Epidemiology of acute heart failure admissions in Iceland: phenotype distribution and prognostic implications by Agnarsson, H R, Hansen, J S, Gunnarsson, D A, Einarsson, H, Gunnthorsdottir, I, Ingimarsdottir, I

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Increased risk of inflammatory bowel disease among patients treated with rituximab in Iceland from 2001 to 2018 by Kristjánsson, Valdimar B., Lund, Sigrún H., Gröndal, Gerður, Sveinsdóttir, Signý V., Agnarsson, Hjálmar R., Jónasson, Jón G., Björnsson, Einar S.

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The Role of Th17/Tc17 Peripheral Blood T cells in Psoriasis and Their Positive Therapeutic Response by Eysteinsdóttir, J. H., Sigurgeirsson, B., Ólafsson, J. H., Fridriksson, Th, Agnarsson, B. A., Davíðsson, S., Valdimarsson, H., Lúðvíksson, B. R.

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Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations by TIRKKONEN, M, JOHANNSSON, O, KALLIONIEMI, O.-P, AGNARSSON, B. A, OLSSON, H, INGVARSSON, S, KARHU, R, TANNER, M, ISOLA, J, BARKARDOTTIR, R. B, BORG, A

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Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer by Stacey, Simon N, Kehr, Birte, Gudmundsson, Julius, Zink, Florian, Jonasdottir, Aslaug, Gudjonsson, Sigurjon A, Sigurdsson, Asgeir, Halldorsson, Bjarni V, Agnarsson, Bjarni A, Benediktsdottir, Kristrun R, Aben, Katja K H, Vermeulen, Sita H, Cremers, Ruben G, Panadero, Angeles, Helfand, Brian T, Cooper, Phillip R, Donovan, Jenny L, Hamdy, Freddie C, Jinga, Viorel, Okamoto, Ichiro, Jonasson, Jon G, Tryggvadottir, Laufey, Johannsdottir, Hrefna, Kristinsdottir, Anna M, Masson, Gisli, Magnusson, Olafur T, Iordache, Paul D, Helgason, Agnar, Helgason, Hannes, Sulem, Patrick, Gudbjartsson, Daniel F, Kong, Augustine, Jonsson, Eirikur, Barkardottir, Rosa B, Einarsson, Gudmundur V, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Mates, Ioan N, Neal, David E, Catalona, William J, Mayordomo, José I, Kiemeney, Lambertus A, Thorleifsson, Gudmar, Stefansson, Kari

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Integrating economics into fisheries science and advice: progress, needs, and future opportunities by Thébaud, O, Nielsen, J R, Motova, A, Curtis, H, Bastardie, F, Blomqvist, G E, Daurès, F, Goti, L, Holzer, J, Innes, J, Muench, A, Murillas, A, Nielsen, R, Rosa, R, Thunberg, E, Villasante, S, Virtanen, J, Waldo, S, Agnarsson, S, Castilla Espino, D, Curtin, R, DePiper, G, Doering, R, Ellefsen, H, García del Hoyo1, J J, Gourguet, S, Greene, P, Hamon, K G, Haynie, A, Kellner, J B, Kuikka, S, Le Gallic, B, Macher, C, Prellezo, R, Santiago Castro-Rial, J, Sys, K, van Oostenbrugge, H, Vastenhoud, B M J

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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction by ANTONIOU, Antonis C, BEESLEY, Jonathan, ISAACS, Claudine, GANZ, Patricia A, TOMLINSON, Gail, OLOPADE, Olufunmilayo I, COUCH, Fergus J, XIANSHU WANG, LINDOR, Noralane M, PANKRATZ, Vernon S, RADICE, Paolo, MANOUKIAN, Siranoush, MCGUFFOG, Lesley, PEISSEL, Bernard, ZAFFARONI, Daniela, BARILE, Monica, VIEL, Alessandra, ALLAVENA, Anna, DALL' OLIO, Valentina, PETERLONGO, Paolo, SZABO, Csilla I, ZIKAN, Michal, CLAES, Kathleen, SINILNIKOVA, Olga M, POPPE, Bruce, FORETOVA, Lenka, MAI, Phuong L, GREENE, Mark H, RENNERT, Gad, LEJBKOWICZ, Flavio, GLENDON, Gord, OZCELIK, Hilmi, ANDRULIS, Irene L, THOMASSEN, Mads, HEALEY, Sue, GERDES, Anne-Marie, SUNDE, Lone, CRUGER, Dorthe, JENSEN, Uffe Birk, CALIGO, Maria, FRIEDMAN, Eitan, KAUFMAN, Bella, LAITMAN, Yael, MILGROM, Roni, DUBROVSKY, Maya, NEUHAUSEN, Susan L, COHEN, Shimrit, BORG, Ake, JERNSTRÖM, Helena, LINDBLOM, Annika, RANTALA, Johanna, STENMARK-ASKMALM, Marie, MELIN, Beatrice, NATHANSON, Kate, DOMCHEK, Susan, JAKUBOWSKA, Ania, YUAN CHUN DING, REBBECK, Timothy R, WEITZEL, Jeffrey N, LYNCH, Henry T

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

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Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignanc... by Karppinen, S-M, Barkardottir, R B, Backenhorn, K, Sydenham, T, Syrjäkoski, K, Schleutker, J, Ikonen, T, Pylkäs, K, Rapakko, K, Erkko, H, Johannesdottir, G, Gerdes, A-M, Thomassen, M, Agnarsson, B A, Grip, M, Kallioniemi, A, Kere, J, Aaltonen, L A, Arason, A, Møller, P, Kruse, T A, Borg, Å, Winqvist, R

