Search Results

Hydrothermal Alteration in the New Deep Geothermal Well GIL-1 (Strasbourg Area, France)

by Glaas, Carole, Patrier, Patricia, Vidal, Jeanne, Beaufort, Daniel, Girard, Jean-François, Genter, Albert
Published 2020

Hydrothermal Alteration in the New Deep Geothermal Well GIL-1 (Strasbourg Area, France)

by Glaas, Carole, Patrier, Patricia, Vidal, Jeanne, Beaufort, Daniel, Girard, Jean-François, Genter, Albert
Published 2020

Hydrothermal Alteration in the New Deep Geothermal Well GIL-1 (Strasbourg Area, France)

by Glaas, Carole, Patrier, Patricia, Vidal, Jeanne, Beaufort, Daniel, Girard, Jean-François, Genter, Albert
Published 2020

Hydrothermal Alteration in the New Deep Geothermal Well GIL-1 (Strasbourg Area, France)

by Glaas, Carole, Patrier, Patricia, Vidal, Jeanne, Beaufort, Daniel, Girard, Jean-François, Genter, Albert
Published 2020

Hydrothermal Alteration in the New Deep Geothermal Well GIL-1 (Strasbourg Area, France)

by Glaas, Carole, Patrier, Patricia, Vidal, Jeanne, Beaufort, Daniel, Girard, Jean-François, Genter, Albert
Published 2020

Genetic Obesity and the Risk of Atrial Fibrillation

by Chatterjee, Neal A., Giulianini, Franco, Geelhoed, Bastiaan, Lunetta, Kathryn L., Misialek, Jeffrey R., Niemeijer, Maartje N., Rienstra, Michiel, Rose, Lynda M., Smith, Albert V., Arking, Dan E., Ellinor, Patrick T., Heeringa, Jan, Lin, Honghuang, Lubitz, Steven A., Soliman, Elsayed Z., Verweij, Niek, Alonso, Alvaro, Benjamin, Emelia J., Gudnason, Vilmundur, Stricker, Bruno H. C., Van Der Harst, Pim, Chasman, Daniel I., Albert, Christine M.
Published in Circulation (2017)

Genetic Obesity and the Risk of Atrial Fibrillation- Causal Estimates from Mendelian Randomization

by Chatterjee, Neal A, Giulianini, Franco, Geelhoed, Bastiaan, Lunetta, Kathryn L, Misialek, Jeffrey R, Niemeijer, Maartje N, Rienstra, Michiel, Rose, Lynda M, Smith, Albert V, Arking, Dan E, Ellinor, Patrick T, Heeringa, Jan, Lin, Honghuang, Lubitz, Steven A, Soliman, Elsayed Z, Verweij, Niek, Alonso, Alvaro, Benjamin, Emelia J, Gudnason, Vilmundur, Stricker, Bruno H, van der Harst, Pim, Chasman, Daniel I, Albert, Christine M
Published in Circulation (2017)

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

by Guo, Y. (Yanjun), Rist, P. M. (Pamela M.), Daghlas, I. (Iyas), Giulianini, F. (Franco), Kurth, T. (Tobias), Chasman, D. I. (Daniel, I)
Published 2020

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L., Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G., Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H., Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C., de la Chapelle, Albert, Jonasson, Jon G., Goldberg, Richard M., Stefansson, Kari
Published in Nature Communications (2017)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L, Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G, Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H, Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C, de la Chapelle, Albert, Jonasson, Jon G, Goldberg, Richard M, Stefansson, Kari
Published in Nature Communications (2017)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L. Frankel, Sylvia Einarsdottir, Asgeir Sigurdsson, Heather Hampel, Petur Snaebjornsson, Gisli Masson, Daniel Weng, Reynir Arngrimsson, Birte Kehr, Ahmet Yilmaz, Stefan Haraldsson, Patrick Sulem, Tryggvi Stefansson, Peter G. Shields, Fridbjorn Sigurdsson, Tanios Bekaii-Saab, Pall H. Moller, Margret Steinarsdottir, Kristin Alexiusdottir, Megan Hitchins, Colin C. Pritchard, Albert de la Chapelle, Jon G. Jonasson, Richard M. Goldberg, Kari Stefansson
Published in Nature Communications (2017)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L., Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G., Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H., Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C., de la Chapelle, Albert, Jonasson, Jon G., Goldberg, Richard M., Stefansson, Kari
Published in Nature Communications (2017)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L., Einarsdóttir, Sylvía, Sigurðsson, Ásgeir, Hampel, Heather, Snaebjornsson, Petur, Másson, Gísli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, sulem, patrick, Stefansson, Tryggvi, Shields, Peter G., Sigurðsson, Fridbjörn, Bekaii-Saab, Tanios, Moller, Pall H., Steinarsdóttir, Margrét, Alexíusdóttir, Kristín, Hitchins, Megan, Pritchard, Colin C., de la Chapelle, Albert, Jónasson, Jón Gunnlaugur, Goldberg, Richard M., Stefansson, Kari
Published in Nature Communications (2017)

