@article{petersen_lyerly_mckendry_islam_brown-guedira_cowger_dong_murphy_2017, title={Validation of Fusarium Head Blight Resistance QTL in US Winter Wheat}, volume={57}, ISSN={["1435-0653"]}, DOI={10.2135/cropsci2015.07.0415}, abstractNote={Fusarium head blight (FHB), primarily caused by Fusarium graminearum Schwabe [telemorph: Gibberella zeae Schw. (Petch)], can significantly reduce the grain quality of wheat (Triticum aestivum L.) due to mycotoxin contamination. Two US soft red winter wheat cultivars, Bess and NC-Neuse, have moderate resistance to FHB. The objective of this study was to validate genomic regions associated with FHB resistance identified in previous studies involving NC-Neuse and the cultivar Truman, a full-sib of Bess. A total of 98 doubled haploid lines derived from the cross Bess × NC-Neuse were evaluated in inoculated, mist-irrigated field nurseries. The lines were evaluated for FHB incidence, severity, Fusarium-damaged kernels, and deoxynivalenol content in seven environments between 2011 and 2014. A 3338-cM linkage map was developed based on 4014 simple sequence repeat and single nucleotide polymorphism markers. Twelve quantitative trait loci (QTL) associated with FHB resistance were identified. NC-Neuse alleles provided resistance at QTL on five chromosomes and Bess alleles provided resistance at QTL on five other chromosomes. Alignment of linkage maps revealed that five of these QTL were overlapping with previously identified regions. Quantitative trait loci on chromosomes 1A, 4A, and 6A identified in this study overlapped with QTL regions identified in NC-Neuse, and QTL identified on chromosomes 2B and 3B overlapped with QTL regions identified in Truman. A preliminary test using Kompetitive Allele-Specific polymerase chain reaction assays on recent Uniform Southern Winter Wheat Scab Nursery entries showed that the assays developed for Qfhb.nc-2B.1 may be good candidates for use in marker-assisted selection.}, number={1}, journal={CROP SCIENCE}, author={Petersen, Stine and Lyerly, Jeanette H. and McKendry, Anne L. and Islam, M. Sariful and Brown-Guedira, Gina and Cowger, Christina and Dong, Yanhong and Murphy, J. Paul}, year={2017}, pages={1–12} }
 @article{petersen_lyerly_maloney_brown-guedira_cowger_costa_dong_murphy_2016, title={Mapping of Fusarium Head Blight Resistance Quantitative Trait Loci in Winter Wheat Cultivar NC-Neuse}, volume={56}, ISSN={["1435-0653"]}, DOI={10.2135/cropsci2015.05.0312}, abstractNote={Fusarium head blight (FHB), primarily caused by Fusarium graminearum , can significantly reduce the grain quality of wheat ( Triticum aestivum L.) due to mycotoxin contamination. The objective of this study was to identify quantitative trait loci (QTL) for FHB resistance in the moderately resistant soft red winter wheat cultivar NC‐Neuse. A total of 170 recombinant inbred lines (RILs) from a cross between NC‐Neuse and the susceptible cultivar AGS 2000 were evaluated in inoculated, mist‐irrigated field nurseries. The lines were evaluated for FHB incidence (INC), severity (SEV), Fusarium ‐damaged kernels (FDK), and deoxynivalenol (DON) content in seven environments between 2011 and 2014. A 3,419 cM linkage map was developed based on 1839 simple sequence repeat (SSR), diversity array technology (DArT), and single nucleotide polymorphism (SNP) markers. Seven FHB resistance QTL on chromosomes 1A, 1B, 1D, 2A, 4A, 5B, and 6A were mapped. The QTL alleles conferring resistance on 1A, 1B, 2A, 4A, and 6A originated from NC‐Neuse, while the alleles associated with resistance on 1D and 5B originated from AGS 2000. Quantitative trait loci effects ranged from 9 to 12% for INC, from 6 to 11% for SEV, from 8 to 20% for FDK, and from 6 to 18% for DON. The QTL on 5B co‐localized with the Vrn‐B1 locus. Kompetitive Allele‐Specific PCR (KASP) assays were developed for each NC‐Neuse QTL region. A preliminary test using these assays on recent Uniform Southern Winter Wheat Nursery (USWWN) entries indicated Qfhb.nc‐1A, Qfhb.nc‐1B, and Qfhb.nc‐6A as likely the best candidates for use in marker‐assisted selection.}, number={4}, journal={CROP SCIENCE}, author={Petersen, Stine and Lyerly, Jeanette H. and Maloney, Peter V. and Brown-Guedira, Gina and Cowger, Christina and Costa, Jose M. and Dong, Yanhong and Murphy, J. Paul}, year={2016}, pages={1473–1483} }
