Relatedness disequilibrium regression estimates heritability without environmental bias

por Young, Alexander I., Frigge, Michael L., Gudbjartsson, Daniel F., Thorleifsson, Gudmar, Bjornsdottir, Gyda, Sulem, Patrick, Masson, Gisli, Thorsteinsdottir, Unnur, Stefansson, Kari, Kong, Augustine
Publicado en Nat Genet (2018)

Localization of a Gene for Migraine without Aura to Chromosome 4q21

por Björnsson, Ásgeir, Gudmundsson, Grétar, Gudfinnsson, Einar, Hrafnsdóttir, María, Benedikz, John, Skúladóttir, Svanhildur, Kristjánsson, Kristleifur, Frigge, Michael L., Kong, Augustine, Stefánsson, Kári, Gulcher, Jeffrey R.
Publicado 2003

Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland

por 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.
Publicado 2003

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3

por Stefánsson, Stefán Einar, Jónsson, Helgi, Ingvarsson, Thorvaldur, Manolescu, Ileana, Jónsson, Hjörtur H., Ólafsdóttir, Guðbjörg, Pálsdóttir, Ebba, Stefánsdóttir, Gerður, Sveinbjörnsdóttir, Guðfinna, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári
Publicado 2003

A Major Susceptibility Gene for Asthma Maps to Chromosome 14q24

por 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
Publicado 2002

A Susceptibility Gene for Psoriatic Arthritis Maps to Chromosome 16q: Evidence for Imprinting

por Karason, Ari, Gudjonsson, Johann E., Upmanyu, Ruchi, Antonsdottir, Arna A., Hauksson, Valdimar B., Runasdottir, E. Hjaltey, Jonsson, Hjortur H., Gudbjartsson, Daniel F., Frigge, Michael L., Kong, Augustine, Stefansson, Kari, Valdimarsson, Helgi, Gulcher, Jeffrey R.
Publicado 2003

Selection against variants in the genome associated with educational attainment

por Kong, Augustine, Frigge, Michael L., Thorleifsson, Gudmar, Stefansson, Hreinn, Young, Alexander I., Zink, Florian, Jonsdottir, Gudrun A., Okbay, Aysu, Sulem, Patrick, Masson, Gisli, Gudbjartsson, Daniel F., Helgason, Agnar, Bjornsdottir, Gyda, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado en Proc Natl Acad Sci U S A (2017)

Localization of a Gene for Peripheral Arterial Occlusive Disease to Chromosome 1p31

por Gudmundsson, Gudmundur, Matthiasson, Stefan E., Arason, Haukur, Johannsson, Halldor, Runarsson, Freyr, Bjarnason, Hjördis, Helgadottir, Katrin, Thorisdottir, Steinthora, Ingadottir, Gudrun, Lindpaintner, Klaus, Sainz, Jesus, Gudnason, Vilmundur, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefansson, Kari
Publicado 2002

Detection of sharing by descent, long-range phasing and haplotype imputation

por Kong, Augustine, Masson, Gisli, Frigge, Michael L., Gylfason, Arnaldur, Zusmanovich, Pasha, Thorleifsson, Gudmar, Olason, Pall I., Ingason, Andres, Steinberg, Stacy, Rafnar, Thorunn, Sulem, Patrick, Mouy, Magali, Jonsson, Frosti, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Stefansson, Hreinn, Stefansson, Kari
Publicado en Nat Genet (2008)

Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

por Styrkarsdottir, Unnur, Cazier, Jean-Baptiste, Kong, Augustine, Rolfsson, Ottar, Larsen, Helene, Bjarnadottir, Emma, Johannsdottir, Vala D, Sigurdardottir, Margret S, Bagger, Yu, Christiansen, Claus, Reynisdottir, Inga, Grant, Struan F. A, Jonasson, Kristjan, Frigge, Michael L, Gulcher, Jeffrey R, Sigurdsson, Gunnar, Stefansson, Kari
Publicado 2003

Reproductive fitness and genetic risk of psychiatric disorders in the general population

por Mullins, Niamh, Ingason, Andrés, Porter, Heather, Euesden, Jack, Gillett, Alexandra, Ólafsson, Sigurgeir, Gudbjartsson, Daniel F., Lewis, Cathryn M., Sigurdsson, Engilbert, Saemundsen, Evald, Gudmundsson, Ólafur Ó, Frigge, Michael L., Kong, Augustine, Helgason, Agnar, Walters, G. Bragi, Gustafsson, Omar, Stefansson, Hreinn, Stefansson, Kari
Publicado en Nat Commun (2017)

Rate of de novo mutations, father’s age, and disease risk

por Kong, Augustine, Frigge, Michael L., Masson, Gisli, Besenbacher, Soren, Sulem, Patrick, Magnusson, Gisli, Gudjonsson, Sigurjon A., Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Wong, Wendy, Sigurdsson, Gunnar, Walters, G. Bragi, Steinberg, Stacy, Helgason, Hannes, Thorleifsson, Gudmar, Gudbjartsson, Daniel F., Helgason, Agnar, Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2012

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

por Zink, Florian, Stacey, Simon N., Norddahl, Gudmundur L., Frigge, Michael L., Magnusson, Olafur T., Jonsdottir, Ingileif, Thorgeirsson, Thorgeir E., Sigurdsson, Asgeir, Gudjonsson, Sigurjon A., Gudmundsson, Julius, Jonasson, Jon G., Tryggvadottir, Laufey, Jonsson, Thorvaldur, Helgason, Agnar, Gylfason, Arnaldur, Sulem, Patrick, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Masson, Gisli, Kong, Augustine, Stefansson, Kari
Publicado en Blood (2017)

