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J. Pfeifer · SciRah

Researcher profile · Semantic Scholar

J. Pfeifer

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J. Pfeifer — researcher profile on SciRah

h-index: 54
Works: 195
Citations: 11K

Most-cited papers

Soft Tissue Sarcoma, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology.
M. von Mehren, R. Randall, Robert S. Benjamin, Sarah G. Boles +26 more
2016The Journal of the National Comprehensive Cancer Network928 citations Open access
Semantic Scholar
Guidelines for Validation of Next-Generation Sequencing–Based Oncology Panels
L. Jennings, M. Arcila, C. Corless, S. Kamel-Reid +5 more
2017Journal of Molecular Diagnostics684 citations Open access
Semantic Scholar
Soft Tissue Sarcoma, Version 2.2016, NCCN Clinical Practice Guidelines in Oncology.
M. von Mehren, R. Randall, R. Benjamin, Sarah G. Boles +25 more
2016The Journal of the National Comprehensive Cancer Network247 citations Open access
Semantic Scholar
Clinical next‐generation sequencing in patients with non–small cell lung cancer
I. Hagemann, S. Devarakonda, Christina M. Lockwood, David H. Spencer +14 more
2015Cancer214 citations
Semantic Scholar
Validation of a next-generation sequencing assay for clinical molecular oncology.
C. Cottrell, H. Al-Kateb, Andrew J. Bredemeyer, E. Duncavage +28 more
2014Journal of Molecular Diagnostics188 citations Open access
Semantic Scholar
Neratinib Efficacy and Circulating Tumor DNA Detection of HER2 Mutations in HER2 Nonamplified Metastatic Breast Cancer
Cynthia X. Ma, R. Bose, Feng Gao, R. Freedman +26 more
2017Clinical Cancer Research178 citations Open access
Semantic Scholar
Computational Pathology
D. Louis, Michael D. Feldman, Alexis B. Carter, A. Dighe +12 more
2015Archives of Pathology & Laboratory Medicine142 citations Open access
Semantic Scholar
Detection of FLT3 internal tandem duplication in targeted, short-read-length, next-generation sequencing data.
David H. Spencer, H. Abel, Christina M. Lockwood, J. Payton +5 more
2013Journal of Molecular Diagnostics141 citations Open access
Semantic Scholar
Performance of common analysis methods for detecting low-frequency single nucleotide variants in targeted next-generation sequence data.
David H. Spencer, M. Tyagi, Francesco Vallania, Andrew J. Bredemeyer +3 more
2014Journal of Molecular Diagnostics137 citations Open access
Semantic Scholar
ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
Chang Liu, X. Yang, B. Duffy, T. Mohanakumar +3 more
2013Nucleic Acids Research117 citations Open access
Semantic Scholar
Preanalytics and Precision Pathology: Pathology Practices to Ensure Molecular Integrity of Cancer Patient Biospecimens for Precision Medicine.
C. Compton, J. Robb, Matthew W. Anderson, A. Berry +18 more
2019Archives of Pathology & Laboratory Medicine110 citations Open access
Semantic Scholar
Soft tissue sarcoma, version 2.2014.
M. von Mehren, R. Randall, Robert S. Benjamin, Sarah G. Boles +24 more
2014The Journal of the National Comprehensive Cancer Network105 citations Open access
Semantic Scholar
Genomic heterogeneity of ALK fusion breakpoints in non-small-cell lung cancer
Jason N. Rosenbaum, R. Bloom, Jason T. Forys, J. Hiken +13 more
2018Modern Pathology92 citations Open access
Semantic Scholar
Next-Generation Sequencing Informatics: Challenges and Strategies for Implementation in a Clinical Environment.
Somak Roy, W. LaFramboise, Y. Nikiforov, M. Nikiforova +5 more
2016Archives of Pathology & Laboratory Medicine90 citations
Semantic Scholar
MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors.
Katherine E. Schwetye, J. Pfeifer, E. Duncavage
2014Human Pathology80 citations
Semantic Scholar
Identification of major factors associated with failed clinical molecular oncology testing performed by next generation sequencing (NGS)
