G. Kakourou

发表

Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK

S. Dhanjal, J. Harper, A. Doshi, 2008, Neuromuscular Disorders.

Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2

S. Dhanjal, J. Harper, A. Doshi, 2007, Prenatal diagnosis.

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.

M. Tzetis, E. Kanavakis, S. Kitsiou-Tzeli, 2012, Gene.

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).

J. Traeger-Synodinos, M. Tzetis, S. Kitsiou-Tzeli, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pre-implantation HLA matching: The production of a Saviour Child.

J. Traeger-Synodinos, C. Vrettou, Maria Moutafi, 2017, Best practice & research. Clinical obstetrics & gynaecology.

A Generic, Flexible Protocol for Preimplantation Human Leukocyte Antigen Typing Alone or in Combination with a Monogenic Disease, for Rapid Case Work-up and Application

J. Traeger-Synodinos, E. Kanavakis, C. Vrettou, 2014, Hemoglobin.

Prenatal and preimplantation diagnosis of hemoglobinopathies

J. Traeger-Synodinos, C. Vrettou, G. Kakourou, 2018, International journal of laboratory hematology.

Preimplantation genetic testing for aneuploidy by microarray analysis of polar bodies in advanced maternal age: a randomized clinical trial

P. Bossuyt, L. Gianaroli, K. Sermon, 2018, Human reproduction.

Hemoglobinopathies and preimplantation diagnostics

J. Traeger-Synodinos, C. Vrettou, G. Kakourou, 2022, International journal of laboratory hematology.

Analysis of glycosidases activity in Chlamydia trachomatis L2 serotype

G. Kakourou, P. Greenwell, S. Rughooputh, 2007 .

Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays.

J. Harper, A. Doshi, P. Serhal, 2009, Human reproduction.

ESHRE survey results and good practice 1 recommendations on Chromosomal 2 Mosaicism 3

J. Vermeesch, C. Rubio, A. Capalbo, 2022 .

ESHRE survey results and good practice recommendations on managing chromosomal mosaicism

J. Vermeesch, C. Rubio, A. Capalbo, 2022, Human reproduction open.

ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders

C. Moutou, V. Goossens, J. Dreesen, 2020, Human reproduction open.

Investigation of gene expression profiles before and after embryonic genome activation and assessment of functional pathways at the human metaphase II oocyte and blastocyst stage.

Georgia Kakourou, Paul Serhal, Pinar Tulay, 2013, Fertility and sterility.

Microsatellite Markers Within the α-Globin Gene Cluster for Robust Preimplantation Genetic Diagnosis of Severe α-Thalassemia Syndromes in Mediterranean Populations

J. Traeger-Synodinos, E. Kanavakis, C. Vrettou, 2012, Hemoglobin.

The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study

S. Kahraman, C. Giménez, J. Traeger-Synodinos, 2018, Human reproduction.

Preimplantation genetic diagnosis for retinoblastoma predisposition

S. Dhanjal, J. Harper, A. Doshi, 2006, British Journal of Ophthalmology.

, Alpesh retinoblastoma predisposition Preimplantation genetic diagnosis for

S. Dhanjal, J. Harper, P. Serhal, 2007 .

Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 2016, Systems biology in reproductive medicine.

An Update on Non-invasive Approaches for Genetic Testing of the Preimplantation Embryo

J. Traeger-Synodinos, C. Vrettou, G. Kakourou, 2022, Current genomics.

Contributing to the on-going debate around the clinical application of preimplantation embryo selection based on polygenic risk scores (PGT-P).

J. Traeger-Synodinos, P. Makrythanasis, C. Vrettou, 2023, European journal of human genetics : EJHG.

Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.

S. Dhanjal, P. Serhal, J. Delhanty, 2010, Fertility and sterility.

Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR.

M. Tzetis, E. Kanavakis, G. Kakourou, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.

S. Dhanjal, P. Serhal, J. Delhanty, 2010, Fertility and sterility.