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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.

Requested Article:

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

Showing 19 citing articles:

Autophagy-induced NR2F1 activation promotes the apoptosis of lens epithelial cells and facilitates cataract-associated fibrosis through targeting STAT3
Hangjia Zuo, Xianyang Liu, Bingjing Lv, et al.
Genes & Diseases (2025), pp. 101549-101549
Open Access
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
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
The Natural Course of Bosch‐Boonstra‐Schaaf Optic Atrophy Syndrome
Ilia Valentin, Pilar Caro, Christine Fischer, et al.
Clinical Genetics (2025)
Open Access
New Insights into the Diverse Functions of the NR2F Nuclear Orphan Receptor Family
Tajana Sajinovic, Gottfried Baier
Frontiers in Bioscience-Landmark (2023) Vol. 28, Iss. 1
Open Access | Times Cited: 8
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
Disrupted protein interaction dynamics in a genetic neurodevelopmental disorder revealed by structural bioinformatics and genetic code expansion
Valerio Marino, Wanchana Phromkrasae, Michele Bertacchi, et al.
Protein Science (2024) Vol. 33, Iss. 4
Open Access | Times Cited: 1
Mitochondrial regulation of adult hippocampal neurogenesis: Insights into neurological function and neurodevelopmental disorders
Sara Bonzano, Eleonora Dallorto, Serena Bovetti, et al.
Neurobiology of Disease (2024) Vol. 199, pp. 106604-106604
Open Access | Times Cited: 1
FGF8-mediated gene regulation affects regional identity in human cerebral organoids
Michele Bertacchi, Gwendoline Maharaux, Agnès Loubat, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 1
Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic
Bela Parekh, Adelyn Beil, Bridget Blevins, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 726-726
Open Access | Times Cited: 3
ERK signaling drives evolutionary expansion of the mammalian cerebral cortex
Meng-Ge Sun, Yanjing Gao, Zhenmeiyu Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
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
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia
Maria Asif, Arwa Ishaq A. Khayyat, Salem Alawbathani, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 7, pp. 101143-101143
Open Access
Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch–Boonstra–Schaaf Optic Atrophy Syndrome
Nenad Hrvatin, Nina Pereza, Tea Čaljkušić‐Mance, et al.
Clinical Genetics (2024)
Closed Access
Structural interhemispheric connectivity defects in mouse models of BBSOAS: Insights from high spatial resolution 3D white matter tractography
Jean-Christophe Deloulme, Maxime Leclercq, Olivier Deschaux, et al.
Neurobiology of Disease (2024) Vol. 193, pp. 106455-106455
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
Pathophysiological Mechanism of Neurodevelopmental Disorders—Overview
Koh‐ichi Nagata
Cells (2022) Vol. 11, Iss. 24, pp. 4082-4082
Open Access | Times Cited: 1
Integrated genetic code expansion and structural bioinformatics reveal disrupted supramolecular assembly in a genetic disorder
Valerio Marino, Wanchana Phromkrasae, Michele Bertacchi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
FGF8-mediated gene regulation affects regional identity in human cerebral organoids
Michele Bertacchi, Gwendoline Maharaux, Agnès Loubat, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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