1. A 19-SNP coronary heart disease gene score profile in subjects with type 2 diabetes: the coronary heart disease risk in type 2 diabetes (CoRDia study) study baseline characteristics. Issue 1 (December 2016) Authors: Beaney, Katherine; Ward, Claire; Bappa, Dauda; McGale, Nadine; Davies, Anna; Hirani, Shashivadan; Li, KaWah; Howard, Philip; Vance, Dwaine; Crockard, Martin; Lamont, John; Newman, Stanton; Humphries, Steve Journal: Cardiovascular diabetology Issue: Volume 15:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. Issue 9965 (24th January 2015) Authors: Swerdlow, Daniel I; Preiss, David; Kuchenbaecker, Karoline B; Holmes, Michael V; Engmann, Jorgen E L; Shah, Tina; Sofat, Reecha; Stender, Stefan; Johnson, Paul C D; Scott, Robert A; Leusink, Maarten; Verweij, Niek; Sharp, Stephen J; Guo, Yiran; Giambartolomei, Claudia; Chung, Christina; Peasey, A... Journal: Lancet Issue: Volume 385:Issue 9965(2015) Page Start: 351 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease Risk. (April 2015) Authors: Guardiola, Montse; Exeter, Holly J.; Perret, Claire; Folkersen, Lasse; van't Hooft, Ferdinand; Eriksson, Per; Franco-Cereceda, Anders; Paulsson-Berne, Gabrielle; Palmen, Jutta; Li, KaWah; Cooper, Jackie A.; Khaw, Kay-Tee; Mallat, Ziad; Ninio, Ewa; Karabina, Sonia-Athina; Humphries, Steve E.; Boek... Journal: Circulation Issue: Volume 8:Number 2(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries. (6th January 2020) Authors: Futema, Marta; Shah, Sonia; Cooper, Jackie A; Li, KaWah; Whittall, Ros A; Sharifi, Mahtab; Goldberg, Olivia; Drogari, Euridiki; Mollaki, Vasiliki; Wiegman, Albert; Defesche, Joep; D'Agostino, Maria N; D'Angelo, Antonietta; Rubba, Paolo; Fortunato, Giuliana; Waluś-Miarka, Małgorzata; Hegele, Rober... Journal: Clinical chemistry Issue: Volume 61:Number 1(2015) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations. Issue 8 (1st July 2014) Authors: Futema, Marta; Plagnol, Vincent; Li, KaWah; Whittall, Ros A; Neil, H Andrew W; Seed, Mary; Bertolini, Stefano; Calandra, Sebastiano; Descamps, Olivier S; Graham, Colin A; Hegele, Robert A; Karpe, Fredrik; Durst, Ronen; Leitersdorf, Eran; Lench, Nicholas; Nair, Devaki R; Soran, Handrean; Van Bockx... Journal: Journal of medical genetics Issue: Volume 51:Issue 8(2014) Page Start: 537 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