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:
Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression
Marwa Ben Jdila, Chahnez Triki, Rania Ghorbel, et al.
Clinica Chimica Acta (2020) Vol. 508, pp. 287-294
Closed Access | Times Cited: 5
Marwa Ben Jdila, Chahnez Triki, Rania Ghorbel, et al.
Clinica Chimica Acta (2020) Vol. 508, pp. 287-294
Closed Access | Times Cited: 5
Showing 5 citing articles:
Unveiling Molecular Dynamics of MeCp2 , CDKL5 and BDNF in the Hippocampus of Individuals With Intractable Mesial Temporal Lobe Epilepsy
NoorMohammad Meshkinkhood, Parastoo Barati Dowom, Farshid Noorbakhsh, et al.
Journal of Cellular and Molecular Medicine (2025) Vol. 29, Iss. 3
Open Access
NoorMohammad Meshkinkhood, Parastoo Barati Dowom, Farshid Noorbakhsh, et al.
Journal of Cellular and Molecular Medicine (2025) Vol. 29, Iss. 3
Open Access
Intellectual disability: dendritic anomalies and emerging genetic perspectives
Tam Quach, Harrison J. Stratton, Rajesh Khanna, et al.
Acta Neuropathologica (2020) Vol. 141, Iss. 2, pp. 139-158
Open Access | Times Cited: 32
Tam Quach, Harrison J. Stratton, Rajesh Khanna, et al.
Acta Neuropathologica (2020) Vol. 141, Iss. 2, pp. 139-158
Open Access | Times Cited: 32
The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defects
Laura Mary, Delphine Leclerc, David Gilot, et al.
Human Mutation (2022) Vol. 43, Iss. 9, pp. 1125-1148
Open Access | Times Cited: 12
Laura Mary, Delphine Leclerc, David Gilot, et al.
Human Mutation (2022) Vol. 43, Iss. 9, pp. 1125-1148
Open Access | Times Cited: 12
Mutation in the β‐tubulin gene TUBB4A results in epileptic encephalopathy associated with hypomyelinated leucodystrophy: Unexpected findings reveal genetic mosaicism
Marwa Ben Jdila, Fatma Kammoun, Rania Abdelmaksoud‐Dammak, et al.
International Journal of Developmental Neuroscience (2023) Vol. 83, Iss. 6, pp. 532-545
Closed Access | Times Cited: 1
Marwa Ben Jdila, Fatma Kammoun, Rania Abdelmaksoud‐Dammak, et al.
International Journal of Developmental Neuroscience (2023) Vol. 83, Iss. 6, pp. 532-545
Closed Access | Times Cited: 1
Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers
Arun Meyyazhagan, Balamuralikrishnan Balasubramanian, Kathannan Sankar, et al.
Epilepsy & Behavior (2020) Vol. 111, pp. 107277-107277
Closed Access | Times Cited: 2
Arun Meyyazhagan, Balamuralikrishnan Balasubramanian, Kathannan Sankar, et al.
Epilepsy & Behavior (2020) Vol. 111, pp. 107277-107277
Closed Access | Times Cited: 2
