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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:

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

Showing 13 citing articles:

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
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
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
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
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
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
Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White–Sutton Syndrome: Case Report and Review of the Literature
Gabriele Trimarchi, Stefano Giuseppe Caraffi, Francesca Clementina Radio, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 950-950
Open Access | Times Cited: 6
Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report
Bernadette Donnarumma, Maria Pia Riccio, Gaetano Terrone, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2021) Vol. 47, Iss. 1
Open Access | Times Cited: 6
White–Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations
Sevim Türay, Recep Eröz
Acta Neurologica Belgica (2021) Vol. 121, Iss. 3, pp. 749-755
Closed Access | Times Cited: 3
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
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
White-Sutton Syndrome
Nurit Assia Batzir, Janson J. White, V. Reid Sutton
(2021)
Closed Access
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