Delisting STAP1

Taking One Step Back in Familial Hypercholesterolemia

(2020) Natalia Loaiza et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Editorial

(2019) Robert A. Hegele   CURRENT OPINION IN LIPIDOLOGY

Evaluation of the role of STAP1 in Familial Hypercholesterolemia

(2019) Magdalena Danyel et al.   Scientific Reports

Predicted pathogenic mutations in STAP1 are not associated with clinically defined familial hypercholesterolemia

(2019) Itziar Lamiquiz-Moneo et al.   ATHEROSCLEROSIS

The complex molecular genetics of familial hypercholesterolaemia

(2018) Amanda J. Berberich et al.   Nature Reviews Cardiology

Clinical Genetic Testing for Familial Hypercholesterolemia

(2018) Amy C. Sturm et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A rare STAP1 mutation incompletely associated with familial hypercholesterolemia

(2018) Francisco Blanco-Vaca et al.   CLINICA CHIMICA ACTA

ClinVar database of global familial hypercholesterolemia-associated DNA variants

(2018) Michael A. Iacocca et al.   HUMAN MUTATION

Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained ClinicallyHighlights

(2016) Jian Wang et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

The Agenda for Familial Hypercholesterolemia

(2015) Samuel S. Gidding et al.   CIRCULATION

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction

(2015) Ingrid Brænne et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations in STAP1 Are Associated With Autosomal Dominant Hypercholesterolemia

(2014) Sigrid W. Fouchier et al.   CIRCULATION RESEARCH

FH4= STAP1 . Another Gene for Familial Hypercholesterolemia?

(2014) Ian N.M. Day   CIRCULATION RESEARCH

Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries

(2014) M. Futema et al.   CLINICAL CHEMISTRY

Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

(2014) M. Cuchel et al.   EUROPEAN HEART JOURNAL

Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

(2013) Nathan O. Stitziel et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

APOE p.Leu167del mutation in familial hypercholesterolemia

(2013) Zuhier Awan et al.   ATHEROSCLEROSIS

Genetics 101 for Cardiologists: Rare Genetic Variants and Monogenic Cardiovascular Disease

(2012) Sali M.K. Farhan et al.   CANADIAN JOURNAL OF CARDIOLOGY

Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia

(2010) J. Rios et al.   HUMAN MOLECULAR GENETICS