Quadricuspid Aortic Valve

por Holm, Hilma, Jacobson, Stuart, Reul, George J., Stainback, Raymond F.
Publicado 2004

Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden

por Christiansen, Morten Krogh, Nissen, Louise, Winther, Simon, Møller, Peter Loof, Frost, Lars, Johansen, Jane Kirk, Jensen, Henrik Kjærulf, Guðbjartsson, Daníel, Holm, Hilma, Stefánsson, Kári, Bøtker, Hans Erik, Bøttcher, Morten, Nyegaard, Mette
Publicado en J Am Heart Assoc (2020)

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease

por Patel, Riyaz S., Su, Shaoyong, Neeland, Ian J., Ahuja, Ayushi, Veledar, Emir, Zhao, Jinying, Helgadottir, Anna, Holm, Hilma, Gulcher, Jeffrey R., Stefansson, Kari, Waddy, Salina, Vaccarino, Viola, Zafari, A. Maziar, Quyyumi, Arshed A.
Publicado 2010

Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

por Helgadottir, Anna, Sulem, Patrick, Thorgeirsson, Gudmundur, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Jensson, Brynjar Ö, Arnadottir, Gudny A, Olafsson, Isleifur, Eyjolfsson, Gudmundur I, Sigurdardottir, Olof, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari
Publicado en Eur Heart J (2018)

Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

por Ivarsdottir, Erna V., Benonisdottir, Stefania, Thorleifsson, Gudmar, Sulem, Patrick, Oddsson, Asmundur, Styrkarsdottir, Unnur, Kristmundsdottir, Snaedis, Arnadottir, Gudny A., Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Zoega, Gunnar M., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonasson, Fridbert, Holm, Hilma, Stefansson, Kari
Publicado en Nat Commun (2019)

Common and rare variants associated with kidney stones and biochemical traits

por Oddsson, Asmundur, Sulem, Patrick, Helgason, Hannes, Edvardsson, Vidar O., Thorleifsson, Gudmar, Sveinbjörnsson, Gardar, Haraldsdottir, Eik, Eyjolfsson, Gudmundur I., Sigurdardottir, Olof, Olafsson, Isleifur, Masson, Gisli, Holm, Hilma, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Indridason, Olafur S., Palsson, Runolfur, Stefansson, Kari
Publicado en Nat Commun (2015)

Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults

por Björnsson, Eythór, Thorleifsson, Guðmar, Helgadóttir, Anna, Guðnason, Thórarinn, Guðbjartsson, Tómas, Andersen, Karl, Grétarsdóttir, Sólveig, Ólafsson, Ísleifur, Tragante, Vinicius, Ólafsson, Ólafur Hreiðar, Jónsdóttir, Birna, Eyjólfsson, Guðmundur I., Sigurðardóttir, Ólöf, Thorgeirsson, Guðmundur, Guðbjartsson, Daníel F., Thorsteinsdóttir, Unnur, Hólm, Hilma, Stefánsson, Kári
Publicado en JAMA Cardiol (2019)

A missense variant in PLEC increases risk of atrial fibrillation

por Thorolfsdottir, Rosa B., Sveinbjornsson, Gardar, Sulem, Patrick, Helgadottir, Anna, Gretarsdottir, Solveig, Benonisdottir, Stefania, Magnusdottir, Audur, Davidsson, Olafur B., Rajamani, Sridharan, Roden, Dan M., Darbar, Dawood, Pedersen, Terje R., Sabatine, Marc S., Jonsdottir, Ingileif, Arnar, David O., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Kari
Publicado en J Am Coll Cardiol (2017)

Predicting the probability of death using proteomics

por Eiriksdottir, Thjodbjorg, Ardal, Steinthor, Jonsson, Benedikt A., Lund, Sigrun H., Ivarsdottir, Erna V., Norland, Kristjan, Ferkingstad, Egil, Stefansson, Hreinn, Jonsdottir, Ingileif, Holm, Hilma, Rafnar, Thorunn, Saemundsdottir, Jona, Norddahl, Gudmundur L., Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F., Sulem, Patrick, Thorsteinsdottir, Unnur, Stefansson, Kari, Ulfarsson, Magnus O.
Publicado en Commun Biol (2021)

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

por Gudbjartsson, Daniel F., Holm, Hilma, Indridason, Olafur S., Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C. H., den Heijer, Martin, Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S., Eyjolfsson, Gudmundur I., Kiemeney, Lambertus A., Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2010

A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta

por Bjornsson, Thorsteinn, Thorolfsdottir, Rosa B, Sveinbjornsson, Gardar, Sulem, Patrick, Norddahl, Gudmundur L, Helgadottir, Anna, Gretarsdottir, Solveig, Magnusdottir, Audur, Danielsen, Ragnar, Sigurdsson, Emil L, Adalsteinsdottir, Berglind, Gunnarsson, Sverrir I, Jonsdottir, Ingileif, Arnar, David O, Helgason, Hrodmar, Gudbjartsson, Tomas, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Holm, Hilma, Stefansson, Kari
Publicado en Eur Heart J (2018)

Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

por Gudbjartsson, Daniel F., Holm, Hilma, Indridason, Olafur S., Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C. H., den Heijer, Martin, Wetzels, Jack F. M., Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S., Eyjolfsson, Gudmundur I., Kiemeney, Lambertus A., Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2010

