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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:

Deletion of Autism Risk Gene Shank3 Disrupts Prefrontal Connectivity
Marco Pagani, Alice Bertero, Adam Liska, et al.
Journal of Neuroscience (2019) Vol. 39, Iss. 27, pp. 5299-5310
Open Access | Times Cited: 98

Showing 26-50 of 98 citing articles:

Interneuron development and dysfunction
Jiaxin Yang, Xiong Yang, Ke Tang
FEBS Journal (2021) Vol. 289, Iss. 8, pp. 2318-2336
Open Access | Times Cited: 36
Abnormal whisker-dependent behaviors and altered cortico-hippocampal connectivity in Shank3b−/− mice
Luigi Balasco, Marco Pagani, Luca Pangrazzi, et al.
Cerebral Cortex (2021) Vol. 32, Iss. 14, pp. 3042-3056
Open Access | Times Cited: 34
Modeling Brain Dysconnectivity in Rodents
Alessandro Gozzi, Valerio Zerbi
Biological Psychiatry (2022) Vol. 93, Iss. 5, pp. 419-429
Open Access | Times Cited: 23
Sex-biasing influence of autism-associated Ube3a gene overdosage at connectomic, behavioral, and transcriptomic levels
Caterina Montani, Luigi Balasco, Marco Pagani, et al.
Science Advances (2024) Vol. 10, Iss. 28
Open Access | Times Cited: 5
Autism-associated Nf1 deficiency disrupts corticocortical and corticostriatal functional connectivity in human and mouse
Ben Shofty, Eyal Bergmann, Gil Zur, et al.
Neurobiology of Disease (2019) Vol. 130, pp. 104479-104479
Open Access | Times Cited: 40
Individual variability in functional connectivity architecture of the mouse brain
Eyal Bergmann, Xenia Gofman, Alexandra Kavushansky, et al.
Communications Biology (2020) Vol. 3, Iss. 1
Open Access | Times Cited: 36
LMT USV Toolbox, a Novel Methodological Approach to Place Mouse Ultrasonic Vocalizations in Their Behavioral Contexts—A Study in Female and Male C57BL/6J Mice and in Shank3 Mutant Females
Fabrice de Chaumont, Nathalie Lemière, Sabrina Coqueran, et al.
Frontiers in Behavioral Neuroscience (2021) Vol. 15
Open Access | Times Cited: 28
CDKL5 sculpts functional callosal connectivity to promote cognitive flexibility
Patricia N. Awad, Valerio Zerbi, Erin Johnson‐Venkatesh, et al.
Molecular Psychiatry (2023) Vol. 29, Iss. 6, pp. 1698-1709
Open Access | Times Cited: 12
Bridging the translational gap: what can synaptopathies tell us about autism?
Ciara J. Molloy, Jennifer Cooke, Nicholas J. F. Gatford, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 12
Neuron type-specific proteomics reveals distinct Shank3 proteoforms in iSPNs and dSPNs lead to striatal synaptopathy in Shank3B–/– mice
Yizhi Wang, Tamara Perez‐Rosello, Samuel N. Smukowski, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 8, pp. 2372-2388
Open Access | Times Cited: 4
Shank2/3 double knockout-based screening of cortical subregions links the retrosplenial area to the loss of social memory in autism spectrum disorders
Débora Garrido, Stefania Beretta, Stefanie Grabrucker, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 12, pp. 4994-5006
Open Access | Times Cited: 16
Understanding the role of AMPA receptors in autism: insights from circuit and synapse dysfunction
Andrés Jiménez-Gómez, Megan X. Nguyen, Jason S. Gill
Frontiers in Psychiatry (2024) Vol. 15
Open Access | Times Cited: 3
Dysfunctional d-aspartate metabolism in BTBR mouse model of idiopathic autism
Tommaso Nuzzo, Masae Sekine, Daniela Punzo, et al.
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics (2020) Vol. 1868, Iss. 12, pp. 140531-140531
Open Access | Times Cited: 24
Phospholipid scramblase Xkr8 is required for developmental axon pruning via phosphatidylserine exposure
Urtė Neniškytė, Ugnė Kuliešiūtė, Augustė Vadišiūtė, et al.
The EMBO Journal (2023) Vol. 42, Iss. 14
Open Access | Times Cited: 8
Acute and Repeated Intranasal Oxytocin Differentially Modulate Brain-wide Functional Connectivity
Marco Pagani, Alessia De Felice, Caterina Montani, et al.
Neuroscience (2020) Vol. 445, pp. 83-94
Open Access | Times Cited: 22
Inhibitory regulation of calcium transients in prefrontal dendritic spines is compromised by a nonsense Shank3 mutation
Farhan Ali, Ling-Xiao Shao, Danielle M. Gerhard, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 6, pp. 1945-1966
Open Access | Times Cited: 22
Copy number variants in neurexin genes: phenotypes and mechanisms
Marc V. Fuccillo, ChangHui Pak
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 64-70
Open Access | Times Cited: 19
The Neurological Manifestations of Phelan-McDermid Syndrome
Yitzchak Frank
Pediatric Neurology (2021) Vol. 122, pp. 59-64
Closed Access | Times Cited: 19
Neurobiological mechanisms of electroconvulsive therapy for depression: Insights into hippocampal volumetric increases from clinical and preclinical studies
Yoshifumi Abe, Vera Jane Erchinger, Olga Therese Ousdal, et al.
Journal of Neurochemistry (2024)
Open Access | Times Cited: 2
Mice lackingAstn2have ASD-like behaviors and altered cerebellar circuit properties
Michalina Hanzel, Kayla Fernando, Susan E. Maloney, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Postnatal immune activation causes social deficits in a mouse model of tuberous sclerosis: Role of microglia and clinical implications
Manuel F. López‐Aranda, Ishanu Chattopadhyay, Gayle M. Boxx, et al.
Science Advances (2021) Vol. 7, Iss. 38
Open Access | Times Cited: 17
16p11.2 deletion mice exhibit compromised fronto-temporal connectivity, GABAergic dysfunction, and enhanced attentional ability
Rebecca L. Openshaw, David M. Thomson, Greg C. Bristow, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 6
Cellular and molecular mechanisms underlying autism spectrum disorders and associated comorbidities: A pathophysiological review
Hussain Al Dera
Biomedicine & Pharmacotherapy (2022) Vol. 148, pp. 112688-112688
Open Access | Times Cited: 10
Severe white matter damage in SHANK3 deficiency: a human and translational study
Sarah Jesse, Hans‐Peter Müller, Michael Schoen, et al.
Annals of Clinical and Translational Neurology (2019) Vol. 7, Iss. 1, pp. 46-58
Open Access | Times Cited: 17
Neural Stem Cells from Shank3-ko Mouse Model Autism Spectrum Disorders
Chiara Grasselli, Annalucia Carbone, Patrizio Panelli, et al.
Molecular Neurobiology (2019) Vol. 57, Iss. 3, pp. 1502-1515
Closed Access | Times Cited: 17

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