about
Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary historyInferring haplotypes at the NAT2 locus: the computational approach.Gene expression and hepatitis C virus infectionRapid birth-and-death evolution of the xenobiotic metabolizing NAT gene family in vertebrates with evidence of adaptive selectionSelecting predictive markers for pharmacogenetic traits: tagging vs. data-mining approaches.Data-mining methods as useful tools for predicting individual drug response: application to CYP2D6 data.Evaluating NAT2PRED for inferring the individual acetylation status from unphased genotype dataArylamine N-acetyltransferase 2 (NAT2) genetic diversity and traditional subsistence: a worldwide population surveyNF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype.CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy.Insights into HLA-G Genetics Provided by Worldwide Haplotype DiversityPositive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humansAssociation of IL-4 and IL-10 maternal haplotypes with immune responses to P. falciparum in mothers and newbornsSPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.Identification of a Major Dimorphic Region in the Functionally Critical N-Terminal ID1 Domain of VAR2CSA.Variation in NAT2 acetylation phenotypes is associated with differences in food-producing subsistence modes and ecoregions in Africa.Soluble human leukocyte antigen -G during pregnancy and infancy in Benin: Mother/child resemblance and association with the risk of malaria infection and low birth weight.Proteomic analysis of Plasmodium falciparum parasites from patients with cerebral and uncomplicated malariaUnravelling the genetic basis of variable clinical expression in neurofibromatosis 1.Parental genotypes in the risk of a complex disease.Detection and characterization of NF1 microdeletions by custom high resolution array CGH.ANRIL, a long, noncoding RNA, is an unexpected major hotspot in GWAS.Genetic diversity of VAR2CSA ID1-DBL2Xb in worldwide Plasmodium falciparum populations: impact on vaccine design for placental malaria.Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens.HLA-E coding and 3' untranslated region variability determined by next-generation sequencing in two West-African population samples.Genetic analysis of ID1-DBL2X predicts its validity as a vaccine candidate in Colombia and supports at least two independently introduced Plasmodium falciparum populations in the region.Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis.Familial Aggregation and Heritability of Wuchereria bancrofti Infection.A homogenizing process of selection has maintained an "ultra-slow" acetylation NAT2 variant in humans.NF1 single and multi-exons copy number variations in neurofibromatosis type 1.Association between ABCB1 C3435T polymorphism and increased risk of cannabis dependence.Worldwide HLA-E nucleotide and haplotype variability reveals a conserved gene for coding and 3' untranslated regions.MDM2 as a modifier gene in retinoblastoma.Worldwide genetic variation at the 3' untranslated region of the HLA-G gene: balancing selection influencing genetic diversity.Insights on the HLA-G evolutionary history provided by a nearby Alu insertion.Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease”.Differential protein expression profiles between Plasmodium falciparum parasites isolated from subjects presenting with pregnancy-associated malaria and uncomplicated malaria in Benin.Association of HLA-G 3'UTR polymorphisms with response to malaria infection: a first insight.NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience.Balancing immunity and tolerance: genetic footprint of natural selection in the transcriptional regulatory region of HLA-G.
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