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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:

De Novo Coding Variants Are Strongly Associated with Tourette Disorder
A. Jeremy Willsey, Thomas Fernandez, Dongmei Yu, et al.
Neuron (2017) Vol. 94, Iss. 3, pp. 486-499.e9
Open Access | Times Cited: 173

Showing 1-25 of 173 citing articles:

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: 401
Psychiatric genetics and the structure of psychopathology
Jordan W. Smoller, Ole A. Andreassen, Howard J. Edenberg, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 3, pp. 409-420
Open Access | Times Cited: 362
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Dongmei Yu, Jae Hoon Sul, Fotis Tsetsos, et al.
American Journal of Psychiatry (2019) Vol. 176, Iss. 3, pp. 217-227
Open Access | Times Cited: 338
Genetic Testing in Neurodevelopmental Disorders
Juliann M. Savatt, Scott M. Myers
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 152
Tourette syndrome: clinical features, pathophysiology, and treatment
Kara A. Johnson, Yulia Worbe, Kelly D. Foote, et al.
The Lancet Neurology (2022) Vol. 22, Iss. 2, pp. 147-158
Open Access | Times Cited: 80
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Alden Y. Huang, Dongmei Yu, Lea K. Davis, et al.
Neuron (2017) Vol. 94, Iss. 6, pp. 1101-1111.e7
Open Access | Times Cited: 162
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders
A. Jeremy Willsey, Montana T. Morris, Sheng Wang, et al.
Cell (2018) Vol. 174, Iss. 3, pp. 505-520
Open Access | Times Cited: 127
A framework for the investigation of rare genetic disorders in neuropsychiatry
Stephan Sanders, Mustafa Şahin, Joseph Hostyk, et al.
Nature Medicine (2019) Vol. 25, Iss. 10, pp. 1477-1487
Open Access | Times Cited: 116
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
Sheng Wang, Jeffrey D. Mandell, Yogesh Kumar, et al.
Cell Reports (2018) Vol. 24, Iss. 13, pp. 3441-3454.e12
Open Access | Times Cited: 114
Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms
Devanand S. Manoli, Matthew W. State
American Journal of Psychiatry (2021) Vol. 178, Iss. 1, pp. 30-38
Open Access | Times Cited: 103
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders
Hoang T. Nguyen, Julien Bryois, April Kim, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 97
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism
Carolina Cappi, Melody Oliphant, Zsanett Péter, et al.
Biological Psychiatry (2019) Vol. 87, Iss. 12, pp. 1035-1044
Open Access | Times Cited: 89
Physiological roles of mammalian transmembrane adenylyl cyclase isoforms
Katrina F. Ostrom, Justin LaVigne, Tarsis F. Brust, et al.
Physiological Reviews (2021) Vol. 102, Iss. 2, pp. 815-857
Open Access | Times Cited: 86
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
Margot A. Cousin, Blake A. Creighton, Keith A. Breau, et al.
Nature Genetics (2021) Vol. 53, Iss. 7, pp. 1006-1021
Open Access | Times Cited: 75
European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part I: assessment
Natalia Szejko, Sally Robinson, Andreas Hartmann, et al.
European Child & Adolescent Psychiatry (2021) Vol. 31, Iss. 3, pp. 383-402
Open Access | Times Cited: 72
Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants
Matthew Halvorsen, Jack Samuels, Ying Wang, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 8, pp. 1071-1076
Closed Access | Times Cited: 66
Protein phosphatase 2A – structure, function and role in neurodevelopmental disorders
Priyanka Sandal, Chian Ju Jong, Ronald A. Merrill, et al.
Journal of Cell Science (2021) Vol. 134, Iss. 13
Open Access | Times Cited: 57
Genome interpretation using in silico predictors of variant impact
Panagiotis Katsonis, Kevin Wilhelm, Amanda M. Williams, et al.
Human Genetics (2022) Vol. 141, Iss. 10, pp. 1549-1577
Open Access | Times Cited: 54
Neurodevelopmental Disorders

American Psychiatric Association Publishing eBooks (2022)
Closed Access | Times Cited: 54
Adhesion G protein-coupled receptors: structure, signaling, physiology, and pathophysiology
Trisha Lala, Randy A. Hall
Physiological Reviews (2022) Vol. 102, Iss. 4, pp. 1587-1624
Open Access | Times Cited: 44
Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs
Ipsita Agarwal, Zachary L. Fuller, Simon Myers, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 36
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci
Nora I. Strom, Zachary F. Gerring, Marco Galimberti, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 12
Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies
Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice
Cara Nasello, Lauren A. Poppi, Junbing Wu, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 19
Open Access | Times Cited: 10
Structure of the extracellular region of the adhesion GPCR CELSR1 reveals a compact module which regulates G protein-coupling
Sumit J. Bandekar, Krassimira Garbett, Szymon P. Kordon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
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