Associated Papers
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
Tadros R et al.
Nature Genetics, 2025
39966646 (PubMed )
Supplement: 41588_2025_2087_MOESM3_ESM.pdf
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Young WJ et al.
Nature Communications, 2022
36050321 (PubMed )
Supplement: 41467_2022_32821_MOESM4_ESM.xlsx › Data_12a
Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
Khan S et al.
Bmc Research Notes, 2021
33743798 (PubMed )
Supplement: 13104_2021_5514_MOESM4_ESM.zip › Supplementary_File_1A-1.xlsx › Supplementary_File_1A-1.exonic_
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
33770142 (PubMed )
Supplement: pone.0249324.s003.xlsx › 8774__IV-2_
High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune profile, clinical outcome and sensitivity to targeted therapies.
Toulmonde M et al.
Ebiomedicine, 2020
33254023 (PubMed )
Supplement: mmc5.xlsx › UPS_somatic_mutations_filtered
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
27512948 (PubMed )
Supplement: PATH-240-315-s015.xlsx › Table_S2
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-A8-A06O-01A.domain
RING finger protein RNF207, a novel regulator of cardiac excitation.
Roder K et al.
The Journal of Biological Chemistry, 2014
Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.
Priest JR et al.
Heart Rhythm, 2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Arking DE et al.
Nature Genetics, 2014
Single-nucleotide variations in cardiac arrhythmias: prospects for genomics and proteomics based biomarker discovery and diagnostics.
Abunimer A et al.
Genes, 2014
Arrhythmia risk in long QT syndrome: beyond the disease-causative mutation.
Giudicessi JR et al.
Circulation. Cardiovascular Genetics, 2013
Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes.
Giudicessi JR et al.
Translational Research : the Journal of Laboratory and Clinical Medicine, 2013
Common genetic variants associated with sudden cardiac death: the FinSCDgen study.
Lahtinen AM et al.
Plos One, 2012
22844511 (PubMed )
Supplement: pone.0041675.s005.pdf
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Pfeufer A et al.
Nature Genetics, 2009
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