Found 11 results
Filters: Author is Dina, Christian [Clear All Filters]
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2020. Correction: The genetic history of France. European Journal of Human Genetics. :1–1.
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2019. Genetic Association Analyses Highlight \textitIL6} , \textitALPL} , and \textitNAV1} As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis. Circulation: Genomic and Precision Medicine. 12:431–441.
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2018. The impact of a fine-scale population stratification on rare variant association test results. PLOS ONE. 13:e0207677.
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2018. Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm. The American Journal of Human Genetics. 102:133–141.
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2017. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease. PLOS ONE. 12:e0179364.
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2016. De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene \textitCHAMP1} Cause Syndromic Intellectual Disability. Human Mutation. 37:354–358.
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2016. Dysfunction of the Voltage‐Gated K $^\textrm+}$ Channel β2 Subunit in a Familial Case of Brugada Syndrome. Journal of the American Heart Association. 5
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2016. Search 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 Genetics. 9:86–94.
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2016. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I. International Journal of Cardiology. 207:349–358.
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2015. Fine-scale human genetic structure in Western France. European Journal of Human Genetics. 23:831–836.
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2015. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human Molecular Genetics. 24:2757–2763.