 @article{petersen_lyerly_worthington_parks_cowger_marshall_brown-guedira_murphy_2015, title={Mapping of powdery mildew resistance gene Pm53 introgressed from Aegilops speltoides into soft red winter wheat}, volume={128}, ISSN={["1432-2242"]}, DOI={10.1007/s00122-014-2430-8}, abstractNote={A powdery mildew resistance gene was introgressed from Aegilops speltoides into winter wheat and mapped to chromosome 5BL. Closely linked markers will permit marker-assisted selection for the resistance gene. Powdery mildew of wheat (Triticum aestivum L.) is a major fungal disease in many areas of the world, caused by Blumeria graminis f. sp. tritici (Bgt). Host plant resistance is the preferred form of disease prevention because it is both economical and environmentally sound. Identification of new resistance sources and closely linked markers enable breeders to utilize these new sources in marker-assisted selection as well as in gene pyramiding. Aegilops speltoides (2n = 2x = 14, genome SS), has been a valuable disease resistance donor. The powdery mildew resistant wheat germplasm line NC09BGTS16 (NC-S16) was developed by backcrossing an Ae. speltoides accession, TAU829, to the susceptible soft red winter wheat cultivar 'Saluda'. NC-S16 was crossed to the susceptible cultivar 'Coker 68-15' to develop F2:3 families for gene mapping. Greenhouse and field evaluations of these F2:3 families indicated that a single gene, designated Pm53, conferred resistance to powdery mildew. Bulked segregant analysis showed that multiple simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers specific to chromosome 5BL segregated with the resistance gene. The gene was flanked by markers Xgwm499, Xwmc759, IWA6024 (0.7 cM proximal) and IWA2454 (1.8 cM distal). Pm36, derived from a different wild wheat relative (T. turgidum var. dicoccoides), had previously been mapped to chromosome 5BL in a durum wheat line. Detached leaf tests revealed that NC-S16 and a genotype carrying Pm36 differed in their responses to each of three Bgt isolates. Pm53 therefore appears to be a new source of powdery mildew resistance.}, number={2}, journal={THEORETICAL AND APPLIED GENETICS}, author={Petersen, Stine and Lyerly, Jeanette H. and Worthington, Margaret L. and Parks, Wesley R. and Cowger, Christina and Marshall, David S. and Brown-Guedira, Gina and Murphy, J. Paul}, year={2015}, month={Feb}, pages={303–312} }
 @inproceedings{petersen_j.h. lyerly_r.a. navarro_g. brown-guedira_c.a. griffey_murphy_2014, title={Fusarium Head Blight resistance QTL in the NC-Neuse / AGS2000 recombinant inbred population}, booktitle={National Fusarium Head Blight Forum}, author={Petersen, S. and J.H. Lyerly, P.V. Maloney and R.A. Navarro, C. Cowger and G. Brown-Guedira, J.M. Costa and C.A. Griffey and Murphy, J. P.}, year={2014} }
 @article{worthington_lyerly_petersen_brown-guedira_marshall_cowger_parks_murphy_2014, title={MlUM15: an Aegilops neglecta-derived powdery mildew resistance gene in common wheat}, volume={54}, number={4}, journal={Crop Science}, author={Worthington, M. and Lyerly, J. and Petersen, S. and Brown-Guedira, G. and Marshall, D. and Cowger, C. and Parks, R. and Murphy, J. P.}, year={2014}, pages={1397–1406} }
 @inproceedings{petersen_j.h. lyerly_r. navarro_g. brown-guedira_murphy_2014, title={Validation of Fusarium head blight resistance QTL using the NC-Neuse / Bess doubled haploid population}, booktitle={National Fusarium Head Blight Forum}, author={Petersen, S. and J.H. Lyerly, A.L. McKendry and R. Navarro, C. Cowger and G. Brown-Guedira, S. Islam and Murphy, J. P.}, year={2014} }
 @inproceedings{petersen_worthington_lyerly_parks_cowger_brown-guedira_marshall_murphy_2013, title={Mapping powdery mildew resistance introgressed from Triticum speltoides}, booktitle={Small Grain Workers Conference}, author={Petersen, S. and Worthington, M. and Lyerly, J. and Parks, R. and Cowger, C. and Brown-Guedira, G. L. and Marshall, D. and Murphy, J. P.}, year={2013} }
