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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:

Multidisciplinary Management of Costello Syndrome: Current Perspectives
Chiara Leoni, Germana Viscogliosi, Marco Tartaglia, et al.
Journal of Multidisciplinary Healthcare (2022) Vol. Volume 15, pp. 1277-1296
Open Access | Times Cited: 16

Showing 16 citing articles:

Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies
Melissa R. Perrino, Anirban Das, Sarah Scollon, et al.
Clinical Cancer Research (2024) Vol. 30, Iss. 21, pp. 4834-4843
Closed Access | Times Cited: 6
Costello Syndrome and Ophthalmologic Issues: Unveiling the Unseen
Sofia Peschiaroli, Germana Viscogliosi, Annabella Salerni, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Management of nutritional and gastrointestinal issues in RASopathies: A narrative review
Roberta Onesimo, Valentina Giorgio, Germana Viscogliosi, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 478-493
Closed Access | Times Cited: 10
Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment
Atilano Carcavilla, Ana Cambra Conejero, José L. Santomé, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 15, pp. 5003-5003
Open Access | Times Cited: 4
Adult syndromology: challenges, opportunities and perspectives
Ariane Schmetz, María Juliana Ballesta‐Martínez, Bertrand Isidor, et al.
Medizinische Genetik (2024) Vol. 36, Iss. 2, pp. 95-102
Open Access | Times Cited: 1
The Surgical Management of Severe Scoliosis in Immature Patient with a Very Rare Disease Costello Syndrome—Clinical Example and Brief Literature Review
Paweł Grabala, P.M. Kowalski, Marek J. Rudziński, et al.
Life (2024) Vol. 14, Iss. 6, pp. 740-740
Open Access | Times Cited: 1
Endocrine system involvement in patients with RASopathies: A case series
Maria Siano, Rosario Pivonello, M Salerno, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 7
Bone health in RASopathies
David A. Stevenson, Germana Viscogliosi, Chiara Leoni
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 459-470
Closed Access | Times Cited: 7
Dermatological manifestations, management, and care in RASopathies
Maria Inês Kavamura, Chiara Leoni, Giovanni Neri
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 452-458
Closed Access | Times Cited: 7
Skeletal defects and bone metabolism in Noonan, Costello and cardio-facio-cutaneous syndromes
Anna Papadopoulou, Evangelia Bountouvi
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 2
Clarifying main nutritional aspects and resting energy expenditure in children with Smith-Magenis syndrome
Francesco Proli, Elisabetta Sforza, Andrea Faragalli, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 10, pp. 4563-4571
Open Access
Costello Syndrome
Yoko Aoki, Tetsuya Niihori
(2024), pp. 133-151
Closed Access
Speech-Language Pathology in the RASopathies
Heather L. Thompson
(2024), pp. 653-678
Closed Access
Epilepsy in the RASopathies
Danilo Bernardo
(2024), pp. 635-651
Closed Access
A very mild phenotype in six individuals of a three‐generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS‐related RASopathy distinct from Costello syndrome
Tanja Frey, Ivan Ivanovski, Angela Bahr, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 8, pp. 2074-2082
Open Access | Times Cited: 1
PATIENT WITH COSTELLO SYNDROME: LITERATURE REVIEW AND CLINICAL CASE
Анна Никитична Завьялова, I. A. Lisitsa, О. В. Лисовский, et al.
Children s medicine of the North-West (2023) Vol. 11, Iss. 4, pp. 99-109
Open Access | Times Cited: 1
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