Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes
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Published in Journal of the American College of Cardiology (17.12.2019)
Published in Journal of the American College of Cardiology (17.12.2019)
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Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Flannick, Jason, Thorleifsson, Gudmar, Beer, Nicola L, Jacobs, Suzanne B R, Grarup, Niels, Burtt, Noël P, Mahajan, Anubha, Fuchsberger, Christian, Atzmon, Gil, Benediktsson, Rafn, Blangero, John, Bowden, Don W, Brandslund, Ivan, Brosnan, Julia, Burslem, Frank, Chambers, John, Cho, Yoon Shin, Christensen, Cramer, Douglas, Desirée A, Duggirala, Ravindranath, Dymek, Zachary, Farjoun, Yossi, Fennell, Timothy, Fontanillas, Pierre, Forsén, Tom, Gabriel, Stacey, Glaser, Benjamin, Gudbjartsson, Daniel F, Hanis, Craig, Hansen, Torben, Hreidarsson, Astradur B, Hveem, Kristian, Ingelsson, Erik, Isomaa, Bo, Johansson, Stefan, Jørgensen, Torben, Jørgensen, Marit Eika, Kathiresan, Sekar, Kong, Augustine, Kooner, Jaspal, Kravic, Jasmina, Laakso, Markku, Lee, Jong-Young, Lind, Lars, Lindgren, Cecilia M, Linneberg, Allan, Masson, Gisli, Meitinger, Thomas, Mohlke, Karen L, Molven, Anders, Morris, Andrew P, Potluri, Shobha, Rauramaa, Rainer, Ribel-Madsen, Rasmus, Richard, Ann-Marie, Rolph, Tim, Salomaa, Veikko, Segrè, Ayellet V, Skärstrand, Hanna, Steinthorsdottir, Valgerdur, Stringham, Heather M, Sulem, Patrick, Tai, E Shyong, Teo, Yik Ying, Teslovich, Tanya, Thorsteinsdottir, Unnur, Trimmer, Jeff K, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Vaziri-Sani, Fariba, Voight, Benjamin F, Wilson, James G, Boehnke, Michael, McCarthy, Mark I, Njølstad, Pål R, Pedersen, Oluf, Groop, Leif, Cox, David R, Stefansson, Kari, Altshuler, David
Published in Nature genetics (01.04.2014)
Published in Nature genetics (01.04.2014)
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Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Sulem, Patrick, Helgason, Hannes, Grarup, Niels, Sigurdsson, Asgeir, Helgadottir, Hafdis T, Johannsdottir, Hrefna, Magnusson, Olafur T, Gudjonsson, Sigurjon A, Justesen, Johanne M, Harder, Marie N, Jørgensen, Marit E, Christensen, Cramer, Brandslund, Ivan, Sandbæk, Annelli, Lauritzen, Torsten, Vestergaard, Henrik, Linneberg, Allan, Jørgensen, Torben, Hansen, Torben, Daneshpour, Maryam S, Fallah, Mohammad-Sadegh, Hreidarsson, Astradur B, Sigurdsson, Gunnar, Azizi, Fereidoun, Benediktsson, Rafn, Masson, Gisli, Helgason, Agnar, Kong, Augustine, Gudbjartsson, Daniel F, Pedersen, Oluf, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature genetics (01.03.2014)
Published in Nature genetics (01.03.2014)
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Parental origin of sequence variants associated with complex diseases
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Published in Nature (London) (17.12.2009)
Published in Nature (London) (17.12.2009)
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The number of adults with incident type 1 diabetes phenotype in Iceland is half the number in children – A population based study
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Published in Diabetes research and clinical practice (01.05.2019)
