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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:

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: 115

Showing 1-25 of 115 citing articles:

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: 358
Phase Separation as a Missing Mechanism for Interpretation of Disease Mutations
Brian Tsang, Iva Pritišanac, Stephen W. Scherer, et al.
Cell (2020) Vol. 183, Iss. 7, pp. 1742-1756
Open Access | Times Cited: 221
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Themasap A. Khan, Omer Revah, Aaron Gordon, et al.
Nature Medicine (2020) Vol. 26, Iss. 12, pp. 1888-1898
Open Access | Times Cited: 159
Insufficient Evidence for “Autism-Specific” Genes
Scott M. Myers, Thomas D. Challman, Raphael Bernier, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 5, pp. 587-595
Open Access | Times Cited: 150
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: 79
The foundation and architecture of precision medicine in neurology and psychiatry
Harald Hampel, Peng Gao, Jeffrey L. Cummings, et al.
Trends in Neurosciences (2023) Vol. 46, Iss. 3, pp. 176-198
Open Access | Times Cited: 67
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P. Schaaf, Catalina Betancur, Ryan K. C. Yuen, et al.
Nature Reviews Genetics (2020) Vol. 21, Iss. 6, pp. 367-376
Open Access | Times Cited: 121
Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome
Élise Douard, Abderrahim Zeribi, Catherine Schramm, et al.
American Journal of Psychiatry (2020) Vol. 178, Iss. 1, pp. 87-98
Open Access | Times Cited: 73
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
American Journal of Psychiatry (2022) Vol. 179, Iss. 3, pp. 189-203
Open Access | Times Cited: 47
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: 35
Examining the role of common variants in rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky, et al.
Nature (2024)
Open Access | Times Cited: 10
Functional neurogenomics in autism spectrum disorders: A decade of progress
Lucy Bicks, Daniel H. Geschwind
Current Opinion in Neurobiology (2024) Vol. 86, pp. 102858-102858
Closed Access | Times Cited: 8
From Serendipity to Precision: Integrating AI, Multi-Omics, and Human-Specific Models for Personalized Neuropsychiatric Care
Masaru Tanaka
Biomedicines (2025) Vol. 13, Iss. 1, pp. 167-167
Open Access | Times Cited: 1
Rare Genetic Diseases: Nature's Experiments on Human Development
Chelsea E. Lee, Kaela S. Singleton, Melissa Wallin, et al.
iScience (2020) Vol. 23, Iss. 5, pp. 101123-101123
Open Access | Times Cited: 68
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia
Clara Moreau, Sebastian Urchs, Kuldeep Kumar, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 57
Dissecting autism and schizophrenia through neuroimaging genomics
Clara Moreau, Armin Raznahan, Pierre Bellec, et al.
Brain (2021) Vol. 144, Iss. 7, pp. 1943-1957
Open Access | Times Cited: 43
A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders
CM Díaz-Caneja, Matthew W. State, RJ Hagerman, et al.
European Neuropsychopharmacology (2021) Vol. 48, pp. 49-88
Open Access | Times Cited: 42
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Ania Fiksinski, Gil D. Hoftman, Jacob Vorstman, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 1, pp. 341-353
Open Access | Times Cited: 34
Multimodal charting of molecular and functional cell states via in situ electro-sequencing
Qiang Li, Zuwan Lin, Ren Liu, et al.
Cell (2023) Vol. 186, Iss. 9, pp. 2002-2017.e21
Closed Access | Times Cited: 18
Comparing ability and norm-referenced scores as clinical trial outcomes for neurodevelopmental disabilities: a simulation study
Cristan Farmer, Audrey Thurm, Jesse D. Troy, et al.
Journal of Neurodevelopmental Disorders (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 16
Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Patrick Campbell, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction
Kathryn Post, Manuel Belmadani, Payel Ganguly, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 48
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
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, et al.
Nature Human Behaviour (2023) Vol. 7, Iss. 6, pp. 1001-1017
Open Access | Times Cited: 13
Genetic pathways involved in human speech disorders
Joery den Hoed, Simon E. Fisher
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 103-111
Open Access | Times Cited: 35
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