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OpenAlex Citation Counts

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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:

Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism
Neelroop Parikshak, Vivek Swarup, T. Grant Belgard, et al.
Nature (2016) Vol. 540, Iss. 7633, pp. 423-427
Open Access | Times Cited: 652

Showing 1-25 of 652 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: 2035
The functions and unique features of long intergenic non-coding RNA
Julia D. Ransohoff, Yuning Wei, Paul A. Khavari
Nature Reviews Molecular Cell Biology (2017) Vol. 19, Iss. 3, pp. 143-157
Open Access | Times Cited: 1163
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: 1069
Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
Gil Sharon, Nikki Jamie Cruz, Dae‐Wook Kang, et al.
Cell (2019) Vol. 177, Iss. 6, pp. 1600-1618.e17
Open Access | Times Cited: 905
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: 884
Selenium Drives a Transcriptional Adaptive Program to Block Ferroptosis and Treat Stroke
Ishraq Alim, Joseph T. Caulfield, Yingxin Chen, et al.
Cell (2019) Vol. 177, Iss. 5, pp. 1262-1279.e25
Open Access | Times Cited: 789
Single-cell genomics identifies cell type–specific molecular changes in autism
Dmitry Velmeshev, Lucas Schirmer, Diane Jung, et al.
Science (2019) Vol. 364, Iss. 6441, pp. 685-689
Open Access | Times Cited: 771
Microglial signatures and their role in health and disease
Oleg Butovsky, Howard L. Weiner
Nature reviews. Neuroscience (2018) Vol. 19, Iss. 10, pp. 622-635
Open Access | Times Cited: 763
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: 396
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, et al.
Cell (2019) Vol. 178, Iss. 4, pp. 850-866.e26
Open Access | Times Cited: 396
An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms
Javier Tapial, Kevin Ha, Timothy Sterne-Weiler, et al.
Genome Research (2017) Vol. 27, Iss. 10, pp. 1759-1768
Open Access | Times Cited: 392
Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility
Towfique Raj, Yang Li, Garrett Wong, et al.
Nature Genetics (2018) Vol. 50, Iss. 11, pp. 1584-1592
Open Access | Times Cited: 382
The Role of m6A/m-RNA Methylation in Stress Response Regulation
Mareen Engel, Carola Eggert, Paul M. Kaplick, et al.
Neuron (2018) Vol. 99, Iss. 2, pp. 389-403.e9
Open Access | Times Cited: 339
Histone Acetylome-wide Association Study of Autism Spectrum Disorder
Wenjie Sun, Jérémie Poschmann, Ricardo Cruz-Herrera del Rosario, et al.
Cell (2016) Vol. 167, Iss. 5, pp. 1385-1397.e11
Open Access | Times Cited: 283
Transcriptome and epigenome landscape of human cortical development modeled in organoids
Anahita Amiri, Gianfilippo Coppola, Soraya Scuderi, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 274
Long-term maturation of human cortical organoids matches key early postnatal transitions
Aaron Gordon, Se‐Jin Yoon, Stephen Tran, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 3, pp. 331-342
Open Access | Times Cited: 271
A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles
Nancy Y. A. Sey, Benxia Hu, Won Mah, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 583-593
Open Access | Times Cited: 261
Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons
Simon T. Schafer, Apuã C.M. Paquola, Shani Stern, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 2, pp. 243-255
Open Access | Times Cited: 258
Meta-Analysis of the Alzheimer’s Disease Human Brain Transcriptome and Functional Dissection in Mouse Models
Ying‐Wooi Wan, Rami Al‐Ouran, Carl Grant Mangleburg, et al.
Cell Reports (2020) Vol. 32, Iss. 2, pp. 107908-107908
Open Access | Times Cited: 251
Cross Talk: The Microbiota and Neurodevelopmental Disorders
John R. Kelly, Chiara Minuto, John F. Cryan, et al.
Frontiers in Neuroscience (2017) Vol. 11
Open Access | Times Cited: 248
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: 240
Germline Chd8 haploinsufficiency alters brain development in mouse
Andrea Gompers, Linda Su-Feher, Jacob Ellegood, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 8, pp. 1062-1073
Open Access | Times Cited: 231
Widespread RNA editing dysregulation in brains from autistic individuals
Stephen Tran, Hyun-Ik Jun, Jae Hoon Bahn, et al.
Nature Neuroscience (2018) Vol. 22, Iss. 1, pp. 25-36
Open Access | Times Cited: 197
Synaptic and transcriptionally downregulated genes are associated with cortical thickness differences in autism
Rafael Romero-García, Varun Warrier, Edward T. Bullmore, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 7, pp. 1053-1064
Open Access | Times Cited: 186
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies
Kátia de Paiva Lopes, Gijsje J. L. Snijders, Jack Humphrey, et al.
Nature Genetics (2022) Vol. 54, Iss. 1, pp. 4-17
Open Access | Times Cited: 168
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