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M Aurel Nagy

Explore the profile of M Aurel Nagy including associated specialties, affiliations and a list of published articles. Areas
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Articles 22
Citations 1123
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Recent Articles
1.
Ivanchenko M, Booth K, Karavitaki K, Antonellis L, Nagy M, Peters C, et al.
bioRxiv . 2025 Jan; PMID: 39763983
Mutations in the gene cause the most common form of human hereditary hearing loss, known as DFNB1. is expressed in two cell groups of the cochlea-epithelial cells of the organ...
2.
Nagy M, Price S, Wang K, Gill S, Ren E, Jayne L, et al.
Proc Natl Acad Sci U S A . 2024 Nov; 121(49):e2418024121. PMID: 39602276
Spinal motor neuron (MN) dysfunction is the cause of a number of clinically significant movement disorders. Despite the recent approval of gene therapeutics targeting these MN-related disorders, there are no...
3.
Peer A, Nagy M, Levin M
JAMA . 2024 Nov; 332(21):1845-1846. PMID: 39504042
No abstract available.
4.
Nagy M, Price S, Wang K, Gill S, Ren E, McElrath L, et al.
bioRxiv . 2024 Sep; PMID: 39282347
Spinal motor neuron (MN) dysfunction is the cause of a number of clinically significant movement disorders. Despite the recent approval of gene therapeutics targeting these MN-related disorders, there are no...
5.
Nagy M, Cunnane M, Juliano A, Wiggs J, Caruso P, Gaier E
J Neuroophthalmol . 2024 Jun; PMID: 38880955
Background: Genetic optic atrophies comprise phenotypically heterogenous disorders of mitochondrial function. We aimed to correlate quantitative neuroimaging findings of the optic nerves in these disorders with clinical measures. Methods: From...
6.
Pollina E, Gilliam D, Landau A, Lin C, Pajarillo N, Davis C, et al.
Nature . 2023 Feb; 614(7949):732-741. PMID: 36792830
Neuronal activity is crucial for adaptive circuit remodelling but poses an inherent risk to the stability of the genome across the long lifespan of postmitotic neurons. Whether neurons have acquired...
7.
Nagy M, Lin M, Wolkow N, Gaier E
Pediatr Dermatol . 2021 Dec; 38(6):1608-1609. PMID: 34931368
No abstract available.
8.
Turrero Garcia M, Stegmann S, Lacey T, Reid C, Hrvatin S, Weinreb C, et al.
Elife . 2021 Dec; 10. PMID: 34851821
The septum is a ventral forebrain structure known to regulate innate behaviors. During embryonic development, septal neurons are produced in multiple proliferative areas from neural progenitors following transcriptional programs that...
9.
Girskis K, Stergachis A, DeGennaro E, Doan R, Qian X, Johnson M, et al.
Neuron . 2021 Sep; 109(20):3239-3251.e7. PMID: 34478631
Human accelerated regions (HARs) are the fastest-evolving regions of the human genome, and many are hypothesized to function as regulatory elements that drive human-specific gene regulatory programs. We interrogate the...
10.
Yap E, Pettit N, Davis C, Nagy M, Harmin D, Golden E, et al.
Nature . 2020 Dec; 590(7844):115-121. PMID: 33299180
Behavioural experiences activate the FOS transcription factor in sparse populations of neurons that are critical for encoding and recalling specific events. However, there is limited understanding of the mechanisms by...