Jean François Deleuze


Ontology type: schema:Person     


Person Info

NAME

Jean François

SURNAME

Deleuze

Publications in SciGraph latest 50 shown

  • 2019-12 Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations in SCIENTIFIC REPORTS
  • 2018-12 Genetic variants of RNASE3 (ECP) and susceptibility to severe malaria in Senegalese population in MALARIA JOURNAL
  • 2018-12 Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress in NATURE COMMUNICATIONS
  • 2018-12 Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing in TRANSLATIONAL PSYCHIATRY
  • 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 Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk in SCIENTIFIC REPORTS
  • 2017-12 Identification and characterization of two functional variants in the human longevity gene FOXO3 in NATURE COMMUNICATIONS
  • 2017-12 A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus in NPJ GENOMIC MEDICINE
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-07 HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy in ACTA NEUROPATHOLOGICA
  • 2017-05-10 Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression in NATURE COMMUNICATIONS
  • 2017-04 Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy in ACTA NEUROPATHOLOGICA
  • 2017 Locus-Specific DNA Methylation Analysis and Applications to Plants in PLANT EPIGENETICS
  • 2016-12 Toxoplasma gondii exposure may modulate the influence of TLR2 genetic variation on bipolar disorder: a gene–environment interaction study in INTERNATIONAL JOURNAL OF BIPOLAR DISORDERS
  • 2016-11 Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-07 EGR2 mutation enhances phenotype spectrum of Dejerine–Sottas syndrome in JOURNAL OF NEUROLOGY
  • 2016-02-24 Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents in NATURE COMMUNICATIONS
  • 2015-09 De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease in MOLECULAR PSYCHIATRY
  • 2010-11 Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level in GENOME BIOLOGY
  • 2006-04 Remission from Kaposi's sarcoma on HAART is associated with suppression of HIV replication and is independent of protease inhibitor therapy in BRITISH JOURNAL OF CANCER
  • 1999-03 No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia in EUROPEAN JOURNAL OF HUMAN GENETICS
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