H. Al-Kateb, Tudung T. Nguyen, K. Steger-May, J. Pfeifer
2015Molecular Oncology78 citations Open access
Semantic Scholar
The Cancer Immunotherapy Biomarker Testing Landscape.
Eric E. Walk, S. Yohe, A. Beckman, Andrew Schade +3 more
2019Archives of Pathology & Laboratory Medicine74 citations Open access
Semantic Scholar
BRAF V600E mutational status in pediatric thyroid cancer
L. Henke, S. Perkins, J. Pfeifer, Chan-chung Ma +3 more
2014Pediatric Blood & Cancer74 citations
Semantic Scholar
Odontoblast TRPC5 channels signal cold pain in teeth
Laura Bernal, P. Sotelo-Hitschfeld, C. König, Viktor Sinica +20 more
2021Science Advances73 citations Open access
Semantic Scholar
Detection of gene rearrangements in targeted clinical next-generation sequencing.
H. Abel, H. Al-Kateb, C. Cottrell, Andrew J. Bredemeyer +6 more
2014Journal of Molecular Diagnostics72 citations Open access
Semantic Scholar
Serum squamous cell carcinoma antigen as an early indicator of response during therapy of cervical cancer
S. Markovina, Song-Yan Wang, L. Henke, C. Luke +13 more
2017British Journal of Cancer70 citations Open access
Semantic Scholar
BRAF mutation is not predictive of long-term outcome in papillary thyroid carcinoma
L. Henke, J. Pfeifer, Chan-chung Ma, S. Perkins +8 more
2015Cancer Medicine70 citations Open access
Semantic Scholar
A novel histological index for evaluation of environmental enteric dysfunction identifies geographic-specific features of enteropathy among children with suboptimal growth
Ta-Chiang Liu, Kelley VanBuskirk, S. Ali, M. Kelly +15 more
2020PLoS Neglected Tropical Diseases66 citations Open access
Semantic Scholar
Retinoblastoma gene mutations detected by whole exome sequencing of Merkel cell carcinoma
P. Cimino, Diane Robirds, Sheryl R. Tripp, J. Pfeifer +2 more
2014Modern Pathology64 citations Open access
Semantic Scholar
Lymphovascular Space Invasion in Microcystic Elongated and Fragmented (MELF)-Pattern Well-differentiated Endometrioid Adenocarcinoma is Associated With a Higher Rate of Lymph Node Metastasis
J. Hertel, P. Huettner, J. Pfeifer
2014International Journal of Gynecological Pathology63 citations
Semantic Scholar
Select autophagy genes maintain quiescence of tissue-resident macrophages and increase susceptibility to Listeria monocytogenes
Ya-Ting Wang, Konstantin Zaitsev, Qun Lu, Shan Li +16 more
2020Nature Microbiology46 citations Open access
Semantic Scholar
Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing.
Paul J. Lee, Naomi Yoo, I. Hagemann, J. Pfeifer +3 more
2017Experimental and molecular pathology (Print)41 citations
Semantic Scholar
Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing.
Jennifer K Sehn, David H. Spencer, J. Pfeifer, Andrew J. Bredemeyer +3 more
2015American Journal of Clinical Pathology37 citations Open access
Semantic Scholar
A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing.
E. Duncavage, H. Abel, J. Merker, J. B. Bodner +3 more
2016Archives of Pathology & Laboratory Medicine36 citations
Semantic Scholar
Histopathology of Third Trimester Placenta from SARS-CoV-2-Positive Women
Mai He, Priya Skaria, K. Kreutz, Ling Chen +6 more
2020medRxiv35 citations Open access
Semantic Scholar
Mucosal melanoma: correlation of clinicopathologic, prognostic, and molecular features
A. Gru, Nils Becker, L. Dehner, J. Pfeifer
2014Melanoma research35 citations
Semantic Scholar
Tumor Mutation Burden and Checkpoint Immunotherapy Markers in Primary and Metastatic Synovial Sarcoma.
Mai He, B. Abro, Madhurima Kaushal, Ling Chen +6 more
2020Human Pathology33 citations
Semantic Scholar
Rate of occult specimen provenance complications in routine clinical practice.
J. Pfeifer, Jingxia Liu
2013American Journal of Clinical Pathology32 citations Open access
Semantic Scholar
Use of short tandem repeat analysis in unusual presentations of trophoblastic tumors and their mimics.