Localization of a Susceptibility Gene for Type 2 Diabetes to Chromosome 5q34–q35.2

por Reynisdottir, Inga, Thorleifsson, Gudmar, Benediktsson, Rafn, Sigurdsson, Gunnar, Emilsson, Valur, Einarsdottir, Anna Sigurlin, Hjorleifsdottir, Eyrun Edda, Orlygsdottir, Gudbjorg Th., Bjornsdottir, Gudrun Thora, Saemundsdottir, Jona, Halldorsson, Skarphedinn, Hrafnkelsdottir, Soffia, Sigurjonsdottir, Steinunn Bjorg, Steinsdottir, Svana, Martin, Mitchell, Kochan, Jarema P., Rhees, Brian K., Grant, Struan F. A., Frigge, Michael L., Kong, Augustine, Gudnason, Vilmundur, Stefansson, Kari, Gulcher, Jeffrey R.
Publicado 2003

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

por Bjornsdottir, Gyda, Benonisdottir, Stefania, Sveinbjornsson, Gardar, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Walters, G. Bragi, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Vikingsson, Arnor, Hansdottir, Ragnheidur, Karlsson, Karl O., Rafnar, Thorunn, Jonsdottir, Ingileif, Frigge, Michael L., Kong, Augustine, Oddsson, Asmundur, Masson, Gisli, Magnusson, Olafur T., Gudbjartsson, Tomas, Stefansson, Hreinn, Sulem, Patrick, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Thorgeirsson, Thorgeir E., Stefansson, Kari
Publicado en Nat Commun (2017)

Localization of a Susceptibility Gene for Common Forms of Stroke to 5q12

por 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.
Publicado 2002

Parental origin of sequence variants associated with complex diseases

por Kong, Augustine, Steinthorsdottir, Valgerdur, Masson, Gisli, Thorleifsson, Gudmar, Sulem, Patrick, Besenbacher, Soren, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Kristinsson, Kari Th., Jonasdottir, Adalbjorg, Frigge, Michael L., Gylfason, Arnaldur, Olason, Pall I., Gudjonsson, Sigurjon A., Sverrisson, Sverrir, Stacey, Simon N., Sigurgeirsson, Bardur, Benediktsdottir, Kristrun R., Sigurdsson, Helgi, Jonsson, Thorvaldur, Benediktsson, Rafn, Olafsson, Jon H., Johannsson, Oskar Th., Hreidarsson, Astradur B., Sigurdsson, Gunnar, Ferguson-Smith, Anne C., Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2009

A sequence variant associating with educational attainment also affects childhood cognition

por Gunnarsson, Bjarni, Jónsdóttir, Guðrún A., Björnsdóttir, Gyða, Konte, Bettina, Sulem, Patrick, Kristmundsdóttir, Snædís, Kehr, Birte, Gústafsson, Ómar, Helgason, Hannes, Iordache, Paul D., Ólafsson, Sigurgeir, Frigge, Michael L., Þorleifsson, Guðmar, Arnarsdóttir, Sunna, Stefánsdóttir, Berglind, Giegling, Ina, Djurovic, Srdjan, Sundet, Kjetil S., Espeseth, Thomas, Melle, Ingrid, Hartmann, Annette M., Thorsteinsdottir, Unnur, Kong, Augustine, Guðbjartsson, Daníel F., Ettinger, Ulrich, Andreassen, Ole A., Dan Rujescu, Halldórsson, Jónas G., Stefánsson, Hreinn, Halldórsson, Bjarni V., Stefánsson, Kári
Publicado en Sci Rep (2016)

Epigenetic and genetic components of height regulation

por Benonisdottir, Stefania, Oddsson, Asmundur, Helgason, Agnar, Kristjansson, Ragnar P., Sveinbjornsson, Gardar, Oskarsdottir, Arna, Thorleifsson, Gudmar, Davidsson, Olafur B., Arnadottir, Gudny A., Sulem, Gerald, Jensson, Brynjar O., Holm, Hilma, Alexandersson, Kristjan F., Tryggvadottir, Laufey, Walters, G. Bragi, Gudjonsson, Sigurjon A., Ward, Lucas D., Sigurdsson, Jon K., Iordache, Paul D., Frigge, Michael L., Rafnar, Thorunn, Kong, Augustine, Masson, Gisli, Helgason, Hannes, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Kari
Publicado en Nat Commun (2016)

Whole genome characterization of sequence diversity of 15,220 Icelanders

por Jónsson, Hákon, Sulem, Patrick, Kehr, Birte, Kristmundsdottir, Snaedis, Zink, Florian, Hjartarson, Eirikur, Hardarson, Marteinn T., Hjorleifsson, Kristjan E., Eggertsson, Hannes P., Gudjonsson, Sigurjon Axel, Ward, Lucas D., Arnadottir, Gudny A., Helgason, Einar A., Helgason, Hannes, Gylfason, Arnaldur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Rafnar, Thorunn, Besenbacher, Soren, Frigge, Michael L., Stacey, Simon N., Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Masson, Gisli, Kong, Augustine, Halldorsson, Bjarni V., Helgason, Agnar, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado en Sci Data (2017)