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Author Details

Adrian M St??tz
St. Anna Children's Cancer Research Institute (CCRI)
1997
55
33
Nathan Sheffield (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
34050156Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden.Nat Commun2021
34782764Chromothripsis followed by circular recombination drives oncogene amplification in human cancer.Nat Genet2021
34426444Quantification of Translocation-Specific ctDNA Provides an Integrating Parameter for Early Assessment of Treatment Response and Risk Stratification in Ewing Sarcoma.Clin Cancer Res2021
32268084Genome-wide Screens Implicate Loss of Cullin Ring Ligase 3 in Persistent Proliferation and Genome Instability in TP53-Deficient Cells.Cell Rep2020
32796846A scalable CRISPR/Cas9-based fluorescent reporter assay to study DNA double-strand break repair choice.Nat Commun2020
30537516Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories.Cancer Cell2018
27869826Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking.Nat Genet2017
28818866Systematic Identification of Determinants for Single-Strand Annealing-Mediated Deletion Formation in <i>Saccharomyces cerevisiae</i>.G3 (Bethesda)2017
26993771Immortalization capacity of HPV types is inversely related to chromosomal instability.Oncotarget2016
26615982MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.Hum Mutat2016
27121553Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).Genes Chromosomes Cancer2016
27161561Next-generation sequencing-based detection of germline L1-mediated transductions.BMC Genomics2016
26028266Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.Nat Commun2015
26432246An integrated map of structural variation in 2,504 human genomes.Nature2015
26294725Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation.Haematologica2015
26346554Erratum: analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.Nat Commun2015
26415501A cell-based model system links chromothripsis with hyperploidy.Mol Syst Biol2015
26121404Assembly and diploid architecture of an individual human genome via single-molecule technologies.Nat Methods2015
26214592Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.Nat Genet2015
24452265SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome.Genes Immun2014
25344728Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads.Nat Biotechnol2014
25043047Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.Nature2014
24972766The activating STAT5B N642H mutation is a common abnormality in pediatric T-cell acute lymphoblastic leukemia and confers a higher risk of relapse.Haematologica2014
24754353A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.Bipolar Disord2014
24553142Epigenomic alterations define lethal CIMP-positive ependymomas of infancy.Nature2014
23222910Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing.Genome Res2013
23817572Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.Nat Genet2013
24014587Primate genome architecture influences structural variation mechanisms and functional consequences.Proc Natl Acad Sci U S A2013
23665482Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype.Matrix Biol2013
23410972Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer.Cancer Cell2013
23550136The genomic and transcriptomic landscape of a HeLa cell line.G3 (Bethesda)2013
23561803Whole-exome sequencing links caspase recruitment domain 11 (CARD11) inactivation to severe combined immunodeficiency.J Allergy Clin Immunol2013
22170014Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study.Eur J Appl Physiol2012
22962449DELLY: structural variant discovery by integrated paired-end and split-read analysis.Bioinformatics2012
22832583Dissecting the genomic complexity underlying medulloblastoma.Nature2012
22832581Subgroup-specific structural variation across 1,000 medulloblastoma genomes.Nature2012
22912860An improved protocol for sequencing of repetitive genomic regions and structural variations using mutagenesis and next generation sequencing.PLoS One2012
22265402Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.Cell2012
20980461Molecular mechanisms for activation of the agouti-related protein and stimulation of appetite.Diabetes2011
21876680A comprehensive map of mobile element insertion polymorphisms in humans.PLoS Genet2011
21293372Mapping copy number variation by population-scale genome sequencing.Nature2011
20037582Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library.Nat Biotechnol2010
21085617Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.PLoS Comput Biol2010
20468057Case-control association study of TGOLN2 in attempted suicide.Am J Med Genet B Neuropsychiatr Genet2010
18984674KIF5B gene sequence variation and response of cardiac stroke volume to regular exercise.Physiol Genomics2009
19384345Functional identification of the promoter of SLC4A5, a gene associated with cardiovascular and metabolic phenotypes in the HERITAGE Family Study.Eur J Hum Genet2009
17372310Circadian expression of genes regulating food intake.Obesity (Silver Spring)2007
15682447CD45 isoform expression is associated with different susceptibilities of human naive and effector CD4+ T cells to respond to IL-4.Eur J Immunol2005
16141394Selective tissue uptake of agouti-related protein(82-131) and its modulation by fasting.Endocrinology2005
15961186The agouti-related protein and its role in energy homeostasis.Peptides2005
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Collaborators

Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 38
Tobias Rausch
University of Heidelberg
Co-authored papers 14
Benjamin Raeder
Co-authored papers 10
Joachim Weischenfeldt
University of Copenhagen
Co-authored papers 8
Andreas E Kulozik
Co-authored papers 8
Paul A Northcott
St Jude Children's Research Hospital
Co-authored papers 8
Stefan M Pfister
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 8
Roland Eils
Berlin Institute of Health (BIH) and Charite
Co-authored papers 7
Andrey Korshunov
Institute of Pathology, University Hospital Heidelberg
Co-authored papers 6
Natalie J??ger
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 6
Peter Lichter
German Cancer Research Center (DKFZ)
Co-authored papers 6
Michael D Taylor
The Hospital for Sick Children
Co-authored papers 6
Sebastian M Waszak
University of California san francisco
Co-authored papers 6
David T W Jones
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 6
Benedikt Brors
German Cancer Research Center (DKFZ)
Co-authored papers 6
Hans-J??rg Warnatz
Max Planck Institute for Molecular Genetics
Co-authored papers 6
Marcel Kool
Hopp Children's Cancer Center (KiTZ)
Co-authored papers 6
Marie-Laure Yaspo
Max Planck Institute for Molecular Genetics
Co-authored papers 6
Mark Gerstein
Yale University
Co-authored papers 5
Hendrik Witt
Co-authored papers 5
Jan Koster
Amsterdam University Medical Centers location AMC
Co-authored papers 5
Christof von Kalle
Berlin Institute of Health at Charite-Universitatsmedizin Berlin
Co-authored papers 5
David J H Shih
University of Texas MD Anderson Cancer Center Houston
Co-authored papers 5
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
Co-authored papers 5
Andreas von Deimling
Co-authored papers 5
Olaf Witt
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 5
Marc Remke
and Clinical Immunology, Heinrich Heine University, University Hospital Dusseldorf
Co-authored papers 5
Chris Lawerenz
German Cancer Research Center (DKFZ)
Co-authored papers 5
Huriye Seker-Cin
Institute of Pathology, Heidelberg University Hospital
Co-authored papers 5
Vyacheslav Amstislavskiy
Max-Planck-Institute for Molecular Genetics
Co-authored papers 4
Release 1.2