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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:

Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS
Wouter J. Peyrot, Alkes L. Price
Nature Genetics (2021) Vol. 53, Iss. 4, pp. 445-454
Open Access | Times Cited: 94

Showing 1-25 of 94 citing articles:

Genetic heterogeneity and subtypes of major depression
Thuy-Dung Nguyen, Arvid Harder, Ying Xiong, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 3, pp. 1667-1675
Open Access | Times Cited: 71
A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer’s disease and gastrointestinal tract disorders
Emmanuel O Adewuyi, Eleanor K. O’Brien, Dale R. Nyholt, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 71
Multi-omic insight into the molecular networks of mitochondrial dysfunction in the pathogenesis of inflammatory bowel disease
Jie Chen, Xixian Ruan, Yuhao Sun, et al.
EBioMedicine (2023) Vol. 99, pp. 104934-104934
Open Access | Times Cited: 46
The Landscape of Shared and Divergent Genetic Influences across 14 Psychiatric Disorders
Andrew D. Grotzinger, Josefin Werme, Wouter J. Peyrot, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 2
Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders
Phil H. Lee, Yen‐Chen Anne Feng, Jordan W. Smoller
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 20-31
Open Access | Times Cited: 125
Dissecting polygenic signals from genome-wide association studies on human behaviour
Abdel Abdellaoui, Karin J. H. Verweij
Nature Human Behaviour (2021) Vol. 5, Iss. 6, pp. 686-694
Closed Access | Times Cited: 86
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Manuel Mattheisen, Jakob Grove, Thomas D. Als, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1470-1478
Open Access | Times Cited: 52
Expression and functions of adenylyl cyclases in the CNS
Karan Devasani, Yao Yao
Fluids and Barriers of the CNS (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 45
Genetic architecture distinguishes tinnitus from hearing loss
Royce E. Clifford, Adam X. Maihofer, Chris Chatzinakos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
The effects of genetic and modifiable risk factors on brain regions vulnerable to ageing and disease
Jordi Manuello, Joosung Min, Paul J. McCarthy, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
A genome‐wide association meta‐analysis of all‐cause and vascular dementia
Bernard Fongang
Alzheimer s & Dementia (2024) Vol. 20, Iss. 9, pp. 5973-5995
Open Access | Times Cited: 10
Systematic dissection of pleiotropic loci and critical regulons in excitatory neurons and microglia relevant to neuropsychiatric and ocular diseases
Yunlong Ma, Dingping Jiang, Jingjing Li, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Innate and adaptive immune abnormalities underlying autoimmune diseases: the genetic connections
Xinxin Chi, Miaozhen Huang, Hailin Tu, et al.
Science China Life Sciences (2023) Vol. 66, Iss. 7, pp. 1482-1517
Open Access | Times Cited: 21
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
Younghun Han, Jinyoung Byun, Catherine Zhu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 18
Recent advances in understanding the genetic basis of systemic lupus erythematosus
Eunji Ha, Sang‐Cheol Bae, Kwang-Woo Kim
Seminars in Immunopathology (2021) Vol. 44, Iss. 1, pp. 29-46
Closed Access | Times Cited: 41
A comprehensive gene-centric pleiotropic association analysis for 14 psychiatric disorders with GWAS summary statistics
Haojie Lu, Jiahao Qiao, Zhonghe Shao, et al.
BMC Medicine (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 41
Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells
Mary-Ellen Lynall, Blagoje Soskic, James Hayhurst, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 23
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder
Sonja LaBianca, Isabell Brikell, Dorte Helenius, et al.
Nature Genetics (2023) Vol. 56, Iss. 2, pp. 234-244
Open Access | Times Cited: 14
Identifying shared genetic loci and common risk genes of rheumatoid arthritis associated with three autoimmune diseases based on large-scale cross-trait genome-wide association studies
Yaping Wen, Zu‐Guo Yu
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 12
A dimensional perspective on the genetics of obsessive-compulsive disorder
Nora I. Strom, Takahiro Soda, Carol A. Mathews, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 25
Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective
Ron Nudel, Wesley K. Thompson, Anders D. Børglum, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 18
Identifying genetic differences between bipolar disorder and major depression through multiple genome-wide association analyses
Georgia Panagiotaropoulou, Kajsa-Lotta Georgii Hellberg, Jonathan R. I. Coleman, et al.
The British Journal of Psychiatry (2025), pp. 1-12
Closed Access
An evolutionary perspective on the genetics of anorexia nervosa
Édith Breton, Tobias Kaufmann
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
The INO80E at 16p11.2 locus increases risk of schizophrenia in humans and induces schizophrenia-like phenotypes in mice
Bo Hu, Mei-Yu Yin, Chuyi Zhang, et al.
EBioMedicine (2025) Vol. 114, pp. 105645-105645
Closed Access
Association between mental disorders and trigeminal neuralgia: a cohort study and Mendelian randomization analysis
Jianke Wang, Mingxiao Li, Ze Zhang, et al.
The Journal of Headache and Pain (2025) Vol. 26, Iss. 1
Open Access
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