Thomas M Morgan

Summary

Affiliation: Vanderbilt University
Country: USA

Publications

  1. ncbi Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study
    Thomas M Morgan
    Department of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Conn 06510, USA
    JAMA 297:1551-61. 2007
  2. ncbi Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome
    Thomas M Morgan
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA
    BMC Med Genet 9:66. 2008
  3. ncbi Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth
    Jevon Plunkett
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA
    BMC Med Genomics 3:62. 2010
  4. ncbi Vaccines are not associated with metabolic events in children with urea cycle disorders
    Thomas M Morgan
    Department of Pediatrics Division of Genetics and Genomic Medicine, Vanderbilt University School of Medicine, DD 2205 Medical Center North, Nashville, TN 37232 2578, USA
    Pediatrics 127:e1147-53. 2011
  5. ncbi Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome
    Thomas M Morgan
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA
    BMC Med Genet 12:127. 2011
  6. ncbi Genetic risk score does not correlate with body mass index of Latina women in a clinical trial
    Kimberly R Coenen
    Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee, USA
    Clin Transl Sci 4:323-7. 2011
  7. ncbi Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype
    Tracy L McGregor
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA
    BMC Med Genet 12:92. 2011
  8. ncbi Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
    Betul Bakkaloglu
    Program on Neurogenetics, Department of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA
    Am J Hum Genet 82:165-73. 2008

Collaborators

Detail Information

Publications8

  1. ncbi Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study
    Thomas M Morgan
    Department of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Conn 06510, USA
    JAMA 297:1551-61. 2007
    ..Given the numerous, yet inconsistent, reports of genetic variants being associated with acute coronary syndromes (ACS), there is a need for comprehensive validation of ACS susceptibility genotypes...
  2. ncbi Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome
    Thomas M Morgan
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA
    BMC Med Genet 9:66. 2008
    ..Many candidate genes have been reported to be risk factors for acute coronary syndrome (ACS), but their impact on clinical prognosis following ACS is unknown...
  3. ncbi Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth
    Jevon Plunkett
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA
    BMC Med Genomics 3:62. 2010
    ..We hypothesize that higher primate-specific gene evolution may lead to these differences and target genes involved in human preterm birth, an area of global health significance...
  4. ncbi Vaccines are not associated with metabolic events in children with urea cycle disorders
    Thomas M Morgan
    Department of Pediatrics Division of Genetics and Genomic Medicine, Vanderbilt University School of Medicine, DD 2205 Medical Center North, Nashville, TN 37232 2578, USA
    Pediatrics 127:e1147-53. 2011
    ..Patients with UCDs are subject to hyperammonemic episodes (HAEs) after infection, fever, or other stressors...
  5. ncbi Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome
    Thomas M Morgan
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA
    BMC Med Genet 12:127. 2011
    ..Genome-wide association studies (GWAS) have identified new candidate genes for the occurrence of acute coronary syndrome (ACS), but possible effects of such genes on survival following ACS have yet to be investigated...
  6. ncbi Genetic risk score does not correlate with body mass index of Latina women in a clinical trial
    Kimberly R Coenen
    Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee, USA
    Clin Transl Sci 4:323-7. 2011
    ..We conclude that an eight locus GRS has no clinical utility for explaining obesity or predicting response to intervention in Latina women participating in a clinical trial...
  7. ncbi Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype
    Tracy L McGregor
    Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA
    BMC Med Genet 12:92. 2011
    ..We hypothesized that common polymorphisms in the five human lysyl oxidase genes (LOX, LOXL1, LOXL2, LOXL3, and LOXL4) may be associated with the phenotype of adolescent idiopathic scoliosis...
  8. ncbi Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
    Betul Bakkaloglu
    Program on Neurogenetics, Department of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA
    Am J Hum Genet 82:165-73. 2008
    ....