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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Dec 01, 2023. (Total: 4776 publications since 2011)
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Records 1-8 (of 8 Records)
Query Trace: Cordovado S[original query]
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 Miyono M, Foster Stephanie L, Cordovado Suzanne K. Journal of inborn errors of metabolism and screening 4 .
Journal of inborn errors of metabolism and screening 4
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.
Baker Mei W, Atkins Anne E, Cordovado Suzanne K, Hendrix Miyono, Earley Marie C, Farrell Philip M. Genet. Med. 2015 Feb 12. .
Genet. Med. 2015 Feb 12.
Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines.
Greene Christopher N, Cordovado Suzanne K, Turner Daniel P, Keong Lisa M, Shulman Dorothy, Mueller Patricia W. Molecular genetics and metabolism reports 2014 1312-323 .
Molecular genetics and metabolism reports 2014 1312-323
Developmental genetics of secretory vesicle acidification during Caenorhabditis elegans spermatogenesis.
Gleason Elizabeth J, Hartley Paul D, Henderson Melissa, Hill-Harfe Katherine L, Price Paul W, Weimer Robby M, Kroft Tim L, Zhu Guang-Dan, Cordovado Suzanne, L'Hernault Steven W. Genetics 2012 Jun 191(2) 477-91 .
Genetics 2012 Jun 191(2) 477-91
CFTR mutation analysis and haplotype associations in CF patients.
Cordovado S K, Hendrix M, Greene C N, Mochal S, Earley M C, Farrell P M, Kharrazi M, Hannon W H, Mueller P W. Mol. Genet. Metab. 2012 Feb 105(2) 249-54 .
Mol. Genet. Metab. 2012 Feb 105(2) 249-54
Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening.
Earley Marie C, Laxova Anita, Farrell Philip M, Driscoll-Dunn Rena, Cordovado Suzanne, Mogayzel Peter J, Konstan Michael W, Hannon W Harry. Clin. Chim. Acta 2011 Jul 15. 412(15-16) 1376-81 .
Clin. Chim. Acta 2011 Jul 15. 412(15-16) 1376-81
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