mild intellectual disability (ID) and language impairment (LI), usually showing no congenital malformations or...
14.
Kawazoe T, Tobisawa S, Sugaya K, Uruha A, Miyamoto K, Komori T, et al.
Intern Med
. 2021 Aug;
61(4):547-552.
PMID: 34433719
We herein report a case of myoclonic epilepsy with ragged-red fibers (MERRF) harboring a novel variant in mitochondrial cysteine transfer RNA (MT-TC). A 68-year-old woman presented with progressive myoclonic epilepsy...
15.
Ishigaki H, Sato N, Kimura Y, Takeshita E, Komaki H, Chiba E, et al.
Brain Dev
. 2021 May;
43(9):931-938.
PMID: 34049744
Background: Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) is a progressive neurodegenerative disorder with stroke-like lesions. The common MRI findings are gyral swelling and high signal intensity on...
16.
Akamatsu T, Sugiyama T, Oshima T, Aoki Y, Mizukami A, Goishi K, et al.
Am J Pathol
. 2021 May;
191(7):1303-1313.
PMID: 33964218
Neonatal hypoxic-ischemic encephalopathy (nHIE) is a major neonatal brain injury. Despite therapeutic hypothermia, mortality and sequelae remain severe. The lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is associated with the pathophysiology...
17.
Ibayashi K, Fujino Y, Mimaki M, Fujimoto K, Matsuda S, Goto Y
J Epidemiol
. 2021 Apr;
33(2):68-75.
PMID: 33907064
Background: To provide a better healthcare system for patients with mitochondrial diseases, it is important to understand the basic epidemiology of these conditions, including the number of patients affected. However,...
18.
Bonora E, Chakrabarty S, Kellaris G, Tsutsumi M, Bianco F, Bergamini C, et al.
Brain
. 2021 Apr;
144(5):1451-1466.
PMID: 33855352
Abnormal gut motility is a feature of several mitochondrial encephalomyopathies, and mutations in genes such as TYMP and POLG, have been linked to these rare diseases. The human genome encodes...
19.
Abe-Hatano C, Iida A, Kosugi S, Momozawa Y, Terao C, Ishikawa K, et al.
Am J Med Genet A
. 2021 Feb;
185(5):1468-1480.
PMID: 33624935
Intellectual disability (ID) is characterized by significant limitations in both intellectual functioning and adaptive behaviors, originating before the age of 18 years. However, the genetic etiologies of ID are still...
20.
Kageyama Y, Deguchi Y, Hattori K, Yoshida S, Goto Y, Inoue K, et al.
Brain Behav
. 2021 Feb;
11(4):e02075.
PMID: 33599392
Objective: Our previous metabolomics study showed that the plasma nervonic acid levels were higher in patients with major depressive disorder (MDD) than those in healthy controls and patients with bipolar...