Torthaí cuardaigh - Mehta, Arpit

Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-asso... de réir Pastori, Chiara, Peschansky, Veronica J., Barbouth, Deborah, Mehta, Arpit, Silva, Jose P., Wahlestedt, Claes

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Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice de réir Yu, Hong, Mehta, Arpit, Wang, Gaofeng, Hauswirth, William W., Chiodo, Vince, Boye, Sanford L., Guy, John

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Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease de réir Nuytemans, Karen, Bademci, Guney, Inchausti, Vanessa, Dressen, Amy, Kinnamon, Daniel D., Mehta, Arpit, Wang, Liyong, Züchner, Stephan, Beecham, Gary W., Martin, Eden R., Scott, William K., Vance, Jeffery M.

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Regulation of AKT signaling by Id1 controls t(8;21) leukemia initiation and progression de réir Wang, Lan, Man, Na, Sun, Xiao-Jian, Tan, Yurong, Cao, Marta Garcia, Liu, Fan, Hatlen, Megan, Xu, Haiming, Huang, Gang, Mattlin, Meredith, Mehta, Arpit, Rampersaud, Evadnie, Benezra, Robert, Nimer, Stephen D.

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Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform de réir Hedges, Dale J., Guettouche, Toumy, Yang, Shan, Bademci, Guney, Diaz, Ashley, Andersen, Ashley, Hulme, William F., Linker, Sara, Mehta, Arpit, Edwards, Yvonne J. K., Beecham, Gary W., Martin, Eden R., Pericak-Vance, Margaret A., Zuchner, Stephan, Vance, Jeffery M., Gilbert, John R.

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Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease de réir Young, Juan I., Sivasankaran, Sathesh K., Wang, Lily, Ali, Aleena, Mehta, Arpit, Davis, David A., Dykxhoorn, Derek M., Petito, Carol K., Beecham, Gary W., Martin, Eden R., Mash, Deborah C., Pericak-Vance, Margaret, Scott, William K., Montine, Thomas J., Vance, Jeffery M.

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