1. 10 Disease penetrance in asymptomatic carriers of familial cardiomyopathy variants. (6th June 2022) Authors: Mahmood, Adil; Morris-Rosendahl, Deborah; Edwards, Matthew; Fleming, Andrew; Homfray, Tessa; Mason, Samantha; Quinn, Ellie; Ware, James; Baksi, John; Prasad, Sanjay; Pantazis, Antonis; Halliday, Brian Journal: Heart Issue: Volume 108(2022)Supplement 1 Page Start: A9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 209 Whole Exome Sequencing Identifies Genetic Cause of Histiocytoid Cardiomyopathy. (3rd June 2016) Authors: Rea, Gillian; Homfray, Tessa; Till, Jan; Roses-Noguer, Ferran; Buchan, Rachel J; Wilkinson, Sam; Walsh, Roddy; McKee, Shane; Stewart, Fiona J; Murday, Victoria; Taylor, Robert W; John Baksi, A; Prasad, Sanjay K; Barton, Paul JR; Ware, James S; Cook, Stuart A Journal: Heart Issue: Volume 102(2016)Supplement 6 Page Start: A138 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 280 Role of the electrocardiogram in differentiating genotype positive dilated cardiomyopathy from cardiac remodelling in athletes. (8th December 2021) Authors: Zaffalon, Denise; Papatheodorou, Efstathios; Merghani, Ahmed; Dhutia, Harshil; Moccia, Eleonora; Malhotra, Aneil; Miles, Christopher J.; Attard, Virginia; Homfray, Tessa; Sharma, Rajan; Gigli, Marta; Dal Ferro, Matteo; Merlo, Marco; Papadakis, Michael; Sinagra, Gianfranco; Sharma, Sanjay; Finocch... Journal: European heart journal supplements Issue: Volume 23(2021)Supplement G Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype. (21st January 2015) Authors: Terhal, Paulien A.; Nievelstein, Rutger Jan A. J.; Verver, Eva J. J.; Topsakal, Vedat; van Dommelen, Paula; Hoornaert, Kristien; Le Merrer, Martine; Zankl, Andreas; Simon, Marleen E. H.; Smithson, Sarah F.; Marcelis, Carlo; Kerr, Bronwyn; Clayton‐Smith, Jill; Kinning, Esther; Mansour, Sahar; Elms... Journal: American journal of medical genetics Issue: Volume 167:Number 3(2015:Mar.) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cerebro–costo–mandibular syndrome: Clinical, radiological, and genetic findings. Issue 5 (12th March 2016) Authors: Tooley, Madeleine; Lynch, Danielle; Bernier, Francois; Parboosingh, Jillian; Bhoj, Elizabeth; Zackai, Elaine; Calder, Alistair; Itasaki, Nobue; Wakeling, Emma; Scott, Richard; Lees, Melissa; Clayton‐Smith, Jill; Blyth, Moira; Morton, Jenny; Shears, Debbie; Kini, Usha; Homfray, Tessa; Clarke, Angu... Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: 1115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Consensus document on optimal management of patients with common arterial trunk. (21st May 2021) Authors: Hazekamp, Mark G; Barron, David J; Dangel, Joanna; Homfray, Tessa; Jongbloed, Monique R M; Voges, Inga Journal: European journal of cardio-thoracic surgery Issue: Volume 60:Number 1(2021) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cover Image, Volume 170A, Number 5, May 2016. Issue 5 (14th April 2016) Authors: Tooley, Madeleine; Lynch, Danielle; Bernier, Francois; Parboosingh, Jillian; Bhoj, Elizabeth; Zackai, Elaine; Calder, Alistair; Itasaki, Nobue; Wakeling, Emma; Scott, Richard; Lees, Melissa; Clayton‐Smith, Jill; Blyth, Moira; Morton, Jenny; Shears, Debbie; Kini, Usha; Homfray, Tessa; Clarke, Angu... Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing. (3rd December 2017) Authors: Stals, Karen L.; Wakeling, Matthew; Baptista, Júlia; Caswell, Richard; Parrish, Andrew; Rankin, Julia; Tysoe, Carolyn; Jones, Garan; Gunning, Adam C.; Lango Allen, Hana; Bradley, Lisa; Brady, Angela F.; Carley, Helena; Carmichael, Jenny; Castle, Bruce; Cilliers, Deirdre; Cox, Helen; Deshpande, Ch... Journal: Prenatal diagnosis Issue: Volume 38:Number 1(2018) Page Start: 33 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion. Issue 12 (18th September 2018) Authors: Sheikh, Nabeel; Papadakis, Michael; Wilson, Mathew; Malhotra, Aneil; Adamuz, Carmen; Homfray, Tessa; Monserrat, Lorenzo; Behr, Elijah R.; Sharma, Sanjay Journal: Circulation Issue: Volume 138:Issue 12(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Diagnostic yield of hypertrophic cardiomyopathy in first-degree relatives of decedents with idiopathic left ventricular hypertrophy. Issue 4 (3rd February 2020) Authors: Finocchiaro, Gherardo; Dhutia, Harshil; Gray, Belinda; Ensam, Bode; Papatheodorou, Stathis; Miles, Chris; Malhotra, Aneil; Fanton, Zeph; Bulleros, Paulo; Homfray, Tessa; Witney, Adam A; Bunce, Nicholas; Anderson, Lisa J; Ware, James S; Sharma, Rajan; Tome, Maite; Behr, Elijah R; Sheppard, Mary N;... Journal: Europace Issue: Volume 22:Issue 4(2020) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