Louis Muglia

Male risk taking, female odors, and the role of estrogen receptors.

Behavioral Studies and Genetic Alterations in Corticotropin-Releasing Hormone (CRH) Neurocircuitry: Insights into Human Psychiatric Disorders.

Site-specific modulation of brain glucocorticoid receptor and corticotropin-releasing hormone expression using lentiviral vectors.

Fetal programming and environmental exposures: implications for prenatal care and preterm birth.

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

Amniotic fluid: the use of high-dimensional biology to understand fetal well-being.

Adjunctive therapies to cerclage for the prevention of preterm birth: a systematic review.

The genomics of preterm birth: from animal models to human studies.

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

Disrupting hypothalamic glucocorticoid receptors causes HPA axis hyperactivity and excess adiposity.

Fine-mapping an association of FSHR with preterm birth in a Finnish population.

Influenza vaccine in pregnancy: policy and research strategies.

Rictor/mTORC2 facilitates central regulation of energy and glucose homeostasis.

Dissection of glucocorticoid receptor-mediated inhibition of the hypothalamic-pituitary-adrenal axis by gene targeting in mice.

50 years ago in the Journal of Pediatrics: The epidemiology of prematurity.

Influence of interpregnancy interval on neonatal morbidity.

Genomics of preterm birth.

Detecting endogenous retrovirus-driven tissue-specific gene transcription.

Air pollution and stillbirth risk: exposure to airborne particulate matter during pregnancy is associated with fetal death.

Ontogeny of hypothalamic glucocorticoid receptor-mediated inhibition of the hypothalamic-pituitary-adrenal axis in mice.

Genetic Approaches to Hypothalamic-Pituitary-Adrenal Axis Regulation.

CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth.

Hypoplastic left heart syndrome is associated with structural and vascular placental abnormalities and leptin dysregulation.

Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis.

Enhancing Pediatric Fellows' Research Training: Development of an Office of Pediatric Clinical Fellowships.

The genetics of preterm birth: Progress and promise.

Systems biology evaluation of cell-free amniotic fluid transcriptome of term and preterm infants to detect fetal maturity.

GEneSTATION 1.0: a synthetic resource of diverse evolutionary and functional genomic data for studying the evolution of pregnancy-associated tissues and phenotypes.

Ambient Temperature and the Risk of Preterm Birth in Guangzhou, China (2001-2011).

Racial disparity in previable birth.

Exposure to airborne particulate matter during pregnancy is associated with preterm birth: a population-based cohort study.

Evolutionary triangulation: informing genetic association studies with evolutionary evidence.

Comparing human and macaque placental transcriptomes to disentangle preterm birth pathology from gestational age effects.

Recurrence of Preterm Birth and Early Term Birth.

Infant Mortality, Cause of Death, and Vital Records Reporting in Ohio, United States.

Racial Differences in the Influence of Interpregnancy Interval on Fetal Growth.

Effect of Modifiable Risk Factors on Preterm Birth: A Population Based-Cohort.

Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.

Comparing oxytocin and cortisol regulation in a double-blind, placebo-controlled, hydrocortisone challenge pilot study in children with autism and typical development.

Finding lost genes in GWAS via integrative-omics analysis reveals novel sub-networks associated with preterm birth.

Infant mortality in coroner/medical examiner investigations.

Evaluation of Fellows' CrossTalk Effectiveness in Promoting Transdisciplinary Networking and Research.

Introduction to evolutionary genomic approaches to human disease.

Signatures of natural selection on genetic variants affecting complex human traits.

The influence of interpregnancy interval on infant mortality.

Single-cell transcriptomics of the human placenta: inferring the cell communication network of the maternal-fetal interface.

Time-Variant Genetic Effects as a Cause for Preterm Birth: Insights from a Population of Maternal Cousins in Sweden.

Risk of preterm birth by maternal age at first and second pregnancy and race/ethnicity.

Combined sewer overflow events and childhood emergency department visits: A case-crossover study.

