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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:

Exome sequencing explained: a practical guide to its clinical application
Eleanor G. Seaby, Reuben J. Pengelly, Sarah Ennis
Briefings in Functional Genomics (2015) Vol. 15, Iss. 5, pp. 374-384
Open Access | Times Cited: 93

Showing 26-50 of 93 citing articles:

A decade of whole-exome sequencing in Brazilian Neurology: from past insights to future perspectives
Caio Robledo D’Angioli Costa Quaio, Thiago Yoshinaga Tonholo Silva, Orlando Graziani Póvoas Barsottini, et al.
Arquivos de Neuro-Psiquiatria (2025) Vol. 83, Iss. 04, pp. 001-014
Open Access
Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
Kristin McDonald Gibson, Addie I. Nesbitt, Kajia Cao, et al.
Genetics in Medicine (2017) Vol. 20, Iss. 3, pp. 329-336
Open Access | Times Cited: 32
Thrombotic microangiopathy following haematopoietic stem cell transplant
Eleanor G. Seaby, Rodney D. Gilbert
Pediatric Nephrology (2017) Vol. 33, Iss. 9, pp. 1489-1500
Open Access | Times Cited: 31
Exome-wide association study of treatment-resistant depression suggests novel treatment targets
Shrey Shah, Teja N. Peddada, Christopher Song, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 8
Molecular Basis of Müllerian Agenesis Causing Congenital Uterine Factor Infertility—A Systematic Review
Rajani Dube, Subhranshu Sekhar Kar, Malay Jhancy, et al.
International Journal of Molecular Sciences (2023) Vol. 25, Iss. 1, pp. 120-120
Open Access | Times Cited: 8
Evaluation of Whole-Exome Enrichment Solutions: Lessons from the High-End of the Short-Read Sequencing Scale
Ana Díaz-de Usera, José M. Lorenzo-Salazar, Luis A. Rubio‐Rodríguez, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 11, pp. 3656-3656
Open Access | Times Cited: 19
Personalized HLA typing leads to the discovery of novel HLA alleles and tumor‐specific HLA variants
Irantzu Anzar, Angelina Sverchkova, Pubudu Samarakoon, et al.
HLA (2022) Vol. 99, Iss. 4, pp. 313-327
Open Access | Times Cited: 12
ESR1 Gene Mutations and Liquid Biopsy in ER-Positive Breast Cancers: A Small Step Forward, a Giant Leap for Personalization of Endocrine Therapy?
Margaux Betz, Vincent Massard, Pauline Gilson, et al.
Cancers (2023) Vol. 15, Iss. 21, pp. 5169-5169
Open Access | Times Cited: 7
Impact of patient education videos on genetic counseling outcomes after exome sequencing
Rebecca Hernan, Megan T. Cho, Ashley Wilson, et al.
Patient Education and Counseling (2019) Vol. 103, Iss. 1, pp. 127-135
Open Access | Times Cited: 19
Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach
Chao Wu, Batsal Devkota, Perry Evans, et al.
European Journal of Human Genetics (2019) Vol. 27, Iss. 4, pp. 612-620
Open Access | Times Cited: 18
Reflexive standardization and the resolution of uncertainty in the genomics clinic
Adam Hedgecoe, Kathleen Job, Angus Clarke
Social Studies of Science (2023) Vol. 53, Iss. 3, pp. 358-378
Open Access | Times Cited: 6
The effect of missing data on evolutionary analysis of sequence capture bycatch, with application to an agricultural pest
Leo Featherstone, Angela McGaughran
Molecular Genetics and Genomics (2024) Vol. 299, Iss. 1
Open Access | Times Cited: 2
In silico identification of pseudo-exon activation events in personal genome and transcriptome data
Narumi Sakaguchi, Mikita Suyama
RNA Biology (2020) Vol. 18, Iss. 3, pp. 382-390
Open Access | Times Cited: 16
Comparison of Mendeliome exome capture kits for use in clinical diagnostics
Reuben J. Pengelly, Daniel Ward, David Hunt, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 15
AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis
Gaia Andreoletti, Eleanor G. Seaby, Jennifer M. Dewing, et al.
Journal of Medical Genetics (2016) Vol. 54, Iss. 4, pp. 269-277
Open Access | Times Cited: 14
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH
Annalisa Vetro, Didier Goidin, Iván Lesende, et al.
Clinical Genetics (2017) Vol. 93, Iss. 3, pp. 545-556
Open Access | Times Cited: 14
A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotyping
Luke O’Gorman, Chelsea Norman, L. Michaels, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 13
Predictive Modelling in Clinical Bioinformatics: Key Concepts for Startups
Ricardo J. Pais
BioTech (2022) Vol. 11, Iss. 3, pp. 35-35
Open Access | Times Cited: 8
Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing
Swati Tomar, Raman Sethi, Poh San Lai
European Journal of Human Genetics (2019) Vol. 27, Iss. 9, pp. 1389-1397
Open Access | Times Cited: 11
Implementation of Exome Sequencing to Identify Rare Genetic Diseases
Prajna Udupa, Debasish Kumar Ghosh
Methods in molecular biology (2023), pp. 79-98
Closed Access | Times Cited: 4
Chromosomal single-strand break repair and neurological disease: Implications on transcription and emerging genomic tools
Arwa A. Abugable, Sarah Antar, Sherif F. El‐Khamisy
DNA repair (2024) Vol. 135, pp. 103629-103629
Open Access | Times Cited: 1
Development of a coding SNP panel for tracking the origin of whole-exome sequencing samples
Yong Huang, Yuanyuan Xiao, Shengqiu Qu, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Advocating Targeted Sequential Screening over Whole Exome Sequencing in 21-Hydroxylase Deficiency
Lavanya Ravichandran, Shriti Paul, A Rekha, et al.
The Indian Journal of Pediatrics (2024)
Closed Access | Times Cited: 1
Detection of Genetic Variations in Children with Tetralogy of Fallot Using Whole Exome Sequencing Technology Integrated Bioinformatics Analysis
Khalid Mohamoud Abdullahi, Ahmed Faisal Ali, Mohamed Mohamoud Adan, et al.
Genetic Testing and Molecular Biomarkers (2024) Vol. 28, Iss. 12, pp. 474-484
Closed Access | Times Cited: 1
First Responder to Genomic Information: A Guide for Primary Care Providers
Susanne B. Haga
Molecular Diagnosis & Therapy (2019) Vol. 23, Iss. 4, pp. 459-466
Open Access | Times Cited: 7

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