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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:

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, Hilary C. Martin, Stefano Lise, et al.
Nature Genetics (2015) Vol. 47, Iss. 7, pp. 717-726
Open Access | Times Cited: 355

Showing 1-25 of 355 citing articles:

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
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, et al.
Nature Genetics (2016) Vol. 48, Iss. 12, pp. 1581-1586
Closed Access | Times Cited: 765
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
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
Jessica X. Chong, Kati J. Buckingham, Shalini N. Jhangiani, et al.
The American Journal of Human Genetics (2015) Vol. 97, Iss. 2, pp. 199-215
Open Access | Times Cited: 655
Non-coding genetic variants in human disease: Figure 1.
Feng Zhang, James R. Lupski
Human Molecular Genetics (2015) Vol. 24, Iss. R1, pp. R102-R110
Open Access | Times Cited: 567
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M. Clark, Zornitza Stark, Lauge Farnaes, et al.
npj Genomic Medicine (2018) Vol. 3, Iss. 1
Open Access | Times Cited: 517
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
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Anath C. Lionel, Gregory Costain, Nasim Monfared, et al.
Genetics in Medicine (2017) Vol. 20, Iss. 4, pp. 435-443
Open Access | Times Cited: 485
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
Katharina Schwarze, James Buchanan, Jenny C. Taylor, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 10, pp. 1122-1130
Open Access | Times Cited: 454
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: 408
Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine
Dimitri J. Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
npj Genomic Medicine (2016) Vol. 1, Iss. 1
Open Access | Times Cited: 341
Clinical exome sequencing: results from 2819 samples reflecting 1000 families
Daniel Trujillano, Aida M. Bertoli‐Avella, Krishna Kumar Kandaswamy, et al.
European Journal of Human Genetics (2016) Vol. 25, Iss. 2, pp. 176-182
Open Access | Times Cited: 328
Presentation of Hypoparathyroidism: Etiologies and Clinical Features
Dolores Shoback, John P. Bilezikian, Aline G. Costa, et al.
The Journal of Clinical Endocrinology & Metabolism (2016) Vol. 101, Iss. 6, pp. 2300-2312
Open Access | Times Cited: 314
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: 312
Epidemiology and Diagnosis of Hypoparathyroidism
B.L. Clarke, Edward M. Brown, Michael T. Collins, et al.
The Journal of Clinical Endocrinology & Metabolism (2016) Vol. 101, Iss. 6, pp. 2284-2299
Open Access | Times Cited: 302
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants
Stephen F. Kingsmore, Julie A. Cakici, Michelle M. Clark, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 4, pp. 719-733
Open Access | Times Cited: 291
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report
Damian Smedley, Katherine R. Smith, A. Martı́n, et al.
New England Journal of Medicine (2021) Vol. 385, Iss. 20, pp. 1868-1880
Open Access | Times Cited: 276
A Genetic-Pathophysiological Framework for Craniosynostosis
Stephen R.F. Twigg, Andrew O.M. Wilkie
The American Journal of Human Genetics (2015) Vol. 97, Iss. 3, pp. 359-377
Open Access | Times Cited: 244
High-throughput Phenotyping of Lung Cancer Somatic Mutations
Alice H. Berger, Angela N. Brooks, Xiaoyun Wu, et al.
Cancer Cell (2016) Vol. 30, Iss. 2, pp. 214-228
Open Access | Times Cited: 202
The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants
Josh E Petrikin, Julie A. Cakici, Michelle M. Clark, et al.
npj Genomic Medicine (2018) Vol. 3, Iss. 1
Open Access | Times Cited: 196
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom
Katharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Genetics in Medicine (2019) Vol. 22, Iss. 1, pp. 85-94
Open Access | Times Cited: 194
Medial Arterial Calcification
Peter Lanzer, Fadil Hannan, Jan D. Lanzer, et al.
Journal of the American College of Cardiology (2021) Vol. 78, Iss. 11, pp. 1145-1165
Open Access | Times Cited: 193
Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges
Menelaos Pipis, Alexander M. Rossor, Matilde Laurà, et al.
Nature Reviews Neurology (2019) Vol. 15, Iss. 11, pp. 644-656
Closed Access | Times Cited: 189
Next-Generation Sequencing — An Overview of the History, Tools, and “Omic” Applications
Jerzy K. Kulski
InTech eBooks (2016)
Open Access | Times Cited: 186
Hypoparathyroidism
Michael Mannstadt, John P. Bilezikian, Rajesh V. Thakker, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Closed Access | Times Cited: 181
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