Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer by Patel, K M, van der Vos, K E, Smith, C G, Mouliere, F, Tsui, D, Morris, J, Chandrananda, D, Marass, F, van den Broek, D, Neal, D E, Gnanapragasam, V J, Forshew, T, van Rhijn, B W, Massie, C E, Rosenfeld, N, van der Heijden, M S

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CTNNB1 mutations are clonal in adamantinomatous craniopharyngioma by Apps, J. R., Stache, C., Gonzalez‐Meljem, J. M., Gutteridge, A., Chalker, J., Jacques, T. S., Forshew, T., Hölsken, A., Martinez‐Barbera, J. P.

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58: Proffered Paper: Noninvasive monitoring of tumour mutations and dynamics in circulating DNA of non-small cell lung cancer patients treated with EGFR inhibitors by Tsui, D, Wong, A.S.C, Murtaza, M, Forshew, T, Soo, R, Lim, H.L, Goh, B.C, Gale, D, Chin, T.M, Rosenfeld, N

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876 Non-invasive Monitoring of Metastatic Breast Cancer by Circulating Tumour DNA – a Comparison With Circulating Tumour Cells by Dawson, S, Tsui, D, Murtaza, M, Biggs, H, Chin, S.F, Gale, D, Forshew, T, Wallis, M, Caldas, C, Rosenfeld, N

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Mapping of a novel locus for achromatopsia (ACHM4) to 1 p and identification of a germline mutation in the α subunit of cone transducin (GNAT2) by ALIGIANIS, I. A, FORSHEW, T, JOHNSON, S, MICHAELIDES, M, JOHNSON, C. A, TREMBATH, R. C, HUNT, D. M, MOORE, A. T, MAHER, E. R

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Three different brain tumours evolving from a common origin by Forshew, T, Lewis, P, Waldman, A, Peterson, D, Glaser, M, Brock, C, Sheer, D, Mulholland, P J

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Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism by Forshew, T, Khaliq, S, Tee, L, Smith, U, Johnson, C A, Mehdi, S Q, Maher, E R

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SCAMP: a spreadsheet to collate autozygosity mapping projects by Forshew, T, Johnson, C A

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P2.01-78 Validation of InVisionFirst ctDNA NGS Profiling via ddPCR Testing in Patients with Non-Small Cell Lung Cancer (NSCLC) by Pritchett, M., Baker-Neblett, K., Mileham, K., Plagnol, V., Howarth, K., Forshew, T., Jones, G., Morris, C.

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Rasagiline for amyotrophic lateral sclerosis: A randomized, controlled trial by Statland, Jeffrey M., Moore, Dan, Wang, Yunxia, Walsh, Maureen, Mozaffar, Tahseen, Elman, Lauren, Nations, Sharon P., Mitsumoto, Hiroshi, Fernandes, J. Americo, Saperstein, David, Hayat, Ghazala, Herbelin, Laura, Karam, Chafic, Katz, Jonathan, Wilkins, Heather M., Agbas, Abdulbaki, Swerdlow, Russell H., Santella, Regina M., Dimachkie, Mazen M., Barohn, Richard J., Barohn, Richard J., Swerdlow, Russell, Wang, Yunxia, Statland, Jeffrey, Dimachkie, Mazen M., Glenn, Melanie, Pasnoor, Mamatha, Walsh, Maureen, Emmons, Kelley, Johns, Kathryn, Harness, Yolanda, Herbelin, Laura, Katz, Jonathan, Miller, Robert G, Forshew, Dallas, Engel, Marguerite, Mozaffar, Tahseen, Goyal, Namita, Cash, Tiyonnoh, Mathew, Veena, Martin, Veronica, Saperstein, David, Levine, Todd, Flynne, Lynn, Karam, Chafic, Dimtrov, Diana, Elman, Lauren, McCluskey, Leo, Almasy, Kelly, Kelley, Mary, Fernandes, J. Americo M., Thaisetthawatkul, Pariwat, Peterson, Carolyn, Cowardin, Cindy, Heires, Peggy, Nations, Sharon, Trivedi, Jaya, Gorham, Nina F., Hopkins, Steve, Hayat, Ghazala, Brown, Susan, Mitsumoto, Hiroshi, Aziz‐Zaman, Sonya, Hupf, Jonathan, Armstrong, Nicole, McHale, Brittany, Wilkins, Heather, Agbas, Abdulbaki, Sage, Jessica, Hall, Sharice, Santella, Regina, Gurvich, Irina, Amato, Anthony, Bedlack, Richard, Jackson, Carlayne, Cutter, Gary, Wolfe, Gil, Simpson, Ericka

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Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III by Kaufmann, Petra, Thompson, John L.P., Levy, Gilberto, Buchsbaum, Richard, Shefner, Jeremy, Krivickas, Lisa S., Katz, Jonathan, Rollins, Yvonne, Barohn, Richard J., Jackson, Carlayne E., Tiryaki, Ezgi, Lomen-Hoerth, Catherine, Armon, Carmel, Tandan, Rup, Rudnicki, Stacy A., Rezania, Kourosh, Sufit, Robert, Pestronk, Alan, Novella, Steven P., Heiman-Patterson, Terry, Kasarskis, Edward J., Pioro, Erik P., Montes, Jacqueline, Arbing, Rachel, Vecchio, Darleen, Barsdorf, Alexandra, Mitsumoto, Hiroshi, Levin, Bruce

