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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:

Clinical overview on RASopathies
Martin Zenker
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 414-424
Open Access | Times Cited: 49

Showing 1-25 of 49 citing articles:

Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study
Michele Santoro, Ingeborg Barišić, Alessio Coi, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access | Times Cited: 1
Novel therapeutic perspectives in Noonan syndrome and RASopathies
Céline Saint-Laurent, Laurène Mazeyrie, Armelle Yart, et al.
European Journal of Pediatrics (2023) Vol. 183, Iss. 3, pp. 1011-1019
Open Access | Times Cited: 18
Roadmap to advance therapeutics for SYNGAP1-related disorder: a patient organization perspective from SynGAP Research Fund
J. Michael Graglia, Aaron J. Harding, Kathryn A. Helde
Therapeutic Advances in Rare Disease (2025) Vol. 6
Open Access
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes
Michael C. Sierant, Sheng Chih Jin, Kaya Bilgüvar, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 13
Open Access
Cardiovascular aspects of Noonan syndrome and related disorders
Martin Zenker, Cordula M. Wolf
Medizinische Genetik (2025) Vol. 37, Iss. 2, pp. 113-124
Closed Access
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations
Jonas Windrich, Peter Braubach, Florian Länger, et al.
American Journal of Respiratory and Critical Care Medicine (2024) Vol. 209, Iss. 10, pp. 1266-1268
Open Access | Times Cited: 4
The Diagnostic and Therapeutic Implications of Phenocopies and Mimics of Hypertrophic Cardiomyopathy
Athanasios Bakalakos, Emanuele Monda, Perry Elliott
Canadian Journal of Cardiology (2024) Vol. 40, Iss. 5, pp. 754-765
Open Access | Times Cited: 4
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant
Andrea Gazzin, Federico Fornari, Marcello Niceta, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 964-971
Closed Access | Times Cited: 4
Undiagnosed RASopathies in infertile men
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities
Elżbieta Katarzyna Biernacka, Tadeusz Osadnik, Zofia T. Bilińska, et al.
Kardiologia Polska (2024) Vol. 82, Iss. 5, pp. 569-593
Open Access | Times Cited: 3
Germline mutations in a G protein identify signaling cross-talk in T cells
Hyoungjun Ham, Huie Jing, Ian T. Lamborn, et al.
Science (2024) Vol. 385, Iss. 6715
Closed Access | Times Cited: 3
Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome
Emanuele Coccia, Lara Valeri, Roberta Zuntini, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 549-549
Open Access | Times Cited: 8
Abnormalities of pubertal development and gonadal function in Noonan syndrome
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 7
The Cardiofaciocutaneous Syndrome: From Genetics to Prognostic–Therapeutic Implications
Giovanna Scorrano, Emanuele David, Elisa Calì, et al.
Genes (2023) Vol. 14, Iss. 12, pp. 2111-2111
Open Access | Times Cited: 6
Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features
Manuela Priolo, Cecilia Mancini, Francesca Clementina Radio, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 2, pp. 160-166
Open Access | Times Cited: 4
Melanoma and LEOPARD Syndrome: Understanding the Role of PTPN11 Mutations in Melanomagenesis
Rodolfo David Palacios‐Diaz, Mónica Pozuelo‐Ruiz, Blanca de Unamuno‐Bustos, et al.
Acta Dermato Venereologica (2024) Vol. 104, pp. adv14720-adv14720
Open Access | Times Cited: 1
RASopathies: Evolving Concepts in Pathogenetics, Clinical Features, and Management
Jigna Padhiyar, Rahul Mahajan, Maitreyee Panda
Indian Dermatology Online Journal (2024) Vol. 15, Iss. 3, pp. 392-404
Open Access | Times Cited: 1
Neurofibromatosis type 1
Jordan J. Cole, Rosalie E. Ferner, David H. Gutmann
Elsevier eBooks (2024), pp. 231-249
Closed Access | Times Cited: 1
Mosaic KRAS Mutation in Schimmelpenning–Feuerstein–Mims Syndrome With Overlapping Oculoectodermal Syndrome and Encephalocraniocutaneous Lipomatosis Features
Hanna Hyvönen, Kettunen Kaisa, Avela Kristiina, et al.
Pediatric Dermatology (2024)
Closed Access | Times Cited: 1
Hypertrophic neuropathy: a possible cause of pain in children with Noonan syndrome and related disorders
Fieke Draaisma, Corrie E. Erasmus, Hilde M. H. Braakman, et al.
European Journal of Pediatrics (2023) Vol. 182, Iss. 8, pp. 3789-3793
Open Access | Times Cited: 3
Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies
Carolyn R. Serbinski, April Vanderwal, Sarah E. Chadwell, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 2, pp. 195-202
Open Access | Times Cited: 2
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
Co-Occurring Thrombotic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in a Child Carrying the Pathogenic SHOC2 c.4A>G (p.Ser2Gly) Variant
Lijun Liu, Chanchan Hu, Zhenjie Chen, et al.
American Journal of Case Reports (2023) Vol. 24
Open Access | Times Cited: 2
NeuroTri2-VISDOT: An open-access tool to harness the power of second trimester human single cell data to inform models of Mendelian neurodevelopmental disorders
Kelly James Clark, Emily E. Lubin, Elizabeth M. Gonzalez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The first case of a point pathogenic variant in the RREB1 gene in Noonan‐like Rasopathy
Olga Shatokhina, Fatima Bostanova, Maria Bulakh, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 573-580
Closed Access
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