V. Velissariou

发表

Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature

C. Sismani, P. Patsalis, P. Evangelidou, 2013, BioMed research international.

Distinctive pattern of first trimester maternal serum biochemical markers in trisomy 22 pregnancies

S. Sifakis, V. Velissariou, M. Karkaletsi, 2008, Prenatal diagnosis.

Noninvasive Cell-Free DNA Prenatal Testing for Fetal Aneuploidy in Maternal Blood

P. Patsalis, V. Velissariou, 2017 .

Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21

Alex Karagrigoriou, Nigel P Carter, N. Carter, 2011, Nature Medicine.

Comparison of next generation sequencing-based and methylated DNA immunoprecipitation-based approaches for fetal aneuploidy non-invasive prenatal testing

P. Patsalis, V. Velissariou, G. Christopoulou, 2015 .

Variability of ffDNA in maternal plasma does not prevent correct classification of trisomy 21 using MeDIP‐qPCR methodology

P. Patsalis, E. Tsaliki, C. Spyrou, 2013, Prenatal diagnosis.

Letter to the editor of Prenatal Diagnosis Technical Concerns on the Clinical Validation of the NIFTY Test

P. Patsalis, V. Velissariou, G. Christopoulou, 2013 .

A new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR

P. Patsalis, A. Karagrigoriou, E. Tsaliki, 2012, Expert opinion on biological therapy.

Mapping interleukin enhancer binding factor 2 gene (ILF2) to human chromosome 1 (1q11-qter and 1p11-p12) by polymerase chain reaction amplification of human-rodent somatic cell hybrid DNA templates.

N. Vamvakopoulos, Z. Mamuris, V. Velissariou, 1996, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21

N. Carter, P. Patsalis, A. Karagrigoriou, 2011, Nature Medicine.

MeDIP real‐time qPCR of maternal peripheral blood reliably identifies trisomy 21

K. Lamnissou, P. Patsalis, A. Karagrigoriou, 2012, Prenatal diagnosis.

Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test

P. Patsalis, K. Tsangaras, S. Vittas, 2019, Molecular Cytogenetics.

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis

M. Petersen, V. Velissariou, E. Katsarou, 2002, European Journal of Human Genetics.

Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis

P. Patsalis, V. Velissariou, M. Petersen, 2001, Prenatal diagnosis.

Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14

T. Liehr, A. Efthymiadou, D. Chrysis, 2020, Cytogenetic and Genome Research.

Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases

C. Sismani, P. Patsalis, K. Tsangaras, 2019, Molecular Cytogenetics.

Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients

C. Sismani, N. Moschonas, P. Patsalis, 1998, Clinical genetics.

Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome

A. Tsezou, P. Patsalis, V. Velissariou, 1997, Clinical genetics.

Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.

A. Latos-Bieleńska, P. Patsalis, K. Tsangaras, 2016, Clinical chemistry.

Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.

C. Kanaka-Gantenbein, V. Velissariou, S. Christopoulou, 2006, European journal of medical genetics.

Genetic skeletal disorders of the fetus and infant: pathologic and molecular findings in a series of 41 cases.

A. Karantanas, E. Patsouris, A. Konstantinidou, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Outcome of pregnancies with trisomy 2 cells in chorionic villi

I. Staboulidou, K. Nicolaides, S. Sifakis, 2010, Prenatal diagnosis.

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2

N. Tommerup, T. Liehr, M. Bak, 2013, European Journal of Human Genetics.

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

C. Sismani, P. Patsalis, I. Georgiou, 2010, Molecular Cytogenetics.

The Replacement of Cytogenetic Analysis by Direct Chorionic Villi Sampling Preparation with Quantitative Fluorescence PCR

S. Sifakis, V. Velissariou, G. Christopoulou, 2009, Gynecologic and Obstetric Investigation.

Prenatal Diagnosis of Trisomy 2 Mosaicism: A Case Report

S. Sifakis, M. Petersen, V. Velissariou, 2004, Fetal Diagnosis and Therapy.

Ring-14 and trisomy 14q in the same child.

V. Velissariou, C. Pangalos, M. Ghica, 1984, Annales de genetique.

Prenatal diagnosis of achondroplasia presenting with multiple‐suture synostosis: a novel association

V. Velissariou, T. Antoniadi, C. Karadimas, 2006, Prenatal diagnosis.

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.

The secretory proteins of the larval salivary gland of Drosophila melanogaster

M. Ashburner, V. Velissariou, 1980, Chromosoma.

Cytogenetic and genetic mapping of a salivary gland secretion protein in Drosophila melanogaster

M. Ashburner, V. Velissariou, 2004, Chromosoma.

Unbalanced X;9 translocation in an infertile male with de novo duplication Xp22.31p22.33

S. Gagos, S. Karras, V. Velissariou, 2019, Journal of Assisted Reproduction and Genetics.

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

N. Agnantis, G. Fountzilas, A. Apessos, 2005, BMC Cancer.

Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population

C. Sismani, T. Liehr, M. Hempel, 2020, Journal of Human Genetics.

A Prenatally Ascertained De Novo Terminal Deletion of Chromosomal Bands 1q43q44 Associated with Multiple Congenital Abnormalities in a Female Fetus

C. Sismani, A. Konstantinidou, P. Evangelidou, 2015, Case reports in genetics.

Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: novel association with Pectus carinatum in a molecularly confirmed case and review of the fetal phenotype.

A. Konstantinidou, V. Velissariou, Jason Tasoulas, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.

C. Sismani, P. Patsalis, C. Bartsocas, 2007, European journal of medical genetics.

A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus.

C. Sismani, A. Konstantinidou, P. Patsalis, 2013, Gene.

Human amniotic fluid stimulates the proliferation of human fetal and adult skin fibroblasts: The roles of bFGF and PDGF and of the ERK and Akt signaling pathways

D. Kletsas, H. Pratsinis, V. Velissariou, 2010, Wound Repair and Regeneration.

Hydrops Fetalis, Thickened Placenta and Other Sonographic Findings in a Low-Level Trisomy 21 Mosaicism: A Case Report

S. Sifakis, O. Koukoura, V. Velissariou, 2008, Fetal Diagnosis and Therapy.

Comment on “Technical concerns on the clinical validation of the NIFTY test”

P. Patsalis, V. Velissariou, G. Christopoulou, 2013, Prenatal diagnosis.

Prenatal diagnosis of hypochondroplasia: Report of two cases

S. Sifakis, G. Nasioulas, V. Velissariou, 2006, American journal of medical genetics. Part A.

A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis

C. Yapijakis, D. Vassilopoulos, V. Velissariou, 2002, Prenatal diagnosis.

Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.

A. Tsezou, M. Tzetis, E. Kanavakis, 2012, European journal of medical genetics.

Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases

C. Sismani, P. Patsalis, K. Tsangaras, 2019, Molecular Cytogenetics.

Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test

P. Patsalis, K. Tsangaras, S. Vittas, 2019, Molecular Cytogenetics.

Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population

C. Sismani, T. Liehr, M. Hempel, 2020, Journal of Human Genetics.

Clinical and molecular description of the prenatal diagnosis of a fetus with a maternally inherited microduplication 22q11.2 of 2.5 Mb.

C. Sismani, V. Velissariou, G. Christopoulou, 2013, Gene.

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.

Prenatal diagnosis of a de novo partial trisomy 10p12.1–12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH

C. Sismani, P. Patsalis, G. Koumbaris, 2008, Prenatal diagnosis.