Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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 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

Showing 17 citing articles:

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
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
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
POGZ targeted by LINC01355/miR-27b-3p retards thyroid cancer progression via interplaying with MAD2L2
Jiancan Lu, Xinglu Zhou, Hongling Zhu, et al.
3 Biotech (2025) Vol. 15, Iss. 4
Closed Access
CRISPRi-based screen of autism spectrum disorder risk genes in microglia uncovers roles of ADNP in microglia endocytosis and synaptic pruning
Olivia M. Teter, Amanda McQuade, Venus Hagan, et al.
Molecular Psychiatry (2025)
Open Access
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
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
Identification of a molecular network regulated by multiple ASD high risk genes
Lei Wan, Guojun Yang, Zhen Yan
Human Molecular Genetics (2024) Vol. 33, Iss. 13, pp. 1176-1185
Closed Access | Times Cited: 2
Tau, ADNP, and sex
Illana Gozes
Cytoskeleton (2023) Vol. 81, Iss. 1, pp. 16-23
Open Access | Times Cited: 5
CRISPRi-based screen of Autism Spectrum Disorder risk genes in microglia uncovers roles ofADNPin microglia endocytosis and uptake of synaptic material
Olivia M. Teter, Amanda McQuade, Venus Hagan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders
Marta Iannuccelli, Alessandro Vitriolo, Luana Licata, et al.
Molecular Psychiatry (2023) Vol. 29, Iss. 1, pp. 186-196
Open Access | Times Cited: 3
CellGO: a novel deep learning-based framework and webserver for cell-type-specific gene function interpretation
Peilong Li, Junfeng Wei, Ying Zhu
Briefings in Bioinformatics (2023) Vol. 25, Iss. 1
Open Access | Times Cited: 2
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
Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances
Yuan Zhang, Rui Tang, Zhimin Hu, et al.
Journal of Integrative Neuroscience (2024) Vol. 23, Iss. 10
Open Access
Epigenetic Mechanisms of Autism Spectrum Disorders
Zhen Yan
(2024), pp. 1-14
Closed Access
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
CellGO: A novel deep learning-based framework and webserver for cell type-specific gene function interpretation
Peilong Li, Junfeng Wei, Ying Zhu
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top