
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:
A screen of 1,049 schizophrenia and 30 Alzheimer's‐associated variants for regulatory potential
Leslie Myint, Ruihua Wang, Leandros Boukas, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2019) Vol. 183, Iss. 1, pp. 61-73
Open Access | Times Cited: 44
Leslie Myint, Ruihua Wang, Leandros Boukas, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2019) Vol. 183, Iss. 1, pp. 61-73
Open Access | Times Cited: 44
Showing 1-25 of 44 citing articles:
Linear models enable powerful differential activity analysis in massively parallel reporter assays
Leslie Myint, Dimitrios Avramopoulos, Loyal A. Goff, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 378
Leslie Myint, Dimitrios Avramopoulos, Loyal A. Goff, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 378
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 24
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 24
Genetic insights into immune mechanisms of Alzheimer’s and Parkinson’s disease
Alexi Nott, Inge R. Holtman
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 20
Alexi Nott, Inge R. Holtman
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 20
Functional characterization of human genomic variation linked to polygenic diseases
Tania Fabo, Paul A. Khavari
Trends in Genetics (2023) Vol. 39, Iss. 6, pp. 462-490
Open Access | Times Cited: 19
Tania Fabo, Paul A. Khavari
Trends in Genetics (2023) Vol. 39, Iss. 6, pp. 462-490
Open Access | Times Cited: 19
Massively parallel techniques for cataloguing the regulome of the human brain
Kayla G. Townsley, Kristen Brennand, Laura M. Huckins
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1509-1521
Open Access | Times Cited: 49
Kayla G. Townsley, Kristen Brennand, Laura M. Huckins
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1509-1521
Open Access | Times Cited: 49
Massively Parallel Reporter Assays: Defining Functional Psychiatric Genetic Variants Across Biological Contexts
Bernard Mulvey, Tomás Lagunas, Joseph D. Dougherty
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 76-89
Open Access | Times Cited: 44
Bernard Mulvey, Tomás Lagunas, Joseph D. Dougherty
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 76-89
Open Access | Times Cited: 44
Focus on your locus with a massively parallel reporter assay
Jessica C. McAfee, Jessica Bell, Oleh Krupa, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 24
Jessica C. McAfee, Jessica Bell, Oleh Krupa, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 24
ω-3PUFAs Improve Cognitive Impairments Through Ser133 Phosphorylation of CREB Upregulating BDNF/TrkB Signal in Schizophrenia
Cuiping Guo, Yi Liu, Maosheng Fang, et al.
Neurotherapeutics (2020) Vol. 17, Iss. 3, pp. 1271-1286
Open Access | Times Cited: 35
Cuiping Guo, Yi Liu, Maosheng Fang, et al.
Neurotherapeutics (2020) Vol. 17, Iss. 3, pp. 1271-1286
Open Access | Times Cited: 35
High-throughput assays to assess variant effects on disease
Kaiyue Ma, L. Gauthier, Frances Cheung, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 4
Kaiyue Ma, L. Gauthier, Frances Cheung, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 4
An in vivo systemic massively parallel platform for deciphering animal tissue-specific regulatory function
Ashley R. Brown, Grant A Fox, Irene M. Kaplow, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Ashley R. Brown, Grant A Fox, Irene M. Kaplow, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Methods for Functional Characterization of Genetic Polymorphisms of Non-Coding Regulatory Regions of the Human Genome
А. Н. Уварова, Е А Ткаченко, Ekaterina M. Stasevich, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 6, pp. 1002-1013
Open Access | Times Cited: 3
А. Н. Уварова, Е А Ткаченко, Ekaterina M. Stasevich, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 6, pp. 1002-1013
Open Access | Times Cited: 3
Transcriptional-regulatory convergence across functional MDD risk variants identified by massively parallel reporter assays
Bernard Mulvey, Joseph D. Dougherty
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 17
Bernard Mulvey, Joseph D. Dougherty
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 17
DeepPerVar: a multi-modal deep learning framework for functional interpretation of genetic variants in personal genome
Ye Wang, Li Chen
Bioinformatics (2022) Vol. 38, Iss. 24, pp. 5340-5351
Open Access | Times Cited: 12
Ye Wang, Li Chen
Bioinformatics (2022) Vol. 38, Iss. 24, pp. 5340-5351
Open Access | Times Cited: 12
Just a SNP Away: The Future of in vivo Massively Parallel Reporter Assay
Katherine Degner, Jessica Bell, Sean D Jones, et al.
Cell Insight (2024) Vol. 4, Iss. 1, pp. 100214-100214
Open Access | Times Cited: 2
Katherine Degner, Jessica Bell, Sean D Jones, et al.
