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)

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|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

Ayşe Nazlı Başak

Tobias B Haack

Suzanne Lesage

Kailash P Bhatia

Henry Houlden

Alexis Brice

Dario R Alessi

Hermann Steller

Andrey Y Abramov

Aida M Bertoli-Avella

Frequent Collaborators

Ayşe Nazlı Başak

Tobias B Haack

Suzanne Lesage

Kailash P Bhatia