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Brain : a Journal of Neurology|May 13, 2005
Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?Gianpiero L Cavalleri, John M Lynch, Chantal Depondt, et al.Plos Genetics|September 3, 2015
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage SensitivitySlavé Petrovski, Ayal B Gussow, Quanli Wang, et al.American Journal of Human Genetics|May 15, 2010
Inferring genetic ancestry: opportunities, challenges, and implicationsCharmaine D Royal, John Novembre, Stephanie M Fullerton, et al.American Journal of Human Genetics|February 22, 2023
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK BiobankAbhishek Nag, Ryan S Dhindsa, Lawrence Middleton, et al.Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.Genome Research|June 16, 2004
Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance geneNicole Soranzo, Gianpiero L Cavalleri, Michael E Weale, et al.Nature Reviews. Genetics|April 10, 2008
Genome-wide association studies for complex traits: consensus, uncertainty and challengesMark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, et al.Journal of Medical Genetics|May 15, 2012
Clinical application of exome sequencing in undiagnosed genetic conditionsAnna C Need, Vandana Shashi, Yuki Hitomi, et al.Epilepsy Research|June 30, 2006
Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPsPeter Kinirons, Gianpiero L Cavalleri, Amre Shahwan, et al.Human Mutation|December 16, 2011
HGV2011: personalized genomic medicine meets the incidentalomeMelissa A Wilson Sayres, Anthony J Brookes, Stephen J Chanock, et al.Pageof 34