Associated Papers
Putative protective genomic variation in the Lithuanian population.
Žukauskaitė G et al.
Genetics and Molecular Biology, 2024
Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension.
van Duijvenboden S et al.
American Journal of Human Genetics, 2023
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.
Stanzick KJ et al.
Nature Communications, 2021
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Koyama S et al.
Nature Genetics, 2020
An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
Zhao J et al.
Genome Medicine, 2018
29378629 (PubMed )
Supplement: 13073_2018_513_MOESM4_ESM.xlsx › Sheet1
Functional Validation of a Common Nonsynonymous Coding Variant in ZC3HC1 Associated With Protection From Coronary Artery Disease.
Linseman T et al.
Circulation. Cardiovascular Genetics, 2017
Interpreting functional effects of coding variants: challenges in proteome-scale prediction, annotation and assessment.
Shameer K et al.
Briefings in Bioinformatics, 2016
Association of genetic variants with atrial fibrillation.
Yamase Y et al.
Biomedical Reports, 2016
Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.
Brænne I et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2015
Association of Zinc Finger, C3HC-Type Containing 1 (ZC3HC1) rs11556924 Genetic Variant With Hypertension in a Finnish Population, the TAMRISK Study.
Kunnas T et al.
Medicine, 2015
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Holehouse AS et al.
Plos One, 2015
26659599 (PubMed )
Supplement: pone.0144692.s002.xlsx › suppTable_2.txt
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A0CT-01A.domain
The ZC3HC1 rs11556924 polymorphism is associated with increased carotid intima-media thickness in patients with rheumatoid arthritis.
López-Mejías R et al.
Arthritis Research & Therapy, 2013
From genome-wide association studies to functional genomics: new insights into cardiovascular disease.
McPherson R
The Canadian Journal of Cardiology, 2013
Next-generation sequencing identifies transportin 3 as the causative gene for LGMD1F.
Torella A et al.
Plos One, 2013
23667635 (PubMed )
Supplement: pone.0063536.s006.xlsx › LGMD1F_HET_in_all
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Schunkert H et al.
Nature Genetics, 2011
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