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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:

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

Showing 1-25 of 40 citing articles:

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: 424
Autism genes converge on asynchronous development of shared neuron classes
Bruna Paulsen, Silvia Velasco, Amanda J. Kedaigle, et al.
Nature (2022) Vol. 602, Iss. 7896, pp. 268-273
Open Access | Times Cited: 307
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
Britt Mossink, Moritz Negwer, Dirk Schubert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2517-2563
Open Access | Times Cited: 80
The Mechanisms of CHD8 in Neurodevelopment and Autism Spectrum Disorders
Orly Weissberg, Evan Elliott
Genes (2021) Vol. 12, Iss. 8, pp. 1133-1133
Open Access | Times Cited: 45
FoxG1 regulates the formation of cortical GABAergic circuit during an early postnatal critical period resulting in autism spectrum disorder-like phenotypes
Goichi Miyoshi, Yoshifumi Ueta, Akiyo Natsubori, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 44
Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice
Robert Ellingford, Martyna J. Panasiuk, Emilie Rabesahala de Meritens, et al.
Molecular Psychiatry (2021) Vol. 26, Iss. 7, pp. 3614-3624
Open Access | Times Cited: 36
Pleiotropy of autism-associated chromatin regulators
Micaela Lasser, Nawei Sun, Yuxiao Xu, et al.
Development (2023) Vol. 150, Iss. 14
Open Access | Times Cited: 15
Cognitive impairment and transcriptomic profile in hippocampus of young mice after multiple neonatal exposures to sevoflurane
Shaoyong Song, Xiaowen Meng, Zhengyuan Xia, et al.
Aging (2019) Vol. 11, Iss. 19, pp. 8386-8417
Open Access | Times Cited: 42
Sentinels of chromatin: chromodomain helicase DNA-binding proteins in development and disease
Andrej Alendar, Anton Berns
Genes & Development (2021) Vol. 35, Iss. 21-22, pp. 1403-1430
Open Access | Times Cited: 31
Molecular and network disruptions in neurodevelopment uncovered by single cell transcriptomics analysis of CHD8 heterozygous cerebral organoids
Maider Astorkia, Yang Liu, Erika Pedrosa, et al.
Heliyon (2024) Vol. 10, Iss. 14, pp. e34862-e34862
Open Access | Times Cited: 4
Chromatin Remodeler CHD8 in Autism and Brain Development
Anke Hoffmann, Dietmar Spengler
Journal of Clinical Medicine (2021) Vol. 10, Iss. 2, pp. 366-366
Open Access | Times Cited: 25
Excitatory neuronal CHD8 in the regulation of neocortical development and sensory-motor behaviors
Hanseul Kweon, Won Beom Jung, Geun Ho Im, et al.
Cell Reports (2021) Vol. 34, Iss. 8, pp. 108780-108780
Open Access | Times Cited: 24
CHD8suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
Emanuela Kerschbamer, Michele Arnoldi, Takshashila Tripathi, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 22, pp. 12809-12828
Open Access | Times Cited: 17
Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA binding and long-term behavioral consequences
Nathan Kopp, Kayla R. Nygaard, Yating Liu, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 9, pp. 1498-1519
Open Access | Times Cited: 27
Developmental pyrethroid exposure and age influence phenotypes in a Chd8 haploinsufficient autism mouse model
Jessica A. Jiménez, Jeremy M. Simon, Wenxin Hu, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 14
Human brain organoids reveal accelerated development of cortical neuron classes as a shared feature of autism risk genes
Bruna Paulsen, Silvia Velasco, Amanda J. Kedaigle, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 19
Single-Cell Transcriptomics Supports a Role of CHD8 in Autism
Anke Hoffmann, Dietmar Spengler
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 6, pp. 3261-3261
Open Access | Times Cited: 16
Neurodevelopmental functions of CHD8: new insights and questions
M. Albert Basson
Biochemical Society Transactions (2024) Vol. 52, Iss. 1, pp. 15-27
Open Access | Times Cited: 2
The CHD Protein Kismet Restricts the Synaptic Localization of Cell Adhesion Molecules at the Drosophila Neuromuscular Junction
Ireland R. Smith, Emily Hendricks, Nina K. Latcheva, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 5, pp. 3074-3074
Open Access | Times Cited: 2
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
The autism risk factor CHD8 is a chromatin activator in human neurons and functionally dependent on the ERK-MAPK pathway effector ELK1
Bahareh Haddad Derafshi, Tamás Dankó, Soham Chanda, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 9
Age-differential sexual dimorphism in CHD8-S62X-mutant mouse behaviors
Soo Yeon Lee, Hanseul Kweon, Hyojin Kang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 8
Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma
Alessandro Vaisfeld, Serena Spartano, Giuseppe Gobbi, et al.
Epilepsia (2020) Vol. 62, Iss. 1, pp. 25-40
Open Access | Times Cited: 11
Chromodomain helicase DNA-binding proteins and neurodevelopmental disorders
Heba Yasin, Farah Zahir
Journal of Translational Genetics and Genomics (2020)
Open Access | Times Cited: 9
Age-differential sexual dimorphisms in CHD8-S62X-mutant mouse synapses and transcriptomes
Soo Yeon Lee, Hanseul Kweon, Hyojin Kang, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 3
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