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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:

NR5A1 c.991‐1G > C splice‐site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance
Maris Laan, Laura Kasak, Kęstutis Timinskas, et al.
Clinical Endocrinology (2020) Vol. 94, Iss. 4, pp. 656-666
Open Access | Times Cited: 17

Showing 17 citing articles:

A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases
Pablo Román-Naranjo, Alberto M. Parra‐Perez, José A. López‐Escámez
Journal of Biomedical Informatics (2023) Vol. 143, pp. 104429-104429
Open Access | Times Cited: 22
Toward clinical exomes in diagnostics and management of male infertility
Kristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 877-895
Closed Access | Times Cited: 8
Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases Database
Charlotte Nachtegael, Barbara Gravel, Arnau Dillen, et al.
Database (2022) Vol. 2022
Open Access | Times Cited: 27
PPI3D: a web server for searching, analyzing and modeling protein–protein, protein–peptide and protein–nucleic acid interactions
Justas Dapkūnas, Albertas Timinskas, Kliment Olechnovič, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. W1, pp. W264-W271
Open Access | Times Cited: 5
Faster and more accurate pathogenic combination predictions with VarCoPP2.0
Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 11
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years
Arvand Akbari, Laura Kasak, Maris Laan
Andrology (2025)
Closed Access
Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study
Chrysanthi Kouri, Idoia Martinez de la Piscina, Rawda Naamneh-Elzenaty, et al.
EBioMedicine (2025) Vol. 113, pp. 105624-105624
Open Access
Undiagnosed RASopathies in infertile men
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
Translational aspects of novel findings in genetics of male infertility—status quo 2021
Maris Laan, Laura Kasak, Margus Punab
British Medical Bulletin (2021) Vol. 140, Iss. 1, pp. 5-22
Open Access | Times Cited: 21
Current perspectives in hypospadias research: A scoping review of articles published in 2021 (Review)
Horea Gozar, Zsolt Bara, Emilia Dicu, et al.
Experimental and Therapeutic Medicine (2023) Vol. 25, Iss. 5
Open Access | Times Cited: 8
Genomic technologies and the diagnosis of 46, XY differences of sex development
Firman Prathama Idris, Andrew Sinclair, Katie L. Ayers
Andrology (2024)
Open Access | Times Cited: 2
Early Gonadal Development and Sex Determination in Mammal
Yanshe Xie, Changhua Wu, Zicong Li, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 14, pp. 7500-7500
Open Access | Times Cited: 8
Case Report: Longitudinal follow-up and testicular sperm extraction in a patient with a pathogenic NR5A1 (SF-1) frameshift variant: p.(Phe70Serfs*5)
Jordan Teoli, Delphine Mallet, Lucie Renault, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 4
NR5A1/SF-1 Collaborates with Inhibin α and the Androgen Receptor
Rawda Naamneh Elzenaty, Chrysanthi Kouri, Idoia Martinez de la Piscina, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 10109-10109
Open Access | Times Cited: 1
Clinical spectrum and molecular basis in 19 Chinese patients with 46, XY disorder of sexual development caused by NR5A1 mutations
Yue Xu, Xuemeng Liu, Yang Liu, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
A systematic review on machine learning approaches in the diagnosis of rare genetic diseases
Pablo Román-Naranjo, AM Parra-Perez, José A. López‐Escámez
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Genetic Aspects of Hypospadias
Loes F.M. van der Zanden
Springer eBooks (2022), pp. 271-283
Closed Access
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