TP53 mutation analyses on breast carcinomas: a study of paraffin-embedded archival material.

Por Gretarsdottir, S., Tryggvadottir, L., Jonasson, J. G., Sigurdsson, H., Olafsdottir, K., Agnarsson, B. A., Ogmundsdottir, H., Eyfjörd, J. E.
Publicado em 1996

A Drastic Reduction in the Life Span of Cystatin C L68Q Carriers Due to Life-Style Changes during the Last Two Centuries

Por Palsdottir, Astridur, Helgason, Agnar, Palsson, Snaebjorn, Bjornsson, Hans Tomas, Bragason, Birkir Thor, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Olafsson, Elias, Stefansson, Kari
Publicado em 2008

Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population

Por Helgadottir, A., Gretarsdottir, S., St. Clair, D., Manolescu, A., Cheung, J., Thorleifsson, G., Pasdar, A., Grant, S. F. A., Whalley, L. J., Hakonarson, H., Thorsteinsdottir, U., Kong, A., Gulcher, J., Stefansson, K., MacLeod, M. J.
Publicado em 2005

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 no PLoS Genet (2015)

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 em 2002

European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations

Por Styrkarsdottir, Unnur, Halldorsson, Bjarni V., Gudbjartsson, Daniel F., Tang, Nelson L. S., Koh, Jung-Min, Xiao, Su-mei, Kwok, Timothy C. Y., Kim, Ghi Su, Chan, Juliana C. N., Cherny, Stacey, Lee, Seung Hun, Kwok, Anthony, Ho, Suzanne, Gretarsdottir, Solveig, Pop Kostic, Jelena, Palsson, Stefan Th., Sigurdsson, Gunnar, Sham, Pak C., Kim, Beom-Jun, Kung, Annie W. C., Kim, Shin-Yoon, Woo, Jean, Leung, Ping-C., Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado em 2010

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 em 2011

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

Por Thorgeirsson, T E, Steinberg, S, Reginsson, G W, Bjornsdottir, G, Rafnar, T, Jonsdottir, I, Helgadottir, A, Gretarsdottir, S, Helgadottir, H, Jonsson, S, Matthiasson, S E, Gislason, T, Tyrfingsson, T, Gudbjartsson, T, Isaksson, H J, Hardardottir, H, Sigvaldason, A, Kiemeney, L A, Haugen, A, Zienolddiny, S, Wolf, H J, Franklin, W A, Panadero, A, Mayordomo, J I, Hall, I P, Rönmark, E, Lundbäck, B, Dirksen, A, Ashraf, H, Pedersen, J H, Masson, G, Sulem, P, Thorsteinsdottir, U, Gudbjartsson, D F, Stefansson, K
Publicado no Mol Psychiatry (2016)

Shared genetic susceptibility to ischemic stroke and coronary artery disease – a genome-wide analysis of common variants

Por Dichgans, Martin, Malik, Rainer, König, Inke R., Rosand, Jonathan, Clarke, Robert, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Mitchell, Braxton D., Assimes, Themistocles L., Levi, Christopher, O′Donnell, Christopher J., Fornage, Myriam, Thorsteinsdottir, Unnur, Psaty, Bruce M., Hengstenberg, Christian, Seshadri, Sudha, Erdmann, Jeanette, Bis, Joshua C., Peters, Annette, Boncoraglio, Giorgio B., März, Winfried, Meschia, James F., Kathiresan, Sekar, Ikram, M. Arfan, McPherson, Ruth, Stefansson, Kari, Sudlow, Cathie, Reilly, Muredach P., Thompson, John R., Sharma, Pankaj, Hopewell, Jemma C., Chambers, John C., Watkins, Hugh, Rothwell, Peter M., Roberts, Robert, Markus, Hugh S., Samani, Nilesh J., Farrall, Martin, Schunkert, Heribert
Publicado em 2013

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Por Gudbjartsson, Daniel F., Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G. Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin, 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, 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
Publicado em 2009

