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.

Requested Article:

KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders
Xinchen Teng, Abdel Aouacheria, Loïc Lionnard, et al.
CNS Neuroscience & Therapeutics (2019) Vol. 25, Iss. 7, pp. 887-902
Open Access | Times Cited: 93

Showing 1-25 of 93 citing articles:

MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies
Arjun Bhattacharya, Yun Li, Michael I. Love
PLoS Genetics (2021) Vol. 17, Iss. 3, pp. e1009398-e1009398
Open Access | Times Cited: 66

Single-nucleus transcriptomic profiling of human orbitofrontal cortex reveals convergent effects of aging and psychiatric disease
Anna S. Fröhlich, Nathalie Gerstner, Miriam Gagliardi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 2021-2032
Open Access | Times Cited: 10

Structure and dynamics of a pentameric KCTD5/CUL3/Gβγ E3 ubiquitin ligase complex
Duc Minh Nguyen, D. Rath, Dominic Devost, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 17
Open Access | Times Cited: 9

The emerging role of the KCTD proteins in cancer
Annapaola Angrisani, A. Di Fiore, Enrico De Smaele, et al.
Cell Communication and Signaling (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 50

Structural basis for the ubiquitination of G protein βγ subunits by KCTD5/Cullin3 E3 ligase
Wentong Jiang, Wei Wang, Yinfei Kong, et al.
Science Advances (2023) Vol. 9, Iss. 28
Open Access | Times Cited: 20

Multiple potassium channel tetramerization domain (KCTD) family members interact with Gβγ, with effects on cAMP signaling
Douglas C. Sloan, Casey E. Cryan, Brian S. Muntean
Journal of Biological Chemistry (2023) Vol. 299, Iss. 3, pp. 102924-102924
Open Access | Times Cited: 19

KCTD13-mediated ubiquitination and degradation of GluN1 regulates excitatory synaptic transmission and seizure susceptibility
Juan Gu, Pingyang Ke, Haokun Guo, et al.
Cell Death and Differentiation (2023) Vol. 30, Iss. 7, pp. 1726-1741
Closed Access | Times Cited: 17

Integrated drug profiling and CRISPR screening identify BCR::ABL1-independent vulnerabilities in chronic myeloid leukemia
Shady Adnan Awad, Olli Dufva, Jay Klievink, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 5, pp. 101521-101521
Open Access | Times Cited: 7

Nacc1 mutation in mice models rare neurodevelopmental disorder with underlying synaptic dysfunction
Mark A. Deehan, Josine Marie Kothuis, Ellen Sapp, et al.
Journal of Neuroscience (2024) Vol. 44, Iss. 14, pp. e1610232024-e1610232024
Open Access | Times Cited: 6

Clustering by phenotype and genome-wide association study in autism
Akira Narita, Masato Nagai, Satoshi Mizuno, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 46

Utility of Protein Microarrays for Detection of Classified and Novel Antibodies in Autoimmune Neurologic Disease
Andrew McKeon, Connie Lesnick, Nisa Vorasoot, et al.
Neurology Neuroimmunology & Neuroinflammation (2023) Vol. 10, Iss. 5
Open Access | Times Cited: 13

Astrocyte-derived extracellular vesicles enhance the survival and electrophysiological function of human cortical neurons in vitro
Changho Chun, Alec S.T. Smith, Hyejin Kim, et al.
Biomaterials (2021) Vol. 271, pp. 120700-120700
Open Access | Times Cited: 28

Targeting E3 ubiquitin ligases and their adaptors as a therapeutic strategy for metabolic diseases
Yelin Jeong, Ah‐Reum Oh, Young Hoon Jung, et al.
Experimental & Molecular Medicine (2023) Vol. 55, Iss. 10, pp. 2097-2104
Open Access | Times Cited: 12

Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases
Margaret Guo, David L. Reynolds, Cheen Euong Ang, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1876-1891
Closed Access | Times Cited: 12

Neuronal-specific TNFAIP1 ablation attenuates postoperative cognitive dysfunction via targeting SNAP25 for K48-linked ubiquitination
Wei Wang, Wenwei Gao, Ping Gong, et al.
Cell Communication and Signaling (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 12

Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia
Weili Wang, Lilan Su, Lanlan Meng, et al.
Human Reproduction (2023) Vol. 38, Iss. 7, pp. 1399-1411
Closed Access | Times Cited: 11

KCTD7‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature
Sangeetha Yoganathan, Robyn Whitney, Maya Thomas, et al.
Epilepsia (2024) Vol. 65, Iss. 3, pp. 709-724
Closed Access | Times Cited: 4

A Comprehensive Analysis of the Structural Recognition between KCTD Proteins and Cullin 3
Nicole Balasco, Luciana Esposito, Giovanni Smaldone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1881-1881
Open Access | Times Cited: 4

Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes
Roberta Leone, Cecilia Zuglian, Riccardo Brambilla, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 4

Identification and study of mood-related biomarkers and potential molecular mechanisms in type 2 diabetes mellitus
Menglong Wang, T.C. Wang, Liu Yang, et al.
Journal of Molecular Histology (2025) Vol. 56, Iss. 2
Closed Access

Androgen receptor ubiquitination links KCTD13 to genitourinary tract defects
Ahmed Chahdi, Carolina J. Jorgez, Jill A. Rosenfeld, et al.
The FASEB Journal (2025) Vol. 39, Iss. 4
Closed Access

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