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Inherited BRCA2 mutation associated with high grade breast cancer by AGNARSSON, B. A, JONASSON, J. G, BJÖRNSDOTTIR, I. B, BARKARDOTTIR, R. B, EGILSSON, V, SIGURDSSON, H

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Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers by Vigorito, Elena, Kuchenbaecker, Karoline B, Beesley, Jonathan, Adlard, Julian, Agnarsson, Bjarni A, Andrulis, Irene L, Arun, Banu K, Barjhoux, Laure, Belotti, Muriel, Benitez, Javier, Berger, Andreas, Bojesen, Anders, Bonanni, Bernardo, Brewer, Carole, Caldes, Trinidad, Caligo, Maria A, Campbell, Ian, Chan, Salina B, Claes, Kathleen B M, Cohn, David E, Cook, Jackie, Daly, Mary B, Damiola, Francesca, Davidson, Rosemarie, Pauw, Antoine de, Delnatte, Capucine, Diez, Orland, Domchek, Susan M, Dumont, Martine, Durda, Katarzyna, Dworniczak, Bernd, Easton, Douglas F, Eccles, Diana, Edwinsdotter Ardnor, Christina, Eeles, Ros, Ejlertsen, Bent, Ellis, Steve, Evans, D Gareth, Feliubadalo, Lidia, Fostira, Florentia, Foulkes, William D, Friedman, Eitan, Frost, Debra, Gaddam, Pragna, Ganz, Patricia A, Garber, Judy, Garcia-Barberan, Vanesa, Gauthier-Villars, Marion, Gehrig, Andrea, Gerdes, Anne-Marie, Giraud, Sophie, Godwin, Andrew K, Goldgar, David E, Hake, Christopher R, Hansen, Thomas V O, Healey, Sue, Hodgson, Shirley, Hogervorst, Frans B L, Houdayer, Claude, Hulick, Peter J, Imyanitov, Evgeny N, Isaacs, Claudine, Izatt, Louise, Izquierdo, Angel, Jacobs, Lauren, Jakubowska, Anna, Janavicius, Ramunas, Jaworska-Bieniek, Katarzyna, Jensen, Uffe Birk, John, Esther M, Vijai, Joseph, Karlan, Beth Y, Kast, Karin, Khan, Sofia, Kwong, Ava, Laitman, Yael, Lester, Jenny, Lesueur, Fabienne, Liljegren, Annelie, Lubinski, Jan, Mai, Phuong L, Manoukian, Siranoush, Mazoyer, Sylvie, Meindl, Alfons, Mensenkamp, Arjen R, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Ong, Kai-Ren, Osorio, Ana, Park, Sue Kyung, Paulsson-Karlsson, Ylva, Pedersen, Inge Sokilde, Peissel, Bernard, Peterlongo, Paolo, Pfeiler, Georg

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers by Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans Mw, Nelen, Marcel R, Ausems, Margreet Gem, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J

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Deletions on Chromosome 4 in Sporadic and BRCA Mutated Tumors and Association with Pathological Variables by JOHANNSDOTTIR, Hrefna K, JOHANNESDOTTIR, Gudrun, NEVANLINNA, Heli, BARKARDOTTIR, Rosa B, AGNARSSON, Bjarni A, EEROLA, Hannaleena, ARASON, Adalgeir, JOHANNSSON, Oskar Th, HEIKKILÄ, Päivi, EGILSSON, Valgardur, OLSSON, Hakan, BORG, Ake

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Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer by SIGBJÖRNSDOTTIR, B. I, RAGNARSSON, G, AGNARSSON, B. A, CHEN HUIPING, BARKARDOTTIR, R. B, EGILSSON, V, INGVARSSON, S

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2mutation carriers by Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans MW, Nelen, Marcel R, Ausems, Margreet GEM, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J

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Lymphoid tumours of the ocular adnexa: a morphologic and genotypic study of 15 cases by Agnarsson, AB, Sigurdardottir, M, Sigurdsson, H, BjAdork Bakardottir, R, Kristjandottir, S

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Mapping loss of heterozygosity at chromosome 13q: loss at 13q12-q13 is associated with breast tumour progression and poor prognosis by Eiriksdottir, G, Johannesdottir, G, Ingvarsson, S, Björnsdottir, I.B, Jonasson, J.G, Agnarsson, B.A, Hallgrimsson, J, Gudmundsson, J, Egilsson, V, Sigurdsson, H, Barkardottir, R.B

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Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer: results from a genome-wide association study by Gudmundsson, J, Sulem, P, Rafnar, T, Bergthorsson, J, Manolescu, A, Sigurdsson, A, Stacey, S, Thorlacius, S, Agnarsson, B, Benediktsdottir, K, Schaid, D, Xu, JF, Gronberg, H, Isaacs, W, Smith, J, Mayordomo, J, Thibodeau, S, Catalona, W, Jonsson, E, Einarsson, G, Kiemeney, L, Barkardottir, R, Gulcher, J, Thorsteinsdottir, U, Kong, A, Stefansson, K

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Lymphoid tumours of the ocular adnexa: a morphologic and genotypic study of 15 cases by Sigurdardottir, Margret, Sigurdsson, Haraldur, Barkardottir, Rosa Björk, Kristjansdottir, Sigrun, Agnarsson, Bjarni A.

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