Search Results

A strong heritability of psoriatic arthritis over four generations--the Reykjavik Psoriatic Arthritis Study

by Karason, A, Love, T J, Gudbjornsson, B
Published in Rheumatology (2009)

A major susceptibility gene for asthma maps to chromosome 14q24

by Hakonarson, Hakon, Bjornsdottir, Unnur S, Halapi, Eva, Palsson, Snaebjorn, Adalsteinsdottir, Elva, Gislason, David, Finnbogason, Gudmundur, Gislason, Thorarinn, Kristjansson, Kristleifur, Arnason, Thor, Birkisson, Illugi, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefansson, Kari
Published in The American Journal of Human Genetics (2008)

The Ethics of Big Data in Genomics: The Instructive Icelandic Saga of the Incidentalome

by Gitter, Donna M.
Published 2019

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.

by 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, Stefansson, Kari
Published in Nature Genetics (2009)

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.

by Thorleifsson, Gudmar, Holm, Hilma, Edvardsson, Vidar, Walters, G Bragi, Styrkarsdottir, Unnur, Gudbjartsson, Daniel F, Sulem, Patrick, Halldorsson, Bjarni V, de Vegt, Femmie, d'Ancona, Frank C H, den Heijer, Martin, Franzson, Leifur, Christiansen, Claus, Alexandersen, Peter, Rafnar, Thorunn, Kristjansson, Kristleifur, Sigurdsson, Gunnar, Kiemeney, Lambertus A, Bodvarsson, Magnus, Indridason, Olafur S, Palsson, Runolfur, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2009)

Genetic determinants of hair, eye and skin pigmentation in Europeans

by Sulem, Patrick, Gudbjartsson, Daniel F, Stacey, Simon N, Helgason, Agnar, Rafnar, Thorunn, Magnusson, Kristinn P, Manolescu, Andrei, Karason, Ari, Palsson, Arnar, Thorleifsson, Gudmar, Jakobsdottir, Margret, Steinberg, Stacy, Pálsson, Snaebjörn, Jonasson, Fridbert, Sigurgeirsson, Bardur, Thorisdottir, Kristin, Ragnarsson, Rafn, Benediktsdottir, Kristrun R, Aben, Katja K, Kiemeney, Lambertus A, Olafsson, Jon H, Gulcher, Jeffrey, Kong, Augie, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2008)

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

by Stefansson, Hreinn, Sarginson, Jane, Kong, Augustine, Yates, Phil, Steinthorsdottir, Valgerdur, Gudfinnsson, Einar, Gunnarsdottir, Steinunn, Walker, Nicholas, Petursson, Hannes, Crombie, Caroline, Ingason, Andres, Gulcher, Jeffrey R, Stefansson, Kari, St Clair, David
Published 2010

Rare genetic variants affecting platelet count: Results from a genome-wide association study

by Jóhann Hauksson 1992-
Published 2019

Composition of the founding population of Iceland: Biological distance and morphological variation in early historic Atlantic Europe

by Hallgrímsson, Benedikt, Ó Donnabháin, Barra, Walters, G. Bragi, Cooper, David M.L., Guđbjartsson, Daníel, Stefánsson, Kari
Published in American Journal of Physical Anthropology (2003)

Pediatric delirium in autism spectrum disorders. Clinical and genetic polymorphism, connection with ontogenetic epileptic encephalopathies, schizophrenia, bipolar disorder

by Martsenkovsky, I.A., Martsenkovska, I.I., Makarenko, H.V., Skrypnyk, T.O., Zdoryk, I.F.
Published 2021

Pediatric delirium in autism spectrum disorders. Clinical and genetic polymorphism, connection with ontogenetic epileptic encephalopathies, schizophrenia, bipolar disorder

by Martsenkovsky, I.A., Martsenkovska, I.I., Makarenko, H.V., Skrypnyk, T.O., Zdoryk, I.F.
Published 2021

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)

Genetics of cardiovascular diseases: lessons learned from a decade of genomics research in Iceland.

by Arnar, David O, Andersen, Karl, Thorgeirsson, Gudmundur
Published in Scandinavian Cardiovascular Journal (2017)

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)

Anxiety with panic disorder linked to chromosome 9q in Iceland

by Thorgeirsson, Thorgeir E, Oskarsson, Högni, Desnica, Natasa, Kostic, Jelena Pop, Stefansson, Jon G, Kolbeinsson, Halldor, Lindal, Eirikur, Gagunashvili, Nikolai, Frigge, Michael L, Kong, Augustine, Stefansson, Kari, Gulcher, Jeffrey R
Published in The American Journal of Human Genetics (2007)

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

by Stefansdottir, Vigdis, Thorolfsdottir, Eirny, Hognason, Hakon B., Patch, Christine, van El, Carla, Hentze, Sabine, Cordier, Christophe, Mendes, Álvaro, Jonsson, Jon J.
Published in European Journal of Human Genetics (2020)

Genetic factors contribute to the risk of developing endometriosis.

by Stefansson, H, Geirsson, R T, Steinthorsdottir, V, Jonsson, H, Manolescu, A, Kong, A, Ingadottir, G, Gulcher, J, Stefansson, K
Published in Human Reproduction (2008)

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

by Sulem, P, Gudbjartsson, D F, Rafnar, T, Holm, H, Olafsdottir, E J, Olafsdottir, G H, Jonsson, T, Alexandersen, P, Feenstra, B, Boyd, H A, Aben, K K, Verbeek, A L, Roeleveld, N, Jonasdottir, A, Styrkarsdottir, U, Steinthorsdottir, V, Karason, A, Stacey, S N, Gudmundsson, J, Jakobsdottir, M, Thorleifsson, G, Hardarson, G, Gulcher, J, Kong, A, Kiemeney, LA, Melbye, M, Christiansen, C, Tryggvadottir, L, Thorsteinsdottir, U, Stefansson, K
Published in Nature Genetics (2009)

Several common variants modulate heart rate, PR interval and QRS duration

by Holm, Hilma, Gudbjartsson, Daniel F, Arnar, David O, Thorleifsson, Gudmar, Thorgeirsson, Gudmundur, Stefansdottir, Hrafnhildur, Gudjonsson, Sigurjon A, Jonasdottir, Aslaug, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Løchen, Maja-Lisa, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature Genetics (2010)

Additional file 19 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis