Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
Gretarsdottir, Solveig, Thorleifsson, Gudmar, Manolescu, Andrei, Styrkarsdottir, Unnur, Helgadottir, Anna, Gschwendtner, Andreas, Kostulas, Konstantinos, Kuhlenbäumer, Gregor, Bevan, Steve, Jonsdottir, Thorbjorg, Bjarnason, Hjordis, Saemundsdottir, Jona, Palsson, Stefan, Arnar, David O., Holm, Hilma, Thorgeirsson, Gudmundur, Valdimarsson, Einar Mar, Sveinbjörnsdottir, Sigurlaug, Gieger, Christian, Berger, Klaus, Wichmann, H-Erich, Hillert, Jan, Markus, Hugh, Gulcher, Jeffrey Robert, Ringelstein, E. Bernd, Kong, Augustine, Dichgans, Martin, Gudbjartsson, Daniel Fannar, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Annals of neurology (01.10.2008)
Published in Annals of neurology (01.10.2008)
Get full text
Journal Article
Familial Aggregation of Parkinson's Disease in Iceland
Sveinbjörnsdóttir, Sigurlaug, Hicks, Andrew A, Jónsson, Thorlákur, Pétursson, Hjörvar, Guðmundsson, Grétar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefánsson, Kári
Published in The New England journal of medicine (14.12.2000)
Published in The New England journal of medicine (14.12.2000)
Get full text
Journal Article
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke
Gretarsdottir, Solveig, Gulcher, Jeffrey R, Thorleifsson, Gudmar, Reynisdottir, Sigridur Th, Manolescu, Andrei, Jonsdottir, Sif, Jonsdottir, Thorbjörg, Gudmundsdottir, Thorunn, Bjarnadottir, Sigrun M, Einarsson, Olafur B, Gudjonsdottir, Herdis M, Hawkins, Malcolm, Gudmundsson, Gudmundur, Gudmundsdottir, Hrefna, Andrason, Hjalti, Gudmundsdottir, Asta S, Sigurdardottir, Matthildur, Chou, Thomas T, Nahmias, Joseph, Goss, Shyamali, Sveinbjörnsdottir, Sigurlaug, Valdimarsson, Einar M, Jakobsson, Finnbogi, Agnarsson, Uggi, Gudnason, Vilmundur, Thorgeirsson, Gudmundur, Fingerle, Jurgen, Gurney, Mark, Gudbjartsson, Daniel, Frigge, Michael L, Kong, Augustine, Stefansson, Kari
Published in Nature genetics (01.10.2003)
Published in Nature genetics (01.10.2003)
Get full text
Journal Article
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease
Huttenlocher, Johanna, Stefansson, Hreinn, Steinberg, Stacy, Helgadottir, Hafdis T, Sveinbjörnsdóttir, Sigurlaug, Riess, Olaf, Bauer, Peter, Stefansson, Kari
Published in Human molecular genetics (01.10.2015)
Published in Human molecular genetics (01.10.2015)
Get full text
Journal Article
Case–control studies on ceruloplasmin and superoxide dismutase (SOD1) in neurodegenerative diseases: A short review
Torsdottir, Gudlaug, Kristinsson, Jakob, Snaedal, Jón, Sveinbjörnsdóttir, Sigurlaug, Gudmundsson, Grétar, Hreidarsson, Stefán, Jóhannesson, Torkell
Published in Journal of the neurological sciences (15.12.2010)
Published in Journal of the neurological sciences (15.12.2010)
Get full text
Journal Article
Conference Proceeding
A susceptibility gene for late-onset idiopathic Parkinson's disease
Hicks, Andrew A., Pétursson, Hjörvar, Jónsson, Thorlákur, Stefánsson, Hreinn, Jóhannsdóttir, Hrefna S., Sainz, Jesus, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári, Sveinbjörnsdóttir, Sigurlaug
Published in Annals of neurology (01.11.2002)
Published in Annals of neurology (01.11.2002)
Get full text
Journal Article
Midlife migraine and late-life parkinsonism: AGES-Reykjavik study
Scher, Ann I, Ross, G Webster, Sigurdsson, Sigurdur, Garcia, Melissa, Gudmundsson, Larus S, Sveinbjörnsdóttir, Sigurlaug, Wagner, Amy K, Gudnason, Vilmundur, Launer, Lenore J
Published in Neurology (30.09.2014)
Published in Neurology (30.09.2014)
Get more information
Journal Article
Prevalence study of primary dystonia in Iceland
Asgeirsson, Hilmir, Jakobsson, Finnbogi, Hjaltason, Haukur, Jonsdottir, Helga, Sveinbjornsdottir, Sigurlaug
Published in Movement disorders (01.03.2006)
Published in Movement disorders (01.03.2006)
Get full text
Journal Article
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke
Gretarsdottir, Solveig, Thorleifsson, Gudmar, Reynisdottir, Sigridur Th, Manolescu, Andrei, Jonsdottir, Sif, Jonsdottir, Thorbjörg, Gudmundsdottir, Thorunn, Bjarnadottir, Sigrun M, Einarsson, Olafur B, Gudjonsdottir, Herdis M, Hawkins, Malcolm, Gudmundsson, Gudmundur, Gudmundsdottir, Hrefna, Andrason, Hjalti, Gudmundsdottir, Asta S, Sigurdardottir, Matthildur, Chou, Thomas T, Nahmias, Joseph, Goss, Shyamali, Sveinbjörnsdottir, Sigurlaug, Valdimarsson, Einar M, Jakobsson, Finnbogi, Agnarsson, Uggi, Gudnason, Vilmundur, Thorgeirsson, Gudmundur, Fingerle, Jurgen, Gurney, Mark, Gudbjartsson, Daniel, Frigge, Michael L, Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R
Published in Nature genetics (01.10.2003)
Published in Nature genetics (01.10.2003)
Get full text
Journal Article
Localization of a Susceptibility Gene for Common Forms of Stroke to 5q12
Gretarsdottir, Solveig, Sveinbjörnsdottir, Sigurlaug, Jonsson, Hjörtur H., Jakobsson, Finnbogi, Einarsdottir, Elisabet, Agnarsson, Uggi, Shkolny, Dana, Einarsson, Gisli, Gudjonsdottir, Herdis M., Valdimarsson, Einar M., Einarsson, Olafur B., Thorgeirsson, Gudmundur, Hadzic, Radinka, Jonsdottir, Sif, Reynisdottir, Sigridur Th, Bjarnadottir, Sigrun M., Gudmundsdottir, Thorunn, Gudlaugsdottir, Gudrun J., Gill, Ramanjit, Lindpaintner, Klaus, Sainz, Jesus, Hannesson, Helgi H., Sigurdsson, Gunnar Th, Frigge, Michael L., Kong, Augustine, Gudnason, Vilmundur, Stefansson, Kari, Gulcher, Jeffrey R.
Published in American journal of human genetics (01.03.2002)
Published in American journal of human genetics (01.03.2002)
Get full text
Journal Article
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls, Michael A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, J, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W
Published in The Lancet (British edition) (19.02.2011)
Published in The Lancet (British edition) (19.02.2011)
Get full text
Journal Article
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya, Murphy, Natalie A, Gibbs, J. Raphael, Ryten, Mina, Ferrari, Raffaele, Bras, Jose, Guerreiro, Rita, Williams, Julie, Sims, Rebecca, Lubbe, Steven, Hernandez, Dena G, Mok, Kin Y, Robak, Laurie, Campbell, Roy H, Rogaeva, Ekaterina, Traynor, Bryan J, Chia, Ruth, Chung, Sun Ju, Hardy, John A, Brice, Alexis, Wood, Nicholas W, Houlden, Henry, Shulman, Joshua M, Morris, Huw R, Gasser, Thomas, Krüger, Rejko, Heutink, Peter, Sharma, Manu, Simón-Sánchez, Javier, Nalls, Mike A, Singleton, Andrew B, Scholz, Sonja W
Published in Neurobiology of aging (01.09.2017)
Published in Neurobiology of aging (01.09.2017)
Get full text
Journal Article
