Gordon Gong

Summary

Affiliation: Creighton University
Country: USA

Publications

  1. ncbi request reprint Fine mapping of susceptibility genes by Lewontin's linkage disequilibrium measure with application to Alzheimer's disease
    Gordon Gong
    Creighton University Osteoporosis Research Center, 601 North 30th Street, Suite 6730, Omaha, NE 68131, USA
    Chin Med J (Engl) 115:1233-40. 2002
  2. ncbi request reprint Association between bone mineral density and candidate genes in different ethnic populations and its implications
    G Gong
    Creighton University Osteoporosis Research Center, 601 North 30th Street, Suite 6730, Omaha, NE 68131, USA
    Calcif Tissue Int 72:113-23. 2003
  3. ncbi request reprint Genetic dissection of myocilin glaucoma
    Gordon Gong
    Osteoporosis Research Center, Creighton University Omaha, NE 68131, USA
    Hum Mol Genet 13:R91-102. 2004
  4. pmc Race, ethnicity and prevalence of primary open-angle glaucoma
    Omofolasade Kosoko-Lasaki
    Department of Surgery, Creighton University, Omaha, NE 68178, USA
    J Natl Med Assoc 98:1626-9. 2006
  5. ncbi request reprint American founder mutation for Lynch syndrome. Prevalence estimates and implications
    Henry T Lynch
    Department of Preventive Medicine and Public Health, Creighton University, Omaha, Nebraska 68178, USA
    Cancer 106:448-52. 2006
  6. ncbi request reprint Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer families
    Henry T Lynch
    Department of Preventive Medicine and Public Health, Creighton University, 2500 California Plaza, Omaha, Nebraska 68178, USA
    Cancer Genet Cytogenet 165:91-7. 2006
  7. ncbi request reprint Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications
    Henry T Lynch
    Department of Preventive Medicine, Creighton University School of Medicine, 2500 California Plaza, Omaha, NE 68178, USA
    Eur J Hum Genet 14:390-402. 2006
  8. pmc Family information service participation increases the rates of mutation testing among members of families with BRCA1/2 mutations
    Henry T Lynch
    Department of Preventive Medicine, Creighton University School of Medicine, Omaha, Nebraska 68178, USA
    Breast J 15:S20-4. 2009
  9. doi request reprint Origins and prevalence of the American Founder Mutation of MSH2
    Mark Clendenning
    Human Cancer Genetics Program, The Ohio State University, Columbus, Ohio 43210, USA
    Cancer Res 68:2145-53. 2008
  10. pmc Inherited, familial and sporadic primary open-angle glaucoma
    Gordon Gong
    West Texas EXPORT Center, F Marie Hall Institute for Rural and Community Health, Texas Tech University Health Science Center, Lubbock, TX 79409 USA
    J Natl Med Assoc 99:559-63. 2007

