Jason D. Peterson

发表

Redefining the Human Oral Mycobiome with Improved Practices in Amplicon-based Taxonomy: Discovery of Malassezia as a Prominent Commensal

Linda D. Strausbaugh, Thomas Heider, P. Diaz, 2014, PloS one.

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

Casey S. Greene, Richard J. Barth, Gregory J. Tsongalis, 2016, Oncotarget.

Variant call concordance between two laboratory-developed, solid tumor targeted genomic profiling assays using distinct workflows and sequencing instruments.

G. Tsongalis, J. Peterson, Jason D. Peterson, 2017, Experimental and molecular pathology.

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

C. Amos, W. Wells, L. Strausbaugh, 2014, Clinical chemistry and laboratory medicine.

Use of Biosynthetic Controls as Performance Standards for Next-Generation Sequencing Assays of Somatic Tumors: A Multilaboratory Study.

Bharathi Anekella, Helen Fernandes, Andrea Ferreira-Gonzalez, 2017, The journal of applied laboratory medicine.

Identifying Associations between Somatic Mutations and Clinicopathologic Findings in Lung Cancer Pathology Reports

Saeed Hassanpour, Gregory J Tsongalis, Christopher I Amos, 2018, Methods of Information in Medicine.

Molecular profiling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing.

C. Amos, G. Tsongalis, A. Suriawinata, 2015, Experimental and molecular pathology.

Molecular pro fi ling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing

C. Amos, G. Tsongalis, A. Suriawinata, 2015 .

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

G. Tsongalis, Jason D. Peterson, F. D. De Abreu, 2018, Neoplasia.

Clinical Genotyping of Non–Small Cell Lung Cancers Using Targeted Next-Generation Sequencing: Utility of Identifying Rare and Co-mutations in Oncogenic Driver Genes1

C. Amos, K. Dragnev, L. Tafe, 2016, Neoplasia.

Effective quality management practices in routine clinical next-generation sequencing

C. Amos, W. Wells, G. Tsongalis, 2016, Clinical chemistry and laboratory medicine.

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

C. Amos, W. Wells, T. Gardner, 2014, Clinical chemistry.

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

Gregory J Tsongalis, Jason D Peterson, Xiaoying Liu, 2015, The oncologist.

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

I. Gorlov, K. Dragnev, L. Tafe, 2020, Practical laboratory medicine.

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

C. Amos, L. Tafe, G. Tsongalis, 2016, Cancer genetics.

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

L. Tafe, W. Wells, R. Barth, 2015, Human pathology.

Metastatic Alveolar Rhabdomyosarcoma to the Breast: Case Report and Literature Review

G. Tsongalis, Xiaoying Liu, J. Peterson, 2013 .

Somatic mutation analysis in melanoma using targeted next generation sequencing.

Shaofeng Yan, Allen P. Miraflor, Gregory J Tsongalis, 2017, Experimental and molecular pathology.

The Pitfalls of Companion Diagnostics: Evaluation of Discordant EGFR Mutation Results from a Clinical Laboratory and a Central Laboratory.

C. Amos, K. Dragnev, G. Tsongalis, 2016, The Journal of molecular diagnostics : JMD.

Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing.

G. Tsongalis, Jason D. Peterson, B. L. Soares, 2016, American journal of clinical pathology.

Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.

L. Tafe, G. Tsongalis, T. Miller, 2016, Experimental and molecular pathology.

Variant call concordance between two laboratory-developed, solid tumor targeted genomic profiling assays using distinct workflows and sequencing instruments.

G. Tsongalis, Jason D. Peterson, F. D. De Abreu, 2017, Experimental and molecular pathology.

Molecular profiling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing.

G. Tsongalis, A. Suriawinata, Jason D. Peterson, 2015, Experimental and molecular pathology.

Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing.

G. Tsongalis, Jason D. Peterson, B. L. Soares, 2016, American journal of clinical pathology.