Detalhe da pesquisa
1.
Heritability of cognitive and emotion processing during functional MRI in a twin sample.
Hum Brain Mapp
; 45(1): e26557, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38224545
2.
Change in Cerebrospinal Fluid Tau Microtubule Binding Region Detects Symptom Onset, Cognitive Decline, Tangles, and Atrophy in Dominantly Inherited Alzheimer's Disease.
Ann Neurol
; 93(6): 1158-1172, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36843330
3.
Brain network decoupling with increased serum neurofilament and reduced cognitive function in Alzheimer's disease.
Brain
; 146(7): 2928-2943, 2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36625756
4.
Investigation of sex differences in mutation carriers of the Dominantly Inherited Alzheimer Network.
Alzheimers Dement
; 20(1): 47-62, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37740921
5.
Presenilin-1 mutation position influences amyloidosis, small vessel disease, and dementia with disease stage.
Alzheimers Dement
; 20(4): 2680-2697, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38380882
6.
α-Synuclein seed amplification assay detects Lewy body co-pathology in autosomal dominant Alzheimer's disease late in the disease course and dependent on Lewy pathology burden.
Alzheimers Dement
; 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38666355
7.
T1 and FLAIR signal intensities are related to tau pathology in dominantly inherited Alzheimer disease.
Hum Brain Mapp
; 44(18): 6375-6387, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37867465
8.
Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sample.
Psychol Med
; 53(4): 1215-1223, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37010213
9.
Negative association between anterior insula activation and resilience during sustained attention: an fMRI twin study.
Psychol Med
; 53(7): 3187-3199, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37449488
10.
Autosomal dominant and sporadic late onset Alzheimer's disease share a common in vivo pathophysiology.
Brain
; 145(10): 3594-3607, 2022 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35580594
11.
Higher systolic blood pressure in early-mid adulthood is associated with poorer cognitive performance in those with a dominantly inherited Alzheimer's disease mutation but not in non-carriers. Results from the DIAN study.
Alzheimers Dement
; 19(11): 4999-5009, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37087693
12.
Plasma glial fibrillary acidic protein in autosomal dominant Alzheimer's disease: Associations with Aß-PET, neurodegeneration, and cognition.
Alzheimers Dement
; 19(7): 2790-2804, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36576155
13.
Pattern and implications of neurological examination findings in autosomal dominant Alzheimer disease.
Alzheimers Dement
; 19(2): 632-645, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35609137
14.
Biomarker clustering in autosomal dominant Alzheimer's disease.
Alzheimers Dement
; 19(1): 274-284, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35362200
15.
Covariance-based vs. correlation-based functional connectivity dissociates healthy aging from Alzheimer disease.
Neuroimage
; 261: 119511, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35914670
16.
CSF Tau phosphorylation at Thr205 is associated with loss of white matter integrity in autosomal dominant Alzheimer disease.
Neurobiol Dis
; 168: 105714, 2022 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35358703
17.
Alzheimer's disease research progress in Australia: The Alzheimer's Association International Conference Satellite Symposium in Sydney.
Alzheimers Dement
; 18(1): 178-190, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34058063
18.
Different rates of cognitive decline in autosomal dominant and late-onset Alzheimer disease.
Alzheimers Dement
; 18(10): 1754-1764, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34854530
19.
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
J Psychiatry Neurosci
; 46(2): E247-E257, 2021 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33729739
20.
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Brain
; 143(3): 783-799, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32185393