Miroslav Dumić

Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Maria I. New, Moolamannil Abraham, Brian D. Gonzalez et al. · Proceedings of the National Academy of Sciences · 2013 · 361 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Justyna Ruminska, Martin Kaufmann et al. · Journal of the American Society of Nephrology · 2015 · 282 citations · Full text

Medicine, Endocrinology, Genetics +17

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Martin Zenker, Julia Mayerle, Markus M. Lerch et al. · Nature Genetics · 2005 · 272 citations

Life Sciences, Genetics, Molecular Biology +14

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Ahmed Khattab, Shozeb Haider, Ameet Kumar et al. · Proceedings of the National Academy of Sciences · 2017 · 156 citations · Full text

Medicine, Endocrinology, Genetics +14

Hormones and handedness

Robert D. Nass, Susan W. Baker, Phyllis Speiser et al. · Neurology · 1987 · 149 citations

Medicine, Endocrinology, Human Genetics +9