Year |
Citation |
Score |
2020 |
Scott SA, Scott ER, Seki Y, Chen AJ, Wallsten R, Owusu Obeng A, Botton MR, Cody N, Shi H, Zhao G, Brake P, Nicoletti P, Yang Y, Delio M, Shi L, et al. Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection. Clinical and Translational Science. PMID 32931151 DOI: 10.1111/Cts.12844 |
0.351 |
|
2018 |
Scott ER, Birch A, Mclellan A, Housman L, Gross SJ, Edelmann L. Whole Genome Sequencing Coverage & Quality at Prenatal Carrier Screening Loci: An Analysis of 15,496 gnomAD Genomes [23K] Obstetrics & Gynecology. 131. DOI: 10.1097/01.Aog.0000533525.00973.75 |
0.308 |
|
2017 |
Credle JJ, Itoh CY, Yuan T, Sharma R, Scott ER, Workman RE, Fan Y, Housseau F, Llosa NJ, Bell WR, Miller H, Zhang SX, Timp W, Larman HB. Multiplexed analysis of fixed tissue RNA using Ligation in situ Hybridization. Nucleic Acids Research. 45: e128. PMID 28854731 DOI: 10.1093/Nar/Gkx471 |
0.601 |
|
2017 |
Yang Y, Botton MR, Scott ER, Scott SA. Sequencing the CYP2D6 gene: from variant allele discovery to clinical pharmacogenetic testing. Pharmacogenomics. PMID 28470112 DOI: 10.2217/Pgs-2017-0033 |
0.342 |
|
2015 |
Bloss CS, Zeeland AA, Topol SE, Darst BF, Boeldt DL, Erikson GA, Bethel KJ, Bjork RL, Friedman JR, Hwynn N, Patay BA, Pockros PJ, Scott ER, Simon RA, Williams GW, et al. A genome sequencing program for novel undiagnosed diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25790160 DOI: 10.1038/Gim.2015.21 |
0.316 |
|
2014 |
Larman HB, Scott ER, Wogan M, Oliveira G, Torkamani A, Schultz PG. Sensitive, multiplex and direct quantification of RNA sequences using a modified RASL assay. Nucleic Acids Research. 42: 9146-57. PMID 25063296 DOI: 10.1093/Nar/Gku636 |
0.551 |
|
Show low-probability matches. |