Sequence variants with large effects on cardiac electrophysiology and disease

por Norland, Kristjan, Sveinbjornsson, Gardar, Thorolfsdottir, Rosa B., Davidsson, Olafur B., Tragante, Vinicius, Rajamani, Sridharan, Helgadottir, Anna, Gretarsdottir, Solveig, van Setten, Jessica, Asselbergs, Folkert W., Sverrisson, Jon Th., Stephensen, Sigurdur S., Oskarsson, Gylfi, Sigurdsson, Emil L., Andersen, Karl, Danielsen, Ragnar, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Arnar, David O., Sulem, Patrick, Holm, Hilma, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado en Nat Commun (2019)

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

por Gretarsdottir, Solveig, Helgason, Hannes, Helgadottir, Anna, Sigurdsson, Asgeir, Thorleifsson, Gudmar, Magnusdottir, Audur, Oddsson, Asmundur, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, de Graaf, Jacqueline, Daneshpour, Maryam S., Hedayati, Mehdi, Azizi, Fereidoun, Grarup, Niels, Jørgensen, Torben, Vestergaard, Henrik, Hansen, Torben, Eyjolfsson, Gudmundur, Sigurdardottir, Olof, Olafsson, Isleifur, Kiemeney, Lambertus A., Pedersen, Oluf, Sulem, Patrick, Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F., Holm, Hilma, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado en PLoS Genet (2015)

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

por Kristjansson, Ragnar P., Oddsson, Asmundur, Helgason, Hannes, Sveinbjornsson, Gardar, Arnadottir, Gudny A., Jensson, Brynjar O., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Bragi Walters, G., Sulem, Gerald, Oskarsdottir, Arna, Benonisdottir, Stefania, Davidsson, Olafur B., Masson, Gisli, Th Magnusson, Olafur, Holm, Hilma, Sigurdardottir, Olof, Jonsdottir, Ingileif, Eyjolfsson, Gudmundur I., Olafsson, Isleifur, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari
Publicado en Nat Commun (2016)

A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

por Oskarsson, Gudjon R., Kristjansson, Ragnar P., Lee, Amy L., Sveinbjornsson, Gardar, Magnusson, Magnus K., Ivarsdottir, Erna V., Benonisdottir, Stefania, Oddsson, Asmundur, Davidsson, Olafur B., Saemundsdottir, Jona, Halldorsson, Gisli H., Arthur, Joseph, Arnadottir, Gudny A., Masson, Gisli, Jensson, Brynjar O., Holm, Hilma, Olafsson, Isleifur, Onundarson, Pall T., Gudbjartsson, Daniel F., Norddahl, Gudmundur L., Thorsteinsdottir, Unnur, Sulem, Patrick, Stefansson, Kari
Publicado en Commun Biol (2018)

Sequence variant at 4q25 near PITX2 associates with appendicitis

por Kristjansson, Ragnar P., Benonisdottir, Stefania, Oddsson, Asmundur, Galesloot, Tessel E., Thorleifsson, Gudmar, Aben, Katja K., Davidsson, Olafur B., Jonsson, Stefan, Arnadottir, Gudny A., Jensson, Brynjar O., Walters, G. Bragi, Sigurdsson, Jon K., Sigurdsson, Snaevar, Holm, Hilma, Arnar, David O., Thorgeirsson, Gudmundur, Alexiusdottir, Kristin, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Kiemeney, Lambertus A., Jonsson, Thorvaldur, Gudbjartsson, Daniel F., Rafnar, Thorunn, Sulem, Patrick, Stefansson, Kari
Publicado en Sci Rep (2017)

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

por Surakka, Ida, Fritsche, Lars G., Zhou, Wei, Backman, Joshua, Kosmicki, Jack A., Lu, Haocheng, Brumpton, Ben, Nielsen, Jonas B., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Wolford, Brooke, Graham, Sarah E., Chen, Y. Eugene, Lee, Seunggeun, Kang, Hyun Min, Langhammer, Arnulf, Forsmo, Siri, Åsvold, Bjørn O., Styrkarsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel, Stefansson, Kari, Baras, Aris, Abecasis, Goncalo R., Hveem, Kristian, Willer, Cristen J.
Publicado en Nat Commun (2020)

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

por Ivarsdottir, Erna V., Holm, Hilma, Benonisdottir, Stefania, Olafsdottir, Thorhildur, Sveinbjornsson, Gardar, Thorleifsson, Gudmar, Eggertsson, Hannes P., Halldorsson, Gisli H., Hjorleifsson, Kristjan E., Melsted, Pall, Gylfason, Arnaldur, Arnadottir, Gudny A., Oddsson, Asmundur, Jensson, Brynjar O., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Juliusdottir, Thorhildur, Stefansdottir, Lilja, Tragante, Vinicius, Halldorsson, Bjarni V., Petersen, Hannes, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Sulem, Patrick, Hinriksdottir, Ingibjorg, Jonsdottir, Ingileif, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado en Commun Biol (2021)

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

por Holm, Hilma, Gudbjartsson, Daniel F, Sulem, Patrick, Masson, Gisli, Helgadottir, Hafdis Th, Zanon, Carlo, Magnusson, Olafur Th, Helgason, Agnar, Saemundsdottir, Jona, Gylfason, Arnaldur, Stefansdottir, Hrafnhildur, Gretarsdottir, Solveig, Matthiasson, Stefan E, Thorgeirsson, Guðmundur, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Stefansson, Hreinn, Werge, Thomas, Rafnar, Thorunn, Kiemeney, Lambertus A, Parvez, Babar, Muhammad, Raafia, Roden, Dan M, Darbar, Dawood, Thorleifsson, Gudmar, Walters, G Bragi, Kong, Augustine, Thorsteinsdottir, Unnur, Arnar, David O, Stefansson, Kari
Publicado 2011