Susan Stuckless

Summary

Affiliation: Memorial University of Newfoundland
Country: Canada

Publications

  1. doi request reprint BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families
    C Fischer
    Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 366, Heidelberg, Germany
    Clin Genet 82:478-83. 2012
  2. doi request reprint Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation
    S Stuckless
    Department of Clinical Epidemiology Department of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Genet 82:439-45. 2012
  3. doi request reprint Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation
    S Stuckless
    Clinical Epidemiology Unit, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Genet 83:359-64. 2013
  4. ncbi request reprint The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
    Susan Stuckless
    Department of Clinical Epidemiology, Faculty of Medicine, Memorial University of Newfoundland, St John s, NL, Canada
    Fam Cancer 6:1-12. 2007
  5. ncbi request reprint High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes
    Michael O Woods
    Discipline of Genetics, Department of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Cancer Res 11:6853-61. 2005
  6. doi request reprint A histology-based model for predicting microsatellite instability in colorectal cancers
    Angela Hyde
    Discipline of Genetics, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Am J Surg Pathol 34:1820-9. 2010
  7. pmc A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features
    Bridget A Fernandez
    Discipline of Genetics, Memorial University of Newfoundland, St John s, NL, Canada
    Respir Res 13:64. 2012
  8. doi request reprint Bias in clinical studies of genetic diseases
    Susan Stuckless
    Department of Medicine, Memorial University of Newfoundland, St John s, Canada
    Methods Mol Biol 473:171-86. 2009

Collaborators

Detail Information

Publications8

  1. doi request reprint BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families
    C Fischer
    Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 366, Heidelberg, Germany
    Clin Genet 82:478-83. 2012
    ..In families with BRCA1/2-negative index patient we recommend a second screening if another patient with a high probability of carrying a BRCA1/2 mutation is available...
  2. doi request reprint Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation
    S Stuckless
    Department of Clinical Epidemiology Department of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Genet 82:439-45. 2012
    ..CRC development may be further reduced by decreasing the screening interval to 1 year and improving quality of colonoscopy...
  3. doi request reprint Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation
    S Stuckless
    Clinical Epidemiology Unit, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Genet 83:359-64. 2013
    ....
  4. ncbi request reprint The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
    Susan Stuckless
    Department of Clinical Epidemiology, Faculty of Medicine, Memorial University of Newfoundland, St John s, NL, Canada
    Fam Cancer 6:1-12. 2007
    ..The incidence of CRC in MSH2 mutation carriers, exposed to the same environment, is not modified by the specific mutation, although there is a suggestion that type of mutation may influence development of some extracolonic cancers...
  5. ncbi request reprint High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes
    Michael O Woods
    Discipline of Genetics, Department of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Clin Cancer Res 11:6853-61. 2005
    ..Our purpose was to determine the proportion of hereditary colorectal cancer and to determine the genetic basis of disease in both population and clinically referred cohorts from Newfoundland...
  6. doi request reprint A histology-based model for predicting microsatellite instability in colorectal cancers
    Angela Hyde
    Discipline of Genetics, Memorial University of Newfoundland, St John s, Newfoundland, Canada
    Am J Surg Pathol 34:1820-9. 2010
    ..4% and a specificity of 53.9%. In the validation cohort, sensitivity was 96.9% and specificity 76.6%. We conclude that PREDICT is a good predictor of MSI-H CRC...
  7. pmc A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features
    Bridget A Fernandez
    Discipline of Genetics, Memorial University of Newfoundland, St John s, NL, Canada
    Respir Res 13:64. 2012
    ..Individuals with Familial Pulmonary Fibrosis (FPF) have at least one affected first or second-degree relative and account for 0.5-20% of cases...
  8. doi request reprint Bias in clinical studies of genetic diseases
    Susan Stuckless
    Department of Medicine, Memorial University of Newfoundland, St John s, Canada
    Methods Mol Biol 473:171-86. 2009
    ..This chapter reviews the epidemiological concepts of selection bias, information bias, and confounding and discusses ways in which these sources of bias can be minimized...