1. Analysis of cell‐free fetal DNA for non‐invasive prenatal diagnosis in a family with neonatal diabetes. Issue 4 (31st July 2016) Authors: De Franco, E.; Caswell, R.; Houghton, J. A. L.; Iotova, V.; Hattersley, A. T.; Ellard, S. Journal: Diabetic medicine Issue: Volume 34:Issue 4(2017) Page Start: 582 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical phenotype associated with reported GCK exon 10 deletions: clinical judgement is needed alongside appropriate genetic investigations. Issue 8 (16th July 2013) Authors: Thanabalasingham, G.; Kaur, K.; Talbot, F.; Colclough, K.; Mathews, A.; Taylor, J.; Ellard, S.; Owen, K. R. Journal: Diabetic medicine Issue: Volume 30:Issue 8(2013:Aug.) Page Start: e233 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency. Issue 5 (28th February 2013) Authors: De, E.; Shaw‐Smith, C.; Flanagan, S. E.; Edghill, E. L.; Wolf, J.; Otte, V.; Ebinger, F.; Varthakavi, P.; Vasanthi, T.; Edvardsson, S.; Hattersley, A. T.; Ellard, S. Journal: Diabetic medicine Issue: Volume 30:Issue 5(2013:May) Page Start: e197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. Issue 4 (2nd August 2020) Authors: Robinson, H.K.; Zaklyazminskaya, E.; Povolotskaya, I.; Surikova, Y.; Mallin, L.; Armstrong, C.; Mabin, D.; Benke, P.J.; Chrisant, M.R.; McDonald, M.; Marboe, C.C.; Agre, K.E.; Deyle, D.R.; McWalter, K.; Douglas, G.; Balashova, M.S.; Kaimonov, V.; Shirokova, N.; Pomerantseva, E.; Turner, C.L. Journal: Clinical genetics Issue: Volume 98:Issue 4(2020) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. HNF1B deletions in patients with young‐onset diabetes but no known renal disease. Issue 1 (13th December 2012) Authors: Edghill, E. L.; Stals, K.; Oram, R. A.; Shepherd, M. H.; Hattersley, A. T.; Ellard, S. Journal: Diabetic medicine Issue: Volume 30:Issue 1(2013:Jan.) Page Start: 114 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity‐onset diabetes of the young, and incretin response. Issue 3 (March 2014) Authors: Arya, V. B.; Rahman, S.; Senniappan, S.; Flanagan, S. E.; Ellard, S.; Hussain, K. Journal: Diabetic medicine Issue: Volume 31:Issue 3(2014:Mar.) Page Start: e11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A–MODY cohort. Issue 7 (17th November 2015) Authors: Bacon, S.; Kyithar, M. P.; Rizvi, S. R.; Donnelly, E.; McCarthy, A.; Burke, M.; Colclough, K.; Ellard, S.; Byrne, M. M. Journal: Diabetic medicine Issue: Volume 33:Issue 7(2016:Jul.) Page Start: 976 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The evolving course of HNF4A hyperinsulinaemic hypoglycaemia—a case series. Issue 1 (12th December 2013) Authors: McGlacken‐Byrne, S. M.; Hawkes, C. P.; Flanagan, S. E.; Ellard, S.; McDonnell, C. M.; Murphy, N. P. Journal: Diabetic medicine Issue: Volume 31:Issue 1(2014:Jan.) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. TRNA methyltransferase homologue gene TRMT10A mutation in young adult‐onset diabetes with intellectual disability, microcephaly and epilepsy. Issue 9 (September 2016) Authors: Yew, T. W.; McCreight, L.; Colclough, K.; Ellard, S.; Pearson, E. R. Journal: Diabetic medicine Issue: Volume 33:Issue 9(2016:Sep.) Page Start: e21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population. Issue 12 (25th July 2019) Authors: Yaghootkar, H.; Abbasi, F.; Ghaemi, N.; Rabbani, A.; Wakeling, M. N.; Eshraghi, P.; Enayati, S.; Vakili, S.; Heidari, S.; Patel, K.; Sayarifard, F.; Borhan‐Dayani, S.; McDonald, T. J.; Ellard, S.; Hattersley, A. T.; Amoli, M. M.; Vakili, R.; Colclough, K. Journal: Diabetic medicine Issue: Volume 36:Issue 12(2019) Page Start: 1694 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