D W Hadley

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc Colonoscopy use following mutation detection in Lynch syndrome: exploring a role for cancer screening in adaptation
    D W Hadley
    Social Network Methods Section, Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, Bethesda, MD 20892, USA
    Clin Genet 79:321-8. 2011
  2. doi request reprint Generation after generation: exploring the psychological impact of providing genetic services through a cascading approach
    Donald W Hadley
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892 2073, USA
    Genet Med 12:808-15. 2010
  3. doi request reprint Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndrome
    Donald W Hadley
    Social and Behavioral Research Branch, National Institutes of Health, 31 Center Drive, MSC 2073, Building 31, Room B1B37F, Bethesda, MD 20892 2073, USA
    J Clin Oncol 26:948-54. 2008
  4. pmc The impact of familial environment on depression scores after genetic testing for cancer susceptibility
    S Ashida
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
    Clin Genet 75:43-9. 2009
  5. pmc Communicating genetic and genomic information: health literacy and numeracy considerations
    D H Lea
    National Human Genome Research Institute, NIH, Bethesda, MD 20892 2070, USA
    Public Health Genomics 14:279-89. 2011
  6. ncbi request reprint Family history: the three-generation pedigree
    Daniel J Wattendorf
    Department of Family Medicine, Uniformed Services University of the Health Sciences, F Edward Hebert School of Medicine, Bethesda, Maryland, USA
    Am Fam Physician 72:441-8. 2005
  7. ncbi request reprint Genetic testing in Parkinson's disease
    Aideen McInerney-Leo
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20952, USA
    Mov Disord 20:1-10. 2005
  8. ncbi request reprint Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer
    Donald W Hadley
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 10 Center Dr, MSC 1852, Building 10, Room 10C103, Bethesda, MD 20892 1852, USA
    Arch Intern Med 163:573-82. 2003
  9. ncbi request reprint Case 47: dural ectasia associated with Marfan syndrome
    Nicola C Ho
    Section of Human Genetics and Integrative Medicine, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
    Radiology 223:767-71. 2002
  10. ncbi request reprint Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    David Ng
    Medical Genetics Branch, NHGRI, National Institutes of Health, Bethesda, Maryland 20892 4472, USA
    Am J Med Genet 110:308-14. 2002

