Detalhe da pesquisa
1.
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
; 611(7934): 115-123, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36180795
2.
Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.
Ann Neurol
; 95(2): 325-337, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37787451
3.
Genetic Risk Score Improves Risk Stratification for Anticoagulation-Related Intracerebral Hemorrhage.
Stroke
; 54(3): 791-799, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36756894
4.
Genetic Architecture of Stroke of Undetermined Source: Overlap with Known Stroke Etiologies and Associations with Modifiable Risk Factors.
Ann Neurol
; 91(5): 640-651, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35178771
5.
Genetically predicted on-statin LDL response is associated with higher intracerebral haemorrhage risk.
Brain
; 145(8): 2677-2686, 2022 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35598204
6.
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
Brain
; 145(3): 1029-1037, 2022 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983064
7.
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
; 612(7938): E7, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36376532
8.
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4.
Genet Med
; 24(11): 2308-2317, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36056923
9.
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Neurogenetics
; 22(1): 71-79, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486633
10.
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Genet Med
; 22(11): 1851-1862, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32713943
11.
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.
Brain
; 141(12): 3331-3342, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30476002
12.
Beyond the Limits of Visual Learning: Prediction of Time From Onset From Noncontrast CT of Acute Ischemic Stroke.
Stroke
; 54(1): e7-e8, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36475469
13.
Hereditary ataxias and paraparesias: clinical and genetic update.
Curr Opin Neurol
; 31(4): 462-471, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29847346
14.
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Genet Med
; 23(10): 2021, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33353973
15.
Genetic variation supports a causal role for valproate in prevention of ischemic stroke.
Int J Stroke
; 19(1): 84-93, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37489815
16.
Educational attainment, severity and short-term prognosis of intracerebral haemorrhage.
BMJ Neurol Open
; 6(1): e000593, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38736584
17.
Genetic and non-genetic components of family history of stroke and heart disease: a population-based study among adopted and non-adopted individuals.
medRxiv
; 2023 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37398414
18.
Genetic and Nongenetic Components of Stroke Family History: A Population Study of Adopted and Nonadopted Individuals.
J Am Heart Assoc
; 12(20): e031566, 2023 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37830349
19.
Pleiotropy analysis between lobar intracerebral hemorrhage and CSF ß-amyloid highlights new and established associations.
Int J Stroke
; 18(7): 804-811, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36705426
20.
Genetic variation supports a causal role for valproate in prevention of ischemic stroke.
medRxiv
; 2023 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36865155