Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion von Hickman, Richard A., Dewan, Ramita, Cortes, Etty, Traynor, Bryan J., Marder, Karen, Vonsattel, Jean-Paul

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ATXN2 intermediate expansions in amyotrophic lateral sclerosis von Glass, Jonathan D, Dewan, Ramita, Ding, Jinhui, Gibbs, J Raphael, Dalgard, Clifton, Keagle, Pamela J, Shankaracharya, García-Redondo, Alberto, Traynor, Bryan J, Chia, Ruth, Landers, John E

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Highlighting the clinical potential of HTT repeat expansions in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von Dewan, Ramita, Scholz, Sonja W., Chiò, Adriano, Traynor, Bryan J.

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Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas von Pemov, Alexander, Dewan, Ramita, Hansen, Nancy F., Chandrasekharappa, Settara C., Ray-Chaudhury, Abhik, Jones, Kristine, Luo, Wen, Heiss, John D., Mullikin, James C., Chittiboina, Prashant, Stewart, Douglas R., Asthagiri, Ashok R.

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In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees von Pemov, Alexander, Pathak, Anand, Jones, Samantha J., Dewan, Ramita, Merberg, Jessica, Karra, Sirisha, Kim, Jung, Arons, Evgeny, Ravichandran, Sarangan, Luke, Brian T., Suman, Shalabh, Yeager, Meredith, Dyer, Martin J. S., Lynch, Henry T., Greene, Mark H., Caporaso, Neil E., Kreitman, Robert J., Goldin, Lynn R., Spinelli, John J., Brooks-Wilson, Angela, McMaster, Mary L., Stewart, Douglas R.

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The Association of CD81 Polymorphisms with Alloimmunization in Sickle Cell Disease von Girot, Robert, Vukmanovic, Stanislav, Rajagopal, Krishnamoorthy, Maury, Jacqueline, Lasserre, Jacqueline, Luban, Naomi L. C., Dewan, Ramita, Le Bouder, Gama P., Tamouza, Ryad, Tatari-Calderone, Zohreh, Lionnet, François

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Age-related accumulation of T cells with markers of relatively stronger autoreactivity leads to functional erosion of T cells von Tatari-Calderone, Zohreh, Stojakovic, Milica, Dewan, Ramita, Le Bouder, Gama, Jankovic, Dragana, Vukmanovic, Stanislav

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Canagliflozin Associated with MELAS Pseudoexacerbation (S5.005) von Dewan, Ramita, Stack, Christopher, Cole, John

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Unrelenting Posterior Circulation TIAs Improved by Left Vertebral Angioplasty and Stenting (P4.216) von Dewan, Ramita, Stack, Christopher, Cole, John

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Man’s Best Friend: A Survey of Academic Neurologists and Subsequent Review of the Literature Exploring Seizure Dogs (P4.275) von Stack, Christopher, Dewan, Ramita, Sanchez, Ana

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Investigating RFC1 expansions in sporadic amyotrophic lateral sclerosis von Abramzon, Yevgenya, Dewan, Ramita, Cortese, Andrea, Resnick, Susan, Ferrucci, Luigi, Houlden, Henry, Traynor, Bryan J.

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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation von Kolmogorov, Mikhail, Billingsley, Kimberley J., Mastoras, Mira, Meredith, Melissa, Monlong, Jean, Lorig-Roach, Ryan, Asri, Mobin, Alvarez Jerez, Pilar, Malik, Laksh, Dewan, Ramita, Reed, Xylena, Genner, Rylee M., Daida, Kensuke, Behera, Sairam, Shafin, Kishwar, Pesout, Trevor, Prabakaran, Jeshuwin, Carnevali, Paolo, Yang, Jianzhi, Rhie, Arang, Scholz, Sonja W., Traynor, Bryan J., Miga, Karen H., Jain, Miten, Timp, Winston, Phillippy, Adam M., Chaisson, Mark, Sedlazeck, Fritz J., Blauwendraat, Cornelis, Paten, Benedict

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CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype von Dewan, Ramita, Jaunmuktane, Zane, Garcia‐Segura, Monica Emili, Strand, Catherine, Wild, Edward, Villar, Joaquin, Dalgard, Clifton L., Tabrizi, Sarah J., Traynor, Bryan J., Proukakis, Christos

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Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types von Saez-Atienzar, Sara, Bandres-Ciga, Sara, Langston, Rebekah G., Kim, Jonggeol J., Choi, Shing Wan, Reynolds, Regina H., Abramzon, Yevgeniya, Dewan, Ramita, Ahmed, Sarah, Landers, John E., Chia, Ruth, Ryten, Mina, Cookson, Mark R., Nalls, Michael A., Chio, Adriano, Traynor, Bryan J.