Cell Insight (2024) Vol. 4, Iss. 1, pp. 100214-100214
Open Access | Times Cited: 2
A functional schizophrenia-associated genetic variant near the TSNARE1 and ADGRB1 genes
Marah H. Wahbeh, Rachel J. Boyd, Christian Yovo, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100303-100303
Open Access | Times Cited: 2
Marah H. Wahbeh, Rachel J. Boyd, Christian Yovo, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100303-100303
Open Access | Times Cited: 2
Modeling common and rare genetic risk factors of neuropsychiatric disorders in human induced pluripotent stem cells
Abdurrahman W. Muhtaseb, Jubao Duan
Schizophrenia Research (2022)
Open Access | Times Cited: 9
Abdurrahman W. Muhtaseb, Jubao Duan
Schizophrenia Research (2022)
Open Access | Times Cited: 9
Using Stem Cell Models to Explore the Genetics Underlying Psychiatric Disorders: Linking Risk Variants, Genes, and Biology in Brain Disease
Kristen Brennand
American Journal of Psychiatry (2022) Vol. 179, Iss. 5, pp. 322-328
Closed Access | Times Cited: 8
Kristen Brennand
American Journal of Psychiatry (2022) Vol. 179, Iss. 5, pp. 322-328
Closed Access | Times Cited: 8
Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
Alex M. Casella, Carlo Colantuoni, Seth A. Ament
PLoS Computational Biology (2022) Vol. 18, Iss. 9, pp. e1010430-e1010430
Open Access | Times Cited: 8
Alex M. Casella, Carlo Colantuoni, Seth A. Ament
PLoS Computational Biology (2022) Vol. 18, Iss. 9, pp. e1010430-e1010430
Open Access | Times Cited: 8
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 8
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 8
Excitatory Neurons Derived from Human-Induced Pluripotent Stem Cells Show Transcriptomic Differences in Alzheimer’s Patients from Controls
Ram Sagar, Ioannis Azoidis, Cristina Zivko, et al.
Cells (2023) Vol. 12, Iss. 15, pp. 1990-1990
Open Access | Times Cited: 4
Ram Sagar, Ioannis Azoidis, Cristina Zivko, et al.
Cells (2023) Vol. 12, Iss. 15, pp. 1990-1990
Open Access | Times Cited: 4
Multiplexed functional genomic assays to decipher the noncoding genome
Yonatan A. Cooper, Qiuyu Guo, Daniel H. Geschwind
Human Molecular Genetics (2022) Vol. 31, Iss. R1, pp. R84-R96
Open Access | Times Cited: 7
Yonatan A. Cooper, Qiuyu Guo, Daniel H. Geschwind
Human Molecular Genetics (2022) Vol. 31, Iss. R1, pp. R84-R96
Open Access | Times Cited: 7
Identification, Design, and Application of Noncoding Cis-Regulatory Elements
Lingna Xu, Yuwen Liu
Biomolecules (2024) Vol. 14, Iss. 8, pp. 945-945
Open Access | Times Cited: 1
Lingna Xu, Yuwen Liu
Biomolecules (2024) Vol. 14, Iss. 8, pp. 945-945
Open Access | Times Cited: 1
WEVar: a novel statistical learning framework for predicting noncoding regulatory variants
Ye Wang, Yuchao Jiang, Bing Yao, et al.
Briefings in Bioinformatics (2021) Vol. 22, Iss. 6
Open Access | Times Cited: 8
Ye Wang, Yuchao Jiang, Bing Yao, et al.
Briefings in Bioinformatics (2021) Vol. 22, Iss. 6
Open Access | Times Cited: 8
The Genetics of Coronary Artery Disease: A Vascular Perspective
Leon N. K. Quaye, Catherine E. Dalzell, Panos Deloukas, et al.
Cells (2023) Vol. 12, Iss. 18, pp. 2232-2232
Open Access | Times Cited: 3
Leon N. K. Quaye, Catherine E. Dalzell, Panos Deloukas, et al.
Cells (2023) Vol. 12, Iss. 18, pp. 2232-2232
Open Access | Times Cited: 3
PALM: a powerful and adaptive latent model for prioritizing risk variants with functional annotations
Xinyi Yu, Jiashun Xiao, Mingxuan Cai, et al.
Bioinformatics (2023) Vol. 39, Iss. 2
Open Access | Times Cited: 2
Xinyi Yu, Jiashun Xiao, Mingxuan Cai, et al.
Bioinformatics (2023) Vol. 39, Iss. 2
Open Access | Times Cited: 2