Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Nov 04, 2024. (Total: 6390 publications)
   dataset
Filtered By:
Records 1-17 (of 17 Records)
Query Trace: Gallagher M[original query]
Folate-related gene variants in Irish families affected by neural tube defects.
Fisk Green R , Byrne J , Crider KS , Gallagher M , Koontz D , Berry RJ .
Front Genet 2013 4 223
Author Correction: Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants
Welch NL , Zhu M , Hua C , Weller J , Mirhashemi ME , Nguyen TG , Mantena S , Bauer MR , Shaw BM , Ackerman CM , Thakku SG , Tse MW , Kehe J , Uwera MM , Eversley JS , Bielwaski DA , McGrath G , Braidt J , Johnson J , Cerrato F , Moreno GK , Krasilnikova LA , Petros BA , Gionet GL , King E , Huard RC , Jalbert SK , Cleary ML , Fitzgerald NA , Gabriel SB , Gallagher GR , Smole SC , Madoff LC , Brown CM , Keller MW , Wilson MM , Kirby MK , Barnes JR , Park DJ , Siddle KJ , Happi CT , Hung DT , Springer M , MacInnis BL , Lemieux JE , Rosenberg E , Branda JA , Blainey PC , Sabeti PC , Myhrvold C .
Nat Med 2023
Multiple lineages of monkeypox virus detected in the United States, 2021-2022.
Gigante CM , Korber B , Seabolt MH , Wilkins K , Davidson W , Rao AK , Zhao H , Smith TG , Hughes CM , Minhaj F , Waltenburg MA , Theiler J , Smole S , Gallagher GR , Blythe D , Myers R , Schulte J , Stringer J , Lee P , Mendoza RM , Griffin-Thomas LA , Crain J , Murray J , Atkinson A , Gonzalez AH , Nash J , Batra D , Damon I , McQuiston J , Hutson CL , McCollum AM , Li Y .
Science 2022 378 (6619) eadd4153 type
Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants.
Welch NL , Zhu M , Hua C , Weller J , Mirhashemi ME , Nguyen TG , Mantena S , Bauer MR , Shaw BM , Ackerman CM , Thakku SG , Tse MW , Kehe J , Uwera MM , Eversley JS , Bielwaski DA , McGrath G , Braidt J , Johnson J , Cerrato F , Moreno GK , Krasilnikova LA , Petros BA , Gionet GL , King E , Huard RC , Jalbert SK , Cleary ML , Fitzgerald NA , Gabriel SB , Gallagher GR , Smole SC , Madoff LC , Brown CM , Keller MW , Wilson MM , Kirby MK , Barnes JR , Park DJ , Siddle KJ , Happi CT , Hung DT , Springer M , MacInnis BL , Lemieux JE , Rosenberg E , Branda JA , Blainey PC , Sabeti PC , Myhrvold C .
Nat Med 2022 28 (5) 1083-1094
Evaluation of DNA extraction methods for the detection of Cytomegalovirus in dried blood spots.
Koontz D , Baecher K , Amin M , Nikolova S , Gallagher M , Dollard S .
J Clin Virol 2015 66 95-9
A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples.
Koontz D , Baecher K , Kobrynski L , Nikolova S , Gallagher M .
J Mol Diagn 2014 16 (5) 533-540
Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Jenkins MM , Reefhuis J , Gallagher ML , Mulle JG , Hoffmann TJ , Koontz DA , Sturchio C , Rasmussen SA , Witte JS , Richter P , Honein MA .
Am J Med Genet A 2014 164A (6) 1454-63
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Jiang B , Ryan KA , Hamedani A , Cheng Y , Sparks MJ , Koontz D , Bean CJ , Gallagher M , Hooper WC , McArdle PF , O'Connell JR , Stine OC , Wozniak MA , Stern BJ , Mitchell BD , Kittner SJ , Cole JW .
Stroke 2014 45 (4) 961-7
Qualitative assessment of study materials and communication strategies used in studies that include DNA collection.
Jenkins MM , Reed-Gross E , Barfield WD , Prue CE , Gallagher ML , Rasmussen SA , Honein MA .
Am J Med Genet A 2011 155A (11) 2721-31
Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects.
Gallagher ML , Sturchio C , Smith A , Koontz D , Jenkins MM , Honein MA , Rasmussen SA .
Birth Defects Res A Clin Mol Teratol 2011 91 (7) 642-8
Maternal attitudes toward DNA collection for gene-environment studies: a qualitative research study
Jenkins MM , Reed-Gross E , Rasmussen SA , Barfield WD , Prue CE , Gallagher ML , Honein MA .
Am J Med Genet A 2009 149A (11) 2378-86
Rapid detection of the CYP2A6*12 hybrid allele by Pyrosequencing technology
Koontz DA , Huckins JJ , Spencer A , Gallagher ML .
BMC Med Genet 2009 10 80
Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
Chang Man-Huei, Lindegren Mary Lou, Butler Mary A, Chanock Stephen J, Dowling Nicole F, Gallagher Margaret, Moonesinghe Ramal, Moore Cynthia A, Ned Renée M, Reichler Mary R, Sanders Christopher L, Welch Robert, Yesupriya Ajay, Khoury Muin J, . American journal of epidemiology 2008 169(1) 54-66 .
American journal of epidemiology 2008 169(1) 54-66 type
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 J M, Sanders Christopher L, Koontz Deborah, Nikolova Stanimila, Erickson J David, Steinberg Karen. The American journal of clinical nutrition 2008 88(1) 232-46 .
The American journal of clinical nutrition 2008 88(1) 232-46 type
HFE genotype and transferrin saturation in the United States.
Cogswell Mary E, Gallagher Margaret L, Steinberg Karen K, Caudill PhD Samuel P, Looker Anne C, Bowman Barbara A, Gunter Elaine W, Franks Adele L, Satten Glen A, Khoury Muin J, Grummer-Strawn Laurence M. Genetics in medicine : official journal of the American College of Medical Genetics 2003 5(4) 304-10 .
Genetics in medicine : official journal of the American College of Medical Genetics 2003 5(4) 304-10 type
DNA banking for epidemiologic studies: a review of current practices.
Steinberg Karen, Beck Jeanne, Nickerson Deborah, Garcia-Closas Montserrat, Gallagher Margaret, Caggana Michele, Reid Yvonne, Cosentino Mark, Ji Jay, Johnson Delene, Hayes Richard B, Earley Marie, Lorey Fred, Hannon Harry, Khoury Muin J, Sampson Eric. Epidemiology (Cambridge, Mass.) 2002 13(3) 246-54 .
Epidemiology (Cambridge, Mass.) 2002 13(3) 246-54 type
Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States.
Steinberg K K, Cogswell M E, Chang J C, Caudill S P, McQuillan G M, Bowman B A, Grummer-Strawn L M, Sampson E J, Khoury M J, Gallagher M L. JAMA 2001 285(17) 2216-22 .
JAMA 2001 285(17) 2216-22 type
TOP