Published in Diabetes research and clinical practice (01.05.2019)
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Sequence variants associating with urinary biomarkers
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Published in Human molecular genetics (01.04.2019)
Published in Human molecular genetics (01.04.2019)
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Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability
Ivarsdottir, Erna V, Steinthorsdottir, Valgerdur, Daneshpour, Maryam S, Thorleifsson, Gudmar, Sulem, Patrick, Holm, Hilma, Sigurdsson, Snaevar, Hreidarsson, Astradur B, Sigurdsson, Gunnar, Bjarnason, Ragnar, Thorsson, Arni V, Benediktsson, Rafn, Eyjolfsson, Gudmundur, Sigurdardottir, Olof, Olafsson, Isleifur, Zeinali, Sirous, Azizi, Fereidoun, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F, Stefansson, Kari
Published in Nature genetics (01.09.2017)
Published in Nature genetics (01.09.2017)
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott, Laura J, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Johnson, Andrew D, Eicher, John D, Lee, Yeji, Ma, Clement, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Van Zuydam, Natalie R, Chen, Han, Voight, Ben F, Grallert, Harald, Müller-Nurasyid, Martina, Karssen, Lennart C, van Leeuwen, Elisabeth M, Willems, Sara M, Fuchsberger, Christian, Teslovich, Tanya M, Chanda, Pritam, Dina, Christian, Yengo, Loic, Jiang, Longda, Sparso, Thomas, Kestler, Hans A, Eisele, Lewin, Strawbridge, Rona J, Benediktsson, Rafn, Kong, Augustine, Sigurðsson, Gunnar, Kerrison, Nicola D, Luan, Jian'an, Roden, Michael, Thorand, Barbara, Fox, Caroline, Liu, Ching-Ti, Rybin, Denis, Tuomi, Tiinamaija, Couper, David J, Jørgensen, Torben, Linneberg, Allan, Cornelis, Marilyn C, Hunter, David J, Kraft, Peter, Sun, Qi, Perry, John R B, Wood, Andrew R, Zeggini, Eleftheria, Chines, Peter S, Stringham, Heather M, Mühleisen, Thomas W, Nöthen, Markus M, Pechlivanis, Sonali, Humphries, Steve E, Tremoli, Elena, Klopp, Norman, Mӓnnistö, Satu, Charpentier, Guillaume, Eury, Elodie, Gigante, Bruna, Leander, Karin, Bottinger, Erwin P, Blüher, Matthias, Kovacs, Peter, Scapoli, Chiara, Erbel, Raimund, Jöckel, Karl-Heinz, Moebus, Susanne, de Faire, Ulf, Hamsten, Anders, Stumvoll, Michael, Donnelly, Peter J, Frayling, Timothy M, Hattersley, Andrew T, Salomaa, Veikko, Pedersen, Nancy L, Mohlke, Karen L, Barroso, Inês, Lannfelt, Lars, Ingelsson, Erik, Lind, Lars, Lindgren, Cecilia M, Froguel, Philippe, Palli, Domenico, van der Schouw, Yvonne T, Altshuler, David, Groop, Leif C, van Duijn, Cornelia M, Florez, Jose C, Meigs, James B, Boerwinkle, Eric, Strauch, Konstantin, Metspalu, Andres, Morris, Andrew D, Hu, Frank B, Thorsteinsdottir, Unnur, Dupuis, Josée, Morris, Andrew P, Prokopenko, Inga
Published in Diabetes (New York, N.Y.) (01.11.2017)
Published in Diabetes (New York, N.Y.) (01.11.2017)