 @inproceedings{petersen_maloney_lyerly_navarro_cowger_brown-guedira_costa_murphy_2013, title={QTL Associated with Fusarium Head Blight Resistance in the NC-NEUSE X AGS 2000 Recombinant Inbred Population}, booktitle={Proceedings of the 2013 National Fusarium Head Blight Forum}, author={Petersen, S. and Maloney, P. V. and Lyerly, J. H. and Navarro, R. A. and Cowger, C. and Brown-Guedira, G. and Costa, J. M. and Murphy, J. P.}, year={2013} }
 @article{maloney_lyerly_wooten_anderson_livingston_brown-guedira_marshall_murphy_2011, title={Marker Development and Quantitative Trait Loci in a Fall-Sown Oat Recombinant Inbred Population}, volume={51}, ISSN={["1435-0653"]}, DOI={10.2135/cropsci2010.04.0224}, abstractNote={Marker-assisted selection for improved winter survival in oat (Avena sativa L.) is difficult because the number of simple sequence repeat (SSR) markers available in this species is limited. The objectives of this research were to increase the number of SSR markers on the 'Fulghum' x 'Norline' recombinant inbred population genetic map and to scan for quantitative trait loci (QTL) associated with winter field survival, crown freezing tolerance, vernalization response, and heading date. New SSR markers were developed from 'Kanota' and 'Ogle' genomic DNA libraries enriched for eight microsatellite motifs. New primers were evaluated for amplification, reproducibility, and polymorphism in 11 oat lines. Simple sequence repeat markers showing high-quality polymorphism between Fulghum and Norline were subsequently examined in 128 recombinant inbred lines. Sixty-five new SSR, four single nucleotide polymorphism (SNP), and one cleaved amplified polymorphic sequence (CAPS) markers were added to the Fulghum x Norline linkage map. This brought the total number of markers mapped on the population to 101. Phenotypic data for winter hardiness component traits in the population were obtained in previous field and controlled chamber experiments. All previously mapped markers and new SSR markers were evaluated and QTL identified. Marker loci on linkage group FN1_3_38 accounted for multiple QTL associated with winter hardiness component traits. The addition of new SSR markers to the Fulghum x Norline map in regions with winter hardiness component trait QTL will enhance marker assisted selection for these important traits.}, number={2}, journal={CROP SCIENCE}, author={Maloney, P. V. and Lyerly, J. H. and Wooten, D. R. and Anderson, J. M. and Livingston, D. P., III and Brown-Guedira, G. and Marshall, D. and Murphy, J. P.}, year={2011}, month={Mar}, pages={490–502} }
 @article{miranda_bland_cambron_lyerly_johnson_buntin_murphy_2010, title={Genetic Mapping of an Aegilops tauschii-derived Hessian Fly Resistance Gene in Common Wheat}, volume={50}, ISSN={["0011-183X"]}, DOI={10.2135/cropsci2009.05.0278}, abstractNote={Hessian fly [Mayetiola destructor (Say)] is a major threat to wheat (Triticum aestivum L.) production in the eastern United States. Cultivar releases containing major Hessian fly resistance genes have proven effective in minimizing losses caused by this pest. Nevertheless, the ephemeral nature of major gene resistance necessitates the identification of novel sources of resistance. Hessian fly resistance from Aegilops tauschii Coss. (2n = 2x = 14; genome DD) was introgressed into the genetic background of the soft red winter wheat cultivar Saluda during the development of the germplasm line NC09MDD14. Our genetic characterization and linkage mapping studies showed that resistance to Hessian Fly biotype L in NC09MDD14 was monogenic and the most likely order of the linked microsatellite markers was: Xcfd13- 4.2 cM-Xcfd42-1.8 cM-Xgdm141-4.9 cM-Xgdm36-1.5 cM- NC09MDD14 Hf gene/Xcfd132- 13.4 cM-Xcfd19. This linkage map situated the NCD-09MDD14 Hf gene on the short arm of chromosome 6D, within the same deletion bin as the named gene H13. No recombinants between H13 and the NCD09MDD14 Hf gene were found in an allelism study that included 170 F 2 individuals from the cross between NCD09MDD14 and Molly (H13). The Hessian fly resistance gene present in the germplasm line NC09MDD14 could be an allele of H13, but unlike H13, the gene in NC09MDD14 provides resistance against biotype vrH13.}, number={2}, journal={CROP SCIENCE}, author={Miranda, L. M. and Bland, D. E. and Cambron, S. E. and Lyerly, J. H. and Johnson, J. and Buntin, G. D. and Murphy, J. P.}, year={2010}, pages={612–616} }
