| Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency MI New, M Abraham, B Gonzalez, M Dumic, M Razzaghy-Azar, D Chitayat, ... Proceedings of the National Academy of Sciences 110 (7), 2611-2616, 2013 | 368 | 2013 |
| Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome) M Zenker, J Mayerle, MM Lerch, A Tagariello, K Zerres, PR Durie, M Beier, ... Nature genetics 37 (12), 1345-1350, 2005 | 294 | 2005 |
| Autosomal-recessive mutations in SLC34A1 encoding sodium-phosphate cotransporter 2A cause idiopathic infantile hypercalcemia KP Schlingmann, J Ruminska, M Kaufmann, I Dursun, M Patti, B Kranz, ... Journal of the American Society of Nephrology 27 (2), 604-614, 2016 | 242 | 2016 |
| A Mutation (Pro-30 to Leu) in CYP21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele MT Tusie-Luna, PW Speiser, M Dumic, MI New, PC White Molecular endocrinology 5 (5), 685-692, 1991 | 216 | 1991 |
| Hormones and handedness: Left‐hand bias in female congenital adrenal hyperplasia patients R Nass, S Baker, P Speiser, R Virdis, A Balsamo, E Cacciari, A Loche, ... Neurology 37 (4), 711-711, 1987 | 182 | 1987 |
| Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome. DB Grant, ND Barnes, M Dumic, M Ginalska-Malinowska, PJ Milla, ... Archives of Disease in Childhood 68 (6), 779-782, 1993 | 169 | 1993 |
| Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency RC Wilson, S Nimkarn, M Dumic, J Obeid, M Azar, H Najmabadi, F Saffari, ... Molecular genetics and metabolism 90 (4), 414-421, 2007 | 157 | 2007 |
| Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency A Khattab, S Haider, A Kumar, S Dhawan, D Alam, R Romero, J Burns, ... Proceedings of the National Academy of Sciences 114 (10), E1933-E1940, 2017 | 121 | 2017 |
| Thyroid diseases in a school population with thyromegaly. J Jaksić, M Dumić, B Filipović, J Ille, M Cvijetić, G Gjurić Archives of disease in childhood 70 (2), 103-106, 1994 | 116 | 1994 |
| Incidence of type 1 diabetes mellitus in 0 to 14‐yr‐old children in Croatia–2004 to 2012 study N Rojnic Putarek, J Ille, A Spehar Uroic, V Skrabic, G Stipancic, N Krnic, ... Pediatric diabetes 16 (6), 448-453, 2015 | 64 | 2015 |
| Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri‐Weill dyschondrosteosis KU Schneider, A Marchini, N Sabherwal, R Röth, B Niesler, T Marttila, ... Human mutation 26 (1), 44-52, 2005 | 61 | 2005 |
| Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome M Dumic, N Barišic, V Kusec, K Stingl, M Skegro, A Stanimirovic, ... European journal of pediatrics 171, 1453-1459, 2012 | 54 | 2012 |
| Premature thelarche: a possible adrenal disorder. M Dumic, M Tajic, D Mardesic, Z Kalafatic Archives of Disease in Childhood 57 (3), 200-203, 1982 | 53 | 1982 |
| Characteristics of the craniofacial complex in Turner syndrome J Dumancic, Z Kaic, ML Varga, T Lauc, M Dumic, SA Milosevic, H Brkic Archives of oral biology 55 (1), 81-88, 2010 | 52 | 2010 |
| Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations S Nimkarn, BI Cerame, JQ Wei, M Dumic, R Zunec, L Brkljacic, V Skrabic, ... The Journal of Clinical Endocrinology & Metabolism 84 (1), 378-381, 1999 | 51 | 1999 |
| Report of fertility in a woman with a predominantly 46, XY karyotype in a family with multiple disorders of sexual development M Dumic, K Lin-Su, NI Leibel, S Ciglar, G Vinci, R Lasan, S Nimkarn, ... The Journal of Clinical Endocrinology & Metabolism 93 (1), 182-189, 2008 | 45 | 2008 |
| An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population M Dumić, L Brkljačić, PW Speiser, E Wood, C Crawford, V Plavšić, ... European Journal of Endocrinology 122 (6), 703-710, 1990 | 43 | 1990 |
| Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency M Dumic, N Janjanin, J Ille, R Zunec, A Špehar, G Zlopasa, I Francetic, ... Journal of Pediatric Endocrinology and Metabolism 18 (9), 887-896, 2005 | 39 | 2005 |
| Testicular adrenal rest tumors in congenital adrenal hyperplasia—cross-sectional study of 51 Croatian male patients M Dumic, V Duspara, Z Grubic, SK Oguic, V Skrabic, V Kusec European journal of pediatrics 176, 1393-1404, 2017 | 37 | 2017 |
| Polymorphism of apolipoprotein E, lipoprotein (a), and other lipoproteins in children with type I diabetes B Salzer, A Stavljenić, G Jürgens, M Dumić, A Radica Clinical chemistry 39 (7), 1427-1432, 1993 | 32 | 1993 |
Jelena DumancicProfessor, doctor of dental medicine, University of Zagreb School of Dental MedicineVerified email at sfzg.unizg.hr