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan, Anubha, Go, Min Jin, Gaulton, Kyle J, Prokopenko, Inga, Wang, Xu, Abecasis, Goncalo R, Balkau, Beverley, Barnett, Anthony H, Beilby, John, Bell, Graeme I, Burtt, Noël, Chang, Li-Ching, Chen, Han, Chidambaram, Manickam, Chines, Peter S, Cho, Nam H, Cho, Young Min, van Dam, Rob M, Danesh, John, Dedoussis, George, Doney, Alex S, Donnelly, Peter J, Emilsson, Valur, Eriksson, Johan G, Florez, Jose C, Forsen, Tom, Fox, Caroline, Fraser, Ross M, Gigante, Bruna, Grant, George B, Grundberg, Elin, Hamsten, Anders, Hara, Kazuo, Hattersley, Andrew T, Herder, Christian, Hveem, Kristian, Hydrie, Zafar I, Ingelsson, Erik, Islam, Muhammed, Jackson, Anne U, Jafar, Tazeen, Kadowaki, Takashi, Kang, Hyun Min, Kao, Wen Hong L, Kato, Norihiro, Kelly, Ann M, Kim, Sangsoo, Kong, Augustine, Kraft, Peter, Kravic, Jasmina, Kumar, Ashish, Kuusisto, Johanna, Lagou, Vasiliki, Langenberg, Claudia, Lee, Jen-Mai, Li, Yun, Lindholm, Eero, Loos, Ruth J F, Maeda, Shiro, Mägi, Reedik, Männisto, Satu, Matthews, David R, Morris, Andrew D, Navarro, Pau, Pankow, James S, Park, Kyong Soo, Platou, Carl G, Qi, Lu, Rauramaa, Rainer, Raychaudhuri, Soumya, Rybin, Denis, Saaristo, Timo E, Saltevo, Juha, Segrè, Ayellet V, Sennblad, Bengt, Sigurđsson, Gunnar, Stefansson, Kari, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Stringham, Heather M, Suo, Chen, Thorleifsson, Gudmar, Tremoli, Elena, Tsai, Fuu Jen, Tuomilehto, Jaakko, Veglia, Fabrizio, Wareham, Nicholas J, Wilsgaard, Tom, Wilson, James F, Wong, Tien Yin, Wu, Ying, Yamamoto, Ken, Zhang, Fan, Zheng, Wei, Bowden, Donald W, Cox, Nancy J, Cruz, Miguel, Seielstad, Mark, Parra, Esteban J, Morris, Andrew P
Published in Nature genetics (01.03.2014)
Published in Nature genetics (01.03.2014)
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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
MORRIS, Andrew P, VOIGHT, Benjamin F, PROKOPENKO, Inga, HYUN MIN KANG, DINA, Christian, ESKOE, Tonu, FRASER, Ross M, KANONI, Stavroula, KUMAR, Ashish, LAGOU, Vasiliki, LANGENBERG, Claudia, LUAN, Jian'an, TESLOVICH, Tanya M, LINDGREN, Cecilia M, MÜLLER-NURASYID, Martina, PECHLIVANIS, Sonali, RAYNER, N. William, SCOTT, Laura J, WILTSHIRE, Steven, YENGO, Loic, KINNUNEN, Leena, ROSSIN, Elizabeth J, RAYCHAUDHURI, Soumya, FERREIRA, Teresa, JOHNSON, Andrew D, DIMAS, Antigones, LOOS, Ruthj F, VEDANTAM, Sailaja, HAN CHEN, FLOREZ, Jose C, FOX, Caroline, LIU, Ching-Ti, RYBIN, Denis, COUPER, David J, SEGRE, Ayellet V, KAO, Wen Hong L, MAN LI, CORNELIS, Marilyn C, KRAFT, Peter, QI SUN, VAN DAM, Rob M, STRINGHAM, Heather M, CHINES, Peter S, FISCHER, Krista, FONTANILLAS, Pierre, STEINTHORSDOTTIR, Valgerdur, HOLMEN, Oddgeir L, HUNT, Sarah E, JACKSON, Anne U, KONG, Augustine, LAWRENCE, Robert, MEYER, Julia, PERRY, John R. B, PLATOU, Carl G. P, POTTER, Simon, REHNBERG, Emil, STRAWBRIDGE, Rona J, KHAN, Hassan, GRALLERT, Harald, MAHAJAN, Anubha
Published in Nature genetics (01.09.2012)
Published in Nature genetics (01.09.2012)
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
Mägi, Reedik, Robertson, Neil, Prokopenko, Inga, Green, Todd, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Kwan, Phoenix, Lu, Yingchang, van de Bunt, Martijn, Chalisey, Anil, Abecasis, Gonçalo R, Charpentier, Guillaume, Chines, Peter S, Doney, Alex S F, Edkins, Sarah, Esko, Tonu, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Gieger, Christian, Hassinen, Maija, Have, Christian T, Herder, Christian, Hreidarsson, Astradur B, Hunter, David J, Jørgensen, Marit E, Jørgensen, Torben, Kong, Augustine, Kraft, Peter, Kravic, Jasmina, Liang, Liming, Lindholm, Eero, Liu, Ching-Ti, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Müller-Nurasyid, Martina, Navarro, Carmen, Oskolkov, Nikolay