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:
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes
Marcello Scala, Nathalie Drouot, Suzanna C. MacLennan, et al.
Human Mutation (2022) Vol. 43, Iss. 9, pp. 1299-1313
Open Access | Times Cited: 8
Marcello Scala, Nathalie Drouot, Suzanna C. MacLennan, et al.
Human Mutation (2022) Vol. 43, Iss. 9, pp. 1299-1313
Open Access | Times Cited: 8
Showing 8 citing articles:
The spectrum of pre‐mRNA splicing in autism
Eden Engal, Zhenwei Zhang, Ophir Geminder, et al.
Wiley Interdisciplinary Reviews - RNA (2024) Vol. 15, Iss. 2
Open Access | Times Cited: 3
Eden Engal, Zhenwei Zhang, Ophir Geminder, et al.
Wiley Interdisciplinary Reviews - RNA (2024) Vol. 15, Iss. 2
Open Access | Times Cited: 3
Comprehensively analysis of splicing factors to construct prognosis prediction classifier in prostate cancer
He Zhang, Jianfei Tian, Sixin Ren, et al.
Journal of Cellular and Molecular Medicine (2023) Vol. 27, Iss. 18, pp. 2684-2700
Open Access | Times Cited: 5
He Zhang, Jianfei Tian, Sixin Ren, et al.
Journal of Cellular and Molecular Medicine (2023) Vol. 27, Iss. 18, pp. 2684-2700
Open Access | Times Cited: 5
Exome sequencing data screening to identify undiagnosed Aromatic l-amino acid decarboxylase deficiency in neurodevelopmental disorders
Antonella Riva, Michele Iacomino, Chiara Piccardo, et al.
Biochemical and Biophysical Research Communications (2023) Vol. 673, pp. 131-136
Closed Access | Times Cited: 4
Antonella Riva, Michele Iacomino, Chiara Piccardo, et al.
Biochemical and Biophysical Research Communications (2023) Vol. 673, pp. 131-136
Closed Access | Times Cited: 4
Investigation of RNA-binding protein NOVA1 in silico: Comparison of the modern human V197 with the archaic I197 variant present in Neanderthals
Julia Liang, Eleni Pitsillou, Tom C. Karagiannis
Computers in Biology and Medicine (2024) Vol. 183, pp. 109278-109278
Open Access | Times Cited: 1
Julia Liang, Eleni Pitsillou, Tom C. Karagiannis
Computers in Biology and Medicine (2024) Vol. 183, pp. 109278-109278
Open Access | Times Cited: 1
A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1‐associated neurodevelopmental disorder
Ahmed Waqas, Romana Liaqat, Sidrah Shaheen, et al.
International Journal of Developmental Neuroscience (2022) Vol. 83, Iss. 2, pp. 191-200
Closed Access | Times Cited: 3
Ahmed Waqas, Romana Liaqat, Sidrah Shaheen, et al.
International Journal of Developmental Neuroscience (2022) Vol. 83, Iss. 2, pp. 191-200
Closed Access | Times Cited: 3
Derivation of an induced pluripotent stem cell line (FDCHi014-A) from PBMCs of a seven-year-old patient with a truncating NOVA2 variant (c.625del)
Tingting Yin, Yanyan Qian, Feng Zhang, et al.
Stem Cell Research (2024) Vol. 76, pp. 103369-103369
Open Access
Tingting Yin, Yanyan Qian, Feng Zhang, et al.
Stem Cell Research (2024) Vol. 76, pp. 103369-103369
Open Access
