1. Comethyl: a network-based methylome approach to investigate the multivariate nature of health and disease. Issue 2 (17th January 2022) Authors: Mordaunt, Charles E; Mouat, Julia S; Schmidt, Rebecca J; LaSalle, Janine M Journal: Briefings in bioinformatics Issue: Volume 23:Issue 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders. (October 2015) Authors: LaSalle, Janine M; Reiter, Lawrence T; Chamberlain, Stormy J Journal: Epigenomics Issue: Volume 7:Number 7(2015) Page Start: 1213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. How has the study of the human placenta aided our understanding of partially methylated genes?. (December 2013) Authors: Schroeder, Diane I; LaSalle, Janine M Journal: Epigenomics Issue: Volume 5:Number 6(2013) Page Start: 645 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Imprinting effects of UBE3A loss on synaptic gene networks and Wnt signaling pathways. (18th October 2019) Authors: Lopez, S Jesse; Laufer, Benjamin I; Beitnere, Ulrika; Berg, Elizabeth L; Silverman, Jill L; O'Geen, Henriette; Segal, David J; LaSalle, Janine M Journal: Human molecular genetics Issue: Volume 28:Number 22(2019) Page Start: 3842 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in Down syndrome DNA methylation profiles. (1st October 2020) Authors: Laufer, Benjamin I; Hwang, Hyeyeon; Jianu, Julia M; Mordaunt, Charles E; Korf, Ian F; Hertz-Picciotto, Irva; LaSalle, Janine M Journal: Human molecular genetics Issue: Volume 29:Number 21(2020) Page Start: 3465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome. (21st August 2018) Authors: Vogel Ciernia, Annie; Yasui, Dag H; Pride, Michael C; Durbin-Johnson, Blythe; Noronha, Adriana B; Chang, Alene; Knotts, Trina A; Rutkowsky, Jennifer R; Ramsey, Jon J; Crawley, Jacqueline N; LaSalle, Janine M Journal: Human molecular genetics Issue: Volume 27:Number 23(2018:Dec. 01) Page Start: 4077 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study. (22nd April 2019) Authors: Zhu, Yihui; Mordaunt, Charles E; Yasui, Dag H; Marathe, Ria; Coulson, Rochelle L; Dunaway, Keith W; Jianu, Julia M; Walker, Cheryl K; Ozonoff, Sally; Hertz-Picciotto, Irva; Schmidt, Rebecca J; LaSalle, Janine M Journal: Human molecular genetics Issue: Volume 28:Number 16(2019) Page Start: 2659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prader–Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN. (14th August 2018) Authors: Coulson, Rochelle L; Powell, Weston T; Yasui, Dag H; Dileep, Gayathri; Resnick, James; LaSalle, Janine M Journal: Human molecular genetics Issue: Volume 27:Number 23(2018:Dec. 01) Page Start: 4051 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