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Heart (British Cardiac Society)|April 2, 2010
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresiaKlaartje van Engelen, Ana Topf, Bernard D Keavney, et al.
Human Mutation|January 26, 2012
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformationHuay L Tan, Elise Glen, Ana Töpf, et al.
Plos One|August 6, 2014
Functionally significant, rare transcription factor variants in tetralogy of FallotAna Töpf, Helen R Griffin, Elise Glen, et al.
Plos Genetics|February 10, 2026
A machine learning classifier to identify and prioritise genes associated with murine cardiac developmentMitra Kabir, Verity Hartill, Gist H Farr, et al.
Nature Communications|November 14, 2018
Author Correction: Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networksMun-Kit Choy, Biola M Javierre, Simon G Williams, et al.
Nature Communications|June 30, 2018
Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networksMun-Kit Choy, Biola M Javierre, Simon G Williams, et al.
Bioinformatics (Oxford, England)|December 3, 2019
The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discriminationKathryn A McGurk, Arianna Dagliati, Davide Chiasserini, et al.
European Heart Journal. Cardiovascular Imaging|November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriersMatthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease PhenotypesAldo Córdova-Palomera, Catherine Tcheandjieu, Jason A Fries, et al.
Circulation. Genomic and Precision Medicine|October 7, 2022
Investigation of Copy Number Variation in South African Patients With Congenital Heart DefectsNicole A Saacks, James Eales, Timothy F Spracklen, et al.
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