Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank
Yang, Quan-He, Botto, Lorenzo D, Gallagher, Margaret, Friedman, JM, Sanders, Christopher L, Koontz, Deborah, Nikolova, Stanimila, Erickson, J. David, Steinberg, Karen
Published in The American journal of clinical nutrition (01.07.2008)
Published in The American journal of clinical nutrition (01.07.2008)
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Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk
Jenkins, Mary M., Reefhuis, Jennita, Gallagher, Margaret L., Mulle, Jennifer G., Hoffmann, Thomas J., Koontz, Deborah A., Sturchio, Cynthia, Rasmussen, Sonja A., Witte, John S., Richter, Patricia, Honein, Margaret A.
Published in American journal of medical genetics. Part A (01.06.2014)
Published in American journal of medical genetics. Part A (01.06.2014)
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Influence of 5,10-Methylenetetrahydrofolate Reductase Polymorphism on Whole-Blood Folate Concentrations Measured by LC-MS/MS, Microbiologic Assay, and Bio-Rad Radioassay
Fazili, Zia, Pfeiffer, Christine M, Zhang, Mindy, Jain, Ram B, Koontz, Deborah
Published in Clinical chemistry (Baltimore, Md.) (01.01.2008)
Published in Clinical chemistry (Baltimore, Md.) (01.01.2008)
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Genetic Studies of a Cluster of Acute Lymphoblastic Leukemia Cases in Churchill County, Nevada
Steinberg, Karen K., Relling, Mary V., Margaret L. Gallagher, Christopher N. Greene, Carol S. Rubin, Deborah French, Holmes, Adrianne K., William L. Carroll, Deborah A. Koontz, Sampson, Eric J., Satten, Glen A.
Published in Environmental health perspectives (01.01.2007)
Published in Environmental health perspectives (01.01.2007)
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Rapid detection of the CYP2A612 hybrid allele by Pyrosequencing technology
Koontz, Deborah A, Huckins, Jacqueline J, Spencer, Antonina, Gallagher, Margaret L
Published in BMC medical genetics (24.08.2009)
Published in BMC medical genetics (24.08.2009)
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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain
Mecocci, P, MacGarvey, U, Kaufman, A E, Koontz, D, Shoffner, J M, Wallace, D C, Beal, M F
Published in Annals of neurology (01.10.1993)
Published in Annals of neurology (01.10.1993)
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Mitochondrial diabetes revisited
Ballinger, Scott W, Shoffner, John M, Gebhart, Susan, Koontz, Deborah A, Wallace, Douglas C
Published in Nature genetics (01.08.1994)
Published in Nature genetics (01.08.1994)
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Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation
Shoffner, J M, Brown, M D, Stugard, C, Jun, A S, Pollock, S, Haas, R H, Kaufman, A, Koontz, D, Kim, Y, Graham, J R
Published in Annals of neurology (01.08.1995)
Published in Annals of neurology (01.08.1995)
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A Pyrosequencing-Based Assay for the Rapid Detection of the 22q11.2 Deletion in DNA from Buccal and Dried Blood Spot Samples
Koontz, Deborah, Baecher, Kirsten, Kobrynski, Lisa, Nikolova, Stanimila, Gallagher, Margaret
Published in The Journal of molecular diagnostics : JMD (01.09.2014)
Published in The Journal of molecular diagnostics : JMD (01.09.2014)
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Prothrombin G20210A Mutation Is Associated With Young-Onset Stroke: The Genetics of Early-Onset Stroke Study and Meta-Analysis
Jiang, Baijia, Ryan, Kathleen A, Hamedani, Ali, Cheng, Yuching, Sparks, Mary J, Koontz, Deborah, Bean, Christopher J, Gallagher, Margaret, Hooper, W Craig, McArdle, Patrick F, O’Connell, Jeffrey R, Stine, O Colin, Wozniak, Marcella A, Stern, Barney J, Mitchell, Braxton D, Kittner, Steven J, Cole, John W
Published in Stroke (1970) (01.04.2014)
Published in Stroke (1970) (01.04.2014)
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Abstract T P289: Genetic Variation in the Sulfonylurea Receptor 1 (Sur1)-regulated NCCa-ATP Channel and Stroke Outcome: The Genetics of Early Onset Stroke Study
Cole, John W, Ryan, Kathleen A, Cheng, Yu-Ching, Koontz, Deborah, Bean, Christopher J, Gallagher, Margaret, Hooper, W C, McArdle, Patrick, O’Connell, Jeffrey R, Stine, O. C, Wozniak, Marcella A, Stern, Barney J, Mitchell, Braxton D, Kittner, Steven J, Simard, J M
Published in Stroke (1970) (01.02.2014)
Published in Stroke (1970) (01.02.2014)
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Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects
Gallagher, Margaret L, Sturchio, Cynthia, Smith, Ashley, Koontz, Deborah, Jenkins, Mary M, Honein, Margaret A, Rasmussen, Sonja A
Published in Birth defects research. A Clinical and molecular teratology (01.07.2011)
Published in Birth defects research. A Clinical and molecular teratology (01.07.2011)
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Abstract WP210: Prothrombin G20210A Mutation and Ischemic Stroke Risk in European Ancestry: The Genetics of Early Onset Stroke Study and Meta-Analysis of 2304 Young-Onset Stroke Cases
Jiang, Baijia, Hamedani, Ali, Cheng, Yuching, Koontz, Deborah, Bean, Christopher J, Gallagher, Margaret, Hooper, W C, Sparks, Mary J, McArdle, Patrick, O’Connell, Jeffrey R, Stine, O C, Wozniak, Marcella A, Stern, Barney J, Mitchell, Braxton D, Kittner, Steven J, Cole, John W
Published in Stroke (1970) (01.02.2013)
Published in Stroke (1970) (01.02.2013)
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Rapid detection of the CYP2A612 hybrid allele by Pyrosequencing.sup.[R] .sup.technology
Koontz, Deborah A, Huckins, Jacqueline J, Spencer, Antonina, Gallagher, Margaret L
Published in BMC medical genetics (24.08.2009)
Published in BMC medical genetics (24.08.2009)
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Journal Article
Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank12
Yang, Quan-He, Botto, Lorenzo D, Gallagher, Margaret, Friedman, JM, Sanders, Christopher L, Koontz, Deborah, Nikolova, Stanimila, Erickson, J David, Steinberg, Karen
Published in The American journal of clinical nutrition (01.07.2008)
Published in The American journal of clinical nutrition (01.07.2008)
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Journal Article