The University of Iowa

Neonatal Biorepository

Publications that include phenotype or genotype data from the Neonatal Biorepository are listed below. This list is not exhaustive.

All future publications that use data from the Neonatal Biorepository will be included on this webpage. We ask all individuals utilizing Neonatal Biorepository data to keep our team apprised of any manuscript submissions, conference presentations, and grant applications. Tracking the ways in which the Neonatal Biorepository assists in scientific and professional endeavors is essential to maintaining this important resource.

Genetic variants associated with patent ductus arteriosus in extremely preterm infants

2019 March

Development and validation of a clinical model for preconception and early pregnancy risk prediction of gestational diabetes mel

2019 April 12

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

2019 May

The Association of Polymorphisms in Circadian Clock and Lipid Metabolism Genes With 2nd Trimester Lipid Levels and Preterm Birth

2019 June 13

CYP2C9*2 is associated with indomethacin treatment failure for patent ductus arteriosus

2019 August

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

2019 September 2

Genetic Risk Scores for Maternal Lipid Levels and Their Association with Preterm Birth

2019 October

Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn

2018 January

Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genet

2018 Feb 15

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

2018 July 12

A functional ATG16L1 (T300A) variant is associated with necrotizing enterocolitis in premature infants

2017 April

Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus

2017 November

A Potential Role for the NOD1 Variant (rs6958571) in Gram-Positive Blood Stream Infection in ELBW Infants

2017

Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population

2017 September

Quality of EHR data extractions for studies of preterm birth in a tertiary care center: guidelines for obtaining reliable data

2016 April 29

Predicting gestational age using neonatal metabolic markers

2016 April

Pregnancy-Related Changes of Amino Acid and Acylcarnitine Concentrations: The Impact of Obesity

2016 April

Polymorphisms in NR5A2, gene encoding liver receptor homolog-1 are associated with preterm birth

2016 May

Maternal and neonatal epidemiological features in clinical subtypes of preterm birth

2016 October

Structural and genomic variation in preterm birth

2016 December

Integrated genomic analyses in bronchopulmonary dysplasia

2015 March

Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy

2015 March

Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants

2015 March

Candidate gene study for smoking, alcohol use, and body weight in a sample of pregnant women

2015 May

Determining the prevalence of cytomegalovirus infection in a cohort of preterm infants

2015

Genes and environment in neonatal intraventricular hemorrhage

2015 December

Metabolic heritability at birth: implications for chronic disease research

2014 August

Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone

2014 September

Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age

2014 October

Clinical and environmental influences on metabolic biomarkers collected for newborn screening

2013 January

Investigation of genetic risk factors for chronic adult diseases for association with preterm birth

2013 January

Candidate gene linkage approach to identify DNA variants that predispose to preterm birth

2013 Feb

The heritability of metabolic profiles in newborn twins

2013 March

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

2013 April 16

Genetic associations with neonatal thyroid-stimulating hormone levels

2013 April

Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm b

2013 May

A proposed method to predict preterm birth using clinical data, standard maternal serum screening, and cholesterol

2013 June

Association of amino acids with common complications of prematurity

2013 June

Environmental risk factors and perinatal outcomes in preterm newborns, according to family recurrence of prematurity

2013 June

Genome-wide analysis of DNA methylation in human amnion

2013

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

2013 July 26

Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth

2013 August

The influence of maternal disease on metabolites measured as part of newborn screening

2013 September

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

2013 October 28

Candidate gene analysis: severe intraventricular hemorrhage in inborn preterm neonates

2013 November

Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP5

2013 December 17

Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns

2012

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

2012 January

Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn

2012 Feburary

Transcriptome landscape of the human placenta

2012 March 27

Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates

2012 May

Noninvasive whole-genome sequencing of a human fetus

2012 June 6

Non-invasive fetal genome sequencing: opportunities and challenges

2012 October

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

2012 November

Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis

2011 Feburary 3

Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birth

2011 March

Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity

2011 March

Cytochrome P450 (CYP2D6) genotype is associated with elevated systolic blood pressure in preterm infants after discharge from th

2011 July

Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage i

2011 July

Patterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus

2010 October

Role of polymorphic variants as genetic modulators of infection in neonatal sepsis

2010 October

Genetic contributions to the development of retinopathy of prematurity

2009 Feburary

Determination of genetic predisposition to patent ductus arteriosus in preterm infants

2009 April

Maternal contributions to preterm delivery

2009 December 1

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

2008 March

Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery

2007 November

Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth

2007 November