Published in Am J Hum Genet on May 01, 2008
Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet (2015) 1.74
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. Hum Mol Genet (2008) 1.46
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A high-resolution recombination map of the human genome. Nat Genet (2002) 28.66
A fine-scale map of recombination rates and hotspots across the human genome. Science (2005) 26.82
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Detecting recent positive selection in the human genome from haplotype structure. Nature (2002) 22.00
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Whole-genome patterns of common DNA variation in three human populations. Science (2005) 21.22
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The fine-scale structure of recombination rate variation in the human genome. Science (2004) 17.05
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Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science (2001) 7.87
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome. Am J Hum Genet (2006) 7.70
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Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs. Am J Hum Genet (2000) 3.59
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Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. Proc Natl Acad Sci U S A (1997) 3.32
Heterogeneous mutation processes in human microsatellite DNA sequences. Nat Genet (2000) 2.98
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Biases and reconciliation in estimates of linkage disequilibrium in the human genome. Am J Hum Genet (2006) 2.26
Using nuclear haplotypes with microsatellites to study gene flow between recently separated Cichlid species. Mol Ecol (2004) 1.99
High-resolution SNPs and microsatellite haplotypes point to a single, recent entry of Native American Y chromosomes into the Americas. Mol Biol Evol (2003) 1.85
Mutation patterns at dinucleotide microsatellite loci in humans. Am J Hum Genet (2002) 1.71
The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories. Hum Mol Genet (2003) 1.66
Messages through bottlenecks: on the combined use of slow and fast evolving polymorphic markers on the human Y chromosome. Am J Hum Genet (2000) 1.65
Y-chromosomal microsatellite mutation rates: differences in mutation rate between and within loci. Hum Mutat (2004) 1.60
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome. Am J Hum Genet (2003) 1.58
STRP screening sets for the human genome at 5 cM density. BMC Genomics (2003) 1.53
Linkage disequilibrium testing when linkage phase is unknown. Genetics (2004) 1.41
Whole genome association study of rheumatoid arthritis using 27 039 microsatellites. Hum Mol Genet (2005) 1.36
Insights into recombination from patterns of linkage disequilibrium in humans. Genetics (2004) 1.29
Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome. PLoS Genet (2006) 1.27
The D' measure of overall gametic disequilibrium between pairs of multiallelic loci. Evolution (2000) 1.20
SNPSTRs: empirically derived, rapidly typed, autosomal haplotypes for inference of population history and mutational processes. Genome Res (2002) 1.16
Comparison of the power and accuracy of biallelic and microsatellite markers in population-based gene-mapping methods. Am J Hum Genet (1999) 1.16
Markov chain Monte Carlo analysis of human Y-chromosome microsatellites provides evidence of biased mutation. Proc Natl Acad Sci U S A (1999) 1.15
Mutation rates at two human Y-chromosomal microsatellite loci using small pool PCR techniques. Hum Mol Genet (2001) 1.09
Microsatellites are subject to directional evolution. Nat Genet (1996) 1.06
Precision and accuracy of divergence time estimates from STR and SNPSTR variation. Mol Biol Evol (2004) 0.98
On Fisher's exact test for detecting gametic disequilibrium between DNA polymorphisms. Ann Hum Genet (1997) 0.90
Integrating patterns of polymorphism at SNPs and STRs. Trends Genet (2006) 0.90
The effective size of the Icelandic population and the prospects for LD mapping: inference from unphased microsatellite markers. Eur J Hum Genet (2006) 0.87
Can long-range microsatellite data be used to predict short-range linkage disequilibrium? Hum Mol Genet (2002) 0.84
Power of genome-wide linkage disequilibrium testing by using microsatellite markers. J Hum Genet (2003) 0.82
Clinical applications of Genome Polymorphism Scans. Biol Direct (2006) 0.76
Genetic structure of human populations. Science (2002) 30.91
A human genome diversity cell line panel. Science (2002) 14.11
The genetic structure and history of Africans and African Americans. Science (2009) 10.65
Lineage-specific biology revealed by a finished genome assembly of the mouse. PLoS Biol (2009) 5.45
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species. Gigascience (2013) 4.11
The genetic structure of Pacific Islanders. PLoS Genet (2008) 3.31
Lifestyle transitions in plant pathogenic Colletotrichum fungi deciphered by genome and transcriptome analyses. Nat Genet (2012) 2.92
Validation of rice genome sequence by optical mapping. BMC Genomics (2007) 2.44
Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. Am J Hum Genet (2002) 2.29
Low levels of genetic divergence across geographically and linguistically diverse populations from India. PLoS Genet (2006) 2.26
A 360-kb interchromosomal duplication of the human HYDIN locus. Genomics (2006) 1.91
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits. Hum Mol Genet (2007) 1.77
Single-molecule approach to bacterial genomic comparisons via optical mapping. J Bacteriol (2004) 1.76
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family. Am J Hum Genet (2004) 1.72
Prospects for association mapping in classical inbred mouse strains. Genetics (2007) 1.71
STRP screening sets for the human genome at 5 cM density. BMC Genomics (2003) 1.53
Markers that discriminate between European and African ancestry show limited variation within Africa. Hum Genet (2002) 1.27
Mutant deoxynucleotide carrier is associated with congenital microcephaly. Nat Genet (2002) 1.25
Quantitative trait locus analysis of atherosclerosis in an intercross between C57BL/6 and C3H mice carrying the mutant apolipoprotein E gene. Genetics (2005) 1.24
Quantifying the increase in average human heterozygosity due to urbanisation. Eur J Hum Genet (2008) 1.17
A novel locus for adolescent idiopathic scoliosis on chromosome 12p. J Orthop Res (2009) 1.13
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects. Eur J Hum Genet (2008) 0.98
The Iceland map. Nat Genet (2002) 0.96
Searching the genomes of inbred mouse strains for incompatibilities that reproductively isolate their wild relatives. J Hered (2007) 0.94
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis. Pediatr Nephrol (2002) 0.85
Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders. Hum Mutat (2006) 0.81
Read all about it: The Lancet's Paper of the Year, 2003. Lancet (2003) 0.79
Channel glass-based detection of human short insertion/deletion polymorphisms by tandem hybridization. Mol Biotechnol (2007) 0.78
A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations. Genet Med (2011) 0.75
Practical matters. CHA scales back zero-tolerance on uninsured. Interview by Vince Galloro. Mod Healthc (2002) 0.75
Health care: essential building block of a free society. Origins (1999) 0.75
Not secular. Tradition and law dictate special status for Catholic healthcare. Mod Healthc (2012) 0.75
A comparison of hybridization efficiency between flat glass and channel glass solid supports. Mol Biotechnol (2007) 0.75