Emily M. Coonrod, Ph.D. - Publications

Affiliations: 
2006 University of Utah, Salt Lake City, UT 
Area:
Cell Biology, Molecular Biology

15 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Buchbinder D, Baker R, Lee YN, Ravell J, Zhang Y, McElwee J, Nugent D, Coonrod EM, Durtschi JD, Augustine NH, Voelkerding KV, Csomos K, Rosen L, Browne S, Walter JE, et al. Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disorders. Journal of Clinical Immunology. 35: 119-24. PMID 25516070 DOI: 10.1007/S10875-014-0121-5  0.307
2015 Profaizer T, Coonrod EM, Delgado JC, Kumánovics A. Report on the effects of fragment size, indexing, and read length on HLA sequencing on the Illumina MiSeq Human Immunology. 76: 897-902. DOI: 10.1016/J.Humimm.2015.08.002  0.317
2014 Coonrod EM, Durtschi JD, VanSant Webb C, Voelkerding KV, Kumánovics A. Next-generation sequencing of custom amplicons to improve coverage of HaloPlex multigene panels. Biotechniques. 57: 204-7. PMID 25312090 DOI: 10.2144/000114217  0.363
2014 Swoboda KJ, Margraf RL, Carey JC, Zhou H, Newcomb TM, Coonrod E, Durtschi J, Mallempati K, Kumanovics A, Katz BE, Voelkerding KV, Opitz JM. A novel germline PIGA mutation in Ferro-Cerebro-Cutaneous syndrome: a neurodegenerative X-linked epileptic encephalopathy with systemic iron-overload. American Journal of Medical Genetics. Part A. 164: 17-28. PMID 24259288 DOI: 10.1002/Ajmg.A.36189  0.343
2014 Profaizer T, Coonrod EM, Delgado J, Kumanovics A. P096 Human Immunology. 75: 118. DOI: 10.1016/J.Humimm.2014.08.158  0.322
2013 Coonrod EM, Graham LA, Carpp LN, Carr TM, Stirrat L, Bowers K, Bryant NJ, Stevens TH. Homotypic vacuole fusion in yeast requires organelle acidification and not the V-ATPase membrane domain. Developmental Cell. 27: 462-8. PMID 24286827 DOI: 10.1016/J.Devcel.2013.10.014  0.311
2013 Durtschi J, Margraf RL, Coonrod EM, Mallempati KC, Voelkerding KV. VarBin, a novel method for classifying true and false positive variants in NGS data. Bmc Bioinformatics. 14: S2. PMID 24266885 DOI: 10.1186/1471-2105-14-S13-S2  0.303
2013 Chen K, Coonrod EM, Kumánovics A, Franks ZF, Durtschi JD, Margraf RL, Wu W, Heikal NM, Augustine NH, Ridge PG, Hill HR, Jorde LB, Weyrich AS, Zimmerman GA, Gundlapalli AV, et al. Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency. American Journal of Human Genetics. 93: 812-24. PMID 24140114 DOI: 10.1016/J.Ajhg.2013.09.009  0.321
2013 Coonrod EM, Margraf RL, Russell A, Voelkerding KV, Reese MG. Clinical analysis of genome next-generation sequencing data using the Omicia platform. Expert Review of Molecular Diagnostics. 13: 529-40. PMID 23895124 DOI: 10.1586/14737159.2013.811907  0.321
2013 Coonrod EM, Durtschi JD, Margraf RL, Voelkerding KV. Developing genome and exome sequencing for candidate gene identification in inherited disorders: an integrated technical and bioinformatics approach. Archives of Pathology & Laboratory Medicine. 137: 415-33. PMID 22770468 DOI: 10.5858/Arpa.2012-0107-Ra  0.346
2012 Coonrod EM, Margraf RL, Voelkerding KV. Translating exome sequencing from research to clinical diagnostics. Clinical Chemistry and Laboratory Medicine. 50: 1161-8. PMID 22850020 DOI: 10.1515/Cclm-2011-0841  0.371
2010 Coonrod EM, Stevens TH. The yeast vps class E mutants: the beginning of the molecular genetic analysis of multivesicular body biogenesis. Molecular Biology of the Cell. 21: 4057-60. PMID 21115849 DOI: 10.1091/Mbc.E09-07-0603  0.31
2008 Neubert C, Graham LA, Black-Maier EW, Coonrod EM, Liu TY, Stierhof YD, Seidel T, Stevens TH, Schumacher K. Arabidopsis has two functional orthologs of the yeast V-ATPase assembly factor Vma21p. Traffic (Copenhagen, Denmark). 9: 1618-28. PMID 18694437 DOI: 10.1111/J.1600-0854.2008.00799.X  0.347
2007 Coonrod EM, Karren MA, Shaw JM. Ugo1p is a multipass transmembrane protein with a single carrier domain required for mitochondrial fusion. Traffic (Copenhagen, Denmark). 8: 500-11. PMID 17451553 DOI: 10.1111/J.1600-0854.2007.00550.X  0.483
2005 Karren MA, Coonrod EM, Anderson TK, Shaw JM. The role of Fis1p-Mdv1p interactions in mitochondrial fission complex assembly. The Journal of Cell Biology. 171: 291-301. PMID 16247028 DOI: 10.1083/Jcb.200506158  0.472
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