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:
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
Dóra Nagy, Sarah Verheyen, Kristen Wigby, et al.
Genes (2022) Vol. 13, Iss. 1, pp. 154-154
Open Access | Times Cited: 11
Showing 11 citing articles:
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
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
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
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
Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0315597-e0315597
Open Access
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
Jing Duan, Yuanzhen Ye, Jianxiang Liao, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 7
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
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
JRK binds satellite III DNA and is necessary for the heat shock response
R. Waldron, Maria de los Angeles Becerra Rodriguez, John M. Williams, et al.
Cell Biology International (2024) Vol. 48, Iss. 8, pp. 1212-1222
Open Access | Times Cited: 1
R. Waldron, Maria de los Angeles Becerra Rodriguez, John M. Williams, et al.
Cell Biology International (2024) Vol. 48, Iss. 8, pp. 1212-1222
Open Access | Times Cited: 1
NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes
Ayaz Khan, Shixiong Tian, Muhammad Tariq, et al.
Molecular Genetics and Genomics (2022) Vol. 297, Iss. 6, pp. 1601-1613
Closed Access | Times Cited: 4
Ayaz Khan, Shixiong Tian, Muhammad Tariq, et al.
Molecular Genetics and Genomics (2022) Vol. 297, Iss. 6, pp. 1601-1613
Closed Access | Times Cited: 4
INVESTIGATION OF POGZ GENE VARIANTS IN NON-SYNDROMIC AUTISM SPECTRUM DISORDER
Jülide Tozkır, Gökberk Yıldırım, Selma Demır, et al.
Nöro Psikiyatri Arşivi (2024)
Closed Access
Jülide Tozkır, Gökberk Yıldırım, Selma Demır, et al.
Nöro Psikiyatri Arşivi (2024)
Closed Access
Auditory Neuropathy Spectrum Disorder in the White Sutton Syndrome
Lucia Belen Musumano, Virginia Fancello, Laura Negossi, et al.
The Journal of International Advanced Otology (2023) Vol. 19, Iss. 3, pp. 260-262
Open Access | Times Cited: 1
Lucia Belen Musumano, Virginia Fancello, Laura Negossi, et al.
The Journal of International Advanced Otology (2023) Vol. 19, Iss. 3, pp. 260-262
Open Access | Times Cited: 1
Congenital hypogonadotropic hypogonadism in a patient with a de novoPOGZmutation
Nazli Eskici, Shrinidhi Madhusudan, Kirsi Vaaralahti, et al.
European Journal of Endocrinology (2023) Vol. 189, Iss. 2, pp. 271-280
Open Access | Times Cited: 1
Nazli Eskici, Shrinidhi Madhusudan, Kirsi Vaaralahti, et al.
European Journal of Endocrinology (2023) Vol. 189, Iss. 2, pp. 271-280
Open Access | Times Cited: 1
A Novel POGZ Variant in a Patient with Intellectual Disability and Obesity
Sebastián Giraldo-Ocampo, Rafael Adrián Pacheco-Orozco, Harry Pachajoa
The Application of Clinical Genetics (2022) Vol. Volume 15, pp. 63-68
Open Access | Times Cited: 2
Sebastián Giraldo-Ocampo, Rafael Adrián Pacheco-Orozco, Harry Pachajoa
The Application of Clinical Genetics (2022) Vol. Volume 15, pp. 63-68
Open Access | Times Cited: 2
