
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:
The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome
Erkut Ilaslan, Renata Markosyan, Patrick Sproll, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 21, pp. 8403-8403
Open Access | Times Cited: 10
Erkut Ilaslan, Renata Markosyan, Patrick Sproll, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 21, pp. 8403-8403
Open Access | Times Cited: 10
Showing 10 citing articles:
Genetic control of typical and atypical sex development
Alejandra P. Reyes, Nayla Y. León, Emily R. Frost, et al.
Nature Reviews Urology (2023) Vol. 20, Iss. 7, pp. 434-451
Closed Access | Times Cited: 26
Alejandra P. Reyes, Nayla Y. León, Emily R. Frost, et al.
Nature Reviews Urology (2023) Vol. 20, Iss. 7, pp. 434-451
Closed Access | Times Cited: 26
FKBP4 integrates FKBP4/Hsp90/IKK with FKBP4/Hsp70/RelA complex to promote lung adenocarcinoma progression via IKK/NF-κB signaling
Shuai Zong, Yulian Jiao, Xin Liu, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 6
Open Access | Times Cited: 34
Shuai Zong, Yulian Jiao, Xin Liu, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 6
Open Access | Times Cited: 34
FK506-binding proteins: Emerging target and therapeutic opportunity in multiple tumors
Hang Ke, Zihan Chen, Long Chen, et al.
International Journal of Biological Macromolecules (2025), pp. 141914-141914
Open Access
Hang Ke, Zihan Chen, Long Chen, et al.
International Journal of Biological Macromolecules (2025), pp. 141914-141914
Open Access
The clinical diversity and molecular etiology in 46, XY disorders of sex development patients without uterus
Leilei Ding, Min Luo, Shan Deng, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Leilei Ding, Min Luo, Shan Deng, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Androgen insensitivity and the evolving genetic heterogeneity
Nadine Hornig, Rafael Loch Batista
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 102000-102000
Closed Access
Nadine Hornig, Rafael Loch Batista
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 102000-102000
Closed Access
Mutations in Hsp90 Cochaperones Result in a Wide Variety of Human Disorders
Jill L. Johnson
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 15
Jill L. Johnson
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 15
Four novel mutations in the androgen receptor gene from Vietnamese patients with androgen insensitivity syndrome
Thu Hien Nguyen, Duc Quan Nguyen, Lien Nguyen Thi Kim, et al.
Genes & Genomics (2022) Vol. 45, Iss. 4, pp. 467-474
Closed Access | Times Cited: 3
Thu Hien Nguyen, Duc Quan Nguyen, Lien Nguyen Thi Kim, et al.
Genes & Genomics (2022) Vol. 45, Iss. 4, pp. 467-474
Closed Access | Times Cited: 3
Effect of Larval Rearing Temperature on Steroidogenesis Pathway Development in Early Life History in Winter Flounder (Pseudopleuronectes Americanus)
Nina Bellenger, Étienne Audet‐Walsh, Lucas Germain, et al.
(2024)
Closed Access
Nina Bellenger, Étienne Audet‐Walsh, Lucas Germain, et al.
(2024)
Closed Access
Novel pathogenic variants in the androgen receptor gene associated with androgen insensitivity syndrome identified through exome sequencing and in silico analysis
Cui Li, Xiaoyan Wang, Xiang Wang, et al.
Gene (2023) Vol. 860, pp. 147225-147225
Closed Access | Times Cited: 1
Cui Li, Xiaoyan Wang, Xiang Wang, et al.
Gene (2023) Vol. 860, pp. 147225-147225
Closed Access | Times Cited: 1
The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation and Neuromuscular Pathology
L. V. Popovych, Andriy Shatillo, Nataliya Zelinska, et al.
Cytology and Genetics (2022) Vol. 56, Iss. 5, pp. 417-422
Closed Access
L. V. Popovych, Andriy Shatillo, Nataliya Zelinska, et al.
Cytology and Genetics (2022) Vol. 56, Iss. 5, pp. 417-422
Closed Access
Pubertal And Gonadal Outcomes In 46,XY Individuals With Partial Androgen Insensitivity Syndrome Raised As Girls
Guilherme Guaragna‐Filho, Gil Guerra‐Júnior, Rieko Tadokoro‐Cuccaro, et al.
Research Square (Research Square) (2021)
Open Access
Guilherme Guaragna‐Filho, Gil Guerra‐Júnior, Rieko Tadokoro‐Cuccaro, et al.
Research Square (Research Square) (2021)
Open Access