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:
RNA-sequencing improves diagnosis for neurodevelopmental disorders by identifying pathogenic non-coding variants and reinterpretation of coding variants
Jordy Dekker, Rachel Schot, Michiel Bongaerts, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Jordy Dekker, Rachel Schot, Michiel Bongaerts, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Showing 3 citing articles:
Beyond genomics: using RNA-seq from dried blood spots to unlock the clinical relevance of splicing variation in a diagnostic setting
Aida M. Bertoli‐Avella, Mandy Radefeldt, Ruslan Al‐Ali, et al.
European Journal of Human Genetics (2025)
Open Access
Aida M. Bertoli‐Avella, Mandy Radefeldt, Ruslan Al‐Ali, et al.
European Journal of Human Genetics (2025)
Open Access
High‐yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing
Hannie Douben, Mark Nellist, Leontine van Unen, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 2130-2140
Open Access | Times Cited: 10
Hannie Douben, Mark Nellist, Leontine van Unen, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 2130-2140
Open Access | Times Cited: 10
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome
Hannie Douben, Marianne Hoogeveen‐Westerveld, Mark Nellist, et al.
Human Mutation (2023) Vol. 2023, pp. 1-14
Open Access | Times Cited: 2
Hannie Douben, Marianne Hoogeveen‐Westerveld, Mark Nellist, et al.
Human Mutation (2023) Vol. 2023, pp. 1-14
Open Access | Times Cited: 2
