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For: Pozner T, Regensburger M, Engelhorn T, Winkler J, Winner B. Janus-faced spatacsin (SPG11): involvement in neurodevelopment and multisystem neurodegeneration. Brain 2020;143:2369-79. [PMID: 32355960 DOI: 10.1093/brain/awaa099] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 7.5] [Reference Citation Analysis]
Number Citing Articles
1 Luo A, Xu Z, Liao S. Clinical characteristics and gene mutation analysis of a family with hereditary spastic paraplegia type 11.. [DOI: 10.21203/rs.3.rs-2269224/v1] [Reference Citation Analysis]
2 Regensburger M, Krumm L, Schmidt MA, Schmid A, Spatz IT, Marterstock DC, Kopp C, Kohl Z, Doerfler A, Karrasch T, Winner B, Winkler J. Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia. Nutrients 2022;14:4803. [DOI: 10.3390/nu14224803] [Reference Citation Analysis]
3 Utz KS, Kohl Z, Marterstock DC, Doerfler A, Winkler J, Schmidt M, Regensburger M. Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia. Orphanet J Rare Dis 2022;17:301. [PMID: 35906604 DOI: 10.1186/s13023-022-02451-1] [Reference Citation Analysis]
4 Rattay TW, Schöls L, Zeltner L, Rohrschneider WK, Ernemann U, Lindig T. "Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers. J Neurol 2022. [PMID: 35614164 DOI: 10.1007/s00415-022-11198-5] [Reference Citation Analysis]
5 Meyyazhagan A, Orlacchio A. Hereditary Spastic Paraplegia: An Update. Int J Mol Sci 2022;23:1697. [PMID: 35163618 DOI: 10.3390/ijms23031697] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 10.0] [Reference Citation Analysis]
6 Daida K, Nishioka Y, Li Y, Yoshino H, Funayama M, Hattori N, Nishioka K. A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene. eNeurologicalSci 2022;26:100391. [PMID: 35036589 DOI: 10.1016/j.ensci.2021.100391] [Reference Citation Analysis]
7 Singer HS, Mink JW, Gilbert DL, Jankovic J. Hereditary Spastic Paraplegia. Movement Disorders in Childhood 2022. [DOI: 10.1016/b978-0-12-820552-5.00021-8] [Reference Citation Analysis]
8 Elsayed LEO, Eltazi IZ, Ahmed AE, Stevanin G. Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview. Front Mol Biosci 2021;8:690899. [PMID: 34901147 DOI: 10.3389/fmolb.2021.690899] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
9 Lehky T, Grunseich C. Juvenile Amyotrophic Lateral Sclerosis: A Review. Genes (Basel) 2021;12:1935. [PMID: 34946884 DOI: 10.3390/genes12121935] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
10 Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, Asadollahi R, Rauch A, Winner B. Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in. Stem Cell Res 2021;56:102520. [PMID: 34479069 DOI: 10.1016/j.scr.2021.102520] [Reference Citation Analysis]
11 Deneubourg C, Ramm M, Smith LJ, Baron O, Singh K, Byrne SC, Duchen MR, Gautel M, Eskelinen EL, Fanto M, Jungbluth H joint contribution. The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy. Autophagy 2021;:1-22. [PMID: 34130600 DOI: 10.1080/15548627.2021.1943177] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
12 Güner F, Pozner T, Krach F, Prots I, Loskarn S, Schlötzer-Schrehardt U, Winkler J, Winner B, Regensburger M. Axon-Specific Mitochondrial Pathology in SPG11 Alpha Motor Neurons. Front Neurosci 2021;15:680572. [PMID: 34326717 DOI: 10.3389/fnins.2021.680572] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Gupta M, Liu X, Teraoka SN, Wright JA, Gatti RA, Quinlan A, Concannon P. Genes affecting ionizing radiation survival identified through combined exome sequencing and functional screening. Hum Mutat 2021;42:1124-38. [PMID: 34153142 DOI: 10.1002/humu.24241] [Reference Citation Analysis]
14 Toupenet Marchesi L, Leblanc M, Stevanin G. Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia. Cells 2021;10:1678. [PMID: 34359848 DOI: 10.3390/cells10071678] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
15 Karpe Y, Chen Z, Li XJ. Stem Cell Models and Gene Targeting for Human Motor Neuron Diseases. Pharmaceuticals (Basel) 2021;14:565. [PMID: 34204831 DOI: 10.3390/ph14060565] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
16 Lallemant-Dudek P, Darios F, Durr A. Recent advances in understanding hereditary spastic paraplegias and emerging therapies. Fac Rev 2021;10:27. [PMID: 33817696 DOI: 10.12703/r/10-27] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]