Associated Papers
Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS.
Abner E et al.
Nature Communications, 2025
41062462 (PubMed )
Supplement: 41467_2025_64006_MOESM6_ESM.xlsx › Figure1a
The genetic architecture of fibromyalgia across 2.5 million individuals.
Kerrebijn I et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
41001472 (PubMed )
Supplement: media-2.xlsx › S3
Large-scale whole-exome sequencing of neuropsychiatric diseases and traits in 350,770 adults.
Deng YT et al.
Nature Human Behaviour, 2024
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_8
Somatic signature of brain-specific single nucleotide variations in sporadic Alzheimer's disease.
Parcerisas A et al.
Journal of Alzheimer's Disease : Jad, 2014
25024348 (PubMed )
Supplement: sj-xls-6-alz-10.3233_jad-140891.xls › P3H
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