Associated Papers
Improved Genetic Characterization of Hypercholesterolemia in Latvian Patients with Familial Hypercholesterolemia: A Combined Monogenic and Polygenic Approach Using Whole-Genome Sequencing.
Atava I et al.
International Journal of Molecular Sciences, 2024
39769230 (PubMed )
Supplement: ijms-25-13466-s001.zip › ijms-3363591-supplementary.pdf
Low-Cost High-Throughput Genotyping for Diagnosing Familial Hypercholesterolemia.
Ibrahim S et al.
Circulation. Genomic and Precision Medicine, 2023
37675602 (PubMed )
Supplement: hcg-16-462-s001.pdf
Use of plasma metabolomics to analyze phenotype-genotype relationships in young hypercholesterolemic females.
Zhang X et al.
Journal of Lipid Research, 2018
Genetics, Lifestyle, and Low-Density Lipoprotein Cholesterol in Young and Apparently Healthy Women.
Balder JW et al.
Circulation, 2018
29459468 (PubMed )
Supplement: circ_circulationaha-2017-032479_supp1.pdf
Genomic and epigenomic analysis of high-risk prostate cancer reveals changes in hydroxymethylation and TET1.
Spans L et al.
Oncotarget, 2016
27014907 (PubMed )
Supplement: oncotarget-07-24326-s004.xlsx › Blad1
Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents.
Merlevede J et al.
Nature Communications, 2016
26908133 (PubMed )
Supplement: ncomms10767-s2.xls › Feuille1
High-resolution melting analysis for detection of familial ligand-defective apolipoprotein B-100 mutations.
Liyanage KE et al.
Annals of Clinical Biochemistry, 2008
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