Publications of Marie-Laure Yaspo-Lehrach
All genres
Journal Article (80)
41.
Journal Article
ChIP-Seq and RNA-Seq Analyses Identify Components of the Wnt and Fgf Signaling Pathways as Prep1 Target Genes in Mouse Embryonic Stem Cells. PLoS One (2015)
42.
Journal Article
47 (1), pp. 22 - 30 (2015)
BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence. Nature Genetics 43.
Journal Article
16 (1), 16:1018 (2015)
Erratum to: 'The direction of cross affects obesity after puberty in male but not female offspring'. BMC Genomics 44.
Journal Article
9 (10), e111006 (2014)
Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains. PLoS One 45.
Journal Article
9 (9), pp. 1104 - 1114 (2014)
Personalized medicine approaches for colon cancer driven by genomics and systems biology: OncoTrack. Biotechnology Journal 46.
Journal Article
15, 15:675 (2014)
Influence of RNA extraction methods and library selection schemes on RNA-seq data. BMC Genomics 47.
Journal Article
42 (14), e110 (2014)
ARH-seq: identification of differential splicing in RNA-seq data. Nucleic Acids Research (London) 48.
Journal Article
511 (7510), pp. 428 - 434 (2014)
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma. Nature 49.
Journal Article
15 (6), R88 (2014)
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 50.
Journal Article
510 (7506), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 51.
Journal Article
5, 5:3934 (2014)
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature Communications 52.
Journal Article
26 (510), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 53.
Journal Article
7 (325), rs3 (2014)
Parallel profiling of the transcriptome, cistrome, and epigenome in the cellular response to ionizing radiation. Science Signaling 54.
Journal Article
342 (6154), p. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 55.
Journal Article
155 (3), pp. 567 - 81 (2013)
Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 56.
Journal Article
45 (8), pp. 927 - 32 (2013)
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma. Nature Genetics 57.
Journal Article
3 (4), pp. 1321 - 33 (2013)
Analysis of the DNA-binding profile and function of TALE homeoproteins reveals their specialization and specific interactions with Hox genes/proteins. Cell Reports 58.
Journal Article
23 (2), pp. 159 - 70 (2013)
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer. Cancer Cell 59.
Journal Article
491 (7422), pp. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature 60.
Journal Article
422 (4), pp. 643 - 646 (2012)
A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods. Biochemical and Biophysical Research Communications