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:
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
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
Showing 7 citing articles:
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
Cutaneous adverse reactions resulting from targeted cancer therapies: histopathologic and clinical findings
Dylan Haynes, Eric E. Morgan, Emily Y. Chu
Human Pathology (2023) Vol. 140, pp. 129-143
Closed Access | Times Cited: 5
Dylan Haynes, Eric E. Morgan, Emily Y. Chu
Human Pathology (2023) Vol. 140, pp. 129-143
Closed Access | Times Cited: 5
Noonan Syndrome with Multiple Lentigines
Myles C. Hodgson, Saravanakkumar Chennappan, Maria I. Kontaridis
(2024), pp. 107-132
Closed Access | Times Cited: 1
Myles C. Hodgson, Saravanakkumar Chennappan, Maria I. Kontaridis
(2024), pp. 107-132
Closed Access | Times Cited: 1
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome
Lucrezia Perri, Germana Viscogliosi, Valentina Trevisan, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024)
Open Access
Lucrezia Perri, Germana Viscogliosi, Valentina Trevisan, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024)
Open Access
An Unexpected Finding of a PTPN11 Germline Mutation in a Patient With a Melanocytic Lesion With a Somatic MAP2K1 Mutation. Coincidence or Not?
Sven van der Woude, Jolien S. Klein Wassink‐Ruiter, Joost Kluiver, et al.
Journal of Cutaneous Pathology (2024)
Open Access
Sven van der Woude, Jolien S. Klein Wassink‐Ruiter, Joost Kluiver, et al.
Journal of Cutaneous Pathology (2024)
Open Access
