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Cancer-associated splicing variant of tumor suppressor AIMP2/p38: pathological implication in tumorigenesis

PLoS genetics, 2011-03, Vol.7 (3), p.e1001351

2011

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Re: Carrier Screening is a Deficient Strategy for Determining Sperm Donor Eligibility and Reducing Risk of Disease in Recipient Children (From: Silver AJ, Larson JL, Silver MJ, et al. Genet Test Mol Biomarkers 2016;20:276-284)

Genetic testing and molecular biomarkers, 2016-08, Vol.20 (8), p.413

2016

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Stability of Repetitive-Sequence PCR Patterns with Respect to Culture Age and Subculture Frequency

Journal of Clinical Microbiology, 2003-06, Vol.41 (6), p.2694-2696

2003

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Model for Predicting the Impact of Gadolinium on Plasma Calcium Measured by the o-Cresolphthalein Method

Clinical chemistry (Baltimore, Md.), 2004-04, Vol.50 (4), p.741-746

2004

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Document-level classification of CT pulmonary angiography reports based on an extension of the ConText algorithm

Journal of biomedical informatics, 2011-10, Vol.44 (5), p.728-737

2011

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Experience With Voice Recognition in Surgical Pathology at a Large Academic Multi-Institutional Center

American journal of clinical pathology, 2010, Vol.133 (1), p.156-159

2010

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Systematic identification of DNA variants associated with ultraviolet radiation using a novel Geographic-Wide Association Study (GeoWAS)

BMC medical genetics, 2013-06, Vol.14 (1), p.62-62, Article 62

2013

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TMA-TAB: A spreadsheet-based document for exchange of tissue microarray data based on the tissue microarray-object model

Journal of biomedical informatics, 2010-06, Vol.43 (3), p.435-441

2010

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Cancer-Associated Splicing Variant of Tumor Suppressor AIMP2/p38: Pathological Implication in Tumorigenesis: e1001351

PLoS genetics, 2011-03, Vol.7 (3)

2011

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Coanalysis of GWAS with eQTLs reveals disease-tissue associations

AMIA Summits on Translational Science proceedings, 2012, Vol.2012, p.35-41

2012

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Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification

Clinical chemistry (Baltimore, Md.), 2018-07, Vol.64 (7), p.1063-1073

2018

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Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment

PeerJ (San Francisco, CA), 2017-02, Vol.5, p.e3046-e3046, Article e3046

2017

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Abstract NG01: Evolution of neoantigen landscape during immune checkpoint blockade in non-small cell lung cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.NG01-NG01

2017

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals

Cancer-associated splicing variant of tumor suppressor AIMP2/p38: pathological implication in tumorigenesis

Re: Carrier Screening is a Deficient Strategy for Determining Sperm Donor Eligibility and Reducing Risk of Disease in Recipient Children (From: Silver AJ, Larson JL, Silver MJ, et al. Genet Test Mol Biomarkers 2016;20:276-284)

Stability of Repetitive-Sequence PCR Patterns with Respect to Culture Age and Subculture Frequency

Model for Predicting the Impact of Gadolinium on Plasma Calcium Measured by the o-Cresolphthalein Method

Document-level classification of CT pulmonary angiography reports based on an extension of the ConText algorithm

Experience With Voice Recognition in Surgical Pathology at a Large Academic Multi-Institutional Center

Systematic identification of DNA variants associated with ultraviolet radiation using a novel Geographic-Wide Association Study (GeoWAS)

TMA-TAB: A spreadsheet-based document for exchange of tissue microarray data based on the tissue microarray-object model

Cancer-Associated Splicing Variant of Tumor Suppressor AIMP2/p38: Pathological Implication in Tumorigenesis: e1001351

Coanalysis of GWAS with eQTLs reveals disease-tissue associations

Evolution of Neoantigen Landscape during Immune Checkpoint Blockade in Non-Small Cell Lung Cancer

Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification

Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment

Abstract NG01: Evolution of neoantigen landscape during immune checkpoint blockade in non-small cell lung cancer

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