Ayten Güleç

4PUBLICATIONS
50CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Sep 01, 2026
From Leukaemia to MOGAD, From Refractive Error to Dural Fistula: Torticollis as the Presenting Sign of Serious Disease in Children.

|Jul 19, 2026
"Severe intellectual disability with cardiac and dermatologic involvement due to homozygous METTL23 frameshift mutation: a case report of two Turkish sisters".

|Jul 22, 2024
Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy.

Angela Clara-Hwang, Stefani Stefani, Tracy Lau

|Feb 20, 2024
Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth.

Frederike L Harms, Jessica Erin Rexach, Stephanie Efthymiou

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Frequent Collaborators

3 joint publications

Stephanie Efthymiou

3 joint publications

Hüseyin Per

2 joint publications

Busra Aynekin

1 joint publications

Frederike L Harms