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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:

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

A cross-disorder dosage sensitivity map of the human genome
Ryan L. Collins, Joseph Glessner, Eleonora Porcu, et al.
Cell (2022) Vol. 185, Iss. 16, pp. 3041-3055.e25
Open Access | Times Cited: 226
seqr : A web‐based analysis and collaboration tool for rare disease genomics
Lynn Pais, Hana Snow, Ben Weisburd, et al.
Human Mutation (2022)
Open Access | Times Cited: 73
The female protective effect against autism spectrum disorder
Emilie M. Wigdor, Daniel J. Weiner, Jakob Grove, et al.
Cell Genomics (2022) Vol. 2, Iss. 6, pp. 100134-100134
Open Access | Times Cited: 72
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
Siavash Fazel Darbandi, Joon‐Yong An, Kenneth Lim, et al.
Cell Reports (2024) Vol. 43, Iss. 6, pp. 114329-114329
Open Access | Times Cited: 9
Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders
David Exposito-Alonso, Beatriz Rico
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 391-422
Closed Access | Times Cited: 28
Developmental Variability in Autism Across 17 000 Autistic Individuals and 4000 Siblings Without an Autism Diagnosis
Susan S. Kuo, Celia van der Merwe, Jack Fu, et al.
JAMA Pediatrics (2022) Vol. 176, Iss. 9, pp. 915-915
Open Access | Times Cited: 27
Novel Approaches for Treating Pediatric Psychiatric Disorders
Niki Sabetfakhri, Edwin H. Cook
Oxford University Press eBooks (2025), pp. 919-932
Closed Access
Diagnosis and Epidemiology of Pediatric Psychiatric Disorders
Magdalena Janecka, Artemis Briasouli, Vahe Khachadourian, et al.
Oxford University Press eBooks (2025), pp. 815-825
Closed Access
Tourette Syndrome and Chronic Tic Disorders
Matthew Halvorsen
Psychiatric Clinics of North America (2025)
Closed Access
CRISPR activation rescues abnormalities in SCN2A haploinsufficiency-associated autism spectrum disorder
Serena Tamura, Andrew D. Nelson, Perry W.E. Spratt, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 16
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Calwing Liao, Mariana Moysés‐Oliveira, Celine E.F. De Esch, et al.
Cell Genomics (2023) Vol. 3, Iss. 4, pp. 100277-100277
Open Access | Times Cited: 10
Autism genes converge on microtubule biology and RNA-binding proteins during excitatory neurogenesis
Nawei Sun, Noam Teyssier, Belinda Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy
Johannes Luppe, Heinrich Sticht, François Lecoquierre, et al.
European Journal of Human Genetics (2022) Vol. 31, Iss. 3, pp. 345-352
Open Access | Times Cited: 12
Dynamic proteomic and phosphoproteomic atlas of corticostriatal axons in neurodevelopment
Vasin Dumrongprechachan, Ryan Salisbury, Lindsey M. Butler, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 11
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders
Chelsea Lowther, Mana M. Mehrjouy, Ryan L. Collins, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 10
Genetics of bipolar disorder: insights into its complex architecture and biology from common and rare variants
Tomonori Hara, Yuji Owada, Atsushi Takata
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 183-191
Closed Access | Times Cited: 10
The genetics of cortical organisation and development: a study of 2,347 neuroimaging phenotypes
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 10
Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies
Chelsea Lowther, Elise Valkanas, Jessica L. Giordano, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 12
Analysis of exome sequencing data implicates rare coding variants in STAG1 and ZNF136 in schizophrenia
Sophie L. Chick, Peter Holmans, Detelina Grozeva, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Genome-wide prediction of dominant and recessive neurodevelopmental disorder risk genes
Ryan S. Dhindsa, Blake Weido, Justin Dhindsa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
A minimal role for synonymous variation in human disease
Ryan S. Dhindsa, Quanli Wang, Dimitrios Vitsios, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 6
Tissue and cell-type specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
Derek J.C. Tai, Parisa Razaz, Serkan Erdin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 5
Identification of a transcriptional signature found in multiple models of ASD and related disorders
Samuel Thudium, Katherine C. Palozola, Éloïse L'Her, et al.
Genome Research (2022) Vol. 32, Iss. 9, pp. 1642-1654
Open Access | Times Cited: 5
Physical and functional convergence of the autism risk genesScn2aandAnk2in neocortical pyramidal cell dendrites
Andrew D. Nelson, Amanda M. Catalfio, Julie M. Gupta, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
Polygenic architecture of rare coding variation across 400,000 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
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