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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:

Neurodevelopmental Disorders: From Genetics to Functional Pathways
Ilaria Parenti, Luis G. Rabaneda, Hanna Schoen, et al.
Trends in Neurosciences (2020) Vol. 43, Iss. 8, pp. 608-621
Open Access | Times Cited: 417

Showing 26-50 of 417 citing articles:

The Role of Bcl11 Transcription Factors in Neurodevelopmental Disorders
Franziska A. Seigfried, Stefan Britsch
Biology (2024) Vol. 13, Iss. 2, pp. 126-126
Open Access | Times Cited: 8
CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs)
Maria Cristina Aspromonte, Alessio Del Conte, Shaowen Zhu, et al.
Human Genetics (2025)
Open Access | Times Cited: 1
Disrupted visual attention relates to cognitive development in infants with Neurofibromatosis Type 1
Jannath Begum Ali, Luke Mason, Tony Charman, et al.
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access | Times Cited: 1
AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
Kei Hori, Kazumi Shimaoka, Mikio Hoshino
Cells (2021) Vol. 11, Iss. 1, pp. 11-11
Open Access | Times Cited: 47
Allostery, and how to define and measure signal transduction
Ruth Nussinov, Chung‐Jung Tsai, Hyunbum Jang
Biophysical Chemistry (2022) Vol. 283, pp. 106766-106766
Open Access | Times Cited: 36
The hidden link between circadian entropy and mental health disorders
Amal Alachkar, Justine Lee, Kalyani Asthana, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 34
Stem Cell–Based Organoid Models of Neurodevelopmental Disorders
Lu Wang, Charlotte Owusu-Hammond, David Sievert, et al.
Biological Psychiatry (2023) Vol. 93, Iss. 7, pp. 622-631
Open Access | Times Cited: 20
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
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
Markéta Wayhelová, Vladimíra Vallová, Petr Brož, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 7
A comprehensive review on DDX3X liquid phase condensation in health and neurodevelopmental disorders
Ivan Rosa e Silva, Juliana Helena Costa Smetana, Juliana Ferreira de Oliveira
International Journal of Biological Macromolecules (2024) Vol. 259, pp. 129330-129330
Closed Access | Times Cited: 6
Drug development advances in human genetics‐based targets
X. Zhang, Wenjun Yu, Yan Li, et al.
MedComm (2024) Vol. 5, Iss. 2
Open Access | Times Cited: 6
Modelling human brain development and disease with organoids
Marcella Birtele, Madeline A. Lancaster, Giorgia Quadrato
Nature Reviews Molecular Cell Biology (2024)
Closed Access | Times Cited: 6
Structural and Functional Aspects of the Neurodevelopmental Gene NR2F1: From Animal Models to Human Pathology
Chiara Tocco, Michele Bertacchi, Michèle Studer
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 39
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders
Xiangbin Jia, S. Zhang, Senwei Tan, et al.
Science Advances (2022) Vol. 8, Iss. 33
Open Access | Times Cited: 25
Developmental disorders caused by haploinsufficiency of transcriptional regulators: a perspective based on cell fate determination
Roman Zug
Biology Open (2022) Vol. 11, Iss. 1
Open Access | Times Cited: 23
Epilepsy-Related CDKL5 Deficiency Slows Synaptic Vesicle Endocytosis in Central Nerve Terminals
Christiana Kontaxi, Daniela Ivanova, Elizabeth C. Davenport, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 11, pp. 2002-2020
Open Access | Times Cited: 14
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder
Dmitrijs Rots, Taryn E. Jakub, Crystal Keung, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 6, pp. 963-978
Open Access | Times Cited: 14
Processed foods and diet quality in pregnancy may affect child neurodevelopment disorders: a narrative review
Roberta Zupo, Fabio Castellana, Giovanni Boero, et al.
Nutritional Neuroscience (2023) Vol. 27, Iss. 4, pp. 361-381
Closed Access | Times Cited: 13
Tackling myelin deficits in neurodevelopmental disorders using drug delivery systems
May Rokach, Corinne Portioli, Sayanti Brahmachari, et al.
Advanced Drug Delivery Reviews (2024) Vol. 207, pp. 115218-115218
Closed Access | Times Cited: 5
Presynaptic perspective: Axonal transport defects in neurodevelopmental disorders
Gui-Jing Xiong, Zu‐Hang Sheng
The Journal of Cell Biology (2024) Vol. 223, Iss. 6
Open Access | Times Cited: 5
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus
Phan Q. Duy, Bettina Jux, Shujuan Zhao, et al.
Brain (2024) Vol. 147, Iss. 12, pp. 4292-4305
Closed Access | Times Cited: 5
Single cell spatial biology over developmental time can decipher pediatric brain pathologies
Ruth Nussinov, Bengi Ruken Yavuz, Hyunbum Jang
Neurobiology of Disease (2024) Vol. 199, pp. 106597-106597
Open Access | Times Cited: 5
Effectiveness of pharmacological interventions for managing ADHD symptoms in individuals with autism spectrum disorder: A systematic review and meta-analysis
Paulo Levi Bezerra Martins, Gustavo César Parente Torquato, Gabriel Alberto Pinheiro Fernandes Dias, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2024) Vol. 134, pp. 111089-111089
Closed Access | Times Cited: 5
NUBP2 deficiency disrupts the centrosome‐check point in the brain and causes primary microcephaly
Rebecca Rushforth, Hanan E. Shamseldin, Nicole Costantino, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Naa15 Haploinsufficiency and De Novo Missense Variants Associate With Neurodevelopmental Disorders and Interfere With Neurogenesis and Neuron Development
Mei He, Bing Du, Guodong Chen, et al.
Autism Research (2025)
Closed Access

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