Elisavet Siomou

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

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases

Ioannis Papoulidis, Alexandros Sotiriadis, Elisavet Siomou et al. · Prenatal Diagnosis · 2015 · 29 citations

Dual testing with QF‐PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF‐PCR as a stand‐alone test according to referral indications

Ioannis Papoulidis, Elisavet Siomou, Alexandros Sotiriadis et al. · Prenatal Diagnosis · 2012 · 22 citations · Full text

Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report

Ioannis Papoulidis, Eirini Oikonomidou, Sandro Orrù et al. · Molecular Medicine Reports · 2013 · 22 citations · Full text

Genetics, Pathology, Tar Syndrome +21

Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study

Alexandros Sotiriadis, Ioannis Papoulidis, Elisavet Siomou et al. · Prenatal Diagnosis · 2017 · 18 citations