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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:

An examination of multiple classes of rare variants in extended families with bipolar disorder
Claudio Toma, Alex D. Shaw, Richard J. N. Allcock, et al.
Translational Psychiatry (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Genetic contributions to bipolar disorder: current status and future directions
Kevin S. O’Connell, Brandon J. Coombes
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2156-2167
Open Access | Times Cited: 68
Amygdala and anterior cingulate transcriptomes from individuals with bipolar disorder reveal downregulated neuroimmune and synaptic pathways
Peter P. Zandi, Andrew E. Jaffe, Fernando S. Goes, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 3, pp. 381-389
Open Access | Times Cited: 51
The genetic etiology of eosinophilic esophagitis
Leah C. Kottyan, Sreeja Parameswaran, Matthew T. Weirauch, et al.
Journal of Allergy and Clinical Immunology (2020) Vol. 145, Iss. 1, pp. 9-15
Open Access | Times Cited: 70
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
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Claudio Toma, Kerrie D. Pierce, Alex D. Shaw, et al.
PLoS Genetics (2018) Vol. 14, Iss. 12, pp. e1007535-e1007535
Open Access | Times Cited: 41
Missing a beat
Michael J. McCarthy
Psychiatric Genetics (2018) Vol. 29, Iss. 2, pp. 29-36
Closed Access | Times Cited: 40
Heterogeneity analysis provides evidence for a genetically homogeneous subtype of bipolar-disorder
Caroline C. McGrouther, Aaditya V. Rangan, Arianna Di Florio, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0314288-e0314288
Open Access
Genetic Variation across Phenotypic Severity of Autism
Claudio Toma
Trends in Genetics (2020) Vol. 36, Iss. 4, pp. 228-231
Open Access | Times Cited: 28
Genomic and neuroimaging approaches to bipolar disorder
Mojtaba Oraki Kohshour, Sergi Papiol, Christopher R. K. Ching, et al.
BJPsych Open (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 18
De novo variation in bipolar disorder
Fernando S. Goes, Mehdi Pirooznia, Martin Tehan, et al.
Molecular Psychiatry (2019) Vol. 26, Iss. 8, pp. 4127-4136
Closed Access | Times Cited: 28
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes
Bàrbara Torrico, Alex D. Shaw, Roberto Mosca, et al.
Journal of Psychiatry and Neuroscience (2019) Vol. 44, Iss. 5, pp. 350-359
Open Access | Times Cited: 27
Anorexia nervosa is associated with Neuronatin variants
Laura Lombardi, Corinne Blanchet, Karine Poirier, et al.
Psychiatric Genetics (2019) Vol. 29, Iss. 4, pp. 103-110
Closed Access | Times Cited: 23
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Xiaoming Jia, Fernando S. Goes, Adam E. Locke, et al.
Molecular Psychiatry (2021) Vol. 26, Iss. 9, pp. 5239-5250
Open Access | Times Cited: 20
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder
Sonia Hesam-Shariati, Bronwyn J. Overs, Gloria Roberts, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 11
Neurotransmission-related gene expression in the frontal pole is altered in subjects with bipolar disorder and schizophrenia
Adriana Medina, Megan Hastings Hagenauer, David M. Krolewski, et al.
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 6
Cholesterol alterations in fragile X syndrome, autism spectrum disorders and other neurodevelopmental disorders
Sérine Benachenhou, Asma Laroui, Olivier Dionne, et al.
International review of neurobiology (2023), pp. 115-139
Closed Access | Times Cited: 6
De Novo Gene Variants and Familial Bipolar Disorder
Claudio Toma, Alex D. Shaw, Bronwyn J. Overs, et al.
JAMA Network Open (2020) Vol. 3, Iss. 5, pp. e203382-e203382
Open Access | Times Cited: 15
dbBIP: a comprehensive bipolar disorder database for genetic research
Xiaoyan Li, Shunshuai Ma, Wenhui Yan, et al.
Database (2022) Vol. 2022
Open Access | Times Cited: 8
Progress and Implications from Genetic Studies of Bipolar Disorder
Lingzhuo Kong, Yiqing Chen, Yuting Shen, et al.
Neuroscience Bulletin (2024) Vol. 40, Iss. 8, pp. 1160-1172
Closed Access | Times Cited: 1
Human-Induced Pluripotent Stem Cell (iPSC)-Derived GABAergic Neuron Differentiation in Bipolar Disorder
Daniel J. Schill, Durga Attili, Cynthia J. DeLong, et al.
Cells (2024) Vol. 13, Iss. 14, pp. 1194-1194
Open Access | Times Cited: 1
Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorder
Naushaba Hasin, Lace M. Riggs, Tatyana Shekhtman, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 9, pp. 3842-3856
Open Access | Times Cited: 7
Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer
Claudio Toma, Marcos Díaz‐Gay, Sebastià Franch‐Expósito, et al.
International Journal of Cancer (2019) Vol. 146, Iss. 6, pp. 1568-1577
Open Access | Times Cited: 9
CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations
Hojka Gregorič Kumperščak, Danijela Krgović, Maja Drobnič Radobuljac, et al.
Frontiers in Psychiatry (2021) Vol. 11
Open Access | Times Cited: 8
Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder
Guang Yang, H. M. Arif Ullah, Ethan Parker, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 6, pp. 2525-2539
Open Access | Times Cited: 3
Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome
Elisa Courtois, Mark Schmid, Orly Wajsbrot, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 8
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