Emmanouil Manolakos

Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3

Annalisa Vetro, Mohammadreza Dehghani, Lilia Kraoua et al. · European Journal of Human Genetics · 2014 · 108 citations · Full text

Spermatogenesis, Biology, Developmental Biology +13

High frequency of the <i>TARDBP</i> p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis

Sandro Orrù, Emmanouil Manolakos, Nicola Orrù et al. · Clinical Genetics · 2011 · 56 citations · Full text

Neurological Disorder, Genetics, Genetic Epidemiology +26

A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth

Ioannis Papoulidis, Emmanouil Manolakos, Elisavet Siomou et al. · Prenatal Diagnosis · 2010 · 45 citations

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature

Emmanouil Manolakos, Annalisa Vetro, Antonios Garas et al. · Experimental and Therapeutic Medicine · 2014 · 41 citations · Full text

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Nehir Edibe Kurtas, Luciano Xumerle, Lorena Leonardelli et al. · Human Mutation · 2018 · 41 citations · Full text

Chromatin, Developmental Biology, Trisomy Rescue +14