
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:
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, et al.
Nature Genetics (2018) Vol. 50, Iss. 3, pp. 381-389
Open Access | Times Cited: 1528
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, et al.
Nature Genetics (2018) Vol. 50, Iss. 3, pp. 381-389
Open Access | Times Cited: 1528
Showing 1-25 of 1528 citing articles:
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove, Stephan Ripke, Thomas D. Als, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 431-444
Open Access | Times Cited: 2051
Jakob Grove, Stephan Ripke, Thomas D. Als, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 431-444
Open Access | Times Cited: 2051
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 502-508
Open Access | Times Cited: 1799
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 502-508
Open Access | Times Cited: 1799
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Niamh Mullins, Andreas J. Forstner, Kevin S. O’Connell, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 817-829
Open Access | Times Cited: 1097
Niamh Mullins, Andreas J. Forstner, Kevin S. O’Connell, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 817-829
Open Access | Times Cited: 1097
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Michael J. Gandal, Pan Zhang, Evi Hadjimichael, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 1076
Michael J. Gandal, Pan Zhang, Evi Hadjimichael, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 1076
Comprehensive functional genomic resource and integrative model for the human brain
Daifeng Wang, Shuang Liu, Jonathan Warrell, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 887
Daifeng Wang, Shuang Liu, Jonathan Warrell, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 887
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse
Frank Koopmans, Pim van Nierop, Maria Andres‐Alonso, et al.
Neuron (2019) Vol. 103, Iss. 2, pp. 217-234.e4
Open Access | Times Cited: 782
Frank Koopmans, Pim van Nierop, Maria Andres‐Alonso, et al.
Neuron (2019) Vol. 103, Iss. 2, pp. 217-234.e4
Open Access | Times Cited: 782
Transcriptome-scale spatial gene expression in the human dorsolateral prefrontal cortex
Kristen R. Maynard, Leonardo Collado‐Torres, Lukas M. Weber, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 3, pp. 425-436
Open Access | Times Cited: 769
Kristen R. Maynard, Leonardo Collado‐Torres, Lukas M. Weber, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 3, pp. 425-436
Open Access | Times Cited: 769
The genetic architecture of the human cerebral cortex
Katrina L. Grasby, Neda Jahanshad, Jodie N. Painter, et al.
Science (2020) Vol. 367, Iss. 6484
Open Access | Times Cited: 717
Katrina L. Grasby, Neda Jahanshad, Jodie N. Painter, et al.
Science (2020) Vol. 367, Iss. 6484
Open Access | Times Cited: 717
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 707
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 707
Brain cell type–specific enhancer–promoter interactome maps and disease - risk association
Alexi Nott, Inge R. Holtman, Nicole G. Coufal, et al.
Science (2019) Vol. 366, Iss. 6469, pp. 1134-1139
Open Access | Times Cited: 611
Alexi Nott, Inge R. Holtman, Nicole G. Coufal, et al.
Science (2019) Vol. 366, Iss. 6469, pp. 1134-1139
Open Access | Times Cited: 611
Genetic identification of brain cell types underlying schizophrenia
Nathan Skene, Julien Bryois, Trygve E. Bakken, et al.
Nature Genetics (2018) Vol. 50, Iss. 6, pp. 825-833
Open Access | Times Cited: 586
Nathan Skene, Julien Bryois, Trygve E. Bakken, et al.
Nature Genetics (2018) Vol. 50, Iss. 6, pp. 825-833
Open Access | Times Cited: 586
Comparative genetic architectures of schizophrenia in East Asian and European populations
Max Lam, Chia‐Yen Chen, Zhiqiang Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1670-1678
Open Access | Times Cited: 580
Max Lam, Chia‐Yen Chen, Zhiqiang Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1670-1678
Open Access | Times Cited: 580
Brain organoids: advances, applications and challenges
Xuyu Qian, Hongjun Song, Guo‐li Ming
Development (2019) Vol. 146, Iss. 8
Open Access | Times Cited: 544
Xuyu Qian, Hongjun Song, Guo‐li Ming
Development (2019) Vol. 146, Iss. 8
Open Access | Times Cited: 544
Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study
Robyn E. Wootton, Rebecca C. Richmond, Bobby Stuijfzand, et al.
