H Hampel

Summary

Affiliation: The Ohio State University
Country: USA

Publications

  1. ncbi request reprint Hereditary colorectal cancer: risk assessment and management
    H Hampel
    Clinical Cancer Genetics Program, Arthur G James Cancer Hospital and Richard J Solove Research Institute, Ohio State University, Columbus 43210 1240, USA
    Clin Genet 58:89-97. 2000
  2. pmc Referral for cancer genetics consultation: a review and compilation of risk assessment criteria
    H Hampel
    Clinical Cancer Genetics Program, The Ohio State University, Columbus, Ohio 43221, USA
    J Med Genet 41:81-91. 2004
  3. pmc Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment
    J Westman
    Human Cancer Genetics Program, Arthur G James Cancer Hospital and Richard J Solove Research Institute, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA
    J Med Genet 37:354-60. 2000
  4. ncbi request reprint Genetic testing for cancer predisposition
    C Eng
    Clinical Cancer Genetics and Human Cancer Genetics Programs, Comprehensive Cancer Center, and Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, Ohio 43210, USA
    Annu Rev Med 52:371-400. 2001
  5. ncbi request reprint Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2
    R E Pyatt
    Department of Pathology, Ohio State University, Columbus, Ohio, USA
    Clin Genet 63:215-8. 2003
  6. pmc Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
    X P Zhou
    Clinical Cancer Genetics and Human Cancer Genetics Programs, Comprehensive Cancer Center, and the Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA
    Am J Hum Genet 69:704-11. 2001
  7. ncbi request reprint Correlation between patient weight and defects in DNA mismatch repair: is this the link between an increased risk of previous cancer in thinner women with endometrial cancer?
    D E Cohn
    Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Ohio State University College of Medicine, Columbus, Ohio, USA
    Int J Gynecol Cancer 18:136-40. 2008
  8. doi request reprint A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
    M Clendenning
    Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA
    J Med Genet 45:340-5. 2008
  9. ncbi request reprint Utilization of genetic counseling services by surgical oncologists: education a must
    D M Agnese
    Clin Genet 70:524-5. 2006
  10. pmc The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
    W D Foulkes
    Department of Medicine, Sir Mortimer B Davis Jewish General Hospital, Montreal, Quebec, Canada, H3G 1A4
    Am J Hum Genet 71:1395-412. 2002

Collaborators

Detail Information

Publications14

  1. ncbi request reprint Hereditary colorectal cancer: risk assessment and management
    H Hampel
    Clinical Cancer Genetics Program, Arthur G James Cancer Hospital and Richard J Solove Research Institute, Ohio State University, Columbus 43210 1240, USA
    Clin Genet 58:89-97. 2000
    ....
  2. pmc Referral for cancer genetics consultation: a review and compilation of risk assessment criteria
    H Hampel
    Clinical Cancer Genetics Program, The Ohio State University, Columbus, Ohio 43221, USA
    J Med Genet 41:81-91. 2004
    ..To assist health care professionals in deciding when a cancer genetics consultation is appropriate, available reports were critically reviewed in order to develop a single set of risk assessment criteria...
  3. pmc Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment
    J Westman
    Human Cancer Genetics Program, Arthur G James Cancer Hospital and Richard J Solove Research Institute, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA
    J Med Genet 37:354-60. 2000
    ..A computer based touchscreen family cancer history questionnaire was developed and implemented to facilitate the provision of cancer risk assessments for the ambulatory and outpatient populations of a free standing cancer hospital...
  4. ncbi request reprint Genetic testing for cancer predisposition
    C Eng
    Clinical Cancer Genetics and Human Cancer Genetics Programs, Comprehensive Cancer Center, and Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, Ohio 43210, USA
    Annu Rev Med 52:371-400. 2001
    ..Thorough medical care requires the identification of families likely to have a hereditary cancer susceptibility syndrome for referral to cancer genetics professionals...
  5. ncbi request reprint Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2
    R E Pyatt
    Department of Pathology, Ohio State University, Columbus, Ohio, USA
    Clin Genet 63:215-8. 2003
    ....
  6. pmc Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
    X P Zhou
    Clinical Cancer Genetics and Human Cancer Genetics Programs, Comprehensive Cancer Center, and the Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH 43210, USA
    Am J Hum Genet 69:704-11. 2001
    ..Thus, germline BMPR1A mutations cause a significant proportion of cases of JPS and might define a small subset of cases of CS/BRRS with specific colonic phenotype...
  7. ncbi request reprint Correlation between patient weight and defects in DNA mismatch repair: is this the link between an increased risk of previous cancer in thinner women with endometrial cancer?
    D E Cohn
    Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Ohio State University College of Medicine, Columbus, Ohio, USA
    Int J Gynecol Cancer 18:136-40. 2008
    ....
  8. doi request reprint A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
    M Clendenning
    Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA
    J Med Genet 45:340-5. 2008
    ..This disparity is primarily due to complications in the study of this gene caused by interference from pseudogene sequences...
  9. ncbi request reprint Utilization of genetic counseling services by surgical oncologists: education a must
    D M Agnese
    Clin Genet 70:524-5. 2006
  10. pmc The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
    W D Foulkes
    Department of Medicine, Sir Mortimer B Davis Jewish General Hospital, Montreal, Quebec, Canada, H3G 1A4
    Am J Hum Genet 71:1395-412. 2002
    ....
  11. ncbi request reprint Increased frequency of a new polymorphism in the cell division cycle 2 (cdc2) gene in patients with Alzheimer's disease and frontotemporal dementia
    A Johansson
    Department of Clinical Neuroscience, The Sahlgrenska Academy at Goteborg University, Goteborg, Sweden
    Neurosci Lett 340:69-73. 2003
    ..In the combined tauopathy (AD and FTD) group the odds ratio (OR) was 1.77 (95% CI 1.19-2.63) for the Ex6+7II genotype. Our findings suggest that the Ex6+7I allele is associated with tauopathies, both AD and FTD...
  12. ncbi request reprint Polymorphisms in the apolipoprotein E (APOE) gene in gerontopsychiatric patients
    P Zill
    Psychiatric Hospital, Ludwig Maximilians University, Munich Nussbaumstrasse 7, 80336 Munich, Germany
    Eur Arch Psychiatry Clin Neurosci 251:24-8. 2001
    ..However, if we combine our results with three previous published positive reports there seems to be an association between the -491A/T polymorphism and AD, though its size is less than found in the original publication...
  13. pmc MSH6 missense mutations are often associated with no or low cancer susceptibility
    R Kariola
    Department of Biological and Environmental Sciences, Genetics, University of Helsinki, FI 00014 Helsinki, Finland
    Br J Cancer 91:1287-92. 2004
    ....
  14. ncbi request reprint [Presenile dementia in memory clinics--incidence rates and clinical features]
    H Bickel
    Klinik und Poliklinik fur Psychiatrie und Psychotherapie der Technischen Universitat Munchen, Germany
    Nervenarzt 77:1079-85. 2006
    ..3/100,000. It can be concluded that memory clinics fulfill an important function in the care of patients with presenile dementia, since they are highly utilized by younger patients in early stages of the illness...