| Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population S Amenta, C Sofocleous, A Kolialexi, L Thomaidis, S Giouroukos, ... Pediatric research 57 (6), 789-795, 2005 | 69 | 2005 |
| A Substitution Involving the NLGN4 Gene Associated with Autistic Behavior in the Greek Population A Pampanos, K Volaki, E Kanavakis, O Papandreou, S Youroukos, ... Genetic testing and molecular biomarkers 13 (5), 611-615, 2009 | 61 | 2009 |
| Predictors of severity and outcome of global developmental delay without definitive etiologic yield: a prospective observational study L Thomaidis, GZ Zantopoulos, S Fouzas, L Mantagou, C Bakoula, ... BMC pediatrics 14, 1-7, 2014 | 39 | 2014 |
| The use of array-CGH in a cohort of Greek children with developmental delay E Manolakos, A Vetro, K Kefalas, SM Rapti, E Louizou, A Garas, G Kitsos, ... Molecular Cytogenetics 3, 1-8, 2010 | 37 | 2010 |
| Does early intervention work? A controlled trial L Thomaidis, E Kaderoglou, M Stefou, S Damianou, C Bakoula Infants & Young Children 12 (3), 17-22, 2000 | 34 | 2000 |
| A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype I Papoulidis, E Papageorgiou, E Siomou, E Oikonomidou, L Thomaidis, ... Gene 536 (2), 441-443, 2014 | 33 | 2014 |
| Unexpected results in the constitution of small supernumerary marker chromosomes A Vetro, E Manolakos, MB Petersen, L Thomaidis, T Liehr, G Croci, ... European journal of medical genetics 55 (3), 185-190, 2012 | 29 | 2012 |
| Cognitive and psychosocial development of HIV pediatric patients receiving highly active anti-retroviral therapy: a case-control study L Thomaidis, G Bertou, E Critselis, V Spoulou, DA Kafetzis, ... BMC pediatrics 10, 1-9, 2010 | 26 | 2010 |
| A female with Coffin-Lowry syndrome and" cataplexy". H Fryssira, S Kountoupi, JP Delaunoy, L Thomaidis Genetic counseling (Geneva, Switzerland) 13 (4), 405-409, 2002 | 25 | 2002 |
| Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: A case report I Papoulidis, E Oikonomidou, S Orru, E Siomou, M Kontodiou, ... Molecular Medicine Reports 9 (1), 163-165, 2014 | 24 | 2014 |
| Attention Deficit/Hyperactivity Disorder (ADHD) symptoms and cognitive skills of preschool children. L Thomaidis, A Choleva, M Janikian, G Bertou, A Tsitsika, ... Psychiatrike= Psychiatriki 28 (1), 28-36, 2017 | 22 | 2017 |
| Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation L Thomaidis, S Kitsiou-Tzeli, E Critselis, H Drandakis, V Touliatou, ... World journal of pediatrics 8, 309-316, 2012 | 21 | 2012 |
| Tetrasomy 9p mosaicism associated with a normal phenotype in two cases I Papoulidis, M Kontodiou, M Tzimina, I Saitis, AB Hamid, E Klein, ... Cytogenetic and Genome Research 136 (4), 237-241, 2012 | 21 | 2012 |
| Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) E Manolakos, S Orru, R Neroutsou, K Kefalas, E Louizou, I Papoulidis, ... Molecular cytogenetics 2, 1-5, 2009 | 17 | 2009 |
| Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH E Manolakos, K Kefalas, A Vetro, E Oikonomidou, G Daskalakis, N Psara, ... Molecular Cytogenetics 6, 1-5, 2013 | 15 | 2013 |
| A 725 kb deletion at 22q13. 1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 E Siomou, E Manolakos, M Petersen, L Thomaidis, Y Gyftodimou, S Orru, ... European Journal of Medical Genetics 55 (11), 641-645, 2012 | 15 | 2012 |
| Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: the value of fluorescence in situ hybridization E Manolakos, K Kefalas, R Neroutsou, M Lagou, N Kosyakova, E Ewers, ... Molecular Medicine Reports 3 (6), 1015-1022, 2010 | 15 | 2010 |
| Deletion 2q31. 2‐q31. 3 in a 4‐year‐old girl with microcephaly and severe mental retardation E Manolakos, A Vetro, K Kefalas, L Thomaidis, G Aperis, S Sotiriou, ... American Journal of Medical Genetics-Part A 155 (6), 1476, 2011 | 12 | 2011 |
| Interstitial deletion at 11q14. 2-11q22. 1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male I Papoulidis, V Paspaliaris, E Siomou, S Orru, R Murru, S Sifakis, ... Molecular Cytogenetics 8, 1-7, 2015 | 11 | 2015 |
| Cohen syndrome: two new cases in siblings L Thomaidis, H Fryssira, E Katsarou, C Metaxotou European journal of pediatrics 158, 838-841, 1999 | 11 | 1999 |
