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:
Nonsense-mediated mRNA decay in neuronal physiology and neurodegeneration
Marija Petrić Howe, Rickie Patani
Trends in Neurosciences (2023) Vol. 46, Iss. 10, pp. 879-892
Open Access | Times Cited: 14
Marija Petrić Howe, Rickie Patani
Trends in Neurosciences (2023) Vol. 46, Iss. 10, pp. 879-892
Open Access | Times Cited: 14
Showing 14 citing articles:
Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders
Anne T. Berg, Christopher H. Thompson, Leah Schust Myers, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2761-2774
Open Access | Times Cited: 8
Anne T. Berg, Christopher H. Thompson, Leah Schust Myers, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2761-2774
Open Access | Times Cited: 8
Alternative Splicing Alterations in Patients With Amyotrophic Lateral Sclerosis: Link to the Disruption of TAR DNA‐Binding Protein 43 kDa Functions
Takashi Miwa, E. Takeuchi, Kotaro Ogawa, et al.
Neurology and Clinical Neuroscience (2025)
Open Access
Takashi Miwa, E. Takeuchi, Kotaro Ogawa, et al.
Neurology and Clinical Neuroscience (2025)
Open Access
Longitudinal multi-omics in alpha-synuclein Drosophila model discriminates disease- from age-associated pathologies in Parkinson’s disease
Justin Moore, Timothy Wu, Justin Dhindsa, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access
Justin Moore, Timothy Wu, Justin Dhindsa, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access
A mutation in the low-complexity domain of splicing factor hnRNPA1 linked to amyotrophic lateral sclerosis disrupts distinct neuronal RNA splicing networks
Yeon J. Lee, Donald C. Rio
Genes & Development (2024) Vol. 38, Iss. 1-2, pp. 11-30
Open Access | Times Cited: 4
Yeon J. Lee, Donald C. Rio
Genes & Development (2024) Vol. 38, Iss. 1-2, pp. 11-30
Open Access | Times Cited: 4
Genomics of diffusion-imaging integrating GWAS, exome data and single-cell sequencing unravels lifespan determinants of cerebral small vessel disease
Stéphanie Debette, Yasaman Saba, Hideaki Suzuki, et al.
Research Square (Research Square) (2025)
Closed Access
Stéphanie Debette, Yasaman Saba, Hideaki Suzuki, et al.
Research Square (Research Square) (2025)
Closed Access
MicroRNA-mediated regulation of nonsense-mediated mRNA decay factors: Insights into microRNA prediction tools and profiling techniques
Priyanka Yadav, Raja Tamilselvan, H. Mani, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2024) Vol. 1867, Iss. 2, pp. 195022-195022
Closed Access | Times Cited: 3
Priyanka Yadav, Raja Tamilselvan, H. Mani, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2024) Vol. 1867, Iss. 2, pp. 195022-195022
Closed Access | Times Cited: 3
Patrick Smith, Zachary T. Campbell
Wiley Interdisciplinary Reviews - RNA (2024) Vol. 15, Iss. 2
Closed Access | Times Cited: 2
Genetic analysis of psychosis Biotypes: shared Ancestry-adjusted polygenic risk and unique genomic associations
Cuihua Xia, Ney Alliey‐Rodriguez, Carol A. Tamminga, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 2
Cuihua Xia, Ney Alliey‐Rodriguez, Carol A. Tamminga, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 2
Rapid UPF1 depletion illuminates the temporal dynamics of the NMD-regulated transcriptome in human cells
Volker Boehm, Damaris Wallmeroth, Paul O. Wulf, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Volker Boehm, Damaris Wallmeroth, Paul O. Wulf, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
A frameshift mutation in the murinePrkragene causes dystonia and exhibits abnormal cerebellar development and reduced eIF2α phosphorylation.
Samuel B. Burnett, Allison M. Culver, Tricia A. Simon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Samuel B. Burnett, Allison M. Culver, Tricia A. Simon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
ZMAT2 condensates regulate the alternative splicing of TRIM28 to reduce cellular ROS accumulation, thereby promoting the proliferation of HCC cells
Ya-Ning Zhu, Jiong Li, Sang Li, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
Ya-Ning Zhu, Jiong Li, Sang Li, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
A frameshift mutation in the murine Prkra gene exhibits cerebellar abnormality and reduced eIF2α phosphorylation
Samuel B. Burnett, Allison M. Culver, Tricia A. Simon, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 11
Closed Access | Times Cited: 1
Samuel B. Burnett, Allison M. Culver, Tricia A. Simon, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 11
Closed Access | Times Cited: 1
UPF1 is required for gene expression in mitochondria and for the elimination of paternal mtDNA
Matthew Wright, Anand K. Singh, Hannah L Dixon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Matthew Wright, Anand K. Singh, Hannah L Dixon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Unveiling RNA Dysfunction: A Key Player in Neurodegeneration
Pranjali Pandey, Tanisha Mukherjee, Oliva Modak, et al.
(2024), pp. 241-270
Closed Access
Pranjali Pandey, Tanisha Mukherjee, Oliva Modak, et al.
(2024), pp. 241-270
Closed Access
