
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:
Formation of tRNA Wobble Inosine in Humans Is Disrupted by a Millennia-Old Mutation Causing Intellectual Disability
Jillian Ramos, Lu Han, Yan Li, et al.
Molecular and Cellular Biology (2019) Vol. 39, Iss. 19
Open Access | Times Cited: 33
Jillian Ramos, Lu Han, Yan Li, et al.
Molecular and Cellular Biology (2019) Vol. 39, Iss. 19
Open Access | Times Cited: 33
Showing 1-25 of 33 citing articles:
The life and times of a tRNA
Eric M. Phizicky, Anita K. Hopper
RNA (2023) Vol. 29, Iss. 7, pp. 898-957
Open Access | Times Cited: 72
Eric M. Phizicky, Anita K. Hopper
RNA (2023) Vol. 29, Iss. 7, pp. 898-957
Open Access | Times Cited: 72
Human transfer RNA modopathies: diseases caused by aberrations in transfer RNA modifications
Takeshi Chujo, Kazuhito Tomizawa
FEBS Journal (2021) Vol. 288, Iss. 24, pp. 7096-7122
Open Access | Times Cited: 105
Takeshi Chujo, Kazuhito Tomizawa
FEBS Journal (2021) Vol. 288, Iss. 24, pp. 7096-7122
Open Access | Times Cited: 105
Inosine in Biology and Disease
Sundaramoorthy Srinivasan, Adrian Gabriel Torres, Lluı́s Ribas de Pouplana
Genes (2021) Vol. 12, Iss. 4, pp. 600-600
Open Access | Times Cited: 87
Sundaramoorthy Srinivasan, Adrian Gabriel Torres, Lluı́s Ribas de Pouplana
Genes (2021) Vol. 12, Iss. 4, pp. 600-600
Open Access | Times Cited: 87
tRNA Modifications and Modifying Enzymes in Disease, the Potential Therapeutic Targets
Weifang Cui, Deze Zhao, Junjie Jiang, et al.
International Journal of Biological Sciences (2023) Vol. 19, Iss. 4, pp. 1146-1162
Open Access | Times Cited: 24
Weifang Cui, Deze Zhao, Junjie Jiang, et al.
International Journal of Biological Sciences (2023) Vol. 19, Iss. 4, pp. 1146-1162
Open Access | Times Cited: 24
DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modification
Jenna M. Lentini, Hessa S. Alsaif, Eissa Faqeih, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 62
Jenna M. Lentini, Hessa S. Alsaif, Eissa Faqeih, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 62
tRNA-derived fragments: A new class of non-coding RNA with key roles in nervous system function and dysfunction
Steven G. Fagan, Mark Helm, Jochen H.M. Prehn
Progress in Neurobiology (2021) Vol. 205, pp. 102118-102118
Closed Access | Times Cited: 46
Steven G. Fagan, Mark Helm, Jochen H.M. Prehn
Progress in Neurobiology (2021) Vol. 205, pp. 102118-102118
Closed Access | Times Cited: 46
An intellectual disability‐associated missense variant in TRMT1 impairs tRNA modification and reconstitution of enzymatic activity
Kejia Zhang, Jenna M. Lentini, Christopher T. Prevost, et al.
Human Mutation (2020) Vol. 41, Iss. 3, pp. 600-607
Open Access | Times Cited: 45
Kejia Zhang, Jenna M. Lentini, Christopher T. Prevost, et al.
Human Mutation (2020) Vol. 41, Iss. 3, pp. 600-607
Open Access | Times Cited: 45
Broadly applicable oligonucleotide mass spectrometry for the analysis of RNA writers and erasers in vitro
Felix Hagelskamp, Kayla Borland, Jillian Ramos, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 7, pp. e41-e41
Open Access | Times Cited: 34
Felix Hagelskamp, Kayla Borland, Jillian Ramos, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 7, pp. e41-e41
Open Access | Times Cited: 34
The structure of the mouse ADAT2/ADAT3 complex reveals the molecular basis for mammalian tRNA wobble adenosine-to-inosine deamination
Elizabeth Ramos‐Morales, Efil Bayam, Jordi Del-Pozo-Rodríguez, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 11, pp. 6529-6548
Open Access | Times Cited: 28
Elizabeth Ramos‐Morales, Efil Bayam, Jordi Del-Pozo-Rodríguez, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 11, pp. 6529-6548
Open Access | Times Cited: 28
The tRNA regulome in neurodevelopmental and neuropsychiatric disease
Jennifer Blaze, Schahram Akbarian
Molecular Psychiatry (2022) Vol. 27, Iss. 8, pp. 3204-3213
Open Access | Times Cited: 22
Jennifer Blaze, Schahram Akbarian
Molecular Psychiatry (2022) Vol. 27, Iss. 8, pp. 3204-3213
Open Access | Times Cited: 22
Proteolytic cleavage and inactivation of the TRMT1 tRNA modification enzyme by SARS-CoV-2 main protease
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
eLife (2024) Vol. 12
Open Access | Times Cited: 4
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
eLife (2024) Vol. 12
Open Access | Times Cited: 4
Crystal structure of the yeast heterodimeric ADAT2/3 deaminase
Xiwen Liu, Ruoyu Chen, Yujie Sun, et al.
