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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:

Genotype‐cardiac phenotype correlations in a large single‐center cohort of patients affected by RASopathies: Clinical implications and literature review
Chiara Leoni, Rita Blandino, Angelica Bibiana Delogu, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 431-445
Closed Access | Times Cited: 43

Showing 26-50 of 43 citing articles:

Monogenic diseases associated with cardiomyopathy genes and their phenotypic manifestations
А. Н. Кучер, М. С. Назаренко
Bulletin of Siberian Medicine (2024) Vol. 23, Iss. 1, pp. 156-165
Open Access
Functional CRISPR repair of induced pluripotent stem cells from patients with Noonan syndrome-associated cardiac hypertrophy
Lennart Roos
(2024)
Open Access
Cardiac Phenotype and Gene Mutations in RASopathies
Maria Felicia Faienza, Giovanni Meliota, Donatella Mentino, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1015-1015
Open Access
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
New Insights Into the Spectrum of RASopathies: Clinical and Genetic Data in a Cohort of 121 Spanish Patients
Ana Isabel Sánchez Barbero, Irene Valenzuela, Paula Fernández‐Álvarez, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
Cardiovascular Disease in the RASopathies
Kathryn C. Chatfield
(2024), pp. 551-569
Closed Access
A Case Report of Noonan Syndrome in Newborn Infant and Literature Review
婷婷 冯
Advances in Clinical Medicine (2024) Vol. 14, Iss. 12, pp. 1072-1077
Closed Access
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review
Flaminia Pugnaloni, Roberta Onesimo, Rita Blandino, et al.
Genes (2023) Vol. 14, Iss. 1, pp. 146-146
Open Access | Times Cited: 1
The Genetics of Canine Pulmonary Valve Stenosis
Samantha L. Kovacs, Brian A. Scansen, Joshua A. Stern
Veterinary Clinics of North America Small Animal Practice (2023) Vol. 53, Iss. 6, pp. 1379-1391
Closed Access | Times Cited: 1
Decision: Precision diagnostics in children — R1/PR7

(2023)
Open Access
Recommendation: Precision diagnostics in children — R1/PR6

(2023)
Open Access
Author comment: Precision diagnostics in children — R1/PR5
Paul Dimitri
(2023)
Open Access
Genotype-Phenotype Correlation in Noonan Syndrome – Focus on LZTR1 and its Substrates
Alexandra Viktoria Busley
(2023)
Open Access
A rare case of Noonan syndrome associated with biallelic variants in the LZTR1
Л. А. Гандаева, В. Г. Каверина, Е. Н. Басаргина, et al.
L O Badalyan Neurological Journal (2023) Vol. 4, Iss. 3, pp. 120-129
Open Access
Emerging Hypotheses on the Pathogenesis of Rasopathy-Associated Cardiomyopathies
Shun Nakagama, Masataka Yamasaki, Masamichi Ito, et al.
Pediatric Cardiology and Cardiac Surgery (2023) Vol. 39, Iss. 4, pp. 192-199
Open Access
Decision: Precision diagnostics in children — R0/PR4

(2022)
Open Access
Recommendation: Precision diagnostics in children — R0/PR3

(2022)
Open Access
Review: Precision diagnostics in children — R0/PR2

(2022)
Open Access
Author comment: Precision diagnostics in children — R0/PR1
Paul Dimitri
(2022)
Open Access
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