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Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study

PloS one, 2016-05, Vol.11 (5), p.e0156261-e0156261

2016

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Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

Scientific reports, 2021-08, Vol.11 (1), p.17115-17115, Article 17115

2021

Volltextzugriff (PDF)

Rare variants analyses suggest novel cleft genes in the African population

Scientific reports, 2024-06, Vol.14 (1), p.14279-10, Article 14279

2024

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Impaired FGF signaling contributes to cleft lip and palate

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4512-4517

2007

Volltextzugriff (PDF)

Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects

Birth defects research. Part C. Embryo today, 2008-03, Vol.84 (1), p.16-29

2008

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Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure

PloS one, 2013-12, Vol.8 (12), p.e82554-e82554

2013

Volltextzugriff (PDF)

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

PloS one, 2016-04, Vol.11 (4), p.e0152576

2016

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

PloS one, 2017-09, Vol.12 (9), p.e0184358-e0184358

2017

Volltextzugriff (PDF)

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

PloS one, 2012-09, Vol.7 (9), p.e45441-e45441

2012

Volltextzugriff (PDF)

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

PloS one, 2013-04, Vol.8 (4), p.e61781

2013

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X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia

PloS one, 2012-06, Vol.7 (6), p.e39240-e39240

2012

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The Impact of Maternal Smoking during Pregnancy on Early Child Neurodevelopment

Journal of human capital, 2011-06, Vol.5 (2), p.207-254

2011

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A cohort study of recurrence patterns among more than 54000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

Journal of medical genetics, 2010-03, Vol.47 (3), p.162

2010

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Genome-Wide Analysis of DNA Methylation in Human Amnion

TheScientificWorld, 2013-01, Vol.2013 (1), p.678156-678156

2013

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A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

PloS one, 2013-07, Vol.8 (7), p.e69333

2013

Volltextzugriff (PDF)

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

Scientific reports, 2022-07, Vol.12 (1), p.11743-11743, Article 11743

2022

Volltextzugriff (PDF)

Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa

AJOB empirical bioethics, 2024-01, Vol.15 (2), p.133-146

2024

Volltextzugriff (PDF)

Validation of gestational age determination from ultrasound or a metabolic gestational age algorithm using exact date of conception in a cohort of newborns conceived using assisted reproduction technologies

AJOG global reports, 2022-11, Vol.2 (4), p.100091-100091, Article 100091

2022

Volltextzugriff (PDF)

Correction: Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants

Journal of perinatology, 2021-02, Vol.41 (2), p.361-361

2021

Volltextzugriff (PDF)

Abstract 2467: Association of specificity protein 1 and survivin expression in medulloblastoma: Identifying effective therapeutic targets

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.2467-2467

2016

Volltextzugriff (PDF)

Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries

Science advances, 2023-05, Vol.9 (21), p.eade7692

2023

Volltextzugriff (PDF)

Protein Kinase C Phosphorylation Modulates N- and C-Terminal Regulatory Activities of the PITX2 Homeodomain Protein

Biochemistry (Easton), 2005-03, Vol.44 (10), p.3942-3954

2005

Volltextzugriff (PDF)

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

Frontiers in genetics, 2013, Vol.4, p.196

2013

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Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study

Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

Rare variants analyses suggest novel cleft genes in the African population

Impaired FGF signaling contributes to cleft lip and palate

Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects

Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

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

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

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

X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia

The Impact of Maternal Smoking during Pregnancy on Early Child Neurodevelopment

A cohort study of recurrence patterns among more than 54000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

Genome-Wide Analysis of DNA Methylation in Human Amnion

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa

Validation of gestational age determination from ultrasound or a metabolic gestational age algorithm using exact date of conception in a cohort of newborns conceived using assisted reproduction technologies

Correction: Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants

Abstract 2467: Association of specificity protein 1 and survivin expression in medulloblastoma: Identifying effective therapeutic targets

Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries

Protein Kinase C Phosphorylation Modulates N- and C-Terminal Regulatory Activities of the PITX2 Homeodomain Protein

Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate

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

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