Lista de obras - Bjarke Feenstra - Dominio Público Uruguay

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

artículo científico publicado en 2014

A quantitative trait locus mixture model that avoids spurious LOD score peaks

artículo científico publicado en 2004

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight.

artículo científico publicado en 2013

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders

artículo científico publicado en 2017

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Co-occurrence of infantile hypertrophic pyloric stenosis and congenital heart defects: a nationwide cohort study

artículo científico publicado en 2019

Common variants associated with general and MMR vaccine-related febrile seizures

artículo científico publicado en 2014

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

artículo científico publicado en 2012

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

artículo científico publicado en 2016

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

artículo científico publicado en 2022

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

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Detectable clonal mosaicism from birth to old age and its relationship to cancer

artículo científico publicado en 2012

Detecting Sample Misidentifications in Genetic Association Studies ⬇️

artículo científico publicado el 1 de enero de 2012

Determination of NAT2 acetylation status in the Greenlandic population

artículo científico publicado en 2015

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs

artículo científico publicado en 2020

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Familial aggregation of tonsillectomy in early childhood and adolescence.

artículo científico publicado en 2018

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

artículo científico publicado en 2019

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

artículo científico publicado en 2017

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

artículo científico publicado en 2016

Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

scientific article published on 25 November 2020

Genetic regulation of gene expression in the epileptic human hippocampus

artículo científico publicado en 2017

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia

artículo científico publicado en 2012

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

artículo científico publicado en 2012

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome partitioning of genetic variation for complex traits using common SNPs

artículo científico publicado en 2011

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

Genome-wide association study identifies four loci associated with eruption of permanent teeth

artículo científico publicado en 2011

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

artículo científico publicado en 2009

Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy

artículo científico publicado en 2016

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

artículo científico publicado en 2018

Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups

scientific journal article

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

article

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

artículo científico publicado en 2018

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

artículo científico publicado en 2013

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

artículo científico publicado en 2019

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

artículo científico publicado en 2014

Improving vaccine safety through a better understanding of vaccine adverse events

artículo científico publicado en 2015

Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations

artículo científico publicado en 2006

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Maternal contributions to preterm delivery

artículo científico publicado en 2009

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

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

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

No association between age at menarche and sex of offspring

No observed association for mitochondrial SNPs with preterm delivery and related outcomes

artículo científico publicado en 2012

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

artículo científico publicado en 2020

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis

scientific journal article

Replication of a genome-wide association study of birth weight in preterm neonates

artículo científico publicado en 2011

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

artículo científico publicado en 2011

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

artículo científico publicado en 2017

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

artículo científico publicado en 2013

Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

artículo científico publicado en 2010

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders

scientific article published on 24 January 2020

The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches

artículo científico publicado en 2010

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Use of macrolides in mother and child and risk of infantile hypertrophic pyloric stenosis: nationwide cohort study

artículo científico publicado en 2014

Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies

artículo científico publicado en 2012

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

artículo científico publicado en 2019

X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study

artículo científico publicado en 2013

[Genome-wide association studies]

artículo científico publicado en 2008

Lista de obras de Bjarke Feenstra

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

A quantitative trait locus mixture model that avoids spurious LOD score peaks

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight.

Associations of autozygosity with a broad range of human phenotypes

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders

Characterization of large structural genetic mosaicism in human autosome

Co-occurrence of infantile hypertrophic pyloric stenosis and congenital heart defects: a nationwide cohort study

Common variants associated with general and MMR vaccine-related febrile seizures

Common variants at 12q15 and 12q24 are associated with infant head circumference

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

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

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

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Defining the role of common variation in the genomic and biological architecture of adult human height

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Detecting Sample Misidentifications in Genetic Association Studies ⬇️

Determination of NAT2 acetylation status in the Greenlandic population

Directional dominance on stature and cognition in diverse human populations

Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

Familial aggregation of tonsillectomy in early childhood and adolescence.

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

Genetic regulation of gene expression in the epileptic human hippocampus

Genetic studies of body mass index yield new insights for obesity biology

Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Genome partitioning of genetic variation for complex traits using common SNPs

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

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

Genome-wide association study identifies 48 common genetic variants associated with handedness

Genome-wide association study identifies four loci associated with eruption of permanent teeth

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

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

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

Improving vaccine safety through a better understanding of vaccine adverse events

Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Maternal contributions to preterm delivery

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

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.

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

No association between age at menarche and sex of offspring

No observed association for mitochondrial SNPs with preterm delivery and related outcomes

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis

Replication of a genome-wide association study of birth weight in preterm neonates

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders

The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Use of macrolides in mother and child and risk of infantile hypertrophic pyloric stenosis: nationwide cohort study

Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration