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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2004 1
2005 2
2006 2
2009 2
2010 2
2011 2
2012 2
2013 2
2014 1
2015 1
2016 2
2017 2
2018 3
2019 2
2020 3
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27 results
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Page 1
Transplant Virus Detection Using Multiplex Targeted Sequencing.
Tan SK, Shen P, Lefterova MI, Sahoo MK, Fung E, Odegaard JI, Davis RW, Pinsky BA, Scharfe C. Tan SK, et al. Among authors: Scharfe C. J Appl Lab Med. 2018 Mar;2(5):757-769. doi: 10.1373/jalm.2017.024521. J Appl Lab Med. 2018. PMID: 31245786 Free PMC article.
Acylcarnitine Profiles Reflect Metabolic Vulnerability for Necrotizing Enterocolitis in Newborns Born Premature.
Sylvester KG, Kastenberg ZJ, Moss RL, Enns GM, Cowan TM, Shaw GM, Stevenson DK, Sinclair TJ, Scharfe C, Ryckman KK, Jelliffe-Pawlowski LL. Sylvester KG, et al. Among authors: Scharfe C. J Pediatr. 2017 Feb;181:80-85.e1. doi: 10.1016/j.jpeds.2016.10.019. Epub 2016 Nov 8. J Pediatr. 2017. PMID: 27836286 Free PMC article.
Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis.
Lefterova MI, Shen P, Odegaard JI, Fung E, Chiang T, Peng G, Davis RW, Wang W, Kharrazi M, Schrijver I, Scharfe C. Lefterova MI, et al. Among authors: Scharfe C. J Mol Diagn. 2016 Mar;18(2):267-82. doi: 10.1016/j.jmoldx.2015.11.005. Epub 2016 Feb 1. J Mol Diagn. 2016. PMID: 26847993 Free PMC article.
Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemia.
Peng G, Shen P, Gandotra N, Le A, Fung E, Jelliffe-Pawlowski L, Davis RW, Enns GM, Zhao H, Cowan TM, Scharfe C. Peng G, et al. Among authors: Scharfe C. Version 2. Genet Med. 2019 Apr;21(4):896-903. doi: 10.1038/s41436-018-0272-5. Epub 2018 Sep 13. Genet Med. 2019. PMID: 30209273 Free PMC article.
A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases.
Wilson KD, Shen P, Fung E, Karakikes I, Zhang A, InanlooRahatloo K, Odegaard J, Sallam K, Davis RW, Lui GK, Ashley EA, Scharfe C, Wu JC. Wilson KD, et al. Among authors: Scharfe C. Circ Res. 2015 Sep 11;117(7):603-11. doi: 10.1161/CIRCRESAHA.115.306723. Epub 2015 Aug 11. Circ Res. 2015. PMID: 26265630 Free PMC article.
Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project.
Karaa A, Rahman S, Lomb├Ęs A, Yu-Wai-Man P, Sheikh MK, Alai-Hansen S, Cohen BH, Dimmock D, Emrick L, Falk MJ, McCormack S, Mirsky D, Moore T, Parikh S, Shoffner J, Taivassalo T, Tarnopolsky M, Tein I, Odenkirchen JC, Goldstein A; Mito Working Group Member Participants:. Karaa A, et al. J Inherit Metab Dis. 2017 May;40(3):403-414. doi: 10.1007/s10545-017-0035-5. Epub 2017 Mar 16. J Inherit Metab Dis. 2017. PMID: 28303425
Multiplex target capture with double-stranded DNA probes.
Shen P, Wang W, Chi AK, Fan Y, Davis RW, Scharfe C. Shen P, et al. Among authors: Scharfe C. Genome Med. 2013 May 29;5(5):50. doi: 10.1186/gm454. eCollection 2013. Genome Med. 2013. PMID: 23718862 Free PMC article.
Rare variant detection using family-based sequencing analysis.
Peng G, Fan Y, Palculict TB, Shen P, Ruteshouser EC, Chi AK, Davis RW, Huff V, Scharfe C, Wang W. Peng G, et al. Among authors: Scharfe C. Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3985-90. doi: 10.1073/pnas.1222158110. Epub 2013 Feb 20. Proc Natl Acad Sci U S A. 2013. PMID: 23426633 Free PMC article.
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