Publications

2022

Miller C, Walker J, Jensen T, Hopper W, Fulton R, Painter J, Sekeres M, Ley T, Spencer D, Goll J, Walter M. Failure to detect mutations in U2AF1 due to changes in the GRCh38 reference sequence. J Mol Diagn. 2022 Mar;24(3):219-223. doi: 10.1016/j.jmoldx.2021.10.013. Epub 2022 Jan 15. PMID: 35041928.
https://www.jmdjournal.org/article/S1525-1578(22)00005-8/fulltext

2019

Sekeres MA, Gore SD, Stablein DM, DiFronzo N, Abel GA, DeZern AE, Troy JD, Rollison DE, Thomas JW, Waclawiw MA, Liu JJ, Al Baghdadi T, Walter MJ, Bejar R, Gorak EJ, Starczynowski DT, Foran JM, Cerhan JR, Moscinski LC, Komrokji RS, Deeg HJ, Epling-Burnette PK. The National MDS Natural History Study: design of an integrated data and sample biorepository to promote research studies in myelodysplastic syndromes. Leuk Lymphoma. 2019 Dec;60(13):3161-3171. doi: 10.1080/10428194.2019.1616186. Epub 2019 May 21. PMID: 31111762.
https://www.tandfonline.com/doi/full/10.1080/10428194.2019.1616186?scroll=top&needAccess=true

2018

Padron E, Ball MC, Teer JK, Painter JS, Yoder SJ, Zhang C, Zhang L, Moscinski LC, Rollison DE, Gore SD, Bejar R, Walter MJ, Sekeres MA, Komrokji RS, Epling-Burnette PK. Germ line tissues for optimal detection of somatic variants in myelodysplastic syndromes. Blood. 1028 May 24;131(21):2402-2405. doi:10.1182/blood-2018-01-827881 Epub 2018 Apr 16. PMID: 29661788 PMC5969383.
http://www.bloodjournal.org/content/131/21/2402.long?sso-checked=true