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Whole exome sequencing and copy-number variation analysis of 20 NF2-associated spinal and cranial meningiomas von Dewan, Ramita, Pemov, Alexander, Hansen, Nancy F, Chandrasekharappa, Settara C, Mullikin, Jim, Boland, Joseph F, Asthagiri, Ashok R, Stewart, Douglas

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Evidence of polyclonality in neurofibromatosis type 2-associated multilobulated vestibular schwannomas von Dewan, Ramita, Pemov, Alex, Kim, H Jeffrey, Morgan, Keaton L, Vasquez, Raul A, Chittiboina, Prashant, Wang, Xiang, Chandrasekharappa, Settara C, Ray-Chaudhury, Abhik, Butman, John A, Stewart, Douglas R, Asthagiri, Ashok R

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Structural variants in Lewy body dementia and frontotemporal dementia spectrum von Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan, Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Ray, Anindita K, Solaiman, Sultana, Jerez, Pilar Alvarez, Malik, Laksh, Dawson, Ted M, Rosenthal, Liana, Albert, Marilyn S., Pletnikova, Olga, Troncoso, Juan C, Masellis, Mario, Keith, Julia, Black, Sandra E., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M., Ghetti, Bernardino Francesco, Landers, John E, Ryten, Mina, Morris, Huw R, Hardy, John A., Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E, Beach, Thomas G, Ferman, Tanis J, Graff‐Radford, Neill R, Boeve, Brad F., Wszolek, Zbigniew, Dickson, Dennis W., Chio, Adriano, Bennett, David A. A, De Jager, Philip L, Ross, Owen A., Dalgard, Clifton L., Gibbs, J. Raphael, Traynor, Bryan J, Scholz, Sonja W

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Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family von Pathak, Anand, Seipel, Katja, Pemov, Alexander, Dewan, Ramita, Brown, Christina, Ravichandran, Sarangan, Luke, Brian T, Malasky, Michael, Suman, Shalabh, Yeager, Meredith, Gatti, Richard A, Caporaso, Neil E, Mulvihill, John J, Goldin, Lynn R, Pabst, Thomas, McMaster, Mary L, Stewart, Douglas R

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Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von Dewan, Ramita, Chia, Ruth, Ding, Jinhui, Hickman, Richard A, Stein, Thor D, Abramzon, Yevgeniya, Ahmed, Sarah, Sabir, Marya S, Portley, Makayla K, Tucci, Arianna, Ibanez, Kristina, Shankaracharya, F.N.U, Keagle, Pamela, Rossi, Giacomina, Caroppo, Paola, Tagliavini, Fabrizio, Waldo, Maria L, Johansson, Per M, Nilsson, Christer F, Rowe, James B, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Jabbari, Edwin, Viollet, Coralie, Glass, Jonathan D, Singleton, Andrew B, Silani, Vincenzo, Ross, Owen A, Ryten, Mina, Torkamani, Ali, Tanaka, Toshiko, Ferrucci, Luigi, Resnick, Susan M, Pickering-Brown, Stuart, Brady, Christopher B, Kowal, Neil, Hardy, John A, Van Deerlin, Vivianna, Vonsattel, Jean Paul, Harms, Matthew B, Morris, Huw R, Ferrari, Raffaele, Landers, John E, Chio, Adriano, Gibbs, J. Raphael, Dalgard, Clifton L, Scholz, Sonja W, Traynor, Bryan J

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Mice Lacking M1 and M3 Muscarinic Acetylcholine Receptors Have Impaired Odor Discrimination and Learning von Chan, Wilson, Singh, Sanmeet, Keshav, Taj, Dewan, Ramita, Eberly, Christian, Maurer, Robert, Nunez-Parra, Alexia, Araneda, Ricardo C

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