Published in Nat Genet on May 08, 2005
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A recombination hotspot in a schizophrenia-associated region of GABRB2. PLoS One (2010) 0.90
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Association of poly-purine/poly-pyrimidine sequences with meiotic recombination hot spots. BMC Genomics (2006) 0.89
Population demographic history can cause the appearance of recombination hotspots. Am J Hum Genet (2012) 0.87
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Structural basis for human PRDM9 action at recombination hot spots. Genes Dev (2016) 0.85
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Whole-genome sequence analyses of Western Central African Pygmy hunter-gatherers reveal a complex demographic history and identify candidate genes under positive natural selection. Genome Res (2016) 0.79
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The fine-scale structure of recombination rate variation in the human genome. Science (2004) 17.05
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The effects of human population structure on large genetic association studies. Nat Genet (2004) 14.88
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A common sequence motif associated with recombination hot spots and genome instability in humans. Nat Genet (2008) 8.64
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nat Genet (2010) 8.48
Comparison of fine-scale recombination rates in humans and chimpanzees. Science (2005) 7.86
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination. Science (2009) 7.35
Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip. PLoS Genet (2009) 6.61
Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. PLoS Genet (2009) 6.36
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas. Nat Genet (2012) 6.25
Intense and highly localized gene conversion activity in human meiotic crossover hot spots. Nat Genet (2004) 6.06
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Inference of population structure using dense haplotype data. PLoS Genet (2012) 4.87
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A statistical method for predicting classical HLA alleles from SNP data. Am J Hum Genet (2008) 4.65
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet (2013) 4.62
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Nat Genet (2009) 4.61
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat Genet (2010) 4.42
Genome-wide and fine-resolution association analysis of malaria in West Africa. Nat Genet (2009) 4.30
Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot. Nat Genet (2002) 4.07
The influence of recombination on human genetic diversity. PLoS Genet (2006) 4.04
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet (2012) 3.40
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet (2010) 3.34
PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans. Nat Genet (2010) 3.33
Bayesian refinement of association signals for 14 loci in 3 common diseases. Nat Genet (2012) 3.31
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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nat Genet (2013) 2.87
A fine-scale chimpanzee genetic map from population sequencing. Science (2012) 2.83
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer. Nature (2012) 2.66
HAPGEN2: simulation of multiple disease SNPs. Bioinformatics (2011) 2.58
Multiple instances of ancient balancing selection shared between humans and chimpanzees. Science (2013) 2.32
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Effects of cis and trans genetic ancestry on gene expression in African Americans. PLoS Genet (2008) 2.09
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Recombination and population structure in Salmonella enterica. PLoS Genet (2011) 1.61
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Application of coalescent methods to reveal fine-scale rate variation and recombination hotspots. Genetics (2004) 1.59
People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population. Eur J Hum Genet (2011) 1.58
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Gang membership, violence, and psychiatric morbidity. Am J Psychiatry (2013) 1.54
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nat Genet (2012) 1.52
Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event. Nat Genet (2012) 1.43
Three- and four-dimensional arterial and venous perforasomes of the internal mammary artery perforator flap. Plast Reconstr Surg (2009) 1.41
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. Am J Hum Genet (2011) 1.35
Presynaptic NMDARs in the hippocampus facilitate transmitter release at theta frequency. Neuron (2010) 1.33
Quantifying the underestimation of relative risks from genome-wide association studies. PLoS Genet (2011) 1.30
The role of hyaluronic acid in wound healing: assessment of clinical evidence. Am J Clin Dermatol (2005) 1.29
Intermediate forms of Charcot-Marie-Tooth neuropathy: a review. Neuromolecular Med (2006) 1.28
The rise and fall of a human recombination hot spot. Nat Genet (2009) 1.25
High recombination rate in herpes simplex virus type 1 natural populations suggests significant co-infection. Infect Genet Evol (2004) 1.23
A robust clustering algorithm for identifying problematic samples in genome-wide association studies. Bioinformatics (2011) 1.19
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14. Brain (2013) 1.18
New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP). Neurogenetics (2008) 1.17
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. Nat Genet (2013) 1.15
Disease model distortion in association studies. Genet Epidemiol (2011) 1.14
Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development. PLoS Genet (2012) 1.14
Economic instruments for obesity prevention: results of a scoping review and modified Delphi survey. Int J Behav Nutr Phys Act (2011) 1.05
A model-based approach to capture genetic variation for future association studies. Genome Res (2006) 1.05
Human telomeres that carry an integrated copy of human herpesvirus 6 are often short and unstable, facilitating release of the viral genome from the chromosome. Nucleic Acids Res (2013) 1.04
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Genomic tools for evolution and conservation in the chimpanzee: Pan troglodytes ellioti is a genetically distinct population. PLoS Genet (2012) 1.00
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PRDM9 marks the spot. Nat Genet (2010) 0.98
Three- and four-dimensional computed tomography angiographic studies of commonly used abdominal flaps in breast reconstruction. Plast Reconstr Surg (2009) 0.98
Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion. Am J Hum Genet (2003) 0.98
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