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Publications by Janis Klovins
Next-Generation-Sequencing-Based Identification of Familial Hypercholesterolemia-Related Mutations in Subjects With Increased LDL–C Levels in a Latvian Population
BMC Medical Genetics
Genetics
Genes Reveal Traces of Common Recent Demographic History for Most of the Uralic-Speaking Populations
Genome Biology
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Identification of TAZ Mutations in Pediatric Patients With Cardiomyopathy by Targeted Next-Generation Sequencing in a Chinese Cohort
Orphanet Journal of Rare Diseases
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“Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-Like Disease”
Pediatric Rheumatology
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Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation
Scientific Reports
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Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing
Molecular Medicine Reports
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Molecular Biology
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ApoB Metabolism in Familial Hypercholesterolemia. Inconsistencies With the LDL Receptor Paradigm
Arteriosclerosis and Thrombosis: A Journal of Vascular Biology
A Chinese Homozygote of Familial Hypercholesterolemia: Identification of a Novel C263R Mutation in the LDL Receptor Gene
Journal of Human Genetics
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Next Generation Sequencing in Synovial Sarcoma Reveals Novel Gene Mutations
Oncotarget
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Coupling Chemical Mutagenesis to Next Generation Sequencing for the Identification of Drug Resistance Mutations in Leishmania
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Identification of Novel GNAS Mutations in Intramuscular Myxoma Using Next-Generation Sequencing With Single-Molecule Tagged Molecular Inversion Probes
Diagnostic Pathology
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