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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:

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development
Khouloud Rjiba, Soumaya Mougou-Zerelli, Imen hadj Hamida, et al.
Reproductive Biology and Endocrinology (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 9

Showing 9 citing articles:

SOX on tumors, a comfort or a constraint?
Junqing Jiang, Yufei Wang, Mengyu Sun, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 7
Molecular genetic diagnosis and surgical management in a cohort of children with 46,XY disorders/differences of sex development
Y.S. Wong, Ho‐Ming Luk, Ho Chung Yau, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
Role of the SOX family in cancer immune evasion: Emerging player and promising therapeutic opportunities
Jin-ke Li, Yawen Xu, Ying Han, et al.
Medicine (2025) Vol. 104, Iss. 5, pp. e41393-e41393
Open Access
Sox8: a multifaceted transcription factor in development and disease
María Nazareth González‐Alvarado, Jessica Aprato
Biology Open (2025) Vol. 14, Iss. 2
Open Access
Diverse genetic causes of amenorrhea in an ethnically homogeneous cohort and an evolving approach to diagnosis
Shabnam Bakhshalizadeh, Fateme Afkhami, Katrina M. Bell, et al.
Molecular and Cellular Endocrinology (2024) Vol. 587, pp. 112212-112212
Open Access | Times Cited: 2
Whole‐genome resequencing reveals novel sex‐related markers and candidate gene in the Chinese soft‐shelled turtle (Pelodiscus sinensis)
Dan Zeng, Mengying Chen, Jiawei Zeng, et al.
Journal of the World Aquaculture Society (2024)
Open Access
<i>PTPN11</i> and <i>FLNA</i> variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features
Yuki Muranishi, Tomoyo Itonaga, Kenji Ihara, et al.
Clinical Pediatric Endocrinology (2024) Vol. 33, Iss. 3, pp. 169-173
Open Access
Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling
Paranchai Boonsawat, Reza Asadollahi, Dunja Niedrist, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 9, pp. 1994-2011
Open Access
Genetic control of fetal sex development
Gabby Atlas, Katie L. Ayers, Rajini Sreenivasan, et al.
Elsevier eBooks (2024)
Closed Access
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