Hϋlya Kayserili

29PUBLICATIONS
246CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Anthropological geneticsGenome structure and regulation
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Publications (29)

|Aug 04, 2026
Hereditary Polyneuropathy Experience of a Tertiary Single-Center in Türkiye: Beyond the Tip of the Iceberg.

|Jul 24, 2026
Integrated D4Z4 structural, epigenetic and exome-based evaluation of facioscapulohumeral muscular dystrophy in a tertiary referral cohort from Türkiye.

|Dec 14, 2025
Cascade counselling and testing. Recommendations of the European Society of Human Genetics.

Guido de Wert, Carla G van El, Angus Clarke

|Apr 02, 2025
Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients.

Gozde Tutku Turgut, Umut Altunoglu, Şahin Avcı

|Mar 17, 2025
Clinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in Females.

Umut Altunoglu, Birsen Karaman, Yasemin Alanay

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

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Frequent Collaborators

6 joint publications

Zehra Oya Uyguner

6 joint publications

Umut Altunoglu

5 joint publications

Nathalie Escande-Beillard

5 joint publications

Şahin Avcı