A Genome-wide Gene-Expression Analysis and Database in Transgenic Mice during Development of Amyloid or Tau Pathology von Matarin, Mar, Salih, Dervis A., Yasvoina, Marina, Cummings, Damian M., Guelfi, Sebastian, Liu, Wenfei, Nahaboo Solim, Muzammil A., Moens, Thomas G., Paublete, Rocio Moreno, Ali, Shabinah S., Perona, Marina, Desai, Roshni, Smith, Kenneth J., Latcham, Judy, Fulleylove, Michael, Richardson, Jill C., Hardy, John, Edwards, Frances A.

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A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release von Matarín, Mar, PhD, Brown, W Mark, MA, Scholz, Sonja, MD, Simón-Sánchez, Javier, BS, Fung, Hon-Chung, MD, Hernandez, Dena, MS, Gibbs, J Raphael, BS, De Vrieze, Fabienne Wavrant, PhD, Crews, Cynthia, Britton, Angela, MS, Langefeld, Carl D, PhD, Brott, Thomas G, MD, Brown, Robert D, MD, Worrall, Bradford B, MD, Frankel, Michael, MD, Silliman, Scott, MD, Case, L Douglas, PhD, Singleton, Andrew, Dr, Hardy, John A, PhD, Rich, Stephen S, PhD, Meschia, James F, MD

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Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke von Gschwendtner, Andreas, Bevan, Steve, Cole, John W., Plourde, Anna, Matarin, Mar, Ross-Adams, Helen, Meitinger, Thomas, Wichmann, Erich, Mitchell, Braxton D., Furie, Karen, Slowik, Agnieszka, Rich, Stephen S., Syme, Paul D., MacLeod, Mary J., Meschia, James F., Rosand, Jonathan, Kittner, Steve J., Markus, Hugh S., Müller-Myhsok, Bertram, Dichgans, Martin

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Doublecortin-expressing cell types in temporal lobe epilepsy von Liu, Joan Y W, Matarin, Mar, Reeves, Cheryl, McEvoy, Andrew W, Miserocchi, Anna, Thompson, Pamela, Sisodiya, Sanjay M, Thom, Maria

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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals von Simon-Sanchez, Javier, Scholz, Sonja, Fung, Hon-Chung, Matarin, Mar, Hernandez, Dena, Gibbs, J. Raphael, Britton, Angela, de Vrieze, Fabienne Wavrant, Peckham, Elizabeth, Gwinn-Hardy, Katrina, Crawley, Anthony, Keen, Judith C., Nash, Josefina, Borgaonkar, Digamber, Hardy, John, Singleton, Andrew

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Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data von Schymick, Jennifer C, BS, Scholz, Sonja W, MD, Fung, Hon-Chung, MD, Britton, Angela, MS, Arepalli, Sampath, MS, Gibbs, J Raphael, BS, Lombardo, Federica, PhD, Matarin, Mar, PhD, Kasperaviciute, Dalia, PhD, Hernandez, Dena G, MSc, Crews, Cynthia, Bruijn, Lucie, PhD, Rothstein, Jeffrey, MD, Mora, Gabriele, MD, Restagno, Gabriella, MD, Chiò, Adriano, MD, Singleton, Andrew, PhD, Hardy, John, PhD, Traynor, Bryan J, MD

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Poorer cognitive performance in humans with mild cognitive impairment carrying the T variant of the Glu/Asp NOS3 polymorphism von Solé-Padullés, Cristina, Bartrés-Faz, David, Junqué, Carme, Via, Marc, Matarı́n, Mar, González-Pérez, Emili, Moral, Pedro, Moya, Antoni, Clemente, Immaculada C

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Functional and magnetic resonance imaging correlates of corpus callosum in normal pressure hydrocephalus before and after shunting von Mataró, Maria, Matarín, Mar, Poca, Maria Antonia, Pueyo, Roser, Sahuquillo, Juan, Barrios, Maite, Junqué, Carme

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Post-surgical changes in brain metabolism detected by magnetic resonance spectroscopy in normal pressure hydrocephalus: results of a pilot study von del Mar Matarín, María, Pueyo, Roser, Poca, María Antonia, Falcón, Carles, Mataró, María, Bargalló, Núria, Sahuquillo, Juan, Junqué, Carme

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Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics von Nalls, Michael A, Simon-Sanchez, Javier, Gibbs, J Raphael, Paisan-Ruiz, Coro, Bras, Jose Tomas, Tanaka, Toshiko, Matarin, Mar, Scholz, Sonja, Weitz, Charles, Harris, Tamara B, Ferrucci, Luigi, Hardy, John, Singleton, Andrew B

