Mustafa Tekin

29PUBLICATIONS
111CO-AUTHORS
Molecular targetsNumerical modelling and mechanical characterisationGene mappingGene expression (incl. microarray and other genome-wide approaches)Forensic epidemiology
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Publications (29)

|Mar 19, 2026
CDK4 and CDK6 variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosis.

Esra Isik, Mohammad Faraz Zafeer, Guney Bademci

|Nov 26, 2025
Glucocorticoid treatment rescues early lethality in a mouse model of geleophysic dysplasia.

Alejo Antonio Morales, Vladimir Camarena, Katherina Walz

|Oct 13, 2025
A Novel Missense Variant in LMX1A Leads to Autosomal Dominant Nonsyndromic Hearing Loss.

Ryan Chen, Dayna Morel Swols, Guney Bademci

|Jan 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

Maggie T Arriaga, Rodrigo Mendez, Rachel A Ungar

|Dec 04, 2024
Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network Study.

Queenie K-G Tan, Allyn McConkie-Rosell, Rachel M Brown

|Oct 14, 2024
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network.

Nicholas A Borja, Rory J Tinker, Stephanie A Bivona

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Frequent Collaborators

9 joint publications

Guney Bademci

5 joint publications

Duygu Duman

4 joint publications

Nicholas Borja

3 joint publications

LeShon Peart