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Şenol Demir

6PUBLICATIONS

31CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Regenerative medicine (incl. stem cells)Neurology and neuromuscular diseasesGene and molecular therapy

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Publications (6)

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|Mar 09, 2026

Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non-Suppressed TSH.

Hilal Sekizkardes, Mehmet Eltan, Senol Demir

|Dec 08, 2025

Autosomal Dominant Transmission Reframes Reproductive Counseling in Myhre Syndrome: A Novel Family and Literature Review.

Maggie R Brand, Eva Vanbelleghem, Alison C Kay

|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

|Jan 06, 2025

Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye

Ömer Doğru, Ceren Alavanda, 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

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Frequent Collaborators

3 joint publications

Eva Vanbelleghem

3 joint publications

Bert Callewaert

3 joint publications

Esra Arslan Ateş

2 joint publications

Tim Van Damme

2 joint publications

Kathleen Claes

2 joint publications

Julie De Backer

2 joint publications

Ilse Meerschaut

2 joint publications

Alicia M Hinze

2 joint publications

Natalia Gomez-Ospina

2 joint publications

Valérie Cormier-Daire

Frequent Collaborators

3 joint publications

Eva Vanbelleghem

3 joint publications

Bert Callewaert

3 joint publications

Esra Arslan Ateş

2 joint publications

Tim Van Damme

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