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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:

Prevalence and architecture of de novo mutations in developmental disorders

Nature (2017) Vol. 542, Iss. 7642, pp. 433-438
Open Access | Times Cited: 1360

Showing 1-25 of 1360 citing articles:

Predicting Splicing from Primary Sequence with Deep Learning
Kishore Jaganathan, Sofia Kyriazopoulou Panagiotopoulou, Jeremy F. McRae, et al.
Cell (2019) Vol. 176, Iss. 3, pp. 535-548.e24
Open Access | Times Cited: 1968
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, et al.
Cell (2020) Vol. 180, Iss. 3, pp. 568-584.e23
Open Access | Times Cited: 1898
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, et al.
Nature Genetics (2018) Vol. 50, Iss. 3, pp. 381-389
Open Access | Times Cited: 1534
Accurate proteome-wide missense variant effect prediction with AlphaMissense
Jun Cheng, Guido Novati, Joshua Pan, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 882
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 713
Structural variation in the 3D genome
Malte Spielmann, Darío G. Lupiáñez, Stefan Mundlos
Nature Reviews Genetics (2018) Vol. 19, Iss. 7, pp. 453-467
Closed Access | Times Cited: 638
A brief history of human disease genetics
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 615
Paediatric genomics: diagnosing rare disease in children
Caroline F. Wright, David Fitzpatrick, Helen V. Firth
Nature Reviews Genetics (2018) Vol. 19, Iss. 5, pp. 253-268
Closed Access | Times Cited: 530
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, et al.
Nature (2020) Vol. 586, Iss. 7831, pp. 757-762
Open Access | Times Cited: 503
Genetics and Genomics of Congenital Heart Disease
Samir Zaidi, Martina Brueckner
Circulation Research (2017) Vol. 120, Iss. 6, pp. 923-940
Open Access | Times Cited: 481
Neurodevelopmental Disorders: From Genetics to Functional Pathways
Ilaria Parenti, Luis G. Rabaneda, Hanna Schoen, et al.
Trends in Neurosciences (2020) Vol. 43, Iss. 8, pp. 608-621
Open Access | Times Cited: 428
Dendritic structural plasticity and neuropsychiatric disease
Marc P. Forrest, Euan Parnell, Peter Penzes
Nature reviews. Neuroscience (2018) Vol. 19, Iss. 4, pp. 215-234
Open Access | Times Cited: 424
Predicting the clinical impact of human mutation with deep neural networks
Laksshman Sundaram, Hong Gao, Samskruthi Reddy Padigepati, et al.
Nature Genetics (2018) Vol. 50, Iss. 8, pp. 1161-1170
Open Access | Times Cited: 402
Variant interpretation using population databases: Lessons from gnomAD
Sanna Gudmundsson, Moriel Singer‐Berk, Nicholas A. Watts, et al.
Human Mutation (2021) Vol. 43, Iss. 8, pp. 1012-1030
Open Access | Times Cited: 401
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 664-685
Open Access | Times Cited: 400
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, et al.
Cell (2019) Vol. 178, Iss. 4, pp. 850-866.e26
Open Access | Times Cited: 396
AP-1 Transcription Factors and the BAF Complex Mediate Signal-Dependent Enhancer Selection
Thomas Vierbuchen, Emi Ling, Christopher Cowley, et al.
Molecular Cell (2017) Vol. 68, Iss. 6, pp. 1067-1082.e12
Open Access | Times Cited: 393
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
Regional missense constraint improves variant deleteriousness prediction
Kaitlin E. Samocha, Jack A. Kosmicki, Konrad J. Karczewski, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 359
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: 320
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders
Caroline F. Wright, Jeremy F. McRae, Stephen Clayton, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 10, pp. 1216-1223
Open Access | Times Cited: 313
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Mari Niemi, Hilary C. Martin, Daniel L Rice, et al.
Nature (2018) Vol. 562, Iss. 7726, pp. 268-271
Open Access | Times Cited: 303
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
Joon‐Yong An, Kevin Lin, Lingxue Zhu, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 302
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
Naomi R. Wray, Cisca Wijmenga, Patrick F. Sullivan, et al.
Cell (2018) Vol. 173, Iss. 7, pp. 1573-1580
Open Access | Times Cited: 292
Predicting Polygenic Risk of Psychiatric Disorders
Alicia R. Martin, Mark J. Daly, Elise Robinson, et al.
Biological Psychiatry (2018) Vol. 86, Iss. 2, pp. 97-109
Open Access | Times Cited: 292
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