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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 26-50 of 64 citing articles:

Atypical 7q11.23 deletions excluding ELN gene result in Williams–Beuren syndrome craniofacial features and neurocognitive profile
Viola Alesi, Sara Loddo, Valeria Orlando, et al.
American Journal of Medical Genetics Part A (2020) Vol. 185, Iss. 1, pp. 242-249
Closed Access | Times Cited: 13
Static and Motion Facial Analysis for Craniofacial Assessment and Diagnosing Diseases
Harold Matthews, Guido de Jong, Thomas Maal, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 19-42
Open Access | Times Cited: 8
Can artificial intelligence save medical genetics?
Benjamin D. Solomon
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 397-399
Closed Access | Times Cited: 11
Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review
Xin Lv, Xiao Yang, Linlin Li, et al.
Medicine (2023) Vol. 102, Iss. 43, pp. e34852-e34852
Open Access | Times Cited: 4
Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians
Nop Khongthon, Midi Theeraviwatwong, Khunton Wichajarn, et al.
The Application of Clinical Genetics (2024) Vol. Volume 17, pp. 107-115
Open Access | Times Cited: 1
Deletions and Other Structural Abnormalities of the Autosomes
Laura K. Conlin, Ada J. S. Chan, Beverly S. Emanuel, et al.
Elsevier eBooks (2024), pp. 179-225
Closed Access | Times Cited: 1
Facial analysis technology for the detection of Down syndrome in the Democratic Republic of the Congo
Antonio R. Porras, Matthew S. Bramble, Kizito Mosema Be Amoti, et al.
European Journal of Medical Genetics (2021) Vol. 64, Iss. 9, pp. 104267-104267
Open Access | Times Cited: 10
Celiac disease prevalence and predisposing‐HLA in a cohort of 93 Williams‐Beuren syndrome patients
Cecilia Ghisleni, Barbara Parma, Paola Cianci, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 1, pp. 84-89
Closed Access | Times Cited: 7
3D facial morphometry in Italian patients affected by Aicardi syndrome
Silvia Masnada, Daniele Gibelli, Claudia Dolci, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 10, pp. 2325-2332
Open Access | Times Cited: 9
Clinical application of chromosomal microarray analysis for the diagnosis of Williams–Beuren syndrome in Chinese Han patients
Yu Xia, Shufang Huang, Yueheng Wu, et al.
Molecular Genetics & Genomic Medicine (2018) Vol. 7, Iss. 2
Open Access | Times Cited: 9
Application of facial analysis Technology in Clinical Genetics: Considerations for diverse populations
Paul Kruszka, Cedrik Tekendo‐Ngongang
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Closed Access | Times Cited: 3
Noonan syndrome on the African Continent
Cedrik Tekendo‐Ngongang, Paul Kruszka
Birth Defects Research (2020) Vol. 112, Iss. 10, pp. 718-724
Closed Access | Times Cited: 8
A study on facial features of children with Williams syndrome in China based on three‐dimensional anthropometric measurement technology
Chai Ji, Dan Yao, Ming‐Yan Li, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 9, pp. 2102-2109
Closed Access | Times Cited: 6
Structural genomic variants in thoracic aortic disease
Josephina Meester, Anne Hebert, Bart Loeys
Current Opinion in Cardiology (2023)
Open Access | Times Cited: 2
First description of frequent occurrence of supernumerary lumbar ribs and transitional vertebrae in children with Williams–Beuren syndrome
Annette Schmitz, Elke Reutershahn, Peter Seiffert, et al.
Pediatric Radiology (2022) Vol. 53, Iss. 2, pp. 244-248
Closed Access | Times Cited: 4
Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of the oldest patient and a review of the adult phenotype
Marianna Farnè, Laura Bernardini, Anna Capalbo, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 692-707
Open Access | Times Cited: 5
Introducing in AJMG Part A: Case reports in diverse populations
Katta M. Girisha, Ambroise Wonkam, Maximilian Muenke
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 7, pp. 1547-1548
Open Access | Times Cited: 4
Machine Learning Models identify Signature Genes as potential Biomarkers for Hypertrophic Cardiomyopathy from Williams Syndrome
Hongxiao Yu, Xiping Liu, Manfang Sun, et al.
Research Square (Research Square) (2024)
Open Access
Optimization and evaluation of facial recognition models for Williams-Beuren syndrome
Pingchuan Huang, J Huang, Yulu Huang, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 9, pp. 3797-3808
Closed Access
Williams–Beuren syndrome diagnosis in an infant with atypical chromosome 7 microdeletion
Adekunle Olowu
BMJ Case Reports (2024) Vol. 17, Iss. 7, pp. e260312-e260312
Open Access
Delayed diagnosis of Williams–Beuren syndrome in an adolescent of Jamaican descent: examining racial disparities in genetics education
Nina B. Gold, Katherine A. Nash, Joanna Perdomo, et al.
Clinical Dysmorphology (2020) Vol. 30, Iss. 1, pp. 69-70
Closed Access | Times Cited: 3
Williams‐Beuren syndrome associated with hammock mitral valve: First case report
Kevin Velarde‐Acosta, Roberto Baltodano‐Arellano, Ángela Cachicatari-Beltrán, et al.
Echocardiography (2023) Vol. 40, Iss. 3, pp. 285-288
Closed Access | Times Cited: 1
A Large Turkish Cohort of Williams Syndrome: The Evaluation of Facial, Cardiovascular, and Neuropsychiatric Features
Serdar Bozlak, Dilek Uludağ Alkaya, Büşra Kasap, et al.
Turkish Archives of Pediatrics (2023) Vol. 58, Iss. 2, pp. 182-188
Open Access | Times Cited: 1
Diversity of Participants in Williams Syndrome Intervention Studies
Eva Shin, Caitlin Ravichandran, Danielle Renzi, et al.
Journal of Autism and Developmental Disorders (2023) Vol. 54, Iss. 10, pp. 3888-3898
Closed Access | Times Cited: 1
Lessons Learned from the Point-of-Care Use of a Facial Analysis Technology
Jon Soo Kim, Hansol Ko, H. Woo, et al.
Annals of Child Neurology (2023) Vol. 31, Iss. 4, pp. 271-275
Open Access | Times Cited: 1

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