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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:

Adult Ube3a Gene Reinstatement Restores the Electrophysiological Deficits of Prefrontal Cortex Layer 5 Neurons in a Mouse Model of Angelman Syndrome
Diana C. Rotaru, Geeske M. van Woerden, Ilse Wallaard, et al.
Journal of Neuroscience (2018) Vol. 38, Iss. 37, pp. 8011-8030
Open Access | Times Cited: 71

Showing 1-25 of 71 citing articles:

Synaptopathology Involved in Autism Spectrum Disorder
Shiqi Guang, Nan Pang, Xiaolu Deng, et al.
Frontiers in Cellular Neuroscience (2018) Vol. 12
Open Access | Times Cited: 247
Development of prefrontal cortex
Sharon M. Kolk, Pasko Rakić
Neuropsychopharmacology (2021) Vol. 47, Iss. 1, pp. 41-57
Open Access | Times Cited: 209
Cortical interneurons in autism
Anis Contractor, Iryna M. Ethell, Carlos Portera‐Cailliau
Nature Neuroscience (2021) Vol. 24, Iss. 12, pp. 1648-1659
Open Access | Times Cited: 118
Daily Oscillation of the Excitation-Inhibition Balance in Visual Cortical Circuits
Michelle Bridi, Fang-Jiao Zong, Min Xia, et al.
Neuron (2019) Vol. 105, Iss. 4, pp. 621-629.e4
Open Access | Times Cited: 129
Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice
Jun Mukai, Enrico Cannavò, Gregg W. Crabtree, et al.
Neuron (2019) Vol. 104, Iss. 3, pp. 471-487.e12
Open Access | Times Cited: 113
Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome
Rossella Avagliano Trezza, Monica Sonzogni, Stijn N. V. Bossuyt, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 8, pp. 1235-1247
Closed Access | Times Cited: 86
An ASO therapy for Angelman syndrome that targets an evolutionarily conserved region at the start of the UBE3A-AS transcript
Scott V. Dindot, Sarah Christian, William J. Murphy, et al.
Science Translational Medicine (2023) Vol. 15, Iss. 688
Open Access | Times Cited: 42
The Autism and Angelman Syndrome Protein Ube3A/E6AP: The Gene, E3 Ligase Ubiquitination Targets and Neurobiological Functions
Natasha Khatri, Heng‐Ye Man
Frontiers in Molecular Neuroscience (2019) Vol. 12
Open Access | Times Cited: 75
Angelman Syndrome: From Mouse Models to Therapy
Diana C. Rotaru, Edwin Mientjes, Ype Elgersma
Neuroscience (2020) Vol. 445, pp. 172-189
Open Access | Times Cited: 61
Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome
Elizabeth L. Berg, Michael C. Pride, Stela P. Petkova, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 57
RNA interference (RNAi)-based therapeutics for treatment of rare neurologic diseases
Noélle D. Germain, Wendy K. Chung, Patrick D. Sarmiere
Molecular Aspects of Medicine (2022) Vol. 91, pp. 101148-101148
Closed Access | Times Cited: 31
Angelman syndrome: a journey through the brain
Carina Maranga, Tiago G. Fernandes, Evguenia Bekman, et al.
FEBS Journal (2020) Vol. 287, Iss. 11, pp. 2154-2175
Open Access | Times Cited: 48
Therapeutic strategies for autism: targeting three levels of the central dogma of molecular biology
Derek Hong, Lilia M. Iakoucheva
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 16
Resolving the Synaptic versus Developmental Dichotomy of Autism Risk Genes
Whitney E. Heavner, Stephen Smith
Trends in Neurosciences (2020) Vol. 43, Iss. 4, pp. 227-241
Open Access | Times Cited: 37
Cell-Type Specificity of Genomic Imprinting in Cerebral Cortex
Susanne Laukoter, Florian M. Pauler, Robert Beattie, et al.
Neuron (2020) Vol. 107, Iss. 6, pp. 1160-1179.e9
Open Access | Times Cited: 35
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndrome
Dongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 11
Genetic backgrounds have unique seizure response profiles and behavioral outcomes following convulsant administration
Nycole A. Copping, Anna Adhikari, Stela P. Petkova, et al.
Epilepsy & Behavior (2019) Vol. 101, pp. 106547-106547
Open Access | Times Cited: 32
Visual Sequences Drive Experience-Dependent Plasticity in Mouse Anterior Cingulate Cortex
Michael S. Sidorov, Hyojin Kim, Marie Rougié, et al.
Cell Reports (2020) Vol. 32, Iss. 11, pp. 108152-108152
Open Access | Times Cited: 28
Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations
Stijn N. V. Bossuyt, A. Mattijs Punt, Ilona J. de Graaf, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 6, pp. 430-442
Open Access | Times Cited: 25
Regional and cellular organization of the autism-associated protein UBE3A/E6AP and its antisense transcript in the brain of the developing rhesus monkey
Chavely Gonzalez Ramirez, Sarah G. Salvador, Ridthi Kartik Rekha Patel, et al.
Frontiers in Neuroanatomy (2024) Vol. 18
Open Access | Times Cited: 3
UBE3A controls axon initial segment in the cortical pyramidal neurons
Xinlang Liu, Zikang Jiang, Yoshinori Otani, et al.
Biochemical and Biophysical Research Communications (2025), pp. 151429-151429
Closed Access
Activity-dependent degradation of Kv4.2 contributes to synaptic plasticity and behavior in Angelman syndrome model mice
Jiahua Hu, Cole Malloy, Ying Liu, et al.
Cell Reports (2025) Vol. 44, Iss. 5, pp. 115583-115583
Closed Access
Molecular mechanisms for targeted ASD treatments
Bernadette Basilico, Jasmin Morandell, Gaia Novarino
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 126-137
Open Access | Times Cited: 27
Dosage-sensitive genes in autism spectrum disorders: From neurobiology to therapy
Sehrish Javed, Tharushan Selliah, Yu‐Ju Lee, et al.
Neuroscience & Biobehavioral Reviews (2020) Vol. 118, pp. 538-567
Closed Access | Times Cited: 22
Acetate supplementation restores cognitive deficits caused by ARID1A haploinsufficiency in excitatory neurons
Pei‐Pei Liu, Shang‐Kun Dai, Ting‐Wei Mi, et al.
EMBO Molecular Medicine (2022) Vol. 14, Iss. 12
Open Access | Times Cited: 14
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