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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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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: Apr 22, 2024
. (Total: 5878 publications)
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Year
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Records 1-25 (of 25 Records)
Query Trace:
Satten GA[original query]
Interaction of HLA-DRB1 * 1501 and TNF-Alpha in a Population-based Case-control Study of Multiple Sclerosis.
Williamson DM
,
Marrie RA , Ashley-Koch A ,
Satten GA
.
Immunol Infect Dis 2013 1 (1) 10-17
Heavy metals, organic solvents, and multiple sclerosis: An exploratory look at gene-environment interactions.
Napier MD , Poole C ,
Satten GA
,
Ashley-Koch A , Marrie RA ,
Williamson DM
.
Arch Environ Occup Health 2016 71 (1) 26-34
What Can We Learn about the Bias of Microbiome Studies from Analyzing Data from Mock Communities?
Li M ,
Tyx RE
,
Rivera AJ
,
Zhao N , Satten GA .
Genes (Basel) 2022 13 (10)
Associations between microbial communities and key chemical constituents in U.S. domestic moist snuff.
Tyxobert RE
,
Rivera AJ
,
Satten GA
,
Keong LM ,
Kuklenyik P
,
Lee GE ,
Lawler TS
,
Kimbrell JB
,
Stanfill SB
,
Valentin-Blasini L
,
Watson CH
.
PLoS One 2022 17 (5) e0267104
Constraining PERMANOVA and LDM to within-set comparisons by projection improves the efficiency of analyses of matched sets of microbiome data.
Zhu Z ,
Satten GA
,
Mitchell C , Hu YJ .
Microbiome 2021 9 (1) 133
A Bottom-up Approach to Testing Hypotheses That Have a Branching Tree Dependence Structure, with Error Rate Control.
Li Y , Hu YJ ,
Satten GA
.
J Am Stat Assoc 2020 117 (538) 664-677
Testing hypotheses about the microbiome using the linear decomposition model (LDM).
Hu YJ ,
Satten GA
.
Bioinformatics 2020 36 (14) 4106-4115
Stability of the vaginal, oral, and gut microbiota across pregnancy among African American women: the effect of socioeconomic status and antibiotic exposure.
Dunlop AL , Knight AK ,
Satten GA
,
Cutler AJ , Wright ML , Mitchell RM , Read TD , Mulle J , Hertzberg VS , Hill CC , Smith AK , Corwin EJ .
PeerJ 2019 7 e8004
Robust Inference of Population Structure from Next-Generation Sequencing Data with Systematic Differences in Sequencing.
Liao P ,
Satten GA
,
Hu YJ .
Bioinformatics 2017 34 (7) 1157-1163
PhredEM: a phred-score-informed genotype-calling approach for next-generation sequencing studies.
Liao P ,
Satten GA
,
Hu YJ .
Genet Epidemiol 2017 41 (5) 375-387
Restoring the Duality between Principal Components of a Distance Matrix and Linear Combinations of Predictors, with Application to Studies of the Microbiome.
Satten GA
,
Tyx RE
,
Rivera AJ
,
Stanfill S
.
PLoS One 2017 12 (1) e0168131
Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease.
Shaw KA , Bertha M , Hofmekler T , Chopra P , Vatanen T , Srivatsa A , Prince J , Kumar A , Sauer C , Zwick ME ,
Satten GA
,
Kostic AD , Mulle JG , Xavier RJ , Kugathasan S .
Genome Med 2016 8 (1) 75
Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls.
Hu YJ , Liao P , Johnston HR , Allen AS ,
Satten GA
.
PLoS Genet 2016 12 (5) e1006040
Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis.
Tyx RE
,
Stanfill SB
,
Keong LM
,
Rivera AJ
,
Satten GA
,
Watson CH
.
PLoS One 2016 11 (1) e0146939
A statistical approach for rare-variant association testing in affected sibships.
Epstein MP , Duncan R , Ware EB , Jhun MA , Bielak LF , Zhao W , Smith JA , Peyser PA , Kardia SL ,
Satten GA
.
Am J Hum Genet 2015 96 (4) 543-54
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees.
Bickeboller H , Bailey JN , Beyene J , Cantor RM , Cordell HJ , Culverhouse RC , Engelman CD , Fardo DW , Ghosh S , Konig IR , Lorenzo Bermejo J , Melton PE , Santorico SA ,
Satten GA
,
Sun L , Tintle NL , Ziegler A , MacCluer JW , Almasy L .
BMC Proc 2014 8 S1
Population-based association and gene by environment interactions in Genetic Analysis Workshop 18.
Satten GA
,
Biswas S , Papachristou C , Turkmen A , Konig IR .
Genet Epidemiol 2014 38 Suppl 1 S49-56
Utilizing population controls in rare-variant case-parent association tests.
Jiang Y ,
Satten GA
,
Han Y , Epstein MP , Heinzen EL , Goldstein DB , Allen AS .
Am J Hum Genet 2014 94 (6) 845-53
Robust regression analysis of copy number variation data based on a univariate score.
Satten GA
,
Allen AS , Ikeda M , Mulle JG , Warren ST .
PLoS One 2014 9 (2) e86272
A permutation procedure to correct for confounders in case-control studies, including tests of rare variation.
Epstein MP , Duncan R , Jiang Y , Conneely KN , Allen AS ,
Satten GA
.
Am J Hum Genet 2012 91 (2) 215-23
Age-associated DNA methylation in pediatric populations.
Alisch RS , Barwick BG , Chopra P , Myrick LK ,
Satten GA
,
Conneely KN , Warren ST .
Genome Res 2012 22 (4) 623-32
Control for confounding in case-control studies using the stratification score, a retrospective balancing score.
Allen AS ,
Satten GA
.
Am J Epidemiol 2011 173 (7) 752-60
Score-based adjustment for confounding by population stratification in genetic association studies
Allen A , Epstein MP ,
Satten GA
.
Genet Epidemiol 2010 34 (5) 383-5
SNPs in CAST are associated with Parkinson disease: a confirmation study
Allen AS ,
Satten GA
.
Am J Med Genet B Neuropsychiatr Genet 2010 153B (4) 973-9
A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity
Liu Y , Li YJ ,
Satten GA
,
Allen AS , Tzeng JY .
Ann Hum Genet 2009 73 520-6
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 22, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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