Detalhe da pesquisa
1.
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.
Brain
; 145(6): 1992-2007, 2022 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511193
2.
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Kidney Int
; 102(3): 624-639, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35716955
3.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int
; 99(4): 926-939, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33137338
4.
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Stroke
; 51(7): 2111-2121, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32517579
5.
Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.
Genet Med
; 20(11): 1414-1422, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29543232
6.
Targeted next-generation sequencing makes new molecular diagnoses and expands genotype-phenotype relationship in Ehlers-Danlos syndrome.
Genet Med
; 18(11): 1119-1127, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27011056
7.
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease.
Nat Med
; 29(4): 950-962, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37069360
8.
Telomere length and brain aging: A systematic review and meta-analysis.
Ageing Res Rev
; 80: 101679, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35777725
9.
Leukocyte Telomere Length Is Related to Brain Parenchymal Fraction and Attention/Speed in the Elderly: Results of the Austrian Stroke Prevention Study.
Front Psychiatry
; 11: 100, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32180739
10.
Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton.
Front Genet
; 10: 856, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31608108
11.
Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.
Front Genet
; 10: 732, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31475037