E
Edward S. Stenroos
Researcher at Rutgers University
Publications - 25
Citations - 9283
Edward S. Stenroos is an academic researcher from Rutgers University. The author has contributed to research in topics: Autism & Allele. The author has an hindex of 16, co-authored 25 publications receiving 8654 citations. Previous affiliations of Edward S. Stenroos include University of Medicine and Dentistry of New Jersey.
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Journal ArticleDOI
Risk of autistic disorder in affected offspring of mothers with a glutathione S-transferase P1 haplotype.
Tanishia A. Williams,Audrey E. Mars,Steven Buyske,Edward S. Stenroos,Rong Wang,Marivic F. Factura-Santiago,George H. Lambert,William G. Johnson +7 more
TL;DR: Overtransmission of the GSTP1*A haplotype to case mothers suggests that action in the mother during pregnancy likely increases the likelihood of AD in her fetus, which could lead to the design of strategies for prevention or treatment.
Journal ArticleDOI
Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
Steven Buyske,Tanishia A. Williams,Audrey E. Mars,Edward S. Stenroos,Sue X. Ming,Rong Wang,Madhura Sreenath,Marivic F Factura,Chitra Reddy,George H. Lambert,William G. Johnson +10 more
TL;DR: The likelihood ratio test has the advantage that it can incorporate complete and incomplete case-parent trios as well as independent cases and controls and will be useful for such a locus analyzed as part of a larger case-parents study design.
Journal ArticleDOI
Genetic variant of glutathione peroxidase 1 in autism
Xue Ming,William G. Johnson,Edward S. Stenroos,Audrey E. Mars,George H. Lambert,Steven Buyske +5 more
TL;DR: Investigation of a GCG repeat polymorphism of a human glutathione peroxidase polyalanine repeat in 103 trios of AD suggests that possessing this ALA6 allele may be protective for AD.
Journal ArticleDOI
Common dihydrofolate reductase 19-base pair deletion allele: a novel risk factor for preterm delivery.
William G. Johnson,Theresa O. Scholl,John R. Spychala,Steven Buyske,Edward S. Stenroos,Xinhua Chen +5 more
TL;DR: The DHFR 19-base pair deletion allele may be a risk factor for preterm delivery or low birth weight in the presence of low dietary folate in women with both a DHFR deletion allele and low folate intake.
Journal ArticleDOI
HLA-DR4 as a Risk Allele for Autism Acting in Mothers of Probands Possibly During Pregnancy
William G. Johnson,Steven Buyske,Audrey E. Mars,Madhura Sreenath,Edward S. Stenroos,Tanishia A. Williams,Rosanne Stein,George H. Lambert +7 more
TL;DR: The HLA-DR4 gene may act in mothers of children with autism during pregnancy to contribute to autism in their offspring, and significant transmission disequilibrium was seen, supporting a role for HLA -DR4 as an autism risk factor acting in mothers during pregnancy.