Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?

por Mitrakos, Anastasios, Kosma, Konstantina, Makrythanasis, Periklis, Tzetis, Maria
Publicado 2023

An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

por Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Gianikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen
Publicado 2015

Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

por Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen
Publicado 2015

Association of Polymorphisms in the Promoter Region of NOS2A Gene with Primary Knee Osteoarthritis in the Greek Population

por Leonidou, Andreas, Lepetsos, Panagiotis, Kenanidis, Eustathios, Macheras, George, Tzetis, Maria, Potoupnis, Michael, Tsiridis, Eleftherios
Publicado 2020

Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion

por Tzeravini, Evangelia, Samara, Stamatia, Kouramba, Anna, Vakrinos, Georgios, Efthimiou, Athina, Tzetis, Maria, Androutsakos, Theodoros
Publicado 2022

Can trophectoderm RNA analysis predict human blastocyst competency?

por Ntostis, Panagiotis, Kokkali, Georgia, Iles, David, Huntriss, John, Tzetis, Maria, Picton, Helen, Pantos, Konstantinos, Miller, David
Publicado 2019

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

por Tsipi, Maria, Tzetis, Maria, Kosma, Konstantina, Moschos, Marilita, Braoudaki, Maria, Poulou, Myrto, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia
Publicado 2016

Integration of Transcriptome and MicroRNA Profile Analysis of iMSCs Defines Their Rejuvenated State and Conveys Them into a Novel Resource for Cell Therapy in Osteoarthritis

por Konteles, Vasileios, Papathanasiou, Ioanna, Tzetis, Maria, Goussetis, Evgenios, Trachana, Varvara, Mourmoura, Evanthia, Balis, Charalampos, Malizos, Konstantinos, Tsezou, Aspasia
Publicado 2023

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients

por Delaveri, Aikaterini, Rapti, Aggeliki, Poulou, Myrto, Fylaktou, Eirini, Tsipi, Maria, Roussos, Charis, Makrythanasis, Periklis, Kanavakis, Emmanuel, Tzetis, Maria
Publicado 2014

Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek Children

por NASI, Lamprini, ALEXOPOULOS, Alexios, KOKKINOU, Eleftheria, ROKA, Kleoniki, TZETIS, Maria, TSIPI, Maria, KAKOUROU, Talia, KANAKA-GANTENBEIN, Christina, CHROUSOS, George, KATTAMIS, Antonis, PONS, Roser
Publicado 2023

The effects of aging on molecular modulators of human embryo implantation

por Ntostis, Panagiotis, Swanson, Grace, Kokkali, Georgia, Iles, David, Huntriss, John, Pantou, Agni, Tzetis, Maria, Pantos, Konstantinos, Picton, Helen M., Krawetz, Stephen A., Miller, David
Publicado 2021

Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases

por Tilemis, Faidon-Nikolaos, Marinakis, Nikolaos M., Veltra, Danai, Svingou, Maria, Kekou, Kyriaki, Mitrakos, Anastasios, Tzetis, Maria, Kosma, Konstantina, Makrythanasis, Periklis, Traeger-Synodinos, Joanne, Sofocleous, Christalena
Publicado 2023

Rapid clinical-scale propagation of mesenchymal stem cells using cultures initiated with immunoselected bone marrow CD105(+) cells

por Spiropoulos, Antonia, Theodosaki, Maria, Stefanaki, Kalliopi, Paterakis, George, Tzetis, Maria, Giannikou, Krinio, Petrakou, Eftichia, Dimopoulou, Maria N, Papassotiriou, Ioannis, Roma, Eleptheria S, Kanavakis, Emmanuel, Graphakos, Stelios, Goussetis, Evgenios
Publicado 2011

NFB-17. "Optic Pathway findings in children with Neurofibromatosis type-1 (NF-1)

por Roka, Kleoniki, Kokkinou, Eleftheria, Gavra, Maria, Tsina, Efthymia, Mparka, Konstantina, Zarafonitis, Georgios, Kosma, Konstantina, Makrythanasis, Periklis, Tzetis, Maria, Chasiotou, Maria, Kanaka-Gantenbein, Christina, Pons, Roser, Kattamis, Antonis
Publicado 2022

The lysine‐specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer

por Rampias, Theodoros, Karagiannis, Dimitris, Avgeris, Margaritis, Polyzos, Alexander, Kokkalis, Antonis, Kanaki, Zoi, Kousidou, Evgenia, Tzetis, Maria, Kanavakis, Emmanouil, Stravodimos, Konstantinos, Manola, Kalliopi N, Pantelias, Gabriel E, Scorilas, Andreas, Klinakis, Apostolos
Publicado 2019

A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication...

por Kolaitis, Gerasimos, Bouwkamp, Christian G., Papakonstantinou, Alexia, Otheiti, Ioanna, Belivanaki, Maria, Haritaki, Styliani, Korpa, Terpsihori, Albani, Zinovia, Terzioglou, Elena, Apostola, Polyxeni, Skamnaki, Aggeliki, Xaidara, Athena, Kosma, Konstantina, Kitsiou-Tzeli, Sophia, Tzetis, Maria
Publicado 2016

The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus

por Girardet, Anne, Viart, Victoria, Plaza, Stéphanie, Daina, Gemma, De Rycke, Martine, Des Georges, Marie, Fiorentino, Francesco, Harton, Gary, Ishmukhametova, Aliya, Navarro, Joaquima, Raynal, Caroline, Renwick, Pamela, Saguet, Florielle, Schwarz, Martin, SenGupta, Sioban, Tzetis, Maria, Roux, Anne-Françoise, Claustres, Mireille
Publicado 2016

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

por O’Rawe, Jason A., Wu, Yiyang, Dörfel, Max J., Rope, Alan F., Au, P.Y. Billie, Parboosingh, Jillian S., Moon, Sungjin, Kousi, Maria, Kosma, Konstantina, Smith, Christopher S., Tzetis, Maria, Schuette, Jane L., Hufnagel, Robert B., Prada, Carlos E., Martinez, Francisco, Orellana, Carmen, Crain, Jonathan, Caro-Llopis, Alfonso, Oltra, Silvestre, Monfort, Sandra, Jiménez-Barrón, Laura T., Swensen, Jeffrey, Ellingwood, Sara, Smith, Rosemarie, Fang, Han, Ospina, Sandra, Stegmann, Sander, Den Hollander, Nicolette, Mittelman, David, Highnam, Gareth, Robison, Reid, Yang, Edward, Faivre, Laurence, Roubertie, Agathe, Rivière, Jean-Baptiste, Monaghan, Kristin G., Wang, Kai, Davis, Erica E., Katsanis, Nicholas, Kalscheuer, Vera M., Wang, Edith H., Metcalfe, Kay, Kleefstra, Tjitske, Innes, A. Micheil, Kitsiou-Tzeli, Sophia, Rosello, Monica, Keegan, Catherine E., Lyon, Gholson J.
Publicado 2015