
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:
Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates
Melissa J MacPherson, Sarah L. Erickson, Drayden Kopp, et al.
Cell Reports (2021) Vol. 35, Iss. 10, pp. 109226-109226
Open Access | Times Cited: 27
Melissa J MacPherson, Sarah L. Erickson, Drayden Kopp, et al.
Cell Reports (2021) Vol. 35, Iss. 10, pp. 109226-109226
Open Access | Times Cited: 27
Showing 1-25 of 27 citing articles:
Emily Fisher, Jian Feng
Wiley Interdisciplinary Reviews - RNA (2022) Vol. 13, Iss. 6
Closed Access | Times Cited: 30
Accurate long-read transcript discovery and quantification at single-cell, pseudo-bulk and bulk resolution with Isosceles
Michał Kabza, Alexander J. Ritter, Ashley Byrne, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Michał Kabza, Alexander J. Ritter, Ashley Byrne, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Neonatal Encephalopathy
Anastasia Ambrose, Vanda McNiven, Diane Wilson, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Closed Access
Anastasia Ambrose, Vanda McNiven, Diane Wilson, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Closed Access
Identifying Genetic Predisposition to Dozer Lamb Syndrome: A Semi-Lethal Muscle Weakness Disease in Sheep
Morgan R Stegemiller, Margaret A. Highland, Kathleen M. Ewert, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 83-83
Open Access
Morgan R Stegemiller, Margaret A. Highland, Kathleen M. Ewert, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 83-83
Open Access
Control of striatal circuit development by the chromatin regulator Zswim6
Kyuhyun Choi, Nathan T. Henderson, Emily R. Feierman, et al.
Science Advances (2025) Vol. 11, Iss. 3
Open Access
Kyuhyun Choi, Nathan T. Henderson, Emily R. Feierman, et al.
Science Advances (2025) Vol. 11, Iss. 3
Open Access
Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity lead to neurodevelopmental disorder and obesity
Ange‐Line Bruel, Anneke T. Vulto-vanSilfhout, Frédéric Bilan, et al.
European Journal of Human Genetics (2025)
Closed Access
Ange‐Line Bruel, Anneke T. Vulto-vanSilfhout, Frédéric Bilan, et al.
European Journal of Human Genetics (2025)
Closed Access
Loss of RNA-binding protein CELF2 promotes acute leukemia development via FAT10-mTORC1
Tengxiao Guo, Yuxia Wang, Xiaolu Sun, et al.
Oncogene (2024) Vol. 43, Iss. 19, pp. 1476-1487
Open Access | Times Cited: 3
Tengxiao Guo, Yuxia Wang, Xiaolu Sun, et al.
Oncogene (2024) Vol. 43, Iss. 19, pp. 1476-1487
Open Access | Times Cited: 3
The role of CELF family in neurodevelopment and neurodevelopmental disorders
Siwan Peng, Xinyi Cai, Junpeng Chen, et al.
Neurobiology of Disease (2024) Vol. 197, pp. 106525-106525
Open Access | Times Cited: 3
Siwan Peng, Xinyi Cai, Junpeng Chen, et al.
Neurobiology of Disease (2024) Vol. 197, pp. 106525-106525
Open Access | Times Cited: 3
MECP2-related pathways are dysregulated in a cortical organoid model of myotonic dystrophy
Kathryn H. Morelli, Wenhao Jin, Shashank Shathe, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 651
Open Access | Times Cited: 15
Kathryn H. Morelli, Wenhao Jin, Shashank Shathe, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 651
Open Access | Times Cited: 15
CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice
Xinyu Duan, Xiaoxia Peng, Xiangbin Jia, et al.
Molecular Neurobiology (2024)
Closed Access | Times Cited: 2
Xinyu Duan, Xiaoxia Peng, Xiangbin Jia, et al.
Molecular Neurobiology (2024)
Closed Access | Times Cited: 2
Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy
Thiéry De Serres‐Bérard, Marion Pierre, Mohamed Chahine, et al.
Neurobiology of Disease (2021) Vol. 160, pp. 105532-105532
Open Access | Times Cited: 15
Thiéry De Serres‐Bérard, Marion Pierre, Mohamed Chahine, et al.
Neurobiology of Disease (2021) Vol. 160, pp. 105532-105532
Open Access | Times Cited: 15
Evolution of the Neocortex Through RNA-Binding Proteins and Post-transcriptional Regulation
Iva Salamon, Mladen‐Roko Rašin
Frontiers in Neuroscience (2022) Vol. 15
Open Access | Times Cited: 10
Iva Salamon, Mladen‐Roko Rašin
Frontiers in Neuroscience (2022) Vol. 15
Open Access | Times Cited: 10
Loss of CELF2 promotes skin tumorigenesis and increases drug resistance
Bindeshwar Sah, Jasvinder A. Singh, Yao Shen, et al.
International Journal of Dermatology (2024)
Open Access | Times Cited: 1
Bindeshwar Sah, Jasvinder A. Singh, Yao Shen, et al.
