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:

KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism
Francesco Miceli, Charissa Millevert, Maria Virginia Soldovieri, et al.
EBioMedicine (2022) Vol. 81, pp. 104130-104130
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Ludovica Montanucci, David Lewis‐Smith, Ryan L. Collins, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 30
The current landscape of epilepsy genetics: where are we, and where are we going?
Sarah M. Ruggiero, Julie Xian, Ingo Helbig
Current Opinion in Neurology (2023)
Open Access | Times Cited: 28
KCNQ2/3 Gain-of-Function Variants and Cell Excitability: Differential Effects in CA1 versus L2/3 Pyramidal Neurons
Nissi Varghese, Bruno Moscoso, Ana G. Chavez, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 38, pp. 6479-6494
Open Access | Times Cited: 26
The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
Nicola Specchio, Valentina Di Micco, Eleonora Aronica, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Potassium channelopathies associated with epilepsy-related syndromes and directions for therapeutic intervention
Valentin K. Gribkoff, Raymond J. Winquist
Biochemical Pharmacology (2023) Vol. 208, pp. 115413-115413
Closed Access | Times Cited: 19
Functional evaluation of epilepsy‐associated KCNT1 variants in multiple cellular systems reveals a predominant gain of function impact on channel properties
Christopher A. Hinckley, Zhonghua Zhu, J Chu, et al.
Epilepsia (2023) Vol. 64, Iss. 8, pp. 2126-2136
Closed Access | Times Cited: 16
Genetic Background of Epilepsy and Antiepileptic Treatments
Kinga K. Borowicz-Reutt, Julia Czernia, Marlena Krawczyk
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16280-16280
Open Access | Times Cited: 15
Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes
Kathryn J. Peall, Michael J. Owen, Jérémy Hall
Nature Reviews Neurology (2023) Vol. 20, Iss. 1, pp. 7-21
Closed Access | Times Cited: 13
Small molecule inhibits KCNQ channels with a non-blocking mechanism
Junnan Li, Zhenni Yang, Shao-ying Zhang, et al.
Nature Chemical Biology (2025)
Closed Access
Amitriptyline use in individuals with KCNQ2/3 gain‐of‐function variants: A retrospective cohort study
Matthias De Wachter, Charissa Millevert, Joost Nicolai, et al.
Epilepsia (2025)
Open Access
Biophysical and structural mechanisms of epilepsy-associated mutations in the S4-S5 Linker of KCNQ2 channels
Inn‐Chi Lee, Yen-Yu Yang, Hsueh‐Kai Chang, et al.
Channels (2025) Vol. 19, Iss. 1
Open Access
Is Precision Therapy in Infantile-Onset Epileptic Encephalopathies Still Too Far to Call Upon?
Raffaele Falsaperla, Vincenzo Sortino, Piero Pavone
Applied Sciences (2025) Vol. 15, Iss. 5, pp. 2372-2372
Open Access
Unraveling the genetic basis of epilepsy: Recent advances and implications for diagnosis and treatment
Rekha Dwivedi, Meenakshi Kaushik, Manjari Tripathi, et al.
Brain Research (2024) Vol. 1843, pp. 149120-149120
Closed Access | Times Cited: 3
ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy
Charissa Millevert, Sarah Weckhuysen
Epileptic Disorders (2023) Vol. 25, Iss. 4, pp. 445-453
Open Access | Times Cited: 8
Neurocardiac pathologies associated with potassium channelopathies
Veronica Singh, David S. Auerbach
Epilepsia (2024) Vol. 65, Iss. 9, pp. 2537-2552
Closed Access | Times Cited: 2
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2 -developmental encephalopathy
Mario Nappi, Giulio Alberini, Alessandro Berselli, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 49
Closed Access | Times Cited: 2
Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatment
Allan Bayat, Stefano Iavarone, Francesco Miceli, et al.
Neurotherapeutics (2023) Vol. 21, Iss. 1, pp. e00296-e00296
Open Access | Times Cited: 5
Phox2b-expressing neurons contribute to breathing problems in Kcnq2 loss- and gain-of-function encephalopathy models
Jaseph Soto‐Perez, Colin Cleary, Cleyton R. Sobrinho, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 4
CONSTITUTIVE OPENING OF THE Kv7.2 PORE ACTIVATION GATE CAUSESKCNQ2-DEVELOPMENTAL ENCEPHALOPATHY
Mario Nappi, Giulio Alberini, Alessandro Berselli, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization
Swee‐Hee Wong, Ying‐Ming Liou, Jiann‐Jou Yang, et al.
Epilepsy & Behavior (2024) Vol. 156, pp. 109798-109798
Closed Access | Times Cited: 1
Proteomic-Based Approach Reveals the Involvement of Apolipoprotein A-I in Related Phenotypes of Autism Spectrum Disorder in the BTBR Mouse Model
Qi Li, Yaxin Shi, Xiang Li, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 23, pp. 15290-15290
Open Access | Times Cited: 6
Improved classification and pathogenicity assessment by comprehensive functional studies in a large data set of KCNQ2 variants
Yuwei Zhang, Yuqing Xue, Yu Ma, et al.
Life Sciences (2023) Vol. 339, pp. 122378-122378
Closed Access | Times Cited: 2
Novel KCNQ2 missense variant expands the genotype spectrum of DEE7
Chao Wang, Jin Zhai, YongJun Chen
Neurological Sciences (2024)
Closed Access
Donepezil as a new therapeutic potential in KCNQ2- and KCNQ3-related autism
Andreea Nissenkorn, Lior Bar, Ariel Ben-Bassat, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access
Page 1 - Next Page

Scroll to top