Lista de obras -

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

artículo científico publicado en 2009

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

artículo científico publicado en 2019

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

artículo científico publicado en 2013

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2017

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

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

Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

artículo científico publicado en 2016

Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios.

artículo científico publicado en 2017

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate

artículo científico publicado en 2015

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

artículo científico publicado en 2018

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

artículo científico publicado en 2017

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci

artículo científico publicado en 2015

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

artículo científico publicado en 2017

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Integration of DNA sample collection into a multi-site birth defects case-control study

artículo científico publicado en 2002

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

artículo científico publicado en 2019

Maternal underweight and obesity and risk of orofacial clefts in a large international consortium of population-based studies

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Non-invasive fetal genome sequencing: opportunities and challenges

artículo científico publicado en 2012

Noninvasive whole-genome sequencing of a human fetus.

artículo científico publicado en 2012

Parent's age and the risk of oral clefts

artículo científico publicado en 2005

Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort

artículo científico publicado en 2010

Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.

artículo científico publicado en 2015

Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.

artículo científico publicado en 2013

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

artículo científico publicado en 2013

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

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

artículo científico publicado en 2010

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

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

scientific article published on 12 July 2018

Lista de obras de

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

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

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

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

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

Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.

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

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios.

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Integration of DNA sample collection into a multi-site birth defects case-control study

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 underweight and obesity and risk of orofacial clefts in a large international consortium of population-based studies

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

Non-invasive fetal genome sequencing: opportunities and challenges

Noninvasive whole-genome sequencing of a human fetus.

Parent's age and the risk of oral clefts

Recurrence risk for offspring of twins discordant for oral cleft: a population-based cohort study of the Danish 1936-2004 cleft twin cohort

Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.

Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.

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

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

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

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth