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Myrto Poulou
Observed names:
M Poulou,
M. Poulou,
Mirto Poulou
Institution:
Institute of Child Health
Observed institutions:
National and Kapodistrian University of Athens,
Children's Hospital Agia Sophia,
Institute of Child Health
ORCID:
0000-0002-4324-8896
Observed ORCID:
0000-0002-4324-8896
OpenAlex ID:
A5045387414
Serum microRNA array analysis identifies miR-140-3p, miR-33b-3p and miR-671-3p as potential osteoarthritis biomarkers involved in metabolic processes
2017
·
E. Ntoumou
, M. Tzetis
, et al.
·
Clinical Epigenetics
·
158
PDF
Melanocortin Receptor-1 Gene Polymorphisms and the Risk of Cutaneous Melanoma in a Low-Risk Southern European Population
2006
·
Alexander J. Stratigos
, Gerasimos Dimisianos
, et al.
·
Journal of Investigative Dermatology
·
100
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA
2018
·
Maria Tsipi
, Myrto Poulou
, et al.
·
Journal of the Neurological Sciences
·
46
A study of a single variant allele (rs1426654) of the pigmentation‐related gene SLC24A5 in Greek subjects
2008
·
Gerasimos Dimisianos
, Irene Stefanaki
, et al.
·
Experimental Dermatology
·
22
PDF
Association of the CALM1 Core Promoter Polymorphism with Knee Osteoarthritis in Patients of Greek Origin
2008
·
Myrto Poulou
, Marios Kaliakatsos
, et al.
·
Genetic Testing
·
21
Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene
2012
·
Myrto Poulou
, Irini Fylaktou
, et al.
·
Journal of Cystic Fibrosis
·
13
Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing
2015
·
Georgia Kakourou
, Christina Vrettou
, et al.
·
Systems Biology in Reproductive Medicine
·
12
PDF
Cystic Fibrosis Conductance Regulator, Tumor Necrosis Factor, Interferon Alpha-10, Interferon Alpha-17, and Interferon Gamma Genotyping as Potential Risk Markers in Pulmonary Sarcoidosis Pathogenesis in Greek Patients
2010
·
Periklis Makrythanasis
, Maria Tzetis
, et al.
·
Genetic Testing and Molecular Biomarkers
·
7
Reprogramming of bone marrow derived mesenchymal stromal cells to human induced pluripotent stem cells from pediatric patients with hematological diseases using a commercial mRNA kit
2019
·
Irene Sfougataki
, Ioannis Grafakos
, et al.
·
Blood Cells Molecules and Diseases
·
6
BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients
2014
·
Aikaterini Delaveri
, Aggeliki Rapti
, et al.
·
Meta Gene
·
6
PDF
Are ALOX5AP gene SNPs a risk or protective factor for stroke?
2014
·
Apostolis Papapostolou
, Kostas Spengos
, et al.
·
Gene
·
6
Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR
2014
·
Myrto Poulou
, Aspasia Destouni
, et al.
·
Journal of Cystic Fibrosis
·
6
PDF
Multi-allele genotyping platform for the simultaneous detection of mutations in the Wilson disease related ATP7B gene
2015
·
Maria Amvrosiadou
, Margarita Petropoulou
, et al.
·
Journal of Chromatography B
·
5
Frequencies of pathogenic CFTR variants in Greek cystic fibrosis patients with allergic bronchopulmonary aspergillosis and Aspergillus fumigatus chronic colonization: A retrospective cohort study
2022
·
Maria Noni
, Anna Katelari
, et al.
·
Journal de Mycologie Médicale
·
4
Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases
2016
·
Maria Tsipi
, Maria Tzetis
, et al.
·
Meta Gene
·
4
PDF
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome
2011
·
Flora Tzifi
, Roser Pons
, et al.
·
Pediatric Neurology
·
4
Second line chemotherapy with methotrexate and gemcitabine in patients with relapsing head and neck cancer.
2006
·
E Xydakis
, E Repassos
, et al.
·
PubMed
·
4
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical Features
2016
·
Evanthia A. Makrygianni
, George K. Papadimas
, et al.
·
Pediatric Neurology
·
3
Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD)
2015
·
A. Destouni
, M. Poulou
, et al.
·
Journal of Cystic Fibrosis
·
3
PDF
Genotyping Efficiency of 2 Primer Sets and an Unlabeled Oligonucleotide Probe for the p.Phe508del in Exon 10 of the CFTR Gene as Determined with High-Resolution Melting Analysis
2012
·
Myrto Poulou
, Aspasia Destouni
, et al.
·
Clinical Chemistry
·
2
Characterization of the Mitochondrial Genome Landscape in Induced Mscs (imscs) Derived From OA and Healthy Donors
2022
·
A. Destouni
, E. Mourmoura
, et al.
·
Osteoarthritis and Cartilage
·
1
PDF
Differential and Common Signatures of miRNA Expression and Methylation in Childhood Central Nervous System Malignancies: An Experimental and Computational Approach
2021
·
George I. Lambrou
, Myrto Poulou
, et al.
·
Cancers
·
1
PDF
Carrier Screening for Cystic Fibrosis: Past, Present and Future
2017
·
Myrto Poulou
, Maria Tzetis
·
OBM Genetics
·
1
PDF
373 p.F508del homozygosity and the genotype-phenotype relationship in Northern Greece
2011
·
M. Fotoulaki
, K. Vasilaki
, et al.
·
Journal of Cystic Fibrosis
·
1
PDF
DBS Direct Elution and Multiplex Digital PCR for SMN1 and SMN2 Copy-Number and CFTR Variant Detection: Development and Validation of a Molecular Screening Workflow
2026
·
Eleftheria Dikoglou-Tzanetatou
, Iro Skopa
, et al.
·
Diagnostics
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Works count:
35
Citation count:
436
H-index:
7
I10-index:
7
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