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:
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
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
Showing 15 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
Beth A. Kozel, Boaz Barak, Chong Ae Kim, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 178
Growth, body composition, and endocrine issues in Williams syndrome
Takara L. Stanley, Aaron Leong, Barbara R. Pober
Current Opinion in Endocrinology Diabetes and Obesity (2020) Vol. 28, Iss. 1, pp. 64-74
Open Access | Times Cited: 40
Takara L. Stanley, Aaron Leong, Barbara R. Pober
Current Opinion in Endocrinology Diabetes and Obesity (2020) Vol. 28, Iss. 1, pp. 64-74
Open Access | Times Cited: 40
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
Fang-Fang Li, Weijun Chen, Dan Yao, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 12
Open Access | Times Cited: 25
A Case Report of Williams Syndrome in a Child and Literature Review
洪柱 梁
Medical Diagnosis (2025) Vol. 15, Iss. 02, pp. 135-139
Closed Access
洪柱 梁
Medical Diagnosis (2025) Vol. 15, Iss. 02, pp. 135-139
Closed Access
Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders
Jianrong Zhou, Ying Zheng, Guiying Liang, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 15
Jianrong Zhou, Ying Zheng, Guiying Liang, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 15
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
Xin Lv, Xiao Yang, Linlin Li, et al.
Medicine (2023) Vol. 102, Iss. 43, pp. e34852-e34852
Open Access | Times Cited: 4
Brazilian growth charts for Williams–Beuren Syndrome at ages 2 to 18 years
Amanda de Sousa Lima Strafacci, Fábio Bertapelli, Chong Ae Kim, et al.
Jornal de Pediatria (2024) Vol. 100, Iss. 3, pp. 277-282
Open Access | Times Cited: 1
Amanda de Sousa Lima Strafacci, Fábio Bertapelli, Chong Ae Kim, et al.
Jornal de Pediatria (2024) Vol. 100, Iss. 3, pp. 277-282
Open Access | Times Cited: 1
Case report: Development of central precocious puberty in a girl with late-diagnosed simple virilizing congenital adrenal hyperplasia complicated with Williams syndrome
Eun Young Joo, Myung Ji Yoo, Su Jin Kim, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 1
Eun Young Joo, Myung Ji Yoo, Su Jin Kim, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 1
Early Neurobehavioral Characterization of the CD Mouse Model of Williams–Beuren Syndrome
Silvia Giannoccaro, C. Ferraguto, Valeria Petroni, et al.
Cells (2023) Vol. 12, Iss. 3, pp. 391-391
Open Access | Times Cited: 3
Silvia Giannoccaro, C. Ferraguto, Valeria Petroni, et al.
Cells (2023) Vol. 12, Iss. 3, pp. 391-391
Open Access | Times Cited: 3
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
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
Caracterização Clínica e Genética de Pacientes com Suspeita da Síndrome de Williams-Beuren (SWB) no Brasil
Fernanda Ramos Barbosa de Oliveira, Bruno Faulin Gamba, Deise Helena de Souza, et al.
Ensaios e Ciência C Biológicas Agrárias e da Saúde (2022) Vol. 26, Iss. 1, pp. 02-09
Open Access | Times Cited: 1
Fernanda Ramos Barbosa de Oliveira, Bruno Faulin Gamba, Deise Helena de Souza, et al.
Ensaios e Ciência C Biológicas Agrárias e da Saúde (2022) Vol. 26, Iss. 1, pp. 02-09
Open Access | Times Cited: 1
Effectiveness of smartphone app-based anxiety therapy in Williams Beuren syndrome: a single-case, multiple-baseline study (Preprint)
Natacha Lehman, David Geneviève, Raphaël Trouillet
(2023)
Closed Access
Natacha Lehman, David Geneviève, Raphaël Trouillet
(2023)
Closed Access
Atypical Deletion of Williams-Beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders
Jianrong Zhou, Ying Zheng, Guiying Liang, et al.
Research Square (Research Square) (2020)
Open Access
Jianrong Zhou, Ying Zheng, Guiying Liang, et al.
Research Square (Research Square) (2020)
Open Access
Ensaios Ciências, Fernanda Ramos Barbosa de Oliveira, Bruno Faulin Gamba, et al.
Ensaios e Ciência C Biológicas Agrárias e da Saúde (2022) Vol. 26, Iss. 1
Open Access
Atypical Deletion of Williams-beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders
Jianrong Zhou, Ying Zheng, Gui‐Ying Liang, et al.
Research Square (Research Square) (2021)
Open Access
Jianrong Zhou, Ying Zheng, Gui‐Ying Liang, et al.
Research Square (Research Square) (2021)
Open Access
