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:

Reverse GWAS: Using genetics to identify and model phenotypic subtypes
Andy Dahl, Na Cai, Arthur Ko, et al.
PLoS Genetics (2019) Vol. 15, Iss. 4, pp. e1008009-e1008009
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Reviewing the genetics of heterogeneity in depression: operationalizations, manifestations and etiologies
Na Cai, Karmel W. Choi, Eiko I. Fried
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R10-R18
Open Access | Times Cited: 133
Advances in asthma and allergic disease genetics: Is bigger always better?
Nathan Schoettler, Elke Rodríguez, Stephan Weidinger, et al.
Journal of Allergy and Clinical Immunology (2019) Vol. 144, Iss. 6, pp. 1495-1506
Open Access | Times Cited: 82
A Robust Method Uncovers Significant Context-Specific Heritability in Diverse Complex Traits
Andy Dahl, Khiem Nguyen, Na Cai, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 1, pp. 71-91
Open Access | Times Cited: 74
Open problems in human trait genetics
Nadav Brandes, Omer Weissbrod, Michal Linial
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 63
Mendelian randomization highlights significant difference and genetic heterogeneity in clinically diagnosed Alzheimer’s disease GWAS and self-report proxy phenotype GWAX
Haijie Liu, Yang Hu, Yan Zhang, et al.
Alzheimer s Research & Therapy (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 38
Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder
Andrew Dahl, Michael Thompson, Ulzee An, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2082-2093
Open Access | Times Cited: 23
A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context
Apolline Gallois, Joel Mefford, Arthur Ko, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 67
Emerging phenotyping strategies will advance our understanding of psychiatric genetics
Sandra Sanchez‐Roige, Abraham A. Palmer
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 475-480
Open Access | Times Cited: 64
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Adam X. Maihofer, Karmel W. Choi, Jonathan R. I. Coleman, et al.
Biological Psychiatry (2021) Vol. 91, Iss. 7, pp. 626-636
Open Access | Times Cited: 45
Ten challenges for clinical translation in psychiatric genetics
Eske M. Derks, Jackson G. Thorp, Zachary F. Gerring
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1457-1465
Closed Access | Times Cited: 31
Transcriptome-wide association study of treatment-resistant depression and depression subtypes for drug repurposing
Chiara Fabbri, Oliver Pain, Saskia P. Hagenaars, et al.
Neuropsychopharmacology (2021) Vol. 46, Iss. 10, pp. 1821-1829
Open Access | Times Cited: 37
Genetic risk factors of ME/CFS: a critical review
Joshua J Dibble, Simon J. McGrath, Chris P. Ponting
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R117-R124
Open Access | Times Cited: 38
Red Blood Cell-Related Phenotype–Genotype Correlations in Chronic and Acute Critical Illnesses (Traumatic Brain Injury Cohort and COVID-19 Cohort)
Darya A. Kashatnikova, А. С. Грачева, Ivan V. Redkin, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 3, pp. 1239-1239
Open Access
Genetic Influences on Disease Subtypes
Andy Dahl, Noah Zaitlen
Annual Review of Genomics and Human Genetics (2020) Vol. 21, Iss. 1, pp. 413-435
Open Access | Times Cited: 32
Multitrait GWAS to connect disease variants and biological mechanisms
Hanna Julienne, Vincent Laville, Zachary R. McCaw, et al.
PLoS Genetics (2021) Vol. 17, Iss. 8, pp. e1009713-e1009713
Open Access | Times Cited: 25
Discerning asthma endotypes through comorbidity mapping
Gengjie Jia, Xue Zhong, Hae Kyung Im, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 18
Characterizing the effect of background selection on the polygenicity of brain-related traits
Frank R. Wendt, Gita A. Pathak, Cassie Overstreet, et al.
Genomics (2020) Vol. 113, Iss. 1, pp. 111-119
Open Access | Times Cited: 25
A model and test for coordinated polygenic epistasis in complex traits
Brooke Sheppard, Nadav Rappoport, Po−Ru Loh, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 15
Open Access | Times Cited: 21
Recent innovations and in-depth aspects of post-genome wide association study (Post-GWAS) to understand the genetic basis of complex phenotypes
Zahra Mortezaei, Mahmood Tavallaei
Heredity (2021) Vol. 127, Iss. 6, pp. 485-497
Open Access | Times Cited: 19
Polygenic risk modeling with latent trait-related genetic components
Matthew Aguirre, Yosuke Tanigawa, Guhan Venkataraman, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 7, pp. 1071-1081
Open Access | Times Cited: 16
Genetics and epigenetics of allergy
Ioana Agache, Cătălina Cojanu, Alexandru Laculiceanu, et al.
Current Opinion in Allergy and Clinical Immunology (2020) Vol. 20, Iss. 3, pp. 223-232
Closed Access | Times Cited: 15
Vascular Injury in the Zebrafish Tail Modulates Blood Flow and Peak Wall Shear Stress to Restore Embryonic Circular Network
Kyung In Baek, Shyr-Shea Chang, Chih‐Chiang Chang, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 6
Multitrait genetic-phenotype associations to connect disease variants and biological mechanisms
Hanna Julienne, Vincent Laville, Zachary R. McCaw, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 6
Leveraging eQTLs to identify individual-level tissue of interest for a complex trait
Arunabha Majumdar, Claudia Giambartolomei, Na Cai, et al.
PLoS Computational Biology (2021) Vol. 17, Iss. 5, pp. e1008915-e1008915
Open Access | Times Cited: 5
Disaggregating diabetes
Lauren Carruth, Sarah Chard, Heather Howard, et al.
Medicine Anthropology Theory (2019) Vol. 6, Iss. 4
Open Access | Times Cited: 5
Page 1 - Next Page

Scroll to top