A two-tiered mechanism by which Cdc42 controls the localization and activation of an Arp2/3-activating motor complex in yeast

Por Lechler, Terry, Jonsdottir, Gudrun A., Klee, Saskia K., Pellman, David, Li, Rong
Publicado em 2001

A study of the relationships between oligonucleotide properties and hybridization signal intensities from NimbleGen microarray datasets

Por Wei, Hairong, Kuan, Pei Fen, Tian, Shulan, Yang, Chuhu, Nie, Jeff, Sengupta, Srikumar, Ruotti, Victor, Jonsdottir, Gudrun A., Keles, Sunduz, Thomson, James A., Stewart, Ron
Publicado em 2008

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 no Proc Natl Acad Sci U S A (2017)

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

Por Stefansson, Hreinn, Steinberg, Stacy, Petursson, Hjorvar, Gustafsson, Omar, Gudjonsdottir, Iris H, Jonsdottir, Gudrun A, Palsson, Stefan T, Jonsson, Thorlakur, Saemundsdottir, Jona, Bjornsdottir, Gyda, Böttcher, Yvonne, Thorlacius, Theodora, Haubenberger, Dietrich, Zimprich, Alexander, Auff, Eduard, Hotzy, Christoph, Testa, Claudia M, Miyatake, Lisa A, Rosen, Ami R, Kristleifsson, Kristleifur, Rye, David, Asmus, Friedrich, Schöls, Ludger, Dichgans, Martin, Jakobsson, Finnbogi, Benedikz, John, Thorsteinsdottir, Unnur, Gulcher, Jeffrey, Kong, Augustine, Stefansson, Kari
Publicado em 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 no Sci Rep (2016)

Disruption of the neurexin 1 gene is associated with schizophrenia

Por Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P.H., Barnes, Michael R., Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I., Hardarsson, Gudmundur, Jonsdottir, Gudrun A., Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette M., Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A., Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E., Sabatti, Chiara, Ophoff, Roel A., Rietschel, Marcella, Nöthen, Markus M., Stefansson, Kari, Peltonen, Leena, Clair, David St, Stefansson, Hreinn, Collier, David A.
Publicado em 2008