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Author Details

Jared Maguire
2009
16
14
PMIDPaper TitleJournal TitlePublished Year
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30268105Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene.BMC Med Genet2018
29760218Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification.Clin Chem2018
28243543Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment.PeerJ2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
27398621The genetic architecture of type 2 diabetes.Nature2016
27375968Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing.PeerJ2016
23593035Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.PLoS Genet2013
22876189The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.PLoS Genet2012
22843986zCall: a rare variant caller for array-based genotyping: genetics and population analysis.Bioinformatics2012
22495311Patterns and rates of exonic de novo mutations in autism spectrum disorders.Nature2012
21775993Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.Nat Genet2011
21478889A framework for variation discovery and genotyping using next-generation DNA sequencing data.Nat Genet2011
20179022Integrative analysis of the melanoma transcriptome.Genome Res2010
19182786Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing.Nat Biotechnol2009
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The Broad Institute of Harvard and MIT
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Perelman School of Medicine, University of Pennsylvania
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Brigham and Women's Hospital
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