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L, Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G, Sigurdsson, Fridjorn, Bekaii-Saab, Tanios, Moller, Pall H, Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Coiln C, Chapelle, Albert de la, Jonasson, Jon G, Goldberg, Richard M, Stefansson, Kari
Published 2017

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

by Haraldsdottir, Sigurdis, Rafnar, Thorunn, Frankel, Wendy L, Einarsdottir, Sylvia, Sigurdsson, Asgeir, Hampel, Heather, Snaebjornsson, Petur, Masson, Gisli, Weng, Daniel, Arngrimsson, Reynir, Kehr, Birte, Yilmaz, Ahmet, Haraldsson, Stefan, Sulem, Patrick, Stefansson, Tryggvi, Shields, Peter G, Sigurdsson, Fridbjorn, Bekaii-Saab, Tanios, Moller, Pall H, Steinarsdottir, Margret, Alexiusdottir, Kristin, Hitchins, Megan, Pritchard, Colin C, de la Chapelle, Albert, Jonasson, Jon G, Goldberg, Richard M, Stefansson, Kari
Published in Nature Communications (2017)

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

by Jakobsdottir, Johanna, van der Lee, Sven J, Bis, Joshua C, Chouraki, Vincent, Li-Kroeger, David, Yamamoto, Shinya, Grove, Megan L, Naj, Adam, Vronskaya, Maria, Salazar, Jose L, DeStefano, Anita L, Brody, Jennifer A, Smith, Albert V, Amin, Najaf, Sims, Rebecca, Ibrahim-Verbaas, Carla A, Choi, Seung-Hoan, Satizabal, Claudia L, Lopez, Oscar L, Beiser, Alexa, Ikram, M Arfan, Garcia, Melissa E, Hayward, Caroline, Varga, Tibor V, Ripatti, Samuli, Franks, Paul W, Hallmans, Göran, Rolandsson, Olov, Jansson, Jan-Håkon, Porteous, David J, Salomaa, Veikko, Eiriksdottir, Gudny, Rice, Kenneth M, Bellen, Hugo J, Levy, Daniel, Uitterlinden, Andre G, Emilsson, Valur, Rotter, Jerome I, Aspelund, Thor, O’Donnell, Christopher J, Fitzpatrick, Annette L, Launer, Lenore J, Hofman, Albert, Wang, Li-San, Williams, Julie, Schellenberg, Gerard D, Boerwinkle, Eric, Psaty, Bruce M, Seshadri, Sudha, Shulman, Joshua M, Gudnason, Vilmundur, van Duijn, Cornelia M
Published 2016

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.

by Jakobsdottir, Johanna, van der Lee, Sven J, Bis, Joshua C, Chouraki, Vincent, Li-Kroeger, David, Yamamoto, Shinya, Grove, Megan L, Naj, Adam, Vronskaya, Maria, Salazar, Jose L, DeStefano, Anita L, Brody, Jennifer A, Smith, Albert V, Amin, Najaf, Sims, Rebecca, Ibrahim-Verbaas, Carla A, Choi, Seung-Hoan, Satizabal, Claudia L, Lopez, Oscar L, Beiser, Alexa, Ikram, M Arfan, Garcia, Melissa E, Hayward, Caroline, Varga, Tibor V, Ripatti, Samuli, Franks, Paul W, Hallmans, Göran, Rolandsson, Olov, Jansson, Jan-Håkon, Porteous, David J, Salomaa, Veikko, Eiriksdottir, Gudny, Rice, Kenneth M, Bellen, Hugo J, Levy, Daniel, Uitterlinden, Andre G, Emilsson, Valur, Rotter, Jerome I, Aspelund, Thor, Cohorts for Heart and Aging Research in Genomic Epidemiology consortium, Alzheimer’s Disease Genetic Consortium, Genetic and Environmental Risk in Alzheimer’s Disease consortium, O'Donnell, Christopher J, Fitzpatrick, Annette L, Launer, Lenore J, Hofman, Albert, Wang, Li-San, Williams, Julie, Schellenberg, Gerard D, Boerwinkle, Eric, Psaty, Bruce M, Seshadri, Sudha, Shulman, Joshua M, Gudnason, Vilmundur, van Duijn, Cornelia M
Published 2016

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

by 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
Published in Nature Genetics (2011)

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

by 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.
Published in Nature Genetics (2010)

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

by 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.
Published in Nature Genetics (2010)