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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:

Towards precision medicine
Euan A. Ashley
Nature Reviews Genetics (2016) Vol. 17, Iss. 9, pp. 507-522
Closed Access | Times Cited: 866

Showing 1-25 of 866 citing articles:

On the Opportunities and Risks of Foundation Models
Rishi Bommasani, Drew A. Hudson, Ehsan Adeli, et al.
arXiv (Cornell University) (2021)
Open Access | Times Cited: 1575
Current and future perspectives of liquid biopsies in genomics-driven oncology
Ellen Heitzer, Imran S. Haque, Charles E. S. Roberts, et al.
Nature Reviews Genetics (2018) Vol. 20, Iss. 2, pp. 71-88
Closed Access | Times Cited: 1173
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
Dilated cardiomyopathy
Heinz‐Peter Schultheiß, DeLisa Fairweather, Alida L.P. Caforio, et al.
Nature Reviews Disease Primers (2019) Vol. 5, Iss. 1
Open Access | Times Cited: 532
Ligand-Targeted Drug Delivery
Madduri Srinivasarao, Philip S. Low
Chemical Reviews (2017) Vol. 117, Iss. 19, pp. 12133-12164
Closed Access | Times Cited: 490
Liquid Biopsies in Cancer Diagnosis, Monitoring, and Prognosis
Gabriele De Rubis, Sabna Rajeev Krishnan, Mary Bebawy
Trends in Pharmacological Sciences (2019) Vol. 40, Iss. 3, pp. 172-186
Open Access | Times Cited: 461
From Big Data to Precision Medicine
Tim Hulsen, Saumya Shekhar Jamuar, Alan R. Moody, et al.
Frontiers in Medicine (2019) Vol. 6
Open Access | Times Cited: 398
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Quanli Wang, Ryan S. Dhindsa, Keren Carss, et al.
Nature (2021) Vol. 597, Iss. 7877, pp. 527-532
Open Access | Times Cited: 380
Long-Read Sequencing Emerging in Medical Genetics
Tuomo Mantere, Simone Kersten, Alexander Hoischen
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 374
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Mircea Cretu Stancu, Markus J. van Roosmalen, Ivo Renkens, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 362
Detection of long repeat expansions from PCR-free whole-genome sequence data
Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw, et al.
Genome Research (2017) Vol. 27, Iss. 11, pp. 1895-1903
Open Access | Times Cited: 340
Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease
Kimberly Splinter, David R. Adams, Carlos A. Bacino, et al.
New England Journal of Medicine (2018) Vol. 379, Iss. 22, pp. 2131-2139
Open Access | Times Cited: 314
Restructured society and environment: A review on potential technological strategies to control the COVID-19 pandemic
Rajvikram Madurai Elavarasan, Rishi Pugazhendhi
The Science of The Total Environment (2020) Vol. 725, pp. 138858-138858
Open Access | Times Cited: 309
Emerging concepts in liquid biopsies
Samantha Perakis, Michael R. Speicher
BMC Medicine (2017) Vol. 15, Iss. 1
Open Access | Times Cited: 267
Artificial Intelligence and Big Data in Public Health
Kurt K. Benke, Geza Benke
International Journal of Environmental Research and Public Health (2018) Vol. 15, Iss. 12, pp. 2796-2796
Open Access | Times Cited: 259
The Sentieon Genomics Tools - A fast and accurate solution to variant calling from next-generation sequence data
Donald Freed, Rafael Aldana, Jessica A. Weber, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 254
Long-read genome sequencing identifies causal structural variation in a Mendelian disease
Jason D. Merker, Aaron M. Wenger, Tam P. Sneddon, et al.
Genetics in Medicine (2017) Vol. 20, Iss. 1, pp. 159-163
Open Access | Times Cited: 237
An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy
Juliana T. W. Tong, Paul W. R. Harris, Margaret A. Brimble, et al.
Molecules (2021) Vol. 26, Iss. 19, pp. 5847-5847
Open Access | Times Cited: 237
Personalised organs-on-chips: functional testing for precision medicine
Albert van den Berg, Christine L. Mummery, Robert Passier, et al.
Lab on a Chip (2018) Vol. 19, Iss. 2, pp. 198-205
Open Access | Times Cited: 232
Combined CRISPRi/a-Based Chemical Genetic Screens Reveal that Rigosertib Is a Microtubule-Destabilizing Agent
Marco Jost, Yuwen Chen, Luke A. Gilbert, et al.
Molecular Cell (2017) Vol. 68, Iss. 1, pp. 210-223.e6
Open Access | Times Cited: 231
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome
Shruti Marwaha, Joshua W. Knowles, Euan A. Ashley
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 228
A review on longitudinal data analysis with random forest
Jianchang Hu, Silke Szymczak
Briefings in Bioinformatics (2023) Vol. 24, Iss. 2
Open Access | Times Cited: 226
Painting a new picture of personalised medicine for diabetes
Mark I. McCarthy
Diabetologia (2017) Vol. 60, Iss. 5, pp. 793-799
Open Access | Times Cited: 207
Inference in the age of big data: Future perspectives on neuroscience
Danilo Bzdok, B.T. Thomas Yeo
NeuroImage (2017) Vol. 155, pp. 549-564
Open Access | Times Cited: 196
Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore
Degang Wu, Jinzhuang Dou, Xiaoran Chai, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 736-749.e15
Open Access | Times Cited: 191
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