Published in Leg Med (Tokyo) on March 25, 2010
Developing criteria and data to determine best options for expanding the core CODIS loci. Investig Genet (2012) 0.99
Short-read, high-throughput sequencing technology for STR genotyping. Biotech Rapid Dispatches (2012) 0.93
Comments on "Interpreting Y chromosome STR haplotype mixture". Leg Med (Tokyo) (2010) 0.75
Integrative annotation of 21,037 human genes validated by full-length cDNA clones. PLoS Biol (2004) 7.17
Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. Am J Hum Genet (2002) 4.29
Genetic evidence supports demic diffusion of Han culture. Nature (2004) 2.92
The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts. Nucleic Acids Res (2007) 2.07
DNA synthesis and biological security. Nat Biotechnol (2007) 1.91
Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122. Am J Hum Genet (2005) 1.86
The Microbial Rosetta Stone Database: a compilation of global and emerging infectious microorganisms and bioterrorist threat agents. BMC Microbiol (2005) 1.73
Association of apolipoprotein E4 and haplotypes of the apolipoprotein E gene with lobar intracerebral hemorrhage. Stroke (2005) 1.65
Admixture in Hispanics: distribution of ancestral population contributions in the Continental United States. Hum Biol (2003) 1.64
Assessment of optimal size and composition of the U.S. National Registry of hematopoietic stem cell donors. Transplantation (2004) 1.59
Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans. Am J Hum Genet (2004) 1.57
Population genetic analyses of the NGM STR loci. Int J Legal Med (2010) 1.50
V75R576 IL-4 receptor alpha is associated with allergic asthma and enhanced IL-4 receptor function. J Immunol (2002) 1.40
Examining population stratification via individual ancestry estimates versus self-reported race. Cancer Epidemiol Biomarkers Prev (2005) 1.33
Genetic analysis and attribution of microbial forensics evidence. Crit Rev Microbiol (2005) 1.31
Genome-wide structural and evolutionary analysis of the P450 monooxygenase genes (P450ome) in the white rot fungus Phanerochaete chrysosporium: evidence for gene duplications and extensive gene clustering. BMC Genomics (2005) 1.27
Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res (2002) 1.26
Mutation rates at Y chromosome short tandem repeats in Texas populations. Forensic Sci Int Genet (2009) 1.26
Association of Phosphodiesterase 4D with ischemic stroke: a population-based case-control study. Stroke (2005) 1.25
Comparisons of familial DNA database searching strategies. J Forensic Sci (2011) 1.25
Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift. Hum Genet (2003) 1.23
DNA identification by pedigree likelihood ratio accommodating population substructure and mutations. Investig Genet (2010) 1.20
Evidence for a major gene influence on persistent developmental stuttering. Hum Biol (2004) 1.15
Forensics and mitochondrial DNA: applications, debates, and foundations. Annu Rev Genomics Hum Genet (2003) 1.15
An improved method for post-PCR purification for mtDNA sequence analysis. J Forensic Sci (2002) 1.13
A Ser49Cys variant in the ataxia telangiectasia, mutated, gene that is more common in patients with breast carcinoma compared with population controls. Cancer (2004) 1.11
Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles. Forensic Sci Int (2003) 1.11
Epidemiology. DNA identifications after the 9/11 World Trade Center attack. Science (2005) 1.09
Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia. Ann Hum Genet (2012) 1.08
Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. Mol Biol Evol (2004) 1.07
Effect of surgical weight loss on sleep architecture in adolescents with severe obesity. Obes Surg (2008) 1.07
Choosing relatives for DNA identification of missing persons. J Forensic Sci (2010) 1.07
Diisocyanate asthma and gene-environment interactions with IL4RA, CD-14, and IL-13 genes. Ann Allergy Asthma Immunol (2006) 1.06
Association of ApoE genetic variants with obstructive sleep apnea in children. Sleep Med (2007) 1.06
Mutation rate variation at human dinucleotide microsatellites. Genetics (2005) 1.06
Texas population substructure and its impact on estimating the rarity of Y STR haplotypes from DNA evidence*. J Forensic Sci (2009) 1.06
Single nucleotide polymorphism typing with massively parallel sequencing for human identification. Int J Legal Med (2013) 1.06
Toward a system of microbial forensics: from sample collection to interpretation of evidence. Appl Environ Microbiol (2005) 1.05
Assessing a novel room temperature DNA storage medium for forensic biological samples. Forensic Sci Int Genet (2011) 1.03
Unequal contributions of male and female gene pools from parental populations in the African descendants of the city of Melo, Uruguay. Am J Phys Anthropol (2002) 1.01
Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia. PLoS One (2010) 1.01
Temporal-spatial activation of apoptosis and epithelial injury in murine experimental biliary atresia. Hepatology (2008) 1.01
Characterization of human control region sequences of the African American SWGDAM forensic mtDNA data set. Forensic Sci Int (2005) 1.00
Whole-genome amplification: relative efficiencies of the current methods. Leg Med (Tokyo) (2005) 1.00
Developing criteria and data to determine best options for expanding the core CODIS loci. Investig Genet (2012) 0.99
Staging of biliary atresia at diagnosis by molecular profiling of the liver. Genome Med (2010) 0.99
