Detalhe da pesquisa
1.
An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access.
PLoS One
; 17(9): e0272260, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36067162
2.
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.
BMJ Open
; 12(10): e064695, 2022 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36198465