Published in Leg Med (Tokyo) on March 01, 2003
Genetic ancestry of a Moroccan population as inferred from autosomal STRs. Meta Gene (2014) 2.08
An Aboriginal Australian genome reveals separate human dispersals into Asia. Science (2011) 4.84
Natural radioactivity and human mitochondrial DNA mutations. Proc Natl Acad Sci U S A (2002) 2.46
Spontaneous and sporadic trypsinogen mutations in idiopathic pancreatitis. JAMA (2002) 2.38
Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis. Hum Genet (2005) 1.47
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome. Am J Hum Genet (2009) 1.41
Head covering and the risk for SIDS: findings from the New Zealand and German SIDS case-control studies. Pediatrics (2008) 1.40
International Journal of Legal Medicine's manuscript submission and peer-review system goes electronic! Int J Legal Med (2009) 1.38
Sleep environment risk factors for sudden infant death syndrome: the German Sudden Infant Death Syndrome Study. Pediatrics (2009) 1.27
The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation, results and perspectives. Forensic Sci Int (2004) 1.26
Modifiable risk factors for SIDS in Germany: results of GeSID. Acta Paediatr (2005) 1.15
Y-chromosomal microsatellite mutation rates in a population sample from northwestern Germany. Int J Legal Med (2006) 1.07
Leptomeningeal neurons are a common finding in infants and are increased in sudden infant death syndrome. Acta Neuropathol (2009) 1.03
Evaluating length heteroplasmy in the human mitochondrial DNA control region. Int J Legal Med (2010) 1.03
Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study. Int J Legal Med (2005) 1.01
Solution structure and backbone dynamics of human epidermal-type fatty acid-binding protein (E-FABP). Biochem J (2002) 0.98
Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region. Int J Legal Med (2004) 0.97
Meiosis study in a population sample from Afghanistan: allele frequencies and mutation rates of 16 STR loci. Int J Legal Med (2006) 0.95
Identification of the microdeletion breakpoint in a GLRA1null allele of Turkish hyperekplexia patients. Hum Mutat (2006) 0.92
A cautionary note on switching mitochondrial DNA reference sequences in forensic genetics. Forensic Sci Int Genet (2012) 0.91
Allele frequencies of 13 short tandem repeat (STR) loci in the Romanian population. Forensic Sci Int (2004) 0.90
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation. Int J Legal Med (2006) 0.88
Characterisation of variant alleles in the STR systems D2S1338, D3S1358 and D19S433. Int J Legal Med (2005) 0.88
Mitochondrial DNA control region diversity in hairs and body fluids of monozygotic triplets. Int J Legal Med (2003) 0.87
Meiosis study in a population sample from Nigeria: allele frequencies and mutation rates of 16 STR loci. Int J Legal Med (2009) 0.87
Identification of DYS385 allele variants by using shorter amplicons and Northern Thai haplotype data. J Forensic Sci (2003) 0.86
STR analysis of artificially degraded DNA-results of a collaborative European exercise. Forensic Sci Int (2004) 0.86
Mitochondrial control region sequences from a Vietnamese population sample. Int J Legal Med (2007) 0.85
The GEDNAP (German DNA profiling group) blind trial concept. Int J Legal Med (2002) 0.84
Bowel wall hemorrhage after death by hanging. Int J Legal Med (2011) 0.84
Reaction patterns of pulmonary macrophages in protracted asphyxiation. Int J Legal Med (2010) 0.84
Petechial bleedings in sudden infant death. Int J Legal Med (2010) 0.83
Cyclooxygenase-2 in sporadic colorectal polyps: immunohistochemical study and its importance in the early stages of colorectal tumorigenesis. Pathol Res Pract (2005) 0.82
New alleles and mutational events at 14 STR loci from different German populations. Forensic Sci Int Genet (2007) 0.82
Developing equine mtDNA profiling for forensic application. Int J Legal Med (2010) 0.81
Haemorrhages into the back and auxiliary breathing muscles after death by hanging. Int J Legal Med (2011) 0.81
NHE3 in the human brainstem: implication for the pathogenesis of the sudden infant death syndrome (SIDS)? Adv Exp Med Biol (2008) 0.80
Real-time quantitative PCR assay for the detection of Helicobacter pylori: no association with sudden infant death syndrome. Int J Legal Med (2005) 0.79
Synthesis of a psilocin hapten and a protein-hapten conjugate. J Pharm Pharmacol (2002) 0.79
Haplotype-assisted characterization of germline mutations at short tandem repeat loci. Int J Legal Med (2009) 0.79
Cytokines and sudden infant death. Int J Legal Med (2011) 0.79
Ultrasound-accelerated formalin fixation improves the preservation of nucleic acids extraction in histological sections. Int J Legal Med (2009) 0.78
Specific traces in stun gun deployment. Int J Legal Med (2005) 0.77
A collaborative study of the EDNAP group regarding Y-chromosome binary polymorphism analysis. Forensic Sci Int (2005) 0.77
Y-STR haplotypes in populations from the Eastern Mediterranean region of Turkey. Int J Legal Med (2006) 0.77
Novel transcript profiling of diffuse alveolar damage induced by hyperoxia exposure in mice: normalization by glyceraldehyde 3-phosphate dehydrogenase. Int J Legal Med (2008) 0.77
Correction to 'Elevated germline mutation rate in teenage fathers'. Proc Biol Sci (2016) 0.75
Sex chromosome changes after sex-mismatched allogeneic bone marrow transplantation can mislead the chimerism analysis. Pediatr Blood Cancer (2010) 0.75
Cerebral c-jun expression mapping in sudden infant death syndrome. Acta Neuropathol (2003) 0.75
Utilization of lectin-histochemistry in forensic neuropathology: lectin staining provides useful information for postmortem diagnosis in forensic neuropathology. Leg Med (Tokyo) (2003) 0.75
Fatal leaflet escape in an Edwards TEKNA aortic prosthesis. J Heart Valve Dis (2006) 0.75
An economical mtDNA SNP assay detecting different mitochondrial haplogroups in identical HVR 1 samples of Caucasian ancestry. Mitochondrion (2009) 0.75
Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: results of the 2006-2007 EDNAP collaborative exercise. Forensic Sci Int Genet (2007) 0.75
German standards for forensic molecular genetics investigations in cases of mass disaster victim identification (DVI). Forensic Sci Int Genet (2010) 0.75