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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:

Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
Eirene Markenscoff-Papadimitriou, Fadya Binyameen, Sean Whalen, et al.
Cell Reports (2021) Vol. 37, Iss. 10, pp. 110089-110089
Open Access | Times Cited: 49

Showing 1-25 of 49 citing articles:

SH3- and actin-binding domains connect ADNP and SHANK3, revealing a fundamental shared mechanism underlying autism
Yanina Ivashko‐Pachima, Maram Ganaiem, Inbar Ben-Horin-Hazak, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 8, pp. 3316-3327
Closed Access | Times Cited: 41
Neurodevelopmental disorders, like cancer, are connected to impaired chromatin remodelers, PI3K/mTOR, and PAK1-regulated MAPK
Ruth Nussinov, Bengi Ruken Yavuz, M. Kaan Arici, et al.
Biophysical Reviews (2023) Vol. 15, Iss. 2, pp. 163-181
Open Access | Times Cited: 37
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
Genetic architecture of childhood speech disorder: a review
Angela Morgan, David J. Amor, Miya St John, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 5, pp. 1281-1292
Open Access | Times Cited: 10
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
Siavash Fazel Darbandi, Joon‐Yong An, Kenneth Lim, et al.
Cell Reports (2024) Vol. 43, Iss. 6, pp. 114329-114329
Open Access | Times Cited: 9
Adnp-mutant mice with cognitive inflexibility, CaMKIIα hyperactivity, and synaptic plasticity deficits
Heejin Cho, Taesun Yoo, Heera Moon, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 8, pp. 3548-3562
Open Access | Times Cited: 15
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
NAP (Davunetide): The Neuroprotective ADNP Drug Candidate Penetrates Cell Nuclei Explaining Pleiotropic Mechanisms
Maram Ganaiem, Nina D. Gildor, Shula Shazman, et al.
Cells (2023) Vol. 12, Iss. 18, pp. 2251-2251
Open Access | Times Cited: 11
Longitudinal Genotype-Phenotype (Vineland Questionnaire) Characterization of 15 ADNP Syndrome Cases Highlights Mutated Protein Length and Structural Characteristics Correlation with Communicative Abilities Accentuated in Males
Jospeh Levine, Alexandra Lobyntseva, Shula Shazman, et al.
Journal of Molecular Neuroscience (2024) Vol. 74, Iss. 1
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
The KRAB-Zinc Finger protein ZKSCAN3 represses enhancers via embedded retrotransposons
Daniel Moore, Eugenia Wong, Charles Arnal, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
A convergent mechanism of high risk factors ADNP and POGZ in neurodevelopmental disorders
Megan Conrow-Graham, Jamal B. Williams, Jennifer A. Martin, et al.
Brain (2022) Vol. 145, Iss. 9, pp. 3250-3263
Open Access | Times Cited: 17
HMGA2 directly mediates chromatin condensation in association with neuronal fate regulation
Naohiro Kuwayama, Tomoya Kujirai, Yusuke Kishi, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 9
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
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
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
Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis
Francesca Mastropasqua, Marika Oksanen, Cristina Soldini, et al.
Biology Open (2023) Vol. 12, Iss. 10
Open Access | Times Cited: 8
ZNF524 directly interacts with telomeric DNA and supports telomere integrity
Hanna Braun, Ziyan Xu, Fiona Chang, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
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
Curation of causal interactions mediated by genes associated to autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders
Marta Iannuccelli, Alessandro Vitriolo, Luana Licata, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Epigenetic regulation of craniofacial development and disease
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 7
Vineland Adaptive Behavior Scale in a Cohort of Four ADNP Syndrome Patients Implicates Age-Dependent Developmental Delays with Increased Impact of Activities of Daily Living
Joseph Levine, Fahed Hakim, R. Frank Kooy, et al.
Journal of Molecular Neuroscience (2022) Vol. 72, Iss. 8, pp. 1531-1546
Closed Access | Times Cited: 12
Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring
Dóra Nagy, Sarah Verheyen, Kristen Wigby, et al.
Genes (2022) Vol. 13, Iss. 1, pp. 154-154
Open Access | Times Cited: 11
Loss of POGZ alters neural differentiation of human embryonic stem cells
Lu Deng, Sandra P. Mojica-Perez, Ruth D. Azaria, et al.
Molecular and Cellular Neuroscience (2022) Vol. 120, pp. 103727-103727
Open Access | Times Cited: 10
A single-cell atlas of the peripheral immune response in patients with influenza A virus infection
Yin Zhang, Lu Zong, Yuanling Zheng, et al.
iScience (2023) Vol. 26, Iss. 12, pp. 108507-108507
Open Access | Times Cited: 6
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