Aflatoxin M1 absorption and cytotoxicity on human intestinal in vitro model von CALONI, F, STAMMATI, A, FRIGGE, G, DE ANGELIS, I

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Aflatoxin M 1 absorption and cytotoxicity on human intestinal in vitro model von Caloni, F., Stammati, A., Friggè, G., De Angelis, I.

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Absorption of fumonisin B1 and aminopentol on an in vitro model of intestinal epithelium; the role of P-glycoprotein von DE ANGELIS, I, FRIGGE, G, RAIMONDI, F, STAMMATI, A, ZUCCO, F, CALONI, F

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Absorption of Fumonisin B 1 and aminopentol on an in vitro model of intestinal epithelium; the role of P-glycoprotein von De Angelis, I., Friggè, G., Raimondi, F., Stammati, A., Zucco, F., Caloni, F.

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Aflatoxin M sub(1) absorption and cytotoxicity on human intestinal in vitro model von Caloni, F, Stammati, A, Frigge, G, De Angelis, I

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Absorption of Fumonisin B sub(1) and aminopentol on an in vitro model of intestinal epithelium; the role of P-glycoprotein von De Angelis, I, Frigge, G, Raimondi, F, Stammati, A, Zucco, F, Caloni, F

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Rate of de novo mutations and the importance of father’s age to disease risk von Kong, Augustine, Frigge, Michael L., Masson, Gisli, Besenbacher, Soren, Sulem, Patrick, Magnusson, Gisli, Gudjonsson, Sigurjon A., Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Wong, Wendy S. W., Sigurdsson, Gunnar, Walters, G. Bragi, Steinberg, Stacy, Helgason, Hannes, Thorleifsson, Gudmar, Gudbjartsson, Daniel F., Helgason, Agnar, Magnusson, Olafur Th, Thorsteinsdottir, Unnur, Stefansson, Kari

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

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A high-resolution recombination map of the human genome von Kong, Augustine, Gudbjartsson, Daniel F., Sainz, Jesus, Jonsdottir, Gudrun M., Gudjonsson, Sigurjon A., Richardsson, Bjorgvin, Sigurdardottir, Sigrun, Barnard, John, Hallbeck, Bjorn, Masson, Gisli, Shlien, Adam, Palsson, Stefan T., Frigge, Michael L., Thorgeirsson, Thorgeir E., Gulcher, Jeffrey R., Stefansson, Kari

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Fine-scale recombination rate differences between sexes, populations and individuals von Kong, Augustine, Thorleifsson, Gudmar, Gudbjartsson, Daniel F., Masson, Gisli, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Walters, G. Bragi, Jonasdottir, Adalbjorg, Gylfason, Arnaldur, Kristinsson, Kari Th, Gudjonsson, Sigurjon A., Frigge, Michael L., Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari

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Optically excited structural transition in atomic wires on surfaces at the quantum limit von Frigge, T., Hafke, B., Witte, T., Krenzer, B., Streubühr, C., Samad Syed, A., Mikšić Trontl, V., Avigo, I., Zhou, P., Ligges, M., von der Linde, D., Bovensiepen, U., Horn-von Hoegen, M., Wippermann, S., Lücke, A., Sanna, S., Gerstmann, U., Schmidt, W. G.

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The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland von Styrkarsdottir, Unnur, Lund, Sigrun H., Saevarsdottir, Saedis, Magnusson, Magnus I., Gunnarsdottir, Kristbjorg, Norddahl, Gudmundur L., Frigge, Michael L., Ivarsdottir, Erna V., Bjornsdottir, Gyda, Holm, Hilma, Thorgeirsson, Gudmundur, Rafnar, Thorunn, Jonsdottir, Ingileif, Ingvarsson, Thorvaldur, Jonsson, Helgi, Sulem, Patrick, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel, Stefansson, Kari

