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:
Breakpoint analysis for cytogenetically balanced translocation revealed unexpected complex structural abnormalities and suggested the position effect for MEF2C
Takeaki Tamura, Keiko Shimojima Yamamoto, Taichi Imaizumi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 6, pp. 1632-1638
Closed Access | Times Cited: 4
Takeaki Tamura, Keiko Shimojima Yamamoto, Taichi Imaizumi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 6, pp. 1632-1638
Closed Access | Times Cited: 4
Showing 4 citing articles:
De Novo Chromosomes 3q and 5q Chromothripsis Leads to a 5q14.3 Microdeletion Syndrome Presentation: Case Report and Review of the Literature
Melina L. Corriveau, Joshua C. Korb, Sydney L. Michener, et al.
American Journal of Medical Genetics Part A (2025)
Closed Access
Melina L. Corriveau, Joshua C. Korb, Sydney L. Michener, et al.
American Journal of Medical Genetics Part A (2025)
Closed Access
Glass syndrome derived from chromosomal breakage downstream region of SATB2
Keiko Shimojima Yamamoto, Rina Shimomura, Hiromichi Shoji, et al.
Brain and Development (2024) Vol. 46, Iss. 9, pp. 281-285
Closed Access | Times Cited: 2
Keiko Shimojima Yamamoto, Rina Shimomura, Hiromichi Shoji, et al.
Brain and Development (2024) Vol. 46, Iss. 9, pp. 281-285
Closed Access | Times Cited: 2
Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome
Ilaria Bestetti, M. Crippa, Alessandra Sironi, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Ilaria Bestetti, M. Crippa, Alessandra Sironi, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia, and seizures
Takeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 12, pp. 639-644
Closed Access
Takeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 12, pp. 639-644
Closed Access
