Research Article

Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population†‡

  1. Faith Pangilinan1,
  2. Kerry Geiler1,
  3. Jessica Dolle1,
  4. James Troendle2,
  5. Deborah A. Swanson1,
  6. Anne M. Molloy3,
  7. Marie Sutton4,
  8. Mary Conley2,
  9. Peadar N. Kirke4,
  10. John M. Scott5,
  11. James L. Mills2,
  12. Lawrence C. Brody1,*

Article first published online: 16 SEP 2008

DOI: 10.1002/ajmg.a.32504

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 20, pages 2617–2625, 15 October 2008

Additional Information

How to Cite

Pangilinan, F., Geiler, K., Dolle, J., Troendle, J., Swanson, D. A., Molloy, A. M., Sutton, M., Conley, M., Kirke, P. N., Scott, J. M., Mills, J. L. and Brody, L. C. (2008), Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population. Am. J. Med. Genet., 146A: 2617–2625. doi: 10.1002/ajmg.a.32504

Author Information

  1. 1

    Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, Bethesda, Maryland

  2. 2

    Division of Epidemiology, Statistics and Prevention Research, National Institute of Child Health and Human Development, Department of Health and Human Services, National Institutes of Health, Bethesda, Maryland

  3. 3

    Department of Clinical Medicine, Trinity College Dublin, Dublin, Ireland

  4. 4

    Child Health Epidemiology Unit, Health Research Board, Dublin, Ireland

  5. 5

    Department of Biochemistry, Trinity College Dublin, Dublin, Ireland

*Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, Building 50, Room 5306, 50 South Drive, MSC 8004, Bethesda, MD 20892-8004.

  1. †

    This article is a US Government work and, as such, is in the public domain in the United States of America.

  2. ‡

    How to cite this article: Pangilinan F, Geiler K, Dolle J, Troendle J, Swanson DA, Molloy AM, Sutton M, Conley M, Kirke PN, Scott JM, Mills JL, Brody LC. 2008. Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population. Am J Med Genet Part A 146A:2617–2625.

Publication History

  1. Issue published online: 24 SEP 2008
  2. Article first published online: 16 SEP 2008
  3. Manuscript Accepted: 16 JUN 2008
  4. Manuscript Received: 10 APR 2008

Funded by

  • National Human Genome Research Institute, National Institutes of Health
  • National Institute of Child Health and Human Development, National Institutes of Health
  • The Health Research Board, Ireland

SEARCH

SEARCH BY CITATION

ARTICLE TOOLS

View Full Article (HTML) Get PDF (251K)

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Neha Chandel, Ashish Chauhan, Kamlesh Guleria, The p.Pro47Ser Polymorphism of TP53: A Systematic Review, International Journal of Cancer Research, 2013, 9, 1, 1

    CrossRef

  2. 2
    C. Pyrgaki, L. Niswander, Neural Circuit Development and Function in the Brain, 2013,

    CrossRef

  3. 3
    Faith Pangilinan, Anne M Molloy, James L Mills, James F Troendle, Anne Parle-McDermott, Caroline Signore, Valerie B O’Leary, Peter Chines, Jessica M Seay, Kerry Geiler-Samerotte, Adam Mitchell, Julia E VanderMeer, Kristine M Krebs, Angelica Sanchez, Joshua Cornman-Homonoff, Nicole Stone, Mary Conley, Peadar N Kirke, Barry Shane, John M Scott, Lawrence C Brody, Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects, BMC Medical Genetics, 2012, 13, 1, 62

    CrossRef

  4. 4
    József Gábor Joó, Recent perspectives on the genetic background of neural tube defects with special regard to iniencephaly, Expert Review of Molecular Diagnostics, 2009, 9, 3, 281

    CrossRef

  5. 5
    Anne M. Molloy, Lawrence C. Brody, James L. Mills, John M. Scott, Peadar N. Kirke, The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects, Birth Defects Research Part A: Clinical and Molecular Teratology, 2009, 85, 4
    Direct Link:
View Full Article (HTML) Get PDF (251K)