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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:

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

Showing 19 citing articles:

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
Modeling human epigenetic disorders in mice: Beckwith-Wiedemann Syndrome and Silver-Russell Syndrome
Suhee Chang, Marisa S. Bartolomei
Disease Models & Mechanisms (2020)
Open Access | Times Cited: 40
Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management
Kelly A. Duffy, Kelly L. Trout, Jennifer M. Gunckle, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 25
GestaltMML: Enhancing Rare Genetic Disease Diagnosis through Multimodal Machine Learning Combining Facial Images and Clinical Texts.
Da Qin Wu, Jingye Yang, Cong Liu, et al.
PubMed (2024)
Closed Access | Times Cited: 3
Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians
Patrizia Defabianis, Alessandro Mussa, Rossella Ninivaggi, et al.
International Journal of Environmental Research and Public Health (2022) Vol. 19, Iss. 4, pp. 2448-2448
Open Access | Times Cited: 11
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
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith–Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
Maria Luca, Diana Carli, Simona Cardaropoli, et al.
Cancers (2023) Vol. 15, Iss. 3, pp. 773-773
Open Access | Times Cited: 5
Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study
Ruixue Wang, Yongmei Xiao, Dan Li, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2020) Vol. 46, Iss. 1
Open Access | Times Cited: 12
The Prevalence of Difficult Airway in Children With Beckwith-Wiedemann Syndrome: A Retrospective Cohort Study
Luis Sequera‐Ramos, Kelly A. Duffy, John E. Fiadjoe, et al.
Anesthesia & Analgesia (2021)
Open Access | Times Cited: 6
Changes on chromosome 11p15.5 as specific marker for embryonal rhabdomyosarcoma?
Aleš Vícha, Pavla Jenčová, Daniela Novakova‐Kodetova, et al.
Genes Chromosomes and Cancer (2023) Vol. 62, Iss. 12, pp. 732-739
Open Access | Times Cited: 2
Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith–Wiedemann Syndrome
Hwa Young Kim, Choong Ho Shin, Young Ah Lee, et al.
Annals of Laboratory Medicine (2022) Vol. 42, Iss. 6, pp. 668-677
Open Access | Times Cited: 4
Investigation of (epi)genotype causes and follow‐up manifestations in the patients with classical and atypical phenotype ofBeckwith‐Wiedemannspectrum
Beyhan Tüysüz, Nilay Güneş, Filiz Geyik, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 6, pp. 1721-1731
Closed Access | Times Cited: 5
Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
Hela Sassi, Yasmina Elaribi, Houweyda Jilani, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 10
Open Access | Times Cited: 5
Phenotypes and epigenetic errors in patients with Beckwith-Wiedemann syndrome in China
Miaoying Zhang, Chengjun Sun, Renchao Liu, et al.
Translational Pediatrics (2020) Vol. 9, Iss. 5, pp. 653-661
Open Access | Times Cited: 3
The future of commercial genetic testing
Benjamin D. Solomon
Current Opinion in Pediatrics (2023) Vol. 35, Iss. 6, pp. 615-619
Closed Access | Times Cited: 1
Onward and upward
Maximilian Muenke
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 7, pp. 1119-1121
Open Access | Times Cited: 1
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases
Alec Reginald Errol Correa, Puneeta Mishra, Madhulika Kabra, et al.
The Indian Journal of Pediatrics (2020) Vol. 87, Iss. 3, pp. 175-178
Closed Access | Times Cited: 1
Surgical approach to a rare case of Beckwith Wiedemann syndrome with left thigh hyperplasia
Francesco Paolo Gesuete, Marcello Molle, Luigi Cagiano, et al.
JPRAS Open (2023) Vol. 39, pp. 303-306
Open Access
Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant
Hanan H. Afifi, Ghada El‐Kamah, Alaa K. Kamel, et al.
Journal of Pediatric Genetics (2020) Vol. 10, Iss. 02, pp. 131-138
Open Access
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