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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:

SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
Pamela Feliciano, Amy M. Daniels, LeeAnne Green Snyder, et al.
Neuron (2018) Vol. 97, Iss. 3, pp. 488-493
Open Access | Times Cited: 395

Showing 1-25 of 395 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: 2051
Big data approaches to decomposing heterogeneity across the autism spectrum
Michael Lombardo, Meng‐Chuan Lai, Simon Baron‐Cohen
Molecular Psychiatry (2019) Vol. 24, Iss. 10, pp. 1435-1450
Open Access | Times Cited: 410
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: 399
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1320-1331
Open Access | Times Cited: 360
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1305-1319
Open Access | Times Cited: 261
Getting to the Cores of Autism
Lilia M. Iakoucheva, Alysson R. Muotri, Jonathan Sebat
Cell (2019) Vol. 178, Iss. 6, pp. 1287-1298
Open Access | Times Cited: 229
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
Pamela Feliciano, Xueya Zhou, Irina Astrovskaya, et al.
npj Genomic Medicine (2019) Vol. 4, Iss. 1
Open Access | Times Cited: 214
Is Motor Impairment in Autism Spectrum Disorder Distinct From Developmental Coordination Disorder? A Report From the SPARK Study
Anjana Bhat
Physical Therapy (2019) Vol. 100, Iss. 4, pp. 633-644
Open Access | Times Cited: 209
A Saturation Mutagenesis Approach to Understanding PTEN Lipid Phosphatase Activity and Genotype-Phenotype Relationships
Taylor L. Mighell, Sara Evans-Dutson, Brian J. O’Roak
The American Journal of Human Genetics (2018) Vol. 102, Iss. 5, pp. 943-955
Open Access | Times Cited: 186
Motor Impairment Increases in Children With Autism Spectrum Disorder as a Function of Social Communication, Cognitive and Functional Impairment, Repetitive Behavior Severity, and Comorbid Diagnoses: A SPARK Study Report
Anjana Bhat
Autism Research (2020) Vol. 14, Iss. 1, pp. 202-219
Open Access | Times Cited: 177
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 166
Gene–environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach
Varun Warrier, Alex S. F. Kwong, Mannan Luo, et al.
The Lancet Psychiatry (2021) Vol. 8, Iss. 5, pp. 373-386
Open Access | Times Cited: 160
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, et al.
Cell (2022) Vol. 185, Iss. 23, pp. 4409-4427.e18
Open Access | Times Cited: 155
Brief Report: Impact of COVID-19 on Individuals with ASD and Their Caregivers: A Perspective from the SPARK Cohort
L. Casey White, Kiely Law, Amy M. Daniels, et al.
Journal of Autism and Developmental Disorders (2021) Vol. 51, Iss. 10, pp. 3766-3773
Open Access | Times Cited: 145
Toward Neurosubtypes in Autism
Seok‐Jun Hong, Joshua T Vogelstein, Alessandro Gozzi, et al.
Biological Psychiatry (2020) Vol. 88, Iss. 1, pp. 111-128
Open Access | Times Cited: 141
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder
Helen Rankin Willsey, A. Jeremy Willsey, Belinda Wang, et al.
Nature reviews. Neuroscience (2022) Vol. 23, Iss. 6, pp. 323-341
Open Access | Times Cited: 140
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Danny Antaki, James P. Guevara, Adam X. Maihofer, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1284-1292
Open Access | Times Cited: 137
Recent ultra-rare inherited variants implicate new autism candidate risk genes
Amy B. Wilfert, Tychele N. Turner, Shwetha C. Murali, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1125-1134
Open Access | Times Cited: 108
Genetic correlates of phenotypic heterogeneity in autism
Varun Warrier, Xinhe Zhang, Patrick Reed, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1293-1304
Open Access | Times Cited: 103
Comorbidities in autism spectrum disorder and their etiologies
Vahe Khachadourian, Behrang Mahjani, Sven Sandin, et al.
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 100
Molecular and network-level mechanisms explaining individual differences in autism spectrum disorder
A. Buch, Petra E. Vértes, Jakob Seidlitz, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 4, pp. 650-663
Open Access | Times Cited: 82
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
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1483-1493
Open Access | Times Cited: 44
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature (2024) Vol. 632, Iss. 8026, pp. 832-840
Open Access | Times Cited: 28
Interpreting polygenic score effects in sibling analysis
Jason M. Fletcher, Yuchang Wu, Tianchang Li, et al.
PLoS ONE (2024) Vol. 19, Iss. 2, pp. e0282212-e0282212
Open Access | Times Cited: 21
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