Surfactant protein-D and exposure to bioaerosols in wastewater and garbage workers von Tabrizi, R D, Bernard, A, Thommen, A M, De Winter, F, Oppliger, A, Hilfiker, S, Tschopp, Alois, Hotz, Philipp

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Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington's disease: a retrospective cohort analysis von Byrne, Lauren M, MRes, Rodrigues, Filipe B, MD, Blennow, Kaj, Prof, Durr, Alexandra, Prof, Leavitt, Blair R, Prof, Roos, Raymund A C, Prof, Scahill, Rachael I, PhD, Tabrizi, Sarah J, Prof, Zetterberg, Henrik, Prof, Langbehn, Douglas, Prof, Wild, Edward J, Dr

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Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data von Tabrizi, Sarah J, Prof, Scahill, Rachael I, PhD, Owen, Gail, PhD, Durr, Alexandra, MD, Leavitt, Blair R, MDCM, Roos, Raymund A, Prof, Borowsky, Beth, PhD, Landwehrmeyer, Bernhard, Prof, Frost, Chris, Prof, Johnson, Hans, PhD, Craufurd, David, MD, Reilmann, Ralf, MD, Stout, Julie C, Prof, Langbehn, Douglas R, Prof

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Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis von Tabrizi, Sarah J, Prof, Scahill, Rachael I, PhD, Durr, Alexandra, MD, Roos, Raymund AC, MD, Leavitt, Blair R, FRCPC, Jones, Rebecca, MSc, Landwehrmeyer, G Bernhard, MD, Fox, Nick C, MD, Johnson, Hans, PhD, Hicks, Stephen L, PhD, Kennard, Christopher, FRCP, Craufurd, David, FRCPsych, Frost, Chris, PhD, Langbehn, Douglas R, MD, Reilmann, Ralf, MD, Stout, Julie C, PhD

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Tapping linked to function and structure in premanifest and symptomatic Huntington disease von BECHTEL, N, SCAHILL, R. I, SALAT, D. H, DURR, A, LEAVITT, B. R, ROOS, R. A. C, LANDWEHRMEYER, G. B, LANGBEHN, D. R, STOUT, J. C, TABRIZI, S. J, REILMANN, R, ROSAS, H. D, ACHARYA, T, VAN DEN BOGAARD, S. J. A, JAUFFRET, C, SAY, M. J, STURROCK, A, JOHNSON, H, ONORATO, C. E

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Apathy predicts rate of cognitive decline over 24 months in premanifest Huntington's disease von Andrews, S. C., Langbehn, D. R., Craufurd, D., Durr, A., Leavitt, B. R., Roos, R. A., Tabrizi, S. J., Stout, J. C.

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Snowmass white paper: beyond the standard model effects on neutrino flavor von Argüelles, C. A, Barenboim, G, Bustamante, M, Coloma, P, Denton, P. B, Esteban, I, Farzan, Y

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Brain Regions Showing White Matter Loss in Huntington’s Disease Are Enriched for Synaptic and Metabolic Genes von McColgan, Peter, Gregory, Sarah, Seunarine, Kiran K., Razi, Adeel, Papoutsi, Marina, Johnson, Eileanoir, Durr, Alexandra, Roos, Raymund A.C., Leavitt, Blair R., Holmans, Peter, Scahill, Rachael I., Clark, Chris A., Rees, Geraint, Tabrizi, Sarah J., Coleman, A., Decolongon, J., Fan, M., Petkau, T., Jauffret, C., Justo, D., Lehericy, S., Nigaud, K., Valabrègue, R., Schoonderbeek, A., ‘t Hart, E.P., Moss, D. J. Hensman, Ghosh, R., Crawford, H., Papoutsi, M., Berna, C., Mahaleskshmi, D., Reilmann, R., Weber, N., Labuschagne, I., Stout, J., Landwehrmeyer, B., Orth, M., Mayer, I., Johnson, H., Crawfurd, D.