 @article{maxwell_lyerly_srnic_parks_cowger_marshall_brown-guedira_murphy_2010, title={MlAB10: A triticum turgidum subsp dicoccoides derived powdery mildew resistance gene identified in common wheat}, volume={50}, number={6}, journal={Crop Science}, author={Maxwell, J. J. and Lyerly, J. H. and Srnic, G. and Parks, R. and Cowger, C. and Marshall, D. and Brown-Guedira, G. and Murphy, J. P.}, year={2010}, pages={2261–2267} }
 @inproceedings{advances in breeding for winter hardiness in oats_2009, booktitle={Proceedings of the Annual Meeting, American Society of Agronomy}, year={2009} }
 @article{maxwell_lyerly_cowger_marshall_brown-guedira_murphy_2009, title={MlAG12: a Triticum timopheevii-derived powdery mildew resistance gene in common wheat on chromosome 7AL}, volume={119}, ISSN={["1432-2242"]}, DOI={10.1007/s00122-009-1150-y}, abstractNote={Wheat powdery mildew is an economically important disease in cool and humid environments. Powdery mildew causes yield losses as high as 48% through a reduction in tiller survival, kernels per head, and kernel size. Race-specific host resistance is the most consistent, environmentally friendly and, economical method of control. The wheat (Triticum aestivum L.) germplasm line NC06BGTAG12 possesses genetic resistance to powdery mildew introgressed from the AAGG tetraploid genome Triticum timopheevii subsp. armeniacum. Phenotypic evaluation of F(3) families derived from the cross NC06BGTAG12/'Jagger' and phenotypic evaluation of an F(2) population from the cross NC06BGTAG12/'Saluda' indicated that resistance to the 'Yuma' isolate of powdery mildew was controlled by a single dominant gene in NC06BGTAG12. Bulk segregant analysis (BSA) revealed simple sequence repeat (SSR) markers specific for chromosome 7AL segregating with the resistance gene. The SSR markers Xwmc273 and Xwmc346 mapped 8.3 cM distal and 6.6 cM proximal, respectively, in NC06BGTAG12/Jagger. The multiallelic Pm1 locus maps to this region of chromosome 7AL. No susceptible phenotypes were observed in an evaluation of 967 F(2) individuals in the cross NC06BGTAG12/'Axminster' (Pm1a) which indicated that the NC06BGTAG12 resistance gene was allelic or in close linkage with the Pm1 locus. A detached leaf test with ten differential powdery mildew isolates indicated the resistance in NC06BGTAG12 was different from all designated alleles at the Pm1 locus. Further linkage and allelism tests with five other temporarily designated genes in this very complex region will be required before giving a permanent designation to this gene. At this time the gene is given the temporary gene designation MlAG12.}, number={8}, journal={THEORETICAL AND APPLIED GENETICS}, author={Maxwell, Judd J. and Lyerly, Jeanette H. and Cowger, Christina and Marshall, David and Brown-Guedira, Gina and Murphy, J. Paul}, year={2009}, month={Nov}, pages={1489–1495} }
 @inproceedings{murphy_maxwell_miranda_lyerly_parks_srnic_perugini_cowger_marshall_van esbroeck_et al._2009, title={Qualitative powdery mildew mapping update}, booktitle={Eastern Wheat Workers/Southern Small Grain Workers NCERA184 Conference}, publisher={Baltimore, Md.: Eastern Wheat Workers/Southern Small Grain Workers}, author={Murphy, J. P. and Maxwell, J. J. and Miranda, L. M. and Lyerly, J. H. and Parks, W. R. and Srnic, G. and Perugini, L. and Cowger, C. and Marshall, D. and Van Esbroeck, G. and et al.}, year={2009}, pages={28–30} }
