Sumeyra Oguz

5PUBLICATIONS
36CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthGene mappingMedical infection agents (incl. prions)Child and adolescent development
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (5)

|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

Pageof 1

Frequent Collaborators

2 joint publications

Enise Avci Durmuşalioğlu

1 joint publications

G E Utine

1 joint publications

Murat Erdogan

1 joint publications

Aysel Unal