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Publications by Crystal Kelly

Exome Sequencing to Identify De Novo Mutations in Sporadic ALS Trios

Nature Neuroscience

English

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Exome Sequencing of Case-Unaffected-Parents Trios Reveals Recessive and De Novo Genetic Variants in Sporadic ALS

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Sporadic Hypertrophic Cardiomyopathy Due to De Novo Myosin Mutations.

Journal of Clinical Investigation

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Exome Sequencing to Identify Novel Genes in Hypertension

Circulation: Cardiovascular Genetics

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De Novo Mutations in Sporadic Deletional Duchenne Muscular Dystrophy (DMD) Cases

Experimental & Molecular Medicine

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

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Exome Sequencing Identifies Recurrent Somatic RAC1 Mutations in Melanoma

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Exome Sequencing Identified New Mutations in a Marfan Syndrome Family

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

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

BMC Research Notes

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