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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:

Williams–Beuren syndrome in diverse populations
Paul Kruszka, Antonio R. Porras, Deise Helena de Souza, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 5, pp. 1128-1136
Open Access | Times Cited: 64

Showing 1-25 of 64 citing articles:

Williams syndrome
Beth A. Kozel, Boaz Barak, Chong Ae Kim, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 178
The influence of social determinants of health on the genetic diagnostic odyssey: who remains undiagnosed, why, and to what effect?
Yarden S. Fraiman, Monica H. Wojcik
Pediatric Research (2020) Vol. 89, Iss. 2, pp. 295-300
Open Access | Times Cited: 75
Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics
Julie De Backer, Antoine Bondue, Werner Budts, et al.
European Journal of Preventive Cardiology (2019) Vol. 27, Iss. 13, pp. 1423-1435
Open Access | Times Cited: 55
Development and evaluation of a machine learning-based point-of-care screening tool for genetic syndromes in children: a multinational retrospective study
Antonio R. Porras, Kenneth N. Rosenbaum, Carlos Tor-Díez, et al.
The Lancet Digital Health (2021) Vol. 3, Iss. 10, pp. e635-e643
Open Access | Times Cited: 55
Clinical phenotypes study of 231 children with Williams syndrome in China: A single‐center retrospective study
Fang-Fang Li, Weijun Chen, Dan Yao, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 12
Open Access | Times Cited: 25
Automatic Facial Recognition of Williams-Beuren Syndrome Based on Deep Convolutional Neural Networks
Hui Liu, Zihua Mo, Hang Yang, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 28
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome
Laryssa A. Huryn, Taylor Flaherty, Rosalie Nolen, et al.
British Journal of Ophthalmology (2022) Vol. 107, Iss. 10, pp. 1554-1559
Open Access | Times Cited: 22
Photorealistic rendering of fetal faces from raw magnetic resonance imaging data
Thierry Blanc, C. Godard, D. Grévent, et al.
Ultrasound in Obstetrics and Gynecology (2025)
Closed Access
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders
Roos van der Donk, Sandra Jansen, Janneke Schuurs-Hoeijmakers, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 8, pp. 1719-1725
Open Access | Times Cited: 37
Dental-craniofacial manifestation and treatment of rare diseases
En Luo, Hanghang Liu, Qiucheng Zhao, et al.
International Journal of Oral Science (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 34
Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study
Yonit A. Addissie, Paul Kruszka, Angela Troia, et al.
Environmental Health (2020) Vol. 19, Iss. 1
Open Access | Times Cited: 30
Williams syndrome
Rachel Royston, Jane Waite, Patricia Howlin
Current Opinion in Psychiatry (2018) Vol. 32, Iss. 2, pp. 60-66
Open Access | Times Cited: 29
Rubinstein–Taybi syndrome in diverse populations
Cedrik Tekendo‐Ngongang, Babajide Owosela, Nicole Fleischer, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 12, pp. 2939-2950
Closed Access | Times Cited: 25
Genetics and genomics in Peru: Clinical and research perspective
Heinner Guio, Julio A. Poterico, Kelly S. Levano, et al.
Molecular Genetics & Genomic Medicine (2018) Vol. 6, Iss. 6, pp. 873-886
Open Access | Times Cited: 27
The genetic workup for structural congenital heart disease
Teodoro Jerves, Andrea Beaton, Paul Kruszka
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 184, Iss. 1, pp. 178-186
Closed Access | Times Cited: 24
7q11.23 deletion and duplication
Lucy R. Osborne, Carolyn Β. Mervis
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 41-48
Closed Access | Times Cited: 19
Turner syndrome in diverse populations
Paul Kruszka, Yonit A. Addissie, Cedrik Tekendo‐Ngongang, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 2, pp. 303-313
Open Access | Times Cited: 21
Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk
Phoebe C. R. Parrish, Delong Liu, Russell H. Knutsen, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 12, pp. 2035-2050
Open Access | Times Cited: 20
Identifying environmental risk factors and gene–environment interactions in holoprosencephaly
Yonit A. Addissie, Angela Troia, Zoë C. Wong, et al.
Birth Defects Research (2020) Vol. 113, Iss. 1, pp. 63-76
Open Access | Times Cited: 20
Beckwith–Wiedemann syndrome in diverse populations
Kelly A. Duffy, Brian J Sajorda, Alice C. Yu, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 4, pp. 525-533
Open Access | Times Cited: 19
Diversity and dysmorphology
Paul Kruszka, Cedrik Tekendo‐Ngongang, Maximilian Muenke
Current Opinion in Pediatrics (2019) Vol. 31, Iss. 6, pp. 702-707
Closed Access | Times Cited: 19
Objective differential diagnosis of Noonan and Williams–Beuren syndromes in diverse populations using quantitative facial phenotyping
Antonio R. Porras, Marshal Summar, Marius George Linguraru
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 5
Open Access | Times Cited: 15
Growth assessment in children with Williams-Beuren syndrome: a systematic review
Amanda de Sousa Lima Strafacci, Juliana Fernandes de Camargo, Fábio Bertapelli, et al.
Journal of Applied Genetics (2020) Vol. 61, Iss. 2, pp. 205-212
Closed Access | Times Cited: 15
Computational diagnostic methods on 2D photographs: A review of the literature
Quentin Hennocq, Roman Hossein Khonsari, Vincent Benoît, et al.
Journal of Stomatology Oral and Maxillofacial Surgery (2021) Vol. 122, Iss. 4, pp. e71-e75
Open Access | Times Cited: 13
Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative
Christoffer Nellåker, Fowzan S. Alkuraya, Gareth Baynam, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 15
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