Associated Papers
Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease.
Tan M et al.
Frontiers in Genetics, 2022
35910219 (PubMed )
Supplement: DataSheet1.xlsx › Table_S7
Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.
Dron JS et al.
Bmc Medical Genomics, 2020
32041611 (PubMed )
Supplement: 12920_2020_669_MOESM1_ESM.xlsx › Supp_Table_4
Improved plasma cholesterol efflux capacity from human macrophages in patients with hyperalphalipoproteinemia.
El Khoury P et al.
Atherosclerosis, 2014
Functional characterization of novel variants in the CETP promoter and the LIPC gene in subjects with hyperalphalipoproteinemia.
Plengpanich W et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2013
Resequencing CETP, LIPC and LIPG genes in Thai subjects with hyperalphalipoproteinemia.
Khovidhunkit W et al.
The American Journal of Cardiology, 2012
Two novel mutations and functional analyses of the CETP and LIPC genes underlying severe hyperalphalipoproteinemia.
Plengpanich W et al.
Metabolism: Clinical and Experimental, 2009
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