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Tomislav Kokotović
Tomislav Kokotović
Unknown affiliation
Verified email at students.meduniwien.ac.at
Title
Cited by
Cited by
Year
Network analysis reveals rare disease signatures across multiple levels of biological organization
P Buphamalai, T Kokotovic, V Nagy, J Menche
Nature communications 12 (1), 6306, 2021
442021
Changes of AXIN-1 and beta-catenin in neuroepithelial brain tumors
T Nikuševa Martić, N Pećina-Šlaus, V Kušec, T Kokotović, H Mušinović, ...
Pathology & Oncology Research 16, 75-79, 2010
432010
AXIN-1 protein expression and localization in glioblastoma
N Pećina-Šlaus, T Nikuševa Martić, T Kokotović, V Kušec, D Tomas, ...
Collegium antropologicum 35 (1), 101-106, 2011
222011
PRDM12: new opportunity in pain research
S Imhof, T Kokotović, V Nagy
Trends in Molecular Medicine 26 (10), 895-897, 2020
122020
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder
CW Fell, A Hagelkruys, A Cicvaric, M Horrer, L Liu, JSS Li, J Stadlmann, ...
EMBO Molecular Medicine 14 (9), e15829, 2022
72022
PRDM12 is transcriptionally active and required for nociceptor function throughout life
T Kokotović, M Langeslag, EM Lenartowicz, J Manion, CW Fell, ...
Frontiers in Molecular Neuroscience 14, 720973, 2021
62021
Acute poisonings in Croatia: differences in epidemiology, associated comorbidities and final outcomes–a single-centre 15-year follow-up
I Klobučar, I Potočnjak, J Dumančić, K Stemberger, M Čupić, T Kokotović, ...
Clinical toxicology 57 (3), 181-188, 2019
62019
Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability
E Alehabib, T Kokotović, S Ranji-Burachaloo, A Tafakhori, SM Ramshe, ...
Clinical Neurology and Neurosurgery 213, 107108, 2022
32022
Expanding the known phenotype of Mullegama–Klein–Martinez syndrome in male patients
F Freyberger, T Kokotović, G Krnjak, SH Frković, V Nagy
Human genome variation 8 (1), 37, 2021
32021
Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder
G D’Onofrio, A Accogli, M Severino, H Caliskan, T Kokotović, A Blazekovic, ...
Human Genetics 142 (7), 909-925, 2023
22023
FIBCD1 is a conserved receptor for chondroitin sulphate proteoglycans of the brain extracellular matrix and a candidate gene for a complex neurodevelopmental disorder
CW Fell, A Hagelkruys, A Cicvaric, M Horrer, L Liu, JSS Li, J Stadlmann, ...
bioRxiv, 2021.09. 09.459581, 2021
22021
Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function
T Kokotović, EM Lenartowicz, M Langeslag, CI Ciotu, CW Fell, ...
The FEBS Journal 289 (12), 3457-3476, 2022
12022
Tumor suppressor gene Axin 1. Atlas Genet Cytogenet Oncol Haematol. May 2011
N Pećina-Šlaus, T Nikuševa Martić, T Kokotović
Atlas of Genetics and Cytogenetics in Oncology and Haematology, 7-11, 2011
2011
Genetic and protein changes of AXIN1 and beta-catenin in neuroepithelial brain tumors
T Nikuševa Martić, N Pećina-Šlaus, V Kušec, T Kokotović, H Mušinović, ...
FEBS Congress (34; 2009), 243-243, 2009
2009
Investigation of axin expression in neuroepithelial brain tumors
T Kokotović
Young european scientist meeting, Porto, Portugal, YES MEETING, September …, 2008
2008
The role of E-caherin in brain metastases
M Zeljko, N Pećina-Šlaus, T Nikuševa Martić, B Vili, T Kokotović
FENS Forum Geneve 2008, 085.17-085.17, 2008
2008
Genetic changes of CDH1, APC and CTNNB1 found in human brain tumors
N Pećina-Šlaus, T Nikuševa Martić, V Beroš, M Zeljko, T Kokotović
32nd FEBS Congress Molecular Machines (32; 2007), 183-183, 2007
2007
Genes of the WNT Signaling Pathway are Altered in Human Brain Tumors
N Pećina-Šlaus, T Nikuševa Martić, V Beroš, M Zeljko, T Kokotović
Croatian Congress of Neuroscience (2; 2007), 136, 2007
2007
Genetic Alterations of the E-cadherin Gene Found in Brain Metastases
M Zeljko, T Nikuševa Martić, V Beroš, T Kokotović, N Pećina-Šlaus
Croatian Congress of Neuroscience (2; 2007), 137-137, 2007
2007
GFP-protein koji svijetli.
T Kokotović, N Pećina-Šlaus
Priroda (Zagreb) 96 (948), 22-26, 2006
2006
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