Distribution and effects of nonsense polymorphisms in human genes. PLoS One (2008) 0.99
Use of prior odds for missing persons identifications. Investig Genet (2011) 0.98
Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations. Hum Mutat (2010) 0.98
Evaluation of variation in control region sequences for Hispanic individuals in the SWGDAM mtDNA data set. J Forensic Sci (2006) 0.98
Uncertainties in estimating health risks associated with exposure to ionising radiation. J Radiol Prot (2013) 0.98
Association of ALOX5AP with ischemic stroke: a population-based case-control study. Hum Genet (2007) 0.97
Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25. Am J Hum Genet (2004) 0.97
A validation study of the Qiagen Investigator DIPplex® kit; an INDEL-based assay for human identification. Int J Legal Med (2012) 0.97
Twelve short tandem repeat loci Y chromosome haplotypes: genetic analysis on populations residing in North America. Forensic Sci Int (2005) 0.97
Quality sample collection, handling, and preservation for an effective microbial forensics program. Appl Environ Microbiol (2006) 0.96
Canine population data generated from a multiplex STR kit for use in forensic casework. J Forensic Sci (2009) 0.95
Concept, measurement and use of acculturation in health and disease risk studies. Coll Antropol (2010) 0.95
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. J Cyst Fibros (2007) 0.95
Recommendations for consistent treatment of length variants in the human mitochondrial DNA control region. Forensic Sci Int (2002) 0.94
Base composition analysis of human mitochondrial DNA using electrospray ionization mass spectrometry: a novel tool for the identification and differentiation of humans. Anal Biochem (2005) 0.93
Accurate, rapid and high-throughput detection of strain-specific polymorphisms in Bacillus anthracis and Yersinia pestis by next-generation sequencing. Investig Genet (2010) 0.92
Statistical power of association using the extreme discordant phenotype design. Pharmacogenet Genomics (2006) 0.92
Genotypic interaction between DRD4 and DAT1 loci is a high risk factor for attention-deficit/hyperactivity disorder in Chilean families. Am J Med Genet B Neuropsychiatr Genet (2006) 0.92
Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™. BMC Genomics (2015) 0.92
Genetic and environmental risk factors for childhood eczema development and allergic sensitization in the CCAAPS cohort. J Invest Dermatol (2009) 0.92
Characterization of the Caucasian haplogroups present in the SWGDAM forensic mtDNA dataset for 1771 human control region sequences. Scientific Working Group on DNA Analysis Methods. J Forensic Sci (2002) 0.91
Genome-wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence. Arthritis Rheum (2003) 0.91
STRait Razor: a length-based forensic STR allele-calling tool for use with second generation sequencing data. Forensic Sci Int Genet (2013) 0.91
Criteria for validation of methods in microbial forensics. Appl Environ Microbiol (2008) 0.91
p53 codon 72 polymorphism and risk of cervical cancer. Biol Res (2003) 0.90
Genetic admixture in three Mexican Mestizo populations based on D1S80 and HLA-DQA1 loci. Am J Hum Biol (2002) 0.90
Population studies on three Native Alaska population groups using STR loci. Forensic Sci Int (2002) 0.90
Maternity exclusion with a very high autosomal STRs kinship index. Int J Legal Med (2012) 0.90
Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height. PLoS One (2012) 0.89
Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. Genome Res (2002) 0.89
Prototype PowerPlex® Y23 System: A concordance study. Forensic Sci Int Genet (2012) 0.88
A novel SNaPshot assay to detect the mdx mutation. Muscle Nerve (2008) 0.88
Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia. Eur J Hum Genet (2010) 0.88
The Microbial Rosetta Stone: a database system for tracking infectious microorganisms. Int J Legal Med (2008) 0.88
Microbial forensics: the next forensic challenge. Int J Legal Med (2005) 0.88
Aircraft-Assisted Pilot Suicides: Lessons to be Learned. Aviat Space Environ Med (2014) 0.87
Genetic susceptibility to obstructive sleep apnea in the obese child. Sleep Med (2007) 0.87
A shared Y-chromosomal heritage between Muslims and Hindus in India. Hum Genet (2006) 0.87
Patients of African ancestry with hemophagocytic lymphohistiocytosis share a common haplotype of PRF1 with a 50delT mutation. J Pediatr (2006) 0.87
Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing. Croat Med J (2015) 0.87
Developmental validation of short tandem repeat reagent kit for forensic DNA profiling of canine biological material. Croat Med J (2009) 0.87
Base composition profiling of human mitochondrial DNA using polymerase chain reaction and direct automated electrospray ionization mass spectrometry. Anal Chem (2009) 0.86
Minnesota population data on 15 STR loci using the Identifiler kit. J Forensic Sci (2006) 0.85
Massively parallel sequencing of forensically relevant single nucleotide polymorphisms using TruSeq™ forensic amplicon. Int J Legal Med (2014) 0.85
Guatemala mestizo population data on 15 STR loci (Identifiler Kit). J Forensic Sci (2006) 0.85
Re: Leptin and leptin receptor gene polymorphisms in obstructive sleep apnea syndrome. Chest (2008) 0.85
Biocrimes, microbial forensics, and the physician. PLoS Med (2005) 0.85
Haplotype block: a new type of forensic DNA markers. Int J Legal Med (2009) 0.85