Open Access Helper

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:

A novel ELP1 mutation impairs the function of the Elongator complex and causes a severe neurodevelopmental phenotype
Marija Kojic, Nour-el-Hana Abbassi, Ting‐Yu Lin, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 7, pp. 445-453
Open Access | Times Cited: 11

Showing 11 citing articles:

Cryo-EM structures of the human Elongator complex at work
Nour-el-Hana Abbassi, Marcin Jaciuk, David Scherf, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
Familial dysautonomia
Alejandra González‐Duarte, Maria Cotrina-Vidal, Horacio Kaufmann, et al.
Clinical Autonomic Research (2023) Vol. 33, Iss. 3, pp. 269-280
Closed Access | Times Cited: 14
Interneuron odyssey: molecular mechanisms of tangential migration
Ikram Toudji, Asmaa Toumi, Émile Chamberland, et al.
Frontiers in Neural Circuits (2023) Vol. 17
Open Access | Times Cited: 11
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
Ricardo Harripaul, Elisabetta Morini, Monica Salani, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
tRNA modifications tune decoding of codon pairs to prevent cellular quality control responses
Jie Wu, Cristián Eggers, Olga Sin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Lost in translation: How neurons cope with tRNA decoding
Wei Guo, Stefano Russo, Francesca Tuorto
BioEssays (2024) Vol. 46, Iss. 9
Open Access | Times Cited: 1
Neurodevelopmental disorders associated variants inADAT3disrupt the activity of the ADAT2/ADAT3 tRNA deaminase complex and impair neuronal migration
Jordi Del-Pozo-Rodríguez, Peggy Tilly, Romain Lecat, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Loss of Elp1 in cerebellar granule cell progenitors models ataxia phenotype of Familial Dysautonomia
Frederik Arnskötter, Patricia Benites Goncalves da Silva, Mackenna E. Schouw, et al.
Neurobiology of Disease (2024) Vol. 199, pp. 106600-106600
Open Access
The Alteration of Proteomic Profiles in Hippocampus of Type 2 Diabetic Mice Associated With Cognitive Impairment
Yoottana Janthakhin, Sirikran Juntapremjit, Karin Anna Hummel, et al.
Bioinformatics and Biology Insights (2024) Vol. 18
Open Access
The conserved wobble uridine tRNA thiolase Ctu1 is required for angiogenesis and embryonic development
Yangziwei Yu, Chuqiao Wang, Yan Wang, et al.
PLoS ONE (2024) Vol. 19, Iss. 12, pp. e0315854-e0315854
Open Access
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
Ricardo Harripaul, Elisabetta Morini, Monica Salani, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top