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Research outputs

AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model   [2023]

Ruizhi Deng; Eva Medico-Salsench; Anita Nikoncuk; Reshmi Ramakrishnan; Kristina Lanko; Nikolas A Kühn; ... et al; Ivan Čapo  ; (broj, koautora 52)

Genome-wide methylation profiling differentiates benign from aggressive and metastatic pituitary neuroendocrine tumors   [2024]

Jotanovic, Jelena; ...; Popovic, Vera; ...; (broj, koautora 35)

Genome-wide methylation profiling differentiates benign from aggressive and metastatic pituitary neuroendocrine tumors (vol 148, 68, 2024)   [2025]

Jotanovic, Jelena; ...; (broj, koautora 35)

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases   [2020]

Perenthaler, Elena; ...; Capo, Ivan Dj  ; ...; (broj, koautora 69)

Distribution patterns of tau pathology in progressive supranuclear palsy   [2020]

Kovacs, Gabor G.; ...; Ječmenica-Lukić, Milica V.  ; ...; (broj, koautora 23)

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