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Comprehensive profiling of metaplastic breast carcinomas reveals frequent overexpression of programmed death-ligand 1

Journal of clinical pathology, 2017-03, Vol.70 (3), p.255

2017

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High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine

Familial cancer, 2016-07, Vol.15 (3), p.405-412

2016

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NUTM1-rearranged neoplasia: a multi-institution experience yields novel fusion partners and expands the histologic spectrum

Modern pathology, 2019-06, Vol.32 (6), p.764-773

2019

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Pan-tumor survey of ROS1 fusions detected by next-generation RNA and whole transcriptome sequencing

BMC cancer, 2023-10, Vol.23 (1), p.1-1000, Article 1000

2023

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Comprehensive molecular profiling of advanced/metastatic olfactory neuroblastomas

PloS one, 2018-01, Vol.13 (1), p.e0191244-e0191244

2018

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Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

American journal of human genetics, 2011-07, Vol.89 (1), p.28-43

2011

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Potential Novel Therapy Targets in Neuroendocrine Carcinomas of the Breast

Clinical breast cancer, 2019-04, Vol.19 (2), p.131-136

2019

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Molecular Profiling of the Metaplastic Spindle Cell Carcinoma of the Breast Reveals Potentially Targetable Biomarkers

Clinical breast cancer, 2020-08, Vol.20 (4), p.326-331.e1

2020

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Novel therapeutic targets in salivary duct carcinoma uncovered by comprehensive molecular profiling

Cancer medicine (Malden, MA), 2019-12, Vol.8 (17), p.7322-7329

2019

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Pan-tumor survey of RET fusions as detected by next-generation RNA sequencing identified RET fusion positive colorectal carcinoma as a unique molecular subset

Translational oncology, 2023-10, Vol.36, p.101744-101744, Article 101744

2023

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Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1

Oncotarget, 2015-08, Vol.6 (23), p.19819-19825

2015

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Molecular characterization of cancers with NTRK gene fusions

Modern pathology, 2019-01, Vol.32 (1), p.147-153

2019

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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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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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Identification of Novel CDH1-NRG2α and F11R-NRG2α Fusions in NSCLC Plus Additional Novel NRG2α Fusions in Other Solid Tumors by Whole Transcriptome Sequencing

JTO clinical and research reports, 2021-02, Vol.2 (2), p.100132-100132, Article 100132

2021

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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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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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Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing

The Journal of molecular diagnostics : JMD, 2014-09, Vol.16 (5), p.477-480

2014

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Using VAAST to Identify an X-linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

American journal of human genetics, 2011-08, Vol.89 (2), p.345-345

2011

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Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait

Blood, 2010-10, Vol.116 (15), p.2822-2825

2010

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Detection of NRG1 Gene Fusions in Solid Tumors

Clinical cancer research, 2019-08, Vol.25 (16), p.4966-4972

2019

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Cystic fibrosis testing in a referral laboratory: results and lessons from a six-year period

Journal of clinical bioinformatics, 2013-01, Vol.3 (1), p.3-3

2013

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Acquired Tertiary MET Resistance (MET D1228N and a Novel LSM8-MET Fusion) to Selpercatinib and Capmatinib in a Patient With KIF5B-RET–positive NSCLC With Secondary MET Amplification as Initial Resistance to Selpercatinib

Journal of thoracic oncology, 2021-07, Vol.16 (7), p.e51-e54

2021

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Abstract A047: Molecular characterization of the malignancies with targetable NTRK gene fusions

Molecular cancer therapeutics, 2018-01, Vol.17 (1_Supplement), p.A047-A047

2018

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Abstract 1757: Spectrum of BAP1 mutations identified in diverse cancer lineages

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1757-1757

2017

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Comprehensive profiling of metaplastic breast carcinomas reveals frequent overexpression of programmed death-ligand 1

High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine

NUTM1-rearranged neoplasia: a multi-institution experience yields novel fusion partners and expands the histologic spectrum

Pan-tumor survey of ROS1 fusions detected by next-generation RNA and whole transcriptome sequencing

Comprehensive molecular profiling of advanced/metastatic olfactory neuroblastomas

Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

Potential Novel Therapy Targets in Neuroendocrine Carcinomas of the Breast

Molecular Profiling of the Metaplastic Spindle Cell Carcinoma of the Breast Reveals Potentially Targetable Biomarkers

Novel therapeutic targets in salivary duct carcinoma uncovered by comprehensive molecular profiling

Pan-tumor survey of RET fusions as detected by next-generation RNA sequencing identified RET fusion positive colorectal carcinoma as a unique molecular subset

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1

Molecular characterization of cancers with NTRK gene fusions

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes

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

Identification of Novel CDH1-NRG2α and F11R-NRG2α Fusions in NSCLC Plus Additional Novel NRG2α Fusions in Other Solid Tumors by Whole Transcriptome Sequencing

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

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies

Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing

Using VAAST to Identify an X-linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait

Detection of NRG1 Gene Fusions in Solid Tumors

Cystic fibrosis testing in a referral laboratory: results and lessons from a six-year period

Acquired Tertiary MET Resistance (MET D1228N and a Novel LSM8-MET Fusion) to Selpercatinib and Capmatinib in a Patient With KIF5B-RET–positive NSCLC With Secondary MET Amplification as Initial Resistance to Selpercatinib

Abstract A047: Molecular characterization of the malignancies with targetable NTRK gene fusions

Abstract 1757: Spectrum of BAP1 mutations identified in diverse cancer lineages

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