Publications by authors named "Novin Balafkan"

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3D genetic architecture of schizophrenia risk across three neuronal subtypes.
Samuel K Powell, Will Liao, Sadaf Ghorbani, Raymond Rigat, Callan O'Shea, Novin Balafkan

Mol Psychiatry· November 2025

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Dynamic convergence of neurodevelopmental disorder risk genes across neurodevelopment.
Meilin Fernandez Garcia, Kayla Retallick-Townsley, April Pruitt, Elizabeth Davidson, Novin Balafkan

bioRxiv· July 2025

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Distinct Mitochondrial Remodeling During Mesoderm Differentiation in a Human-Based Stem Cell Model.
Sepideh Mostafavi, Novin Balafkan, Ina Katrine Nitschke Pettersen, Gonzalo S Nido, Richard Siller

Front Cell Dev Biol· October 2021

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Disease-specific phenotypes in iPSC-derived neural stem cells with POLG mutations.
Kristina Xiao Liang, Cecilie Katrin Kristiansen, Sepideh Mostafavi, Guro Helén Vatne, Gina Alien Zantingh, Novin Balafkan

EMBO Mol Med· October 2020

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A method for differentiating human induced pluripotent stem cells toward functional cardiomyocytes in 96-well microplates.
Novin Balafkan, Sepideh Mostafavi, Manja Schubert, Richard Siller, Kristina Xiao Liang

Sci Rep· October 2020

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Mitochondrial DNA depletion in sporadic inclusion body myositis.
Padmanabh S Bhatt, Charalampos Tzoulis, Novin Balafkan, Hrvoje Miletic, Gia Tuong Thi Tran

Neuromuscul Disord· March 2019

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Molecular pathogenesis of polymerase γ-related neurodegeneration.
Charalampos Tzoulis, Gia Tuong Tran, Jonathan Coxhead, Bjørn Bertelsen, Peer K Lilleng, Novin Balafkan

Ann Neurol· July 2014

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Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.
Charalampos Tzoulis, Gia Tuong Tran, Thomas Schwarzlmüller, Karsten Specht, Kristoffer Haugarvoll, Novin Balafkan

Brain· August 2013

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Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population.
Novin Balafkan, Charalampos Tzoulis, Bernd Müller, Kristoffer Haugarvoll, Ole-Bjørn Tysnes

Mitochondrion· November 2012

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