N, Palli, Domenico, Perry, John R B, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Stančáková, Alena, Steinbach, Gerald, Strauch, Konstantin, Stringham, Heather M, Thorand, Barbara, Tonjes, Anke, Wiltshire, Steven, Zeggini, Eleftheria, Dunham, Ian, Pasquali, Lorenzo, Loos, Ruth J F, Boerwinkle, Eric, Thorsteinsdottir, Unnur, Stefansson, Kari, Rauramaa, Rainer, Stumvoll, Michael, Pedersen, Nancy L, Keinanen-Kiukaanniemi, Sirkka M, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Laakso, Markku, Jöcke, Karl-Heinz, Ripatti, Samuli, Boehm, Bernhard O, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Hveem, Kristian, Njølstad, Inger, Deloukas, Panagiotis, Frayling, Timothy M, Hattersley, Andrew T, de Faire, Ulf, Hamsten, Anders, Illig, Thomas, Cauchi, Stephane, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Pedersen, Oluf, Morris, Andrew D, Palmer, Collin N A, Kathiresan, Sekar, Melander, Olle, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, McCarthy, Mark I, Morris, Andrew P
Published in Nature genetics (01.12.2015)
Published in Nature genetics (01.12.2015)
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FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Saevarsdottir, Saedis, Olafsdottir, Thorunn A, Ivarsdottir, Erna V, Halldorsson, Gisli H, Gunnarsdottir, Kristbjorg, Sigurdsson, Asgeir, Johannesson, Ari, Sigurdsson, Jon K, Juliusdottir, Thorhildur, Lund, Sigrun H, Arnthorsson, Asgeir O, Styrmisdottir, Edda L, Gudmundsson, Julius, Grondal, Gerdur M, Steinsson, Kristjan, Alfredsson, Lars, Askling, Johan, Benediktsson, Rafn, Bjarnason, Ragnar, Geirsson, Arni J, Gudbjornsson, Bjorn, Gudjonsson, Hallgrimur, Hjaltason, Haukur, Hreidarsson, Astradur B, Klareskog, Lars, Kockum, Ingrid, Kristjansdottir, Helga, Love, Thorvardur J, Ludviksson, Bjorn R, Olsson, Tomas, Onundarson, Pall T, Orvar, Kjartan B, Padyukov, Leonid, Sigurgeirsson, Bardur, Tragante, Vinicius, Bjarnadottir, Kristbjorg, Rafnar, Thorunn, Masson, Gisli, Sulem, Patrick, Gudbjartsson, Daniel F, Melsted, Pall, Thorleifsson, Gudmar, Norddahl, Gudmundur L, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Stefansson, Kari
Published in Nature (London) (27.08.2020)
Published in Nature (London) (27.08.2020)
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Painful autoimmune thyroiditis occurring on amiodarone therapy
Gudbjörnsson, B, Kristinsson, A, Geirsson, G, Hreidarsson, A B
Published in Acta medica Scandinavica (01.01.1987)
Published in Acta medica Scandinavica (01.01.1987)
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Frequency of deletion of short arm satellites in acrocentric chromosomes
Nielsen, Johannes, Friedrich, Ursula, Hreidarsson, Ástrádur B.
Published in Journal of medical genetics (01.06.1974)
Published in Journal of medical genetics (01.06.1974)
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Screening compliance and visual outcome in diabetes
Zoega, Gunnar Már, Gunnarsdóttir, Þóra, Björnsdóttir, Sigríður, Hreiðarsson, Ástradur B., Viggósson, Guðmundur, Stefánsson, Einar
Published in Acta ophthalmologica Scandinavica (01.12.2005)
Published in Acta ophthalmologica Scandinavica (01.12.2005)
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