sameAs
Initial sequencing and analysis of the human genomeDeath and resurrection of the human IRGM geneStable in a genome of instability: an interview with Evan Eichler. Interview by Jane GitschierModernizing reference genome assembliesLineage-specific biology revealed by a finished genome assembly of the mouseThe genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wildA high-resolution integrated map of copy number polymorphisms within and between breeds of the modern domesticated dogAncient human genomes suggest three ancestral populations for present-day EuropeansPopulation stratification of a common APOBEC gene deletion polymorphismGeneration and annotation of the DNA sequences of human chromosomes 2 and 4The DNA sequence of human chromosome 7The DNA sequence and biology of human chromosome 19The genome sequence of taurine cattle: a window to ruminant biology and evolutionFine-scale structural variation of the human genomeResolving the complexity of the human genome using single-molecule sequencingThe bonobo genome compared with the chimpanzee and human genomesInsights into hominid evolution from the gorilla genome sequenceGenetic history of an archaic hominin group from Denisova Cave in SiberiaComparative and demographic analysis of orang-utan genomesThe genome of a songbirdFinding the missing heritability of complex diseasesMapping and sequencing of structural variation from eight human genomesGenome analysis of the platypus reveals unique signatures of evolutionSequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolutionGenome sequence of the Brown Norway rat yields insights into mammalian evolutionMutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problemsDisruptive CHD8 mutations define a subtype of autism early in developmentCloning, sequencing, gene organization, and localization of the human ribosomal protein RPL23A geneThe sequence and analysis of duplication-rich human chromosome 16Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10pA SWI/SNF-related autism syndrome caused by de novo mutations in ADNPA high-coverage genome sequence from an archaic Denisovan individualNext-generation VariationHunter: combinatorial algorithms for transposon insertion discoveryDiversity of human copy number variation and multicopy genesEvolution of human-specific neural SRGAP2 genes by incomplete segmental duplicationMapping copy number variation by population-scale genome sequencingTargeted capture and massively parallel sequencing of 12 human exomesDe novo mutations in epileptic encephalopathiesEstimating the human mutation rate using autozygosity in a founder populationRefinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
P50
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P50
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American scientist
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Amerikaans onderzoeker (1968-)
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eolaĆ MeiriceĆ”nach
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nolavan LamerikƤnik
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Evan E. Eichler
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Evan E. Eichler
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