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter
Published in Genome Biology (30.01.2017)
Published in Genome Biology (30.01.2017)
Get full text
Journal Article
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
KELLER, Margaux F, SAAD, Mohamad, SCHULTE, Claudia, MOSKVINA, Valentina, DURR, Alexandra, HOLMANS, Peter, KILARSKI, Laura L, GUERREIRO, Rita, HERNANDEZ, Dena G, BRICE, Alexis, YLIKOTILA, Pauli, STEFANSSON, Hreinn, BRAS, Jose, MAJAMAA, Kari, MORRIS, Huw R, WILLIAMS, Nigel, GASSER, Thomas, HEUTINK, Peter, WOOD, Nicholas W, HARDY, John, MARTINEZ, Maria, SINGLETON, Andrew B, NALLS, Michael A, BETTELLA, Francesco, NICOLAOU, Nayia, SIMON-SANCHEZ, Javier, MITTAG, Florian, BÜCHEL, Finja, SHARMA, Manu, RAPHAEL GIBBS, J
Published in Human molecular genetics (15.11.2012)
Published in Human molecular genetics (15.11.2012)
Get full text
Journal Article
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Hald, Erin M, So, Wing Yee, Kong, Augustine, Løchen, Maja-Lisa, Kuhlenbäumer, Gregor, Berger, Klaus, Gieger, Christian, Thorleifsson, Gudmar, Sveinbjörnsdóttir, Sigurlaug, Thorsteinsdottir, Unnur, Stoltenberg, Camilla, Kucera, Gayle, Nyrnes, Audhild, Mathiesen, Ellisiv B, Ringelstein, E Bernd, Walters, G Bragi, Bevan, Steve, Gudbjartsson, Daniel F, Stubblefield, Tanya, Holm, Hilma, Gulcher, Jeffrey, Hillert, Jan, Gschwendtner, Andreas, Njølstad, Inger, Carter, Shannon, Wichmann, H-Erich, Wong, Ka Sing, Valdimarsson, Einar M, Arnar, David O, Stefansson, Kari, Baum, Larry, Thorgeirsson, Gudmundur, Kostulas, Konstantinos, Gretarsdottir, Solveig, Chan, Juliana C N, Ng, Maggie C Y, Ma, Ronald C W, Hveem, Kristian, Darbar, Dawood, Markus, Hugh S, Roden, Dan, Wilsgaard, Tom, Dichgans, Martin
Published in Nature genetics (01.08.2009)
Published in Nature genetics (01.08.2009)
Get full text
Journal Article
Familial Aggregation of Parkinson's Disease
de la Fuente-Fernández, Raúl, Calne, Donald B, Kong, Augustine, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári
Published in The New England journal of medicine (12.04.2001)
Published in The New England journal of medicine (12.04.2001)
Get full text
Journal Article
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke
Stefansson, Kari, Helgadottir, Anna, Manolescu, Andrei, Thorleifsson, Gudmar, Gretarsdottir, Solveig, Jonsdottir, Helga, Thorsteinsdottir, Unnur, Samani, Nilesh J, Gudmundsson, Gudmundur, Grant, Struan F A, Thorgeirsson, Gudmundur, Sveinbjornsdottir, Sigurlaug, Valdimarsson, Einar M, Matthiasson, Stefan E, Johannsson, Halldor, Gudmundsdottir, Olof, Gurney, Mark E, Sainz, Jesus, Thorhallsdottir, Margret, Andresdottir, Margret, Frigge, Michael L, Topol, Eric J, Kong, Augustine, Gudnason, Vilmundur, Hakonarson, Hakon, Gulcher, Jeffrey R
Published in Nature genetics (01.03.2004)
Published in Nature genetics (01.03.2004)
Get full text
Journal Article
Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis
Ramasamy, Adaikalavan, Trabzuni, Daniah, Forabosco, Paola, Smith, Colin, Walker, Robert, Dillman, Allissa, Sveinbjornsdottir, Sigurlaug, Hardy, John, Weale, Michael E, Ryten, Mina
Published in Multiple sclerosis and related disorders (01.03.2014)
Published in Multiple sclerosis and related disorders (01.03.2014)
Get full text
Journal Article