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SARS-CoV-2 receptor networks in diabetic and COVID-19-associated kidney disease.
Menon R, Otto EA, Sealfon R, Nair V, Wong AK, Theesfeld CL, Chen X, Wang Y, Boppana AS, Luo J, Yang Y, Kasson PM, Schaub JA, Berthier CC, Eddy S, Lienczewski CC, Godfrey B, Dagenais SL, Sohaney R, Hartman J, Fermin D, Subramanian L, Looker HC, Harder JL, Mariani LH, Hodgin JB, Sexton JZ, Wobus CE, Naik AS, Nelson RG, Troyanskaya OG, Kretzler M. Menon R, et al. Among authors: dagenais sl. Kidney Int. 2020 Dec;98(6):1502-1518. doi: 10.1016/j.kint.2020.09.015. Epub 2020 Oct 8. Kidney Int. 2020. PMID: 33038424 Free PMC article.
SARS-CoV-2 receptor networks in diabetic and COVID-19 associated kidney disease.
Menon R, Otto EA, Sealfon R, Nair V, Wong AK, Theesfeld CL, Chen X, Wang Y, Boppanna A, Luo J, Yang Y, Kasson PM, Schaub JA, Berthier CC, Eddy S, Lienczewski CC, Godfrey B, Dagenais SL, Sohaney R, Hartman J, Fermin D, Subramanian L, Looker HC, Harder JL, Mariani LH, Hodgin JB, Sexton JZ, Wobus CE, Naik AS, Nelson RG, Troyanskaya OG, Kretzler M. Menon R, et al. Among authors: dagenais sl. medRxiv [Preprint]. 2020 Aug 21:2020.05.09.20096511. doi: 10.1101/2020.05.09.20096511. medRxiv. 2020. PMID: 32511461 Free PMC article. Updated. Preprint.
Estimation of DNA contamination and its sources in genotyped samples.
Zajac GJM, Fritsche LG, Weinstock JS, Dagenais SL, Lyons RH, Brummett CM, Abecasis GR. Zajac GJM, et al. Among authors: dagenais sl. Genet Epidemiol. 2019 Dec;43(8):980-995. doi: 10.1002/gepi.22257. Epub 2019 Aug 26. Genet Epidemiol. 2019. PMID: 31452258 Free PMC article.
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2012 Apr;158A(4):839-49. doi: 10.1002/ajmg.a.35229. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407726 Free PMC article.
A novel VEGFR3 mutation causes Milroy disease.
Butler MG, Dagenais SL, Rockson SG, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2007 Jun 1;143A(11):1212-7. doi: 10.1002/ajmg.a.31703. Am J Med Genet A. 2007. PMID: 17458866 Free article.
Mutation of the FOXC2 gene in familial distichiasis.
Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW. Brooks BP, et al. Among authors: dagenais sl. J AAPOS. 2003 Oct;7(5):354-7. doi: 10.1016/s1091-8531(03)00144-7. J AAPOS. 2003. PMID: 14566319
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