International Journal of Dermatology (2024)
Open Access | Times Cited: 1
Excitatory neurons and oligodendrocyte precursor cells are vulnerable to focal cortical dysplasia type IIIa as suggested by single‐nucleus multiomics
Yingying Liu, Yinchao Li, Yaqian Zhang, et al.
Clinical and Translational Medicine (2024) Vol. 14, Iss. 10
Open Access | Times Cited: 1
Yingying Liu, Yinchao Li, Yaqian Zhang, et al.
Clinical and Translational Medicine (2024) Vol. 14, Iss. 10
Open Access | Times Cited: 1
Ubiquitination and deubiquitination of 4E-T regulate neural progenitor cell maintenance and neurogenesis by controlling P-body formation
Shreeya Kedia, Mohamad‐Reza Aghanoori, Kaylan M.L. Burns, et al.
Cell Reports (2022) Vol. 40, Iss. 2, pp. 111070-111070
Open Access | Times Cited: 7
Shreeya Kedia, Mohamad‐Reza Aghanoori, Kaylan M.L. Burns, et al.
Cell Reports (2022) Vol. 40, Iss. 2, pp. 111070-111070
Open Access | Times Cited: 7
Case report: Functional characterization of a novel CHD7 intronic variant in patients with CHARGE syndrome
Cesare Rossi, Sherin Ramadan, Cecilia Evangelisti, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
Cesare Rossi, Sherin Ramadan, Cecilia Evangelisti, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
The Control of Cortical Folding: Multiple Mechanisms, Multiple Models
Alexandra Moffat, Carol Schuurmans
The Neuroscientist (2023) Vol. 30, Iss. 6, pp. 704-722
Open Access | Times Cited: 2
Alexandra Moffat, Carol Schuurmans
The Neuroscientist (2023) Vol. 30, Iss. 6, pp. 704-722
Open Access | Times Cited: 2
Global Exploration of RNA-Binding Proteins in Exercise-Induced Adult Hippocampal Neurogenesis: A Transcriptome Meta-analysis and Computational Study
M. J. Nishanth, Shanker Jha
Biochemical Genetics (2022) Vol. 60, Iss. 6, pp. 2471-2488
Closed Access | Times Cited: 4
M. J. Nishanth, Shanker Jha
Biochemical Genetics (2022) Vol. 60, Iss. 6, pp. 2471-2488
Closed Access | Times Cited: 4
Generation and characterization of a human iPSC line and gene-corrected isogenic line derived from a patient with a CELF2 gene mutation
Michelle Hua, Laura Williams, Kaylan M.L. Burns, et al.
Stem Cell Research (2024) Vol. 76, pp. 103344-103344
Open Access
Michelle Hua, Laura Williams, Kaylan M.L. Burns, et al.
Stem Cell Research (2024) Vol. 76, pp. 103344-103344
Open Access
Expression Proteomics and Histone Analysis Reveal Extensive Chromatin Network Changes and a Role for Histone Tail Trimming during Cellular Differentiation
Giorgio Oliviero, Kieran Wynne, Darrell Andrews, et al.
Biomolecules (2024) Vol. 14, Iss. 7, pp. 747-747
Open Access
Giorgio Oliviero, Kieran Wynne, Darrell Andrews, et al.
Biomolecules (2024) Vol. 14, Iss. 7, pp. 747-747
Open Access
Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity, leads to neurodevelopmental disorder and obesity.
Ange‐Line Bruel, Anneke Vulto‐van Silfhout, Frédéric Bilan, et al.
Research Square (Research Square) (2024)
Closed Access
Ange‐Line Bruel, Anneke Vulto‐van Silfhout, Frédéric Bilan, et al.
Research Square (Research Square) (2024)
Closed Access
Accurate long-read transcript discovery and quantification at single-cell resolution with Isosceles
Michał Kabza, Alexander Ritter, Ashley Byrne, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Michał Kabza, Alexander Ritter, Ashley Byrne, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
A Subphenotype-to-Genotype Approach Reveals Disproportionate Megalencephaly Autism Risk Genes
Sierra S. Nishizaki, Nicholas K. Haghani, Gabriana N. La, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Sierra S. Nishizaki, Nicholas K. Haghani, Gabriana N. La, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Post-transcriptional Gene Regulation During Cortical Development
Lucas D. Serdar, Camila Manso Musso, Debra L. Silver
Springer eBooks (2022), pp. 255-273
Closed Access | Times Cited: 1
Lucas D. Serdar, Camila Manso Musso, Debra L. Silver
Springer eBooks (2022), pp. 255-273
Closed Access | Times Cited: 1
Posttranscriptional Control of Brain Development
Camila Manso Musso, Bianca M. Lupan, Debra L. Silver
(2023), pp. 625-648
Closed Access
Camila Manso Musso, Bianca M. Lupan, Debra L. Silver
(2023), pp. 625-648
Closed Access