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Author Details
Full Name
Jared Maguire
Affiliation
ORCID
Career Start Year
2009
Papers
16
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
29360107
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2018
30268105
Detecting 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 Genet
2018
29760218
Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification.
Clin Chem
2018
28243543
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment.
PeerJ
2017
28341696
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
Diabetes
2017
29257133
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
2017
27398621
The genetic architecture of type 2 diabetes.
Nature
2016
27375968
Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing.
PeerJ
2016
23593035
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.
PLoS Genet
2013
22876189
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet
2012
22843986
zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Bioinformatics
2012
22495311
Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Nature
2012
21775993
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
Nat Genet
2011
21478889
A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Nat Genet
2011
20179022
Integrative analysis of the melanoma transcriptome.
Genome Res
2010
19182786
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing.
Nat Biotechnol
2009
1 - 16 of 16
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