Published in Nat Genet on February 01, 2005
Genetic design and statistical power of nested association mapping in maize. Genetics (2008) 4.92
Analysis of genomic admixture in Uyghur and its implication in mapping strategy. Am J Hum Genet (2008) 2.30
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans. Hum Mol Genet (2010) 2.11
A genome-wide analysis of admixture in Uyghurs and a high-density admixture map for disease-gene discovery. Am J Hum Genet (2008) 1.92
A clarified position for Solanum lycopersicum var. cerasiforme in the evolutionary history of tomatoes (solanaceae). BMC Plant Biol (2008) 1.75
Admixture mapping provides evidence of association of the VNN1 gene with hypertension. PLoS One (2007) 1.31
Mapping genes that predict treatment outcome in admixed populations. Pharmacogenomics J (2010) 1.05
Correcting for measurement error in individual ancestry estimates in structured association tests. Genetics (2007) 1.04
Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markers. BMC Med Genomics (2010) 0.96
A candidate gene based approach validates Md-PG1 as the main responsible for a QTL impacting fruit texture in apple (Malus x domestica Borkh). BMC Plant Biol (2013) 0.95
Biogeographic ancestry, self-identified race, and admixture-phenotype associations in the Heart SCORE Study. Am J Epidemiol (2012) 0.92
The use of plasmodes as a supplement to simulations: A simple example evaluating individual admixture estimation methodologies. Comput Stat Data Anal (2009) 0.92
Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia. BMC Med Genet (2010) 0.86
Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosis. Am J Hum Genet (2006) 0.83
SOD2 polymorphisms: unmasking the effect of polymorphism on splicing. BMC Med Genet (2007) 0.80
What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research. AJOB Prim Res (2012) 0.79
Human population structure, genome autozygosity and human health. Genome Med (2009) 0.77
Extensive copy number variations in admixed Indian population of African ancestry: potential involvement in adaptation. Genome Biol Evol (2014) 0.76
Genomic research, publics and experts in Latin America: Nation, race and body. Soc Stud Sci (2015) 0.75
Mapping asthma-associated variants in admixed populations. Front Genet (2015) 0.75
Building the genomic nation: 'Homo Brasilis' and the 'Genoma Mexicano' in comparative cultural perspective. Soc Stud Sci (2015) 0.75
Investigating the case of human nose shape and climate adaptation. PLoS Genet (2017) 0.75
Global mobility and the break-up of human population isolates - neglected mechanisms in health, demographics, and anthropology. Croat Med J (2015) 0.75
Admixture mapping for hypertension loci with genome-scan markers. Nat Genet (2005) 6.78
Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet (2008) 10.52
The Collaborative Cross, a community resource for the genetic analysis of complex traits. Nat Genet (2004) 9.37
Strategies for mapping and cloning quantitative trait genes in rodents. Nat Rev Genet (2005) 5.57
The nature and identification of quantitative trait loci: a community's view. Nat Rev Genet (2003) 3.96
A highly significant association between a COMT haplotype and schizophrenia. Am J Hum Genet (2002) 3.52
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genet (2008) 3.33
Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. Am J Hum Genet (2007) 3.31
The involvement of ErbB4 with schizophrenia: association and expression studies. Am J Med Genet B Neuropsychiatr Genet (2006) 1.94
Linkage disequilibrium patterns of the human genome across populations. Hum Mol Genet (2003) 1.91
Length distributions of identity by descent reveal fine-scale demographic history. Am J Hum Genet (2012) 1.91
High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues. Genome Res (2009) 1.83
Power and efficiency of the TDT and case-control design for association scans. Behav Genet (2002) 1.75
Using advanced intercross lines for high-resolution mapping of HDL cholesterol quantitative trait loci. Genome Res (2003) 1.66
An integrated in silico gene mapping strategy in inbred mice. Genetics (2006) 1.60
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. PLoS Genet (2012) 1.52
The architecture of long-range haplotypes shared within and across populations. Mol Biol Evol (2011) 1.50
