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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:

Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism
Claudio Peter D’Incal, Kirsten Esther Van Rossem, Kevin De Man, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 23

Showing 23 citing articles:

ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case
Claudio Peter D’Incal, Anke Van Dijck, Joe Ibrahim, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 5
SWI/SNF Complex Connects Signaling and Epigenetic State in Cells of Nervous System
Victor Chmykhalo, Roman V. Deev, Artemy T. Tokarev, et al.
Molecular Neurobiology (2024)
Closed Access | Times Cited: 4
The chromatin remodeler ADNP regulates neurodevelopmental disorder risk genes and neocortical neurogenesis
Samuel Clémot-Dupont, José Alex Lourenço Fernandes, Sarah Larrigan, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 3
Closed Access
Transcriptomic Analysis Uncovers an Unfolded Protein Response in ADNP Syndrome
Anna Bieluszewska, Phillip Wulfridge, Kuo-Chen Fang, et al.
Molecular and Cellular Biology (2025), pp. 1-11
Open Access
Clinical and genetic findings in autism spectrum disorders analyzed using exome sequencing
Ana Blázquez, Laia Rodríguez‐Revenga, María Isabel Álvarez‐Mora, et al.
Frontiers in Psychiatry (2025) Vol. 16
Open Access
Clinical impact and in vitro characterization of ADNP variants in pediatric patients
Chuanhui Ge, Yuxin Tian, Chunchun Hu, et al.
Molecular Autism (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel–Van der Aa syndrome
Claudio Peter D’Incal, Dale Annear, Ellen Elinck, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 6, pp. 630-638
Closed Access | Times Cited: 3
Moderate Physical Activity Increases the Expression of ADNP in Rat Brain
Grazia Maugeri, Agata Grazia D’Amico, Concetta Federico, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 8, pp. 4382-4382
Open Access | Times Cited: 3
Involvement of Vasoactive Intestinal Peptide Family Members in Diabetic Keratopathy
Grazia Maugeri, Agata Grazia D’Amico, Benedetta Magrì, et al.
Applied Sciences (2024) Vol. 14, Iss. 5, pp. 1754-1754
Open Access | Times Cited: 2
Tau, ADNP, and sex
Illana Gozes
Cytoskeleton (2023) Vol. 81, Iss. 1, pp. 16-23
Open Access | Times Cited: 5
Extended phenotypic characterization of a novel Helsmoortel‐van der Aa syndrome case series
Giulia Pascolini, Giovanni Di Zenzo, Annarita Panebianco, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 5
Open Access | Times Cited: 1
The ChAHP chromatin remodelling complex regulates neurodevelopmental disorder risk genes to scale the production of neocortical layers
Samuel Clémot-Dupont, José Alex Lourenço Fernandes, Sarah Larrigan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype
Camilla Sarli, Liselot van der Laan, Jack Reilly, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2024)
Open Access | Times Cited: 1
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
Claudio Peter D’Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Abnormal fetal ultrasound leading to the diagnosis of ADNP syndrome
Jessica Rosenblum, Lennart Van der Veeken, Michaël Aertsen, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 11, pp. 104855-104855
Open Access | Times Cited: 3
Rare variants in 45 genes account for 25% of cases with NDDs in 415 pediatric patients
Maria Cristina Aspromonte, Alessio Del Conte, Roberta Polli, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 2
The Pathogenesis and Differences in molecule of Autism
Jingwen Xie
Theoretical and Natural Science (2024) Vol. 29, Iss. 1, pp. 46-49
Open Access
Putative Role of the Futile Repair Initiated by Human Thymine-DNA Glycosylase in Formation of Programmed Strand Breaks in Neuronal Enhancers
Diana Manapkyzy, Murat Saparbaev, Sabira Taipakova
BIO Web of Conferences (2024) Vol. 100, pp. 03010-03010
Open Access
Chromatin Remodelers in Neuronal Gene Transcription
Karen G. Cornejo, Ramendra N. Saha
(2024), pp. 275-298
Closed Access
ADNP in reverse gear
Claudio Peter D’Incal, R. Frank Kooy
European Journal of Human Genetics (2023) Vol. 31, Iss. 8, pp. 849-850
Closed 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
Patient with Helsmoortel-van der Aa Syndrome and O’Donnell-Luria-Rodan Syndrome: a case report
Ana Beatriz Deleame Medeiros, D. Coutinho, Rafael Patricio dos Santos Alarcón, et al.
Brazilian Journal of Case Reports (2023) Vol. 4, Iss. 2, pp. 9-16
Open Access
Tracing the Invisible Mutant ADNP protein in Helsmoortel- Van der Aa Syndrome patients
Claudio Peter D’Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Research Square (Research Square) (2023)
Open Access
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