Last Updated: 09/26/2026
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Found 29 publications
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection.
Journal: Research square
Published: January 03, 2024
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection.
Journal: medRxiv : the preprint server for health sciences
Published: December 18, 2023
Correlations between causal effect sizes of proximal SNPs vary with functional annotations and implicate stabilizing selection.
Journal: Nature genetics
Published: December 04, 2023
Association of structural variation with cardiometabolic traits in Finns.
Journal: American journal of human genetics
Published: December 12, 2020
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Journal: Nature
Published: November 06, 2019
Mapping and characterization of structural variation in 17,795 human genomes.
Journal: Nature
Published: December 29, 2018
svtools: population-scale analysis of structural variation.
Journal: Bioinformatics (Oxford, England)
Published: December 19, 2018
Exome sequencing of Finnish isolates enhances rare-variant association power.
Journal: Nature
Published: November 05, 2018
Identification of Drivers of Aneuploidy in Breast Tumors.
Journal: Cell reports
Published: July 11, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.
Journal: Nature genetics
Published: May 27, 2017
Potential molecular consequences of transgene integration: The R6/2 mouse example.
Journal: Scientific reports
Published: September 23, 2016
Last Updated: 09/26/2026