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:
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum
Roseline Vibert, Cyril Mignot, Boris Keren, et al.
Clinical Genetics (2021) Vol. 101, Iss. 3, pp. 307-316
Closed Access | Times Cited: 7
Roseline Vibert, Cyril Mignot, Boris Keren, et al.
Clinical Genetics (2021) Vol. 101, Iss. 3, pp. 307-316
Closed Access | Times Cited: 7
Showing 7 citing articles:
Agenesis of the corpus callosum: What to tell expecting parents?
Pascale Tsai, Shiri Shinar
Prenatal Diagnosis (2023) Vol. 43, Iss. 12, pp. 1527-1535
Open Access | Times Cited: 9
Pascale Tsai, Shiri Shinar
Prenatal Diagnosis (2023) Vol. 43, Iss. 12, pp. 1527-1535
Open Access | Times Cited: 9
Chromosome 8p Syndromes Clinical Presentation and Management Guidelines
Kourtney Santucci, Kristina E. Malik, Katie Angione, et al.
Clinical Genetics (2024)
Closed Access | Times Cited: 1
Kourtney Santucci, Kristina E. Malik, Katie Angione, et al.
Clinical Genetics (2024)
Closed Access | Times Cited: 1
Identification of small-sized intrachromosomal segments at the ends of INV–DUP–DEL patterns
Keiko Shimojima Yamamoto, Takeaki Tamura, Nobuhiko Okamoto, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 11, pp. 751-757
Closed Access | Times Cited: 3
Keiko Shimojima Yamamoto, Takeaki Tamura, Nobuhiko Okamoto, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 11, pp. 751-757
Closed Access | Times Cited: 3
Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of “8p Inverted Duplication/Deletion Syndrome”
D. A. Yurchenko, М.Е. Миньженкова, Е. Л. Дадали, et al.
Biomedicines (2022) Vol. 10, Iss. 3, pp. 567-567
Open Access | Times Cited: 4
D. A. Yurchenko, М.Е. Миньженкова, Е. Л. Дадали, et al.
Biomedicines (2022) Vol. 10, Iss. 3, pp. 567-567
Open Access | Times Cited: 4
Detection of an 8p23.1 Inversion Using High-Resolution Optical Genome Mapping
Chunxiang Zhou, Huijun Li, Yiyan Shi, et al.
Maternal-Fetal Medicine (2024) Vol. 6, Iss. 3, pp. 173-177
Open Access
Chunxiang Zhou, Huijun Li, Yiyan Shi, et al.
Maternal-Fetal Medicine (2024) Vol. 6, Iss. 3, pp. 173-177
Open Access
Chromosome engineering to restore euploidy in cells harboring a complex rearrangement of chromosome 8
Sophia N. Lee, Lu Qiao, Sarah Thompson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Sophia N. Lee, Lu Qiao, Sarah Thompson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Chromosomal Microarray Analysis and Prenatal Diagnosis: What Obstetricians Should Know
Heejin Son, E. Choi, Yiyoung Ju, et al.
Perinatology (2022) Vol. 33, Iss. 3, pp. 121-121
Open Access
Heejin Son, E. Choi, Yiyoung Ju, et al.
Perinatology (2022) Vol. 33, Iss. 3, pp. 121-121
Open Access
