Published in Genomics on September 27, 2008
Fine-scaled human genetic structure revealed by SNP microarrays. Genome Res (2009) 1.48
The microbial detection array combined with random Phi29-amplification used as a diagnostic tool for virus detection in clinical samples. PLoS One (2011) 1.00
Characterization of whole genome amplified (WGA) DNA for use in genotyping assay development. BMC Genomics (2012) 0.99
Inter-chromosomal level of genome organization and longevity-related phenotypes in humans. Age (Dordr) (2012) 0.90
Sortilin receptor 1 predicts longitudinal cognitive change. Neurobiol Aging (2013) 0.89
Copy number and loss of heterozygosity detected by SNP array of formalin-fixed tissues using whole-genome amplification. PLoS One (2011) 0.85
Laser capture microdissection (LCM) and whole genome amplification (WGA) of DNA from normal breast tissue --- optimization for genome wide array analyses. BMC Res Notes (2011) 0.84
Variant discovery in targeted resequencing using whole genome amplified DNA. BMC Genomics (2013) 0.77
The International HapMap Project. Nature (2003) 73.65
Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci U S A (2002) 13.58
Variation is the spice of life. Nat Genet (2001) 7.62
Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays. Bioinformatics (2005) 5.01
Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification. Nucleic Acids Res (2004) 3.37
Quality and completeness of SNP databases. Nat Genet (2003) 2.60
Multiple displacement amplification to create a long-lasting source of DNA for genetic studies. Hum Mutat (2006) 1.86
Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplification. Electrophoresis (2005) 1.45
Whole genome-amplified DNA: insights and imputation. Nat Methods (2008) 1.02
Performance of whole-genome amplified DNA isolated from serum and plasma on high-density single nucleotide polymorphism arrays. J Mol Diagn (2008) 0.98
Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science (2010) 18.45
Mobile elements create structural variation: analysis of a complete human genome. Genome Res (2009) 7.06
Genetic evidence for high-altitude adaptation in Tibet. Science (2010) 5.37
Human population genetic structure and inference of group membership. Am J Hum Genet (2003) 4.73
Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Nat Genet (2006) 3.94
Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation. Hum Genomics (2005) 3.77
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency. Am J Hum Genet (2011) 3.43
A probabilistic disease-gene finder for personal genomes. Genome Res (2011) 3.23
High-resolution imaging with adaptive optics in patients with inherited retinal degeneration. Invest Ophthalmol Vis Sci (2007) 3.21
A comprehensive map of mobile element insertion polymorphisms in humans. PLoS Genet (2011) 3.14
Genetic variation among world populations: inferences from 100 Alu insertion polymorphisms. Genome Res (2003) 2.47
A comprehensive analysis of recently integrated human Ta L1 elements. Am J Hum Genet (2002) 2.47
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet (2012) 2.34
Natural selection and molecular evolution in PTC, a bitter-taste receptor gene. Am J Hum Genet (2004) 2.33
High-resolution in vivo imaging of the RPE mosaic in eyes with retinal disease. Invest Ophthalmol Vis Sci (2007) 2.11
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes. Am J Hum Genet (2003) 2.11
Trehalose metabolism and signaling. Annu Rev Plant Biol (2008) 2.09
Retinally stabilized cone-targeted stimulus delivery. Opt Express (2007) 2.06
Microsatellites as EWS/FLI response elements in Ewing's sarcoma. Proc Natl Acad Sci U S A (2008) 2.06
Aphid alarm pheromone produced by transgenic plants affects aphid and parasitoid behavior. Proc Natl Acad Sci U S A (2006) 1.90
Maximum-likelihood estimation of recent shared ancestry (ERSA). Genome Res (2011) 1.88
Alu elements and hominid phylogenetics. Proc Natl Acad Sci U S A (2003) 1.81
A strong signature of balancing selection in the 5' cis-regulatory region of CCR5. Proc Natl Acad Sci U S A (2002) 1.78
Ancestry and disease in the age of genomic medicine. N Engl J Med (2010) 1.71
Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proc Natl Acad Sci U S A (2008) 1.70
Mobile element scanning (ME-Scan) identifies thousands of novel Alu insertions in diverse human populations. Genome Res (2013) 1.66
