Search Results

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L., Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G., Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H., Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C., de la Chapelle, Albert, Jonasson, Jon G., Goldberg, Richard M., Stefansson, Kari
Published in Nature Communications (2017)

Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death.

by Sveinbjornsson, Gardar, Olafsdottir, Eva F, Thorolfsdottir, Rosa B, Davidsson, Olafur B, Helgadottir, Anna, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Bjornsson, Eythor, Jensson, Brynjar O, Arnadottir, Gudny A, Kristinsdottir, Hallfridur, Stephensen, Sigurdur S, Oskarsson, Gylfi, Gudbjartsson, Tomas, Sigurdsson, Emil L, Andersen, Karl, Danielsen, Ragnar, Arnar, David O, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Sulem, Patrick, Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari
Published in Circulation: Genomic and Precision Medicine (2018)

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

by Gudbjartsson, Daniel F, Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Ng, Maggie C Y, Baum, Larry, So, Wing Yee, Wong, Ka Sing, Chan, Juliana C N, Gieger, Christian, Wichmann, H-Erich, Gschwendtner, Andreas, Dichgans, Martin, Kuhlenbäumer, Gregor, Berger, Klaus, Ringelstein, E Bernd, Bevan, Steve, Markus, Hugh S, Kostulas, Konstantinos, Hillert, Jan, Sveinbjörnsdóttir, Sigurlaug, Valdimarsson, Einar M, Løchen, Maja-Lisa, Ma, Ronald C W, Darbar, Dawood, Kong, Augustine, Arnar, David O, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2009)

The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland

by Helgason, Agnar, Palsson, Snaebjorn, Stefansson, Hreinn, St. Clair, David, Andreassen, Ole A., Kong, Augustine, Stefansson, Kari, Price, Alkes, Reich, David Emil
Published in PLoS Genetics (2009)

Familiality of kidney stone disease in Iceland

by Edvardsson, Vidar, Palsson, Runolfur, Indridason, Olafur, Thorvaldsson, Sverrir, Stefansson, Kari
Published in Scandinavian Journal of Urology and Nephrology (2009)

Familiality of kidney stone disease in Iceland

by Edvardsson, Vidar O., Palsson, Runolfur, Indridason, Olafur S., Thorvaldsson, Sverrir, Stefansson, Kari
Published in Scandinavian Journal of Urology and Nephrology (2009)

Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency

by Runolfsdottir, Hrafnhildur L., Sayer, John A., Indridason, Olafur S., Edvardsson, Vidar O., Jensson, Brynjar O., Arnadottir, Gudny A., Gudjonsson, Sigurjon A., Fridriksdottir, Run, Katrinardottir, Hildigunnur, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari, Palsson, Runolfur
Published in European Journal of Human Genetics (2021)

Linkage of essential hypertension to chromosome 18q

by Kristjansson, Kristleifur, Manolescu, Andrei, Kristinsson, Arni, Hardarson, Thordur, Knudsen, Helga, Ingason, Sigurdur, Thorleifsson, Gudmar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefansson, Kari
Published 2008

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

by Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A., Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H., Kristjansson, Ragnar P., Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P., Melsted, Pall, Halldorsson, Bjarni V., Lund, Sigrun H., Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Published in Communications Biology (2020)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L, Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G, Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H, Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C, de la Chapelle, Albert, Jonasson, Jon G, Goldberg, Richard M, Stefansson, Kari
Published in Nature Communications (2017)

Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family

by Amundadottir, Laufey T, Thorvaldsson, Sverrir, Gudbjartsson, Daniel F, Sulem, Patrick, Kristjansson, Kristleifur, Arnason, Sigurdur, Gulcher, Jeffrey R, Bjornsson, Johannes, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in PLoS Medicine (2004)

A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas

by Gudbjartsson, Tomas, Jonasdottir, Thora J, Thoroddsen, Asgeir, Einarsson, Gudmundur V, Jonsdottir, Gudrun M, Kristjansson, Kristleifur, Hardarson, Sverrir, Magnusson, Kjartan, Gulcher, Jeffrey, Stefansson, Kari, Amundadottir, Laufey T
Published in International Journal of Cancer (2008)

Genetics of Psoriasis in Iceland: Evidence for Linkage of Subphenotypes to Distinct Loci

by Karason, Ari, Gudjonsson, Johann E., Jónsson, Hjörtur H., Hauksson, Valdimar B., Hjaltey Runarsdottir, E., Stefansson, Kari, Valdimarsson, Helgi, Gulcher, Jeffrey R.
Published in Journal of Investigative Dermatology (2005)

