Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors von Johannsdottir, Hrefna K., Jonsson, Goran, Johannesdottir, Gudrun, Agnarsson, Bjarni A., Eerola, Hannaleena, Arason, Adalgeir, Heikkila, Paivi, Egilsson, Valgardur, Olsson, Hakan, Johannsson, Oskar Th, Nevanlinna, Heli, Borg, Ake, Barkardottir, Rosa B.

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Deletions on Chromosome 4 in Sporadic and BRCA Mutated Tumors and Association with Pathological Variables von 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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Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease von Steinberg, Stacy, Stefansson, Hreinn, Jonsson, Thorlakur, Johannsdottir, Hrefna, Ingason, Andres, Helgason, Hannes, Sulem, Patrick, Magnusson, Olafur Th, Gudjonsson, Sigurjon A, Unnsteinsdottir, Unnur, Kong, Augustine, Helisalmi, Seppo, Soininen, Hilkka, Lah, James J, Aarsland, Dag, Fladby, Tormod, Ulstein, Ingun D, Djurovic, Srdjan, Sando, Sigrid B, White, Linda R, Knudsen, Gun-Peggy, Westlye, Lars T, Selbæk, Geir, Giegling, Ina, Hampel, Harald, Hiltunen, Mikko, Levey, Allan I, Andreassen, Ole A, Rujescu, Dan, Jonsson, Palmi V, Bjornsson, Sigurbjorn, Snaedal, Jon, Stefansson, Kari

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A susceptibility gene for late-onset idiopathic Parkinson's disease von Hicks, Andrew A., Pétursson, Hjörvar, Jónsson, Thorlákur, Stefánsson, Hreinn, Jóhannsdóttir, Hrefna S., Sainz, Jesus, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári, Sveinbjörnsdóttir, Sigurlaug

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A genome-wide association study yields five novel thyroid cancer risk loci von Gudmundsson, Julius, Thorleifsson, Gudmar, Sigurdsson, Jon K., Stefansdottir, Lilja, Jonasson, Jon G., Gudjonsson, Sigurjon A., Gudbjartsson, Daniel F., Masson, Gisli, Johannsdottir, Hrefna, Halldorsson, Gisli H., Stacey, Simon N., Helgason, Hannes, Sulem, Patrick, Senter, Leigha, He, Huiling, Liyanarachchi, Sandya, Ringel, Matthew D., Aguillo, Esperanza, Panadero, Angeles, Prats, Enrique, Garcia-Castaño, Almudena, De Juan, Ana, Rivera, Fernando, Xu, Li, Kiemeney, Lambertus A., Eyjolfsson, Gudmundur I., Sigurdardottir, Olof, Olafsson, Isleifur, Kristvinsson, Hoskuldur, Netea-Maier, Romana T., Jonsson, Thorvaldur, Mayordomo, Jose I., Plantinga, Theo S., Hjartarson, Hannes, Hrafnkelsson, Jon, Sturgis, Erich M., Thorsteinsdottir, Unnur, Rafnar, Thorunn, de la Chapelle, Albert, Stefansson, Kari

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Association of BRCA2 K3326 With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin von Rafnar, Thorunn, Sigurjonsdottir, Gudbjorg R, Stacey, Simon N, Halldorsson, Gisli, Sulem, Patrick, Pardo, Luba M, Helgason, Hannes, Sigurdsson, Stefan T, Gudjonsson, Thorkell, Tryggvadottir, Laufey, Olafsdottir, Gudridur H, Jonasson, Jon G, Alexiusdottir, Kristin, Sigurdsson, Asgeir, Gudmundsson, Julius, Saemundsdottir, Jona, Sigurdsson, Jon K, Johannsdottir, Hrefna, Uitterlinden, Andre, Vermeulen, Sita H, Galesloot, Tessel E, Allain, Dawn C, Lacko, Martin, Sigurgeirsson, Bardur, Thorisdottir, Kristin, Johannsson, Oskar T, Sigurdsson, Fridbjorn, Ragnarsson, Gunnar B, Isaksson, Helgi, Hardardottir, Hronn, Gudbjartsson, Tomas, Gudbjartsson, Daniel F, Masson, Gisli, Kiemeney, Lambertus A M L, Ewart Toland, Amanda, Nijsten, Tamar, Peters, Wilbert H M, Olafsson, Jon H, Jonsson, Steinn, Thorsteinsdottir, Unnur, Thorleifsson, Gudmar, Stefansson, Kari

