Esra Arslan Ates (Esra Arslan Ateş)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Topics

Epithelial Mesenchymal Transition

Intellectual Disability

Top Venues

European journal of human genetics : EJHG

The Journal of clinical endocrinology and metabolism

Journal of human genetics

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

Publications

Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG 32 (9) (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Esra Arslan Ates, Ayberk Türkyilmaz, Özlem Yıldırım, Ceren Alavanda, Hamza Polat, Şenol Demir, Alper Han Çebi, Bilgen Bilge Geçkinli, Ahmet İlter Güney, Pınar Ata, Ahmet Arman
Secondary findings in 622 Turkish clinical exome sequencing data. Journal of human genetics 66 (11) (2021)
Sare Betul Kaygusuz, Esra Arslan Ates, Maria Lillina Vignola, Burcu Volkan, Bilgen Bilge Geckinli, Serap Turan, Abdullah Bereket, Carles Gaston-Massuet, Tülay Güran
Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects. The Journal of clinical endocrinology and metabolism 106 (10) (2021)