Megan L Grove

Summary

Affiliation: Texas Medical Center
Country: USA

Publications

  1. pmc Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
    Megan L Grove
    School of Public Health, Human Genetics Center, The University of Texas Health Science Center at Houston, Houston, Texas, USA
    PLoS ONE 8:e68095. 2013
  2. pmc Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD
    Joshua W Knowles
    Division of Cardiovascular Medicine, Falk Cardiovascular Research Building, Stanford University School of Medicine, Stanford, CA 94305 5406, USA
    BMC Med Genet 9:23. 2008
  3. pmc Single nucleotide polymorphisms in cholesteryl ester transfer protein gene and recurrent coronary heart disease or mortality in patients with established atherosclerosis
    Salim S Virani
    Health Services Research and Development Center of Excellence, Michael E DeBakey Veterans Affairs Medical Center, Houston, Texas Section of Cardiovascular Research, Department of Internal Medicine, Baylor College of Medicine, Houston, Texas Electronic address
    Am J Cardiol 112:1287-92. 2013
  4. pmc Seafood consumption and blood mercury concentrations in Jamaican children with and without autism spectrum disorders
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences, The University of Texas School of Public Health at Houston, Houston, TX 77030, USA
    Neurotox Res 23:22-38. 2013
  5. ncbi request reprint Role of Metabolic Genes in Blood Arsenic Concentrations of Jamaican Children with and without Autism Spectrum Disorder
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences EHGES, University of Texas School of Public Health at Houston, Houston, TX 77030, USA
    Int J Environ Res Public Health 11:7874-95. 2014
  6. pmc High-resolution identity by descent mapping uncovers the genetic basis for blood pressure differences between spontaneously hypertensive rat lines
    Rebecca Bell
    Institute of Molecular Medicine, University of Texas HSC at Houston, Houston, TX 77030, USA
    Circ Cardiovasc Genet 4:223-31. 2011
  7. pmc Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida
    A J Agopian
    Human Genetics Center, Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, Texas
    Birth Defects Res A Clin Mol Teratol 97:597-601. 2013
  8. pmc Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease
    Salim S Virani
    Center of Excellence, Health Services Research and Development, Michael E DeBakey Veterans Affairs Medical Center, Houston, TX 77030, USA
    Circ J 76:950-6. 2012
  9. pmc Maternal and paternal age are jointly associated with childhood autism in Jamaica
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences EHGES, School of Public Health, The University of Texas Health Science Center at Houston UTHealth, Houston, TX 77030, USA
    J Autism Dev Disord 42:1928-38. 2012
  10. pmc Population-based risk factors for elevated alanine aminotransferase in a South Texas Mexican-American population
    Hui Qi Qu
    University of Texas School of Public Health, Brownsville, Texas, USA
    Arch Med Res 43:482-8. 2012

Collaborators

Detail Information

Publications11

  1. pmc Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium
    Megan L Grove
    School of Public Health, Human Genetics Center, The University of Texas Health Science Center at Houston, Houston, Texas, USA
    PLoS ONE 8:e68095. 2013
    ..The cluster file from this experiment is available at www.chargeconsortium.com/main/exomechip. ..
  2. pmc Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD
    Joshua W Knowles
    Division of Cardiovascular Medicine, Falk Cardiovascular Research Building, Stanford University School of Medicine, Stanford, CA 94305 5406, USA
    BMC Med Genet 9:23. 2008
    ..We tested whether single nucleotide polymorphisms (SNPs) in OLR1 are associated with clinically significant CAD in the Atherosclerotic Disease, VAscular FuNction, & Geneti C Epidemiology (ADVANCE) study...
  3. pmc Single nucleotide polymorphisms in cholesteryl ester transfer protein gene and recurrent coronary heart disease or mortality in patients with established atherosclerosis
    Salim S Virani
    Health Services Research and Development Center of Excellence, Michael E DeBakey Veterans Affairs Medical Center, Houston, Texas Section of Cardiovascular Research, Department of Internal Medicine, Baylor College of Medicine, Houston, Texas Electronic address
    Am J Cardiol 112:1287-92. 2013
    ..In conclusion, genetic CETP variants were not associated with recurrent MI or recurrent revascularization in overall cohort with a possible mortality increase in patients who underwent CABG. ..
  4. pmc Seafood consumption and blood mercury concentrations in Jamaican children with and without autism spectrum disorders
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences, The University of Texas School of Public Health at Houston, Houston, TX 77030, USA
    Neurotox Res 23:22-38. 2013
    ..Based on our findings, we recommend additional education to Jamaican parents regarding potential hazards of elevated blood mercury concentrations, and its association with seafood consumption and type of seafood...
  5. ncbi request reprint Role of Metabolic Genes in Blood Arsenic Concentrations of Jamaican Children with and without Autism Spectrum Disorder
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences EHGES, University of Texas School of Public Health at Houston, Houston, TX 77030, USA
    Int J Environ Res Public Health 11:7874-95. 2014
    ..These findings suggest a possible role of GSTP1 in the detoxification of arsenic. ..
  6. pmc High-resolution identity by descent mapping uncovers the genetic basis for blood pressure differences between spontaneously hypertensive rat lines
    Rebecca Bell
    Institute of Molecular Medicine, University of Texas HSC at Houston, Houston, TX 77030, USA
    Circ Cardiovasc Genet 4:223-31. 2011
    ....
  7. pmc Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida
    A J Agopian
    Human Genetics Center, Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, Texas
    Birth Defects Res A Clin Mol Teratol 97:597-601. 2013
    ..Based on studies in animals and humans, PAX3 and T (brachyury) are candidate genes for spina bifida. However, neither gene has been definitively identified as a risk factor for this condition...
  8. pmc Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease
    Salim S Virani
    Center of Excellence, Health Services Research and Development, Michael E DeBakey Veterans Affairs Medical Center, Houston, TX 77030, USA
    Circ J 76:950-6. 2012
    ....
  9. pmc Maternal and paternal age are jointly associated with childhood autism in Jamaica
    Mohammad H Rahbar
    Division of Epidemiology, Human Genetics, and Environmental Sciences EHGES, School of Public Health, The University of Texas Health Science Center at Houston UTHealth, Houston, TX 77030, USA
    J Autism Dev Disord 42:1928-38. 2012
    ..6, 9.1)] and a difference for maternal age of [6.5 years; 95% CI (4.0, 8.9)]. To avoid multicollinearity in logistic regression, we recommend joint modeling of parental ages as a vector of outcome variables using MGLM...
  10. pmc Population-based risk factors for elevated alanine aminotransferase in a South Texas Mexican-American population
    Hui Qi Qu
    University of Texas School of Public Health, Brownsville, Texas, USA
    Arch Med Res 43:482-8. 2012
    ..We aimed to identify and stratify risk factors associated with elevated ALT in a randomly selected population with a high prevalence of elevated ALT (39%), obesity (49%) and diabetes (30%)...
  11. pmc Genome-wide identification of allelic expression in hypertensive rats
    Renata I Dmitrieva
    Institute of Molecular Medicine and Human Genetics Center, University of Texas Health Science Center, 2121 Holcombe Blvd, Houston, TX 77030, USA
    Circ Cardiovasc Genet 2:106-15. 2009
    ..Inbred animal models can facilitate genetic studies of disease traits. The spontaneously hypertensive rat (SHR) is an inbred model of hypertension that exists in several closely related but genetically distinct lines...