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 road to precision psychiatry: translating genetics into disease mechanisms
Michael J. Gandal, Virpi Leppä, Hyejung Won, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1397-1407
Open Access | Times Cited: 215

Showing 1-25 of 215 citing articles:

Brain charts for the human lifespan
Richard A.I. Bethlehem, Jakob Seidlitz, Simon R. White, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 525-533
Open Access | Times Cited: 1124
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: 1080
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap
Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, et al.
Science (2018) Vol. 359, Iss. 6376, pp. 693-697
Open Access | Times Cited: 957
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: 479
Autism genetics: opportunities and challenges for clinical translation
Jacob Vorstman, Jeremy Parr, Daniel Moreno‐De‐Luca, et al.
Nature Reviews Genetics (2017) Vol. 18, Iss. 6, pp. 362-376
Open Access | Times Cited: 415
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan, Daniel H. Geschwind
Cell (2019) Vol. 177, Iss. 1, pp. 162-183
Open Access | Times Cited: 400
Psychiatric genetics and the structure of psychopathology
Jordan W. Smoller, Ole A. Andreassen, Howard J. Edenberg, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 3, pp. 409-420
Open Access | Times Cited: 360
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
Naomi R. Wray, Cisca Wijmenga, Patrick F. Sullivan, et al.
Cell (2018) Vol. 173, Iss. 7, pp. 1573-1580
Open Access | Times Cited: 292
From Basic Science to Clinical Application of Polygenic Risk Scores
Naomi R. Wray, Tian Lin, Jehannine Austin, et al.
JAMA Psychiatry (2020) Vol. 78, Iss. 1, pp. 101-101
Closed Access | Times Cited: 284
Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms
Rebecca L. Walker, Gokul Ramaswami, Christopher Hartl, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 750-771.e22
Open Access | Times Cited: 243
Could Polygenic Risk Scores Be Useful in Psychiatry?
Graham K. Murray, Tian Lin, Jehannine Austin, et al.
JAMA Psychiatry (2020) Vol. 78, Iss. 2, pp. 210-210
Closed Access | Times Cited: 226
Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap
Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, et al.
FOCUS The Journal of Lifelong Learning in Psychiatry (2019) Vol. 17, Iss. 1, pp. 66-72
Open Access | Times Cited: 208
The polygenic architecture of schizophrenia — rethinking pathogenesis and nosology
Olav B. Smeland, Oleksandr Frei, Anders M. Dale, et al.
Nature Reviews Neurology (2020) Vol. 16, Iss. 7, pp. 366-379
Closed Access | Times Cited: 163
Twelve years of GWAS discoveries for osteoporosis and related traits: advances, challenges and applications
Xiaowei Zhu, Wei-Yang Bai, Hou‐Feng Zheng
Bone Research (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 145
Discovery and implications of polygenicity of common diseases
Peter M. Visscher, Loïc Yengo, Nancy J. Cox, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1468-1473
Open Access | Times Cited: 130
Single-cell genomics and regulatory networks for 388 human brains
Prashant S. Emani, Jason Liu, Declan Clarke, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 43
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 19
3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders
Chun‐Ting Lee, Raphael M. Bendriem, Wells W. Wu, et al.
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 155
Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome
Kiran Girdhar, Gabriel E. Hoffman, Yan Jiang, et al.
Nature Neuroscience (2018) Vol. 21, Iss. 8, pp. 1126-1136
Open Access | Times Cited: 138
Translating genome-wide association findings into new therapeutics for psychiatry
Gerome Breen, Qingqin S. Li, Bryan L. Roth, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1392-1396
Open Access | Times Cited: 126
Risk factors and peripheral biomarkers for schizophrenia spectrum disorders: an umbrella review of meta‐analyses
Lazaros Belbasis, Cristiano A. Köhler, Nikos C. Stefanis, et al.
Acta Psychiatrica Scandinavica (2017) Vol. 137, Iss. 2, pp. 88-97
Open Access | Times Cited: 125
Redefining phenotypes to advance psychiatric genetics: Implications from hierarchical taxonomy of psychopathology.
Monika A. Waszczuk, Nicholas R. Eaton, Robert F. Krueger, et al.
Journal of Abnormal Psychology (2019) Vol. 129, Iss. 2, pp. 143-161
Open Access | Times Cited: 123
Precision Psychiatry Applications with Pharmacogenomics: Artificial Intelligence and Machine Learning Approaches
Eugene Lin, Chieh‐Hsin Lin, Hsien‐Yuan Lane
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 3, pp. 969-969
Open Access | Times Cited: 121
A framework for the investigation of rare genetic disorders in neuropsychiatry
Stephan Sanders, Mustafa Şahin, Joseph Hostyk, et al.
Nature Medicine (2019) Vol. 25, Iss. 10, pp. 1477-1487
Open Access | Times Cited: 116
Polygenic risk score increases schizophrenia liability through cognition-relevant pathways
Timothea Toulopoulou, Xiaowei Zhang, Stacey S. Cherny, et al.
Brain (2018) Vol. 142, Iss. 2, pp. 471-485
Open Access | Times Cited: 93
Page 1 - Next Page

Scroll to top