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OpenAlex Citation Counts

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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.

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Showing 22 citing articles:

Molecular networks of the FOXP2 transcription factor in the brain
Joery den Hoed, Karthikeyan Devaraju, Simon E. Fisher
EMBO Reports (2021) Vol. 22, Iss. 8
Open Access | Times Cited: 41
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
Matteo D’Antonio, Jennifer Nguyen, Timothy D. Arthur, et al.
Cell Reports (2021) Vol. 37, Iss. 7, pp. 110020-110020
Open Access | Times Cited: 36
The functions of FOXP transcription factors and their regulation by post-translational modifications
Congwen Gao, Honglin Zhu, Peng Gong, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2023) Vol. 1866, Iss. 4, pp. 194992-194992
Closed Access | Times Cited: 12
CellLoop: Identifying single-cell 3D genome chromatin loops
Yusen Ye, Yuxuan Hu, Shihua Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Underlying genetic etiologies of congenital diaphragmatic hernia
Daryl A. Scott, Yoel Gofin, Aliska M. Berry, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 3, pp. 373-386
Open Access | Times Cited: 15
Formation of the Mouse Internal Capsule and Cerebral Peduncle: A Pioneering Role for Striatonigral Axons as Revealed inIsl1Conditional Mutants
Jacqueline M. Ehrman, Paloma Merchán, Lisa A. Ehrman, et al.
Journal of Neuroscience (2022) Vol. 42, Iss. 16, pp. 3344-3364
Open Access | Times Cited: 13
Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental Disorders
Insa Halfmeyer, Tobias Bartolomaeus, Bernt Popp, et al.
Genes (2022) Vol. 14, Iss. 1, pp. 30-30
Open Access | Times Cited: 9
Polymorphisms of IFN signaling genes and FOXP4 influence the severity of COVID-19
Feng Zhang, Pingping Zhou, Liangliang Wang, et al.
BMC Infectious Diseases (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Deciphering the role of FOXP4 in long COVID: exploring genetic associations, evolutionary conservation, and drug identification through bioinformatics analysis
Manoj Kumar Gupta, Gayatri Gouda, Ramakrishna Vadde
Functional & Integrative Genomics (2024) Vol. 24, Iss. 5
Closed Access | Times Cited: 1
Downregulation of microRNA‑423‑5p suppresses TGF‑β1‑induced EMT by targeting FOXP4 in airway fibrosis
Yi Chen, Xuan Li, Yishi Li, et al.
Molecular Medicine Reports (2022) Vol. 26, Iss. 1
Open Access | Times Cited: 6
The forkhead box transcription factor FoxP4 regulates thermogenic programs in adipocytes
Luce Pèrié, Narendra Verma, Elisabetta Mueller
Journal of Lipid Research (2021) Vol. 62, pp. 100102-100102
Open Access | Times Cited: 6
Inhibition of Foxp4 Disrupts Cadherin-based Adhesion of Radial Glial Cells, Leading to Abnormal Differentiation and Migration of Cortical Neurons in Mice
Xue Li, Shimin Zou, Xiaomeng Tu, et al.
Neuroscience Bulletin (2023) Vol. 39, Iss. 7, pp. 1131-1145
Closed Access | Times Cited: 2
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions
Elliot Sollis, Joery den Hoed, Martí Quevedo, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 9, pp. 1497-1510
Open Access | Times Cited: 4
Effects of Cortical FoxP1 Knockdowns on Learned Song Preference in Female Zebra Finches
Fabian Heim, Simon E. Fisher, Constance Scharff, et al.
eNeuro (2023) Vol. 10, Iss. 3, pp. ENEURO.0328-22.2023
Open Access | Times Cited: 2
An improved isochronous pulse after lentiviral knock-down of STEP in Area X of juvenile zebra finches
Philipp Norton, Daniel Breslav, Ezequiel Mendoza
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia
Katherine E. Pendleton, Andrés Hernández, Jennifer M. Lyu, et al.
Journal of Pediatric Genetics (2023) Vol. 13, Iss. 01, pp. 029-034
Closed Access | Times Cited: 1
Developmental language disorders and special educational needs: consideration of inclusion in the Norwegian school context
Sobh Chahboun, Harald Wahl, Jana Langner, et al.
Frontiers in Education (2024) Vol. 9
Open Access
FOXP4 differentially controls cold-induced beige adipocyte differentiation and thermogenesis
Fuhua Wang, Shuqin Xu, Tienan Chen, et al.
Development (2022) Vol. 149, Iss. 7
Open Access | Times Cited: 2
Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia
Florencia Del Viso, Dihong Zhou, Isabelle Thiffault, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 1, pp. 259-264
Closed Access | Times Cited: 1
A Replication Study of GWAS-Associated Variants in the TUFM, SH2B1, ZNF638, NEGR1, ATP2A1, EXOC4, and CSE1L Genes and Cognitive Abilities
А. В. Казанцева, Yu. D. Davydova, Р. Ф. Еникеева, et al.
Russian Journal of Genetics (2023) Vol. 59, Iss. 9, pp. 940-948
Closed Access
Replication Study of GWAS-Associated Variants in the <i>TUFM</i>, <i>SH2B1</i>, <i>ZNF638</i>, <i>NEGR1</i>, <i>ATP2A1</i>, <i>EXOC4</i>, and <i>CSE1L</i> Genes and Cognitive Abilities
А. В. Казанцева, Yu. D. Davydova, Р. Ф. Еникеева, et al.
Генетика (2023) Vol. 59, Iss. 9, pp. 1059-1069
Closed Access
FOXP4 differentially controls cold-induced beige adipocyte differentiation and thermogenesis
Fuhua Wang, Shuqin Xu, Tienan Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
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