Psychological Medicine (2019) Vol. 50, Iss. 14, pp. 2435-2443
Open Access | Times Cited: 489
Robyn E. Wootton, Rebecca C. Richmond, Bobby Stuijfzand, et al.
Psychological Medicine (2019) Vol. 50, Iss. 14, pp. 2435-2443
Open Access | Times Cited: 489
A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation
Damon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, et al.
Neuron (2019) Vol. 103, Iss. 5, pp. 785-801.e8
Open Access | Times Cited: 475
Damon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, et al.
Neuron (2019) Vol. 103, Iss. 5, pp. 785-801.e8
Open Access | Times Cited: 475
Single-nucleus chromatin accessibility and transcriptomic characterization of Alzheimer’s disease
Samuel Morabito, Emily Miyoshi, Neethu Michael, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1143-1155
Open Access | Times Cited: 458
Samuel Morabito, Emily Miyoshi, Neethu Michael, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1143-1155
Open Access | Times Cited: 458
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, et al.
Nature Genetics (2023) Vol. 55, Iss. 2, pp. 198-208
Open Access | Times Cited: 380
Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, et al.
Nature Genetics (2023) Vol. 55, Iss. 2, pp. 198-208
Open Access | Times Cited: 380
Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior
Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard, et al.
Science (2019) Vol. 365, Iss. 6456
Open Access | Times Cited: 360
Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard, et al.
Science (2019) Vol. 365, Iss. 6456
Open Access | Times Cited: 360
Human CNS barrier-forming organoids with cerebrospinal fluid production
Laura Pellegrini, Claudia Bonfio, Jessica Chadwick, et al.
Science (2020) Vol. 369, Iss. 6500
Open Access | Times Cited: 353
Laura Pellegrini, Claudia Bonfio, Jessica Chadwick, et al.
Science (2020) Vol. 369, Iss. 6500
Open Access | Times Cited: 353
Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia
Stephan Ripke, James Walters, Michael O’Donovan
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 318
Stephan Ripke, James Walters, Michael O’Donovan
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 318
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions
Solveig K. Sieberts, Thanneer M. Perumal, Minerva M. Carrasquillo, et al.
Scientific Data (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 315
Solveig K. Sieberts, Thanneer M. Perumal, Minerva M. Carrasquillo, et al.
Scientific Data (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 315
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 307
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 307
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Mari Niemi, Hilary C. Martin, Daniel L Rice, et al.
Nature (2018) Vol. 562, Iss. 7726, pp. 268-271
Open Access | Times Cited: 300
Mari Niemi, Hilary C. Martin, Daniel L Rice, et al.
Nature (2018) Vol. 562, Iss. 7726, pp. 268-271
Open Access | Times Cited: 300
Cortical patterning of abnormal morphometric similarity in psychosis is associated with brain expression of schizophrenia-related genes
Sarah E. Morgan, Jakob Seidlitz, Kirstie Whitaker, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 19, pp. 9604-9609
Open Access | Times Cited: 298
Sarah E. Morgan, Jakob Seidlitz, Kirstie Whitaker, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 19, pp. 9604-9609
Open Access | Times Cited: 298
A large-scale genome-wide association study meta-analysis of cannabis use disorder
Emma C. Johnson, Ditte Demontis, Thorgeir E. Thorgeirsson, et al.
The Lancet Psychiatry (2020) Vol. 7, Iss. 12, pp. 1032-1045
Open Access | Times Cited: 297
Emma C. Johnson, Ditte Demontis, Thorgeir E. Thorgeirsson, et al.
The Lancet Psychiatry (2020) Vol. 7, Iss. 12, pp. 1032-1045
Open Access | Times Cited: 297