Abdullah Sezer

23PUBLICATIONS
142CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical virologyGene mappingEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (23)

|Jun 19, 2026
Atypical Biallelic Inheritance in "Dominant" Genes: Evidence From a Large-Scale Consanguineus Exome Cohort.

|May 26, 2026
A comparative analysis of all reported patients with MTHFS-related neurodevelopmental disorder.

|Feb 24, 2026
ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

Zeynep Esener, Murat Öztürk, Esra Habiloğlu

|Jan 30, 2026
Meier-Gorlin syndrome due to a recurrent <i>DONSON</i> variant in a Turkish family: first report of thumb aplasia and long-term growth data.

Abdullah Sezer, Fatma Zehra Yalçın, Abdulkerim Kolkıran

|Dec 09, 2025
A novel NT5C2 Variant in a Family with Spastic Paraplegia and Intellectual Disability.

Deniz Yasar, Abdullah Sezer, Bahadır Konuskan

|Aug 10, 2025
A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With Sarcoglycanopathy.

Abdullah Sezer, Afife Büke, Hasan Hüseyin Kazan

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Frequent Collaborators

6 joint publications

Mustafa Kılıç

3 joint publications

Suzan İcil

3 joint publications

Abdulkerim Kolkıran

3 joint publications

Elifcan Taşdelen