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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:

Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences
Nicolas Lebrun, Claire Mehler‐Jacob, Karine Poirier, et al.
Gene (2018) Vol. 679, pp. 305-313
Closed Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Regulation, functions and transmission of bivalent chromatin during mammalian development
Trisha A. Macrae, Julie Fothergill-Robinson, Miguel Ramalho‐Santos
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 1, pp. 6-26
Closed Access | Times Cited: 116
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J. Jurgens, Ling Xiao, et al.
Nature Genetics (2025)
Closed Access | Times Cited: 3
The impact of rare protein coding genetic variation on adult cognitive function
Chia‐Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 927-938
Open Access | Times Cited: 42
KDM5A mutations identified in autism spectrum disorder using forward genetics
Lauretta El Hayek, İslam Oğuz Tuncay, Nadine Nijem, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 44
Emerging of lysine demethylases (KDMs): From pathophysiological insights to novel therapeutic opportunities
Sarder Arifuzzaman, Mst Reshma Khatun, R Khatun
Biomedicine & Pharmacotherapy (2020) Vol. 129, pp. 110392-110392
Open Access | Times Cited: 43
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
PLoS Genetics (2021) Vol. 17, Iss. 7, pp. e1009679-e1009679
Open Access | Times Cited: 31
Increased burden of rare protein‐truncating variants in constrained, brain‐specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder
Dita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
Genes Brain & Behavior (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 4
Drawing a line between histone demethylase KDM5A and KDM5B: their roles in development and tumorigenesis
Jung Yoo, Go Woon Kim, Yu Hyun Jeon, et al.
Experimental & Molecular Medicine (2022) Vol. 54, Iss. 12, pp. 2107-2117
Open Access | Times Cited: 19
20 years of histone lysine demethylases: From discovery to the clinic and beyond
Zach H. Gray, M. Honer, Pooja Ghatalia, et al.
Cell (2025) Vol. 188, Iss. 7, pp. 1747-1783
Closed Access
Alternative Splicing in Autism Spectrum Disorder: Recent Insights from Mechanisms to Therapy
Michael Zheng, Nengcheng Bao, Zhechao Wang, et al.
Asian Journal of Psychiatry (2025), pp. 104501-104501
Open Access
The histone demethylase KDM5 is required for synaptic structure and function at the Drosophila neuromuscular junction
Helen M. Belálcazar, Emily Hendricks, Sumaira Zamurrad, et al.
Cell Reports (2021) Vol. 34, Iss. 7, pp. 108753-108753
Open Access | Times Cited: 19
Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder
Stephen K. Siecinski, Stephanie N. Giamberardino, Marina Spanos, et al.
Autism Research (2023) Vol. 16, Iss. 3, pp. 502-523
Open Access | Times Cited: 8
Histone demethylases in neurodevelopment and neurodegenerative diseases
Haiying Wang, Beiyi Guo, Xiaoqiang Guo
International Journal of Neuroscience (2023), pp. 1-11
Closed Access | Times Cited: 8
NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia
Mouhamed Alsaqati, Brittany A. Davis, Jamie L. Wood, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 11
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes
Aldesia Provenzano, Andrea La Barbera, Mirko Scagnet, et al.
Human Genetics (2020) Vol. 140, Iss. 4, pp. 625-647
Open Access | Times Cited: 16
Pathogenic KDM5B variants in the context of developmental disorders
Jack Harrington, Gabrielle Wheway, Sandrine Willaime‐Morawek, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2022) Vol. 1865, Iss. 5, pp. 194848-194848
Open Access | Times Cited: 10
The impact of rare protein coding genetic variation on adult cognitive function
Chia‐Yen Chen, Ruoyu Tian, Tian Ge, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 8
A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster
Giuseppe Donato Mangano, Vincenzo Antona, Elisa Calì, et al.
Seizure (2022) Vol. 97, pp. 20-22
Open Access | Times Cited: 7
A Genotype/Phenotype Study of KDM5B-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense Variants
Maria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1033-1033
Open Access | Times Cited: 1
KDM5B protein expressed in viable and fertile ΔARID mice exhibit no demethylase activity
Shirin Jamshidi, Steven Catchpole, Jie Chen, et al.
International Journal of Oncology (2021) Vol. 59, Iss. 5
Open Access | Times Cited: 7
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 4
KDM5 Lysine Demethylases in Pathogenesis, from Basic Science Discovery to the Clinic
Shang‐Min Zhang, Jian Cao, Qin Yan
Advances in experimental medicine and biology (2023), pp. 113-137
Closed Access | Times Cited: 1
Evaluation of DNA repair capacity in parents of pediatric patients diagnosed with autism spectrum disorder using the comet assay procedure
Mansoureh Akouchekian, Rasoul Alizadeh, Fatemeh Beiranvandi, et al.
IBRO Neuroscience Reports (2023) Vol. 15, pp. 304-309
Open Access | Times Cited: 1
Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous KDM5B Variants
Sébastien Lebon, Mathieu Quinodoz, Virginie G. Peter, et al.
Genes (2021) Vol. 12, Iss. 9, pp. 1397-1397
Open Access | Times Cited: 3
Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder
Stephen K. Siecinski, Stephanie N. Giamberardino, Marina Spanos, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
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