Lista de obras - Audrey Sabbagh - Dominio Público Uruguay

A homogenizing process of selection has maintained an "ultra-slow" acetylation NAT2 variant in humans.

artículo científico publicado en 2014

ANRIL, a long, noncoding RNA, is an unexpected major hotspot in GWAS.

scientific article published on 18 October 2010

ANRILou l’étrange histoire d’un grand ARN non codant

scientific article published on 01 June 2010

Arylamine N-acetyltransferase 2 (NAT2) genetic diversity and traditional subsistence: a worldwide population survey

artículo científico publicado en 2011

Association between ABCB1 C3435T polymorphism and increased risk of cannabis dependence

artículo científico publicado en 2009

Association of HLA-G 3' untranslated region polymorphisms with antibody response against Plasmodium falciparum antigens: preliminary results.

artículo científico publicado en 2013

Association of HLA-G 3'UTR polymorphisms with response to malaria infection: a first insight.

artículo científico publicado en 2013

Association of IL-4 and IL-10 maternal haplotypes with immune responses to P. falciparum in mothers and newborns

artículo científico publicado en 2013

Balancing immunity and tolerance: genetic footprint of natural selection in the transcriptional regulatory region of HLA-G.

artículo científico publicado en 2014

CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy

artículo científico publicado en 2012

Data-mining methods as useful tools for predicting individual drug response: application to CYP2D6 data

artículo científico publicado en 2006

Decreasing the effects of horizontal gene transfer on bacterial phylogeny: the Escherichia coli case study

artículo científico publicado en 2004

Detection and characterization of NF1 microdeletions by custom high resolution array CGH.

artículo científico publicado en 2009

Differential protein expression profiles between Plasmodium falciparum parasites isolated from subjects presenting with pregnancy-associated malaria and uncomplicated malaria in Benin

artículo científico publicado en 2013

Evaluating NAT2PRED for inferring the individual acetylation status from unphased genotype data

artículo científico publicado en 2009

Familial Aggregation and Heritability of Wuchereria bancrofti Infection

artículo científico publicado en 2016

Gene expression and hepatitis C virus infection

artículo científico publicado en 2009

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.

artículo científico publicado en 2017

Genetic diversity of VAR2CSA ID1-DBL2Xb in worldwide Plasmodium falciparum populations: impact on vaccine design for placental malaria

artículo científico publicado en 2014

Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens

artículo científico publicado en 2016

HLA-E coding and 3' untranslated region variability determined by next-generation sequencing in two West-African population samples

artículo científico publicado en 2015

HLA-G 3' UTR-2 haplotype is associated with Human African trypanosomiasis susceptibility

artículo científico publicado en 2013

Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis

artículo científico publicado en 2016

Humans and Chimpanzees Display Opposite Patterns of Diversity in Arylamine N-Acetyltransferase Genes

scientific article published on 09 July 2019

Identification of a Major Dimorphic Region in the Functionally Critical N-Terminal ID1 Domain of VAR2CSA.

artículo científico publicado en 2015

Inferring haplotypes at the NAT2 locus: the computational approach

artículo científico publicado en 2005

Insights into HLA-G Genetics Provided by Worldwide Haplotype Diversity

artículo científico publicado en 2014

Insights on the HLA-G evolutionary history provided by a nearby Alu insertion.

artículo científico publicado en 2013

Liver gene expression signature to predict response to pegylated interferon plus ribavirin combination therapy in patients with chronic hepatitis C.

artículo científico publicado en 2007

MDM2 as a modifier gene in retinoblastoma

artículo científico publicado en 2010

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

artículo científico publicado en 2010

NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience

artículo científico publicado en 2013

NF1 single and multi-exons copy number variations in neurofibromatosis type 1.

artículo científico publicado en 2015

Natural Killer Cell Immunoglobulin-like Receptor (KIR) genotypes in Follicular Lymphoma patients: results of a pilot study.

artículo científico publicado en 2013

New method for surname studies of ancient patrilineal population structures, and possible application to improvement of Y-chromosome sampling

artículo científico publicado en 2005

Parental genotypes in the risk of a complex disease

scientific article published on 07 June 2002

Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans

artículo científico publicado en 2012

Present day inbreeding does not forbid the forensic utility of commonly explored STR loci: a case study of native Qataris

artículo científico publicado en 2009

Proteomic analysis of Plasmodium falciparum parasites from patients with cerebral and uncomplicated malaria

artículo científico publicado en 2016

Rapid birth-and-death evolution of the xenobiotic metabolizing NAT gene family in vertebrates with evidence of adaptive selection

artículo científico publicado en 2013

Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease”.

artículo científico publicado en 2002

Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1.

artículo científico publicado en 2011

SNP selection at the NAT2 locus for an accurate prediction of the acetylation phenotype

artículo científico publicado en 2006

SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.

artículo científico publicado en 2009

Selecting predictive markers for pharmacogenetic traits: tagging vs. data-mining approaches.

