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Bruce W. Eckloff

Bruce W. Eckloff

D-Index & Metrics

Molecular Biology

D-Index
44
Citations
6390
World Ranking
2933
National Ranking
1398

Overview

Bruce W. Eckloff is affiliated with the Mayo Clinic in the United States. Their research spans the fields of biochemistry, genetics, and molecular biology, with a notable presence in medicine. The scientist has contributed to the subfields of molecular biology, cancer research, genetics, pathology and forensic medicine, and oncology.

The main topics of their work include cancer genomics and diagnostics, molecular biology techniques and applications, microbial community ecology and physiology, protist diversity and phylogeny, biocrusts and microbial ecology, genetic factors in colorectal cancer, and cancer immunotherapy and biomarkers.

Frequent coauthors of Bruce W. Eckloff are Jin Jen, Samantha J. McDonough, Jesse S. Voss, Benjamin R. Kipp, and Yuguang Liu.

Several publication venues have hosted their work, with multiple papers appearing in the Journal of Molecular Diagnostics. Other frequent venues include BMC Genomics, iScience, Blood Cancer Journal, and Cardiovascular Drugs and Therapy.

Selected recent papers include:

  • RNA-Seq Reveals Differences in Expressed Tumor Mutation Burden in Colorectal and Endometrial Cancers with and without Defective DNA-Mismatch Repair, 2021, Journal of Molecular Diagnostics
  • Comparative evaluation for the globin gene depletion methods for mRNA sequencing using the whole blood-derived total RNAs, 2020, BMC Genomics
  • Whole genome sequencing of cyanobacterium Nostoc sp. CCCryo 231-06 using microfluidic single cell technology, 2022, iScience
  • Next-Generation Sequencing of CYP2C19 in Stent Thrombosis: Implications for Clopidogrel Pharmacogenomics, 2020, Cardiovascular Drugs and Therapy
  • Non-random genetic alterations in the cyanobacterium Nostoc sp. exposed to space conditions, 2022, Scientific Reports

Best Publications

  • The genomic landscape of small intestine neuroendocrine tumors

    Michaela S. Banck;Rahul Kanwar;Amit A. Kulkarni;Ganesh K. Boora

  • Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing.

    Andrew L. Feldman;Ahmet Dogan;David I. Smith;Mark E. Law

  • Human Aromatase: Gene Resequencing and Functional Genomics

    Cynthia X. Ma;Araba A. Adjei;Oreste E. Salavaggione;Josefa Coronel

  • Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas

    George Vasmatzis;Sarah H. Johnson;Ryan A. Knudson;Rhett P. Ketterling

  • Genetic Alterations Associated With Progression From Pancreatic Intraepithelial Neoplasia to Invasive Pancreatic Tumor

    Stephen J. Murphy;Steven N. Hart;Joema Felipe Lima;Benjamin R. Kipp

  • Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes

    Alison Shield;Bianca Thomae;Bruce Eckloff;Eric Wieben

  • Identification of Gene Mutations in Autosomal Dominant Polycystic Kidney Disease through Targeted Resequencing

    Sandro Rossetti;Katharina Hopp;Robert A. Sikkink;Jamie L. Sundsbak

  • Human Arsenic Methyltransferase (AS3MT) Pharmacogenetics GENE RESEQUENCING AND FUNCTIONAL GENOMICS STUDIES

    Thomas C. Wood;Oreste E. Salavagionne;Baidehi Mukherjee;Liewei Wang

  • Gemcitabine Pharmacogenomics: Cytidine Deaminase and Deoxycytidylate Deaminase Gene Resequencing and Functional Genomics

    Judith A. Gilbert;Oreste E. Salavaggione;Yuan Ji;Linda L. Pelleymounter

  • Functional genetic polymorphisms in the aromatase gene CYP19 vary the response of breast cancer patients to neoadjuvant therapy with aromatase inhibitors.

    Liewei Wang;Katarzyna A. Ellsworth;Irene Moon;Linda L. Pelleymounter

  • Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance.

    Manish Kohli;Yeung Ho;David W. Hillman;Jamie L. Van Etten

  • Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients

    Chunling Hu;Steven N. Hart;William R. Bamlet;Raymond M. Moore

  • Integrated mate-pair and RNA sequencing identifies novel, targetable gene fusions in peripheral T-cell lymphoma

    Rebecca L. Boddicker;Gina L. Razidlo;Surendra Dasari;Yu Zeng

  • Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest Elucidation of the Triadin Knockout Syndrome

    Helene M. Altmann;David J. Tester;Melissa L. Will;Sumit Middha

  • Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomics.

    Araba A Adjei;Bianca A Thomae;Janel L Prondzinski;Bruce W Eckloff

  • Glutathione S-transferase omega 1 and omega 2 pharmacogenomics

    Baidehi Mukherjee;Oreste E. Salavaggione;Linda L. Pelleymounter;Irene Moon

  • Multi-Platform Analysis of MicroRNA Expression Measurements in RNA from Fresh Frozen and FFPE Tissues

    Christopher P. Kolbert;Rod M. Feddersen;Fariborz Rakhshan;Diane E. Grill

  • Glutathione s-transferase p1: gene sequence variation and functional genomic studies

    Ann M. Moyer;Oreste E. Salavaggione;Tse Yu Wu;Irene Moon

  • Human sulfotransferase SULT2A1 pharmacogenetics: genotype-to-phenotype studies

    B A Thomae;B W Eckloff;R R Freimuth;E D Wieben

  • A Prospective Genome-Wide Study of Prostate Cancer Metastases Reveals Association of Wnt Pathway Activation and Increased Cell Cycle Proliferation with Primary Resistance to Abiraterone Acetate-Prednisone.

    L. Wang;L. Wang;Scott M Dehm;D. W. Hillman;H. Sicotte

Frequent Co-Authors

Eric D. Wieben
Eric D. Wieben Mayo Clinic
Yan W. Asmann
Yan W. Asmann Mayo Clinic
Liewei Wang
Liewei Wang Mayo Clinic
Jin Jen
Jin Jen Bristol Myers Squibb
Daniel J. Schaid
Daniel J. Schaid Mayo Clinic
George Vasmatzis
George Vasmatzis Mayo Clinic
Brooke L. Fridley
Brooke L. Fridley University of Kansas
david i smith
david i smith Mayo Clinic
James R. Cerhan
James R. Cerhan Mayo Clinic

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