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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 and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort
Hao Chen, Xin Li, Xiaoliang Liu, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 1038
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
Treatment Strategies for Cardiomyopathy in Children: A Scientific Statement From the American Heart Association
Carmel Bogle, Steven D. Colan, Shelley D. Miyamoto, et al.
Circulation (2023) Vol. 148, Iss. 2, pp. 174-195
Open Access | Times Cited: 33
Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations
Jeevana Praharsha Athota, Meenakshi Bhat, Sheela Nampoothiri, et al.
BMC Medical Genetics (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 63
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
Time-dependent effects of BRAF-V600E on cell cycling, metabolism, and function in engineered myocardium
Nicholas Strash, Sophia DeLuca, Geovanni L. Janer Carattini, et al.
Science Advances (2024) Vol. 10, Iss. 4
Open Access | Times Cited: 6
Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes
Cristina Mazzaccara, Raffaella Lombardi, Bruno Mirra, et al.
Biomolecules (2022) Vol. 12, Iss. 10, pp. 1417-1417
Open Access | Times Cited: 23
Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants
Carolin Knauer, Henrike Haltern, Eric Schoger, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 1, pp. 102123-102123
Open Access | Times Cited: 5
RASopathies and cardiac manifestations
Nazia Hilal, Zi Chen, Ming Hui Chen, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 12
Natural history and outcomes in paediatric RASopathy‐associated hypertrophic cardiomyopathy
Olga Boleti, Gabrielle Norrish, Ella Field, et al.
ESC Heart Failure (2024) Vol. 11, Iss. 2, pp. 923-936
Open Access | Times Cited: 4
THE ROLE OF MULTIDISCIPLINARY APPROACH IN THE PROCESS OF DIAGNOSING NEUROFIBROMATOSIS, TYPE 1, IN COMBINATION WITH CONGENITAL HEART PATHOLOGY
M. V. Kuzevanova, А А Конюшевская, G.S. Smyrnova, et al.
Bulletin of Problems Biology and Medicine (2025) Vol. 1, Iss. 1, pp. 43-43
Open Access
Protein-losing enteropathy and multiple vasculature dysplasia in LZTR1-related Noonan syndrome: A case report and review of literature
Qiuju Tian, Lujia Zhang, Qun Zhang, et al.
World Journal of Gastroenterology (2025) Vol. 31, Iss. 17
Closed Access
Identification and validation of pyroptosis-related genes as potential biomarkers for hypertrophic cardiomyopathy: A comprehensive bioinformatics analysis
Xin Tang, Yi Shen, Yun Lu, et al.
Medicine (2024) Vol. 103, Iss. 4, pp. e36799-e36799
Open Access | Times Cited: 3
Comprehensive Transcriptomics Profiling of MicroRNA Reveals Plasma Circulating Biomarkers of Hypertrophic Cardiomyopathy and Dysregulated Signaling Pathways
Lusha W. Liang, Kohei Hasegawa, Matthew J. Maurer, et al.
Circulation Heart Failure (2023) Vol. 16, Iss. 6
Open Access | Times Cited: 7
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
Kirsten M. Farncombe, Emily Thain, Carolina Barnett‐Tapia, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Phenotypic and genotypic spectrum of noonan syndrome: A retrospective analysis of 46 consecutive pediatric patients presented at a regional cardiac center in China
Qinchang Chen, Dian Hong, Yulu Huang, et al.
Heliyon (2024) Vol. 10, Iss. 5, pp. e27038-e27038
Open Access | Times Cited: 2
Phenotype–genotype analysis of 242 individuals with RASopathies: 18‐year experience of a tertiary center in Brazil
Débora Romeo Bertola, Matheus Augusto Araújo Castro, Guilherme Lopes Yamamoto, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 4, pp. 896-911
Closed Access | Times Cited: 18
The molecular functions of RIT1 and its contribution to human disease
Richard Van, Antonio Cuevas-Navarro, Pau Castel, et al.
Biochemical Journal (2020) Vol. 477, Iss. 15, pp. 2755-2770
Open Access | Times Cited: 17
Comprehensive Proteomics Profiling Identifies Patients With Late Gadolinium Enhancement on Cardiac Magnetic Resonance Imaging in the Hypertrophic Cardiomyopathy Population
Bradley Lander, Yanling Zhao, Kohei Hasegawa, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 8
Biventricular outflow tract obstruction due to hypertrophy related to compound heterozygous variants in LZTR1
Shuai Wang, Daoquan Peng
ESC Heart Failure (2024) Vol. 11, Iss. 6, pp. 4450-4455
Open Access | Times Cited: 1
Noonan Syndrome with Multiple Lentigines
Myles C. Hodgson, Saravanakkumar Chennappan, Maria I. Kontaridis
(2024), pp. 107-132
Closed Access | Times Cited: 1
Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations
Giulio Calcagni, M. Cristina Digilio, Bruno Marino, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 11
PTPN11 Gene Mutations and Its Association with the Risk of Congenital Heart Disease
Ziqing Xu, Wei-Cheng Chen, Yujie Li, et al.
Disease Markers (2022) Vol. 2022, pp. 1-11
Open Access | Times Cited: 6
Early Outcomes of Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy in Children With Noonan Syndrome
Shi Chen, Liang Chen, Yong Jiang, et al.
Seminars in Thoracic and Cardiovascular Surgery (2021) Vol. 34, Iss. 2, pp. 655-665
Closed Access | Times Cited: 8
Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
Biyun Feng, Xin Li, Qianwen Zhang, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 3
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