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Locus heterogeneity in autosomal recessive congenital cataracts : linkage to 9q and germline HSF4 mutations by FORSHEW, Tim, JOHNSON, Colin A, MOORE, Anthony T, MAHER, Eamonn R, KHALIQ, Shagufta, PASHA, Shanaz, WILLIS, Catherine, ABBASI, Rashida, TEE, Louise, SMITH, Ursula, TREMBATH, Richard C, SYED QASIM MEHDI

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Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the α subunit of cone transducin (GNAT2) by Aligianis, I A, Forshew, T, Johnson, S, Michaelides, M, Johnson, C A, Trembath, R C, Hunt, D M, Moore, A T, Maher, E R

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A multi-center screening trial of rasagiline in patients with amyotrophic lateral sclerosis: Possible mitochondrial biomarker target engagement by Macchi, Zachary, Wang, Yunxia, Moore, Dan, Katz, Jonathan, Saperstein, David, Walk, David, Simpson, Ericka, Genge, Angela, Bertorini, Tulio, Fernandes, J. Americo, Swenson, Andrea, Elman, Lauren, Dimachkie, Mazen, Herbelin, Laura, Miller, Joann, Lu, Jianghua, Wilkins, Heather, Swerdlow, Russell H., Statland, Jeffrey, Barohn, Richard

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ALS Multicenter Cohort Study of Oxidative Stress (ALS COSMOS): Study methodology, recruitment, and baseline demographic and disease characteristics by Mitsumoto, Hiroshi, Factor-Litvak, Pam, Andrews, Howard, Goetz, Raymond R., Andrews, Leslie, Rabkin, Judith G., McElhiney, Martin, Nieves, Jeri, Santella, Regina M., Murphy, Jennifer, Hupf, Jonathan, Singleton, Jess, Merle, David, Kilty, Mary, Heitzman, Daragh, Bedlack, Richard S., Miller, Robert G., Katz, Jonathan S., Forshew, Dallas, Barohn, Richard J., Sorenson, Eric J., Oskarsson, Bjorn, Fernandes Filho, J. Americo M., Kasarskis, Edward J., Lomen-Hoerth, Catherine, Mozaffar, Tahseen, Rollins, Yvonne D., Nations, Sharon P., Swenson, Andrea J., Shefner, Jeremy M., Andrews, Jinsy A., Koczon-Jaremko, Boguslawa A.

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Randomized phase 2 trial of NP001–a novel immune regulator: Safety and early efficacy in ALS by Miller, Robert G, Block, Gilbert, Barohn, Richard J, Cudkowicz, Merit, Zhang, Jane R, McGrath, Michael S, Appel, Stan H, Katz, Jonathan, Kushner, Giovanna, Wong, Cynthia, Akers, Amy, Zayas-Bazan, Thais, McCoy, Shelly, Goyal, Neelam, Harris, Will, Gonella, Marie, Brooks, Benjamin R, Bravver, Elena, Sanjak, Mohammed, Ward, Amber L, Mehrizi, Amir, Belfiore, Mark, Lary, Cynthia, Nemeth, Joanne, Conway, Jill, Holsten, Scott, Shue, Jamie, Mitsumoto, Hiroshi, Youngman, Regina, Lee, Yei-won, Dalton, Kate, Bedlack, Richard S, Morgenlander, Joel Charles, Boyette, Candace Lee, Grace, Karen L, Thomas Hickey, Patrick, Perry-Trice, Peggy, Berry, James, Atassi, Nazem, Boylan, Kevin, Kennelly, Kathleen, DeSaro, Pamela, Johnston, Amelia, Huser, Angela, Fuqua, Paula, Staggs, Kristin, Babcock, Lorraine, Kryston, Thomas, Bosch, E Peter, Verheijde, Josephus L, Grover, Yvvonne, Lee, Michael S, Musil, Danette J, Whiteman, Dana, Simpson, Ericka P, Pleitez, Milvia Y, Lay, Luis F, Schwartz, Thomas, Blanton, Linda, Lai, Eugene C, Berry, Nicole, Khan, Sara, Chowdhury, Nabi, Goslin, Kimberly, Carter, Gregory T, Ann Kovarik, Mary, Simionescu, Laura, Reale, Melissa A, Markis, Katie, Money, Kristina, Boevin, Travis, Lava, Neil, Glass, Jonathan D, Polak, Meraida, Shaw, Latoya, Bordeau, Jane, Rogers, Susan, Ferguson, Susan, Kelly, Crystal, Mozaffar, Tahseen, Ramsey, Gladys, Tully, Patricia A, Alvarez, Rebecca, Barohn, Richard, Dimachkie, Mazen M, Pasnoor, Mamatha, Herbelin, Laura, Kasarskis, Edward J, Dotson, William F, Sitzlar, Stephen C, Tandy, Tammy, Carrico, Jeffery, Rice, Linda, Chamblin, Lisa, Townsend, Janet, Hanley-Borgia, Lisa, Vanderpool, Kathryn E, Taylor, Deborah G, Hutchinson, Jan, King, Jason T

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ALSUntangled No. 27: Precision Stem Cell by ALSUntangled Group, The ALSUntangled Group

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ALSUntangled No. 29: MitoQ by ALSUntangled Group, The ALSUntangled Group

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ALSUntangled No. 28: Acupuncture by ALSUntangled Group, The ALSUntangled Group

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ALSUntangled No. 24: Vitamin D by ALSUntangled Group, The ALSUntangled Group

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