DANIEL PENNY to Mutation
This is a "connection" page, showing publications DANIEL PENNY has written about Mutation.
Connection Strength
0.298
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Functional changes in pulmonary arterial endothelial cells associated with BMPR2 mutations. PLoS One. 2014; 9(9):e106703.
Score: 0.167
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Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise. Heart Rhythm. 2018 07; 15(7):1042-1050.
Score: 0.053
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Early onset severe pulmonary arterial hypertension with 'two-hit' digenic mutations in both BMPR2 and KCNA5 genes. Int J Cardiol. 2014 Dec 20; 177(3):e167-9.
Score: 0.042
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Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation. Mol Genet Genomic Med. 2019 06; 7(6):e593.
Score: 0.014
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Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals. Circ Arrhythm Electrophysiol. 2017 Apr; 10(4).
Score: 0.012
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Dilated cardiomyopathy and ovarian dysgenesis in a patient with Malouf syndrome: a case report. Mol Med Rep. 2013 Nov; 8(5):1311-4.
Score: 0.010