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:
Deficiency of CHAMP1, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotype
Masayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Brain Communications (2022) Vol. 4, Iss. 5
Open Access | Times Cited: 7
Masayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Brain Communications (2022) Vol. 4, Iss. 5
Open Access | Times Cited: 7
Showing 7 citing articles:
Whole exome/genome sequencing in cyclic vomiting syndrome reveals multiple candidate genes, suggesting a model of elevated intracellular cations and mitochondrial dysfunction
Omri Bar, Laurie Ebenau, Kellee Weiner, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 16
Omri Bar, Laurie Ebenau, Kellee Weiner, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 16
Kinesin-like motor protein KIF23 maintains neural stem and progenitor cell pools in the developing cortex
Sharmin Naher, Kenji Iemura, Satoshi Miyashita, et al.
The EMBO Journal (2024) Vol. 44, Iss. 2, pp. 331-355
Closed Access | Times Cited: 1
Sharmin Naher, Kenji Iemura, Satoshi Miyashita, et al.
The EMBO Journal (2024) Vol. 44, Iss. 2, pp. 331-355
Closed Access | Times Cited: 1
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Discriminative features in White-Sutton syndrome: literature review and first report in Iran
Emran Esmaeilzadeh, Aysan Jafari Harandi, Fatemeh Astaraki, et al.
Psychiatric Genetics (2023)
Closed Access | Times Cited: 2
Emran Esmaeilzadeh, Aysan Jafari Harandi, Fatemeh Astaraki, et al.
Psychiatric Genetics (2023)
Closed Access | Times Cited: 2
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Research Square (Research Square) (2024)
Open Access
Yujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Research Square (Research Square) (2024)
Open Access
Neuron-specific loss of Ppp6c induces neonatal death and decreases the number of cortical neurons and interneurons
Miki Matsuoka, Daisuke Sakai, Hiroshi Shima, et al.
Biochemical and Biophysical Research Communications (2023) Vol. 693, pp. 149353-149353
Closed Access | Times Cited: 1
Miki Matsuoka, Daisuke Sakai, Hiroshi Shima, et al.
Biochemical and Biophysical Research Communications (2023) Vol. 693, pp. 149353-149353
Closed Access | Times Cited: 1
Kinesin family member Kif23 regulates cytokinetic division and maintains neural stem/progenitor cell pool in the developing neocortex
Sharmin Naher, Takako Kikkawa, Kenji Iemura, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Sharmin Naher, Takako Kikkawa, Kenji Iemura, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
