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The Journal of Invasive Cardiology|August 6, 2013
Provision of gastroprotective medication and bleeding risk following acute coronary syndromeAthar Badar, Jennifer Scaife, Andrew T Yan, et al.
Geroscience|April 22, 2023
Activation of telomerase by TA-65 enhances immunity and reduces inflammation post myocardial infarctionBilal Bawamia, Luke Spray, Vincent K Wangsaputra, et al.
Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.
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.
Heart (British Cardiac Society)|October 13, 2010
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variantsHelen R Griffin, Ana Töpf, Elise Glen, et al.
Nanoscale|July 3, 2018
Imaging the magnetic structures of artificial quasicrystal magnets using resonant coherent diffraction of circularly polarized X-raysDaeho Sung, Chulho Jung, Byeong-Gwan Cho, et al.
Physical Review Letters|May 31, 2019
Exploiting Symmetry Mismatch to Control Magnetism in a Ferroelastic HeterostructureEr-Jia Guo, Ryan Desautels, Dongkyu Lee, 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.
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