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Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease.
Zee RY, Hoh J, Cheng S, Reynolds R, Grow MA, Silbergleit A, Walker K, Steiner L, Zangenberg G, Fernandez-Ortiz A, Macaya C, Pintor E, Fernandez-Cruz A, Ott J, Lindpainter K. Zee RY, et al. Among authors: reynolds r. Pharmacogenomics J. 2002;2(3):197-201. doi: 10.1038/sj.tpj.6500101. Pharmacogenomics J. 2002. PMID: 12082592 Clinical Trial.
Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy.
Hoffjan S, Ostrovnaja I, Nicolae D, Newman DL, Nicolae R, Gangnon R, Steiner L, Walker K, Reynolds R, Greene D, Mirel D, Gern JE, Lemanske RF Jr, Ober C. Hoffjan S, et al. Among authors: reynolds r. J Allergy Clin Immunol. 2004 Mar;113(3):511-8. doi: 10.1016/j.jaci.2003.10.044. J Allergy Clin Immunol. 2004. PMID: 15007355
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.
Barcellos LF, Begovich AB, Reynolds RL, Caillier SJ, Brassat D, Schmidt S, Grams SE, Walker K, Steiner LL, Cree BA, Stillman A, Lincoln RR, Pericak-Vance MA, Haines JL, Erlich HA, Hauser SL, Oksenberg JR. Barcellos LF, et al. Among authors: reynolds rl. Ann Neurol. 2004 Jun;55(6):793-800. doi: 10.1002/ana.20092. Ann Neurol. 2004. PMID: 15174013
Testosterone Effects on Short-Term Physical, Hormonal, and Neurodevelopmental Outcomes in Infants with 47,XXY/Klinefelter Syndrome: The TESTO Randomized Controlled Trial.
Davis S, Howell S, Janusz J, Lahlou N, Reynolds R, Thompson T, Swenson K, Wilson R, Ross J, Zeitler P, Tartaglia N. Davis S, et al. Among authors: reynolds r. medRxiv [Preprint]. 2024 Dec 10:2024.12.09.24318726. doi: 10.1101/2024.12.09.24318726. medRxiv. 2024. PMID: 39711709 Free PMC article. Preprint.
2,437 results