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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:

Development and validation of a 4-color multiplexing spinal muscular atrophy (SMA) genotyping assay on a novel integrated digital PCR instrument
Lingxia Jiang, Robert Lin, Steve Gallagher, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 19

Showing 19 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
Current commercial dPCR platforms: technology and market review
Li Ling Tan, Nitin Loganathan, Sushama Agarwalla, et al.
Critical Reviews in Biotechnology (2022) Vol. 43, Iss. 3, pp. 433-464
Closed Access | Times Cited: 53
Disruption of the circadian clock drives Apc loss of heterozygosity to accelerate colorectal cancer
Sung Kook Chun, Bridget M. Fortin, Rachel C. Fellows, et al.
Science Advances (2022) Vol. 8, Iss. 32
Open Access | Times Cited: 50
Newborn screening for spinal muscular atrophy in Japan: One year of experience
Takaaki Sawada, Jun Kido, Keishin Sugawara, et al.
Molecular Genetics and Metabolism Reports (2022) Vol. 32, pp. 100908-100908
Open Access | Times Cited: 21
Next generation sequencing is a highly reliable method to analyze exon 7 deletion of survival motor neuron 1 (SMN1) gene
Sumin Zhao, Yaoshen Wang, Xiuqing Xin, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 15
Technical feasibility of newborn screening for spinal muscular atrophy by next-generation DNA sequencing
Bennett O. V. Shum, Ilya Henner, Anita Cairns, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 9
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
Digital PCR Discriminates between SARS-CoV-2 Omicron Variants and Immune Escape Mutations
Steven C. Holland, LaRinda A. Holland, Matthew F. Smith, et al.
Microbiology Spectrum (2023) Vol. 11, Iss. 4
Open Access | Times Cited: 4
Melt‐Encoded‐Tags for Expanded Optical Readout in Digital PCR (METEOR‐dPCR) Enables Highly Multiplexed Quantitative Gene Panel Profiling
Dongdong Liu, Daniel Muliaditan, Ramya Viswanathan, et al.
Advanced Science (2023) Vol. 10, Iss. 27
Open Access | Times Cited: 4
Next generation multiplexing for digital PCR using a novel melt-based hairpin probe design
Rebecca L. Edwards, Johanna E. Takach, Michael McAndrew, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
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
Increased AID results in mutations at the CRLF2 locus implicated in Latin American ALL health disparities
Valeria Rangel, Jason N. Sterrenberg, A Al Garawi, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Comprehensive Analysis of Retrotransposon Insertions within the Survival Motor Neuron Genes Involved in Spinal Muscular Atrophy
Albano Pinto, Catarina Cunha, Raquel Chaves, et al.
Research Square (Research Square) (2022)
Closed Access | Times Cited: 3
Digital PCR discriminates between SARS-CoV-2 Omicron variants and immune escape mutations
Steven C. Holland, LaRinda A. Holland, Matthew F. Smith, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis
Gülten Tuncel, Burçin Şanlıdağ, Eray Dırık, et al.
Global Medical Genetics (2023) Vol. 10, Iss. 03, pp. 240-246
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
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