
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:
Genetics of 46,XY gonadal dysgenesis
Maëva Elzaïat, Ken McElreavey, Anu Bashamboo
Best Practice & Research Clinical Endocrinology & Metabolism (2022) Vol. 36, Iss. 1, pp. 101633-101633
Open Access | Times Cited: 36
Maëva Elzaïat, Ken McElreavey, Anu Bashamboo
Best Practice & Research Clinical Endocrinology & Metabolism (2022) Vol. 36, Iss. 1, pp. 101633-101633
Open Access | Times Cited: 36
Showing 1-25 of 36 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: 23
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: 23
Toward a Robust Definition of Sport Sex
David J. Handelsman
Endocrine Reviews (2024) Vol. 45, Iss. 5, pp. 709-736
Closed Access | Times Cited: 11
David J. Handelsman
Endocrine Reviews (2024) Vol. 45, Iss. 5, pp. 709-736
Closed Access | Times Cited: 11
A conserved NR5A1-responsive enhancer regulates SRY in testis-determination
Denis Houzelstein, Caroline Eozénou, Carlos F. Lagos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Denis Houzelstein, Caroline Eozénou, Carlos F. Lagos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study
Rawda Naamneh Elzenaty, Idoia Martinez de la Piscina, Chrysanthi Kouri, et al.
The Journal of Clinical Endocrinology & Metabolism (2024)
Open Access | Times Cited: 4
Rawda Naamneh Elzenaty, Idoia Martinez de la Piscina, Chrysanthi Kouri, et al.
The Journal of Clinical Endocrinology & Metabolism (2024)
Open Access | Times Cited: 4
Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
Jiali Chen, Peng Huifang, Yuqing Jiang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 4
Jiali Chen, Peng Huifang, Yuqing Jiang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 4
Altered RNA-processing provides a mechanistic framework delineating human sex reversal associated with pathogenic variants in the RNA-helicase DHX37
Maëva Elzaïat, Estelle Talouarn, Somboon Wankanit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Maëva Elzaïat, Estelle Talouarn, Somboon Wankanit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Infertility management in a patient with Swyer syndrome: a case report
Laura Krygere, Ruta Bartasiene, Agnė Kozlovskaja-Gumbrienė, et al.
Journal of Assisted Reproduction and Genetics (2025)
Open Access
Laura Krygere, Ruta Bartasiene, Agnė Kozlovskaja-Gumbrienė, et al.
Journal of Assisted Reproduction and Genetics (2025)
Open Access
Coexistence of SRY, DHX37 and POR gene variants in a patient with 46,XY disorder of sex development
Ayşe Özden, Hakan Döneray, Ayberk Türkyılmaz, et al.
Journal of Pediatric Endocrinology and Metabolism (2025)
Closed Access
Ayşe Özden, Hakan Döneray, Ayberk Türkyılmaz, et al.
Journal of Pediatric Endocrinology and Metabolism (2025)
Closed Access
The epidemiology of disorders of sex development
Agnethe Berglund, Simon Chang, Marie Lind‐Holst, et al.
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 102002-102002
Closed Access
Agnethe Berglund, Simon Chang, Marie Lind‐Holst, et al.
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 102002-102002
Closed Access
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
Khouloud Rjiba, Soumaya Mougou-Zerelli, Imen hadj Hamida, et al.
Reproductive Biology and Endocrinology (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 9
Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development
Atsushi Hattori, Maki Fukami
Biomolecules (2023) Vol. 13, Iss. 4, pp. 691-691
Open Access | Times Cited: 7
Atsushi Hattori, Maki Fukami
Biomolecules (2023) Vol. 13, Iss. 4, pp. 691-691
Open Access | Times Cited: 7
Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility
Jana Emich, Avinash Gaikwad, Birgit Stallmeyer, et al.
Fertility and Sterility (2022) Vol. 119, Iss. 2, pp. 219-228
Open Access | Times Cited: 8
Jana Emich, Avinash Gaikwad, Birgit Stallmeyer, et al.
