Şenol Demir

7PUBLICATIONS
42CO-AUTHORS
Haematological tumoursEpigenetics (incl. genome methylation and epigenomics)Regenerative medicine (incl. stem cells)Neurology and neuromuscular diseasesGene and molecular therapy
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Publications (7)

|Sep 01, 2026
RNA sequencing detects more challenging cases of somatic hypermutation in the IgHV gene in patients with chronic lymphocytic leukemia.

|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

|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