Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Christine E. Cronk is active.

Publication


Featured researches published by Christine E. Cronk.


Environmental Health Perspectives | 2009

Environment and obesity in the National Children's Study.

Leonardo Trasande; Christine E. Cronk; Maureen S. Durkin; Marianne E. Weiss; Dale A. Schoeller; Elizabeth A. Gall; Jeanne Beauchamp Hewitt; Aaron L. Carrel; Philip J. Landrigan; Matthew W. Gillman

Objective In this review we describe the approach taken by the National Children’s Study (NCS), a 21-year prospective study of 100,000 American children, to understanding the role of environmental factors in the development of obesity. Data sources and extraction We review the literature with regard to the two core hypotheses in the NCS that relate to environmental origins of obesity and describe strategies that will be used to test each hypothesis. Data synthesis Although it is clear that obesity in an individual results from an imbalance between energy intake and expenditure, control of the obesity epidemic will require understanding of factors in the modern built environment and chemical exposures that may have the capacity to disrupt the link between energy intake and expenditure. The NCS is the largest prospective birth cohort study ever undertaken in the United States that is explicitly designed to seek information on the environmental causes of pediatric disease. Conclusions Through its embrace of the life-course approach to epidemiology, the NCS will be able to study the origins of obesity from preconception through late adolescence, including factors ranging from genetic inheritance to individual behaviors to the social, built, and natural environment and chemical exposures. It will have sufficient statistical power to examine interactions among these multiple influences, including gene–environment and gene–obesity interactions. A major secondary benefit will derive from the banking of specimens for future analysis.


Birth Defects Research Part A-clinical and Molecular Teratology | 2011

Modeling geographic risk of complex congenital heart defects in Eastern Wisconsin

Christine E. Cronk; Ronald E. Gangnon; Stacy Cossette; Jane A. McElroy

BACKGROUND Geographic variation may be an indicator of risk factors for birth defects. This study models the geographic distribution of three complex congenital heart defects (CHDs) in eastern Wisconsin, and evaluates effects of demographic census variables linked to geographic location. METHODS Cases of Hypoplastic Left Heart Syndrome (HLHS), Tetralogy of Fallot (TOF) and d-Transposition of the Great Arteries (d-TGAs) born between1995 and 2004 were identified from three medical centers serving eastern Wisconsin. Case diagnoses were assigned by a pediatric cardiologist using echocardiographic records. Births by ZIP code were obtained from the State of Wisconsin. ZIP Code demographic variables were derived from 2000 census data. Numbers of cardiac defects by ZIP code were modeled using cluster analysis and Poisson generalized additive models (GAMs) for spatial coordinates including all and white only cases (excluding trisomies). GAM analyses were repeated adjusting for census variables. RESULTS Four hundred forty-eight cases were ascertained. A significant south-to-north spatial gradient for HLHS, TOF, and combined CHDs, but not d-TGAs was identified. This gradient remained significant when census variables were included in the model for the full sample. In the analysis excluding non-white cases, findings were the same for TOF, combined CHDs, and d-TGAs. However, the geographic gradient for HLHS was not significant in the adjusted model. CONCLUSIONS A south-to-north gradient was apparent for two of three complex CHDs in eastern Wisconsin. For white cases, demographic variation seems to explain some of this spatial gradient in HLHS. Further studies are needed to confirm demographic and other risk factors underlying this geographic gradient.


Ciencia & Saude Coletiva | 2010

Environment and Obesity in the National Children's Study

Leonardo Trasande; Christine E. Cronk; Maureen S. Durkin; Marianne E. Weiss; Dale A. Schoeller; Elizabeth A. Gall; Jeanne Beauchamp Hewitt; Aaron L. Carrel; Philip J. Landrigan; Matthew W. Gillman

We describe the approach taken by the National Childrens Study (NCS) to understanding the role of environmental factors in the development of obesity. We review the literature with regard to the two core hypotheses in the NCS that relate to environmental origins of obesity and describe strategies that will be used to test each hypothesis. Although it is clear that obesity in an individual results from an imbalance between energy intake and expenditure, control of the obesity epidemic will require understanding of factors in the modern built environment and chemical exposures that may have the capacity to disrupt the link between energy intake and expenditure. Through its embrace of the life-course approach to epidemiology, the NCS will be able to study the origins of obesity from preconception through late adolescence, including factors ranging from genetic inheritance to individual behaviors to the social, built, and natural environment and chemical exposures. It will have sufficient statistical power to examine interactions among these multiple influences, including gene-environment and gene-obesity interactions. A major secondary benefit will derive from the banking of specimens for future analysis.


