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:
Mosaic trisomy 12 diagnosed in a female patient: clinical features, genetic analysis, and review of the literature
Daniela Hainz, Marcus Krüger, Daniela Reber, et al.
World Journal of Pediatrics (2021) Vol. 17, Iss. 4, pp. 438-448
Open Access | Times Cited: 6
Daniela Hainz, Marcus Krüger, Daniela Reber, et al.
World Journal of Pediatrics (2021) Vol. 17, Iss. 4, pp. 438-448
Open Access | Times Cited: 6
Showing 6 citing articles:
Mosaic trisomy 12 – A case of a rare phenotypic association and literature review
Greta Senkeviciute, Evelina Dagytė, Vytautas Šliužas, et al.
Brain and Development Case Reports (2025) Vol. 3, Iss. 1, pp. 100058-100058
Open Access
Greta Senkeviciute, Evelina Dagytė, Vytautas Šliužas, et al.
Brain and Development Case Reports (2025) Vol. 3, Iss. 1, pp. 100058-100058
Open Access
Rare structural variants, aneuploidies, and mosaicism in individuals with Mullerian aplasia detected by optical genome mapping
Soumia Brakta, Zoe Hawkins, Nikhil Sahajpal, et al.
Human Genetics (2023) Vol. 142, Iss. 4, pp. 483-494
Closed Access | Times Cited: 6
Soumia Brakta, Zoe Hawkins, Nikhil Sahajpal, et al.
Human Genetics (2023) Vol. 142, Iss. 4, pp. 483-494
Closed Access | Times Cited: 6
Artificial intelligence for prenatal chromosome analysis
Kavitha Boddupally, Esther Rani Thuraka
Clinica Chimica Acta (2023) Vol. 552, pp. 117669-117669
Closed Access | Times Cited: 6
Kavitha Boddupally, Esther Rani Thuraka
Clinica Chimica Acta (2023) Vol. 552, pp. 117669-117669
Closed Access | Times Cited: 6
Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods
Irina Iordănescu, Anca Teodora Neacsu, Andreea Cătană, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
Irina Iordănescu, Anca Teodora Neacsu, Andreea Cătană, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
Prenatal Clinical Presentation and Genetic Analysis of Partial Trisomy 12: A Case Report
Nnenna Mbara, Adegbenro Omotuyi John Fakoya
Cureus (2024)
Open Access
Nnenna Mbara, Adegbenro Omotuyi John Fakoya
Cureus (2024)
Open Access
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
Angélica Martínez‐Hernández, Daniel Martínez-Anaya, Carola Durán‐McKinster, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Angélica Martínez‐Hernández, Daniel Martínez-Anaya, Carola Durán‐McKinster, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 1
