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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:

Detection of SMN1 to SMN2 gene conversion events and partial SMN1 gene deletions using array digital PCR
Deborah L. Stabley, Jennifer Holbrook, Mena Scavina, et al.
Neurogenetics (2021) Vol. 22, Iss. 1, pp. 53-64
Closed Access | Times Cited: 20

Showing 20 citing articles:

Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development
Matthew E.R. Butchbach
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 15, pp. 7896-7896
Open Access | Times Cited: 64
Unraveling the genetic mysteries of spinal muscular atrophy in Chinese families
Shanshan Gao, Duo Chen, Qianqian Li, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Quantitative and structural features of the SMN1 and SMN2 genes in patients with spinal muscular atrophy 5q
A. I. Vlasenko, В. Д. Назаров, С. В. Лапин, et al.
Neuromuscular Diseases (2025) Vol. 14, Iss. 4, pp. 21-28
Open Access
Spinal muscular atrophy: Molecular mechanism of pathogenesis, diagnosis, therapeutics, and clinical trials in the Indian context
Ashutosh Aasdev, R S Sreelekshmi, V Rajesh Iyer, et al.
Journal of Biosciences (2024) Vol. 49, Iss. 1
Closed Access | Times Cited: 4
Diagnosis of Challenging Spinal Muscular Atrophy Cases with Long-Read Sequencing
Ningning Wang, Kexin Jiao, J. He, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 5, pp. 364-373
Closed Access | Times Cited: 1
Detection of male 2+0 and 1+0 carriers for spinal muscular atrophy by digital PCR
Shanshan Gao, Dongping Wu, Shuai Liu, et al.
Clinical Genetics (2023) Vol. 104, Iss. 1, pp. 90-99
Closed Access | Times Cited: 4
Single-Tube Multiplex Digital Polymerase Chain Reaction Assay for Molecular Diagnosis and Prediction of Severity of Spinal Muscular Atrophy
Chianru Tan, Yousheng Yan, Na Guo, et al.
Analytical Chemistry (2022) Vol. 94, Iss. 8, pp. 3517-3525
Closed Access | Times Cited: 6
Comparison of the accuracy of multiplex digital PCR versus multiplex ligation-dependent probe amplification in quantification of the survival of motor neuron genes copy numbers
Yu Jiang, Zhongmin Xia, Yulin Zhou, et al.
Clinica Chimica Acta (2023) Vol. 553, pp. 117708-117708
Closed Access | Times Cited: 2
Comprehensive In Silico Analysis of Retrotransposon Insertions within the Survival Motor Neuron Genes Involved in Spinal Muscular Atrophy
Albano Pinto, Catarina Cunha, Raquel Chaves, et al.
Biology (2022) Vol. 11, Iss. 6, pp. 824-824
Open Access | Times Cited: 4
Development of a low-cost and accurate carrier screening method for spinal muscular atrophy in developing countries
Yu Jiang, Zhenyu Luo, Wenrong Wang, et al.
European Journal of Medical Genetics (2024) Vol. 68, pp. 104921-104921
Open Access
Clinical significance of Spinal Muscular Atrophy carrier detection in Guangdong Province, China: Insights from quantitative polymerase chain reaction and multiplex ligation-dependent probe amplification analysis
Chenxia Xu, Jianming Peng, Xuewei Wu, et al.
Gene Reports (2024) Vol. 37, pp. 102055-102055
Closed Access
Spinal Muscular Atrophy (SMA): Clinical Characteristics, Molecular Mechanisms and Treatment
Gökhan Görgişen
(2024), pp. 153-170
Closed Access
SMA carrier testing using Real-time PCR as a potential preconception screening tool
Noura R. Eissa, Heba Hassan, Sameh Mohamed Senousy, et al.
Egyptian Journal of Medical Human Genetics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 2
Characteristics of genetic changes in the <i>SMN1</i> gene in spinal muscular atrophy 5q
A. V. Dil, В. Д. Назаров, D. V. Sidorenko, et al.
Neuromuscular Diseases (2022) Vol. 12, Iss. 3, pp. 36-44
Open Access | Times Cited: 2


Вестник Российского государственного медицинского университета (2023), Iss. 2023(3)
Open Access
Detection of SMN1 loss with PCR-based screening test
VD Nazarov, C. C. Cherebillo, Lapin Sv, et al.
Bulletin of Russian State Medical University (2023), Iss. 2023(3)
Open Access
Detekciya razlichnyh form poteri gena SMN1 s pomoshch'yu nabora dlya PCR-RV
В. Д. Назаров, К. К. Черебилло, С. В. Лапин, et al.
Вестник Российского государственного медицинского университета (2023), Iss. 2023(3)
Open Access
Current Advances in Genetic Testing for Spinal Muscular Atrophy
Yulin Zhou, Yu Jiang
Current Genomics (2023) Vol. 24, Iss. 5, pp. 273-286
Open Access
Copy number assessment of SMN1 based on real-time PCR with high-resolution melting: fast and highly reliable testing
Ying Xu, Tingting Song, Xiaozhou Wang, et al.
Brain and Development (2022) Vol. 44, Iss. 7, pp. 462-468
Open Access
Copy Number Assessment of SMN1 Based on Real-Time PCR With High-Resolution Melting: Fast and Highly Reliable Testing
Ying Xu, Tingting Song, Xiaozhou Wang, et al.
Research Square (Research Square) (2021)
Open Access
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