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Lipid traits and whole genome sequencing association studies

dc.contributor.authorRossi, Niccolò
dc.contributor.authorBourbon, Mafalda
dc.contributor.authorFalchi, Mario
dc.date.accessioned2017-11-10T12:05:36Z
dc.date.available2017-11-10T12:05:36Z
dc.date.issued2017-10
dc.description.abstractBackground: Genome-wide association studies (GWAS) have significantly advanced the genetic study of complex human traits. With the advent of next generation sequencing technologies, whole genome sequencing based GWAS are expected to provide further opportunities for the discovery of low frequency and rare variants with a large effect size. Moreover heritability of lipid traits has been estimated from 30% to 70 in family-based studies. Given the strong genetic component, twins represent a powerful resource to explore the genetic architecture of dyslipidemias. Objectives: Still a big gap exists between clinical and genetic diagnosis of dyslipidemic disorders. Almost the 60% of the patients with a clinical diagnosis of Familial hypercholesterolemia (FH) still lacks of a genetic diagnosis. It has been suggested that this gap might include a high percentage of individuals with a polygenic or environmental forms of dyslipidemia, while a small percentage of individuals may carry a mutation in some genes not yet known to be associated with FH. Here I present the results of an association analysis of lipids traits and whole genome sequencing data coming from 1762 twins from the TiwnsUK cohort.pt_PT
dc.description.sponsorshipNiccolò Rossi was founded by SFRH/BD/106086/2015.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4823
dc.language.isoengpt_PT
dc.subjectFamilial Hypercholesterolemiapt_PT
dc.subjectDyslipidemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleLipid traits and whole genome sequencing association studiespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBeja, Portugalpt_PT
oaire.citation.title2nd BioSys Retreat, 6-7 October 2017pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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