Jianxin Shi, Peng Li. Genet Epidemiol 2012
Times Cited: 4
Times Cited: 4
Times Cited
Times Co-cited
Similarity
Strong association of de novo copy number mutations with autism.
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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
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Circular binary segmentation for the analysis of array-based DNA copy number data.
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A robust statistical method for case-control association testing with copy number variation.
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Optimal Sparse Segment Identification with Application in Copy Number Variation Analysis.
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Global variation in copy number in the human genome.
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Markov Models for inferring copy number variations from genotype data on Illumina platforms.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
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Microduplications of 16p11.2 are associated with schizophrenia.
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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
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Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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Novel copy number variants in children with autism and additional developmental anomalies.
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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De novo gene disruptions in children on the autistic spectrum.
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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A first-generation linkage disequilibrium map of human chromosome 22.
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Fine-scale structural variation of the human genome.
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Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
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Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
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An algorithm for inferring complex haplotypes in a region of copy-number variation.
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Common deletion polymorphisms in the human genome.
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Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
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MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data.
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Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.
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Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma.
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Comparing CNV detection methods for SNP arrays.
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Large-scale copy number polymorphism in the human genome.
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Copy number variation at 1q21.1 associated with neuroblastoma.
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famCNV: copy number variant association for quantitative traits in families.
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A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.