Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
2022 · Nature Genetics · 140 citations
https://doi.org/10.1038/s41588-021-01007-6
D
Doris Škorić‐Milosavljević
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
14
Papers
565
Citations
11
h-index
11
i10-index
Doris Škorić‐Milosavljević is an academic researcher from Amsterdam University Medical Centers. The author has contributed to research in topics: Cardiac electrophysiology and arrhythmias & Congenital heart defects research & Congenital Heart Disease Studies. The author has an h-index of 11, co-authored 12 publications.
ORCID: 0000-0001-7089-3703Papers by this author
worksEnhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2020 · Genetics in Medicine · 102 citations
https://doi.org/10.1038/s41436-020-00946-5
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
2021 · Circulation Research · 38 citations
https://doi.org/10.1161/circresaha.120.317107
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
2021 · Genetics in Medicine · 0 citations
https://doi.org/10.1038/s41436-021-01279-7
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat