Adrian M Stütz

Ontology type: schema:Person     

Person Info


Adrian M



Publications in SciGraph latest 50 shown

  • 2017-01 Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking in NATURE GENETICS
  • 2016-12 Next-generation sequencing-based detection of germline L1-mediated transductions in BMC GENOMICS
  • 2015-12 Erratum: Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms in NATURE COMMUNICATIONS
  • 2015-12 Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms in NATURE COMMUNICATIONS
  • 2015-10 An integrated map of structural variation in 2,504 human genomes in NATURE
  • 2015-09 Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options in NATURE GENETICS
  • 2015-08 Assembly and diploid architecture of an individual human genome via single-molecule technologies in NATURE METHODS
  • 2014-11 Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads in NATURE BIOTECHNOLOGY
  • 2014-07 Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma in NATURE
  • 2014-04 SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome in GENES & IMMUNITY
  • 2013-08 Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma in NATURE GENETICS
  • 2012-10 ICGC PedBrain - dissecting the genomic complexity underlying medulloblastoma using whole-genome sequencing in BMC PROCEEDINGS
  • 2012-08 Dissecting the genomic complexity underlying medulloblastoma in NATURE
  • 2012-08 Subgroup-specific structural variation across 1,000 medulloblastoma genomes in NATURE
  • 2012-08 Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study in EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
  • 2011-02-03 Mapping copy number variation by population-scale genome sequencing in NATURE
  • 2010-10-28 A map of human genome variation from population-scale sequencing in NATURE
  • 2010-06 Potenzial und Herausforderungen der personalisierten Genomik und des 1000-Genom-Projekts in MEDIZINISCHE GENETIK
  • 2010-01 Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library in NATURE BIOTECHNOLOGY
  • 2009-11 Functional identification of the promoter of SLC4A5, a gene associated with cardiovascular and metabolic phenotypes in the HERITAGE Family Study in EUROPEAN JOURNAL OF HUMAN GENETICS
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