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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:

Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing
Ahmed Alfares, Taghrid Aloraini, Lamia Al subaie, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 11, pp. 1328-1333
Open Access | Times Cited: 143

Showing 1-25 of 143 citing articles:

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
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
Next-Generation Sequencing to Diagnose Suspected Genetic Disorders
David R. Adams, Christine M. Eng
New England Journal of Medicine (2018) Vol. 379, Iss. 14, pp. 1353-1362
Closed Access | Times Cited: 216
Artificial intelligence-based multi-omics analysis fuels cancer precision medicine
Xiujing He, Xiaowei Liu, Fengli Zuo, et al.
Seminars in Cancer Biology (2022) Vol. 88, pp. 187-200
Open Access | Times Cited: 156
Diagnosis, prognosis, and treatment of leukodystrophies
Marjo S. van der Knaap, Raphael Schiffmann, Fanny Mochel, et al.
The Lancet Neurology (2019) Vol. 18, Iss. 10, pp. 962-972
Closed Access | Times Cited: 146
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis
Lisa Ewans, André E. Minoche, Deborah Schofield, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 10, pp. 1121-1131
Open Access | Times Cited: 73
Beyond the exome: What’s next in diagnostic testing for Mendelian conditions
Monica H. Wojcik, Chloe M. Reuter, Shruti Marwaha, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1229-1248
Open Access | Times Cited: 65
Genome Sequencing for Diagnosing Rare Diseases
Monica H. Wojcik, Gabrielle Lemire, Eva Berger, et al.
New England Journal of Medicine (2024) Vol. 390, Iss. 21, pp. 1985-1997
Closed Access | Times Cited: 56
Targeted Sequencing Approach and Its Clinical Applications for the Molecular Diagnosis of Human Diseases
Xiao M. Pei, Martin Ho Yin Yeung, Alex Ngai Nick Wong, et al.
Cells (2023) Vol. 12, Iss. 3, pp. 493-493
Open Access | Times Cited: 48
Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing
David R. Murdock, Hongzheng Dai, Lindsay C. Burrage, et al.
Journal of Clinical Investigation (2020) Vol. 131, Iss. 1
Open Access | Times Cited: 133
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
David Bick, Marilyn C. Jones, Stacie L. Taylor, et al.
Journal of Medical Genetics (2019) Vol. 56, Iss. 12, pp. 783-791
Open Access | Times Cited: 124
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results
Yvonne Bombard, Kyle B. Brothers, Sara Fitzgerald‐Butt, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 4, pp. 578-595
Open Access | Times Cited: 110
Clinical application of next-generation sequencing to the practice of neurology
Jessica E. Rexach, Hane Lee, Julián A. Martínez-Agosto, et al.
The Lancet Neurology (2019) Vol. 18, Iss. 5, pp. 492-503
Open Access | Times Cited: 101
Genome sequencing and implications for rare disorders
Jennifer E. Posey
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 96
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS
André B. P. Kuilenburg, Maja Tarailo‐Graovac, Phillip A. Richmond, et al.
New England Journal of Medicine (2019) Vol. 380, Iss. 15, pp. 1433-1441
Open Access | Times Cited: 86
Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals tested
Lina Basel‐Vanagaite, Naama Orenstein, Keren Markus‐Bustani, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 6, pp. 1443-1451
Open Access | Times Cited: 84
Mapping RNA splicing variations in clinically accessible and nonaccessible tissues to facilitate Mendelian disease diagnosis using RNA-seq
Joseph K. Aicher, Paul Jewell, Jorge Vaquero-Garcia, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 7, pp. 1181-1190
Open Access | Times Cited: 75
Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics
Sateesh Maddirevula, Hiroyuki Kuwahara, Nour Ewida, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 74
Genetic basis of mitochondrial diseases
Mirjana Gušić, Holger Prokisch
FEBS Letters (2021) Vol. 595, Iss. 8, pp. 1132-1158
Closed Access | Times Cited: 61
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy
Siddharth Srivastava, Sara A. Lewis, Julie S. Cohen, et al.
JAMA Neurology (2022) Vol. 79, Iss. 12, pp. 1287-1287
Open Access | Times Cited: 53
Re-analysis of genomic data: An overview of the mechanisms and complexities of clinical adoption
Alan J. Robertson, Natalie B. Tan, Amanda B. Spurdle, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 4, pp. 798-810
Open Access | Times Cited: 41
Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse populations
Claudia Ching Yan Chung, Shirley P.Y. Hue, Nicole Y.T. Ng, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 9, pp. 100896-100896
Open Access | Times Cited: 39
Identification of clinically actionable variants from genome sequencing of families with congenital heart disease
Dimuthu Alankarage, Eddie Ip, Justin O. Szot, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 5, pp. 1111-1120
Open Access | Times Cited: 72
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders
Kathie J. Ngo, Jessica E. Rexach, Hane Lee, et al.
Human Mutation (2019) Vol. 41, Iss. 2, pp. 487-501
Open Access | Times Cited: 71
Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review
Natalie B. Tan, Rachel Stapleton, Zornitza Stark, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 11
Open Access | Times Cited: 69
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