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1.

scientific article published on 05 May 2009

Variation in NAT2 acetylation phenotypes is associated with differences in food-producing subsistence modes and ecoregions in Africa

artículo científico publicado en 2015

Worldwide HLA-E nucleotide and haplotype variability reveals a conserved gene for coding and 3' untranslated regions.

artículo científico publicado en 2014

Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history

artículo científico publicado en 2008

Worldwide genetic variation at the 3' untranslated region of the HLA-G gene: balancing selection influencing genetic diversity.

artículo científico publicado en 2013

Lista de obras de Audrey Sabbagh

A homogenizing process of selection has maintained an "ultra-slow" acetylation NAT2 variant in humans.

ANRIL, a long, noncoding RNA, is an unexpected major hotspot in GWAS.

ANRILou l’étrange histoire d’un grand ARN non codant

Arylamine N-acetyltransferase 2 (NAT2) genetic diversity and traditional subsistence: a worldwide population survey

Association between ABCB1 C3435T polymorphism and increased risk of cannabis dependence

Association of HLA-G 3' untranslated region polymorphisms with antibody response against Plasmodium falciparum antigens: preliminary results.

Association of HLA-G 3'UTR polymorphisms with response to malaria infection: a first insight.

Association of IL-4 and IL-10 maternal haplotypes with immune responses to P. falciparum in mothers and newborns

Balancing immunity and tolerance: genetic footprint of natural selection in the transcriptional regulatory region of HLA-G.

CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy

Data-mining methods as useful tools for predicting individual drug response: application to CYP2D6 data

Decreasing the effects of horizontal gene transfer on bacterial phylogeny: the Escherichia coli case study

Detection and characterization of NF1 microdeletions by custom high resolution array CGH.

Differential protein expression profiles between Plasmodium falciparum parasites isolated from subjects presenting with pregnancy-associated malaria and uncomplicated malaria in Benin

Evaluating NAT2PRED for inferring the individual acetylation status from unphased genotype data

Familial Aggregation and Heritability of Wuchereria bancrofti Infection

Gene expression and hepatitis C virus infection

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.

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

HLA-G 3' UTR-2 haplotype is associated with Human African trypanosomiasis susceptibility

Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis

Humans and Chimpanzees Display Opposite Patterns of Diversity in Arylamine N-Acetyltransferase Genes

Identification of a Major Dimorphic Region in the Functionally Critical N-Terminal ID1 Domain of VAR2CSA.

Inferring haplotypes at the NAT2 locus: the computational approach

Insights into HLA-G Genetics Provided by Worldwide Haplotype Diversity

Insights on the HLA-G evolutionary history provided by a nearby Alu insertion.

Liver gene expression signature to predict response to pegylated interferon plus ribavirin combination therapy in patients with chronic hepatitis C.

MDM2 as a modifier gene in retinoblastoma

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience

NF1 single and multi-exons copy number variations in neurofibromatosis type 1.

Natural Killer Cell Immunoglobulin-like Receptor (KIR) genotypes in Follicular Lymphoma patients: results of a pilot study.

New method for surname studies of ancient patrilineal population structures, and possible application to improvement of Y-chromosome sampling

Parental genotypes in the risk of a complex disease

Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans

Present day inbreeding does not forbid the forensic utility of commonly explored STR loci: a case study of native Qataris

Proteomic analysis of Plasmodium falciparum parasites from patients with cerebral and uncomplicated malaria

Rapid birth-and-death evolution of the xenobiotic metabolizing NAT gene family in vertebrates with evidence of adaptive selection

Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease”.

Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1.

SNP selection at the NAT2 locus for an accurate prediction of the acetylation phenotype

SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.

Selecting predictive markers for pharmacogenetic traits: tagging vs. data-mining approaches.

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

Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1.

Variation in NAT2 acetylation phenotypes is associated with differences in food-producing subsistence modes and ecoregions in Africa

Worldwide HLA-E nucleotide and haplotype variability reveals a conserved gene for coding and 3' untranslated regions.

Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history

Worldwide genetic variation at the 3' untranslated region of the HLA-G gene: balancing selection influencing genetic diversity.