Surgically targeted radiation therapy (STaRT) for recurrent glioblastoma: Initial outcomes from a prospective multicenter registry von Ozair, Ahmad, Brachman, David, Campbell, Lisa, Chen, Clark C, Patel, Toral R., Floyd, John, Hayden, Devon H, Nowlan, Adam W, Wasilewski, Andrea C, Wanebo, John, Shah, Mitesh, Richardson, Angela, Hanft, Simon, Choutka, Ondrej, Shen, Colette, Wardak, Zabi, Lee, Stuart, Ranjan, Tulika, Khosla, Atulya Aman, Ahluwalia, Manmeet Singh

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Racial and ethnic disparities in genomic testing among lung cancer patients: a systematic review von Meernik, Clare, Raveendran, Yadurshini, Kolarova, Michaela, Rahman, Fariha, Olunuga, Ebunoluwa, Hammond, Emmery, Shivaramakrishnan, Akhilesh, Hendren, Steph, Bosworth, Hayden B, Check, Devon K, Green, Michelle, Strickler, John H, Akinyemiju, Tomi

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 von Showguchi-Miyata, Junko, Hosler, Betsy A, Devon, Rebecca S, Skaug, Jennifer, Scherer, Stephen W, Okada, Yoshinori, Hayden, Michael R, Kwiatkowski, Thomas, Hadano, Shinji, Otomo, Asako, Nasir, Jamal, Singaraja, Roshni, Rouleau, Guy A, Brown, Robert H, Ikeda, Joh-E, Sagie, Tally, Yanagisawa, Yoshiko, Miyamoto, Natsuki, Osuga, Hitoshi, Figlewicz, Denise A, Hand, Collette K

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Huntingtin Decreases Susceptibility to a Spontaneous Seizure Disorder in FVN/B Mice von Van Raamsdonk, Jeremy M, Al-Shekaili, Hilal H, Wagner, Laura, Bredy, Tim W, Chan, Laura, Pearson, Jacqueline, Schwab, Claudia, Murphy, Zoe, Devon, Rebecca S, Lu, Ge, Kobor, Michael S, Hayden, Michael R, Leavitt, Blair R

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Association of Race and Ethnicity with Genomic Testing at a Comprehensive Cancer Center in North Carolina von Meernik, Clare, Wang, Frances, Raveendran, Yadurshini, Green, Michelle F, Check, Devon K, Bosworth, Hayden B, Sutton, Linda M, Strickler, John H, Akinyemiju, Tomi F

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An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred von Gros-Louis, François, Meijer, Inge A., Hand, Collette K., Dubé, Marie-Pierre, MacGregor, Daune L., Seni, Marie-Hélène, Devon, Rebecca S., Hayden, Michael R., Andermann, Frederick, Andermann, Eva, Rouleau, Guy A.

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

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