Alisch RS - Search Results

1

Szulwach KE, Jin P, Alisch RS. Szulwach KE, et al. Among authors: alisch rs. Clin Genet. 2009 Mar;75(3):209-19. doi: 10.1111/j.1399-0004.2008.01134.x. Epub 2009 Jan 20. Clin Genet. 2009. PMID: 19159391 Free PMC article. Review.

2

Early-life disruption of epigenetic marks may contribute to the origins of mental illness.

Lee ER, Alisch RS. Lee ER, et al. Among authors: alisch rs. Epigenomics. 2012 Aug;4(4):355-7. doi: 10.2217/epi.12.35. Epigenomics. 2012. PMID: 22920174 No abstract available.

3

Whole genome methylation sequencing in blood from persons with mild cognitive impairment and dementia due to Alzheimer's disease identifies cognitive status.

Madrid A, Papale LA, Bergmann PE, Breen C, Clark LR, Asthana S, Johnson SC, Keleş S, Hogan KJ, Alisch RS. Madrid A, et al. Among authors: alisch rs. bioRxiv [Preprint]. 2024 Sep 27:2024.09.26.615196. doi: 10.1101/2024.09.26.615196. bioRxiv. 2024. Update in: Alzheimers Dement. 2025 Jan 1. doi: 10.1002/alz.14474 PMID: 39386499 Free PMC article. Updated. Preprint.

4

RNA and microRNAs in fragile X mental retardation.

Jin P, Alisch RS, Warren ST. Jin P, et al. Among authors: alisch rs. Nat Cell Biol. 2004 Nov;6(11):1048-53. doi: 10.1038/ncb1104-1048. Nat Cell Biol. 2004. PMID: 15516998 Review.

5

Argonaute2 is essential for mammalian gastrulation and proper mesoderm formation.

Alisch RS, Jin P, Epstein M, Caspary T, Warren ST. Alisch RS, et al. PLoS Genet. 2007 Dec 28;3(12):e227. doi: 10.1371/journal.pgen.0030227. PLoS Genet. 2007. PMID: 18166081 Free PMC article.

6

Genome-wide alterations in hippocampal 5-hydroxymethylcytosine links plasticity genes to acute stress.

Li S, Papale LA, Zhang Q, Madrid A, Chen L, Chopra P, Keleş S, Jin P, Alisch RS. Li S, et al. Among authors: alisch rs. Neurobiol Dis. 2016 Feb;86:99-108. doi: 10.1016/j.nbd.2015.11.010. Epub 2015 Nov 18. Neurobiol Dis. 2016. PMID: 26598390 Free PMC article.

7

Sex-specific hippocampal 5-hydroxymethylcytosine is disrupted in response to acute stress.

Papale LA, Li S, Madrid A, Zhang Q, Chen L, Chopra P, Jin P, Keleş S, Alisch RS. Papale LA, et al. Among authors: alisch rs. Neurobiol Dis. 2016 Dec;96:54-66. doi: 10.1016/j.nbd.2016.08.014. Epub 2016 Aug 26. Neurobiol Dis. 2016. PMID: 27576189 Free PMC article.

8

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus.

Alisch RS, Wang T, Chopra P, Visootsak J, Conneely KN, Warren ST. Alisch RS, et al. BMC Med Genet. 2013 Jan 29;14:18. doi: 10.1186/1471-2350-14-18. BMC Med Genet. 2013. PMID: 23356558 Free PMC article.

9

ATLAS: a system to selectively identify human-specific L1 insertions.

Badge RM, Alisch RS, Moran JV. Badge RM, et al. Among authors: alisch rs. Am J Hum Genet. 2003 Apr;72(4):823-38. doi: 10.1086/373939. Epub 2003 Mar 11. Am J Hum Genet. 2003. PMID: 12632328 Free PMC article.

10

Age-associated DNA methylation in pediatric populations.

Alisch RS, Barwick BG, Chopra P, Myrick LK, Satten GA, Conneely KN, Warren ST. Alisch RS, et al. Genome Res. 2012 Apr;22(4):623-32. doi: 10.1101/gr.125187.111. Epub 2012 Feb 1. Genome Res. 2012. PMID: 22300631 Free PMC article.

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