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Investigation of a Cluster of Sphingomonas koreensis Infections.
Johnson RC, Deming C, Conlan S, Zellmer CJ, Michelin AV, Lee-Lin S, Thomas PJ, Park M, Weingarten RA, Less J, Dekker JP, Frank KM, Musser KA, McQuiston JR, Henderson DK, Lau AF, Palmore TN, Segre JA. Johnson RC, et al. Among authors: lee lin s. N Engl J Med. 2018 Dec 27;379(26):2529-2539. doi: 10.1056/NEJMoa1803238. N Engl J Med. 2018. PMID: 30586509 Free PMC article.
Pericentromeric duplications in the laboratory mouse.
Thomas JW, Schueler MG, Summers TJ, Blakesley RW, McDowell JC, Thomas PJ, Idol JR, Maduro VV, Lee-Lin SQ, Touchman JW, Bouffard GG, Beckstrom-Sternberg SM; NISC Comparative Sequencing Program; Green ED. Thomas JW, et al. Genome Res. 2003 Jan;13(1):55-63. doi: 10.1101/gr.791403. Genome Res. 2003. PMID: 12529306 Free PMC article.
Expanded skin virome in DOCK8-deficient patients.
Tirosh O, Conlan S, Deming C, Lee-Lin SQ, Huang X; NISC Comparative Sequencing Program; Su HC, Freeman AF, Segre JA, Kong HH. Tirosh O, et al. Among authors: lee lin sq. Nat Med. 2018 Dec;24(12):1815-1821. doi: 10.1038/s41591-018-0211-7. Epub 2018 Nov 5. Nat Med. 2018. PMID: 30397357 Free PMC article.
Expanded microbiome niches of RAG-deficient patients.
Blaustein RA, Shen Z, Kashaf SS, Lee-Lin S, Conlan S; NISC Comparative Sequencing Program; Bosticardo M, Delmonte OM, Holmes CJ, Taylor ME, Banania G, Nagao K, Dimitrova D, Kanakry JA, Su H, Holland SM, Bergerson JRE, Freeman AF, Notarangelo LD, Kong HH, Segre JA. Blaustein RA, et al. Among authors: lee lin s. Cell Rep Med. 2023 Oct 17;4(10):101205. doi: 10.1016/j.xcrm.2023.101205. Epub 2023 Sep 26. Cell Rep Med. 2023. PMID: 37757827 Free PMC article.
Integrated genomic and functional analyses of human skin-associated Staphylococcus reveal extensive inter- and intra-species diversity.
Joglekar P, Conlan S, Lee-Lin SQ, Deming C, Kashaf SS; NISC Comparative Sequencing Program; Kong HH, Segre JA. Joglekar P, et al. Among authors: lee lin sq. Proc Natl Acad Sci U S A. 2023 Nov 21;120(47):e2310585120. doi: 10.1073/pnas.2310585120. Epub 2023 Nov 13. Proc Natl Acad Sci U S A. 2023. PMID: 37956283 Free PMC article.
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
Antonellis A, Ellsworth RE, Sambuughin N, Puls I, Abel A, Lee-Lin SQ, Jordanova A, Kremensky I, Christodoulou K, Middleton LT, Sivakumar K, Ionasescu V, Funalot B, Vance JM, Goldfarb LG, Fischbeck KH, Green ED. Antonellis A, et al. Am J Hum Genet. 2003 May;72(5):1293-9. doi: 10.1086/375039. Epub 2003 Apr 10. Am J Hum Genet. 2003. PMID: 12690580 Free PMC article.
23 results