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:
Identification of 3’-UTR single nucleotide variants and prediction of select protein imbalance in mesial temporal lobe epilepsy patients
T K Chaudhuri, Janaki Chintalapati, M.V. Hosur
PLoS ONE (2021) Vol. 16, Iss. 6, pp. e0252475-e0252475
Open Access | Times Cited: 3
T K Chaudhuri, Janaki Chintalapati, M.V. Hosur
PLoS ONE (2021) Vol. 16, Iss. 6, pp. e0252475-e0252475
Open Access | Times Cited: 3
Showing 3 citing articles:
Epileptic Encephalopathy of Unknown Cause in Turkey Indicates a New Homozygous <i>NAPB </i>Gene Variant
Sibğatullah Ali Orak, Dilek Gün Bilgiç, Çisil Çerçi Kubur, et al.
Molecular Syndromology (2024) Vol. 15, Iss. 5, pp. 437-442
Closed Access
Sibğatullah Ali Orak, Dilek Gün Bilgiç, Çisil Çerçi Kubur, et al.
Molecular Syndromology (2024) Vol. 15, Iss. 5, pp. 437-442
Closed Access
Phenotyping of FGF12AV52H mutation in mouse implies a complex FGF12 network
Jianyu Huang, Chongyang Sun, Qian Zhu, et al.
Neurobiology of Disease (2024) Vol. 200, pp. 106637-106637
Open Access
Jianyu Huang, Chongyang Sun, Qian Zhu, et al.
Neurobiology of Disease (2024) Vol. 200, pp. 106637-106637
Open Access
3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay
Xin Bi, Maureen Mulhern, Erica Spiegel, et al.
Genes (2023) Vol. 14, Iss. 9, pp. 1687-1687
Open Access
Xin Bi, Maureen Mulhern, Erica Spiegel, et al.
Genes (2023) Vol. 14, Iss. 9, pp. 1687-1687
Open Access
