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Page 1
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM. Nuytemans K, et al. Among authors: dressen a. Neurology. 2013 Mar 12;80(11):982-9. doi: 10.1212/WNL.0b013e31828727d4. Epub 2013 Feb 13. Neurology. 2013. PMID: 23408866 Free PMC article.
Genomic signatures of a global fitness index in a multi-ethnic cohort of women.
Rampersaud E, Nathanson L, Farmer J, Meshbane K, Belton RL, Dressen A, Cuccaro M, Musto A, Daunert S, Deo S, Hudson N, Vance JM, Seo D, Mendez A, Dykxhoorn DM, Pericak-Vance MA, Goldschmidt-Clermont PJ. Rampersaud E, et al. Among authors: dressen a. Ann Hum Genet. 2013 Mar;77(2):147-57. doi: 10.1111/ahg.12006. Epub 2013 Jan 7. Ann Hum Genet. 2013. PMID: 23289938
Functional analysis of protective IL1RL1 variants associated with asthma risk.
Ramirez-Carrozzi V, Dressen A, Lupardus P, Yaspan B, Pappu R. Ramirez-Carrozzi V, et al. Among authors: dressen a. J Allergy Clin Immunol. 2015 Apr;135(4):1080-1083.e3. doi: 10.1016/j.jaci.2014.10.028. Epub 2014 Dec 4. J Allergy Clin Immunol. 2015. PMID: 25483601 No abstract available.
23 results