BMC Biology (2020) Vol. 18, Iss. 1
Open Access | Times Cited: 28
Xiwen Liu, Ruoyu Chen, Yujie Sun, et al.
BMC Biology (2020) Vol. 18, Iss. 1
Open Access | Times Cited: 28
Human tRNAs with inosine 34 are essential to efficiently translate eukarya-specific low-complexity proteins
Adrian Gabriel Torres, Marta Rodríguez-Escribà, Marina Marcet‐Houben, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 12, pp. 7011-7034
Open Access | Times Cited: 25
Adrian Gabriel Torres, Marta Rodríguez-Escribà, Marina Marcet‐Houben, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 12, pp. 7011-7034
Open Access | Times Cited: 25
Destabilization of mutated human PUS3 protein causes intellectual disability
Ting‐Yu Lin, Robert Śmigiel, Bożena Kuźniewska, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 2063-2078
Open Access | Times Cited: 17
Ting‐Yu Lin, Robert Śmigiel, Bożena Kuźniewska, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 2063-2078
Open Access | Times Cited: 17
Neurological Diseases Caused by Loss of Transfer RNA Modifications: Commonalities in Their Molecular Pathogenesis
Takeshi Chujo, Kazuhito Tomizawa
Journal of Molecular Biology (2025), pp. 169047-169047
Closed Access
Takeshi Chujo, Kazuhito Tomizawa
Journal of Molecular Biology (2025), pp. 169047-169047
Closed Access
Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder
Jillian Ramos, Melissa Proven, Jonatan Halvardson, et al.
RNA (2020) Vol. 26, Iss. 11, pp. 1654-1666
Open Access | Times Cited: 22
Jillian Ramos, Melissa Proven, Jonatan Halvardson, et al.
RNA (2020) Vol. 26, Iss. 11, pp. 1654-1666
Open Access | Times Cited: 22
High-Performance Near-Infrared Fluorescent Secondary Antibodies for Immunofluorescence
Cynthia L. Schreiber, Dong‐Hao Li, Bradley D. Smith
Analytical Chemistry (2021) Vol. 93, Iss. 7, pp. 3643-3651
Open Access | Times Cited: 19
Cynthia L. Schreiber, Dong‐Hao Li, Bradley D. Smith
Analytical Chemistry (2021) Vol. 93, Iss. 7, pp. 3643-3651
Open Access | Times Cited: 19
The Repertoire of RNA Modifications Orchestrates a Plethora of Cellular Responses
Panagiotis G. Adamopoulos, Konstantina Athanasopoulou, Glykeria N. Daneva, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 2387-2387
Open Access | Times Cited: 8
Panagiotis G. Adamopoulos, Konstantina Athanasopoulou, Glykeria N. Daneva, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 2387-2387
Open Access | Times Cited: 8
Proteolytic cleavage and inactivation of the TRMT1 tRNA modification enzyme by SARS-CoV-2 main protease
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 7
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 7
Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variant
Sateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics (2021) Vol. 141, Iss. 2, pp. 209-215
Closed Access | Times Cited: 16
Sateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics (2021) Vol. 141, Iss. 2, pp. 209-215
Closed Access | Times Cited: 16
ADATs: roles in tRNA editing and relevance to disease
Xue-Ling Mao, Gilbert Eriani, Xiao-Long Zhou
Acta Biochimica et Biophysica Sinica (2024)
Open Access | Times Cited: 2
Xue-Ling Mao, Gilbert Eriani, Xiao-Long Zhou
Acta Biochimica et Biophysica Sinica (2024)
Open Access | Times Cited: 2
The role of altered translation in intellectual disability and epilepsy
Taylor J. Malone, Leonard K. Kaczmarek
Progress in Neurobiology (2022) Vol. 213, pp. 102267-102267
Open Access | Times Cited: 10
Taylor J. Malone, Leonard K. Kaczmarek
Progress in Neurobiology (2022) Vol. 213, pp. 102267-102267
Open Access | Times Cited: 10
Proteolytic cleavage and inactivation of the TRMT1 tRNA modification enzyme by SARS-CoV-2 main protease
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Kejia Zhang, Patrick Eldin, Jessica H. Ciesla, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
The CGA codon decoding through tRNAArg (ICG ) supply governed by Tad2/Tad3 in Saccharomyces cerevisiae
M. Wada, Koichi Ito
FEBS Journal (2023) Vol. 290, Iss. 13, pp. 3480-3489
Open Access | Times Cited: 4
M. Wada, Koichi Ito
FEBS Journal (2023) Vol. 290, Iss. 13, pp. 3480-3489
Open Access | Times Cited: 4
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
Wei Guo, Stefano Russo, Francesca Tuorto
BioEssays (2024) Vol. 46, Iss. 9
Open Access | Times Cited: 1