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OpenAlex Citation Counts

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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 genetics of intellectual disability: advancing technology and gene editing
Muhammad Ilyas, Asif Mir, Stéphanie Efthymiou, et al.
F1000Research (2020) Vol. 9, pp. 22-22
Open Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

A literature review of sleep problems and neurodevelopment disorders
Abeer Al Lihabi
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 28
Effect of inbreeding on intellectual disability revisited by trio sequencing
Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, et al.
Clinical Genetics (2018) Vol. 95, Iss. 1, pp. 151-159
Open Access | Times Cited: 70
Neurogenetic disorders across the lifespan: from aberrant development to degeneration
Richard A. Hickman, Sarah A. O’Shea, Mark F. Mehler, et al.
Nature Reviews Neurology (2022) Vol. 18, Iss. 2, pp. 117-124
Open Access | Times Cited: 34
E3 Ubiquitin Ligase TRIP12: Regulation, Structure, and Physiopathological Functions
Manon Brunet, Claire Vargas, Dorian Larrieu, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 22, pp. 8515-8515
Open Access | Times Cited: 47
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: 33
The contribution of whole-exome sequencing to intellectual disability diagnosis and knowledge of underlying molecular mechanisms: A systematic review and meta-analysis
Karen Sánchez-Luquez, Marina Xavier Carpena, Simone de Menezes Karam, et al.
Mutation Research/Reviews in Mutation Research (2022) Vol. 790, pp. 108428-108428
Open Access | Times Cited: 22
Embryo and fetal gene editing: Technical challenges and progress toward clinical applications
Citra Nurfarah Zaini Mattar, Wei Leong Chew, Poh San Lai
Molecular Therapy — Methods & Clinical Development (2024) Vol. 32, Iss. 2, pp. 101229-101229
Open Access | Times Cited: 4
SNV/Indel and CNV Analysis in Trio‐WES for Intellectual and Developmental Disabilities: Diagnostic Yield & Cost‐Effectiveness
Guanhua Qian, Nanyan Yang, Fang Deng, et al.
Clinical Genetics (2025)
Closed Access
Novel heterozygous ASH1L nonsense variant involved in mild intellectual disability
Baoqiong Liao, Wuming Xie, Shuwen He
Frontiers in Neurology (2025) Vol. 16
Open Access
Genetic Analysis and Reporting from Whole-Exome Sequencing Data in 1052 Patients with Intellectual Disability
Xin Pan, Guanhua Qian, Li Liu, et al.
(2025)
Closed Access
Exploring the connection between RNA splicing and intellectual disability
Anthony Caputo, Ashleigh E. Schaffer
Current Opinion in Genetics & Development (2025) Vol. 91, pp. 102322-102322
Open Access
Neurobiological Relationships Between Neurodevelopmental Disorders and Mood Disorders
Amanda Gollo Bertollo, Camila Ferreira Puntel, Brunna Varela da Silva, et al.
Brain Sciences (2025) Vol. 15, Iss. 3, pp. 307-307
Open Access
Inequalities of the Waiting Time for Education Health and Care Plan Provision for Pupils With Intellectual Developmental Disabilities: A Brief Report
Irene Lee, Jeanne Wolstencroft, Harriet Housby, et al.
Journal of Intellectual Disability Research (2025)
Open Access
Selenium, Silver, and Gold Nanoparticles: Emerging Strategies for Hepatic Oxidative Stress and Inflammation Reduction
Karthik K Karunakar, Binoy Varghese Cheriyan, D. Suresh Babu, et al.
Nano TransMed (2025), pp. 100085-100085
Open Access
Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability
Alejandro Brea‐Fernández, Miriam Álvarez-Barona, Jorge Amigo, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 8, pp. 938-945
Open Access | Times Cited: 15
The inequity of education, health and care plan provision for children and young people with intellectual and developmental disabilities
Irene Lee, Jeanne Wolstencroft, Harriet Housby, et al.
Journal of Intellectual Disability Research (2024) Vol. 68, Iss. 10, pp. 1167-1183
Open Access | Times Cited: 3
Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay
Chengyan Li, You Wang, Chao Zeng, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Top2a promotes the development of social behavior via PRC2 and H3K27me3
Yijie Geng, Tejia Zhang, Ivy G. Alonzo, et al.
Science Advances (2022) Vol. 8, Iss. 47
Open Access | Times Cited: 12
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performance
Mira Brazane, Dilyana G. Dimitrova, Julien Pigeon, et al.
Life Science Alliance (2023) Vol. 6, Iss. 4, pp. e202201877-e202201877
Open Access | Times Cited: 7
A Biallelic Truncating Variant in the TPR Domain of GEMIN5 Associated with Intellectual Disability and Cerebral Atrophy
Nazia Ibrahim, Shagufta Naz, Francesca Mattioli, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 707-707
Open Access | Times Cited: 6
Effects of the special olympics unified sports soccer training program on executive function in adolescents with intellectual disabilities
Rang Xiao, Xu Ping, Xuelian Liang, et al.
Journal of Exercise Science & Fitness (2023) Vol. 22, Iss. 2, pp. 103-110
Open Access | Times Cited: 6
Overcoming genetic and cellular complexity to study the pathophysiology of X-linked intellectual disabilities
Dayne Martinez, Evan Jiang, Zhaolan Zhou
Journal of Neurodevelopmental Disorders (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Ubiquitin and Ubiquitin-Like Proteins in the Critical Equilibrium between Synapse Physiology and Intellectual Disability
Alessandra Folci, Filippo Mirabella, Matteo Fossati
eNeuro (2020) Vol. 7, Iss. 4, pp. ENEURO.0137-20.2020
Open Access | Times Cited: 13
Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases
Caroline Racine, Anne‐Sophie Denommé‐Pichon, Camille Engel, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 1, pp. 36-46
Closed Access | Times Cited: 5
Sleep in people with and without intellectual disabilities: a systematic review and meta‐analysis
E. G. Browne, Jeremy King, Andrew Surtees
Journal of Intellectual Disability Research (2023) Vol. 68, Iss. 1, pp. 1-22
Open Access | Times Cited: 5
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