Detail Information

Publications15

  1. ncbi request reprint Fine mapping of susceptibility genes by Lewontin's linkage disequilibrium measure with application to Alzheimer's disease
    Gordon Gong
    Creighton University Osteoporosis Research Center, 601 North 30th Street, Suite 6730, Omaha, NE 68131, USA
    Chin Med J (Engl) 115:1233-40. 2002
    ..To formulate an equation for fine mapping of disease loci under complex conditions and determine the marker-disease distance in a specific case using this equation...
  2. ncbi request reprint Association between bone mineral density and candidate genes in different ethnic populations and its implications
    G Gong
    Creighton University Osteoporosis Research Center, 601 North 30th Street, Suite 6730, Omaha, NE 68131, USA
    Calcif Tissue Int 72:113-23. 2003
    ..Phenotype-genotype associations found in East Asians are unlikely to be due to admixture with Caucasians...
  3. ncbi request reprint Genetic dissection of myocilin glaucoma
    Gordon Gong
    Osteoporosis Research Center, Creighton University Omaha, NE 68131, USA
    Hum Mol Genet 13:R91-102. 2004
    ..Polymorphisms at several loci including MYOC are associated with POAG, and play an important role in the pathogenesis of POAG...
  4. pmc Race, ethnicity and prevalence of primary open-angle glaucoma
    Omofolasade Kosoko-Lasaki
    Department of Surgery, Creighton University, Omaha, NE 68178, USA
    J Natl Med Assoc 98:1626-9. 2006
    ..Recently, some authors pooled data from studies on the Dutch, Australians and Americans of European origin in an attempt to predict the prevalence of primary open-angle glaucoma (POAG) in the United States...
  5. ncbi request reprint American founder mutation for Lynch syndrome. Prevalence estimates and implications
    Henry T Lynch
    Department of Preventive Medicine and Public Health, Creighton University, Omaha, Nebraska 68178, USA
    Cancer 106:448-52. 2006
    ..This test might serve as first-line screening for Lynch syndrome mutations, provided AFM was prevalent, which is assessed in the current study...
  6. ncbi request reprint Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer families
    Henry T Lynch
    Department of Preventive Medicine and Public Health, Creighton University, 2500 California Plaza, Omaha, Nebraska 68178, USA
    Cancer Genet Cytogenet 165:91-7. 2006
    ..Despite these psychological consequences, carriers and noncarriers reported a positive attitude toward genetic testing...
  7. ncbi request reprint Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications
    Henry T Lynch
    Department of Preventive Medicine, Creighton University School of Medicine, 2500 California Plaza, Omaha, NE 68178, USA
    Eur J Hum Genet 14:390-402. 2006
    ....
  8. pmc Family information service participation increases the rates of mutation testing among members of families with BRCA1/2 mutations
    Henry T Lynch
    Department of Preventive Medicine, Creighton University School of Medicine, Omaha, Nebraska 68178, USA
    Breast J 15:S20-4. 2009
    ..FIS attendance significantly increased the rate of mutation testing among high-risk family members...
  9. doi request reprint Origins and prevalence of the American Founder Mutation of MSH2
    Mark Clendenning
    Human Cancer Genetics Program, The Ohio State University, Columbus, Ohio 43210, USA
    Cancer Res 68:2145-53. 2008
    ..The consequences of this finding would be that the AFM is significantly more frequent in the United States than was previously predicted...
  10. pmc Inherited, familial and sporadic primary open-angle glaucoma
    Gordon Gong
    West Texas EXPORT Center, F Marie Hall Institute for Rural and Community Health, Texas Tech University Health Science Center, Lubbock, TX 79409 USA
    J Natl Med Assoc 99:559-63. 2007
    ..We further formulated a mathematic model to estimate disease prevalence and mutation frequency taking both ethnic background and familial aggregation into consideration...
  11. pmc Bone mineral density-affecting genes in Africans
    Gordon Gong
    Center, University of Texas at Houston, Houston, TX, USA
    J Natl Med Assoc 98:1102-8. 2006
    ..We have recently reported the role of environmental exposure in the ethnic diversity of bone mineral density (BMD). Potential genetic difference has not been adequately assessed...
  12. pmc Bone mineral density of recent African immigrants in the United States
    Gordon Gong
    West Texas EXPORT Center, Office of Rural and Community Health, Texas Tech University Health Science Center, Box 45013 STOP 5013, Lubbock, TX 79409, USA
    J Natl Med Assoc 98:746-52. 2006
    ..Racial/ethnic difference in bone mineral density (BMD) exists. The underlying mechanism is unclear and needs investigation...
  13. ncbi request reprint The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features
    Gershon Y Locker
    Evanston Northwestern Healthcare, Feinberg School of Medicine, Northwestern University, 2650 Ridge Ave, Evanston, IL 60201, USA
    Cancer Genet Cytogenet 169:33-8. 2006
    ..We could find no group of Ashkenazi Jews with colorectal cancer for whom screening for I1307K would be clinically useful...
  14. ncbi request reprint Factors associated with undiagnosed open-angle glaucoma: the Thessaloniki Eye Study
    Fotis Topouzis
    II Department of Ophthalmology, Aristotle University of Thessaloniki, General Hospital Papageorgiou, Periferiaki Odos Thessalonikis N Efkarpia 56403, Thessaloniki, Greece
    Am J Ophthalmol 145:327-335. 2008
    ..To identify factors associated with undiagnosed open-angle glaucoma (OAG), primary open-angle glaucoma (POAG), and pseudoexfoliative glaucoma (PEXG) in an elderly population in Thessaloniki, Greece...
  15. pmc A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait
    Randall D Little
    Department of Human Genetics, Genome Therapeutics Corporation, Waltham, MA 02453, USA
    Am J Hum Genet 70:11-9. 2002
    ..Our findings suggest that the HBM mutation confers a unique osteogenic activity in bone remodeling, and this understanding may facilitate the development of novel therapies for the treatment of osteoporosis...