Maria Tzetis

Scopus Author ID Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 11

Top Venues

Expert review of molecular diagnostics

Genes

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Anastasios K Mitrakos, Konstantina Kosma, Periklis Makrythanasis, Maria Tzetis
The Phenotypic Spectrum of 16p11.2 Recurrent Chromosomal Rearrangements. Genes 15 (8) (2024)
Anastasios K Mitrakos, Konstantina Kosma, Periklis Makrythanasis, Maria Tzetis
The Phenotypic Spectrum of 16p11.2 Recurrent Chromosomal Rearrangements. Genes 15 (8) (2024)
Vasileia Christodoulaki, Konstantina Kosma, Nikolaos M Marinakis, Faidon-Nikolaos Tilemis, Nikolaos Stergiou, Afroditi Kampouraki, Charalampos Kapogiannis, Vasiliki Karava, Andromachi Mitsioni, Maria Mila, Christina Kanaka-Gantenbein, Periklis Makrythanasis, Maria Tzetis, Joanne Traeger Synodinos
Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes 15 (8) (2024)
Vasileia Christodoulaki, Konstantina Kosma, Nikolaos M Marinakis, Faidon-Nikolaos Tilemis, Nikolaos Stergiou, Afroditi Kampouraki, Charalampos Kapogiannis, Vasiliki Karava, Andromachi Mitsioni, Maria Mila, Christina Kanaka-Gantenbein, Periklis Makrythanasis, Maria Tzetis, Joanne Traeger Synodinos
Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes 15 (8) (2024)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieves a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics (2023)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics 23 (1) (2023)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics 23 (1) (2023)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics 23 (1) (2023)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics 23 (1) (2023)
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger Synodinos, Christalena Sofocleous
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. Expert review of molecular diagnostics (2023)
Philip Farrell, Claude Férec, Milan Macek, Thomas Frischer, Sabine Renner, Katharina Riss, David Barton, Teresa Repetto, Maria Tzetis, Karine Giteau, Morten Duno, Melissa Rogers, Hara Levy, Mourad Sahbatou, Yann Fichou, Cédric Le Maréchal, French Exome Consortium
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis. European journal of human genetics : EJHG 26 (12) (2018)
Anne Girardet, Victoria Viart, Stéphanie Plaza, Gemma Daina, Martine De Rycke, Marie Des Georges, Francesco Fiorentino, Gary Harton, Aliya Ishmukhametova, Joaquima Navarro, Caroline Raynal, Pamela Renwick, Florielle Saguet, Martin Schwarz, Sioban SenGupta, Maria Tzetis, Anne-Françoise Roux, Mireille Claustres
The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus. European journal of human genetics : EJHG 24 (4) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Maria Tzetis