Published in Forensic Sci Int Genet on April 18, 2008
A method for the analysis of 32 X chromosome insertion deletion polymorphisms in a single PCR. Int J Legal Med (2011) 0.98
Forensic performance of two insertion-deletion marker assays. Int J Legal Med (2012) 0.97
Application of the new insertion-deletion polymorphism kit for forensic identification and parentage testing on the Czech population. Int J Legal Med (2011) 0.95
Comparison of the genetic background of different Colombian populations using the SNPforID 52plex identification panel. Int J Legal Med (2013) 0.95
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? Transfus Med Hemother (2012) 0.93
Maternity exclusion with a very high autosomal STRs kinship index. Int J Legal Med (2012) 0.90
Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory. Transfus Med Hemother (2012) 0.87
Insertion-deletion polymorphisms--utilization on forensic analysis. Int J Legal Med (2011) 0.87
Beyond STRs: The Role of Diallelic Markers in Forensic Genetics. Transfus Med Hemother (2012) 0.86
Haplotype block: a new type of forensic DNA markers. Int J Legal Med (2009) 0.85
Comparative evaluation of alternative batteries of genetic markers to complement autosomal STRs in kinship investigations: autosomal indels vs. X-chromosome STRs. Int J Legal Med (2012) 0.82
SNP Markers as Additional Information to Resolve Complex Kinship Cases. Transfus Med Hemother (2015) 0.82
Forensically relevant SNaPshot(®) assays for human DNA SNP analysis: a review. Int J Legal Med (2016) 0.79
A SNP panel for identity and kinship testing using massive parallel sequencing. Int J Legal Med (2016) 0.78
A single nucleotide polymorphism genotyping platform for the authentication of patient derived xenografts. Oncotarget (2016) 0.75
Kinship Testing Based on SNPs Using Microarray System. Transfus Med Hemother (2016) 0.75
Familial clustering of mice consistent to known pedigrees enabled by the genome profiling (GP) method. Biophysics (Nagoya-shi) (2014) 0.75
Potential forensic use of a 33 X-InDel panel in the Argentinean population. Int J Legal Med (2016) 0.75
Assessment of application value of 19 autosomal short tandem repeat loci of GoldenEye 20A kit in forensic paternity testing. Int J Legal Med (2013) 0.75
The metagenomics RAST server - a public resource for the automatic phylogenetic and functional analysis of metagenomes. BMC Bioinformatics (2008) 29.20
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Falls and major injuries are risk factors for thoracolumbar fractures: cognitive impairment and multiple injuries impede the detection of back pain and tenderness. J Trauma (1995) 1.60
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Rupture of thoracic aorta caused by blunt trauma. A fifteen-year experience. J Thorac Cardiovasc Surg (1990) 1.56
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A brief dementia screener suitable for use by non-specialists in resource poor settings--the cross-cultural derivation and validation of the brief Community Screening Instrument for Dementia. Int J Geriatr Psychiatry (2010) 1.53
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Typing of mitochondrial DNA coding region SNPs of forensic and anthropological interest using SNaPshot minisequencing. Forensic Sci Int (2004) 1.52
The diagnosis of acute acalculous cholecystitis: a comparison of sonography, scintigraphy, and CT. AJR Am J Roentgenol (1986) 1.50
Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel. Forensic Sci Int Genet (2010) 1.48
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Heparinless partial cardiopulmonary bypass for the repair of aortic trauma. J Thorac Cardiovasc Surg (2000) 1.48
Increasing the diagnostic yield of conjunctival biopsy in patients with suspected ocular cicatricial pemphigoid. Ophthalmology (1995) 1.48
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Influence of dose-rate on inflammatory damage and adhesion molecule expression after abdominal radiation in the rat. Int J Radiat Oncol Biol Phys (1999) 1.46
Hemoperitoneum as the sole indicator of abdominal visceral injuries: a potential limitation of screening abdominal US for trauma. Radiology (1999) 1.44
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Considerations by the European DNA profiling (EDNAP) group on the working practices, nomenclature and interpretation of mitochondrial DNA profiles. Forensic Sci Int (2001) 1.43
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DNA commission of the international society for forensic genetics: guidelines for mitochondrial DNA typing. Forensic Sci Int (2000) 1.37
The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript. Hum Mutat (2001) 1.36
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DNA Commission of the International Society for Forensic Genetics (ISFG): recommendations regarding the role of forensic genetics for disaster victim identification (DVI). Forensic Sci Int Genet (2006) 1.28
Artificial recombination in forensic mtDNA population databases. Int J Legal Med (2004) 1.24
Intracranial venous thrombosis in young women. Stroke (1980) 1.22