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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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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: Aug 26, 2024
. (Total: 6271 publications)
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Year
Journal
Records 1-16 (of 16 Records)
Query Trace:
Rajeevan MS[original query]
Identification of Phosphoglycerate Kinase 1 (PGK1) as a reference gene for quantitative gene expression measurements in human blood RNA.
Falkenberg VR
,
Whistler T
,
Murray JR
,
Unger ER
,
Rajeevan MS
.
BMC Res Notes 2011 4 324
Evaluation of DNA extraction from granulocytes discarded in the separation medium after isolation of peripheral blood mononuclear cells and plasma from whole blood.
Murray JR
,
Rajeevan MS
.
BMC Res Notes 2013 6 440
Broad-spectrum detection of HPV in male genital samples using target-enriched whole-genome sequencing
Li T
,
Unger ER
,
Rajeevan MS
.
Viruses 2023 15 (9)
NanoString Technology for Human Papillomavirus Typing.
Rajeevan MS
,
Patel S
,
Li T
,
Unger ER
.
Viruses 2021 13 (2)
Bioinformatics Pipeline for Human Papillomavirus Short Read Genomic Sequences Classification Using Support Vector Machine.
Lomsadze A ,
Li T
,
Rajeevan MS
,
Unger ER
,
Borodovsky M .
Viruses 2020 12 (7)
Universal human papillomavirus typing by whole genome sequencing following target enrichment: evaluation of assay reproducibility and limit of detection.
Li T
,
Unger ER
,
Rajeevan MS
.
BMC Genomics 2019 20 (1) 231
Simultaneous extraction of mRNA and microRNA from whole blood stabilized in tempus tubes.
Richards J
,
Unger ER
,
Rajeevan MS
.
BMC Res Notes 2019 12 (1) 39
Association of chronic fatigue syndrome with premature telomere attrition.
Rajeevan MS
,
Murray J
,
Oakley L
,
Lin JS
,
Unger ER
.
J Transl Med 2018 16 (1) 44
Precision Medicine Requires Precision Laboratories.
Rajeevan MS
,
Li T
,
Unger ER
.
J Mol Diagn 2017 19 (2) 226-229
Pathway-Focused Genetic Evaluation of Immune and Inflammation Related Genes with Chronic Fatigue Syndrome.
Rajeevan MS
,
Dimulescu I
,
Murray J
,
Falkenberg VR
,
Unger ER
.
Hum Immunol 2015 76 (8) 553-60
Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome.
Bhattacharjee M ,
Rajeevan MS
,
Sillanpaa MJ .
Hum Genomics 2015 9 (1) 8
Human papillomavirus prevalence in invasive anal cancers in the United States before vaccine introduction
Steinau M
,
Unger ER
,
Hernandez BY , Goodman MT , Copeland G , Hopenhayn C , Cozen W , Saber MS , Huang Y , Peters ES , Lynch CF , Wilkinson EJ ,
Rajeevan MS
,
Lyu C ,
Saraiya M
.
J Low Genit Tract Dis 2013 17 (4) 397-403
Assuring the quality of next-generation sequencing in clinical laboratory practice.
Gargis AS
,
Kalman L
,
Berry MW , Bick DP , Dimmock DP , Hambuch T , Lu F , Lyon E , Voelkerding KV ,
Zehnbauer BA
,
Agarwala R , Bennett SF ,
Chen B
,
Chin EL , Compton JG , Das S , Farkas DH , Ferber MJ , Funke BH , Furtado MR ,
Ganova-Raeva LM
,
Geigenmuller U , Gunselman SJ , Hegde MR , Johnson PL , Kasarskis A , Kulkarni S , Lenk T , Liu CS , Manion M , Manolio TA , Mardis ER , Merker JD ,
Rajeevan MS
,
Reese MG , Rehm HL , Simen BB , Yeakley JM , Zook JM ,
Lubin IM
.
Nat Biotechnol 2012 30 (11) 1033-6
Convergent genomic studies identify association of GRIK2 and NPAS2 with chronic fatigue syndrome.
Smith AK
,
Fang H ,
Whistler T
,
Unger ER
,
Rajeevan MS
.
Neuropsychobiology 2011 64 (4) 183-94
Functional genomics of serotonin receptor 2A (HTR2A): interaction of polymorphism, methylation, expression and disease association.
Falkenberg VR
,
Gurbaxani BM
,
Unger ER
,
Rajeevan MS
.
Neuromolecular Med 2010 13 (1) 66-76
Identification of a potential molecular link between the glucocorticoid and serotonergic signaling systems
Falkenberg VR
,
Rajeevan MS
.
J Mol Neurosci 2010 41 (2) 322-7
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Page last reviewed:
Feb 1, 2024
Page last updated:
Aug 26, 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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