AB133. SmartLabs—a solution to healthcare

od Elackatt, Niby J., Rajasimha, Harsha K.
Izdano u Ann Transl Med (2015)

Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl(−/−) retinal transcriptomes

od Brooks, Matthew J., Rajasimha, Harsha K., Roger, Jerome E., Swaroop, Anand
Izdano 2011

Transcriptome analysis using next generation sequencing reveals molecular signatures of diabetic retinopathy and efficacy of candidate drugs

od Kandpal, Raj P., Rajasimha, Harsha K., Brooks, Matthew J., Nellissery, Jacob, Wan, Jun, Qian, Jiang, Kern, Timothy S., Swaroop, Anand
Izdano 2012

Developing rods transplanted into the degenerating retina of Crx-knockout mice exhibit neural activity similar to native photoreceptors

od Homma, Kohei, Okamoto, Satoshi, Mandai, Michiko, Gotoh, Norimoto, Rajasimha, Harsha K., Chang, Yi-Sheng, Chen, Shan, Li, Wei, Cogliati, Tiziana, Swaroop, Anand, Takahashi, Masayo
Izdano u Stem Cells (2013)

Differential gene expression and alternative splicing between diploid and tetraploid watermelon

od Saminathan, Thangasamy, Nimmakayala, Padma, Manohar, Sumanth, Malkaram, Sridhar, Almeida, Aldo, Cantrell, Robert, Tomason, Yan, Abburi, Lavanya, Rahman, Mohammad A., Vajja, Venkata G., Khachane, Amit, Kumar, Brajendra, Rajasimha, Harsha K., Levi, Amnon, Wehner, Todd, Reddy, Umesh K.
Izdano u J Exp Bot (2015)

Non-Random mtDNA Segregation Patterns Indicate a Metastable Heteroplasmic Segregation Unit in m.3243A>G Cybrid Cells

od Raap, Anton K., Jahangir Tafrechi, Roshan S., van de Rijke, Frans M., Pyle, Angela, Wählby, Carolina, Szuhai, Karoly, Ravelli, Raimond B. G., de Coo, René F. M., Rajasimha, Harsha K., Nilsson, Mats, Chinnery, Patrick F., Samuels, David C., Janssen, George M. C.
Izdano 2012

Recent Advances in Systems and Network Medicine: Meeting Report from the First International Conference in Systems and Network Medicine

od Kurnat-Thoma, Emma, Baranova, Ancha, Baird, Pat, Brodsky, Elia, Butte, Atul J., Cheema, Amrita K., Cheng, Feixiong, Dutta, Shuchismita, Grant, Christina, Giordano, James, Maitland-van der Zee, Anke H., Fridsma, Douglas B., Jarrin, Robert, Kann, Maricel G., Keeney, Jonathon, Loscalzo, Joseph, Madhavan, Guru, Maron, Bradley A., McBride, Dennis K., McKean, Maeve, Mun, Seong K., Palmer, James C., Patel, Bakul, Parakh, Kapil, Pariser, Anne R., Pristipino, Christian, Radstake, Timothy R.D.J., Rajasimha, Harsha K., Rouse, William B., Rozman, Damjana, Saleh, Alif, Schmidt, Harald H.H.W., Schultz, Nikolaus, Sethi, Tavpritesh, Silverman, Edwin K., Skopac, Jessica, Svab, Igor, Trujillo, Sylvia, Valentine, James E., Verma, Dinesh, West, Bruce J., Vasudevan, Sona
Izdano u Syst Med (New Rochelle) (2020)

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

od Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N., Branham, Kari E., Zipprer, David, Chakarova, Christina F., Sergeev, Yuri V., Campos, Maria M., Othman, Mohammad, Friedman, James S., Maminishkis, Arvydas, Waseem, Naushin H., Brooks, Matthew, Rajasimha, Harsha K., Edwards, Albert O., Lotery, Andrew, Klein, Barbara E., Truitt, Barbara J., Li, Bingshan, Schaumberg, Debra A., Morgan, Denise J., Morrison, Margaux A., Souied, Eric, Tsironi, Evangelia E., Grassmann, Felix, Fishman, Gerald A., Silvestri, Giuliana, Scholl, Hendrik P.N., Kim, Ivana K., Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E., Merriam, John C., Park, Kyu Hyung, Olson, Lana M., Farrer, Lindsay A., Johnson, Matthew P., Peachey, Neal S., Lathrop, Mark, Baron, Robert V., Igo, Robert P., Klein, Ronald, Hagstrom, Stephanie A., Kamatani, Yoichiro, Martin, Tammy M., Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J., Chan, Chi-Chao, Pericak-Vance, Margaret A., Jacobson, Samuel G., Gorin, Michael B., Klein, Michael L., Allikmets, Rando, Iyengar, Sudha K., Weber, Bernhard H., Haines, Jonathan L., Léveillard, Thierry, Deangelis, Margaret M., Stambolian, Dwight, Weeks, Daniel E., Bhattacharya, Shomi S., Chew, Emily Y., Heckenlively, John R., Abecasis, Gonçalo R., Swaroop, Anand
Izdano 2014