This study was performed under the direction of Principal Investigators Jer-Yuarn Wu, PhD and Tsong-Hai Lee, MD, PhD at the following institutions: Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; Chang Gung Memorial Hospital, Linkou Medical Center, and Chang Gung University College of Medicine, Taoyuan, Taiwan.
The CADISP 2015 dataset contains summary-level data.
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Cheng Y-C, et al.
Stroke. 2016 Feb;47(2):307-16. doi: 10.1161/STROKEAHA.115.011328.
PMID:26732560
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Both summary-level and individual-level data were generated for the ICH GWAS 2014 dataset. Individual-level data are available for the GOCHA and ISGC European Centers subjects. Summary-level data are available for the full cohort.
Both summary-level and individual-level data were generated for the GERFHS III 2017 dataset.
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Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.
Prins BP, et al.
Genome Biol. 2018 Jul 17;19(1):87. doi: 10.1186/s13059-018-1457-6
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Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.
Lin H, et al.
Circ Genom Precis Med. 2018;11:e002037. doi: 10.1161/CIRCGEN.117.002037
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Do R, et al.
Nature. 2015 Feb 5;518(7537):102-6. doi: 10.1038/nature13917
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators, et al.
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium.
Weng LC, et al.
Sci Rep. 2017 Sep 12;7(1):11303. doi: 10.1038/s41598-017-09396-7