A Comparative Analysis of Phenotypic Predictors of Mutations in Familial Hypercholesterolemia

Recent advances in genetic testing for familial hypercholesterolemia

(2017) Michael A. Iacocca et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing

(2017) Joshua W. Knowles et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Cost-effectiveness of a cascade screening program for the early detection of familial hypercholesterolemia

(2017) Pablo Lázaro et al.   Journal of Clinical Lipidology

Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217

(2016) Marianne Benn et al.   EUROPEAN HEART JOURNAL

A new electronic screening tool for identifying risk of familial hypercholesterolaemia in general practice

(2016) Lakkhina Troeung et al.   HEART

Familial combined hyperlipidemia and hyperlipoprotein(a) as phenotypic mimics of familial hypercholesterolemia: Frequencies, associations and predictions

(2016) Katrina L. Ellis et al.   Journal of Clinical Lipidology

US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registry

(2016) Zahid S. Ahmad et al.   Journal of Clinical Lipidology

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

(2016) Amit V. Khera et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales

(2015) K. Haralambos et al.   ATHEROSCLEROSIS

The Agenda for Familial Hypercholesterolemia

(2015) Samuel S. Gidding et al.   CIRCULATION

Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment

(2015) Albert Wiegman et al.   EUROPEAN HEART JOURNAL

Prevalence and treatment of familial hypercholesterolaemia in Australian communities

(2015) Gerald F. Watts et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Elevated lipoprotein(a), hypertension and renal insufficiency as predictors of coronary artery disease in patients with genetically confirmed heterozygous familial hypercholesterolemia

(2015) Dick C. Chan et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Mutations in STAP1 Are Associated With Autosomal Dominant Hypercholesterolemia

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

LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias

(2014) Christopher T. Johansen et al.   JOURNAL OF LIPID RESEARCH

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society

(2013) B. G. Nordestgaard et al.   EUROPEAN HEART JOURNAL

Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation

(2013) Gerald F. Watts et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study

(2013) Philippa J Talmud et al.   LANCET

Genetic analysis of familial hypercholesterolaemia in Western Australia

(2012) Amanda J. Hooper et al.   ATHEROSCLEROSIS

Effectiveness of alternative strategies to define index case phenotypes to aid genetic diagnosis of familial hypercholesterolaemia

(2012) Rosemary E J Clarke et al.   HEART

Lipoprotein(a)-cholesterol: A significant component of serum cholesterol

(2011) Kiyoko Kinpara et al.   CLINICA CHIMICA ACTA

Comparison of Genetic Versus Clinical Diagnosis in Familial Hypercholesterolemia

(2008) Fernando Civeira et al.   AMERICAN JOURNAL OF CARDIOLOGY