Related references
Note: Only part of the references are listed.Update of the Portuguese Familial Hypercholesterolaemia Study
A. M. Medeiros et al.
ATHEROSCLEROSIS (2010)
Effect of ABCG1 Gene Promoter-257T>G Polymoirphism on Coronary Artery Disease Severity in Japanese Men
Shoudai Furuyama et al.
JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS (2009)
Mutations in the LDL receptor gene in four Chinese homozygous familial hypercholesterolemia phenotype patients
L. Wang et al.
NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES (2009)
The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder:: Strong evidence of epistatic effects between loci on chromosomes 2q and 6q
Rami Abou Jamra et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Mechanisms of Disease: genetic causes of familial hypercholesterolemia
Anne K. Soutar et al.
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE (2007)
ABCA1 and ABCG1 or ABCG4 act sequentially to remove cellular cholesterol and generate cholesterol-rich HDL
Ashley M. Vaughan et al.
JOURNAL OF LIPID RESEARCH (2006)
Diagnosis and screening for familial hypercholesterolaemia: finding the patients, finding the genes
Deepak Bhatnagar
ANNALS OF CLINICAL BIOCHEMISTRY (2006)
Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico
L Robles-Osorio et al.
ARCHIVES OF MEDICAL RESEARCH (2006)
ABCG1 has a critical role in mediating cholesterol efflux to HDL and preventing cellular lipid accumulation
MA Kennedy et al.
CELL METABOLISM (2005)
High factor VIII levels in venous thromboembolism show linkage to imprinted loci on chromosomes 5 and 11
M Berger et al.
BLOOD (2005)
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
M Abifadel et al.
NATURE GENETICS (2003)
How to model a complex trait - 2. Analysis with two disease loci
K Strauch et al.
HUMAN HEREDITY (2003)
Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemia
H Al-Kateb et al.
CIRCULATION RESEARCH (2002)
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
GR Abecasis et al.
NATURE GENETICS (2002)
Use of homozygosity mapping to identify a region on chromosome 1 bearing a defective gene that causes autosomal recessive homozygous hypercholesterolemia in two unrelated families
ER Eden et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III-IV locus - The NHLBI Family Heart Study
H Coon et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2000)
A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26
M Ciccarese et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Share Paper
