| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel phylogenetic approach for de novo discovery of putative nuclear mitochondrial (pNumt) haplotypes
|
Smart, Utpal
|
|
|
43 |
C |
p.
|
artikel
|
| 2 |
A retrospective study on the transfer, persistence and recovery of sperm and epithelial cells in samples collected in sexual assault casework
|
Fonneløp, Ane Elida
|
|
|
43 |
C |
p.
|
artikel
|
| 3 |
Automated estimation of the number of contributors in autosomal short tandem repeat profiles using a machine learning approach
|
Benschop, Corina C.G.
|
|
|
43 |
C |
p.
|
artikel
|
| 4 |
Base specific variation rates at mtDNA positions 16093 and 16183 in human hairs
|
Desmyter, Stijn
|
|
|
43 |
C |
p.
|
artikel
|
| 5 |
Civil society stakeholder views on forensic DNA phenotyping: Balancing risks and benefits
|
Samuel, Gabrielle
|
|
|
43 |
C |
p.
|
artikel
|
| 6 |
Demonstration of a mitochondrial DNA-compatible workflow for genetically variant peptide identification from human hair samples
|
Catlin, LA
|
|
|
43 |
C |
p.
|
artikel
|
| 7 |
Developmental validation of PACE™: Automated artifact identification and contributor estimation for use with GlobalFiler™ and PowerPlex® fusion 6c generated data
|
Marciano, Michael A.
|
|
|
43 |
C |
p.
|
artikel
|
| 8 |
Development and comprehensive evaluation of a noninvasive prenatal paternity testing method through a scaled trial
|
Chang, Liao
|
|
|
43 |
C |
p.
|
artikel
|
| 9 |
Editorial Board
|
|
|
|
43 |
C |
p.
|
artikel
|
| 10 |
Evaluation of 12 Multi-InDel markers for forensic ancestry prediction in Asian populations
|
Sun, Kuan
|
|
|
43 |
C |
p.
|
artikel
|
| 11 |
HIrisPlex-S system for eye, hair, and skin color prediction from DNA: Massively parallel sequencing solutions for two common forensically used platforms
|
Breslin, Krystal
|
|
|
43 |
C |
p.
|
artikel
|
| 12 |
Massively parallel sequencing of autosomal STRs and identity-informative SNPs highlights consanguinity in Saudi Arabia
|
Khubrani, Yahya M.
|
|
|
43 |
C |
p.
|
artikel
|
| 13 |
Performance of ancestry-informative SNP and microhaplotype markers
|
Cheung, Elaine Y.Y.
|
|
|
43 |
C |
p.
|
artikel
|
| 14 |
Pilot study for forensic evaluations of the Precision ID GlobalFiler™ NGS STR Panel v2 with the Ion S5™ system
|
Tao, Ruiyang
|
|
|
43 |
C |
p.
|
artikel
|
| 15 |
Rapid sperm lysis and novel screening approach for human male DNA via colorimetric loop-mediated isothermal amplification
|
Scott, Anchi
|
|
|
43 |
C |
p.
|
artikel
|
| 16 |
Report from the STRAND Working Group on the 2019 STR sequence nomenclature meeting
|
Gettings, Katherine Butler
|
|
|
43 |
C |
p.
|
artikel
|
| 17 |
Resolving mitochondrial haplogroups B2 and B4 with next-generation mitogenome sequencing to distinguish Native American from Asian haplotypes
|
Wood, Melody R.
|
|
|
43 |
C |
p.
|
artikel
|
| 18 |
RETRACTED: Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel
|
Simayijiang, H.
|
|
|
43 |
C |
p.
|
artikel
|
| 19 |
Secondary DNA transfer by working gloves
|
Otten, Laura
|
|
|
43 |
C |
p.
|
artikel
|
| 20 |
Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation
|
Santori, Montserrat
|
|
|
43 |
C |
p.
|
artikel
|
| 21 |
Testing whether stutter and low-level DNA peaks are additive
|
Buckleton, John S.
|
|
|
43 |
C |
p.
|
artikel
|
| 22 |
The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood
|
Fernlund, Eva
|
|
|
43 |
C |
p.
|
artikel
|
| 23 |
The effect of FBI CODIS Core STR Loci expansion on familial DNA database searching
|
Karantzali, Efthymia
|
|
|
43 |
C |
p.
|
artikel
|
| 24 |
Touch DNA collection – Performance of four different swabs
|
Comte, Jennifer
|
|
|
43 |
C |
p.
|
artikel
|
| 25 |
Transcription and microbial profiling of body fluids using a massively parallel sequencing approach
|
Salzmann, Andrea Patrizia
|
|
|
43 |
C |
p.
|
artikel
|
Tijdschrift beschrijving