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:
Autism-associated protein POGZ controls ESCs and ESC neural induction by association with esBAF
Xiaoyun Sun, Linxi Cheng, Yuhua Sun
Molecular Autism (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 14
Xiaoyun Sun, Linxi Cheng, Yuhua Sun
Molecular Autism (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 14
Showing 14 citing articles:
Molecular landscape of congenital vertebral malformations: recent discoveries and future directions
Anna Szoszkiewicz, Ewelina Bukowska‐Olech, Aleksander Jamsheer
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 4
Anna Szoszkiewicz, Ewelina Bukowska‐Olech, Aleksander Jamsheer
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 4
Genetic and Environmental Factors Co-Contributing to Behavioral Abnormalities in adnp/adnp2 Mutant Zebrafish
Yongxin Wang, Xiaoyun Sun, Bo Xiong, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9469-9469
Open Access | Times Cited: 4
Yongxin Wang, Xiaoyun Sun, Bo Xiong, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9469-9469
Open Access | Times Cited: 4
Retrotransposon: an insight into neurological disorders from perspectives of neurodevelopment and aging
Wenchuan Zhang, Chongtian Huang, Haiyang Yao, et al.
Translational Neurodegeneration (2025) Vol. 14, Iss. 1
Open Access
Wenchuan Zhang, Chongtian Huang, Haiyang Yao, et al.
Translational Neurodegeneration (2025) Vol. 14, Iss. 1
Open Access
O-GlcNAc Transferase Congenital Disorder of Glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome
Johnathan M. Mayfield, Naomi L. Hitefield, Ignacy Czajewski, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107599-107599
Open Access | Times Cited: 3
Johnathan M. Mayfield, Naomi L. Hitefield, Ignacy Czajewski, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107599-107599
Open Access | Times Cited: 3
POGZ suppresses 2C transcriptional program and retrotransposable elements
Xiaoyun Sun, Tianzhe Zhang, Bei Tong, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112867-112867
Open Access | Times Cited: 8
Xiaoyun Sun, Tianzhe Zhang, Bei Tong, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112867-112867
Open Access | Times Cited: 8
Epigenetic regulation of craniofacial development and disease
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 8
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 8
Exploring the molecular pathways linking sleep phenotypes andPOGZ-associated neurodevelopmental disorder
Bruna Pereira Marquezini, Mariana Moysés‐Oliveira, Anna Kloster, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 586-589
Closed Access | Times Cited: 1
Bruna Pereira Marquezini, Mariana Moysés‐Oliveira, Anna Kloster, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 586-589
Closed Access | Times Cited: 1
Deficiency of CHAMP1, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotype
Masayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Brain Communications (2022) Vol. 4, Iss. 5
Open Access | Times Cited: 7
Masayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Brain Communications (2022) Vol. 4, Iss. 5
Open Access | Times Cited: 7
Discriminative features in White-Sutton syndrome: literature review and first report in Iran
Emran Esmaeilzadeh, Aysan Jafari Harandi, Fatemeh Astaraki, et al.
Psychiatric Genetics (2023)
Closed Access | Times Cited: 2
Emran Esmaeilzadeh, Aysan Jafari Harandi, Fatemeh Astaraki, et al.
Psychiatric Genetics (2023)
Closed Access | Times Cited: 2
Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance
Yasaman Arman Fard, Elham Sadeghi, Zohreh Pajoohesh, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024)
Closed Access
Yasaman Arman Fard, Elham Sadeghi, Zohreh Pajoohesh, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024)
Closed Access
A novel nonsense variant in POGZ expanding the spectrum of White-Sutton Syndrome: A case report
Alain Chebly, Nabiha Salem, Romy Moussallem, et al.
Heliyon (2024) Vol. 10, Iss. 21, pp. e40057-e40057
Open Access
Alain Chebly, Nabiha Salem, Romy Moussallem, et al.
Heliyon (2024) Vol. 10, Iss. 21, pp. e40057-e40057
Open Access
Congenital hypogonadotropic hypogonadism in a patient with a de novoPOGZmutation
Nazli Eskici, Shrinidhi Madhusudan, Kirsi Vaaralahti, et al.
European Journal of Endocrinology (2023) Vol. 189, Iss. 2, pp. 271-280
Open Access | Times Cited: 1
Nazli Eskici, Shrinidhi Madhusudan, Kirsi Vaaralahti, et al.
European Journal of Endocrinology (2023) Vol. 189, Iss. 2, pp. 271-280
Open Access | Times Cited: 1
Proteomics and phosphoproteomics profiling in glutamatergic neurons and microglia in an iPSC model of Jansen de Vries Syndrome
Jennifer Aguilan, Erika Pedrosa, Hedwig Dolstra, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Jennifer Aguilan, Erika Pedrosa, Hedwig Dolstra, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
POGZ suppresses 2C transcriptional program and retrotransposable elements
X. Sun, TZ Zhang, LX Cheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
X. Sun, TZ Zhang, LX Cheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
