Delphine Bacq


Ontology type: schema:Person     


Person Info

NAME

Delphine

SURNAME

Bacq

Publications in SciGraph latest 50 shown

  • 2018-12 Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress in NATURE COMMUNICATIONS
  • 2017-12 Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis in NATURE COMMUNICATIONS
  • 2017-12 Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort in NPJ BREAST CANCER
  • 2017-12 Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes in BREAST CANCER RESEARCH
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2016-06 SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease in MOLECULAR PSYCHIATRY
  • 2016-05 Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-11 Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families in NEUROGENETICS
  • 2006-07 Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14 in MOLECULAR PSYCHIATRY
  • 2002-11 The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin in NATURE GENETICS
  • 2002-10 The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin in NATURE GENETICS
  • 2002-04 Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2 in HUMAN GENETICS
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