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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:

Hypertension in Children and Adolescents with Turner Syndrome (TS), Neurofibromatosis 1 (NF1), and Williams Syndrome (WS)
Ramya Sivasubramanian, Kevin Meyers
Current Hypertension Reports (2021) Vol. 23, Iss. 4
Closed Access | Times Cited: 12

Showing 12 citing articles:

Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations
Cristina Peduto, Mariateresa Zanobio, Vincenzo Nigro, et al.
Cancers (2023) Vol. 15, Iss. 4, pp. 1217-1217
Open Access | Times Cited: 25
Feasibility of home blood pressure screening in the paediatric outpatient clinic setting
Jessie Mackay, Jonathan P. Glenning, Brittany M Grantham, et al.
Archives of Disease in Childhood (2025), pp. archdischild-327391
Closed Access
Neurofibromatosis Type 1
Sofia Dhanani, R. Lévy
Elsevier eBooks (2025)
Closed Access
Hereditary Thoracic Aortic Diseases
Gaia Spaziani, Francesca Chiara Surace, Francesca Girolami, et al.
Diagnostics (2024) Vol. 14, Iss. 1, pp. 112-112
Open Access | Times Cited: 1
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series
Paolo Currao, Marta Balzarini, Dario Pruna, et al.
Journal of Child Neurology (2024) Vol. 40, Iss. 1, pp. 49-60
Closed Access | Times Cited: 1
Renal Artery Stenosis and Mid-Aortic Syndrome in Children—A Review
Jakub Pytlos, Aneta Michalczewska, Piotr Majcher, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 22, pp. 6778-6778
Open Access | Times Cited: 1
Proteomic mapping reveals dysregulated angiogenesis in the cerebral arteries of rats with early-onset hypertension
Joakim Bastrup, Thomas A. Jepps
Journal of Biological Chemistry (2023) Vol. 299, Iss. 10, pp. 105221-105221
Open Access | Times Cited: 3
WILLIAMS-BEUREN SYNDROME AND COMBINED PATHOLOGY IN MONOCHORIAL TWINS (LITERATURE REVIEW AND CLINICAL CASE)
I. V. Lastivka, V. V. Antsupova, А. Babintseva, et al.
Neonatology surgery and perinatal medicine (2024) Vol. 14, Iss. 2(52), pp. 135-144
Open Access
Clinical Care for Cardiovascular Disease in Patients With Williams–Beuren Syndrome
R. Thomas Collins, Verena Gravenhorst, Gilles Faury, et al.
Journal of the American Heart Association (2024) Vol. 13, Iss. 19
Open Access
Genotypes and phenotypes of neurofibromatosis type 1 patients in Japan: A Hereditary Tumor Cohort Study
Mashu Futagawa, Tetsuya Okazaki, Eiji Nakata, et al.
Human Genome Variation (2024) Vol. 11, Iss. 1
Open Access
Williams Syndrome
Ana Fish, Barbara R. Pober, Robyn P. Thom
(2024), pp. 41-58
Closed Access
Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension
Yiting Lu, Di Zhang, Xin-Chang Liu, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 2
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