|
Pathak, Shilpa; Miller, James; Morris, Emily C et al. (2018) DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia 59:1011-1019
|
|
Subaran, Ryan L; Conte, Juliette M; Stewart, William C L et al. (2015) Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. Epilepsia 56:188-94
|
|
Lipner, Ettie M; Tomer, Yaron; Noble, Janelle A et al. (2015) Linkage Analysis of Genomic Regions Contributing to the Expression of Type 1 Diabetes Microvascular Complications and Interaction with HLA. J Diabetes Res 2015:694107
|
|
Corso, Barbara; Greenberg, David A (2014) Using linkage analysis to detect gene-gene interaction by stratifying family data on known disease, or disease-associated, alleles. PLoS One 9:e93398
|
|
Chachua, T; Goletiani, C; Maglakelidze, G et al. (2014) Sex-specific behavioral traits in the Brd2 mouse model of juvenile myoclonic epilepsy. Genes Brain Behav 13:702-12
|
|
Tomer, Yaron; Hasham, Alia; Davies, Terry F et al. (2013) Fine mapping of loci linked to autoimmune thyroid disease identifies novel susceptibility genes. J Clin Endocrinol Metab 98:E144-52
|
|
Lipner, E M; Tomer, Y; Noble, J A et al. (2013) HLA class I and II alleles are associated with microvascular complications of type 1 diabetes. Hum Immunol 74:538-44
|
|
Greenberg, David A; Stewart, William C L (2012) How should we be searching for genes for common epilepsy? A critique and a prescription. Epilepsia 53 Suppl 4:72-80
|
|
Strug, Lisa J; Addis, Laura; Chiang, Theodore et al. (2012) The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy. PLoS One 7:e40696
|
|
Stefan, Mihaela; Jacobson, Eric M; Huber, Amanda K et al. (2011) Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon alpha-modulated mechanism. J Biol Chem 286:31168-79
|
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