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm

Por Jones, Gregory T., Bown, Matthew J., Gretarsdottir, Solveig, Romaine, Simon P.R., Helgadottir, Anna, Yu, Grace, Tromp, Gerard, Norman, Paul E., Jin, Cao, Baas, Annette F., Blankensteijn, Jan D., Kullo, Iftikhar J., Phillips, L. Victoria, Williams, Michael J.A., Topless, Ruth, Merriman, Tony R., Vasudevan, Thodor M., Lewis, David R., Blair, Ross D., Hill, Andrew A., Sayers, Robert D., Powell, Janet T., Deloukas, Panagiotis, Thorleifsson, Gudmar, Matthiasson, Stefan E., Thorsteinsdottir, Unnur, Golledge, Jonathan, Ariëns, Robert A., Johnson, Anne, Sohrabi, Soroush, Scott, D. Julian, Carey, David J., Erdman, Robert, Elmore, James R., Kuivaniemi, Helena, Samani, Nilesh J., Stefansson, Kari, van Rij, Andre M.
Publicado em 2013

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12

Por Kilarski, Laura L., Achterberg, Sefanja, Devan, William J., Traylor, Matthew, Malik, Rainer, Lindgren, Arne, Pare, Guillame, Sharma, Pankaj, Slowik, Agniesczka, Thijs, Vincent, Walters, Matthew, Worrall, Bradford B., Sale, Michele M., Algra, Ale, Kappelle, L. Jaap, Wijmenga, Cisca, Norrving, Bo, Sandling, Johanna K., Rönnblom, Lars, Goris, An, Franke, Andre, Sudlow, Cathie, Rothwell, Peter M., Levi, Christopher, Holliday, Elizabeth G., Fornage, Myriam, Psaty, Bruce, Gretarsdottir, Solveig, Thorsteinsdottir, Unnar, Seshadri, Sudha, Mitchell, Braxton D., Kittner, Steven, Clarke, Robert, Hopewell, Jemma C., Bis, Joshua C., Boncoraglio, Giorgio B., Meschia, James, Ikram, M. Arfan, Hansen, Bjorn M., Montaner, Joan, Thorleifsson, Gudmar, Stefanson, Kari, Rosand, Jonathan, de Bakker, Paul I.W., Farrall, Martin, Dichgans, Martin, Markus, Hugh S., Bevan, Steve
Publicado em 2014

Ischemic Stroke Is Associated with the ABO Locus: The EuroCLOT Study

Por Williams, Frances M K, Carter, Angela M, Hysi, Pirro G, Surdulescu, Gabriela, Hodgkiss, Dylan, Soranzo, Nicole, Traylor, Matthew, Bevan, Steve, Dichgans, Martin, Rothwell, Peter M W, Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Arveiler, Dominique, Ferrieres, Jean, Wiklund, Per-Gunnar, Arfan Ikram, M, Hofman, Albert, Boncoraglio, Giorgio B, Parati, Eugenio A, Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Thorleifsson, Gudmar, Stefansson, Kari, Seshadri, Sudha, DeStefano, Anita, Gschwendtner, Andreas, Psaty, Bruce, Longstreth, Will, Mitchell, Braxton D, Cheng, Yu-Ching, Clarke, Robert, Ferrario, Marco, Bis, Joshua C, Levi, Christopher, Attia, John, Holliday, Elizabeth G, Scott, Rodney J, Fornage, Myriam, Sharma, Pankaj, Furie, Karen L, Rosand, Jonathan, Nalls, Mike, Meschia, James, Mosely, Thomas H, Evans, Alun, Palotie, Aarno, Markus, Hugh S, Grant, Peter J, Spector, Tim D
Publicado em 2013

New common variants affecting susceptibility to basal cell carcinoma

Por Stacey, Simon N, Sulem, Patrick, Masson, Gisli, Gudjonsson, Sigurjon A, Thorleifsson, Gudmar, Jakobsdottir, Margret, Sigurdsson, Asgeir, Gudbjartsson, Daniel F, Sigurgeirsson, Bardur, Benediktsdottir, Kristrun R, Thorisdottir, Kristin, Ragnarsson, Rafn, Scherer, Dominique, Hemminki, Kari, Rudnai, Peter, Gurzau, Eugene, Koppova, Kvetoslava, Botella-Estrada, Rafael, Soriano, Virtudes, Juberias, Pablo, Saez, Berta, Gilaberte, Yolanda, Fuentelsaz, Victoria, Corredera, Cristina, Grasa, Matilde, Höiom, Veronica, Lindblom, Annika, Bonenkamp, Johannes J, van Rossum, Michelle M, Aben, Katja K H, de Vries, Esther, Santinami, Mario, Di Mauro, Maria G, Maurichi, Andrea, Wendt, Judith, Hochleitner, Pia, Pehamberger, Hubert, Gudmundsson, Julius, Magnusdottir, Droplaug N, Gretarsdottir, Solveig, Holm, Hilma, Steinthorsdottir, Valgerdur, Frigge, Michael L, Blondal, Thorarinn, Saemundsdottir, Jona, Bjarnason, Hjördis, Kristjansson, Kristleifur, Bjornsdottir, Gyda, Okamoto, Ichiro, Rivoltini, Licia, Rodolfo, Monica, Kiemeney, Lambertus A, Hansson, Johan, Nagore, Eduardo, Mayordomo, José I, Kumar, Rajiv, Karagas, Margaret R, Nelson, Heather H, Gulcher, Jeffrey R, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Olafsson, Jon H, Kong, Augustine, Stefansson, Kari
Publicado em 2009

Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1

Por Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A.W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., McPherson, Ruth, Folkersen, Lasse, Franco-Cereceda, Anders, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicolas, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjærg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J.
Publicado em 2011

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

Por Holliday, Elizabeth G, Maguire, Jane M, Evans, Tiffany-Jane, Koblar, Simon A, Jannes, Jim, Sturm, Jonathan W, Hankey, Graeme J, Baker, Ross, Golledge, Jonathan, Parsons, Mark W, Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D, Lincz, Lisa F, Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Bevan, Steve, Bis, Joshua C, Boerwinkle, Eric, Boncoraglio, Giorgio B, Brott, Thomas G, Brown, Robert D, Cheng, Yu-Ching, Cole, John W, Cotlarciuc, Ioana, Devan, William J, Fornage, Myriam, Furie, Karen L, Grétarsdóttir, Sólveig, Gschwendtner, Andreas, Ikram, M Arfan, Longstreth, W T, Meschia, James F, Mitchell, Braxton D, Mosley, Thomas H, Nalls, Michael A, Parati, Eugenio A, Psaty, Bruce M, Sharma, Pankaj, Stefansson, Kari, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Traylor, Matthew, Verhaaren, Benjamin F J, Wiggins, Kerri L, Worrall, Bradford B, Sudlow, Cathie, Rothwell, Peter M, Farrall, Martin, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S, Scott, Rodney J, Levi, Christopher, Attia, John
Publicado em 2012

Genetic variation at 16q24.2 is associated with small vessel stroke

Por Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W.T., Ikram, M. Arfan, Launer, Lenore J., Seshadri, Sudha, Hamilton‐Bruce, Monica Anne, Jimenez‐Conde, Jordi, Cole, John W., Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P., Sacco, Ralph L., Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K., Johnson, Julie A., Benavente, Oscar R., Wasssertheil‐Smoller, Sylvia, Lee, Jin‐Moo, Pulit, Sara L., Wong, Quenna, Rich, Stephen S., de Bakker, Paul I.W., McArdle, Patrick F., Woo, Daniel, Anderson, Christopher D., Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M., Sharma, Pankaj, Sudlow, Cathie L.M., Rothwell, Peter M., Boncoraglio, Giorgio B., Thijs, Vincent, Levi, Chris, Meschia, James F., Rosand, Jonathan, Kittner, Steven J., Mitchell, Braxton D., Dichgans, Martin, Worrall, Bradford B., Markus, Hugh S.
Publicado no Ann Neurol (2017)

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

Por Traylor, Matthew, Farrall, Martin, Holliday, Elizabeth G, Sudlow, Cathie, Hopewell, Jemma C, Cheng, Yu-Ching, Fornage, Myriam, Ikram, M Arfan, Malik, Rainer, Bevan, Steve, Thorsteinsdottir, Unnur, Nalls, Mike A, Longstreth, WT, Wiggins, Kerri L, Yadav, Sunaina, Parati, Eugenio A, DeStefano, Anita L, Worrall, Bradford B, Kittner, Steven J, Khan, Muhammad Saleem, Reiner, Alex P, Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E Bernd, O'Donnell, Martin, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbäumer, Gregor, Doney, Alexander S F, Vicente, Astrid M, Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sofia A, Palmer, Colin N A, Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, de Bakker, Paul I W, Kostulas, Konstantinos, Ferro, Jose M, van Zuydam, Natalie R, Valdimarsson, Einar, Nordestgaard, Børge G, Lindgren, Arne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Hofman, Albert, Mosley, Thomas H, Mitchell, Braxton D, Furie, Karen, Clarke, Robert, Levi, Christopher, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B, Sharma, Pankaj, Bis, Joshua C, Gretarsdottir, Solveig, Psaty, Bruce M, Rothwell, Peter M, Rosand, Jonathan, Meschia, James F, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S
Publicado em 2012

