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Year
Paper
2022
Kokotović T, Lenartowicz EW, Langeslag M, Ciotu CI, Fell CW, Scaramuzza A, Fischer MJM, Kress M, Penninger JM, Nagy V. Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function. FEBS J. 2022 Jun;289(12):3457-3476. doi: 10.1111/febs.16347. Epub 2022 Feb 16.
Abstract: https://pubmed.ncbi.nlm.nih.gov/35029322/
2022
Alehabib E, Kokotovi T, Ranji-Burachaloo S, Tafakhori A, Ramshe SM, Esmaeilizadeh Z, Darvish H, Movafagh A, Nagy V. Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability. Clin Neurol Neurosurg. 2022 Feb;213:107108. doi: 10.1016/j.clineuro.2021.107108. Epub 2021 Dec 30.
Abstract: https://pubmed.ncbi.nlm.nih.gov/34995834/
2022
Hilgen G, Kartsaki E, Kartysh V, Cessac B, Sernagor E. A novel approach to the functional classification of retinal ganglion cells. Open Biol. 2022 Mar;12(3):210367. doi: 10.1098/rsob.210367. Epub 2022 Mar 9.
Abstract: https://pubmed.ncbi.nlm.nih.gov/35259949/
2022
Kokotovi T, Lenartowicz EM, Langeslag M, Ciotu CI, Fell CW, Scaramuzza A, Fischer MJM, Kress M, Penninger JM, Nagy V. Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function. FEBS J. 2022 Jan 13. doi: 10.1111/febs.16347. Online ahead of print.
Abstract: https://pubmed.ncbi.nlm.nih.gov/35029322/
2021
Fell CW, Nagy V. Cellular Models and High-Throughput Screening for Genetic Causality of Intellectual Disability. Trends Mol Med. 2021 Mar;27(3):220-230. doi: 10.1016/j.molmed.2020.12.003. Epub 2021 Jan 2.
Abstract: https://pubmed.ncbi.nlm.nih.gov/33397633/
2020
Imhof S, Kokotović T, Nagy V. PRDM12: New Opportunity in Pain Research. Trends Mol Med. 2020 Oct;26(10):895-897. doi: 10.1016/j.molmed.2020.07.007. Epub 2020 Aug 20.
Abstract: https://pubmed.ncbi.nlm.nih.gov/32828702/
2019
Nagy V, Hollstein R, Pai TP, Herde MK, Buphamalai P, Moeseneder P,Lenartowicz E, Kavirayani A, Korenke GC, Kozieradzki I, Nitsch R, Cicvaric A,Monje Quiroga FJ, Deardorff MA, Bedoukian EC, Li Y, Yigit G, Menche J, Perçin EF,Wollnik B, Henneberger C, Kaiser FJ, Penninger JM. HACE1 deficiency leads to structural and functional neurodevelopmental defects. Neurol Genet. 2019 Apr29;5(3):e330. doi: 10.1212/NXG.0000000000000330. eCollection 2019 Jun. PubMedPMID: 31321300;
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/6561753
2019
Lee NJ, Clarke IM, Zengin A, Enriquez RF, Nagy V, Penninger JM, Baldock PA,Herzog H. RANK deletion in neuropeptide Y neurones attenuates oestrogen deficiency-related bone loss. J Neuroendocrinol. 2019 Feb;31(2):e12687. doi:10.1111/jne.12687. Epub 2019 Feb 1.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/30633834