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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:

Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
Catarina M. Seabra, Tatsiana Aneichyk, Serkan Erdin, et al.
Molecular Autism (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 16

Showing 16 citing articles:

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, et al.
Cell (2020) Vol. 180, Iss. 3, pp. 568-584.e23
Open Access | Times Cited: 1873
Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency
A. Ayanna Wade, Kenneth Lim, Rinaldo Catta-Preta, et al.
Frontiers in Molecular Neuroscience (2019) Vol. 11
Open Access | Times Cited: 40
Recent Developments in Autism Genetic Research: A Scientometric Review from 2018 to 2022
Mengyu Lim, Alessandro Carollo, Dagmara Dimitriou, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1646-1646
Open Access | Times Cited: 17
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Calwing Liao, Mariana Moysés‐Oliveira, Celine E.F. De Esch, et al.
Cell Genomics (2023) Vol. 3, Iss. 4, pp. 100277-100277
Open Access | Times Cited: 10
Evidence of shared transcriptomic dysregulation of HNRNPU-related disorder between human organoids and embryonic mice
Andrew K. Ressler, Gabriela L.A. Sampaio, Sarah A. Dugger, et al.
iScience (2022) Vol. 26, Iss. 1, pp. 105797-105797
Open Access | Times Cited: 7
RINGs, DUBs and Abnormal Brain Growth—Histone H2A Ubiquitination in Brain Development and Disease
Lucy Anne Doyle, Firuze Unlu Bektas, Eleftheria Chatzantonaki, et al.
Epigenomes (2022) Vol. 6, Iss. 4, pp. 42-42
Open Access | Times Cited: 6
A Novel Genetic Variant in MBD5 Associated with Severe Epilepsy and Intellectual Disability: Potential Implications on Neural Primary Cilia
Mariana Martins, Ana Rafaela Oliveira, Solange Martins, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 16, pp. 12603-12603
Open Access | Times Cited: 3
The impact of psychosocial defeat stress on the bed nucleus of the stria terminalis transcriptome in adult male mice
Anand Gururajan, Thomaz F. S. Bastiaanssen, Ana Paula Ventura Silva, et al.
European Journal of Neuroscience (2021) Vol. 55, Iss. 1, pp. 67-77
Closed Access | Times Cited: 7
Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes
Sureni V. Mullegama, Steven D. Klein, Stephen R. Williams, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Reply to: “Correspondence to bipolar disorder-iPSC derived neural progenitor cells exhibit dysregulation of store-operated Ca2+ entry and accelerated differentiation” by Yde Ohki and colleagues
Tristen Hewitt, Begüm Alural, Natalina Becke, et al.
Molecular Psychiatry (2024)
Closed Access
Association between the copy number variations of Methyl-CpG binding domain family and schizophrenia
Zhouyang Sun, Changgui Kou, Zibo Gao, et al.
Gene (2024) Vol. 930, pp. 148836-148836
Closed Access
A scalable, high-throughput neural development platform identifies shared impact of ASD genes on cell fate and differentiation
Xuran Wang, Matthew A. Lalli, Urvashi Thopte, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Autism and the cell’s antennae
Giorgia Guglielmi
The Transmitter (2022)
Closed Access | Times Cited: 2
Germline mosaicism in a family withMBD5haploinsufficiency
Mehak Bhatia, Gianpiero L. Cavalleri, Máire White, et al.
Molecular Case Studies (2022) Vol. 8, Iss. 7, pp. a006253-a006253
Open Access | Times Cited: 1
Early-Onset Dementia Associated with a Heterozygous, Nonsense, and de novo Variant in the MBD5 Gene
Guillermo González‐Ortega, Sara Llamas‐Velasco, Ana Arteche‐López, et al.
Journal of Alzheimer s Disease (2021) Vol. 84, Iss. 1, pp. 73-78
Closed Access | Times Cited: 1
Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Calwing Liao, Mariana Moysés‐Oliveira, Celine E. de Esch, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
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