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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:

Investigation into the genetics of fetal congenital lymphatic anomalies
Daniella Rogerson, Anna Alkelai, Jessica L. Giordano, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 6, pp. 703-716
Open Access | Times Cited: 17

Showing 17 citing articles:

Hydrops fetalis und fetale Anämie
U. Gembruch
Springer eBooks (2025), pp. 753-799
Closed Access
Chromosomal abnormalities associated with fetal pleural effusion (I): General overview
Chih‐Ping Chen
Taiwanese Journal of Obstetrics and Gynecology (2024) Vol. 63, Iss. 2, pp. 165-167
Open Access | Times Cited: 2
Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies
Chih‐Ping Chen
Taiwanese Journal of Obstetrics and Gynecology (2024) Vol. 63, Iss. 2, pp. 174-177
Open Access | Times Cited: 2
Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations
Chih‐Ping Chen
Taiwanese Journal of Obstetrics and Gynecology (2024) Vol. 63, Iss. 2, pp. 168-173
Open Access | Times Cited: 2
Complex lymphatic anomalies: Molecular landscape and medical management
Alexandra J. Borst, Allison Britt, Denise M. Adams
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151422-151422
Closed Access | Times Cited: 2
Spectrum of lymphatic anomalies in patients with RASA1‐related CM‐AVM
Mia A. Mologousis, Claire A. Ostertag‐Hill, Hilary Haimes, et al.
Pediatric Dermatology (2023) Vol. 40, Iss. 6, pp. 1028-1034
Closed Access | Times Cited: 6
De novo heterozygous missense variants inCELSR1as cause of fetal pleural effusions and progressive fetal hydrops
Maayke A. de Koning, Paula Andrea Pimienta Ramírez, Monique C. Haak, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 549-552
Open Access | Times Cited: 1
Roles for RERE in lymphatic endothelial cell proliferation and survival, and human cystic lymphatic malformations
Daniella Rogerson, Ajit Muley, Jessica L. Giordano, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Another face of RASA1: Report of familial germline variant in RASA1 with dysmorphic features
Esteban Hume, M Cossio, Paula Vargas, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Closed Access
Lymphatic System Development and Function
Harish P. Janardhan, Brianna T. Wachter, Chinmay M. Trivedi
Current Cardiology Reports (2024) Vol. 26, Iss. 11, pp. 1209-1219
Closed Access
Robust Differentiation of Human Pluripotent Stem Cells into Lymphatic Endothelial Cells Using Transcription Factors
Sanjoy Saha, Francine Graham, James Knopp, et al.
Cells Tissues Organs (2024), pp. 1-11
Open Access
Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
Brian Burnett, Christian M. Parobek, Matthew A. Shanahan, et al.
Prenatal Diagnosis (2024)
Closed Access
Endothelial force sensing signals to parenchymal cells to regulate bile and plasma lipids
Laeticia Lichtenstein, Chew W. Cheng, Muath Bajarwan, et al.
Science Advances (2024) Vol. 10, Iss. 39
Open Access
Central Conducting Lymphatic Anomalies
Hui‐Qi Qu, Dong Li, Hákon Hákonarson
(2024), pp. 215-239
Closed Access
Fetal Neck Pathology
Radu Vlădăreanu, Costin Berceanu
Donald School Journal of Ultrasound in Obstetrics & Gynecology (2024) Vol. 18, Iss. 4, pp. 370-391
Open Access
Diagnosis and treatment of lymphatic malformations: experience of the surgical department for newborns and infants
Aleksandra S. Gurskaya, Mariya A. Sulavko, Rimir R. Bayazitov, et al.
Russian Pediatric Journal (2023) Vol. 26, Iss. 4, pp. 242-251
Open Access
Unilateral segmental presentation and a novel EPHB4 gene variant in capillary malformation–arteriovenous malformation type 2
Clara Valente, Margarida Brito Caldeira, Bruno Duarte, et al.
Pediatric Dermatology (2023) Vol. 41, Iss. 2, pp. 344-345
Closed Access
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