Tülay Güran

Mutations in<i>CYP24A1</i>and Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber et al. · New England Journal of Medicine · 2011 · 684 citations · Full text

Medicine, Pediatrics, Pharmacotherapy +17

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

Ender Karaca, Tamar Harel, Davut Pehli̇van et al. · Neuron · 2015 · 340 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Tülay Güran, Federica Buonocore, Nurçin Saka et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 212 citations · Full text

Medicine, Endocrinology, Pediatrics +16

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome

Rathi Prasad, Irene Hadjidemetriou, Avinaash Maharaj et al. · Journal of Clinical Investigation · 2017 · 175 citations · Full text

Medicine, Endocrinology, Molecular Genetics +16

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

Serap Turan, Burcu Topçu, İbrahim Gökçe et al. · Journal of Clinical Research in Pediatric Endocrinology · 2011 · 159 citations · Full text

Medicine, Child Health, Pediatrics +10