Detalhe da pesquisa
1.
Rare variant associations with plasma protein levels in the UK Biobank.
Nature;
622(7982): 339-347, 2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37794183
2.
Functional evaluation of epilepsy-associated KCNT1 variants in multiple cellular systems reveals a predominant gain of function impact on channel properties.
Epilepsia;
64(8): 2126-2136, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37177976
3.
FreeSurfer-based segmentation of hippocampal subfields: A review of methods and applications, with a novel quality control procedure for ENIGMA studies and other collaborative efforts.
Hum Brain Mapp;
43(1): 207-233, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33368865
4.
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.
Acta Neuropathol;
144(1): 107-127, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35551471
5.
The ENIGMA-Epilepsy working group: Mapping disease from large data sets.
Hum Brain Mapp;
2020 May 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32468614
6.
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.
Brain;
141(2): 391-408, 2018 02 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29365066
7.
Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity.
Hum Brain Mapp;
39(11): 4183-4195, 2018 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29947131
8.
Smaller hippocampal CA1 subfield volume in posttraumatic stress disorder.
Depress Anxiety;
35(11): 1018-1029, 2018 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30256497
9.
Temporal Cortex Morphology in Mesial Temporal Lobe Epilepsy Patients and Their Asymptomatic Siblings.
Cereb Cortex;
26(3): 1234-41, 2016 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25576532
10.
Heritability and reliability of automatically segmented human hippocampal formation subregions.
Neuroimage;
128: 125-137, 2016 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26747746
11.
White matter alterations in patients with MRI-negative temporal lobe epilepsy and their asymptomatic siblings.
Epilepsia;
56(10): 1551-61, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26249101
12.
Cerebellum and cognition: evidence for the encoding of higher order rules.
Cereb Cortex;
23(6): 1433-43, 2013 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22617850
13.
Genome-Wide Association Studies of ARIA From the Aducanumab Phase 3 ENGAGE and EMERGE Studies.
Neurology;
102(3): e207919, 2024 Feb 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38165296
14.
Regional increase of cerebral cortex thickness in juvenile myoclonic epilepsy.
Epilepsia;
54(9): e138-41, 2013 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23944956
15.
The genetic regulation of protein expression in cerebrospinal fluid.
EMBO Mol Med;
15(1): e16359, 2023 01 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36504281
16.
The burden of rare protein-truncating genetic variants on human lifespan.
Nat Aging;
2(4): 289-294, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37117740
17.
Microglial activation protects against accumulation of tau aggregates in nondemented individuals with underlying Alzheimer's disease pathology.
Nat Aging;
2(12): 1138-1144, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37118533
18.
Genetic map of regional sulcal morphology in the human brain from UK biobank data.
Nat Commun;
13(1): 6071, 2022 10 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36241887
19.
Genetic variants associated with longitudinal changes in brain structure across the lifespan.
Nat Neurosci;
25(4): 421-432, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35383335
20.
BioInfograph: An Online Tool to Design and Display Multi-Panel Scientific Figure Interactively.
Front Genet;
12: 784531, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35069687