Sümeyra Oğuz

6PUBLICATIONS
56CO-AUTHORS
Genetic immunologyGene expression (incl. microarray and other genome-wide approaches)Infant and child healthGene mappingMedical infection agents (incl. prions)
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Publications (6)

|Sep 29, 2026
Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

|May 15, 2026
Expanding the Neurodevelopmental Spectrum of Xia-Gibbs Syndrome: New Clinical Entities and Novel Variants From a Turkish Cohort.

|Feb 27, 2026
Trisomy 18 and Trisomy 13: A Retrospective Cohort Study at a Tertiary Hospital.

Nihan Uygur Külcü, Nurdan Erol, Sümeyra Oguz

|Jul 31, 2025
Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1.

Burcu Yeter, Yasemin Kendir Demirkol, Esra Usluer

|Apr 17, 2025
A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

Murat Erdogan, Aysel Unal, Muhammet Ensar Dogan

|Oct 18, 2021
Diagnostic yield of microarrays in individuals with non-syndromic developmental delay and intellectual disability.

S Oğuz, U E Arslan, P Ö Ş Kiper

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Frequent Collaborators

2 joint publications

Tahir Atik

2 joint publications

Aysel Unal

2 joint publications

Irem Kalay

2 joint publications

Aslıhan Kıraz