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Publications by Jeremy D. Burgess

African American Exome Sequencing Identifies Potential Risk Variants at Alzheimer Disease Loci

Neurology: Genetics

English

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Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease

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Exome Sequencing Identifies Germline Variants in DIS3 in Familial Multiple Myeloma

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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

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Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease

Annals of Clinical and Translational Neurology

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Exome Sequencing of African-American Prostate Cancer Reveals Loss-Of-Function ERF Mutations

Cancer Discovery

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Whole Exome Sequencing of Rare Variants in EIF4G1 and VPS35 in Parkinson Disease

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Exome Sequencing in Parkinson's Disease

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Exome Sequencing Identifies Recurrent Somatic RAC1 Mutations in Melanoma

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Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia

Hernia : the journal of hernias and abdominal wall surgery

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