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:
The molecular genetics of RASopathies : An update on novel disease genes and new disorders
Marco Tartaglia, Yoko Aoki, Bruce D. Gelb
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 425-439
Open Access | Times Cited: 43
Marco Tartaglia, Yoko Aoki, Bruce D. Gelb
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 425-439
Open Access | Times Cited: 43
Showing 1-25 of 43 citing articles:
Exploring New Drug Repurposing Opportunities for MEK Inhibitors in RASopathies: A Comprehensive Review of Safety, Efficacy, and Future Perspectives of Trametinib and Selumetinib
Andrea Gazzin, Federico Fornari, Simona Cardaropoli, et al.
Life (2024) Vol. 14, Iss. 6, pp. 731-731
Open Access | Times Cited: 6
Andrea Gazzin, Federico Fornari, Simona Cardaropoli, et al.
Life (2024) Vol. 14, Iss. 6, pp. 731-731
Open Access | Times Cited: 6
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: 5
Athanasios Bakalakos, Emanuele Monda, Perry Elliott
Canadian Journal of Cardiology (2024) Vol. 40, Iss. 5, pp. 754-765
Open Access | Times Cited: 5
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 954-963
Closed Access | Times Cited: 4
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 954-963
Closed Access | Times Cited: 4
Nerve Enlargement in Patients with INF2 Variants Causing Peripheral Neuropathy and Focal Segmental Glomerulosclerosis
Tran Thuy Huong Quynh, Linh Tran, Hiroko Ueda, et al.
Biomedicines (2025) Vol. 13, Iss. 1, pp. 127-127
Open Access
Tran Thuy Huong Quynh, Linh Tran, Hiroko Ueda, et al.
Biomedicines (2025) Vol. 13, Iss. 1, pp. 127-127
Open Access
Impact of pubertal timing on growth progression and final height in subjects affected by RASopathies
Federica Tamburrino, Laura Mazzanti, Dino Gibertoni, et al.
Frontiers in Endocrinology (2025) Vol. 15
Open Access
Federica Tamburrino, Laura Mazzanti, Dino Gibertoni, et al.
Frontiers in Endocrinology (2025) Vol. 15
Open Access
Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding—A Comprehensive Review
Gioia Mastromoro, Daniele Guadagnolo, Alessandro De Luca, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 465-465
Open Access
Gioia Mastromoro, Daniele Guadagnolo, Alessandro De Luca, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 465-465
Open Access
Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study and Systematic Review
G.J. Reynolds, Andrea Gazzin, Diana Carli, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3515-3515
Open Access
G.J. Reynolds, Andrea Gazzin, Diana Carli, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3515-3515
Open Access
A Novel Description of Immunodeficiency and Immune Dysregulation in a 14-Year-Old Girl with Noonan Syndrome 13
Saira Tabassum, Sarah Grün, Ben Molloy, et al.
Journal of Clinical Immunology (2025) Vol. 45, Iss. 1
Open Access
Saira Tabassum, Sarah Grün, Ben Molloy, et al.
Journal of Clinical Immunology (2025) Vol. 45, Iss. 1
Open Access
The molecular basis of p21-activated kinase-associated neurodevelopmental disorders: From genotype to phenotype
Manon Dobrigna, Sandrine Poëa‐Guyon, Véronique Rousseau, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
Manon Dobrigna, Sandrine Poëa‐Guyon, Véronique Rousseau, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
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
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
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
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 7
Impact of pathogenic variants of the Ras-Mitogen-activated protein kinase (Ras-MAPK) pathway on major white matter tracts in the human brain
Monica Siqueiros Sanchez, Erpeng Dai, Chloe McGhee, et al.
Brain Communications (2024) Vol. 6, Iss. 4
Open Access | Times Cited: 2
Monica Siqueiros Sanchez, Erpeng Dai, Chloe McGhee, et al.
Brain Communications (2024) Vol. 6, Iss. 4
Open Access | Times Cited: 2
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
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
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
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
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
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome
Yasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Clinical Pediatric Endocrinology (2024) Vol. 33, Iss. 2, pp. 50-58
Open Access | Times Cited: 1
Yasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Clinical Pediatric Endocrinology (2024) Vol. 33, Iss. 2, pp. 50-58
Open Access | Times Cited: 1
Transient Myeloproliferative Disorder (TMD), Acute Lymphoblastic Leukemia (ALL), and Juvenile Myelomonocytic Leukemia (JMML) in a Child with Noonan Syndrome: Sequential Occurrence, Single Center Experience, and Review of the Literature
Marta Arrabito, Nicolò Li Volsi, Manuela La Rosa, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1191-1191
Open Access | Times Cited: 1
Marta Arrabito, Nicolò Li Volsi, Manuela La Rosa, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1191-1191
Open Access | Times Cited: 1
Analysis of the Main Checkpoints of the JNK-MAPK Pathway in HTLV-1-Associated Leukemia/Lymphoma via Boolean Network Simulation
Shayan Mardi, Arash Letafati, Amin Hosseini, et al.
Biochemical Genetics (2024)
Closed Access | Times Cited: 1
Shayan Mardi, Arash Letafati, Amin Hosseini, et al.
Biochemical Genetics (2024)
Closed Access | Times Cited: 1
RAS and SHOC2 Roles in RAF Activation and Therapeutic Considerations
Daniel A. Bonsor, Dhirendra K. Simanshu
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 97-113
Closed Access | Times Cited: 3
Daniel A. Bonsor, Dhirendra K. Simanshu
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 97-113
Closed Access | Times Cited: 3
Complex Roles of PTPN11/SHP2 in Carcinogenesis and Prospect of Targeting SHP2 in Cancer Therapy
Alexander Scheiter, Li‐Chun Lu, Lilian H. Gao, et al.
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 15-33
Closed Access | Times Cited: 3
Alexander Scheiter, Li‐Chun Lu, Lilian H. Gao, et al.
Annual Review of Cancer Biology (2023) Vol. 8, Iss. 1, pp. 15-33
Closed 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
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
High frequency of hotspot mutation in PTPN11 gene among Moroccan patients with Noonan syndrome
Fatima Ouboukss, Najlae Adadi, Saadia Amasdl, et al.
Journal of Applied Genetics (2023) Vol. 65, Iss. 2, pp. 303-308
Closed Access | Times Cited: 2
Fatima Ouboukss, Najlae Adadi, Saadia Amasdl, et al.
Journal of Applied Genetics (2023) Vol. 65, Iss. 2, pp. 303-308
Closed 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
Lijun Liu, Chanchan Hu, Zhenjie Chen, et al.
American Journal of Case Reports (2023) Vol. 24
Open Access | Times Cited: 2
