Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Broad Institute · Harvard University · +67 more institutions
Indexed incrossrefpubmed
Abstract
No abstract available for this paper.
Citation impact
678
total citations
- FWCI
- 63.02
- Percentile
- 100%
- References
- 55
Citations per year
Authors
94- RDRon DoCorresponding
Broad Institute, Harvard University, Massachusetts General Hospital, Center for Human Genetics
- NONathan O. Stitziel
Washington University in St. Louis
- HWHong‐Hee Won
Broad Institute, Harvard University, Massachusetts General Hospital, Center for Human Genetics
- ABAnders Berg Jørgensen
University of Copenhagen, Copenhagen University Hospital, Rigshospitalet
- SDStefano Duga
University of Milan
Topics & keywords
Topics
Keywords
- LDL receptor
- Exome
- Exome sequencing
- Genetics
- Myocardial infarction
- Familial hypercholesterolemia
- PCSK9
- Allele
UN Sustainable Development Goals
- Good health and well-being
No related works found for this paper.
Funding
- MGMassachusetts General HospitalAward: R01HL107816
- CCCleveland Clinic
- FFFoundation for Barnes-Jewish Hospital
- DFDonovan Family Foundation
- FLFondation LeducqAward: T32HL007208
- NINational Institutes of HealthAwards: P01 HL076491, T32HL007604, T32HL007208, P01 HL098055, HL076491
- CICanadian Institutes of Health Research
- MRMedical Research CouncilAward: MR/L003120/1
- NHNational Heart, Lung, and Blood InstituteAwards: P01 HL098055, HL-102924, RC2 HL-102925, P01 HL076491, RC2 HL-103010, R01HL107816, HL-103010, HL-102923, RC2 HL-102924, RC2 HL-102923, RC2 HL-102926, T32HL007208, T32HL007604
- NHNational Human Genome Research InstituteAward: 5U54HG003067