 @article{wooten_livingston_lyerly_holland_jellen_marshall_murphy_2009, title={Quantitative Trait Loci and Epistasis for Oat Winter-Hardiness Component Traits}, volume={49}, ISSN={["1435-0653"]}, url={http://www.scopus.com/inward/record.url?eid=2-s2.0-70749094348&partnerID=MN8TOARS}, DOI={10.2135/cropsci2008.10.0612}, abstractNote={Winter hardiness is a complex trait and poor winter hardiness limits commercial production of winter oat (Avena spp.). The objective of this study was to identify quantitative trait loci (QTL) for fi ve winter-hardiness component traits in a recombinant inbred line population derived from a cross between the winter-tender cultivar Fulghum and the winter-hardy cultivar Norline. Crown freezing tolerance, vernalization response, and photoperiod response were evaluated in controlled environment studies. Heading date and plant height were evaluated over two seasons in Kinston, NC, and winter fi eld survival was evaluated in fi ve environments over two seasons in the mountains of North Carolina and Virginia. A partial genetic linkage map of regions believed to affect winter hardiness was developed using restriction fragment length polymorphism and simple sequence repeat markers. Most QTL were located on linkage groups FN3, FN22, and FN24. Quantitative trait loci were identifi ed for all traits except photoperiod response, and epistatic interactions were identifi ed for winter fi eld survival, crown freezing tolerance, vernalization response, and plant height. Major QTL for winter fi eld survival (R 2 = 35%) and crown freezing tolerance (R 2 = 53%) were identifi ed on linkage group FN3, which was associated with an intergenomic reciprocal translocation between chromosomes 7C and 17.}, number={6}, journal={CROP SCIENCE}, author={Wooten, D. R. and Livingston, D. P., III and Lyerly, H. J. and Holland, J. B. and Jellen, E. N. and Marshall, D. S. and Murphy, J. P.}, year={2009}, pages={1989–1998} }
 @inproceedings{additional markers added to the fulghum/norline genetic map and qtl scan for winter hardiness traits in avena sativa_2008, booktitle={Proceedings, 8th International Oat Conference, Minneapolis, Minn.}, year={2008} }
 @inproceedings{miranda_maxwell_perugini_srnic_shi_lyerly_navarro_cowger_marshall_brown-guedira_et al._2007, title={Genetics and mapping of powdery mildew resistance in North Carolina wheat germplasms}, booktitle={Proceedings of the Annual Meeting, American Society of Agronomy}, author={Miranda, L. and Maxwell, J. and Perugini, L. and Srnic, G. and Shi, A. and Lyerly, J. and Navarro, R. and Cowger, C. and Marshall, D. and Brown-Guedira, G. and et al.}, year={2007} }
 @inproceedings{maxwell_cowger_marshall_kolmer_brown-guedira_lyerly_murphy_2007, title={Powdery mildew and leaf rust resistance in winter wheat germplasm lines}, booktitle={ASA-CSSA-SSSA International Annual Meetings, New Orleans, LA}, author={Maxwell, J. and Cowger, C. and Marshall, D. and Kolmer, J. and Brown-Guedira, G. and Lyerly, J. and Murphy, P.}, year={2007} }
 @inproceedings{murphy_navarro_lyerly_2006, title={2005-06 uniform Southern fusarium head blight screening nursery}, booktitle={Proceedings of the 2006 National Fusarium Head Blight Forum, 2006 Dec. 10-12, Research Triangle Park, NC}, author={Murphy, J. P. and Navarro, R. A. and Lyerly, J. H.}, year={2006}, pages={114} }
 @article{parks_moyer_lyerly_2006, title={Identification of fluorescent AFLP and SSR markers for differentiation and analysis of New Guinea impatiens}, volume={131}, number={5}, journal={Journal of the American Society for Horticultural Science}, author={Parks, E. J. and Moyer, J. W. and Lyerly, J. H.}, year={2006}, pages={622–631} }
 @inproceedings{wooten_livingston_lyerly_murphy_2006, title={Quantitative trait loci for winter hardiness component traits in oat}, booktitle={2006 American Oat Workers Conference, Program book}, publisher={Fargo, ND: American Oat Workers Conference}, author={Wooten, D. R. and Livingston, D. P. and Lyerly, J. H. and Murphy, J. P.}, year={2006}, pages={63} }
 @inproceedings{wooten_livingston_lyerly_murphy_2006, title={Quantitative trait loci for winter hardiness in oat}, booktitle={ASA-CSSA-SSSA International Annual Meetings, November 12-16, 2006, Indianapolis, IN}, author={Wooten, D. R. and Livingston, D. P. and Lyerly, J. H. and Murphy, J. P.}, year={2006} }
