Tuğçe Gül-Demirkale

5PUBLICATIONS
93CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesMedical biochemistry - proteins and peptides (incl. medical proteomics)Family and household studiesBehavioural genetics
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Publications (5)

|May 27, 2026
Computational Short Tandem Repeat Genotyping Reveals Clinically Relevant Expansions in a Large Turkish Neurodegeneration Disease Cohort.

|Apr 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality.

|Aug 16, 2024
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.

Francesca Magrinelli, Christelle Tesson, Plamena R Angelova

|Oct 04, 2021
Early-Onset Parkinson's Disease: A Novel Deletion Comprising the DJ-1 and TNFRSF9 Genes.

Süleyman Güler, Tuğçe Gül, Şükran Güler

|Sep 28, 2020
An unusual familial dementia associated with G131V PRNP mutation.

E Yetim, T Gul, A N Basak

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Frequent Collaborators

5 joint publications

Ayşe Nazlı Başak

3 joint publications

Tobias B Haack

3 joint publications

Suzanne Lesage

3 joint publications

Kailash P Bhatia