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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:

Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome)
Nurit Assia Batzir, Jennifer E. Posey, Xiaofei Song, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 1, pp. 38-52
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

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
Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine
James R. Lupski
Trends in Genetics (2022) Vol. 38, Iss. 6, pp. 554-571
Open Access | Times Cited: 22
Pleiotropy of autism-associated chromatin regulators
Micaela Lasser, Nawei Sun, Yuxiao Xu, et al.
Development (2023) Vol. 150, Iss. 14
Open Access | Times Cited: 15
Broadening the clinical spectrum of White-Sutton syndrome, implications for co-morbidity with celiac disease in a patient with a novel likely pathogenic variant in the POGZ gene
Mirela Tabaku, Sonila Tomori, Ermira Dervishi, et al.
Gene (2025) Vol. 940, pp. 149213-149213
Closed Access
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
Exome Sequencing in 200 Intellectual Disability/Autistic Patients: New Candidates and Atypical Presentations
Floriana Valentino, Lucia Pia Bruno, Gabriella Doddato, et al.
Brain Sciences (2021) Vol. 11, Iss. 7, pp. 936-936
Open Access | Times Cited: 29
The zinc-finger protein POGZ associates with Polycomb repressive complex 1 to regulate bone morphogenetic protein signaling during neuronal differentiation
Jessenia Chavez, Trevor Wolf, Zhuangzhuang Geng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Case Report: White–Sutton syndrome and cannabidiol, an update on a reported patient with a successful response to off--label therapy
Lorenzo Perilli, Samanta Carbone, Michele Minerva, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
Cyclical Vomiting Syndrome in Individuals with Bptf-Haploinsufficiency
Alessandro Ferretti, Margherita Furlan, Kevin E. Glinton, et al.
(2025)
Closed 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
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
Underlying genetic etiologies of congenital diaphragmatic hernia
Daryl A. Scott, Yoel Gofin, Aliska M. Berry, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 3, pp. 373-386
Open Access | Times Cited: 14
White-Sutton syndrome and congenital heart disease: case report and literature review
Jing Duan, Yuanzhen Ye, Jianxiang Liao, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
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
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 novel patient with White–Sutton syndrome refines the mutational and clinical repertoire of the POGZ‐related phenotype and suggests further observations
Giulia Pascolini, Emanuele Agolini, Nicole Fleischer, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 7, pp. 1791-1795
Closed Access | Times Cited: 13
Neuropsychological study in 19 French patients with White‐Sutton syndrome and POGZ mutations
Aurore Garde, Jenny Cornaton, Arthur Sorlin, et al.
Clinical Genetics (2020) Vol. 99, Iss. 3, pp. 407-417
Closed Access | Times Cited: 13
A systematic review of brain MRI findings in monogenic disorders strongly associated with autism spectrum disorder
Veronica Rose, Courtney P. Gilchrist, Simonne E. Collins, et al.
Journal of Child Psychology and Psychiatry (2021) Vol. 62, Iss. 11, pp. 1339-1352
Closed Access | Times Cited: 11
Exploring the molecular pathways linking sleep phenotypes andPOGZ-associated neurodevelopmental disorder
Bruna Pereira Marquezini, Mariana Moysés‐Oliveira, Anna Kloster, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 586-589
Closed Access | Times Cited: 1
Seeing beyond words: Visualizing autism spectrum disorder biomarker insights
Xinyue Xie, Rongyi Zhou, Zihan Fang, et al.
Heliyon (2024) Vol. 10, Iss. 9, pp. e30420-e30420
Open Access | Times Cited: 1
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Further delineation of the clinical spectrum of White–Sutton syndrome: 12 new individuals and a review of the literature
Oliver Murch, Vani Jain, Andreas Benneche, et al.
European Journal of Human Genetics (2021) Vol. 30, Iss. 1, pp. 95-100
Open Access | Times Cited: 10
Deficiency of CHAMP1, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotype
Masayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Brain Communications (2022) Vol. 4, Iss. 5
Open Access | Times Cited: 7
A novel, de novo intronic variant in POGZ causes White–Sutton syndrome
Ashanta Merriweather, David R. Murdock, Jill A. Rosenfeld, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2198-2203
Open Access | Times Cited: 6
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