Collaborators

Detail Information

Publications18

  1. pmc Colonoscopy use following mutation detection in Lynch syndrome: exploring a role for cancer screening in adaptation
    D W Hadley
    Social Network Methods Section, Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, Bethesda, MD 20892, USA
    Clin Genet 79:321-8. 2011
    ..Furthermore, depressive symptoms may interfere with behavioral compliance in some patients, suggesting referral to mental health specialists...
  2. doi request reprint Generation after generation: exploring the psychological impact of providing genetic services through a cascading approach
    Donald W Hadley
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892 2073, USA
    Genet Med 12:808-15. 2010
    ..This study examines whether previous family experiences with genetic services influences levels of psychological well-being of family members receiving services later...
  3. doi request reprint Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndrome
    Donald W Hadley
    Social and Behavioral Research Branch, National Institutes of Health, 31 Center Drive, MSC 2073, Building 31, Room B1B37F, Bethesda, MD 20892 2073, USA
    J Clin Oncol 26:948-54. 2008
    ..This study (1) evaluated women's perceived risks for cancers, (2) compared endometrial cancer screening and colonoscopy, and (3) identified predictors of screening before and after genetic testing...
  4. pmc The impact of familial environment on depression scores after genetic testing for cancer susceptibility
    S Ashida
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
    Clin Genet 75:43-9. 2009
    ..The findings highlight the complexity of familial environment surrounding individuals that undergo genetic testing and suggest the benefits of considering these factors when providing genetic services...
  5. pmc Communicating genetic and genomic information: health literacy and numeracy considerations
    D H Lea
    National Human Genome Research Institute, NIH, Bethesda, MD 20892 2070, USA
    Public Health Genomics 14:279-89. 2011
    ..Public health genomics researchers and practitioners are uniquely positioned to engage in research that explores how different audiences react to and use genomic risk information...
  6. ncbi request reprint Family history: the three-generation pedigree
    Daniel J Wattendorf
    Department of Family Medicine, Uniformed Services University of the Health Sciences, F Edward Hebert School of Medicine, Bethesda, Maryland, USA
    Am Fam Physician 72:441-8. 2005
    ..Major organizations have endorsed using standardized symbols in pedigrees to identify inherited contributions to disease...
  7. ncbi request reprint Genetic testing in Parkinson's disease
    Aideen McInerney-Leo
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20952, USA
    Mov Disord 20:1-10. 2005
    ..We explore the utility, appropriateness, and possible implications of genetic testing for diagnostic and presymptomatic purposes...
  8. ncbi request reprint Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer
    Donald W Hadley
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 10 Center Dr, MSC 1852, Building 10, Room 10C103, Bethesda, MD 20892 1852, USA
    Arch Intern Med 163:573-82. 2003
    ..This study investigated attitudes, intentions, and uptake of genetic testing within newly identified families with hereditary nonpolyposis colorectal cancer...
  9. ncbi request reprint Case 47: dural ectasia associated with Marfan syndrome
    Nicola C Ho
    Section of Human Genetics and Integrative Medicine, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA
    Radiology 223:767-71. 2002
  10. ncbi request reprint Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    David Ng
    Medical Genetics Branch, NHGRI, National Institutes of Health, Bethesda, Maryland 20892 4472, USA
    Am J Med Genet 110:308-14. 2002
    ..In addition, it suggests that Lenz microphthalmia syndrome, previously thought to be a single disorder, may represent an amalgam of two distinct disorders...
  11. ncbi request reprint Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer
    Donald W Hadley
    Genetic Counseling Research Unit, Medical Genetics Branch, National Human Genome Research Institute NIH, 10 Center Drive, MSC 1852, Bldg 10 Room 10 C103, Bethesda, MD 20892 1852, USA
    J Clin Oncol 22:39-44. 2004
    ....
  12. pmc Communication, encouragement, and cancer screening in families with and without mutations for hereditary nonpolyposis colorectal cancer: a pilot study
    Anne L Ersig
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health Bethesda, Maryland, USA
    Genet Med 11:728-34. 2009
    ..Little is known about colonoscopy completion in families suspected of having hereditary nonpolyposis colorectal cancer but without identified mutations...
  13. ncbi request reprint BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention
    Aideen McInerney-Leo
    Medical Genetics Branch, NHGRI, NIH, Bethesda, Maryland 20892, USA
    Am J Med Genet A 130:221-7. 2004
    ..001). Results suggest that a problem-solving counseling intervention may help to enhance psychological well-being following testing and that a personal history of cancer may increase psychological distress associated with genetic testing...
  14. ncbi request reprint Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR
    David Ng
    Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA
    Nat Genet 36:411-6. 2004
    ....
  15. ncbi request reprint Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer families
    B B Biesecker
    Medical Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland, USA 20892 1852, USA
    Am J Med Genet 93:257-63. 2000
    ..A better understanding of factors that influence interest in predictive testing may help to inform the counseling that occurs prior to genetic testing...
  16. ncbi request reprint BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships
    Aideen McInerney-Leo
    Medical Genetics Branch, National Human Genome Research Institute NIH, Bldg 10, 10 Center Drive, Bethesda, MD 20892, USA
    Am J Med Genet A 133:165-9. 2005
    ....
  17. pmc Colon cancer screening practices and disclosure after receipt of positive or inconclusive genetic test results for hereditary nonpolyposis colorectal cancer
    Anne L Ersig
    Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892 2073, USA
    Cancer 115:4071-9. 2009
    ..This study compared endoscopy use and disclosure between individuals with positive and inconclusive genetic test results, within a year after results were received...
  18. ncbi request reprint Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature
    Emily S Doherty
    National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA
    Am J Med Genet A 143:3204-15. 2007
    ..01). Based on our findings, we propose that the clinical management should include audiometric and developmental assessment in addition to standard clinical care and appropriate genetic counseling...