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Author Details

Christian Dina
1994
148
67
PMIDPaper TitleJournal TitlePublished Year
37480873Left Ventricular Abnormal Substrate in Brugada Syndrome.2023
36656928Heritable defects in telomere and mitotic function selectively predispose to sarcomas.Science2023
36873395Genetics and pathophysiology of mitral valve prolapse.2023
37228217On the genes, genealogies, and geographies of Quebec.2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
35132965Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.JCI Insight2022
35819174Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical management.Human Mutation2022
35427703Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosis.International Journal of Cardiology2022
35549293Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study.Circ Genom Precis Med2022
35245370Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.Eur Heart J2022
34461747Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.Circulation. Genomic and precision medicine2021
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
34219138Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome.European Heart Journal2021
34261756Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (<i>HSD17B14</i>) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes.J Am Soc Nephrol2021
32636298Lipoprotein-associated phospholipase A2 activity, genetics and calcific aortic valve stenosis in humans.Heart2020
32161328Correction: The genetic history of France.European Journal of Human Genetics2020
32042083The genetic history of France.European Journal of Human Genetics2020
32760854Genetic and In Vitro Inhibition of and Calcific Aortic Valve Stenosis.JACC: Basic to Translational Science2020
31112420Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse.Circ Genom Precis Med2019
31026275Correction: AVPR1a and SLC6A4 Gene Polymorphisms Are Associated with Creative Dance Performance.PLoS Genetics2019
31114854RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.European Heart Journal2019
29547902SMMB: a stochastic Markov blanket framework strategy for epistasis detection in GWAS.2018
29020406New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.Eur Heart J2018
30521541The impact of a fine-scale population stratification on rare variant association test results.PLoS ONE2018
29304371Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm.American Journal of Human Genetics2018
29029846Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.Lancet Neurol2017
28742119DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease.PLoS ONE2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
26643481Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta.Circulation: Cardiovascular Genetics2016
26751395De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability.Hum Mutat2016
27287695Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.Journal of the American Heart Association2016
26722118Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project.Bioinformatics2016
26820365Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.International Journal of Cardiology2016
25182131Fine-scale human genetic structure in Western France.European Journal of Human Genetics2015
29371517Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.Journal of Cardiovascular Development and Disease2015
25650408Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.Human Molecular Genetics2015
26483167Mitral valve disease--morphology and mechanisms.Nat Rev Cardiol2015
26442103A survey about methods dedicated to epistasis detection.Frontiers in Genetics2015
26258302Mutations in DCHS1 cause mitral valve prolapse.Nature2015
26592308Staphylokinase and ABO group phenotype: new players in Staphylococcus aureus implant-associated infections development.Future Microbiology2015
26301497Genetic association analyses highlight biological pathways underlying mitral valve prolapse.Nat Genet2015
24509480Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.Nat Genet2014
24514567A genome-wide association study of anorexia nervosa.Mol Psychiatry2014
23583979Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.Nat Genet2013
23872634Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.Nat Genet2013
22238593A genome-wide association search for type 2 diabetes genes in African Americans.PLoS One2012
22479202Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.PLoS Genet2012
22885922Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.Nat Genet2012
22286214Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.Nature Genetics2012
22327514Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.Nat Genet2012
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