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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:

How we approach genetics in the diagnosis and management of vascular anomalies
Bhuvana A. Setty, Katie Wusik, Adrienne M. Hammill
Pediatric Blood & Cancer (2022) Vol. 69, Iss. S3
Closed Access | Times Cited: 12

Showing 12 citing articles:

Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache
Luis Fernando Sánchez‐Espino, Marta Ivars, Javier Antoñanzas, et al.
The Application of Clinical Genetics (2023) Vol. Volume 16, pp. 63-81
Open Access | Times Cited: 41
Genetic testing in the evaluation of individuals with clinical diagnosis of atypicalSturge–Webersyndrome
SangEun Yeom, Bernard A. Cohen, Clifford R. Weiss, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 4, pp. 983-994
Open Access | Times Cited: 9
Vascular Anomalies Care in the United States: A Cross-Sectional National Survey
Sally Cohen‐Cutler, Julie Blatt, Sherry Bayliff, et al.
The Journal of Pediatrics (2023) Vol. 261, pp. 113579-113579
Closed Access | Times Cited: 7
Sturge–Weber syndrome: an update for the pediatrician
Emilie Dingenen, Damien Segers, Hannelore De Maeseneer, et al.
World Journal of Pediatrics (2024) Vol. 20, Iss. 5, pp. 435-443
Closed Access | Times Cited: 2
The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms
Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza, Laura Florea, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12199-12199
Open Access | Times Cited: 11
Prevalence and Predictors of Hereditary Hemorrhagic Telangiectasia and Capillary-Malformation Arteriovenous Malformation Syndrome Among Children with Neurovascular Malformations
Elissa Engel, Katie Wusik, Philip Bright, et al.
The Journal of Pediatrics (2023) Vol. 264, pp. 113761-113761
Closed Access | Times Cited: 4
Neonatal Cutaneous Vascular Anomalies
Lauren L. Evans, Lauren Hill, Ann M. Kulungowski
NeoReviews (2024) Vol. 26, Iss. 1, pp. e12-e27
Closed Access | Times Cited: 1
Repurposing of antiangiogenic agents for treatment of vascular anomalies
Julie Blatt, Jennifer Brondon, Elizabeth L. Nieman, et al.
Pharmacology & Therapeutics (2023) Vol. 250, pp. 108520-108520
Closed Access | Times Cited: 2
Prevalence of aortic aneurysms and dissections in patients with systemic vessel aneurysms and dissections; matched case-control study using a national sample cohort
Jihye Song, Yong Cheol Lim, Do Jung Kim
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 1
Medical Management and Therapeutic Updates on Vascular Anomalies of the Head and Neck
Jorie Gatts, Srinivasa R. Chandra, Kiersten Ricci
Oral and Maxillofacial Surgery Clinics of North America (2023) Vol. 36, Iss. 1, pp. 115-123
Closed Access | Times Cited: 1
Sturge-Weber Syndrome: A comprehensive review of clinical features, optimized diagnosis and management strategies
Katarzyna Naja, Alicja Kapciak, Julia Górny, et al.
Quality in Sport (2024) Vol. 36, pp. 56849-56849
Open Access
Introduction: The changing role of the pediatric hematologist/oncologist in the care of people with vascular anomalies
Kristen Snyder, Clifford M. Takemoto
Pediatric Blood & Cancer (2022) Vol. 69, Iss. S3
Open Access
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