Clinical genomics and precision medicine
Author:
Affiliation:
1. Universidade Federal de Minas Gerais, Brazil; Núcleo de Genética Médica, Brazil
2. Universidade Federal de Minas Gerais, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/scielo.php?script=sci_pdf&pid=S1415-47572022000300104&tlng=en
Reference46 articles.
1. Role of whole exome sequencing for unidentified genetic syndromes;Aggarwal S;Curr Opin Obstet Gynecol,2021
2. Polygenic risk scores and the prediction of common diseases;Ala-Korpela M;Int J Epidemiol,2020
3. Opportunities and challenges in long-read sequencing data analysis;Amarasinghe SL;Genome Biol,2020
4. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants;Belkadi A;Proc Natl Acad Sci USA,2015
5. Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases;Bick D;J Med Genet,2019
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1. Whole Genome Sequencing in Era of Newborn Screening;OBM Genetics;2023-10-05
2. Integrating oculomics with genomics reveals imaging biomarkers for preventive and personalized prediction of arterial aneurysms;EPMA Journal;2023-02-13
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