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

Por Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tõnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M, Steves, Claire, Uitterlinden, André G, Hofman, Albert, Tönjes, Anke, Kovacs, Peter, Hottenga, Jouke Jan, Willemsen, Gonneke, Vogelzangs, Nicole, Döring, Angela, Dahmen, Norbert, Nitz, Barbara, Pergadia, Michele L., Saez, Berta, De Diego, Veronica, Lezcano, Victoria, Garcia-Prats, Maria D., Ripatti, Samuli, Perola, Markus, Kettunen, Johannes, Hartikainen, Anna-Liisa, Pouta, Anneli, Laitinen, Jaana, Isohanni, Matti, Huei-Yi, Shen, Allen, Maxine, Krestyaninova, Maria, Hall, Alistair S, Jones, Gregory T., van Rij, Andre M., Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Jonsson, Steinn, Matthiasson, Stefan E., Oskarsson, Hogni, Tyrfingsson, Thorarinn, Kiemeney, Lambertus A., Mayordomo, Jose I., Lindholt, Jes S, Pedersen, Jesper Holst, Franklin, Wilbur A., Wolf, Holly, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Madden, Pamela A.F., Giegling, Ina, Rujescu, Dan, Järvelin, Marjo-Riitta, Salomaa, Veikko, Stumvoll, Michael, Spector, Tim D, Wichmann, H-Erich, Metspalu, Andres, Samani, Nilesh J., Penninx, Brenda W., Oostra, Ben A., Boomsma, Dorret I., Tiemeier, Henning, van Duijn, Cornelia M., Kaprio, Jaakko, Gulcher, Jeffrey R., McCarthy, Mark I., Peltonen, Leena, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado em 2010

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Por Gretarsdottir, Solveig, Baas, Annette F, Thorleifsson, Gudmar, Holm, Hilma, den Heijer, Martin, de Vries, Jean-Paul P M, Kranendonk, Steef E, Zeebregts, Clark J A M, van Sterkenburg, Steven M, Geelkerken, Robert H, van Rij, Andre M, Williams, Michael J A, Boll, Albert P M, Kostic, Jelena P, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Walters, G Bragi, Masson, Gisli, Sulem, Patrick, Saemundsdottir, Jona, Mouy, Magali, Magnusson, Kristinn P, Tromp, Gerard, Elmore, James R, Sakalihasan, Natzi, Limet, Raymond, Defraigne, Jean-Olivier, Ferrell, Robert E, Ronkainen, Antti, Ruigrok, Ynte M, Wijmenga, Cisca, Grobbee, Diederick E, Shah, Svati H, Granger, Christopher B, Quyyumi, Arshed A, Vaccarino, Viola, Patel, Riyaz S, Zafari, A Maziar, Levey, Allan I, Austin, Harland, Girelli, Domenico, Pignatti, Pier Franco, Olivieri, Oliviero, Martinelli, Nicola, Malerba, Giovanni, Trabetti, Elisabetta, Becker, Lewis C, Becker, Diane M, Reilly, Muredach P, Rader, Daniel J, Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Urbonavicius, Sigitas, Lindblad, Bengt, Gottsäter, Anders, Gaetani, Eleonora, Pola, Roberto, Wells, Philip, Rodger, Marc, Forgie, Melissa, Langlois, Nicole, Corral, Javier, Vicente, Vicente, Fontcuberta, Jordi, España, Francisco, Grarup, Niels, Jørgensen, Torben, Witte, Daniel R, Hansen, Torben, Pedersen, Oluf, Aben, Katja K, de Graaf, Jacqueline, Holewijn, Suzanne, Folkersen, Lasse, Franco-Cereceda, Anders, Eriksson, Per, Collier, David A, Stefansson, Hreinn, Steinthorsdottir, Valgerdur, Rafnar, Thorunn, Valdimarsson, Einar M, Magnadottir, Hulda B, Sveinbjornsdottir, Sigurlaug, Olafsson, Isleifur, Magnusson, Magnus Karl, Palmason, Robert, Haraldsdottir, Vilhelmina, Andersen, Karl, Onundarson, Pall T, Thorgeirsson, Gudmundur, Kiemeney, Lambertus A, Powell, Janet T, Carey, David J, Kuivaniemi, Helena, Lindholt, Jes S, Jones, Gregory T, Kong, Augustine, Blankensteijn, Jan D, Matthiasson, Stefan E, Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado em 2010