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

by Gretarsdottir, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J, Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Urbonavicius, Sigitas, Lindblad, Bengt, Gottsäter, Anders, Gaetani, Eleonora, Pola, Roberto, Wells, Philip, Rodger, Marc, Forgie, Melissa, Langlois, Nicole, Corral, Javier, Vicente, Vicente, Fontcuberta, Jordi, España, Francisco, Grarup, Niels, Jørgensen, Torben, Witte, Daniel R, Hansen, Torben, Pedersen, Oluf, Aben, Katja K, de Graaf, Jacqueline, Holewijn, Suzanne, Folkersen, Lasse, Franco-Cereceda, Anders, Eriksson, Per, Collier, David A, Stefansson, Hreinn, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, Valdimarsson, Einar M, Magnadottir, Hulda B, Sveinbjornsdottir, Sigurlaug, Olafsson, Isleifur, Magnusson, Magnus Karl, Palmason, Robert, Haraldsdottir, Vilhelmina, Andersen, Karl, Onundarson, Pall T, Thorgeirsson, Gudmundur, Kiemeney, Lambertus A, Powell, Janet T, Carey, David J, Kuivaniemi, Helena, Lindholt, Jes S., Jones, Gregory T, Kong, Augustine, Blankensteijn, Jan D, Matthiasson, Stefan E, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Weighting sequence variants based on their annotation increases power of whole-genome association studies.

by Sveinbjornsson, Gardar, Albrechtsen, Anders, Zink, Florian, Gudjonsson, Sigurjón A, Oddson, Asmundur, Másson, Gísli, Holm, Hilma, Kong, Augustine, Thorsteinsdottir, Unnur, Sulem, Patrick, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Nature Genetics (2016)

Localization of a gene for migraine without aura to chromosome 4q21.

by Bjornsson, Asgeir, Gudmundsson, Gretar, Gudfinnsson, Einar, Hrafnsdottir, María, Benedikz, John, Skuladottir, Svanhildur, Kristjansson, Kristleifur, Frigge, Michael L, Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R
Published 2008

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.

by Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A, Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H, Kristjansson, Ragnar P, Frigge, Michael L, Stefansdottir, Lilja, Sigurdsson, Jon K, Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P, Melsted, Pall, Halldorsson, Bjarni V, Lund, Sigrun H, Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Published in Communications Biology (2020)

Large-scale whole-genome sequencing of the Icelandic population

by Gudbjartsson, Daniel F, Helgason, Hannes, Gudjonsson, Sigurjon A, Zink, Florian, Oddson, Asmundur, Gylfason, Arnaldur, Besenbacher, Soren, Magnusson, Gisli, Halldorsson, Bjarni V, Hjartarson, Eirikur, Sigurdsson, Gunnar Th, Stacey, Simon N, Frigge, Michael L, Holm, Hilma, Saemundsdottir, Jona, Helgadottir, Hafdis Th, Johannsdottir, Hrefna, Sigfusson, Gunnlaugur, Thorgeirsson, Gudmundur, Sverrisson, Jon Th, Gretarsdottir, Solveig, Walters, G Bragi, Rafnar, Thorunn, Thjodleifsson, Bjarni, Bjornsson, Einar S, Olafsson, Sigurdur, Thorarinsdottir, Hildur, Steingrimsdottir, Thora, Gudmundsdottir, Thora S, Theodors, Asgeir, Jonasson, Jon G, Sigurdsson, Asgeir, Bjornsdottir, Gyda, Jonsson, Jon J, Thorarensen, Olafur, Ludvigsson, Petur, Gudbjartsson, Hakon, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Olafsson, Isleifur, Arnar, David O, Magnusson, Olafur Th, Kong, Augustine, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Sulem, Patrick, Stefansson, Kari
Published in Nature Genetics (2015)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L., Einarsdóttir, Sylvía, Sigurðsson, Ásgeir, Hampel, Heather, Snaebjornsson, Petur, Másson, Gísli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, sulem, patrick, Stefansson, Tryggvi, Shields, Peter G., Sigurðsson, Fridbjörn, Bekaii-Saab, Tanios, Moller, Pall H., Steinarsdóttir, Margrét, Alexíusdóttir, Kristín, Hitchins, Megan, Pritchard, Colin C., de la Chapelle, Albert, Jónasson, Jón Gunnlaugur, Goldberg, Richard M., Stefansson, Kari
Published in Nature Communications (2017)

Abstract 4405: Sequence Variant for Atrial Fibrillation on Chromosome 4q25 near the PITX2 Gene Increases Risk for Recurrent AF

by Gulcher, Jeffrey, Holm, Hilma, Gudbjartsson, Daniel, Arnar, David, Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Circulation (2008)