Carey P. Davis

Most-cited papers

1. A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

   Josephine Purps, S. Siegert, Sascha Willuweit, M. Nagy +159 more

   2014Forensic Science International: Genetics278 citations Open access

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2. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.

   A. Jäger, Michelle L. Alvarez, Carey P. Davis, Ernesto Guzmán +12 more

   2017Forensic Science International: Genetics269 citations Open access

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3. High-quality and high-throughput massively parallel sequencing of the human mitochondrial genome using the Illumina MiSeq.

   J. King, B. LaRue, Nicole M. M. Novroski, Monika Stoljarova +7 more

   2014Forensic Science International: Genetics156 citations

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4. Single nucleotide polymorphism typing with massively parallel sequencing for human identification

   S. Seo, J. King, David H. Warshauer, Carey P. Davis +2 more

   2013Zeitschrift für Rechtsmedizin126 citations

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5. STRait Razor: a length-based forensic STR allele-calling tool for use with second generation sequencing data.

   David H. Warshauer, D. Lin, K. Hari, R. Jain +4 more

   2013Forensic Science International: Genetics105 citations

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6. Extraction platform evaluations: a comparison of AutoMate Express™, EZ1® Advanced XL, and Maxwell® 16 Bench-top DNA extraction systems.

   Carey P. Davis, J. King, B. Budowle, A. Eisenberg +1 more

   2012Legal Medicine49 citations

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7. Prototype PowerPlex® Y23 System: A concordance study.

   Carey P. Davis, Jian-Ye Ge, C. Sprecher, A. Chidambaram +6 more

   2013Forensic Science International: Genetics43 citations

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8. Massively parallel sequencing of forensically relevant single nucleotide polymorphisms using TruSeq™ forensic amplicon

   David H. Warshauer, Carey P. Davis, C. Holt, Yonmee Han +6 more

   2014Zeitschrift für Rechtsmedizin27 citations

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9. Variants observed for STR locus SE33: a concordance study.

   Carey P. Davis, Jian-Ye Ge, J. King, Naseem Malik +3 more

   2012Forensic Science International: Genetics27 citations

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10. Maternity exclusion with a very high autosomal STRs kinship index

    Li Li, Jian-Ye Ge, Suhua Zhang, Jian Guo +7 more

    2012Zeitschrift für Rechtsmedizin26 citations

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11. Sequencing the hypervariable regions of human mitochondrial DNA using massively parallel sequencing: Enhanced data acquisition for DNA samples encountered in forensic testing.

    Carey P. Davis, Dixie Peters, David H. Warshauer, J. King +1 more

    2015Legal Medicine24 citations

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12. Y-STR loci diversity in native Alaskan populations

    Carey P. Davis, Jian-Ye Ge, A. Chidambaram, J. King +6 more

    2011Zeitschrift für Rechtsmedizin16 citations

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13. A case of Amelogenin Y-null: a simple primer binding site mutation or unusual genetic anomaly?

    Carey P. Davis, M. J. Illescas, C. Tirado, R. Lopez +2 more

    2012Legal Medicine9 citations

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14. Deep Sequencing Provides Comprehensive Multiplex Capabilities

    B. Budowle, David H. Warshauer, S. Seo, J. King +2 more

    20135 citations Open access

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15. Multiplex Short Tandem Repeat Amplification of Low Template DNA Samples with the Addition of Proofreading Enzymes *

    Carey P. Davis, Lynzee A. Chelland, Victoria R. Pavlova, M. J. Illescas +2 more

    2011Journal of Forensic Sciences5 citations

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16. Post Rift Oligocene Marine Source Rock, a New Petroleum System in Greater Bangkanai, Upper Kutai, Indonesia

    B. Nugroho, E. Guritno, H. Mustapha, W. Darmawan +2 more

    20161 citations

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17. Abstract 3819: Validation of TruSight Oncology Comprehensive for detecting and reporting clinically relevant mutations

    M. Chavez, S. Chan, Stewart Comer, G. Dakshinamoorthy +7 more

    2026Cancer Research0 citations

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18. Abstract 1136: Analytical evaluation of a whole genome tumor-informed molecular residual disease detection assay with high sensitivity and specificity

    W. Gong, Sung Kim, G. Tagliazucchi, T. U. Dincer +16 more

    2026Cancer Research0 citations

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19. Large panels of SNPs for human identity typing are feasible with current generation sequencing ( CGS ) technology

    S. Seo, J. King, David H. Warshauer, Carey P. Davis +2 more

    20130 citations

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20. Analytical Evaluation of Whole Genome Sequencing 1 for Acute Myeloid Leukemia 2

    W. Gong, Guidantonio Malagoli Tagliazucchi, Stewart Comer, Megha Ghildiyal +19 more

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