Bleeding during pregnancy is associated with familial preterm birth.

Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.

Evolutionarily derived networks to inform disease pathways.

Inhibition of IRAK1 Ubiquitination Determines Glucocorticoid Sensitivity for TLR9-Induced Inflammation in Macrophages.

Comparative transcriptomic analysis of human placentae at term and preterm delivery.

Genetic Associations with Spontaneous Preterm Birth.

Periconception Exposure to Air Pollution and Risk of Congenital Malformations.

Loss of Intercalated Cells (ITCs) in the Mouse Amygdala of Mutants Correlates with Fear, Depression, and Social Interaction Phenotypes.

Implementation of a Regional Perinatal Data Repository from Clinical and Billing Records.

Inverted formin 2 regulates intracellular trafficking, placentation, and pregnancy outcome.

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.

A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth.

Preterm Birth and Gestational Length in Four Race-Nativity Groups, Including Somali Americans.

Natural Selection Has Differentiated the Progesterone Receptor among Human Populations.

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

Genetic studies of gestational duration and preterm birth.

Anthropoid primate-specific retroviral element THE1B controls expression of CRH in placenta and alters gestation length.

Spontaneous premature birth as a target of genomic research.

Uterine distention as a factor in birth timing: retrospective nationwide cohort study in Sweden.

Previous Adverse Outcome of Term Pregnancy and Risk of Preterm Birth in Subsequent Pregnancy.

Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research.

Trimester specific PM exposure and fetal growth in Ohio, 2007-2010.

Hyperadrenocorticism of calorie restriction contributes to its anti-inflammatory action in mice.

Enzymatic Activity of HPGD in Treg Cells Suppresses Tconv Cells to Maintain Adipose Tissue Homeostasis and Prevent Metabolic Dysfunction.

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

Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.

Network as a Biomarker: A Novel Network-Based Sparse Bayesian Machine for Pathway-Driven Drug Response Prediction.

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

Peptide/Receptor Co-evolution Explains the Lipolytic Function of the Neuropeptide TLQP-21.

Eutherian-Specific Gene TRIML2 Attenuates Inflammation in the Evolution of Placentation.

Unique transcriptomic landscapes identified in idiopathic spontaneous and infection related preterm births compared to normal term births.

Early pregnancy loss in 15-hydroxyprostaglandin dehydrogenase knockout (15-HPGD) mice due to requirement for embryo 15-HPGD activity.

Health Advantages and Disparities in Preterm Birth Among Immigrants Despite Disparate Sociodemographic, Behavioral, and Maternal Risk Factors in San Diego, California.

Maternal dietary selenium intake is associated with increased gestational length and decreased risk of preterm delivery.

Chronic psychosocial stress during pregnancy affects maternal behavior and neuroendocrine function and modulates hypothalamic CRH and nuclear steroid receptor expression.

IRAK1 Is a Critical Mediator of Inflammation-Induced Preterm Birth.

Model-Informed Bayesian Estimation Improves the Prediction of Morphine Exposure in Neonates and Infants.

Importance of the environment for gestational duration variability and correlation between relatives - results from the Medical Swedish Birth Registry, 1973-2012.

Accounting for diverse evolutionary forces reveals mosaic patterns of selection on human preterm birth loci.

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.

Changes in data management contribute to temporal variation in gestational duration distribution in the Swedish Medical Birth Registry.

Transcriptome and regulatory maps of decidua-derived stromal cells inform gene discovery in preterm birth.

Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios.

Maternal Dietary Selenium Intake during Pregnancy Is Associated with Higher Birth Weight and Lower Risk of Small for Gestational Age Births in the Norwegian Mother, Father and Child Cohort Study.

Developing a theoretical evolutionary framework to solve the mystery of parturition initiation.

Maternal high-fat-diet exposure is associated with elevated blood pressure and sustained increased leptin levels through epigenetic memory in offspring.

Baby's best Foe-riend: Endogenous retroviruses and the evolution of eutherian reproduction.