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Petros Varnavas
Petros Varnavas
University of Patras
Genetics
Biology
Genetic heterogeneity
Internal medicine
Endocrinology
5
Papers
29
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Next-generation sequencing refines the genetic architecture of Greek GnRH-deficient patients
2019
Endocrine connections
Maria I. Stamou
Petros Varnavas
Lacey Plummer
Vasiliki Koika
Neoklis A. Georgopoulos
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Citations (2)
Genetic architecture of greek patients with isolated GnRH deficiency
2019
Maria I. Stamou
Petros Varnavas
Lacey Plummer
V. Koika
Neoklis A. Georgopoulos
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Isolated GnRH Deficiency: Genotypic and Phenotypic Characteristics of the Genetically Heterogeneous Greek Population.
2017
European Journal of Endocrinology
Maria I. Stamou
Petros Varnavas
Machi Kentrou
Fotini Adamidou
Antonis Voutetakis
Jw Jing
Lacey Plummer
Vasiliki Koika
Neoklis A. Georgopoulos
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Citations (7)
Comparative functional analysis of two fibroblast growth factor receptor 1 (FGFR1) mutations affecting the same residue (R254W and R254Q) in isolated hypogonadotropic hypogonadism (IHH)
2013
Gene
Vasiliki Koika
Petros Varnavas
Helen Valavani
Yisrael Sidis
Lacey Plummer
Andrew A. Dwyer
Richard Quinton
Christine Kanaka-Gantenbein
Nelly Pitteloud
Amalia Sertedaki
Catherine Dacou-Voutetakis
Neoklis A. Georgopoulos
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Citations (16)
Can Kallmann syndrome be occasionally diagnosed during childhood? Genetic diagnosis in a child with associated renal agenesis and mirror movements
2009
Asian Journal of Andrology
Neoklis A. Georgopoulos
Vasiliki Koika
Petros Varnavas
Alexandra Efthymiadou
Dimitra J. Marioli
Stefanos Mantagos
Dionysios Chrysis
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Citations (4)
1