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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:

Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders
Nicola M. Grissom, Sarah E. McKee, Hannah Schoch, et al.
Molecular Psychiatry (2017) Vol. 23, Iss. 3, pp. 544-555
Open Access | Times Cited: 80

Showing 1-25 of 80 citing articles:

Let’s call the whole thing off: evaluating gender and sex differences in executive function
Nicola M. Grissom, Teresa M. Reyes
Neuropsychopharmacology (2018) Vol. 44, Iss. 1, pp. 86-96
Open Access | Times Cited: 229
Behavioral neuroscience of autism
Toru Takumi, Kota Tamada, Fumiyuki Hatanaka, et al.
Neuroscience & Biobehavioral Reviews (2019) Vol. 110, pp. 60-76
Closed Access | Times Cited: 127
16p11.2 Copy Number Variations and Neurodevelopmental Disorders
Benjamin Rein, Zhen Yan
Trends in Neurosciences (2020) Vol. 43, Iss. 11, pp. 886-901
Open Access | Times Cited: 109
Sex Differences in Psychiatric Disease: A Focus on the Glutamate System
Megan M. Wickens, Debra A. Bangasser, Lisa A. Briand
Frontiers in Molecular Neuroscience (2018) Vol. 11
Open Access | Times Cited: 95
Vascular contributions to 16p11.2 deletion autism syndrome modeled in mice
Julie Ouellette, Xavier Toussay, César H. Comin, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 9, pp. 1090-1101
Closed Access | Times Cited: 93
Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice
Joanna Pucilowska, Joseph Vithayathil, Marco Pagani, et al.
Journal of Neuroscience (2018) Vol. 38, Iss. 30, pp. 6640-6652
Open Access | Times Cited: 84
A multidimensional precision medicine approach identifies an autism subtype characterized by dyslipidemia
Yuan Luo, Alal Eran, Nathan Palmer, et al.
Nature Medicine (2020) Vol. 26, Iss. 9, pp. 1375-1379
Closed Access | Times Cited: 72
Divergent Strategies for Learning in Males and Females
Cathy S. Chen, R. Becket Ebitz, Sylvia R. Bindas, et al.
Current Biology (2020) Vol. 31, Iss. 1, pp. 39-50.e4
Open Access | Times Cited: 72
Sex mechanisms as nonbinary influences on cognitive diversity
Nicola M. Grissom, Nic Glewwe, Cathy Chen, et al.
Hormones and Behavior (2024) Vol. 162, pp. 105544-105544
Open Access | Times Cited: 8
Genetic changes linked to two different syndromic forms of autism enhance reinforcement learning in adolescent male but not female mice
Juliana Chase, Jing‐Jing Li, Wan Chen Lin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation
Troy A. McDiarmid, Manuel Belmadani, Joseph Liang, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 117, Iss. 1, pp. 656-667
Open Access | Times Cited: 70
Emerging behavioral and neuroimaging biomarkers for early and accurate characterization of autism spectrum disorders: a systematic review
Chandrakanta Hiremath, John Vijay Sagar Kommu, B. K. Yamini, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 53
Developmental Disruptions of the Dorsal Striatum in Autism Spectrum Disorder
Maya M. Evans, Jaekyoon Kim, Ted Abel, et al.
Biological Psychiatry (2023) Vol. 95, Iss. 2, pp. 102-111
Closed Access | Times Cited: 20
Sex differences and the effects of estradiol on striatal function
John Meitzen, Robert L. Meisel, P. Mermelstein
Current Opinion in Behavioral Sciences (2018) Vol. 23, pp. 42-48
Open Access | Times Cited: 52
Sex-specific Behavioral Features of Rodent Models of Autism Spectrum Disorder
Se Jin Jeon, Edson Luck Gonzales, Darine Froy N. Mabunga, et al.
Experimental Neurobiology (2018) Vol. 27, Iss. 5, pp. 321-343
Open Access | Times Cited: 51
Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion
Vinod Jangir Kumar, Nicola M. Grissom, Sarah E. McKee, et al.
Translational Psychiatry (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 50
The functional neural architecture of dysfunctional reward processing in autism
Hildegard Janouschek, Henry W. Chase, Rachel Sharkey, et al.
NeuroImage Clinical (2021) Vol. 31, pp. 102700-102700
Open Access | Times Cited: 38
The Link Between Autism and Sex-Related Neuroanatomy, and Associated Cognition and Gene Expression
Dorothea L. Floris, Han Peng, Varun Warrier, et al.
American Journal of Psychiatry (2022) Vol. 180, Iss. 1, pp. 50-64
Open Access | Times Cited: 26
Dissecting 16p11.2 hemi-deletion to study sex-specific striatal phenotypes of neurodevelopmental disorders
Jaekyoon Kim, Yann Vanrobaeys, Benjamin A. Kelvington, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 5, pp. 1310-1321
Open Access | Times Cited: 5
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions
Thomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 9, pp. 1474-1486
Open Access | Times Cited: 41
Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma
Laura E. Egolf, Zalman Vaksman, Gonzalo López, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 3, pp. 658-668
Open Access | Times Cited: 41
Gene regulatory mechanisms underlying sex differences in brain development and psychiatric disease
Devanand S. Manoli, Jessica Tollkühn
Annals of the New York Academy of Sciences (2018) Vol. 1420, Iss. 1, pp. 26-45
Open Access | Times Cited: 39
Home-cage hypoactivity in mouse genetic models of autism spectrum disorder
Christopher C. Angelakos, Jennifer C. Tudor, Sarah L. Ferri, et al.
Neurobiology of Learning and Memory (2019) Vol. 165, pp. 107000-107000
Open Access | Times Cited: 37
An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes
Tal Yardeni, Ana G. Cristancho, Almedia J. McCoy, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 6
Open Access | Times Cited: 32
Altered medial prefrontal cortex and dorsal raphé activity predict genotype and correlate with abnormal learning behavior in a mouse model of autism‐associated 2p16.3 deletion
Rebecca Hughes, Jayde Whittingham‐Dowd, Steven J. Clapcote, et al.
Autism Research (2022) Vol. 15, Iss. 4, pp. 614-627
Open Access | Times Cited: 19
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