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The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke von Helgadottir, Anna, Manolescu, Andrei, Thorleifsson, Gudmar, Gretarsdottir, Solveig, Jonsdottir, Helga, Thorsteinsdottir, Unnur, Samani, Nilesh J, Gudmundsson, Gudmundur, Grant, Struan F A, Thorgeirsson, Gudmundur, Sveinbjornsdottir, Sigurlaug, Valdimarsson, Einar M, Matthiasson, Stefan E, Johannsson, Halldor, Gudmundsdottir, Olof, Gurney, Mark E, Sainz, Jesus, Thorhallsdottir, Margret, Andresdottir, Margret, Frigge, Michael L, Topol, Eric J, Kong, Augustine, Gudnason, Vilmundur, Hakonarson, Hakon, Gulcher, Jeffrey R, Stefansson, Kari

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Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits von Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Sulem, Patrick, Gudbjartsson, Daniel F., Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Oddsson, Asmundur, Helgason, Agnar, Magnusson, Olafur T., Walters, G. Bragi, Frigge, Michael L., Helgadottir, Hafdis T., Johannsdottir, Hrefna, Bergsteinsdottir, Kristin, Ogmundsdottir, Margret H., Center, Jacqueline R., Nguyen, Tuan V., Eisman, John A., Christiansen, Claus, Steingrimsson, Erikur, Jonasson, Jon G., Tryggvadottir, Laufey, Eyjolfsson, Gudmundur I., Theodors, Asgeir, Jonsson, Thorvaldur, Ingvarsson, Thorvaldur, Olafsson, Isleifur, Rafnar, Thorunn, Kong, Augustine, Sigurdsson, Gunnar, Masson, Gisli, Thorsteinsdottir, Unnur, Stefansson, Kari

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A common inversion under selection in Europeans von Stefansson, Hreinn, Helgason, Agnar, Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Masson, Gisli, Barnard, John, Baker, Adam, Jonasdottir, Aslaug, Ingason, Andres, Gudnadottir, Vala G, Desnica, Natasa, Hicks, Andrew, Gylfason, Arnaldur, Gudbjartsson, Daniel F, Jonsdottir, Gudrun M, Sainz, Jesus, Agnarsson, Kari, Birgisdottir, Birgitta, Ghosh, Shyamali, Olafsdottir, Adalheidur, Cazier, Jean-Baptiste, Kristjansson, Kristleifur, Frigge, Michael L, Thorgeirsson, Thorgeir E, Gulcher, Jeffrey R, Kong, Augustine, Stefansson, Kari

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MAP1B mutations cause intellectual disability and extensive white matter deficit von Walters, G. Bragi, Gustafsson, Omar, Sveinbjornsson, Gardar, Eiriksdottir, Valgerdur K., Agustsdottir, Arna B., Jonsdottir, Gudrun A., Steinberg, Stacy, Gunnarsson, Arni F., Magnusson, Magnus I., Unnsteinsdottir, Unnur, Lee, Amy L., Jonasdottir, Adalbjorg, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Skuladottir, Astros, Jonsson, Lina, Nawaz, Muhammad S., Sulem, Patrick, Frigge, Mike, Ingason, Andres, Love, Askell, Norddhal, Gudmundur L., Zervas, Mark, Gudbjartsson, Daniel F., Ulfarsson, Magnus O., Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari

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Linkage of osteoporosis to chromosome 20p12 and association to BMP2 von 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

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

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

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Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits von Rafnar, Thorunn, Gunnarsson, Bjarni, Stefansson, Olafur A., Sulem, Patrick, Ingason, Andres, Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Tragante, Vinicius, Steinthorsdottir, Valgerdur, Styrkarsdottir, Unnur, Stacey, Simon N., Gudmundsson, Julius, Arnadottir, Gudny A., Oddsson, Asmundur, Zink, Florian, Halldorsson, Gisli, Sveinbjornsson, Gardar, Kristjansson, Ragnar P., Davidsson, Olafur B., Salvarsdottir, Anna, Thoroddsen, Asgeir, Helgadottir, Elisabet A., Kristjansdottir, Katrin, Ingthorsson, Orri, Gudmundsson, Valur, Geirsson, Reynir T., Arnadottir, Ragnheidur, Gudbjartsson, Daniel F., Masson, Gisli, Asselbergs, Folkert W., Jonasson, Jon G., Olafsson, Karl, Thorsteinsdottir, Unnur, Halldorsson, Bjarni V., Thorleifsson, Gudmar, Stefansson, Kari

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