Detalhe da pesquisa
1.
Disruption of a RAC1-centred network is associated with Alzheimer's disease pathology and causes age-dependent neurodegeneration.
Hum Mol Genet
; 29(5): 817-833, 2020 03 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31942999
2.
Prevalence of dementia in people with intellectual disabilities: Cross-sectional study.
Int J Geriatr Psychiatry
; 35(4): 414-422, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31894597
3.
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia.
J Hum Genet
; 63(12): 1259-1267, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30266950
4.
Japanese and North American Alzheimer's Disease Neuroimaging Initiative studies: Harmonization for international trials.
Alzheimers Dement
; 14(8): 1077-1087, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29753531
5.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Alzheimers Dement
; 13(7): 727-738, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28183528
6.
Evaluation of polygenic risks for narcolepsy and essential hypersomnia.
J Hum Genet
; 61(10): 873-878, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27305985
7.
An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbances.
Neuropathology
; 36(3): 295-304, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26610886
8.
Systematic review and meta-analysis of Japanese familial Alzheimer's disease and FTDP-17.
J Hum Genet
; 60(5): 281-3, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25694106
9.
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
Ann Neurol
; 76(3): 379-92, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25043464
10.
Immune-related pathways including HLA-DRB1(∗)13:02 are associated with panic disorder.
Brain Behav Immun
; 46: 96-103, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25582808
11.
A polymorphism in CCR1/CCR3 is associated with narcolepsy.
Brain Behav Immun
; 49: 148-55, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25986216
12.
Role of the p.E66Q variant of GLA in the progression of chronic kidney disease.
Clin Exp Nephrol
; 19(2): 225-30, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24718812
13.
Relative ratio and level of amyloid-ß 42 surrogate in cerebrospinal fluid of familial Alzheimer disease patients with presenilin 1 mutations.
Neurodegener Dis
; 13(2-3): 166-70, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24192669
14.
Polygenic effects on the risk of Alzheimer's disease in the Japanese population.
Alzheimers Res Ther
; 16(1): 45, 2024 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38414085
15.
Telomelysin shows potent antitumor activity through apoptotic and non-apoptotic cell death in soft tissue sarcoma cells.
Cancer Sci
; 104(9): 1178-88, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23718223
16.
Prevalence and modifiable risk factors for dementia in persons with intellectual disabilities.
Alzheimers Res Ther
; 15(1): 125, 2023 07 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37464412
17.
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.
N Engl J Med
; 360(17): 1729-39, 2009 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-19387015
18.
Different AT(N) profiles and clinical progression classified by two different N markers using total tau and neurofilament light chain in cerebrospinal fluid.
BMJ Neurol Open
; 4(2): e000321, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36046332
19.
A genome-wide CNV association study on panic disorder in a Japanese population.
J Hum Genet
; 56(12): 852-6, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22011818
20.
Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly.
J Med Genet
; 47(8): 538-48, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20577004