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A common variant at 8q24.21 is associated with renal cell cancer von Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F., Masson, Gisli, Petursdottir, Vigdis, Hardarson, Sverrir, Gudjonsson, Sigurjon A., Johannsdottir, Hrefna, Helgadottir, Hafdis Th, Stacey, Simon N., Magnusson, Olafur Th, Helgason, Hannes, Panadero, Angeles, van der Zanden, Loes F., Aben, Katja K. H., Vermeulen, Sita H., Oosterwijk, Egbert, Kong, Augustine, Mayordomo, Jose I., Sverrisdottir, Asgerdur, Jonsson, Eirikur, Gudbjartsson, Tomas, Einarsson, Gudmundur V., Kiemeney, Lambertus A., Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari

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Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer von Rafnar, Thorunn, Sulem, Patrick, Thorleifsson, Gudmar, Vermeulen, Sita H, Helgason, Hannes, Saemundsdottir, Jona, Gudjonsson, Sigurjon A, Sigurdsson, Asgeir, Stacey, Simon N, Gudmundsson, Julius, Johannsdottir, Hrefna, Alexiusdottir, Kristin, Petursdottir, Vigdis, Nikulasson, Sigfus, Geirsson, Gudmundur, Jonsson, Thorvaldur, Aben, Katja K H, Grotenhuis, Anne J, Verhaegh, Gerald W, Dudek, Aleksandra M, Witjes, J Alfred, van der Heijden, Antoine G, Vrieling, Alina, Galesloot, Tessel E, De Juan, Ana, Panadero, Angeles, Rivera, Fernando, Hurst, Carolyn, Bishop, D Timothy, Sak, Sei C, Choudhury, Ananya, Teo, Mark T W, Arici, Cecilia, Carta, Angela, Toninelli, Elena, de Verdier, Petra, Rudnai, Peter, Gurzau, Eugene, Koppova, Kvetoslava, van der Keur, Kirstin A, Lurkin, Irene, Goossens, Mieke, Kellen, Eliane, Guarrera, Simonetta, Russo, Alessia, Critelli, Rossana, Sacerdote, Carlotta, Vineis, Paolo, Krucker, Clémentine, Zeegers, Maurice P, Gerullis, Holger, Ovsiannikov, Daniel, Volkert, Frank, Hengstler, Jan G, Selinski, Silvia, Magnusson, Olafur T, Masson, Gisli, Kong, Augustine, Gudbjartsson, Daniel, Lindblom, Annika, Zwarthoff, Ellen, Porru, Stefano, Golka, Klaus, Buntinx, Frank, Matullo, Giuseppe, Kumar, Rajiv, Mayordomo, José I, Steineck, D Gunnar, Kiltie, Anne E, Jonsson, Eirikur, Radvanyi, François, Knowles, Margaret A, Thorsteinsdottir, Unnur, Kiemeney, Lambertus A, Stefansson, Kari

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Genetic Sharing with Cardiovascular Disease Risk Factors and Diabetes Reveals Novel Bone Mineral Density Loci von Reppe, Sjur, Wang, Yunpeng, Thompson, Wesley K, McEvoy, Linda K, Schork, Andrew J, Zuber, Verena, LeBlanc, Marissa, Bettella, Francesco, Mills, Ian G, Desikan, Rahul S, Djurovic, Srdjan, Gautvik, Kaare M, Dale, Anders M, Andreassen, Ole A

