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miRNA analysis in pancreatic cancer: the Dartmouth experience

Clinical chemistry and laboratory medicine, 2017-05, Vol.55 (5), p.755

2017

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Synchronous Pulmonary Adenofibroma and Solitary Fibrous Tumor: Case Report and Review of the Literature

International journal of surgical pathology, 2019-05, Vol.27 (3), p.322-327

2019

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Frequency of Somatic TP53 Mutations in Combination with Known Pathogenic Mutations in Colon Adenocarcinoma, Non–Small Cell Lung Carcinoma, and Gliomas as Identified by Next-Generation Sequencing

Neoplasia (New York, N.Y.), 2018-03, Vol.20 (3), p.256-262

2018

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Routine use of the Ion Torrent AmpliSeq™ Cancer Hotspot Panel for identification of clinically actionable somatic mutations

Clinical chemistry and laboratory medicine, 2014-05, Vol.52 (5), p.707

2014

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Implementation of a Molecular Tumor Board: The Impact on Treatment Decisions for 35 Patients Evaluated at Dartmouth‐Hitchcock Medical Center

The oncologist (Dayton, Ohio), 2015-09, Vol.20 (9), p.1011-1018

2015

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The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma

Cancer genetics, 2016-05, Vol.209 (5), p.195-198

2016

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Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations

Clinical chemistry (Baltimore, Md.), 2014-07, Vol.60 (7), p.1004-1011

2014

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Molecular profiling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing

Experimental and molecular pathology, 2015-10, Vol.99 (2), p.240-244

2015

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Triple-Negative Breast Cancer: Next-Generation Sequencing for Target Identification

The American journal of pathology, 2017-10, Vol.187 (10), p.2133-2138

2017

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Non–small cell lung cancers with isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations

Human pathology, 2018-08, Vol.78, p.138-143

2018

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Molecular matching and treatment strategies for advanced stage lung cancer at Dartmouth-Hitchcock Medical Center: A three-year review of a Molecular Tumor Board

Practical laboratory medicine, 2020-08, Vol.21, p.e00174-e00174, Article e00174

2020

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Benign phyllodes tumor of the breast recurring as a malignant phyllodes tumor and spindle cell metaplastic carcinoma

Human pathology, 2015-02, Vol.46 (2), p.327-333

2015

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The Emerging Role of the Molecular Diagnostics Laboratory in Breast Cancer Personalized Medicine

The American journal of pathology, 2013-10, Vol.183 (4), p.1075-1083

2013

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Central xanthoma of the jaw in association with Noonan syndrome

Human pathology, 2018-12, Vol.82, p.202-205

2018

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Undifferentiated Sarcoma as Intermediate Step in the Progression of Malignant Melanoma to Rhabdomyosarcoma: Histologic, Immunohistochemical, and Molecular Studies of a New Case of Malignant Melanoma With Rhabdomyosarcomatous Differentiation

The American journal of dermatopathology, 2019-03, Vol.41 (3), p.221-229

2019

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Improving Adequacy of Small Biopsy and Fine-Needle Aspiration Specimens for Molecular Testing by Next-Generation Sequencing in Patients With Lung Cancer: A Quality Improvement Study at Dartmouth-Hitchcock Medical Center

Archives of pathology & laboratory medicine (1976), 2017-03, Vol.141 (3), p.402-409

2017

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Impact of Molecular Sequencing Information as Related to 2008 and 2016 World Health Organization Classification of Acute Myeloid Leukemia and Myelodysplasia

Archives of pathology & laboratory medicine (1976), 2018-09, Vol.142 (9), p.1017-1017

2018

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Variant allele frequencies do not correlate well with myeloblast counts in a clinically validated gene sequencing panel for routine acute myeloid leukemia workup

Leukemia & lymphoma, 2019-08, Vol.60 (10), p.2415-2422

2019

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Effective quality management practices in routine clinical next-generation sequencing

Clinical chemistry and laboratory medicine, 2016-05, Vol.54 (5), p.761

2016

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Somatic mutation analysis in melanoma using targeted next generation sequencing

Experimental and molecular pathology, 2017-10, Vol.103 (2), p.172-177

2017

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Rat-bite fever: An uncommon cause of fever and rash in a 9-year-old patient

JAAD Case Reports, 2015-11, Vol.1 (6), p.371-374

2015

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Regulatory T cells are not a strong predictor of survival for patients with glioblastoma

Neuro-oncology (Charlottesville, Va.), 2015-06, Vol.17 (6), p.801-809

2015

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Determining methylation status of methylguanine DNA methyl transferase (MGMT) from formalin-fixed, paraffin embedded tumor tissue

MethodsX, 2014-01, Vol.1 (C), p.42-48

2014

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miRNA analysis in pancreatic cancer: the Dartmouth experience

Synchronous Pulmonary Adenofibroma and Solitary Fibrous Tumor: Case Report and Review of the Literature

Frequency of Somatic TP53 Mutations in Combination with Known Pathogenic Mutations in Colon Adenocarcinoma, Non–Small Cell Lung Carcinoma, and Gliomas as Identified by Next-Generation Sequencing

Routine use of the Ion Torrent AmpliSeq™ Cancer Hotspot Panel for identification of clinically actionable somatic mutations

A Phase II Trial of Dovitinib in BCG-Unresponsive Urothelial Carcinoma with FGFR3 Mutations or Overexpression: Hoosier Cancer Research Network Trial HCRN 12-157

Implementation of a Molecular Tumor Board: The Impact on Treatment Decisions for 35 Patients Evaluated at Dartmouth‐Hitchcock Medical Center

The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma

Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations

Molecular profiling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing

Triple-Negative Breast Cancer: Next-Generation Sequencing for Target Identification

Non–small cell lung cancers with isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations

Molecular matching and treatment strategies for advanced stage lung cancer at Dartmouth-Hitchcock Medical Center: A three-year review of a Molecular Tumor Board

Benign phyllodes tumor of the breast recurring as a malignant phyllodes tumor and spindle cell metaplastic carcinoma

The Emerging Role of the Molecular Diagnostics Laboratory in Breast Cancer Personalized Medicine

Central xanthoma of the jaw in association with Noonan syndrome

Undifferentiated Sarcoma as Intermediate Step in the Progression of Malignant Melanoma to Rhabdomyosarcoma: Histologic, Immunohistochemical, and Molecular Studies of a New Case of Malignant Melanoma With Rhabdomyosarcomatous Differentiation

Improving Adequacy of Small Biopsy and Fine-Needle Aspiration Specimens for Molecular Testing by Next-Generation Sequencing in Patients With Lung Cancer: A Quality Improvement Study at Dartmouth-Hitchcock Medical Center

Impact of Molecular Sequencing Information as Related to 2008 and 2016 World Health Organization Classification of Acute Myeloid Leukemia and Myelodysplasia

Variant allele frequencies do not correlate well with myeloblast counts in a clinically validated gene sequencing panel for routine acute myeloid leukemia workup

Effective quality management practices in routine clinical next-generation sequencing

Somatic mutation analysis in melanoma using targeted next generation sequencing

Rat-bite fever: An uncommon cause of fever and rash in a 9-year-old patient

Regulatory T cells are not a strong predictor of survival for patients with glioblastoma

Genomic characterization of patient-derived xenograft models established from fine needle aspirate biopsies of a primary pancreatic ductal adenocarcinoma and from patient-matched metastatic sites

Determining methylation status of methylguanine DNA methyl transferase (MGMT) from formalin-fixed, paraffin embedded tumor tissue

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