CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Jan 21, 2025. (Total: 6495 publications)

All Cancer Diabetes Economic Equity Environmental FHH HLBS ID Implementation ND PGx PI Rare RCH dataset

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Records 1-11 (of 11 Records)

Query Trace: Cordovado S[original query]
Can incorporating molecular testing improve the accuracy of newborn screening for congenital adrenal hyperplasia? Sarafoglou K , Gaviglio A , Wolf C , Lorentz CP , Lteif A , Kyllo J , Radloff G , Detwiler Z , Cuthbert CD , Hodges JS , Grosse SD , Greene CN , Cordovado S . J Clin Endocrinol Metab 2024
Assessing the Performance of Dried-Blood-Spot DNA Extraction Methods in Next Generation Sequencing. Hendrix MM , Cuthbert CD , Cordovado SK . Int J Neonatal Screen 2020 6 (2) 1-15
Evaluation of rapid and sensitive DNA extraction methods for detection of cytomegalovirus in dried blood spots. Koontz D , Dollard S , Cordovado S . J Virol Methods 2019 265 117-120
Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis. Hendrix MM , Foster SL , Cordovado SK . J Inborn Errors Metab Screen 2016 4
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study. Baker MW , Atkins AE , Cordovado SK , Hendrix M , Earley MC , Farrell PM . Genet Med 2015 18 (3) 231-8
Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines. Greene CN , Cordovado SK , Turner DP , Keong LM , Shulman D , Mueller PW . Mol Genet Metab Rep 2014 1 312-323
Developmental genetics of secretory vesicle acidification during Caenorhabditis elegans spermatogenesis. Gleason EJ , Hartley PD , Henderson M , Hill-Harfe KL , Price PW , Weimer RM , Kroft TL , Zhu GD , Cordovado S , L'Hernault S W . Genetics 2012 191 (2) 477-91
CFTR mutation analysis and haplotype associations in CF patients. Cordovado SK , Hendrix M , Greene CN , Mochal S , Earley MC , Farrell PM , Kharrazi M , Hannon WH , Mueller PW . Mol Genet Metab 2012 105 (2) 249-54
Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening. Earley MC , Laxova A , Farrell PM , Driscoll-Dunn R , Cordovado S , Mogayzel PJ Jr , Konstan MW , Hannon WH . Clin Chim Acta 2011 412 1376-81
Proficiency testing of human leukocyte antigen-DR and human leukocyte antigen-DQ genetic risk assessment for type 1 diabetes using dried blood spots Dantonio P , Meredith-Molloy N , Hagopian WA , She JX , Akolkar B , Cordovado SK , Hendrix M , Henderson LO , Hannon WH , Vogt RF . J Diabetes Sci Technol 2010 4 (4) 929-941
Novel human leukocyte antigen class I and class II alleles identified by sequence-based typing in the Genetics of Kidneys in Diabetes (GoKinD) study population Cordovado SK , Hancock LN , Hendrix M , Greene CN , Mueller PW . Hum Immunol 2009 70 (9) 747-9