Christopher Phillips
0000-0002-9601-0128
123 papers found
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Eurasiaplex: A forensic SNP assay for differentiating European and South Asian ancestries
Further development of forensic eye color predictive tests
An assessment of Bayesian and multinomial logistic regression classification systems to analyse admixed individuals
Comparative analysis of two indel-based ancestry informative multiplex PCR typing kits
Genetic variability of the SNPforID 52-plex identification SNP panel in Italian population samples
European Network of Forensic Science Institutes (ENFSI): Evaluation of new commercial STR multiplexes that include the European Standard Set (ESS) of markers
Evaluation of forensic and anthropological potential of D9S1120 in Mestizos and Amerindian populations from Mexico
Allele frequencies of 20 STRs from Northwest Spain (Galicia)
Distribution of allele frequencies of 20 STRs loci in a population sample from Calabria, Southern Italy
Analysis of the SNPforID 52-plex markers in four Native American populations from Venezuela
Typing short amplicon binary polymorphisms: Supplementary SNP and Indel genetic information in the analysis of highly degraded skeletal remains
An evaluation of potential allelic association between the STRs vWA and D12S391: Implications in criminal casework and applications to short pedigrees
Revision of the SNPforID 34-plex forensic ancestry test: Assay enhancements, standard reference sample genotypes and extended population studies
Forensic performance of two insertion–deletion marker assays
Differentiation of African Components of Ancestry to Stratify Groups in a Case–Control Study of a Brazilian Urban Population
Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data
The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data
Straightforward Inference of Ancestry and Admixture Proportions through Ancestry-Informative Insertion Deletion Multiplexing
SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction
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