OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function
Aarti Sharma, Alexander K. Lyashchenko, Lei Lü, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 310

Showing 26-50 of 310 citing articles:

TDP‐43 and FUS en route from the nucleus to the cytoplasm
Helena Ederle, Dorothee Dormann
FEBS Letters (2017) Vol. 591, Iss. 11, pp. 1489-1507
Open Access | Times Cited: 150

Hypoexcitability precedes denervation in the large fast-contracting motor units in two unrelated mouse models of ALS
María de Lourdes Martínez-Silva, Rebecca D Imhoff-Manuel, Aarti Sharma, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 142

Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis
Yulei Shang, Eric J. Huang
Brain Research (2016) Vol. 1647, pp. 65-78
Open Access | Times Cited: 138

Nuclear egress of TDP-43 and FUS occurs independently of Exportin-1/CRM1
Helena Ederle, Christina Funk, Claudia Abou‐Ajram, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 137

RNA metabolism in neurodegenerative disease
Elaine Y. Liu, Christopher P. Cali, Edward B. Lee
Disease Models & Mechanisms (2017) Vol. 10, Iss. 5, pp. 509-518
Open Access | Times Cited: 125

RNA-Binding Proteins in Amyotrophic Lateral Sclerosis.
Melody Zhao, Jihye Rachel Kim, Rebekah van Bruggen, et al.
PubMed (2018) Vol. 41, Iss. 9, pp. 818-829
Closed Access | Times Cited: 123

Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis
Jelena Scekic‐Zahirovic, Hajer El Oussini, Sina Mersmann, et al.
Acta Neuropathologica (2017) Vol. 133, Iss. 6, pp. 887-906
Open Access | Times Cited: 120

Pathogenesis of FUS-associated ALS and FTD: insights from rodent models
Matthew Nolan, Kevin Talbot, Olaf Ansorge
Acta Neuropathologica Communications (2016) Vol. 4, Iss. 1
Open Access | Times Cited: 117

TDP-43/FUS in motor neuron disease: Complexity and challenges
Erika N. Guerrero, Haibo Wang, Joy Mitra, et al.
Progress in Neurobiology (2016) Vol. 145-146, pp. 78-97
Open Access | Times Cited: 116

CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs
Lixia Wang, Fei Yi, Lina Fu, et al.
Protein & Cell (2017) Vol. 8, Iss. 5, pp. 365-378
Open Access | Times Cited: 110

Mouse models of ALS: Past, present and future
Cathleen Lutz
Brain Research (2018) Vol. 1693, pp. 1-10
Closed Access | Times Cited: 109

The Role of Post-Translational Modifications on Prion-Like Aggregation and Liquid-Phase Separation of FUS
Shannon N. Rhoads, Zachary Monahan, Debra Yee, et al.
International Journal of Molecular Sciences (2018) Vol. 19, Iss. 3, pp. 886-886
Open Access | Times Cited: 109

Linking hnRNP Function to ALS and FTD Pathology
Maria D. Purice, J. Paul Taylor
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 109

FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosis
Gina Picchiarelli, Maria Demestre, Amila Zuko, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 11, pp. 1793-1805
Open Access | Times Cited: 106

Stress granules at the intersection of autophagy and ALS
Zachary Monahan, Frank Shewmaker, Udai Bhan Pandey
Brain Research (2016) Vol. 1649, pp. 189-200
Open Access | Times Cited: 104

Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice
Anny Devoy, Bernadett Kalmár, Michelle Stewart, et al.
Brain (2017) Vol. 140, Iss. 11, pp. 2797-2805
Open Access | Times Cited: 104

Human sensorimotor organoids derived from healthy and amyotrophic lateral sclerosis stem cells form neuromuscular junctions
João D. Pereira, D Dubreuil, Anna‐Claire Devlin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 101

Gamma motor neurons survive and exacerbate alpha motor neuron degeneration in ALS
Mélanie Lalancette–Hébert, Aarti Sharma, Alexander K. Lyashchenko, et al.
Proceedings of the National Academy of Sciences (2016) Vol. 113, Iss. 51
Open Access | Times Cited: 99

Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes
Shinsuke Ishigaki, Yusuke Fujioka, Yohei Okada, et al.
Cell Reports (2017) Vol. 18, Iss. 5, pp. 1118-1131
Open Access | Times Cited: 97

Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy
Christian M. Simon, Ya Dai, Meaghan Van Alstyne, et al.
Cell Reports (2017) Vol. 21, Iss. 13, pp. 3767-3780
Open Access | Times Cited: 96

The phase separation-dependent FUS interactome reveals nuclear and cytoplasmic function of liquid–liquid phase separation
Stefan Reber, Daniel Jutzi, Helen Lindsay, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 13, pp. 7713-7731
Open Access | Times Cited: 95

Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging
Feng Tian, Wenlong Yang, Daniel A. Mordes, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 92

FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention
Jack Humphrey, Nicol Birsa, Carmelo Milioto, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 12, pp. 6889-6905
Open Access | Times Cited: 90

Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice
Eva So, Jacqueline C. Mitchell, Caroline Memmi, et al.
Human Molecular Genetics (2017) Vol. 27, Iss. 3, pp. 463-474
Open Access | Times Cited: 89

Scroll to top