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Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data von Tabrizi, Sarah J, Prof, Reilmann, Ralf, MD, Roos, Raymund AC, MD, Durr, Alexandra, MD, Leavitt, Blair, FRCP, Owen, Gail, PhD, Jones, Rebecca, MSc, Johnson, Hans, PhD, Craufurd, David, FRCPsych, Hicks, Stephen L, PhD, Kennard, Christopher, FRCP, Landwehrmeyer, Bernhard, MD, Stout, Julie C, PhD, Borowsky, Beth, PhD, Scahill, Rachael I, PhD, Frost, Chris, MA, Langbehn, Douglas R, PhD

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Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities von Tabrizi, Sarah J, Estevez-Fraga, Carlos, van Roon-Mom, Willeke M C, Flower, Michael D, Scahill, Rachael I, Wild, Edward J, Muñoz-Sanjuan, Ignacio, Sampaio, Cristina, Rosser, Anne E, Leavitt, Blair R

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Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data von Tabrizi, Sarah J, Langbehn, Douglas R, Leavitt, Blair R, Roos, Raymund AC, Durr, Alexandra, Craufurd, David, Kennard, Christopher, Hicks, Stephen L, Fox, Nick C, Scahill, Rachael I, Borowsky, Beth, Tobin, Allan J, Rosas, H Diana, Johnson, Hans, Reilmann, Ralf, Landwehrmeyer, Bernhard, Stout, Julie C

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Microglial activation in presymptomatic Huntington's disease gene carriers von Tai, Yen F., Pavese, Nicola, Gerhard, Alexander, Tabrizi, Sarah J., Barker, Roger A., Brooks, David J., Piccini, Paola

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Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series von Koriath, C., Kenny, J., Adamson, G., Druyeh, R., Taylor, W., Beck, J., Quinn, L., Mok, T. H., Dimitriadis, A., Norsworthy, P., Bass, N., Carter, J., Walker, Z., Kipps, C., Coulthard, E., Polke, J. M., Bernal-Quiros, M., Denning, N., Thomas, R., Raybould, R., Williams, J., Mummery, C. J., Wild, E. J., Houlden, H., Tabrizi, S. J., Rossor, M. N., Hummerich, H., Warren, J. D., Rowe, J. B., Rohrer, J. D., Schott, J. M., Fox, N. C., Collinge, J., Mead, S.

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Operationalizing compensation over time in neurodegenerative disease von Gregory, Sarah, Long, Jeffrey D, Klöppel, Stefan, Razi, Adeel, Scheller, Elisa, Minkova, Lora, Papoutsi, Marina, Mills, James A, Durr, Alexandra, Leavitt, Blair R, Roos, Raymund A C, Stout, Julie C, Scahill, Rachael I, Langbehn, Douglas R, Tabrizi, Sarah J, Rees, Geraint

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Pitfalls in the Use of Voxel-Based Morphometry as a Biomarker: Examples from Huntington Disease von HENLEY, S. M. D, RIDGWAY, G. R, SCAHILL, R. I, KLÖPPEL, S, TABRIZI, S. J, FOX, N. C, KASSUBEK, J

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FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington’s disease von Goold, Robert, Hamilton, Joseph, Menneteau, Thomas, Flower, Michael, Bunting, Emma L., Aldous, Sarah G., Porro, Antonio, Vicente, José R., Allen, Nicholas D., Wilkinson, Hilary, Bates, Gillian P., Sartori, Alessandro A., Thalassinos, Konstantinos, Balmus, Gabriel, Tabrizi, Sarah J.

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A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes von Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah A., Hensman Moss, Davina J., Alshammari, Asma M., Flower, Michael D., Durr, Alexandra, Leavitt, Blair R., Roos, Raymund A.C., Holmans, Peter, Jones, Lesley, Langbehn, Douglas R., Kwak, Seung, Tabrizi, Sarah J., Monckton, Darren G.

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Fall in Human Papillomavirus Prevalence Following a National Vaccination Program von Tabrizi, Sepehr N., Brotherton, Julia M. L., Kaldor, John M., Skinner, S. Rachel, Cummins, Eleanor, Liu, Bette, Bateson, Deborah, McNamee, Kathleen, Garefalakis, Maria, Garland, Suzanne M.

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Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease von STURROCK, A, LAULE, C, MACKAY, A. L, LEAVITT, B. R, DECOLONGON, J, DAR SANTOS, R, COLEMAN, A. J, CREIGHTON, S, BECHTEL, N, REILMANN, R, HAYDEN, M. R, TABRIZI, S. J

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The Prevalence of Huntington's Disease von Rawlins, Michael D., Wexler, Nancy S., Wexler, Alice R., Tabrizi, Sarah J., Douglas, Ian, Evans, Stephen J.W., Smeeth, Liam

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