A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients. Schizophr Res (2005) 1.30
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. PLoS Genet (2012) 1.25
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Nat Commun (2013) 1.25
Quantitative technologies for allele frequency estimation of SNPs in DNA pools. Mol Cell Probes (2002) 1.23
Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression. Hum Mol Genet (2011) 1.16
COMT: a common susceptibility gene in bipolar disorder and schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2004) 1.15
Genomics: Gene expression meets genetics. Nature (2003) 1.15
Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2. Genome Res (2010) 1.10
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Genome Biol (2012) 1.08
Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry (2013) 1.05
A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia. Hum Genet (2006) 1.00
Fine-scale maps of recombination rates and hotspots in the mouse genome. Genetics (2012) 0.99
Experimental designs for QTL fine mapping in rodents. Methods Mol Biol (2002) 0.97
The variance of identity-by-descent sharing in the Wright-Fisher model. Genetics (2012) 0.95
Acetylcholinesterase/paraoxonase interactions increase the risk of insecticide-induced Parkinson's disease. FASEB J (2005) 0.93
Correlational analysis for identifying genes whose regulation contributes to chronic neuropathic pain. Mol Pain (2009) 0.93
Global coevolution of human microRNAs and their target genes. Mol Biol Evol (2014) 0.93
The genetic variation of RELN expression in schizophrenia and bipolar disorder. PLoS One (2011) 0.90
Mouse inbred strain sequence information and yin-yang crosses for quantitative trait locus fine mapping. Genetics (2004) 0.90
Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locus. Biol Psychiatry (2008) 0.87
Animal models of psychiatric disease. Curr Opin Genet Dev (2008) 0.87
Human embryonic stem cells from aneuploid blastocysts identified by pre-implantation genetic screening. In Vitro Cell Dev Biol Anim (2010) 0.86
Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population. Hum Genet (2008) 0.86
A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder. Psychiatr Genet (2009) 0.86
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. J Invest Dermatol (2012) 0.86
Sex-specific variability and a 'cage effect' independently mask a neuropathic pain quantitative trait locus detected in a whole genome scan. Eur J Neurosci (2007) 0.86
Mono-nucleotide repeats (MNRs): a neglected polymorphism for generating high density genetic maps in silico. Hum Genet (2004) 0.85
pain1: a neuropathic pain QTL on mouse chromosome 15 in a C3HxC58 backcross. Pain (2005) 0.85
pain2: A neuropathic pain QTL identified on rat chromosome 2. Pain (2007) 0.84
Population-based gene discovery in the post-genomic era. Drug Discov Today (2001) 0.84
An efficient haplotyping method with DNA pools. Nucleic Acids Res (2002) 0.84
Identifying alternative hyper-splicing signatures in MG-thymoma by exon arrays. PLoS One (2008) 0.83
Forensic identification of an individual in complex DNA mixtures. Forensic Sci Int Genet (2010) 0.82
Neurogenomic evidence for a shared mechanism of the antidepressant effects of exercise and chronic fluoxetine in mice. PLoS One (2012) 0.82
Closing in on complex traits. Nat Genet (2006) 0.81
Genetic variants in major depression. Novartis Found Symp (2008) 0.80
Further investigation of the association between rs7341475 and rs17746501 and schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2010) 0.80
Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved? Int J Neuropsychopharmacol (2009) 0.79
Mice congenic for a locus that determines phenotype in the neuroma model of neuropathic pain. Exp Neurol (2006) 0.78
A new in vivo model of pantothenate kinase-associated neurodegeneration reveals a surprising role for transcriptional regulation in pathogenesis. Front Cell Neurosci (2013) 0.77
Genetic dissection of common diseases. Isr Med Assoc J (2002) 0.75
Population-based gene discovery in psychiatric diseases. Expert Rev Neurother (2003) 0.75
Further tests of the association between schizophrenia and single nucleotide polymorphism markers at the catechol-O-methyltransferase locus in an Askenazi Jewish population using microsatellite markers. Psychiatr Genet (2005) 0.75