 @article{srnic_murphy_lyerly_leath_marshall_2005, title={Inheritance and chromosomal assignment of powdery mildew resistance genes in two winter wheat germplasm lines}, volume={45}, ISSN={["1435-0653"]}, DOI={10.2135/cropsci2004.0530}, abstractNote={Powdery mildew of wheat (Triticum aestivum L.), caused by Blumeria graminis DC f. sp. tritici Em. Marchal, occurs annually in eastern North America resulting in reduced grain yield and end‐use quality in susceptible cultivars. The objectives of this study were to determine the inheritance, chromosomal location, and linkage with molecular markers of powdery mildew resistance genes in the two recently released germplasm lines NC96BGTA4 and NC99BGTAG11. Between 99 and 194 F2:3 progenies plus parents in two populations, ‘Saluda’ × NC96BGTA4 and Saluda × NC99BGTAG11, were evaluated in greenhouse and field nurseries for reaction to powdery mildew infection. Results indicated that the germplasm lines each contained a different, partially dominant, major resistance gene. The two segregating populations were subjected to amplified fragment length polymorphism (AFLP) and simple sequence repeat, or microsatellite (SSR) analyses. Both resistance genes were located on the long arm of chromosome 7A. The most likely locus order indicated that the resistance gene in NC96BGTA4 was flanked by the SSR loci Xbarc292 and Xwmc525 The resistance gene in NC99BGTAG11 was most likely flanked by the AFLP markers XE38M54‐196 and XE36M55‐126, and the SSR loci Xgwm332 and Xwmc525 Both genes mapped to a chromosome arm that contains the powdery mildew resistance loci Pm1 and Pm9 The resistance genes in the two germplasms are different from the Pm1a allele. Our mapping results suggested that the resistance genes were not alleles at the Pm1 or Pm9 loci, but further allelism tests are necessary to determine the relationships both between the two genes themselves and between the two genes and named Pm loci on chromosome 7AL.}, number={4}, journal={CROP SCIENCE}, author={Srnic, G and Murphy, JP and Lyerly, JH and Leath, S and Marshall, DS}, year={2005}, pages={1578–1586} }
 @article{garcia_stalker_schroeder_lyerly_kochert_2005, title={RAPD-based linkage map of peanut based on a backcross population between the two diploid species Arachis stenosperma and A. Cardenasii}, volume={32}, DOI={10.3146/0095-3679(2005)32[1:arlmop]2.0.co;2}, abstractNote={Abstract A molecular linkage map based on an interspecific diploid backcross population [Arachis stenosperma × (A. stenosperma × A. cardenasii)] was constructed utilizing RAPD and RFLP markers. One hundred sixty-seven RAPD loci and 39 RFLPs were mapped to 11 linkage groups, covering a total genetic length of 800 cM. Clusters of 2 to18 markers were observed in most linkage groups. Twenty seven percent of the markers showed segregation distortion and mapped to four regions. Thirty-nine RFLP markers shared with a previously published linkage map, based on an A. stenosperma × A. cardenasii F2 population, and six RAPD markers were used to establish correspondence between maps and to compare recombination frequencies between common markers. A generalized reduction in the recombination fraction was observed in the backcross map compared to the F2 map. All common markers mapped to the same linkage groups and mostly in the same order in both maps.}, number={1}, journal={Peanut Science}, author={Garcia, G. M. and Stalker, H. T. and Schroeder, E. and Lyerly, J. H. and Kochert, G.}, year={2005}, pages={1–8} }
 @inproceedings{murphy_navarro_lyerly_2005, title={The 2004-05 uniform Southern fusarium head blight screening nursery}, booktitle={Proceedings of the 2005 National Fusarium Head Blight Forum, 2005 Dec. 11-13, Milwaukee, WI}, publisher={East Lansing: Michigan State University}, author={Murphy, J. P. and Navarro, R. A. and Lyerly, J. H.}, year={2005}, pages={73} }
 @article{lyerly_new_abad_moyer_2003, title={Identification of sweetpotato viruses using an RT- PCR based method}, volume={93}, journal={Phytopathology}, author={Lyerly, J. H. and New, S. L. and Abad, J. A. and Moyer, J. W.}, year={2003}, pages={S55} }
 @article{lyerly_stalker_moyer_hoffman_2002, title={Evaluation of Arachis species for resistance to tomato spotted wilt virus}, volume={29}, DOI={10.3146/pnut.29.2.0001}, abstractNote={Abstract}, journal={Peanut Science}, author={Lyerly, J. H. and Stalker, H. T. and Moyer, J. W. and Hoffman, K.}, year={2002}, pages={79–84} }