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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:

Cardiovascular disease in Noonan syndrome
Mary Ella Pierpont, M. Cristina Digilio
Current Opinion in Pediatrics (2018) Vol. 30, Iss. 5, pp. 601-608
Closed Access | Times Cited: 59

Showing 1-25 of 59 citing articles:

Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP)
Giuseppe Limongelli, Rachele Adorisio, Chiara Baggio, et al.
International Journal of Cardiology (2022) Vol. 357, pp. 55-71
Open Access | Times Cited: 49
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
Hypertrophic Cardiomyopathy in RASopathies
Michele Lioncino, Emanuele Monda, Federica Verrillo, et al.
Heart Failure Clinics (2021) Vol. 18, Iss. 1, pp. 19-29
Open Access | Times Cited: 52
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
Sarah E. Sheppard, Michael March, Christoph Seiler, et al.
JCI Insight (2023) Vol. 8, Iss. 9
Open Access | Times Cited: 19
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Francesco Nappi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1734-1734
Open Access | Times Cited: 6
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 440-451
Closed Access | Times Cited: 19
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 clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age
S. G. Fetisova, Olesya Melnik, Е. С. Васичкина, et al.
Pediatric Research (2025)
Closed Access
A Multidimensional Approach to Understanding Genetic Diversity, Risk Stratification, and Personalized Interventions in Pediatric Hypertrophic Cardiomyopathy
Mona Alromaihi, Faris Alrumaihi, Wanian M. Alwanian, et al.
Current Problems in Cardiology (2025), pp. 103040-103040
Closed Access
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects
Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
Children (2022) Vol. 9, Iss. 6, pp. 772-772
Open Access | Times Cited: 17
Activating Mutation of SHP2 Establishes a Tumorigenic Phonotype Through Cell-Autonomous and Non-Cell-Autonomous Mechanisms
Lei Dong, Da Han, Xinyi Meng, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 21
Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness
Lorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Clinical Genetics (2023) Vol. 104, Iss. 5, pp. 528-541
Open Access | Times Cited: 7
Clinical and functional characterization of a novel RASopathy‐causingSHOC2mutation associated with prenatal‐onset hypertrophic cardiomyopathy
Marialetizia Motta, Aldo Giancotti, Gioia Mastromoro, et al.
Human Mutation (2019)
Open Access | Times Cited: 20
Application of CRISPR-Cas9 gene editing for congenital heart disease
Heeyoung Seok, Rui Deng, Douglas B. Cowan, et al.
Clinical and Experimental Pediatrics (2021) Vol. 64, Iss. 6, pp. 269-279
Open Access | Times Cited: 16
New insights on Noonan syndrome’s clinical phenotype: a single center retrospective study
Francesco Baldo, Alice Fachin, Beatrice Da Re, et al.
BMC Pediatrics (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 12
The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations
Geeske M. van Woerden, Richelle Senden, Charlotte de Konink, et al.
Human Mutation (2022) Vol. 43, Iss. 10, pp. 1377-1395
Open Access | Times Cited: 10
Cardiac transplantation in children with Noonan syndrome
Leslie M. McCallen, Rebecca Ameduri, Susan W. Denfield, et al.
Pediatric Transplantation (2019) Vol. 23, Iss. 6
Closed Access | Times Cited: 17
The Prevalence of Noonan Spectrum Disorders in Pediatric Patients with Pulmonary Valve Stenosis
Janet M. Bell, Ellen M. Considine, Leslie M. McCallen, et al.
The Journal of Pediatrics (2021) Vol. 234, pp. 134-141.e5
Closed Access | Times Cited: 14
Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G
Narasimman Gurusamy, Sheeja Rajasingh, Vinoth Sigamani, et al.
Experimental Cell Research (2021) Vol. 400, Iss. 1, pp. 112508-112508
Open Access | Times Cited: 13
Near Adult Height and Body Mass Index Changes in Growth Hormone Treated Short Children with Noonan Syndrome: The Belgian Experience
Jean De Schepper, Muriel Thomas, Koen Huysentruyt, et al.
Hormone Research in Paediatrics (2024), pp. 1-13
Closed Access | Times Cited: 1
Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a p.Q510P mutation in the PTPN11 gene
Rong Li, Amanda Baskfield, Yongshun Lin, et al.
Stem Cell Research (2018) Vol. 34, pp. 101374-101374
Open Access | Times Cited: 10
Regulatory mechanism of fibrosis-related genes in patients with heart failure
Yijing Tao, Chengjie Gao, Da Qian, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 6
Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (II)
Chih‐Ping Chen
Journal of Medical Ultrasound (2023) Vol. 31, Iss. 1, pp. 13-16
Open Access | Times Cited: 3
Noonan syndrome associated with hypoplastic left heart syndrome
Kendall M. Lawrence, Danielle S. Burstein, Rebecca C. Ahrens‐Nicklas, et al.
Cardiology in the Young (2022) Vol. 33, Iss. 4, pp. 652-654
Closed Access | Times Cited: 5
The added value of the electrocardiogram in Noonan syndrome
Eefke Vos, Erika Leenders, Sterre R. Werkman, et al.
Cardiology in the Young (2021) Vol. 32, Iss. 6, pp. 936-943
Open Access | Times Cited: 6
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