1. Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network. Issue 2 (1st June 2016) Authors: Bush, WS; Crosslin, DR; Owusu‐Obeng, A; Wallace, J; Almoguera, B; Basford, MA; Bielinski, SJ; Carrell, DS; Connolly, JJ; Crawford, D; Doheny, KF; Gallego, CJ; Gordon, AS; Keating, B; Kirby, J; Kitchner, T; Manzi, S; Mejia, AR; Pan, V; Perry, CL Journal: Clinical pharmacology & therapeutics Issue: Volume 100:Issue 2(2016:Aug.) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup. Issue 2 (9th November 2015) Authors: Overby, CL; Heale, B; Aronson, S; Cherry, JM; Dwight, S; Milosavljevic, A; Nelson, T; Niehaus, A; Weaver, MA; Ramos, EM; Williams, MS Journal: Clinical pharmacology & therapeutics Issue: Volume 99:Issue 2(2016:Feb.) Page Start: 157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