Metabolic signalling and carbon partitioning: role of Snf1-related (SnRK1) protein kinase. J Exp Bot (2003) 1.64
Larger genetic differences within africans than between Africans and Eurasians. Genetics (2002) 1.62
Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. Am J Hum Genet (2004) 1.61
Resolving single cone inputs to visual receptive fields. Nat Neurosci (2009) 1.58
A method for detecting recent selection in the human genome from allele age estimates. Genetics (2003) 1.55
Adiponectin increases macrophages cholesterol efflux and suppresses foam cell formation in patients with type 2 diabetes mellitus. Atherosclerosis (2013) 1.54
Tumor necrosis factor-alpha-converting enzyme (ADAM17) mediates GPIbalpha shedding from platelets in vitro and in vivo. Circ Res (2004) 1.54
Mobile element scanning (ME-Scan) by targeted high-throughput sequencing. BMC Genomics (2010) 1.54
Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B. Am J Hum Genet (2003) 1.52
Worldwide haplotype diversity and coding sequence variation at human bitter taste receptor loci. Hum Mutat (2005) 1.50
Fine-scaled human genetic structure revealed by SNP microarrays. Genome Res (2009) 1.48
Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotyping. Genomics (2010) 1.47
Recently integrated Alu elements and human genomic diversity. Mol Biol Evol (2003) 1.46
Balinese Y-chromosome perspective on the peopling of Indonesia: genetic contributions from pre-neolithic hunter-gatherers, Austronesian farmers, and Indian traders. Hum Biol (2005) 1.45
AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees. Am J Hypertens (2010) 1.43
Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations. Am J Hum Genet (2001) 1.43
Insights into the demographic history of African Pygmies from complete mitochondrial genomes. Mol Biol Evol (2010) 1.43
Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome. Curr Biol (2002) 1.43
Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation. Invest Ophthalmol Vis Sci (2008) 1.42
Mobile DNA elements in primate and human evolution. Am J Phys Anthropol (2007) 1.38
Genome-wide analysis of the human Alu Yb-lineage. Hum Genomics (2004) 1.33
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome. Am J Hum Genet (2006) 1.31
Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. Proc Natl Acad Sci U S A (2009) 1.30
High-resolution images of retinal structure in patients with choroideremia. Invest Ophthalmol Vis Sci (2013) 1.27
Benzoxazinoid metabolites regulate innate immunity against aphids and fungi in maize. Plant Physiol (2011) 1.26
Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype. Am J Hum Genet (2003) 1.26
Cone structure in retinal degeneration associated with mutations in the peripherin/RDS gene. Invest Ophthalmol Vis Sci (2011) 1.24
OUTER RETINAL TUBULATION IN ADVANCED AGE-RELATED MACULAR DEGENERATION: Optical Coherence Tomographic Findings Correspond to Histology. Retina (2015) 1.24
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency. Am J Hum Genet (2013) 1.23
Recent horizontal transfer of mellifera subfamily mariner transposons into insect lineages representing four different orders shows that selection acts only during horizontal transfer. Mol Biol Evol (2003) 1.22
Genetic determinants of Tibetan high-altitude adaptation. Hum Genet (2011) 1.21
Variants in TNFAIP3, STAT4, and C12orf30 loci associated with multiple autoimmune diseases are also associated with juvenile idiopathic arthritis. Arthritis Rheum (2009) 1.20
A mobile element-based evolutionary history of guenons (tribe Cercopithecini). BMC Biol (2007) 1.18
LINE-1 preTa elements in the human genome. J Mol Biol (2003) 1.16
HapMap tagSNP transferability in multiple populations: general guidelines. Genomics (2008) 1.16
Variation in the human TAS1R taste receptor genes. Chem Senses (2006) 1.14
Genetic diversity in India and the inference of Eurasian population expansion. Genome Biol (2010) 1.13
Alu repeats increase local recombination rates. BMC Genomics (2009) 1.11
Highly conserved protein kinases involved in the regulation of carbon and amino acid metabolism. J Exp Bot (2003) 1.10
Contrasting effects of natural selection on human and chimpanzee CC chemokine receptor 5. Am J Hum Genet (2004) 1.10
Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data. Hum Genet (2004) 1.09
Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8. Am J Med Genet A (2006) 1.08