Esra Arslan Ates

7PUBLICATIONS
49CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesGene and molecular therapyCancer geneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (7)

|Dec 01, 2025
Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum.

Zehra Manav Yiğit, Aydan Mengübaş Erbaş, Ayberk Türkyılmaz

|Feb 04, 2025
Identification of Novel Variants in the NHS in Four Turkish Patients With Nance-Horan Syndrome.

Ceren Alavanda, Esra Arslan Ateş, Şenol Demir

|Sep 10, 2024
Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens

|Jul 12, 2024
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens

|Jun 23, 2022
Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients.

Esra Arslan Ates, Ayberk Turkyilmaz, Ceren Alavanda

|May 29, 2021
Secondary findings in 622 Turkish clinical exome sequencing data.

Esra Arslan Ateş, Ayberk Türkyilmaz, Özlem Yıldırım

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Frequent Collaborators

3 joint publications

Şenol Demir

2 joint publications

Kathleen Claes

2 joint publications

Bilgen Bilge Geckinli

2 joint publications

Alicia M Hinze