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Sequencing rare and common APOL1 coding variants to determine kidney disease risk.
Limou S, Nelson GW, Lecordier L, An P, O'hUigin CS, David VA, Binns-Roemer EA, Guiblet WM, Oleksyk TK, Pays E, Kopp JB, Winkler CA. Limou S, et al. Among authors: david va. Kidney Int. 2015 Oct;88(4):754-63. doi: 10.1038/ki.2015.151. Epub 2015 May 20. Kidney Int. 2015. PMID: 25993319 Free PMC article.
Mutation in CEP290 discovered for cat model of human retinal degeneration.
Menotti-Raymond M, David VA, Schäffer AA, Stephens R, Wells D, Kumar-Singh R, O'Brien SJ, Narfström K. Menotti-Raymond M, et al. Among authors: david va. J Hered. 2007 May-Jun;98(3):211-20. doi: 10.1093/jhered/esm019. Epub 2007 May 16. J Hered. 2007. PMID: 17507457
A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus).
Kuehn MH, Lipsett KA, Menotti-Raymond M, Whitmore SS, Scheetz TE, David VA, O'Brien SJ, Zhao Z, Jens JK, Snella EM, Ellinwood NM, McLellan GJ. Kuehn MH, et al. Among authors: david va. PLoS One. 2016 May 5;11(5):e0154412. doi: 10.1371/journal.pone.0154412. eCollection 2016. PLoS One. 2016. PMID: 27149523 Free PMC article.
67 results