Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center by Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Nicos Skordis, Leonidas A. Phylactou

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RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report by Vassos Neocleous, Pavlos Fanis, Savvas Frangos, Nicos Skordis, Leonidas A. Phylactou

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Editorial: Genetic, epigenetic and molecular landscaping of puberty by Sasha R. Howard, Sasha R. Howard, Pavlos Fanis, Nicolas C. Nicolaides, Anna Grandone

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The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes by Pavlos Fanis, Nicos Skordis, Nicos Skordis, Nicos Skordis, Meropi Toumba, Meropi Toumba, Michalis Picolos, George A. Tanteles, Vassos Neocleous, Leonidas A. Phylactou

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Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasia by Trine Holm Johannsen, Jakob Albrethsen, Vassos Neocleous, Federico Baronio, Martine Cools, Lise Aksglaede, Niels Jørgensen, Peter Christiansen, Meropi Toumba, Pavlos Fanis, Marie Lindhardt Ljubicic, Anders Juul

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Methylation status of hypothalamic Mkrn3 promoter across puberty by Pavlos Fanis, Maria Morrou, Marios Tomazou, Kyriaki Michailidou, George M. Spyrou, Meropi Toumba, Meropi Toumba, Nicos Skordis, Nicos Skordis, Nicos Skordis, Vassos Neocleous, Leonidas A. Phylactou

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Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia by Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Alexia A. P. Phedonos, Michalis Picolos, Elena Andreou, Tassos C. Kyriakides, George A. Tanteles, Christos Shammas, Leonidas A. Phylactou, Nicos Skordis

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The DNA binding factor Hmg20b is a repressor of erythroid differentiation by Fatemehsadat Esteghamat, Thamar Bryn van Dijk, Harald Braun, Sylvia Dekker, Reinier van der Linden, Jun Hou, Pavlos Fanis, Jeroen Demmers, Wilfred van IJcken, Zeliha Özgür, Rastislav Horos, Farzin Pourfarzad, Marieke von Lindern, Sjaak Philipsen

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Sex-specific transcriptional profiles identified in β-thalassemia patients by Aikaterini Nanou, Chrisavgi Toumpeki, Pavlos Fanis, Nicoletta Bianchi, Lucia Carmela Cosenza, Cristina Zuccato, George Sentis, Giorgos Giagkas, Coralea Stephanou, Marios Phylactides, Soteroula Christou, Michalis Hadjigavriel, Maria Sitarou, Carsten W. Lederer, Roberto Gambari, Marina Kleanthous, Eleni Katsantoni

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