CDC-Authored Genomics and Precision Health Publications Database

---

Last data update: Sep 09, 2024. (Total: 6295 publications)

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

Filtered By: Select to fine-tune your search Year Journal

Records 1-6 (of 6 Records)

Query Trace: Mueller PW[original query]
Fragile X Syndrome: Scientific Background and Screening Technologies. Lyons JI , Kerr G , Mueller PW . J Mol Diagn 2015 17 (5) 463-71
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
Standard enrichment methods for targeted next-generation sequencing in high-repeat genomic regions. Mueller PW , Lyons J , Kerr G , Haase CP , Isett RB . Genet Med 2013 15 (11) 910-1
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
Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey. Chang MH , Yesupriya A , Ned RM , Mueller PW , Dowling NF . BMC Med Genet 2010 11 62
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