Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome
Silvia M. Vidal, Núria Brandi, Paola Pacheco, et al.
European Journal of Paediatric Neurology (2019) Vol. 23, Iss. 4, pp. 609-620
Closed Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies
Alexander J. Sandweiss, Vicky Brandt, Huda Y. Zoghbi
The Lancet Neurology (2020) Vol. 19, Iss. 8, pp. 689-698
Closed Access | Times Cited: 145
Progress on the roles of MEF2C in neuropsychiatric diseases
Zhikun Zhang, Yongxiang Zhao
Molecular Brain (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 40
Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges
Silvia M. Vidal, Clara Xiol, Ainhoa Pascual‐Alonso, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 16, pp. 3925-3925
Open Access | Times Cited: 53
The Role of MEF2 Transcription Factor Family in Neuronal Survival and Degeneration
Malwina Lisek, Oskar Przybyszewski, Ludmiła Żylińska, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3120-3120
Open Access | Times Cited: 15
Cyclin-Dependent Kinase-Like 5 (CDKL5): Possible Cellular Signalling Targets and Involvement in CDKL5 Deficiency Disorder
Syouichi Katayama, Noriyuki Sueyoshi, T. INAZU, et al.
Neural Plasticity (2020) Vol. 2020, pp. 1-14
Open Access | Times Cited: 35
MECP2-Related Disorders in Males
Ainhoa Pascual‐Alonso, Antonio Federico Martínez‐Monseny, Clara Xiol, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 17, pp. 9610-9610
Open Access | Times Cited: 32
Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery
Elisa Calì, Clarissa Rocca, Vincenzo Salpietro, et al.
Frontiers in Neurology (2022) Vol. 12
Open Access | Times Cited: 16
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A ( KIF1A )
Simranpreet Kaur, Nicole J. Van Bergen, Kristen J. Verhey, et al.
Human Mutation (2020) Vol. 41, Iss. 10, pp. 1761-1774
Open Access | Times Cited: 24
Comprehensive investigation of the phenotype of MEF2C‐related disorders in human patients: A systematic review
Jessica A. Cooley Coleman, Sara M. Sarasua, Luigi Boccuto, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3884-3894
Closed Access | Times Cited: 17
Adult Phenotype of SYNGAP1 -DEE
Marlene Rong, Tim A. Benke, Quratulain Zulfiqar Ali, et al.
Neurology Genetics (2023) Vol. 9, Iss. 6
Open Access | Times Cited: 6
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders
Eric Frankel, Avijit Podder, Megan Sharifi, et al.
Cells (2023) Vol. 12, Iss. 10, pp. 1437-1437
Open Access | Times Cited: 5
SCN2A and Its Related Epileptic Phenotypes
Andrea D. Praticò, Alessandro Giallongo, Marta Arrabito, et al.
Journal of Pediatric Neurology (2021) Vol. 21, Iss. 03, pp. 173-185
Closed Access | Times Cited: 11
Zebrafish in understanding molecular pathophysiology, disease modeling, and developing effective treatments for Rett syndrome
Subrata Pramanik, Asis Bala, Ajay Pradhan
The Journal of Gene Medicine (2024) Vol. 26, Iss. 2
Closed Access | Times Cited: 1
Technological Improvements in the Genetic Diagnosis of Rett Syndrome Spectrum Disorders
Clara Xiol, María José Gómez Heredia, Ainhoa Pascual‐Alonso, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 19, pp. 10375-10375
Open Access | Times Cited: 8
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspot
Davide Politano, Simone GANA, Elena PEZZOTTI, et al.
Brain and Development (2022) Vol. 45, Iss. 3, pp. 179-184
Closed Access | Times Cited: 3
Genomic analysis in Chilean patients with suspected Rett syndrome: keep a broad differential diagnosis
Florencia Brito, Catalina Lagos, Jessica Cubillos, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Synaptic Vesicle Cycling Disorders: Cross-Sectional Phenotyping Study of a Gene Functional Network
Josefine Eck, Tess A. Smith, Anna Kolesnik, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
<i>SCN2A</i>-Related Disorders
Megan Abbott, Kevin J. Bender, Andreas Brunklaus, et al.
Cambridge University Press eBooks (2024)
Open Access
KCNQ2 encephalopathy manifesting with Rett-like features
Mario Mastrangelo, Filippo Manti, Maria Teresa Giannini, et al.
Neurology Genetics (2020) Vol. 6, Iss. 5
Open Access | Times Cited: 3
Molecular Modelling Hurdle in the Next-Generation Sequencing Era
Guerau Fernández, Dèlia Yubero, Francesc Palau, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 13, pp. 7176-7176
Open Access | Times Cited: 2
Comprehensive In Silico Functional Prediction Analysis of CDKL5 by Single Amino Acid Substitution in the Catalytic Domain
Yuri Yoshimura, Atsushi Morii, Yuuki Fujino, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12281-12281
Open Access | Times Cited: 2
Identification of disease genes and assessment of eye-related diseases caused by disease genes using JMFC and GDLNN
Samar Jyoti Saikia, S. R. Nirmala
Computer Methods in Biomechanics & Biomedical Engineering (2021) Vol. 25, Iss. 4, pp. 359-370
Closed Access | Times Cited: 2
CDKL5 mutations may mimic Pitt-Hopkins syndrome phenotype
Aurora Currò, Gabriella Doddato, Mirella Bruttini, et al.
European Journal of Medical Genetics (2020) Vol. 64, Iss. 1, pp. 104102-104102
Closed Access | Times Cited: 1
Breathing Disturbances as Comorbidity of Rett Syndrome
С.Л. Куликова, А.В. Кузнецова, М.А. Савченко, et al.
Неврология и нейрохирургия Восточная Европа (2020), Iss. 1, pp. 41-51
Closed Access | Times Cited: 1
MECP2-Related Disorders and Epilepsy Phenotypes
Alessandra Sauna, Laura Sciuto, Roberta Criscione, et al.
Journal of Pediatric Neurology (2021) Vol. 21, Iss. 04, pp. 283-291
Closed Access | Times Cited: 1
Page 1 - Next Page

Scroll to top