Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21

by Matarin, Mar, Brown, W. Mark, Singleton, Andrew, Hardy, John A., Meschia, James F.
Published 2008

Functional and magnetic resonance imaging correlates of corpus callosum in normal pressure hydrocephalus before and after shunting

by Mataró, Maria, Matarín, Mar, Poca, Maria Antonia, Pueyo, Roser, Sahuquillo, Juan, Barrios, Maite, Junqué, Carme
Published 2007

Soluble Fibrinogen Triggers Non-cell Autonomous ER Stress-Mediated Microglial-Induced Neurotoxicity

by Piers, Thomas M., East, Emma, Villegas-Llerena, Claudio, Sevastou, Ioanna G., Matarin, Mar, Hardy, John, Pocock, Jennifer M.
Published in Front Cell Neurosci (2018)

Peripheral Serotonin 1B Receptor Transcription Predicts the Effect of Acute Tryptophan Depletion on Risky Decision-Making

by Faulkner, Paul, Mancinelli, Federico, Lockwood, Patricia L, Matarin, Mar, Dolan, Raymond J, Wood, Nick W, Dayan, Peter, Roiser, Jonathan P
Published in Int J Neuropsychopharmacol (2016)

Doublecortin-expressing cell types in temporal lobe epilepsy

by Liu, Joan Y. W., Matarin, Mar, Reeves, Cheryl, McEvoy, Andrew W., Miserocchi, Anna, Thompson, Pamela, Sisodiya, Sanjay M., Thom, Maria
Published in Acta Neuropathol Commun (2018)

Association of integrin α2 gene variants with ischemic stroke

by Matarin, Mar, Brown, W Mark, Hardy, John A, Rich, Stephen S, Singleton, Andrew B, Brown, Robert D, Brott, Thomas G, Worrall, Bradford B, Meschia, James F
Published 2007

PAX6, brain structure and function in human adults: advanced MRI in aniridia

by Yogarajah, Mahinda, Matarin, Mar, Vollmar, Christian, Thompson, Pamela J., Duncan, John S., Symms, Mark, Moore, Anthony T., Liu, Joan, Thom, Maria, van Heyningen, Veronica, Sisodiya, Sanjay M.
Published in Ann Clin Transl Neurol (2016)

The impact of brain‐derived neurotrophic factor Val66Met polymorphism on cognition and functional brain networks in patients with intractable partial epilepsy

by Sidhu, Meneka K., Thompson, Pamela J., Wandschneider, Britta, Foulkes, Alexandra, de Tisi, Jane, Stretton, Jason, Perona, Marina, Thom, Maria, Bonelli, Silvia B., Burdett, Jane, Williams, Elaine, Duncan, John S., Matarin, Mar
Published in CNS Neurosci Ther (2018)

The TOR1A Polymorphism rs1182 and the Risk of Spread in Primary Blepharospasm

by Defazio, Giovanni, Matarin, Mar, Peckham, Elizabeth L., Martino, Davide, Valente, Enza M., Singleton, Andrew, Crawley, Anthony, Aniello, Maria Stella, Brancati, Francesco, Abbruzzese, Giovanni, Girlanda, Paolo, Livrea, Paolo, Hallett, Mark, Berardelli, Alfredo
Published 2009

Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis

by 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, Robert D., Hardy, John, Worrall, Bradford B.
Published 2011

Siblings with Ischemic Stroke Study (SWISS): Results of a Genome-wide Scan for Stroke Loci

by Meschia, James F., Nalls, Michael, Matarin, Mar, Brott, Thomas G., Brown, Robert D., Hardy, John, Kissela, Brett, Rich, Stephen S., Singleton, Andrew, Hernandez, Dena, Ferrucci, Luigi, Pearce, Kerra, Keller, Margaret, Worrall, Bradford B.
Published 2011

Measures of Autozygosity in Decline: Globalization, Urbanization, and Its Implications for Medical Genetics

by 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.
Published 2009

Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy

by Arrigoni, Francesca I, Matarin, Mar, Thompson, Pamela J, Michaelides, Michel, McClements, Michelle E, Redmond, Elizabeth, Clarke, Lindsey, Ellins, Elizabeth, Mohamed, Saifullah, Pavord, Ian, Hunt, David M, Moore, Anthony T, Halcox, Julian, Sisodiya, Sanjay M
Published 2011

Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy

by Arrigoni, Francesca I, Matarin, Mar, Thompson, Pamela J, Michaelides, Michel, McClements, Michelle E, Redmond, Elizabeth, Clarke, Lindsey, Ellins, Elizabeth, Mohamed, Saifullah, Pavord, Ian, Klein, Nigel, Hunt, David M, Moore, Anthony T, Halcox, Julian, Sisodiya, Sanjay M
Published 2011

Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy

by Schoeler, Natasha E., Leu, Costin, White, Jon, Plagnol, Vincent, Ellard, Sian, Matarin, Mar, Yellen, Gary, Thiele, Elizabeth A., Mackay, Mark, McMahon, Jacinta M., Scheffer, Ingrid E., Sander, Josemir W., Cross, J. Helen, Sisodiya, Sanjay M.
Published in Epilepsy Res (2015)

Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence

by Rainger, Jacqueline K., Bhatia, Shipra, Bengani, Hemant, Gautier, Philippe, Rainger, Joe, Pearson, Matt, Ansari, Morad, Crow, Jayne, Mehendale, Felicity, Palinkasova, Bozena, Dixon, Michael J., Thompson, Pamela J., Matarin, Mar, Sisodiya, Sanjay M., Kleinjan, Dirk A., FitzPatrick, David R.
Published 2014

First effects of rising amyloid-β in transgenic mouse brain: synaptic transmission and gene expression

by Cummings, Damian M., Liu, Wenfei, Portelius, Erik, Bayram, Sevinç, Yasvoina, Marina, Ho, Sui-Hin, Smits, Hélène, Ali, Shabinah S., Steinberg, Rivka, Pegasiou, Chrysia-Maria, James, Owain T., Matarin, Mar, Richardson, Jill C., Zetterberg, Henrik, Blennow, Kaj, Hardy, John A., Salih, Dervis A., Edwards, Frances A.
Published in Brain (2015)

Candidate Gene Polymorphisms for Ischemic Stroke

by Matarin, Mar, Brown, W. Mark, Dena, Hernandez, Britton, Angela, De Vrieze, Fabienne Wavrant, Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Case, L. Douglas, Chanock, Stephen J., Metter, E. Jeffrey, Ferruci, Luigi, Gamble, Dale, Hardy, John A., Rich, Stephen S., Singleton, Andrew, Meschia, James F.
Published 2009

Genetic variability in response to amyloid beta deposition influences Alzheimer’s disease risk

by Salih, Dervis A, Bayram, Sevinc, Guelfi, Sebastian, Reynolds, Regina H, Shoai, Maryam, Ryten, Mina, Brenton, Jonathan W, Zhang, David, Matarin, Mar, Botia, Juan A, Shah, Runil, Brookes, Keeley J, Guetta-Baranes, Tamar, Morgan, Kevin, Bellou, Eftychia, Cummings, Damian M, Escott-Price, Valentina, Hardy, John
Published in Brain Commun (2019)

Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics

by 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
Published 2010