John Aranake-Chrisinger, P. Huettner, A. Hagemann, J. Pfeifer
2016Human Pathology31 citations
Semantic Scholar
Histopathologic, immunophenotypic, and proteomics characteristics of low-grade phyllodes tumor and fibroadenoma: more similarities than differences
Lingxin Zhang, Chen Yang, J. Pfeifer, R. Caprioli +5 more
2020npj Breast Cancer29 citations Open access
Semantic Scholar
Rituximab is associated with improved survival in cardiac allograft patients with antibody‐mediated rejection: a single center review
A. Ravichandran, J. Schilling, E. Novak, J. Pfeifer +2 more
2013Clinical Transplantation28 citations
Semantic Scholar
The Impact of Reducing DNA Input on Next-Generation Sequencing Library Complexity and Variant Detection.
Samantha N. McNulty, Patrick R Mann, J. Robinson, E. Duncavage +1 more
2020Journal of Molecular Diagnostics27 citations Open access
Semantic Scholar
In Silico Proficiency Testing for Clinical Next-Generation Sequencing.
E. Duncavage, H. Abel, J. Pfeifer
2017Journal of Molecular Diagnostics27 citations Open access
Semantic Scholar
Angiosarcoma of the parotid gland with a t(12;22) translocation creating a EWSR1–ATF1 fusion: a diagnostic dilemma
A. Gru, Nils Becker, J. Pfeifer
2013Journal of Clinical Pathology26 citations
Semantic Scholar
Designing and Implementing NGS Tests for Inherited Disorders: A Practical Framework with Step-by-Step Guidance for Clinical Laboratories.
A. Santani, B. Simen, M. Briggs, Matthew S. Lebo +6 more
2019Journal of Molecular Diagnostics25 citations Open access
Semantic Scholar
Tumor mutation burden, DNA mismatch repair status and checkpoint immunotherapy markers in primary and relapsed malignant rhabdoid tumors.
B. Abro, Madhurima Kaushal, Ling Chen, Robert Wu +3 more
2019Pathology, Research and Practice25 citations
Semantic Scholar
Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
L. Henke, J. Pfeifer, Thomas J. Baranski, T. DeWees +1 more
2018Endocrine Connections24 citations Open access
Semantic Scholar
Optimization of Population Frequency Cut-offs for Filtering Common Germline Polymorphisms from Tumor-Only Next-Generation Sequencing Data.
Samantha N. McNulty, B. Parikh, E. Duncavage, Jonathan W. Heusel +1 more
2019Journal of Molecular Diagnostics23 citations Open access
Semantic Scholar
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.
I. Lubin, N. Aziz, L. Babb, D. Ballinger +20 more
2017Journal of Molecular Diagnostics23 citations Open access
Semantic Scholar
Tumor Mutation Burden and Checkpoint Immunotherapy Markers in NUT Midline Carcinoma
Mai He, R. Chernock, Sheng-Mei Zhou, Mercia J. Gondim +2 more
2019Applied immunohistochemistry & molecular morphology (Print)20 citations
Semantic Scholar
American Journal of Clinical Pathology
L. Kroft, H. Steven, J. Guarner, T. Cornish +28 more
201920 citations
Semantic Scholar
Stabilization of disease after targeted therapy in a thymic carcinoma with KIT mutation detected by clinical next-generation sequencing.
I. Hagemann, R. Govindan, Cylen Javidan-Nejad, J. Pfeifer +1 more
2014Journal of Thoracic Oncology20 citations Open access
Semantic Scholar
Clinical Implications of a Targeted RNA Sequencing Panel in the Detection of Gene Fusions in Solid Tumors.
Lu-Lu Sun, Samantha N. McNulty, Michael J. Evenson, Xiao-Pei Zhu +4 more
2021Journal of Molecular Diagnostics19 citations Open access
Semantic Scholar
The business of genomic testing: a survey of early adopters
J. M. Crawford, L. Bry, J. Pfeifer, Samuel K. Caughron +3 more
2014Genetics in Medicine19 citations Open access
Semantic Scholar
Coronary Collaterals Predict Improved Survival and Allograft Function in Patients with Coronary Allograft Vasculopathy
Kory J. Lavine, M. Sintek, E. Novak, G. Ewald +4 more
2013Circulation: Heart Failure19 citations Open access
Semantic Scholar

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