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Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics von Biffi, Alessandro, Anderson, Christopher D., Nalls, Michael A., Rahman, Rosanna, Sonni, Akshata, Cortellini, Lynelle, Rost, Natalia S., Matarin, Mar, Hernandez, Dena G., Plourde, Anna, de Bakker, Paul I.W., Ross, Owen A., Greenberg, Steven M., Furie, Karen L., Meschia, James F., Singleton, Andrew B., Saxena, Richa, Rosand, Jonathan

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PAX6, brain structure and function in human adults: advanced MRI in aniridia von Yogarajah, Mahinda, Matarin, Mar, Vollmar, Christian, Thompson, Pamela J., Duncan, John S., Symms, Mark, Moore, Anthony T., Liu, Joan, Thom, Maria, Heyningen, Veronica, Sisodiya, Sanjay M.

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CSF galanin and cognition after shunt surgery in normal pressure hydrocephalus von Mataró, M, Poca, M A, Del Mar Matarín, M, Catalan, R, Sahuquillo, J, Galard, R

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Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis von Meschia, James F, Singleton, Andrew, Nalls, Michael A, Rich, Stephen S, Sharma, Pankaj, Ferrucci, Luigi, Matarin, Mar, Hernandez, Dena G, Pearce, Kerra, Brott, Thomas G, Brown, Jr, Robert D, Hardy, John, Worrall, Bradford B

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Soluble Fibrinogen Triggers Non-cell Autonomous ER Stress-Mediated Microglial-Induced Neurotoxicity von Piers, Thomas M, East, Emma, Villegas-Llerena, Claudio, Sevastou, Ioanna G, Matarin, Mar, Hardy, John, Pocock, Jennifer M

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Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy von Guelfi, Sebastian, Botia, Juan A, Thom, Maria, Ramasamy, Adaikalavan, Perona, Marina, Stanyer, Lee, Martinian, Lillian, Trabzuni, Daniah, Smith, Colin, Walker, Robert, Ryten, Mina, Reimers, Mark, Weale, Michael E, Hardy, John, Matarin, Mar

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Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank von Wain, Louise V, PhD, Shrine, Nick, PhD, Miller, Suzanne, PhD, Jackson, Victoria E, MSc, Ntalla, Ioanna, PhD, Artigas, María Soler, PhD, Billington, Charlotte K, PhD, Kheirallah, Abdul Kader, BSc, Allen, Richard, MSc, Cook, James P, PhD, Probert, Kelly, BSc, Obeidat, Ma'en, PhD, Bossé, Yohan, PhD, Hao, Ke, ScD, Postma, Dirkje S, Prof, Paré, Peter D, MD, Ramasamy, Adaikalavan, DPhil, Mägi, Reedik, PhD, Mihailov, Evelin, MSc, Reinmaa, Eva, MSc, Melén, Erik, MD, O'Connell, Jared, DPhil, Frangou, Eleni, MSc[Res], Delaneau, Olivier, PhD, Freeman, Colin, PhD, Petkova, Desislava, PhD, McCarthy, Mark, Prof, Sayers, Ian, PhD, Deloukas, Panos, Prof, Hubbard, Richard, Prof, Pavord, Ian, FMedSci, Hansell, Anna L, MBBChir, Thomson, Neil C, Prof, Zeggini, Eleftheria, PhD, Morris, Andrew P, Prof, Marchini, Jonathan, Prof, Strachan, David P, Prof, Tobin, Martin D, Prof, Hall, Ian P, Prof

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Genomewide SNP assay reveals mutations underlying Parkinson disease von Simon-Sanchez, Javier, Scholz, Sonja, del Mar Matarin, Maria, Fung, Hon-Chung, Hernandez, Dena, Gibbs, J Raphael, Britton, Angela, Hardy, John, Singleton, Andrew

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Genotype, haplotype and copy-number variation in worldwide human populations von Jakobsson, Mattias, Scholz, Sonja W., Scheet, Paul, Gibbs, J. Raphael, VanLiere, Jenna M., Fung, Hon-Chung, Szpiech, Zachary A., Degnan, James H., Wang, Kai, Guerreiro, Rita, Bras, Jose M., Schymick, Jennifer C., Hernandez, Dena G., Traynor, Bryan J., Simon-Sanchez, Javier, Matarin, Mar, Britton, Angela, van de Leemput, Joyce, Rafferty, Ian, Bucan, Maja, Cann, Howard M., Hardy, John A., Rosenberg, Noah A., Singleton, Andrew B.

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Corpus callosum functioning in patients with normal pressure hydrocephalus before and after surgery von MATARO, Maria, POCA, Maria Antonia, MATARIN, Mar, SAHUQUILLO, Juan, SEBASTIAN, Nuria, JUNQUE, Carme

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