Associated Papers
Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.
Mitchell J et al.
Nature Communications, 2025
Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.
Mitchell J et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
FinnGen provides genetic insights from a well-phenotyped isolated population.
Kurki MI et al.
Nature, 2023
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution.
Kanai M et al.
Cell Genomics, 2022
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis.
Dhindsa RS et al.
Communications Biology, 2021
Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer.
Zekavat SM et al.
Medrxiv : the Preprint Server for Health Sciences, 2020
33236019 (PubMed )
Supplement: media-2.xlsx › S.Data3
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