| Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families O Rubio-Cabezas, AM Patch, JAL Minton, SE Flanagan, EL Edghill, ... The Journal of Clinical Endocrinology & Metabolism 94 (11), 4162-4170, 2009 | 164 | 2009 |
| SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion FH Sansbury, SE Flanagan, JAL Houghton, FL Shuixian Shen, ... Diabetologia 55, 2381-2385, 2012 | 140 | 2012 |
| Comprehensive screening of eight known causative genes in congenital hypothyroidism with gland-in-situ AK Nicholas, EG Serra, H Cangul, S Alyaarubi, I Ullah, E Schoenmakers, ... The Journal of Clinical Endocrinology & Metabolism 101 (12), 4521-4531, 2016 | 96 | 2016 |
| Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia AM Habeb, MSF Al‐Magamsi, IM Eid, MI Ali, AT Hattersley, K Hussain, ... Pediatric Diabetes 13 (6), 499-505, 2012 | 96 | 2012 |
| Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine‐responsive megaloblastic anaemia C Shaw‐Smith, SE Flanagan, AM Patch, J Grulich‐Henn, AM Habeb, ... Pediatric diabetes 13 (4), 314-321, 2012 | 81 | 2012 |
| High incidence of childhood type 1 diabetes in al‐madinah, north west saudi arabia (2004–2009) AM Habeb, MSF Al‐Magamsi, S Halabi, IM Eid, S Shalaby, O Bakoush Pediatric diabetes 12 (8), 676-681, 2011 | 80 | 2011 |
| Expanding the Clinical Spectrum Associated With GLIS3 Mutations P Dimitri, AM Habeb, F Garbuz, A Millward, S Wallis, K Moussa, T Akcay, ... The Journal of Clinical Endocrinology & Metabolism 100 (10), E1362-E1369, 2015 | 75 | 2015 |
| Endocrinopathies in beta-thalassemia major. Prevalence, risk factors, and age at diagnosis in Northwest Saudi Arabia. AM Habeb, ZM Al-Hawsawi, MM Morsy, AM Al-Harbi, AS Osilan, ... Saudi medical journal 34 (1), 67-73, 2013 | 49 | 2013 |
| Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans AM Habeb, SE Flanagan, A Deeb, I Al-Alwan, H Alawneh, AAL Balafrej, ... Archives of disease in childhood 97 (8), 721-723, 2012 | 44 | 2012 |
| ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents SAW Greeley, M Polak, PR Njølstad, F Barbetti, R Williams, L Castano, ... Pediatric Diabetes 23 (8), 1188, 2022 | 42 | 2022 |
| Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates A Deeb, A Habeb, W Kaplan, S Attia, S Hadi, A Osman, J Al‐Jubeh, ... American Journal of Medical Genetics Part A 170 (3), 602-609, 2016 | 42 | 2016 |
| Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome AM Habeb, SE Flanagan, MA Zulali, MA Abdullah, R Pomahačová, ... Diabetologia 61, 1027-1036, 2018 | 37 | 2018 |
| Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort AM Habeb, A Deeb, M Johnson, M Abdullah, M Abdulrasoul, H Al-Awneh, ... Hormone Research in Paediatrics 83 (3), 190-197, 2015 | 37 | 2015 |
| Reduced frequency and severity of ketoacidosis at diagnosis of childhood type 1 diabetes in Northwest Saudi Arabia AM Ahmed, M Al-Maghamsi, AM Al-Harbi, IM Eid, HH Baghdadi, ... Journal of Pediatric Endocrinology and Metabolism 29 (3), 259-264, 2016 | 36 | 2016 |
| ISPAD Clinical Practice Consensus Guidelines: Fasting during Ramadan by young people with diabetes A Deeb, N Elbarbary, CE Smart, SA Beshyah, A Habeb, S Kalra, ... Pediatric diabetes 21 (1), 5-17, 2020 | 32 | 2020 |
| The spectrum of congenital heart diseases in down syndrome: a retrospective study from Northwest Saudi Arabia MM Morsy, OO Algrigri, SS Salem, MM Abosedera, AR Abutaleb, ... Saudi medical journal 37 (7), 767, 2016 | 30 | 2016 |
| Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review AM Habeb Libyan Journal of Medicine 8 (1), 2013 | 27 | 2013 |
| Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid deficiency type 2 CR Hughes, TT Chung, AM Habeb, F Kelestimur, AJL Clark, LA Metherell The Journal of Clinical Endocrinology & Metabolism 95 (7), 3497-3501, 2010 | 26 | 2010 |
| Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries F Al Juraibah, E Al Amiri, M Al Dubayee, J Al Jubeh, H Al Kandari, ... Archives of Osteoporosis 16, 1-15, 2021 | 20 | 2021 |
| Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRMP6 gene mutation AM Habeb, H Al-Harbi, KP Schlingmann Saudi Journal of Kidney Diseases and Transplantation 23 (5), 1038-1042, 2012 | 20 | 2012 |
