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:
White-Sutton syndrome and congenital heart disease: case report and literature review
Jing Duan, Yuanzhen Ye, Jianxiang Liao, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 7
Jing Duan, Yuanzhen Ye, Jianxiang Liao, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 7
Showing 7 citing articles:
Denovo variants in POGZ and YY1 genes: The novel mega players for neurodevelopmental syndromes in two unrelated consanguineous families
Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0315597-e0315597
Open Access
Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0315597-e0315597
Open Access
CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair
Feng Li, Tianpeng Zhang, Aleem Syed, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Feng Li, Tianpeng Zhang, Aleem Syed, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Case Report: White–Sutton syndrome and cannabidiol, an update on a reported patient with a successful response to off--label therapy
Lorenzo Perilli, Samanta Carbone, Michele Minerva, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
Lorenzo Perilli, Samanta Carbone, Michele Minerva, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
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
Analyses of Conditional Knockout Mice for Pogz, a Responsible Gene for Neurodevelopmental Disorders, in Excitatory and Inhibitory Neurons in the Brain
Nanako Hamada, Takuma Nishijo, Ikuko Iwamoto, et al.
(2024)
Open Access
Nanako Hamada, Takuma Nishijo, Ikuko Iwamoto, et al.
(2024)
Open 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
Analyses of Conditional Knockout Mice for Pogz, a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain
Nanako Hamada, Takuma Nishijo, Ikuko Iwamoto, et al.
Cells (2024) Vol. 13, Iss. 6, pp. 540-540
Open Access
Nanako Hamada, Takuma Nishijo, Ikuko Iwamoto, et al.
Cells (2024) Vol. 13, Iss. 6, pp. 540-540
Open Access
