SWStephanie J. Weinstein

Stephanie J. Weinstein

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Stephanie J. Weinstein has a total of 7 co-authors. Here are the top co-authors by number of shared publications:

  • Deborah M. Winn

    Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, MD 20892; and

    1 shared publication
  • Eleuterio Bravo-Otero

    ** University of Puerto Rico School of Dentistry, San Juan, Puerto Rico 00936

    1 shared publication
  • Gloria Gridley

    Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892

    1 shared publication
  • Lea C. Harty

    Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892

    1 shared publication
  • Linda M. Brown

    Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892

    1 shared publication
  • Richard B. Hayes

    Division of Epidemiology, Department of Population Health, New York University School of Medicine, New York, USA

    1 shared publication

Latest Publications

  • Open Access

    Folate Intake, Serum Homocysteine and Methylenetetrahydrofolate Reductase (MTHFR) C677T Genotype Are Not Associated with Oral Cancer Risk in Puerto Rico

    by Stephanie J. Weinstein, Gloria Gridley, Lea C. Harty, Linda M. Brown, Richard B. Hayes, Scott R. Diehl, Deborah M. Winn, Eleuterio Bravo-Otero

    We examined the relationships between folate and methionine intake, serum homocysteine levels (as a biomarker for folate metabolism), and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism genotype and risk of oral cancer in a population-based, case-control study in Puerto Rico. Structured questionnaires were used to collect information on demographic factors, usual adult diet, and tobacco and alcohol use. Oral epithelial cells and blood samples were collected from a subset of subjects. Analyses were conducted by logistic regression, adjusting for age, sex, lifetime smoking and lifetime alcohol intake, with the following numbers of cases/controls, respectively: dietary data (341/521); MTHFR genotype (148/149); and homocysteine (60/90). Although increased folate intake was associated with decreased oral cancer risk [adjusted odds ratio (OR) in highest vs. lowest quartile = 0.6, 95% confidence interval (CI): 0.4, 1.0, Ptrend = 0.05)], this finding was due almost entirely to folate intake from fruit (adjusted OR = 0.4, 95% CI: 0.2, 0.6; Ptrend = 0.0001), whereas other dietary folate sources showed no clear association. Methionine intake and serum homocysteine levels were not associated with oral cancer risk. Subjects with the MTHFR C677T homozygous variant (TT) genotype had a nonsignificantly lower risk, and risk patterns tended to differ by level of folate, methionine, alcohol intake and smoking, although the power to detect significant associations in subgroups of these variables was low. Risks for oral cancer are not folate specific; preventive recommendations for this disease should emphasize the importance of a healthy diet, including substantial intake of fruits.