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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:

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies, Christian R. Marshall, Susan Walker, et al.
JAMA (2015) Vol. 314, Iss. 9, pp. 895-895
Closed Access | Times Cited: 406

Showing 1-25 of 406 citing articles:

Identification, Evaluation, and Management of Children With Autism Spectrum Disorder
Susan Hyman, Susan E. Levy, Scott M. Myers, et al.
PEDIATRICS (2019) Vol. 145, Iss. 1
Open Access | Times Cited: 1169
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K. C. Yuen, Daniele Merico, Matt Bookman, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 4, pp. 602-611
Open Access | Times Cited: 825
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Siddharth Srivastava, Jamie Love‐Nichols, Kira A. Dies, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 11, pp. 2413-2421
Open Access | Times Cited: 536
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M. Clark, Zornitza Stark, Lauge Farnaes, et al.
npj Genomic Medicine (2018) Vol. 3, Iss. 1
Open Access | Times Cited: 519
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Anath C. Lionel, Gregory Costain, Nasim Monfared, et al.
Genetics in Medicine (2017) Vol. 20, Iss. 4, pp. 435-443
Open Access | Times Cited: 490
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Kandamurugu Manickam, Monica R. McClain, Laurie Demmer, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2029-2037
Open Access | Times Cited: 408
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: 399
Neurodevelopmental disorders—the history and future of a diagnostic concept
Deborah J. Morris‐Rosendahl, Marc-Antoine Crocq
Dialogues in Clinical Neuroscience (2020) Vol. 22, Iss. 1, pp. 65-72
Open Access | Times Cited: 326
Genome-wide characteristics of de novo mutations in autism
Ryan K. C. Yuen, Daniele Merico, Hongzhi Cao, et al.
npj Genomic Medicine (2016) Vol. 1, Iss. 1
Open Access | Times Cited: 218
The road to precision psychiatry: translating genetics into disease mechanisms
Michael J. Gandal, Virpi Leppä, Hyejung Won, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1397-1407
Open Access | Times Cited: 215
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: 215
Environmental factors in the development of autism spectrum disorders
Leanna Sealey, Brandon W. Hughes, Ahila N. Sriskanda, et al.
Environment International (2016) Vol. 88, pp. 288-298
Closed Access | Times Cited: 203
Clinical and Molecular Characteristics of Mitochondrial Dysfunction in Autism Spectrum Disorder
Shannon Rose, Dmitriy Niyazov, Daniel A. Rossignol, et al.
Molecular Diagnosis & Therapy (2018) Vol. 22, Iss. 5, pp. 571-593
Open Access | Times Cited: 201
Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD)
Ann Genovese, Merlin G. Butler
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 13, pp. 4726-4726
Open Access | Times Cited: 201
Artificial intelligence for precision medicine in neurodevelopmental disorders
Mohammed Uddin, Yujiang Wang, Marc Woodbury‐Smith
npj Digital Medicine (2019) Vol. 2, Iss. 1
Open Access | Times Cited: 196
Genome-wide detection of tandem DNA repeats that are expanded in autism
Brett Trost, Worrawat Engchuan, Charlotte Nguyen, et al.
Nature (2020) Vol. 586, Iss. 7827, pp. 80-86
Open Access | Times Cited: 196
Genetics of autism spectrum disorder
Gokul Ramaswami, Daniel H. Geschwind
Handbook of clinical neurology (2018), pp. 321-329
Open Access | Times Cited: 182
Evidence-based support for autistic people across the lifespan: maximising potential, minimising barriers, and optimising the person–environment fit
Meng‐Chuan Lai, Evdokia Anagnostou, Max Wiznitzer, et al.
The Lancet Neurology (2020) Vol. 19, Iss. 5, pp. 434-451
Closed Access | Times Cited: 180
Clinical genetics of craniosynostosis
Andrew O.M. Wilkie, David Johnson, Steven A. Wall
Current Opinion in Pediatrics (2017) Vol. 29, Iss. 6, pp. 622-628
Open Access | Times Cited: 178
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: 157
Emerging biomarkers in autism spectrum disorder: a systematic review
Richard E. Frye, Sarah Vassall, Gurjot Kaur, et al.
Annals of Translational Medicine (2019) Vol. 7, Iss. 23, pp. 792-792
Open Access | Times Cited: 154
Genetic Testing in Neurodevelopmental Disorders
Juliann M. Savatt, Scott M. Myers
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 152
The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations
Ann Genovese, Merlin G. Butler
Genes (2023) Vol. 14, Iss. 3, pp. 677-677
Open Access | Times Cited: 104
The Genetic Architecture of Congenital Diarrhea and Enteropathy
Zeenat Gaibee, Neil Warner, Katlynn Bugda Gwilt, et al.
New England Journal of Medicine (2025) Vol. 392, Iss. 13, pp. 1297-1309
Closed Access | Times Cited: 2
Progress in the genetics of autism spectrum disorder
Marc Woodbury‐Smith, Stephen W. Scherer
Developmental Medicine & Child Neurology (2018) Vol. 60, Iss. 5, pp. 445-451
Open Access | Times Cited: 157
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