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Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases

Genomics and Informatics
EvolutionEcologyGeneticsSystematicsHealth InformaticsBehavior
2012English

Exome Sequencing to Identify Novel Genes in Hypertension

Circulation: Cardiovascular Genetics
2012English

Using Whole-Exome Sequencing to Identify Variants Inherited From Mosaic Parents

European Journal of Human Genetics
Genetics
2014English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2015English

Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic Variants

Frontiers in Neurology
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2019English

Preliminary Evaluation of Exome Sequencing to Identify Genetic Markers of Susceptibility to Tuberculosis Disease

BMC Research Notes
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2015English

Mapping Genetic Variants Associated With Beta-Adrenergic Responses in Inbred Mice

PLoS ONE
Multidisciplinary
2012English

Using Linkage Studies Combined With Whole‐exome Sequencing to Identify Novel Candidate Genes for Familial Colorectal Cancer

International Journal of Cancer
Cancer ResearchOncology
2019English

Whole Exome Sequencing for the Identification of CYP3A7 Variants Associated With Tacrolimus Concentrations in Kidney Transplant Patients

Scientific Reports
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2018English

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