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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
Sandra Jansen, Lisenka E.L.M. Vissers, Bert B.A. de Vries
Brain Sciences (2023) Vol. 13, Iss. 2, pp. 231-231
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Genome sequencing as a generic diagnostic strategy for rare disease
Gaby Schobers, Ronny Derks, Amber den Ouden, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 11
Functional genomics and small molecules in mitochondrial neurodevelopmental disorders
Daniel G. Calame, Lisa Emrick
Neurotherapeutics (2024) Vol. 21, Iss. 1, pp. e00316-e00316
Open Access | Times Cited: 7
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1605-1625
Closed Access | Times Cited: 4
The WAVE complex in developmental and adulthood brain disorders
Hyung‐Goo Kim, Clara Berdasco, Angus C. Nairn, et al.
Experimental & Molecular Medicine (2025)
Open Access
Denovo variants in POGZ and YY1 genes: The novel mega players for neurodevelopmental syndromes in two unrelated consanguineous families
Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0315597-e0315597
Open Access
Generation of induced pluripotent stem cell line ISMMSi060-A from a patient with combined oxidative phosphorylation deficiency 25
S. Salemi, Erdene Baljinnyam, N. Liu, et al.
Stem Cell Research (2025), pp. 103662-103662
Open 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
DNA methylation biomarkers of intellectual/developmental disability across the lifespan
Janine M. LaSalle
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Mainstreaming Diagnostic Genetic Testing and Precision Medicine for Autism Spectrum Disorder
David H. Ledbetter, Brenda Finucane, Daniel Moreno‐De‐Luca, et al.
Psychiatric Clinics of North America (2025)
Closed Access
Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene,FOXG1
Aishwarya Ramamurthy, Masha D Bandouil, Likhita Aluru, et al.
(2025)
Closed Access
SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X‐Linked Intellectual Disability
Arkaprava Roychaudhury, Yu‐Ri Lee, Tae‐Ik Choi, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 914-931
Open Access | Times Cited: 3
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder
María del Rocío Pérez Baca, María Palomares‐Bralo, Michiel Vanhooydonck, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing
Vijay Gupta, Afif Ben‐Mahmoud, Bonsu Ku, et al.
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 7
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature
Valentina Trevisan, Anna Meroni, Chiara Leoni, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 346-346
Open Access | Times Cited: 2
Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot
Anne S. Bassett, Miriam S. Reuter, Sarah Malecki, et al.
CJC Pediatric and Congenital Heart Disease (2023) Vol. 2, Iss. 6, pp. 426-439
Open Access | Times Cited: 5
Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1
Lieke Dillen, Neelam Fatima, Marina P. Hommersom, et al.
Stem Cell Research (2024) Vol. 77, pp. 103442-103442
Open Access | Times Cited: 1
Normal Values for the fT3/fT4 Ratio: Centile Charts (0-29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay
Nina‐Maria Wilpert, Michael Thamm, Michael Thamm, et al.
(2024)
Open Access | Times Cited: 1
Role of mitochondria‐endoplasmic reticulum contacts in neurodegenerative, neurodevelopmental and neuropsychiatric conditions
Serangeli Ilaria, Diamanti Tamara, De Jaco Antonella, et al.
European Journal of Neuroscience (2024) Vol. 60, Iss. 5, pp. 5040-5068
Open Access | Times Cited: 1
Normal Values for the fT3/fT4 Ratio: Centile Charts (0–29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay
Nina‐Maria Wilpert, Michael Thamm, Michael Thamm, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8585-8585
Open Access | Times Cited: 1
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability
Cheol‐Hee Kim, Yu‐Ri Lee, Mervyn G. Thomas, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
Rare splice and missense variants with evidence of pathogenicity in consanguineous families with autosomal recessive intellectual disability from Pakistan
Abdül Waheed, Robert Eveleigh, Danielle Perley, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes and establishment of LEO1 as a novel disease gene
Sarah Weckhuysen, Noor Smal, Fatma Majdoub, et al.
Research Square (Research Square) (2024)
Open Access
Navigating Neurogenetics for Child and Adolescent Psychiatry Practice
Aaron J. Hauptman, Jay A. Salpekar, Julie S. Cohen, et al.
Journal of the American Academy of Child & Adolescent Psychiatry (2024) Vol. 63, Iss. 7, pp. 666-669
Closed Access
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein
Hua Pan, Feng Zhu, Kun Chen, et al.
Journal of Genetics (2024) Vol. 103, Iss. 1
Closed Access
A 10-Year Review on Advancements in Identifying and Treating Intellectual Disability Caused by Genetic Variations
Kexin Hou, Xinyan Zheng
Genes (2024) Vol. 15, Iss. 9, pp. 1118-1118
Open Access
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