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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:

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing
Beryl B. Cummings, Jamie L. Marshall, Taru Tukiainen, et al.
Science Translational Medicine (2017) Vol. 9, Iss. 386
Open Access | Times Cited: 692

Showing 1-25 of 692 citing articles:

Delivery technologies for cancer immunotherapy
Rachel Riley, Carl H. June, Róbert Langer, et al.
Nature Reviews Drug Discovery (2019) Vol. 18, Iss. 3, pp. 175-196
Open Access | Times Cited: 2129
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: 1947
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: 870
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: 606
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: 528
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S. Kremer, Daniel M. Bader, Christian Mertes, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 496
Highly efficient therapeutic gene editing of human hematopoietic stem cells
Yuxuan Wu, Jing Zeng, Benjamin P. Roscoe, et al.
Nature Medicine (2019) Vol. 25, Iss. 5, pp. 776-783
Open Access | Times Cited: 430
Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification
Rick Kamps, Rita D. Brandão, Bianca J.C. van den Bosch, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 2, pp. 308-308
Open Access | Times Cited: 417
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Kandamurugu Manickam, Monica R. McClain, Laurie Demmer, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2029-2037
Open Access | Times Cited: 400
Muscular dystrophies
Eugenio Mercuri, Carsten G. Bönnemann, Francesco Muntoni
The Lancet (2019) Vol. 394, Iss. 10213, pp. 2025-2038
Closed Access | Times Cited: 389
Long-Read Sequencing Emerging in Medical Genetics
Tuomo Mantere, Simone Kersten, Alexander Hoischen
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 371
Engineering microrobots for targeted cancer therapies from a medical perspective
Christine K. Schmidt, Mariana Medina‐Sánchez, Richard J. Edmondson, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 338
The Expanding Landscape of Alternative Splicing Variation in Human Populations
Eddie Park, Zhicheng Pan, Zijun Zhang, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 1, pp. 11-26
Open Access | Times Cited: 318
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M. Werling, Harrison Brand, Joon‐Yong An, et al.
Nature Genetics (2018) Vol. 50, Iss. 5, pp. 727-736
Open Access | Times Cited: 280
Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function
Gökçen Eraslan, Eugene Drokhlyansky, Shankara Anand, et al.
Science (2022) Vol. 376, Iss. 6594
Open Access | Times Cited: 280
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts
Laure Frésard, Craig Smail, Nicole M. Ferraro, et al.
Nature Medicine (2019) Vol. 25, Iss. 6, pp. 911-919
Open Access | Times Cited: 278
Genomic Analysis in the Age of Human Genome Sequencing
Tuuli Lappalainen, Alexandra J. Scott, Margot Brandt, et al.
Cell (2019) Vol. 177, Iss. 1, pp. 70-84
Open Access | Times Cited: 269
Mitochondrial medicine in the omics era
Joyeeta Rahman, Shamima Rahman
The Lancet (2018) Vol. 391, Iss. 10139, pp. 2560-2574
Open Access | Times Cited: 245
Next-Generation Sequencing and Emerging Technologies
Kishore R. Kumar, Mark J. Cowley, Ryan L. Davis
Seminars in Thrombosis and Hemostasis (2019) Vol. 45, Iss. 07, pp. 661-673
Open Access | Times Cited: 239
Therapeutic base editing of human hematopoietic stem cells
Jing Zeng, Yuxuan Wu, Chunyan Ren, et al.
Nature Medicine (2020) Vol. 26, Iss. 4, pp. 535-541
Open Access | Times Cited: 237
Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology
Ann E. Frazier, David R. Thorburn, Alison G. Compton
Journal of Biological Chemistry (2017) Vol. 294, Iss. 14, pp. 5386-5395
Open Access | Times Cited: 229
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: 228
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: 226
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 3, pp. 466-483
Open Access | Times Cited: 208
Genetics of mitochondrial diseases: Identifying mutations to help diagnosis
Sarah L. Stenton, Holger Prokisch
EBioMedicine (2020) Vol. 56, pp. 102784-102784
Open Access | Times Cited: 204
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