International Journal on Disability and Human Development | 2007

Diagnosis, surveillance and screening for fetal alcohol syndrome spectrum disorders: Methods and dilemmas

Christine E. Cronk; Marianne E. Weiss

Fetal Alcohol Spectrum Disorder (FASD) is a prevalent preventable disorder with a significant societal burden related to the cognitive and behavioral disabilities associated with this disorder. This paper reviews the published work on FASD diagnosis, surveillance, and screening programs. Challenges inherent to FASD diagnosis remain and complicate attempts to estimate FAS prevalence. In addition, the drive toward diagnostic accuracy has led to the formulation of screening children at school ages after many disabilities associated with FASD are established. We present the design and selected findings from a regional multi-stage screening project piloted in Wisconsin. Small for gestational age (SGA) newborns with birth head circumference less than 10 percentile were selected in the first screening stages. Those meeting these criteria were evaluated for growth, development and FAS facial features at about 2 years of age. Of newborns meeting the initial screening criteria, 30% demonstrated growth deficits and developmental delays at about 2 years of age. Children with any FAS facial feature (of 177 children assessed, n=13 with 2 or 3 facial findings, n=77 with one facial finding) showed greater deficits in growth and a greater proportion were developmentally delayed. The findings demonstrate the potential value of embedding screening for FAS within a multistage screening method to identify infants at risk for any developmental delay. Because this model would be a part of larger population screening for developmental delay, cost efficiencies could be achieved. Problems relating to protection and confidentiality that inevitably accompany screening to identify FASD would also be reduced.


Birth Defects Research Part A-clinical and Molecular Teratology | 2003

Completeness of state administrative databases for surveillance of congenital heart disease.

Christine E. Cronk; Marsha E. Malloy; Richard E. Miller; Sally A. Meyer; Melissa Cowell; D. Gail McCarver


Alcoholism: Clinical and Experimental Research | 2004

Alcohol dehydrogenase 2*3 affects alterations in offspring facial morphology associated with maternal ethanol intake in pregnancy.

Utpala (“Shonu”) G Das; Christine E. Cronk; Susan S. Martier; Pippa Simpson; D. Gail McCarver


Birth Defects Research Part A-clinical and Molecular Teratology | 2004

Excess birth prevalence of Hypoplastic Left Heart syndrome in eastern Wisconsin for birth cohorts 1997–1999

Christine E. Cronk; Marsha E. Malloy; D. Gail McCarver


WMJ : official publication of the State Medical Society of Wisconsin | 2006

The National Children's Study and the children of Wisconsin.

Leonardo Trasande; Christine E. Cronk; Leuthner; Jeanne Beauchamp Hewitt; Maureen S. Durkin; Jane A. McElroy; Henry A. Anderson; Philip J. Landrigan


Wisconsin medical journal | 2004

The Wisconsin Fetal Alcohol Syndrome Screening Project.

Marianne E. Weiss; Christine E. Cronk; Sandra Mahkorn; Randall Glysch; Sara Zirbel


Journal of registry management | 2011

Exploring the environmental and genetic etiologies of congenital heart defects: the Wisconsin Pediatric Cardiac Registry.

Susan E. Harris; Christine E. Cronk; Laura D. Cassidy; Pippa Simpson; Aoy Tomita-Mitchell

Collaboration


Dive into the Christine E. Cronk's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Jeanne Beauchamp Hewitt

University of Wisconsin–Milwaukee

View shared research outputs
Top Co-Authors

Avatar

D. Gail McCarver

Children's Hospital of Wisconsin

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Philip J. Landrigan

Icahn School of Medicine at Mount Sinai

View shared research outputs
Top Co-Authors

Avatar

Aaron L. Carrel

University of Wisconsin-Madison

View shared research outputs
Top Co-Authors

Avatar

Dale A. Schoeller

University of Wisconsin-Madison

View shared research outputs
Top Co-Authors

Avatar

Elizabeth A. Gall

University of Wisconsin-Madison

View shared research outputs
Researchain Logo
Decentralizing Knowledge