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Septin 9 methylated DNA is a sensitive and specific blood test for colorectal cancer

BMC medicine, 2011-12, Vol.9 (1), p.133-133, Article 133

2011

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Frequency of KRAS, BRAF, and NRAS mutations in colorectal cancer

Genes chromosomes & cancer, 2011-05, Vol.50 (5), p.307-312

2011

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Quantitative evaluation of CpG island methylation in hyperplastic polyps

Modern pathology, 2010-01, Vol.23 (1), p.151-156

2010

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Identification of proteins from formalin-fixed paraffin-embedded cells by LC-MS MS

Laboratory investigation, 2005-11, Vol.85 (11), p.1405-1415

2005

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Advances in detection of hemoglobinopathies

Clinica chimica acta, 2015-01, Vol.439, p.50-57

2015

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Sporadic Microsatellite Instability-High Colon Cancers Rarely Display Immunohistochemical Evidence of Wnt Signaling Activation

The American journal of surgical pathology, 2015-03, Vol.39 (3), p.313-317

2015

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Confirmation of Single Exon Deletions in MLH1 and MSH2 Using Quantitative Polymerase Chain Reaction

The Journal of molecular diagnostics : JMD, 2008-07, Vol.10 (4), p.355-360

2008

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Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes

Human mutation, 2010-05, Vol.31 (5), p.588-593

2010

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Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog

The Journal of molecular diagnostics : JMD, 2018-07, Vol.20 (4), p.512-521

2018

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Avoidance of pseudogene interference in the detection of 3′ deletions in PMS2

Human mutation, 2011-09, Vol.32 (9), p.1063-1071

2011

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Comprehensive identification of proteins in Hodgkin lymphoma-derived Reed–Sternberg cells by LC-MS/MS

Laboratory investigation, 2007-11, Vol.87 (11), p.1113-1124

2007

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The frequency of previously undetectable deletions involving 3′ Exons of the PMS2 gene

Genes chromosomes & cancer, 2013-01, Vol.52 (1), p.107-112

2013

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A PIK3CA Pyrosequencing-Based Assay that Excludes Pseudogene Interference

The Journal of molecular diagnostics : JMD, 2012, Vol.14 (1), p.56-60

2012

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A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curves

The Journal of molecular diagnostics : JMD, 2013-03, Vol.15 (2), p.248-254

2013

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Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies

Pediatric blood & cancer, 2013-11, Vol.60 (11), p.E135-E136

2013

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A Quantitative Allele-Specific PCR Test for the BRAF V600E Mutation Using a Single Heterozygous Control Plasmid for Quantitation

The Journal of molecular diagnostics : JMD, 2013-03, Vol.15 (2), p.248-254

2013

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NF1 exon 22 analysis of individuals with the clinical diagnosis of neurofibromatosis type 1

American journal of medical genetics. Part A, 2010-08, Vol.152A (8), p.1973-1978

2010

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High-Resolution Melting Analysis for Detection of Internal Tandem Duplications

The Journal of molecular diagnostics : JMD, 2004-08, Vol.6 (3), p.211-216

2004

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Hybridization-Induced Dequenching of Fluorescein-Labeled Oligonucleotides: A Novel Strategy for PCR Detection and Genotyping

The American journal of pathology, 2003-07, Vol.163 (1), p.29-35

2003

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Analytical Characteristics of Cleavable Isotope-Coded Affinity Tag-LC-Tandem Mass Spectrometry for Quantitative Proteomic Studies

The Journal of molecular diagnostics : JMD, 2006-09, Vol.8 (4), p.513-520

2006

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Identification of proteins released by follicular lymphoma-derived cells using a mass spectrometry-based approach

Proteomics (Weinheim), 2006-05, Vol.6 (10), p.3223-3230

2006

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Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies: Constitutional Mismatch Repair Deficiency in Childhood

Pediatric blood & cancer, 2013-11, Vol.60 (11), p.E135-E136

2013

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Recurrent and founder mutations in the PMS2 gene

Clinical genetics, 2013-03, Vol.83 (3), p.238-243

2013

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Septin 9 methylated DNA is a sensitive and specific blood test for colorectal cancer

Frequency of KRAS, BRAF, and NRAS mutations in colorectal cancer

Quantitative evaluation of CpG island methylation in hyperplastic polyps

Identification of proteins from formalin-fixed paraffin-embedded cells by LC-MS MS

Advances in detection of hemoglobinopathies

Sporadic Microsatellite Instability-High Colon Cancers Rarely Display Immunohistochemical Evidence of Wnt Signaling Activation

Confirmation of Single Exon Deletions in MLH1 and MSH2 Using Quantitative Polymerase Chain Reaction

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes

Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog

Avoidance of pseudogene interference in the detection of 3′ deletions in PMS2

Comprehensive identification of proteins in Hodgkin lymphoma-derived Reed–Sternberg cells by LC-MS/MS

Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study

The frequency of previously undetectable deletions involving 3′ Exons of the PMS2 gene

A PIK3CA Pyrosequencing-Based Assay that Excludes Pseudogene Interference

A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curves

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies

A Quantitative Allele-Specific PCR Test for the BRAF V600E Mutation Using a Single Heterozygous Control Plasmid for Quantitation

NF1 exon 22 analysis of individuals with the clinical diagnosis of neurofibromatosis type 1

High-Resolution Melting Analysis for Detection of Internal Tandem Duplications

Hybridization-Induced Dequenching of Fluorescein-Labeled Oligonucleotides: A Novel Strategy for PCR Detection and Genotyping

Analytical Characteristics of Cleavable Isotope-Coded Affinity Tag-LC-Tandem Mass Spectrometry for Quantitative Proteomic Studies

Identification of proteins released by follicular lymphoma-derived cells using a mass spectrometry-based approach

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies: Constitutional Mismatch Repair Deficiency in Childhood

Recurrent and founder mutations in the PMS2 gene

Abstract 3575: The OncoNetwork Consortium: A global collaborative research study on the development and verification of an Ion AmpliSeq RNA gene lung fusion panel

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