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Somatic Deletions in Hereditary Breast Cancers Implicate 13q21 as a Putative Novel Breast Cancer Susceptibility Locus von Kainu, Tommi, Juo, Suh-Hang Hank, Desper, Richard, Schaffer, Alejandro A., Gillanders, Elizabeth, Rozenblum, Ester, Freas-Lutz, Diana, Weaver, Don, Stephan, Dietrich, Bailey-Wilson, Joan, Olli-P. Kallioniemi, Trikkonen, Mika, Syrjakoski, Kirsi, Kuukasjarvi, Tuula, Koivisto, Pasi, Karhu, Ritva, Holli, Kaija, Arason, Adalgeir, Johannesdottir, Gudrun, Bergthorsson, Jon Thor, Johannsdottir, Hrefna, Egilsson, Valgardur, Barkardottir, Rosa Bjork, Johannsson, Oskar, Haraldsson, Karin, Sandberg, Therese, Holmberg, Eva, Gronberg, Henrik, Olsson, Hakan, Borg, Ake, Vehmanen, Paula, Eerola, Hannaleena, Heikkila, Paivi, Pyrhonen, Seppo, Nevanlinna, Heli

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A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus von Oei, Ling, Hsu, Yi-Hsiang, Styrkarsdottir, Unnur, Eussen, Bert H, de Klein, Annelies, Peters, Marjolein J, Halldorsson, Bjarni, Liu, Ching-Ti, Alonso, Nerea, Kaptoge, Stephen K, Thorleifsson, Gudmar, Hallmans, Göran, Hocking, Lynne J, Husted, Lise Bjerre, Jameson, Karen A, Kruk, Marcin, Lewis, Joshua R, Patel, Millan S, Scollen, Serena, Svensson, Olle, Trompet, Stella, van Schoor, Natasja M, Zhu, Kun, Buckley, Brendan M, Cooper, Cyrus, Ford, Ian, Goltzman, David, González-Macías, Jesús, Langdahl, Bente Lomholt, Leslie, William D, Lips, Paul, Lorenc, Roman S, Olmos, José M, Pettersson-Kymmer, Ulrika, Reid, David M, Riancho, José A, Slagboom, P Eline, Garcia-Ibarbia, Carmen, Ingvarsson, Thorvaldur, Johannsdottir, Hrefna, Luben, Robert, Medina-Gómez, Carolina, Arp, Pascal, Nandakumar, Kannabiran, Palsson, Stefan Th, Sigurdsson, Gunnar, van Meurs, Joyce B J, Zhou, Yanhua, Hofman, Albert, Jukema, J Wouter, Pols, Huibert A P, Prince, Richard L, Cupples, L Adrienne, Marshall, Christian R, Pinto, Dalila, Sato, Daisuke, Scherer, Stephen W, Reeve, Jonathan, Thorsteinsdottir, Unnur, Karasik, David, Richards, J Brent, Stefansson, Kari, Uitterlinden, André G, Ralston, Stuart H, Ioannidis, John P A, Kiel, Douglas P, Rivadeneira, Fernando, Estrada, Karol

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A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes von ROZENBLUM, Ester, VAHTERISTO, Pia, GOLBERGER, Natalie, ROBBINS, Christiane, PAK, Evgenia, DUTRA, Amalia, GILLANDER, Elizabeth, STEPHAN, Dietrich A, BAILEY-WILSON, Joan, JUO, Suh-Hang Hank, KAINU, Tommi, ARASON, Adalgeir, SANDBERG, Therese, BARKARDOTTIR, Rosa Bjork, NEVANLINNA, Heli, BORG, Ake, KALLIONIEMI, Olli-P, BERGTHORSSON, Jon Thor, SYRJAKOSKI, Kirsi, WEAVER, Don, HARALDSSON, Karin, JOHANNSDOTTIR, Hrefna Kristin, VEHMANEN, Paula, NIGAM, Savita

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Lack of HIN-1 methylation in BRCA1-linked and BRCA1-like breast tumors von KROP, Ian, MAGUIRE, Paula, LINDBLOM, Annika, POLYAK, Kornelia, LAHTI-DOMENICI, Jaana, LODEIRO, Gabriela, RICHARDSON, Andrea, JOHANNSDOTTIR, Hrefna Kristin, NEVANLINNA, Heli, BORG, Ake, GELMAN, Rebecca, BARKARDOTTIR, Rosa Björk

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