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:
A severe case of Bosch–Boonstra–Schaaf optic atrophy syndrome with a novel description of coloboma and septo‐optic dysplasia, owing to a start codon variant in the NR2F1 gene
Gabriella Gazdagh, Rebecca Mawby, Jay Self, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 3, pp. 900-906
Open Access | Times Cited: 8
Gabriella Gazdagh, Rebecca Mawby, Jay Self, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 3, pp. 900-906
Open Access | Times Cited: 8
Showing 8 citing articles:
Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome
Michele Bertacchi, Chiara Tocco, Christian P. Schaaf, et al.
Cells (2022) Vol. 11, Iss. 8, pp. 1260-1260
Open Access | Times Cited: 19
Michele Bertacchi, Chiara Tocco, Christian P. Schaaf, et al.
Cells (2022) Vol. 11, Iss. 8, pp. 1260-1260
Open Access | Times Cited: 19
A pathogenic NR2F1 gene variant disrupts transcriptional activity and causes severe neurodevelopmental delay in Bosch-Boonstra-Schaaf syndrome
Juan Liu, Jihong Hu, Peng Zhou, et al.
Hereditas (2025) Vol. 162, Iss. 1
Open Access
Juan Liu, Jihong Hu, Peng Zhou, et al.
Hereditas (2025) Vol. 162, Iss. 1
Open Access
Biological pathways leading to septo-optic dysplasia: a review
Ludovica Pasca, Davide Politano, Federica Morelli, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Ludovica Pasca, Davide Politano, Federica Morelli, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Unravelling the conundrum of nucleolar NR2F1 localization using antibody-based approaches in vitro and in vivo
Michele Bertacchi, Susanne Theiß, Ayat Ahmed, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
Michele Bertacchi, Susanne Theiß, Ayat Ahmed, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access
Effective treatment of NR2F1-related epilepsy with perampanel
Xiao Li, Kai Gao, Yutang Li, et al.
Acta Epileptologica (2024) Vol. 6, Iss. 1
Open Access | Times Cited: 1
Xiao Li, Kai Gao, Yutang Li, et al.
Acta Epileptologica (2024) Vol. 6, Iss. 1
Open Access | Times Cited: 1
Novel NR2F1 variant identified by whole-exome sequencing in a patient with Bosch–Boonstra–Schaaf optic atrophy syndrome
Ayça Kocaağa, Sevgi Yimenicioğlu, HalukHüseyin Gürsoy
Indian Journal of Ophthalmology (2022) Vol. 70, Iss. 7, pp. 2762-2764
Open Access | Times Cited: 3
Ayça Kocaağa, Sevgi Yimenicioğlu, HalukHüseyin Gürsoy
Indian Journal of Ophthalmology (2022) Vol. 70, Iss. 7, pp. 2762-2764
Open Access | Times Cited: 3
Unravelling the conundrum of nucleolar NR2F1 localization: A comparative analysis of NR2F1 antibody-based approachesin vitroandin vivo
Michele Bertacchi, Susanne Theiß, Ayat Ahmed, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Michele Bertacchi, Susanne Theiß, Ayat Ahmed, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Infantile epileptic spasm syndrome as a new NR2F1 gene phenotype
Yan Liang, Lin Wan, Xinting Liu, et al.
International Journal of Developmental Neuroscience (2023)
Open Access | Times Cited: 1
Yan Liang, Lin Wan, Xinting Liu, et al.
International Journal of Developmental Neuroscience (2023)
Open Access | Times Cited: 1
