Nina Barisic

5PUBLICATIONS
133CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesNeonatologyMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (5)

|Aug 06, 2026
Equivalent gain-of-function variants in KCNK3 and KCNK9 and their contribution to distinct TASK K2P channelopathies.

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

|Sep 28, 2024
Machine Learning for the Identification of Key Predictors to Bayley Outcomes: A Preterm Cohort Study.

Petra Grđan Stevanović, Nina Barišić, Iva Šunić

|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

|Dec 18, 2023
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and Availability.

Victor D Armengol, Basil T Darras, Ahmad A Abulaban

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Frequent Collaborators

4 joint publications

Henry Houlden

3 joint publications

Reza Maroofian

3 joint publications

Suzanne Lesage

3 joint publications

Andrey Y Abramov