| Reprogramming human T cell function and specificity with non-viral genome targeting TL Roth, C Puig-Saus, R Yu, E Shifrut, J Carnevale, PJ Li, J Hiatt, J Saco, ... Nature 559 (7714), 405-409, 2018 | 777 | 2018 |
| Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications RN Naylor, PM John, AN Winn, D Carmody, SAW Greeley, LH Philipson, ... Diabetes care 37 (1), 202-209, 2014 | 141 | 2014 |
| Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach G Alkorta-Aranburu, D Carmody, YW Cheng, V Nelakuditi, L Ma, ... Molecular genetics and metabolism 113 (4), 315-320, 2014 | 115 | 2014 |
| GCK-MODY in the US National Monogenic Diabetes Registry: frequently misdiagnosed and unnecessarily treated D Carmody, RN Naylor, CD Bell, S Berry, JT Montgomery, EC Tadie, ... Acta diabetologica 53, 703-708, 2016 | 83 | 2016 |
| Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes BW Thurber, D Carmody, EC Tadie, AN Pastore, JT Dickens, ... Diabetologia 58, 1430-1435, 2015 | 78 | 2015 |
| Diabetes presentation in infancy: high risk of diabetic ketoacidosis LR Letourneau, D Carmody, K Wroblewski, AM Denson, M Sanyoura, ... Diabetes Care 40 (10), e147-e148, 2017 | 68 | 2017 |
| Sulfonylurea treatment before genetic testing in neonatal diabetes: pros and cons D Carmody, CD Bell, JL Hwang, JT Dickens, DI Sima, DL Felipe, ... The Journal of Clinical Endocrinology & Metabolism 99 (12), E2709-E2714, 2014 | 61 | 2014 |
| Platelet reactivity in type 2 diabetes mellitus: a comparative analysis with survivors of myocardial infarction and the role of glycaemic control D Mylotte, GF Kavanagh, AJ Peace, AF Tedesco, D Carmody, M O’reilly, ... Platelets 23 (6), 439-446, 2012 | 46 | 2012 |
| ADHD, learning difficulties and sleep disturbances associated with KCNJ11‐related neonatal diabetes KA Landmeier, M Lanning, D Carmody, SAW Greeley, ME Msall Pediatric diabetes 18 (7), 518-523, 2017 | 43 | 2017 |
| Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder SA Shalev, Y Tenenbaum‐Rakover, Y Horovitz, VP Paz, H Ye, ... Pediatric diabetes 15 (3), 252-256, 2014 | 41 | 2014 |
| FOXP3 mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked … JL Hwang, SY Park, H Ye, M Sanyoura, AN Pastore, D Carmody, ... Pediatric diabetes 19 (3), 388-392, 2018 | 39 | 2018 |
| Patients with KCNJ11‐related diabetes frequently have neuropsychological impairments compared with sibling controls D Carmody, AN Pastore, KA Landmeier, LR Letourneau, R Martin, ... Diabetic Medicine 33 (10), 1380-1386, 2016 | 37 | 2016 |
| Role of noninsulin therapies alone or in combination in chromosome 6q24-related transient neonatal diabetes: sulfonylurea improves but does not always normalize insulin secretion D Carmody, FA Beca, CD Bell, JL Hwang, JT Dickens, NA Devine, ... Diabetes Care 38 (6), e86-e87, 2015 | 32 | 2015 |
| Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism D Carmody, SY Park, H Ye, ME Perrone, G Alkorta-Aranburu, ... Journal of medical genetics 52 (9), 612-616, 2015 | 30 | 2015 |
| Hypoglycemia in sulfonylurea‐treated KCNJ11‐neonatal diabetes: Mild‐moderate symptomatic episodes occur infrequently but none involving unconsciousness or … MS Lanning, D Carmody, Ł Szczerbiński, LR Letourneau, RN Naylor, ... Pediatric diabetes 19 (3), 393-397, 2018 | 27 | 2018 |
| Low-dose hydrocortisone replacement is associated with improved arterial stiffness index and blood pressure dynamics in severely adrenocorticotrophin-deficient hypopituitary … LA Behan, D Carmody, B Rogers, MJ Hannon, C Davenport, W Tormey, ... European journal of endocrinology 174 (6), 791-799, 2016 | 26 | 2016 |
| A clinical guide to monogenic diabetes D Carmody, J Støy, SAW Greeley, GI Bell, LH Philipson Genetic diagnosis of endocrine disorders, 21-30, 2016 | 26 | 2016 |
| Teenage pregnancy in type 1 diabetes mellitus D Carmody, A Doyle, R GR Firth, MM Byrne, S Daly, F Mc Auliffe, M Foley, ... Pediatric Diabetes 11 (2), 111-115, 2010 | 25 | 2010 |
| Improved molecular diagnosis of patients with neonatal diabetes using a combined next-generation sequencing and MS-MLPA approach G Alkorta-Aranburu, M Sukhanova, D Carmody, T Hoffman, L Wysinger, ... Journal of Pediatric Endocrinology and Metabolism 29 (5), 523-531, 2016 | 24 | 2016 |
| Successful rh IGF 1 treatment for over 5 years in a patient with severe insulin resistance due to homozygous insulin receptor mutation D Carmody, SS Ladsaria, RK Buikema, RK Semple, SAW Greeley Diabetic Medicine 33 (3), e8-e12, 2016 | 20 | 2016 |
