Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine
Zhihui Yang, Danyang Zhou, Huijuan Li, et al.
Molecular Psychiatry (2019) Vol. 25, Iss. 1, pp. 48-66
Closed Access | Times Cited: 72

Showing 1-25 of 72 citing articles:

Elephants as an animal model for self-domestication
Limor Raviv, Sarah L. Jacobson, Joshua M. Plotnik, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 15
Open Access | Times Cited: 24
Proteome-wide Association Study Provides Insights Into the Genetic Component of Protein Abundance in Psychiatric Disorders
Jiewei Liu, Xiaoyan Li, Xiong‐Jian Luo
Biological Psychiatry (2021) Vol. 90, Iss. 11, pp. 781-789
Closed Access | Times Cited: 55
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals
Huijuan Li, Chen Zhang, Li Hui, et al.
JAMA Psychiatry (2020) Vol. 78, Iss. 3, pp. 320-320
Open Access | Times Cited: 50
New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis
Hélène Choquet, Jie Yin, Alice Jacobson, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 46
The genetic relationships between brain structure and schizophrenia
Eva-Maria Stauffer, Richard A. I. Bethlehem, Lena Dorfschmidt, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 21
Translational genomics and beyond in bipolar disorder
Chen Zhang, Xiao Xiao, Tao Li, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 1, pp. 186-202
Closed Access | Times Cited: 42
Phenotypes, mechanisms and therapeutics: insights from bipolar disorder GWAS findings
Ming Li, Tao Li, Xiao Xiao, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 7, pp. 2927-2939
Closed Access | Times Cited: 27
Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathways
Wendiao Zhang, Ming Zhang, Zhenhong Xu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data
Huijuan Li, Na Qu, Li Hui, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 38
Chronic Overlapping Pain Conditions and Nociplastic Pain
Keira J.A. Johnston, Rebecca Signer, Laura M. Huckins
Human Genetics and Genomics Advances (2024) Vol. 6, Iss. 1, pp. 100381-100381
Open Access | Times Cited: 4
Persistent large-scale changes in alternative splicing in prefrontal cortical neuron types following psychedelic exposure
Yungyi Hsiao, Marcos A. Fonseca, Alina S. Tiemroth, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Unraveling ADHD: genes, co-occurring traits, and developmental dynamics
Catriona J Miller, Evgeniia Golovina, Sreemol Gokuladhas, et al.
Life Science Alliance (2025) Vol. 8, Iss. 5, pp. e202403029-e202403029
Open Access
Gut Microbiota and Mental Health: A Comprehensive Review of Gut-Brain Interactions in Mood Disorders
Ishani Mehta, Keshav Juneja, Tharun Nimmakayala, et al.
Cureus (2025)
Open Access
Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder
Wenqiang Li, Xin Cai, Huijuan Li, et al.
Neuropsychopharmacology (2020) Vol. 46, Iss. 6, pp. 1103-1112
Open Access | Times Cited: 29
Genome-wide association study accounting for anticholinergic burden to examine cognitive dysfunction in psychotic disorders
Seenae Eum, S. Kristian Hill, Ney Alliey‐Rodriguez, et al.
Neuropsychopharmacology (2021)
Open Access | Times Cited: 26
An alternative splicing hypothesis for neuropathology of schizophrenia: evidence from studies on historical candidate genes and multi-omics data
Chuyi Zhang, Xiao Xiao, Zhuohua Zhang, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 95-112
Closed Access | Times Cited: 24
Large‐scale collaboration in ENIGMA‐EEG: A perspective on the meta‐analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity
Dirk J. A. Smit, Ole A. Andreassen, Dorret I. Boomsma, et al.
Brain and Behavior (2021) Vol. 11, Iss. 8
Open Access | Times Cited: 24
Coexistence of Multiple Functional Variants and Genes Underlies Genetic Risk Locus 11p11.2 of Alzheimer’s Disease
Min Xu, Qianjin Liu, Rui Bi, et al.
Biological Psychiatry (2023) Vol. 94, Iss. 9, pp. 743-759
Closed Access | Times Cited: 10
NEK4: prediction of available drug targets and common genetic linkages in bipolar disorder and major depressive disorder
Bin Gong, Chenxu Xiao, Yu Feng, et al.
Frontiers in Psychiatry (2025) Vol. 16
Open Access
Genetically regulated eRNA expression predicts chromatin contact frequency and reveals genetic mechanisms at GWAS loci
Michael J. Betti, Phillip Lin, Melinda C. Aldrich, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population
Weipeng Liu, Hao Yan, Danyang Zhou, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 26
Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus
Hong Chang, Xin Cai, Huijuan Li, et al.
Biological Psychiatry (2020) Vol. 89, Iss. 3, pp. 246-255
Closed Access | Times Cited: 25
A Human-Specific Schizophrenia Risk Tandem Repeat Affects Alternative Splicing of a Human-Unique Isoform AS3MTd2d3 and Mushroom Dendritic Spine Density
Xin Cai, Zhihui Yang, Huijuan Li, et al.
Schizophrenia Bulletin (2020) Vol. 47, Iss. 1, pp. 219-227
Open Access | Times Cited: 22
Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci
Weipeng Liu, Wenqiang Li, Xin Cai, et al.
Neuropsychopharmacology (2020) Vol. 45, Iss. 7, pp. 1196-1206
Open Access | Times Cited: 21
Integrative analyses prioritize GNL3 as a risk gene for bipolar disorder
Qingtuan Meng, Le Wang, Rujia Dai, et al.
Molecular Psychiatry (2020) Vol. 25, Iss. 11, pp. 2672-2684
Closed Access | Times Cited: 21
Page 1 - Next Page

Scroll to top