Associated Papers
FinnGen provides genetic insights from a well-phenotyped isolated population.
Kurki MI et al.
Nature, 2023
36653562 (PubMed )
Supplement: 41586_2022_5473_MOESM4_ESM.xlsx › Supplementary_Table_11
Genetic associations of protein-coding variants in human disease.
Sun BB et al.
Nature, 2022
Rare variants in LRRK1 and Parkinson's disease.
Schulte EC et al.
Neurogenetics, 2014
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway.
Haugarvoll K et al.
Neuroscience Letters, 2007
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease.
Taylor JP et al.
Neurogenetics, 2007
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