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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:

Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China
Licong Su, Jing Cheng, Xi Yin, et al.
Andrologia (2017) Vol. 49, Iss. 10, pp. e12763-e12763
Open Access | Times Cited: 8

Showing 8 citing articles:

Identification of gene variants in 130 Han Chinese patients with hypospadias by targeted next‐generation sequencing
Wanyu Zhang, Jinxiu Shi, Chenhui Zhang, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 8
Open Access | Times Cited: 14
Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity Syndrome
Anil Kumar, Rajni Sharma, Mohammed Faruq, et al.
Sexual Development (2021) Vol. 16, Iss. 1, pp. 34-45
Open Access | Times Cited: 11
Application and insights of targeted next-generation sequencing in a large cohort of 46,XY disorders of sex development in Chinese
Hongyu Chen, Guangjie Chen, Fengxia Li, et al.
Biology of Sex Differences (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Functional Effects In Silico Prediction for Androgen Receptor Ligand-Binding Domain Novel I836S Mutation
Alexey Rayevsky, Dmytro Sirokha, Dariia Samofalova, et al.
Life (2021) Vol. 11, Iss. 7, pp. 659-659
Open Access | Times Cited: 8
Complete Androgen Insensitivity Syndrome due to Mutations in the DNA-Binding Domain of the Human Androgen Receptor Gene
Pooja Chauhan, Anjali Rani, Surya Kumar Singh, et al.
Sexual Development (2018) Vol. 12, Iss. 6, pp. 269-274
Closed Access | Times Cited: 8
Yield of modern genetic evaluation for patients with proximal hypospadias and descended gonads
Courtney K. Rowe, Margaret P Adam, Jennifer Ahn, et al.
Journal of Pediatric Urology (2019) Vol. 15, Iss. 5, pp. 527.e1-527.e6
Closed Access | Times Cited: 6
Whole-Exome Sequencing Identified Rare Genetic Variants Associated with Undervirilized Genitalia in Taiwanese Pediatric Patients
Meng‐Che Tsai, Yun-Han Weng, Yu-Fang Lin, et al.
Biomedicines (2023) Vol. 11, Iss. 2, pp. 242-242
Open Access | Times Cited: 2
Identification of the Rare Ala871Glu Mutation in the Androgen Receptor Gene Leading to Complete Androgen Insensitivity Syndrome in an Adolescent Girl with Primary Amenorrhea
Aikaterini Kapama, Dimitrios T. Papadimitriou, George Mastorakos, et al.
Children (2022) Vol. 9, Iss. 12, pp. 1900-1900
Open Access | Times Cited: 1
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