Donald W Hadley

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. pmc Willingness of Mexican-American adults to share family health history with healthcare providers
    Laura M Koehly
    Social and Behavioral Research Branch, National Human Genome Research Institute NIH, 31 Center Drive, Bethesda, MD 20892, USA
    Am J Prev Med 40:633-6. 2011
  8. pmc De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
    Birth Defects Res A Clin Mol Teratol 91:862-5. 2011
  9. pmc Personalized genomic medicine: lessons from the exome
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    Mol Genet Metab 104:189-91. 2011
  10. 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

Collaborators

Detail Information

Publications26

  1. 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...
  2. 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
    ....
  3. 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
    ....
  4. 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...
  5. 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...
  6. 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...
  7. pmc Willingness of Mexican-American adults to share family health history with healthcare providers
    Laura M Koehly
    Social and Behavioral Research Branch, National Human Genome Research Institute NIH, 31 Center Drive, Bethesda, MD 20892, USA
    Am J Prev Med 40:633-6. 2011
    ..Collecting family health history (FHH) information to share with healthcare providers is an important aspect of health-risk assessment...
  8. pmc De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
    Birth Defects Res A Clin Mol Teratol 91:862-5. 2011
    ..The causes of this condition are thought to be heterogeneous but are overall not well understood...
  9. pmc Personalized genomic medicine: lessons from the exome
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA
    Mol Genet Metab 104:189-91. 2011
    ....
  10. 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
  11. 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...
  12. doi request reprint The role of religious and existential well-being in families with Lynch syndrome: prevention, family communication, and psychosocial adjustment
    Bronwyn A Morris
    Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD, USA
    J Genet Couns 22:482-91. 2013
    ..Interventions considering family-level factors may provide efficient pathways to improving psychosocial factors, screening practices, communication about disease risk and genetic testing, and cancer prevention. ..
  13. 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
    ....
  14. pmc Incidental medical information in whole-exome sequencing
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
    Pediatrics 129:e1605-11. 2012
    ....
  15. pmc A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum
    Daniel E Pineda-Alvarez
    Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20814, USA
    Am J Med Genet A 155:2713-20. 2011
    ..These findings contribute to the understanding of the phenotypic variability of the HPE spectrum, and highlight findings in one medically important but often incompletely investigated system...
  16. 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...
  17. 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...
  18. 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...
  19. doi request reprint Analysis of cardiac anomalies in VACTERL association
    Bridget K Cunningham
    Department of Pediatrics, Walter Reed National Military Medical Center Bethesda, Maryland Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland
    Birth Defects Res A Clin Mol Teratol 97:792-7. 2013
    ..Controversy still remains regarding the definition of VATER association and its expansion to VACTERL, the appropriate diagnostic criteria and the overall incidence...
  20. doi request reprint Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog
    Benjamin D Solomon
    Medical Genetics Branch, National Human Genome Research Institute, NationalInstitutes of Health, Bethesda, MD, USA
    J Med Genet 49:473-9. 2012
    ..The severity spectrum is wide, ranging from incompatibility with extrauterine life to isolated midline facial differences...
  21. 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...
  22. 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...
  23. ncbi request reprint Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review
    Noralane M Lindor
    Department of Medical Genetics, Mayo Clinic College of Medicine, Rochester, Minn, USA
    JAMA 296:1507-17. 2006
    ..Potential risk-reducing interventions are recommended for individuals known to have these mutations...
  24. ncbi request reprint How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases
    Cynthia A James
    Department of Medicine, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, MD, USA
    Genet Med 8:234-42. 2006
    ..While the mode of inheritance of a genetic condition has long been considered to have not only medical, but also psychosocial consequences for families, this supposition has never been tested...
  25. ncbi request reprint Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease
    Cynthia A James
    Division of Cardiology, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287 0409, USA
    Am J Med Genet C Semin Med Genet 119:60-9. 2003
    ..Published 2003 Wiley-Liss, Inc...
  26. ncbi request reprint Evaluating the impact of genetic counseling and testing with signal detection methods
    Christina G S Palmer
    Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California, USA
    J Genet Couns 14:17-27. 2005
    ..Signal detection methods are easily implemented and are useful techniques for evaluating the impact of GCT...