Maika Malig

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2020-08-10 An evolutionary driver of interspersed segmental duplications in primates in GENOME BIOLOGY
  • 2020-07-18 Characterization of R-Loop Structures Using Single-Molecule R-Loop Footprinting and Sequencing in RNA-CHROMATIN INTERACTIONS
  • 2017-02-17 The evolution and population diversity of human-specific segmental duplications in NATURE ECOLOGY & EVOLUTION
  • 2017-02-03 Epigenetic origin of evolutionary novel centromeres in SCIENTIFIC REPORTS
  • 2016-08-03 Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility in NATURE
  • 2015-09-30 A global reference for human genetic variation in NATURE
  • 2015-09-30 An integrated map of structural variation in 2,504 human genomes in NATURE
  • 2014-11-10 Resolving the complexity of the human genome using single-molecule sequencing in NATURE
  • 2014-10-23 Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity in GENES & IMMUNITY
  • 2014-10-19 Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability in NATURE GENETICS
  • 2013-07-03 Great ape genetic diversity and population history in NATURE
  • 2012-09-23 Estimating human mutation rate using autozygosity in a founder population in NATURE GENETICS
  • 2012-07-01 Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism in NATURE GENETICS
  • 2012-04-04 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations in NATURE
  • 2010-08-22 A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk in NATURE GENETICS
  • 2010-04-18 Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions in NATURE METHODS
  • 2009-08-30 Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing in NATURE GENETICS
  • 2008-05 Mapping and sequencing of structural variation from eight human genomes in NATURE
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