Greenberg DA - Search Results

1

Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry.

Subaran RL, Conte JM, Stewart WC, Greenberg DA. Subaran RL, et al. Among authors: greenberg da. Epilepsia. 2015 Feb;56(2):188-94. doi: 10.1111/epi.12864. Epub 2014 Dec 8. Epilepsia. 2015. PMID: 25489633 Free PMC article.

2

Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies.

Greenberg DA, Subaran R. Greenberg DA, et al. Epilepsia. 2011 Jan;52(1):1-9. doi: 10.1111/j.1528-1167.2010.02734.x. Epilepsia. 2011. PMID: 21219301 Free PMC article. Review.

3

How should we be searching for genes for common epilepsy? A critique and a prescription.

Greenberg DA, Stewart WC. Greenberg DA, et al. Epilepsia. 2012 Sep;53 Suppl 4(0 4):72-80. doi: 10.1111/j.1528-1167.2012.03616.x. Epilepsia. 2012. PMID: 22946724 Free PMC article. Review.

4

DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians.

Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. Pathak S, et al. Among authors: greenberg da. Epilepsia. 2018 May;59(5):1011-1019. doi: 10.1111/epi.14058. Epub 2018 Apr 2. Epilepsia. 2018. PMID: 29608786 Free PMC article.

5

Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy.

Wang M, Greenberg DA, Stewart WCL. Wang M, et al. Among authors: greenberg da. Epilepsia. 2019 Mar;60(3):539-546. doi: 10.1111/epi.14654. Epub 2019 Feb 4. Epilepsia. 2019. PMID: 30719716

6

In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy.

Wang M, Greenberg DA, Stewart WCL. Wang M, et al. Among authors: greenberg da. Epilepsia. 2019 Sep;60(9):2001-2002. doi: 10.1111/epi.16303. Epub 2019 Jul 29. Epilepsia. 2019. PMID: 31353459 No abstract available.

7

Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data.

Stewart WC, Huang Y, Greenberg DA, Vieland VJ. Stewart WC, et al. Among authors: greenberg da. BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S111. doi: 10.1186/1753-6561-8-S1-S111. eCollection 2014. BMC Proc. 2014. PMID: 25519364 Free PMC article.

8

Brd2 haploinsufficiency extends lifespan and healthspan in C57B6/J mice.

Pathak S, Stewart WCL, Burd CE, Hester ME, Greenberg DA. Pathak S, et al. Among authors: greenberg da. PLoS One. 2020 Jun 19;15(6):e0234910. doi: 10.1371/journal.pone.0234910. eCollection 2020. PLoS One. 2020. PMID: 32559200 Free PMC article.

9

Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension.

Rodriguez-Murillo L, Subaran R, Stewart WC, Pramanik S, Marathe S, Barst RJ, Chung WK, Greenberg DA. Rodriguez-Murillo L, et al. Among authors: greenberg da. J Heart Lung Transplant. 2010 Feb;29(2):174-80. doi: 10.1016/j.healun.2009.08.022. Epub 2009 Oct 28. J Heart Lung Transplant. 2010. PMID: 19864167 Free PMC article.

10

Finding disease genes: a fast and flexible approach for analyzing high-throughput data.

Stewart WC, Drill EN, Greenberg DA. Stewart WC, et al. Among authors: greenberg da. Eur J Hum Genet. 2011 Oct;19(10):1090-4. doi: 10.1038/ejhg.2011.81. Epub 2011 May 25. Eur J Hum Genet. 2011. PMID: 21610749 Free PMC article.

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