Fertility and Sterility (2022) Vol. 119, Iss. 2, pp. 219-228
Open Access | Times Cited: 8
A case of complete androgen insensitivity syndrome combined with bilateral inguinal hernia
R. Zheng, Frank Chen, M. G. Zhao, et al.
Hernia (2024) Vol. 28, Iss. 4, pp. 1477-1480
Closed Access | Times Cited: 1
R. Zheng, Frank Chen, M. G. Zhao, et al.
Hernia (2024) Vol. 28, Iss. 4, pp. 1477-1480
Closed Access | Times Cited: 1
MYRF: A New Regulator of Cardiac and Early Gonadal Development—Insights from Single Cell RNA Sequencing Analysis
Verónica Calonga‐Solís, Helena Fabbri‐Scallet, Fabian Ott, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 16, pp. 4858-4858
Open Access | Times Cited: 7
Verónica Calonga‐Solís, Helena Fabbri‐Scallet, Fabian Ott, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 16, pp. 4858-4858
Open Access | Times Cited: 7
A novel c.64G > T (p.G22C) NR5A1 variant in a Chinese adolescent with 46,XY disorders of sex development: a case report
Dan Zhang, Dajia Wang, Yajie Tong, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 3
Dan Zhang, Dajia Wang, Yajie Tong, et al.
BMC Pediatrics (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 3
Management of a Girl With Delayed Puberty and Elevated Gonadotropins
Sinead McGlacken‐Byrne, John C. Achermann, Gerard Conway
Journal of the Endocrine Society (2022) Vol. 6, Iss. 9
Open Access | Times Cited: 3
Sinead McGlacken‐Byrne, John C. Achermann, Gerard Conway
Journal of the Endocrine Society (2022) Vol. 6, Iss. 9
Open Access | Times Cited: 3
AGENESIA DE CELULAS DE LEYDIG NA PEDIATRIA– REVISÃO DE LITERATURA
Mariana Thees Perillo Rodrigues, Mariana de Melo Gadelha
Revista Contemporânea (2024) Vol. 4, Iss. 4, pp. e3313-e3313
Open Access
Mariana Thees Perillo Rodrigues, Mariana de Melo Gadelha
Revista Contemporânea (2024) Vol. 4, Iss. 4, pp. e3313-e3313
Open Access
Variaciones del desarrollo genital
Claire Bouvattier
EMC - Ginecología-Obstetricia (2024) Vol. 60, Iss. 3, pp. 1-11
Closed Access
Claire Bouvattier
EMC - Ginecología-Obstetricia (2024) Vol. 60, Iss. 3, pp. 1-11
Closed Access
The genotype-phenotype correlation of NR5A1 variants in 46,XY individuals: A study protocol
Renata Thomazini Dallago, Rafael Loch Batista, Berenice B. Mendonça, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Renata Thomazini Dallago, Rafael Loch Batista, Berenice B. Mendonça, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The interpretation of immunometric, chromatographic and mass spectrometric data for steroids in diagnosis of endocrine disorders
John W. Honour
Steroids (2024) Vol. 211, pp. 109502-109502
Closed Access
John W. Honour
Steroids (2024) Vol. 211, pp. 109502-109502
Closed Access
Swyer Syndrome: Clinical Case of Gonadal Dysgenesis in a 15-year-old Girl
И.В. Караченцова, E. V. Sibirskaya, Tatyana G. Dyadik, et al.
Педиатрическая фармакология (2024) Vol. 21, Iss. 4, pp. 344-349
Open Access
И.В. Караченцова, E. V. Sibirskaya, Tatyana G. Dyadik, et al.
Педиатрическая фармакология (2024) Vol. 21, Iss. 4, pp. 344-349
Open Access
Casey Brewer, Alyxis G. Coyan, Nicki Smith, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 11
Open Access
NMF typing and machine learning algorithm-based exploration of preeclampsia-related mechanisms on ferroptosis signature genes
Xuemin Liu, Di Zhang, Hui Qiu
Cell Biology and Toxicology (2024) Vol. 41, Iss. 1
Open Access
Xuemin Liu, Di Zhang, Hui Qiu
Cell Biology and Toxicology (2024) Vol. 41, Iss. 1
Open Access
An Infant With DHX37 Variant: A Novel Etiology of 46,XY DSD and Literature Review
R Sena Turk Yilmaz, Adam B. Hittelman, Alla Vash‐Margita, et al.
JCEM Case Reports (2024) Vol. 3, Iss. 1
Open Access
R Sena Turk Yilmaz, Adam B. Hittelman, Alla Vash‐Margita, et al.
JCEM Case Reports (2024) Vol. 3, Iss. 1
Open Access
Variations du développement génital
Claire Bouvattier
EMC - Gynécologie (2024) Vol. 39, Iss. 1, pp. 1-11
Closed Access
Claire Bouvattier
EMC - Gynécologie (2024) Vol. 39, Iss. 1, pp. 1-11
Closed Access