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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:

Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders
Alexander S. Hatoum, Sarah M. C. Colbert, Emma C. Johnson, et al.
Nature Mental Health (2023) Vol. 1, Iss. 3, pp. 210-223
Open Access | Times Cited: 129

Showing 26-50 of 129 citing articles:

Exploration of Genetic Liability to Insomnia and Substance Use Disorders in Patients With Bipolar Disorder
Lindsay Melhuish Beaupre, Brandon J. Coombes, Anthony Batzler, et al.
Bipolar Disorders (2025)
Closed Access
Genetic, transcriptomic, metabolic, and neuropsychiatric underpinnings of cortical functional gradients
Bin Wan, Yong He, Varun Warrier, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Comparison of the multivariate genetic architecture of eight major psychiatric disorders across sex
Ted Schwaba, Travis T. Mallard, Adam X. Maihofer, et al.
Nature Genetics (2025)
Open Access
Pleiotropic Effects of Grm7/GRM7 in Shaping Neurodevelopmental Pathways and the Neural Substrate of Complex Behaviors and Disorders
Beatrix Gyetvai, Csaba Vadász
Biomolecules (2025) Vol. 15, Iss. 3, pp. 392-392
Open Access
Reevaluating the brain disease model of addiction
Chrysanthi Blithikioti, Eiko I. Fried, Emiliano Albanese, et al.
The Lancet Psychiatry (2025)
Closed Access
Polygenic Risk Score Analysis of Antidepressant Treatment Outcomes: A CAN-BIND-1 Study Report: Analyse des résultats du traitement antidépresseur à l’aide des scores de risque polygéniques : Rapport sur l’étude CAN-BIND-1
Leen Magarbeh, Samar S. M. Elsheikh, Farhana Islam, et al.
The Canadian Journal of Psychiatry (2025)
Closed Access
Polygenic overlap of substance use behaviors and disorders with externalizing and internalizing problems independent of genetic correlations
Laila Al‐Soufi, Guy Hindley, Linn Rødevand, et al.
Psychological Medicine (2025) Vol. 55
Closed Access
Measuring the associations between brain morphometry and polygenic risk scores for substance use disorders in drug-naive adolescents
Sydney Kramer, Mei‐Hsin Su, Mallory Stephenson, et al.
Research Square (Research Square) (2025)
Closed Access
Polygenic Scores and Mood Disorder Onsets in the Context of Family History and Early Psychopathology
Kathryn Freeman, Alyson Zwicker, Janice M. Fullerton, et al.
JAMA Network Open (2025) Vol. 8, Iss. 4, pp. e255331-e255331
Open Access
Epigenetic and genetic profiling of comorbidity patterns among substance dependence diagnoses
Gita A. Pathak, Robert H. Pietrzak, AnnMarie Lacobelle, et al.
Molecular Psychiatry (2025)
Open Access
Apremilast reduces co-occurring alcohol drinking and mechanical allodynia and regulates central amygdala GABAergic transmission
Valentina Vozella, Vittoria Borgonetti, Bryan Cruz, et al.
JCI Insight (2025) Vol. 10, Iss. 8
Open Access
Biological Risk Amplification: Disease Vulnerability

Cambridge University Press eBooks (2025), pp. 117-169
Closed Access
Cell-type brain-region specific changes in prefrontal cortex of a mouse model of alcohol dependence
Nihal A. Salem, L.A. Manzano, Michael W. Keist, et al.
Neurobiology of Disease (2023) Vol. 190, pp. 106361-106361
Open Access | Times Cited: 10
Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults
Wei Q. Deng, Kyla Belisario, Joshua C. Gray, et al.
Genes Brain & Behavior (2023) Vol. 22, Iss. 3
Open Access | Times Cited: 9
Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information
Hüseyin Gedik, Tan Hoang Nguyen, Roseann E. Peterson, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 9
Drugs and Addiction Science: NIDA Celebrates 50 Years of Research and Looks to the Future
Nora D. Volkow
American Journal of Psychiatry (2024) Vol. 181, Iss. 5, pp. 349-352
Closed Access | Times Cited: 3
Shared genetics linking sociability with the brain's default mode network.
Giuseppe Fanelli, Jamie Robinson, Chiara Fabbri, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Generalized genetic liability to substance use disorders
Alex P. Miller, Ryan Bogdan, Arpana Agrawal, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 11
Open Access | Times Cited: 3
PET imaging in rat brain shows opposite effects of acute and chronic alcohol exposure on phosphodiesterase-4B, an indirect biomarker of cAMP activity
Shiyu Tang, Sung Won Kim, Amanda Olsen-Dufour, et al.
Neuropsychopharmacology (2024) Vol. 50, Iss. 2, pp. 444-451
Open Access | Times Cited: 3
Leveraging pleiotropy for the improved treatment of psychiatric disorders
D Woodward, Jackson G. Thorp, Christel M. Middeldorp, et al.
Molecular Psychiatry (2024)
Open Access | Times Cited: 3
Substance use and common contributors to morbidity: A genetics perspective
Sandra Sanchez‐Roige, Rachel L. Kember, Arpana Agrawal
EBioMedicine (2022) Vol. 83, pp. 104212-104212
Open Access | Times Cited: 15
High intensity interval training exercise increases dopamine D2 levels and modulates brain dopamine signaling
John Tyler, Madeline Podaras, Brittany Richardson, et al.
Frontiers in Public Health (2023) Vol. 11
Open Access | Times Cited: 8
The First Exploratory Personalized Medicine Approach to Improve Bariatric Surgery Outcomes Utilizing Psychosocial and Genetic Risk Assessments: Encouraging Clinical Research
Panayotis K. Thanos, Colin Hanna, Abrianna Mihalkovic, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 7, pp. 1164-1164
Open Access | Times Cited: 7
A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorder
Shirley Y. Hill, Joseph Hostyk
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 7
Functional 3’-UTR Variants Identify Regulatory Mechanisms Impacting Alcohol Use Disorder and Related Traits
Andy Chen, Xuhong Yu, Kriti S. Thapa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2

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