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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:

Quantifying prion disease penetrance using large population control cohorts
Eric Vallabh Minikel, Sonia M. Vallabh, Monkol Lek, et al.
Science Translational Medicine (2016) Vol. 8, Iss. 322
Open Access | Times Cited: 417

Showing 1-25 of 417 citing articles:

Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, et al.
Nature (2016) Vol. 536, Iss. 7616, pp. 285-291
Open Access | Times Cited: 9732
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
Alicia R. Martin, Christopher R. Gignoux, Raymond K. Walters, et al.
The American Journal of Human Genetics (2017) Vol. 100, Iss. 4, pp. 635-649
Open Access | Times Cited: 1385
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
William J. Astle, Heather Elding, Tao Jiang, et al.
Cell (2016) Vol. 167, Iss. 5, pp. 1415-1429.e19
Open Access | Times Cited: 1219
Integrative omics for health and disease
Konrad J. Karczewski, M Snyder
Nature Reviews Genetics (2018) Vol. 19, Iss. 5, pp. 299-310
Open Access | Times Cited: 862
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: 603
Infant Gut Microbiome Associated With Cognitive Development
Alexander L. Carlson, Kai Xia, M. Andrea Azcárate-Peril, et al.
Biological Psychiatry (2017) Vol. 83, Iss. 2, pp. 148-159
Open Access | Times Cited: 455
New insights into the generation and role of de novo mutations in health and disease
Rocío Acuña‐Hidalgo, Joris A. Veltman, Alexander Hoischen
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 418
The Rotterdam Study: 2018 update on objectives, design and main results
M. Arfan Ikram, Guy Brusselle, Sarwa Darwish Murad, et al.
European Journal of Epidemiology (2017) Vol. 32, Iss. 9, pp. 807-850
Open Access | Times Cited: 416
Using high-resolution variant frequencies to empower clinical genome interpretation
Nicola Whiffin, Eric Vallabh Minikel, Roddy Walsh, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 10, pp. 1151-1158
Open Access | Times Cited: 407
Objectives, design and main findings until 2020 from the Rotterdam Study
M. Arfan Ikram, Guy Brusselle, Mohsen Ghanbari, et al.
European Journal of Epidemiology (2020) Vol. 35, Iss. 5, pp. 483-517
Open Access | Times Cited: 397
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: 384
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: 299
Prions, prionoids and protein misfolding disorders
Claudia Scheckel, Adriano Aguzzi
Nature Reviews Genetics (2018) Vol. 19, Iss. 7, pp. 405-418
Closed Access | Times Cited: 285
Rheological characterisation of ceramic inks for 3D direct ink writing: A review
Laura del-Mazo-Barbara, Maria‐Pau Ginebra
Journal of the European Ceramic Society (2021) Vol. 41, Iss. 16, pp. 18-33
Open Access | Times Cited: 277
Advanced Materials for Health Monitoring with Skin‐Based Wearable Devices
Han Jin, Yasmin Shibli Abu‐Raya, Hossam Haick
Advanced Healthcare Materials (2017) Vol. 6, Iss. 11
Closed Access | Times Cited: 272
The Genetic Landscape of Diamond-Blackfan Anemia
Jacob C. Ulirsch, Jeffrey M. Verboon, Shideh Kazerounian, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 6, pp. 930-947
Open Access | Times Cited: 227
The biological function of the cellular prion protein: an update
Marie-Angela Wulf, Assunta Senatore, Adriano Aguzzi
BMC Biology (2017) Vol. 15, Iss. 1
Open Access | Times Cited: 226
A Practical Guide for Transparency in Psychological Science
Olivier Klein, Tom E Hardwicke, Frederik Aust, et al.
Collabra Psychology (2018) Vol. 4, Iss. 1
Open Access | Times Cited: 223
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting
Caroline F. Wright, Ben C. West, Marcus A. Tuke, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 2, pp. 275-286
Open Access | Times Cited: 193
Insulin Resistance in Alzheimer's Disease
Laís S. S. Ferreira, Caroline Fernandes, Marcelo N. N. Vieira, et al.
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 190
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation
Joshua L. Traynelis, Michael Silk, Quanli Wang, et al.
Genome Research (2017) Vol. 27, Iss. 10, pp. 1715-1729
Open Access | Times Cited: 174
Evaluating drug targets through human loss-of-function genetic variation
Eric Vallabh Minikel, Konrad J. Karczewski, Hilary C. Martin, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 459-464
Open Access | Times Cited: 160
Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts
Rebecca Kingdom, Caroline F. Wright
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 141
Brainwide silencing of prion protein by AAV-mediated delivery of an engineered compact epigenetic editor
Edwin N. Neumann, Tessa M. Bertozzi, Elaine Wu, et al.
Science (2024) Vol. 384, Iss. 6703
Closed Access | Times Cited: 22
Creutzfeldt–Jakob disease and other prion diseases
Inga Zerr, Anna Ladogana, Simon Mead, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 21
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