Lista de obras - Johannes Waage - Dominio Público Uruguay

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

artículo científico publicado en 2016

A novel common variant in DCST2 is associated with length in early life and height in adulthood

artículo científico publicado en 2014

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

article

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

artículo científico publicado en 2017

Amplification of pico-scale DNA mediated by bacterial carrier DNA for small-cell-number transcription factor ChIP-seq

artículo científico publicado en 2015

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

artículo científico publicado en 2018

C/EBPα is required for long-term self-renewal and lineage priming of hematopoietic stem cells and for the maintenance of epigenetic configurations in multipotent progenitors

artículo científico publicado en 2014

CDHR3 Genetics and Rhinovirus C Respiratory Illnesses

artículo científico publicado en 2017

CDHR3 gene variation and childhood bronchiolitis.

artículo científico publicado en 2017

Consortium genome-wide meta-analysis for childhood dental caries traits

Consortium-based genome-wide meta-analysis for childhood dental caries traits

scholarly article by Simon Haworth published in September 2018

Corrigendum: Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes

artículo científico publicado en 2016

Distinct immune phenotypes in infants developing asthma during childhood

artículo científico publicado en 2020

Domestic dog exposure at birth reduces the incidence of atopic dermatitis.

artículo científico publicado en 2016

Enhancer and Transcription Factor Dynamics during Myeloid Differentiation Reveal an Early Differentiation Block in Cebpa null Progenitors

artículo científico publicado en 2018

Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

article

Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring

artículo científico publicado en 2016

Genetic, Clinical, and Environmental Factors Associated With Persistent Atopic Dermatitis in Childhood

Genetics of allergy and allergic sensitization: common variants, rare mutations

artículo científico publicado en 2015

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

artículo científico publicado en 2015

Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

scholarly article by Johannes Waage et al published August 2018 in Nature Genetics

Genome-wide association study identifies 74 loci associated with educational attainment

artículo científico publicado en 2016

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

High breast milk IL-1β level is associated with reduced risk of childhood eczema.

artículo científico publicado en 2016

Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes

artículo científico publicado en 2014

Incidence and Determinants of Ventilation Tubes in Denmark

artículo científico publicado en 2016

Infant airway microbiota and topical immune perturbations in the origins of childhood asthma

artículo científico publicado en 2019

Large-scale benchmarking reveals false discoveries and count transformation sensitivity in 16S rRNA gene amplicon data analysis methods used in microbiome studies.

artículo científico publicado en 2016

Mammalian tissues defective in nonsense-mediated mRNA decay display highly aberrant splicing patterns

artículo científico publicado en 2012

Maturation of the gut microbiome and risk of asthma in childhood

artículo científico publicado en 2018

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

artículo científico publicado en 2017

NKG2D gene variation and susceptibility to viral bronchiolitis in childhood

article

Prenatal vitamin D supplementation reduces risk of asthma/recurrent wheeze in early childhood: A combined analysis of two randomized controlled trials

artículo científico publicado en 2017

Publisher Correction: Maturation of the gut microbiome and risk of asthma in childhood

artículo científico publicado en 2018

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

artículo científico publicado en 2017

TGIF1 is a negative regulator of MLL-rearranged acute myeloid leukemia

artículo científico publicado en 2014

Temporal mapping of CEBPA and CEBPB binding during liver regeneration reveals dynamic occupancy and specific regulatory codes for homeostatic and cell cycle gene batteries

artículo científico publicado en 2013

The developing hypopharyngeal microbiota in early life

artículo científico publicado en 2016

UBL5 is essential for pre-mRNA splicing and sister chromatid cohesion in human cells

artículo científico publicado en 2014

UPF2 is a critical regulator of liver development, function and regeneration

scientific journal article

UPF2-Dependent Nonsense-Mediated mRNA Decay Pathway Is Essential for Spermatogenesis by Selectively Eliminating Longer 3'UTR Transcripts

artículo científico publicado en 2016

microRNA-9 targets the long non-coding RNA MALAT1 for degradation in the nucleus

artículo científico publicado en 2013

spliceR: an R package for classification of alternative splicing and prediction of coding potential from RNA-seq data

artículo científico publicado en 2014

Lista de obras de Johannes Waage

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

A novel common variant in DCST2 is associated with length in early life and height in adulthood

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

Amplification of pico-scale DNA mediated by bacterial carrier DNA for small-cell-number transcription factor ChIP-seq

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

C/EBPα is required for long-term self-renewal and lineage priming of hematopoietic stem cells and for the maintenance of epigenetic configurations in multipotent progenitors

CDHR3 Genetics and Rhinovirus C Respiratory Illnesses

CDHR3 gene variation and childhood bronchiolitis.

Consortium genome-wide meta-analysis for childhood dental caries traits

Consortium-based genome-wide meta-analysis for childhood dental caries traits

Corrigendum: Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes

Distinct immune phenotypes in infants developing asthma during childhood

Domestic dog exposure at birth reduces the incidence of atopic dermatitis.

Enhancer and Transcription Factor Dynamics during Myeloid Differentiation Reveal an Early Differentiation Block in Cebpa null Progenitors

Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring

Genetic, Clinical, and Environmental Factors Associated With Persistent Atopic Dermatitis in Childhood

Genetics of allergy and allergic sensitization: common variants, rare mutations

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

Genome-wide association study identifies 74 loci associated with educational attainment

Genome-wide associations for birth weight and correlations with adult disease

High breast milk IL-1β level is associated with reduced risk of childhood eczema.

Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes

Incidence and Determinants of Ventilation Tubes in Denmark

Infant airway microbiota and topical immune perturbations in the origins of childhood asthma

Large-scale benchmarking reveals false discoveries and count transformation sensitivity in 16S rRNA gene amplicon data analysis methods used in microbiome studies.

Mammalian tissues defective in nonsense-mediated mRNA decay display highly aberrant splicing patterns

Maturation of the gut microbiome and risk of asthma in childhood

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

NKG2D gene variation and susceptibility to viral bronchiolitis in childhood

Prenatal vitamin D supplementation reduces risk of asthma/recurrent wheeze in early childhood: A combined analysis of two randomized controlled trials

Publisher Correction: Maturation of the gut microbiome and risk of asthma in childhood

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

TGIF1 is a negative regulator of MLL-rearranged acute myeloid leukemia

Temporal mapping of CEBPA and CEBPB binding during liver regeneration reveals dynamic occupancy and specific regulatory codes for homeostatic and cell cycle gene batteries

The developing hypopharyngeal microbiota in early life

UBL5 is essential for pre-mRNA splicing and sister chromatid cohesion in human cells

UPF2 is a critical regulator of liver development, function and regeneration

UPF2-Dependent Nonsense-Mediated mRNA Decay Pathway Is Essential for Spermatogenesis by Selectively Eliminating Longer 3'UTR Transcripts

microRNA-9 targets the long non-coding RNA MALAT1 for degradation in the nucleus

spliceR: an R package for classification of alternative splicing and prediction of coding potential from RNA-seq data