Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3 von Stefánsson, Stefán Einar, Jónsson, Helgi, Ingvarsson, Thorvaldur, Manolescu, Ileana, Jónsson, Hjörtur H., Ólafsdóttir, Guðbjörg, Pálsdóttir, Ebba, Stefánsdóttir, Gerður, Sveinbjörnsdóttir, Guðfinna, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári

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Hand radiology characteristics of patients carrying the T 303 M mutation in the gene for matrilin‐3 von Eliasson, G. J., Verbruggen, G., Stefansson, S. E., Ingvarsson, T., Jonsson, H.

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Genetic variation for survival and shell length of cultured red abalone (Haliotis rufescens) in Iceland von Jonasson, J, Stefansson, SE, Gudnason, A, Steinarsson, A

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The inheritance of hand osteoarthritis in Iceland von Jonsson, Helgi, Manolescu, Ileana, Stefansson, Stefan Einar, Ingvarsson, Thorvaldur, Jonsson, Hjortur H., Manolescu, Andrei, Gulcher, Jeff, Stefansson, Kari

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A large Icelandic family with early osteoarthritis of the hip associated with a susceptibility locus on chromosome 16p von Ingvarsson, Thorvaldur, Stefánsson, Stefán Einar, Gulcher, Jeffrey R., Jónsson, Hjörtur Heiǒar, Jónsson, Helgi, Frigge, Michael L., Pálsdóttir, Ebba, Ólafsdóttir, Guǒbjörg, Jónsdóttir, þorbjörg, Walters, Guǒmundur Bragi, Lohmander, L. Stefan, Stefánsson, Kári

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The inheritance of hip osteoarthritis in Iceland von Ingvarsson, Thorvaldur, Stefánsson, Stefán Einar, Hallgrímsdóttir, Ingileif B., Frigge, Michael L., Jónsson Jr, Halldór, Gulcher, Jeff, Jónsson, Helgi, Ragnarsson, Jón Ingvar, Lohmander, L. Stefan, Stefánsson, Kári

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry von Konte, Bettina, Walters, James T. R., Rujescu, Dan, Legge, Sophie E., Pardiñas, Antonio F., Cohen, Dan, Pirmohamed, Munir, Tiihonen, Jari, Hartmann, Annette M., Bogers, Jan P., van der Weide, Jan, van der Weide, Karen, Putkonen, Anu, Repo-Tiihonen, Eila, Hallikainen, Tero, Silva, Ed, Ingimarsson, Oddur, Sigurdsson, Engilbert, Kennedy, James L., Sullivan, Patrick F., Rietschel, Marcella, Breen, Gerome, Stefansson, Hreinn, Stefansson, Kari, Collier, David A., O’Donovan, Michael C., Giegling, Ina

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A mega-analysis of genome-wide association studies for major depressive disorder von Ripke, Stephan, Wray, Naomi R, Lewis, Cathryn M, Hamilton, Steven P, Weissman, Myrna M, Breen, Gerome, Byrne, Enda M, Blackwood, Douglas H R, Boomsma, Dorret I, Cichon, Sven, Heath, Andrew C, Holsboer, Florian, Lucae, Susanne, Madden, Pamela A F, Martin, Nicholas G, McGuffin, Peter, Muglia, Pierandrea, Noethen, Markus M, Penninx, Brenda P, Pergadia, Michele L, Potash, James B, Rietschel, Marcella, Lin, Danyu, Müller-Myhsok, Bertram, Shi, Jianxin, Steinberg, Stacy, Grabe, Hans J, Lichtenstein, Paul, Magnusson, Patrik, Perlis, Roy H, Preisig, Martin, Smoller, Jordan W, Stefansson, Kari, Uher, Rudolf, Kutalik, Zoltan, Tansey, Katherine E, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, Breuer, René, Castro, Victor M, Churchill, Susanne E, Coryell, William H, Craddock, Nick, Craig, Ian W, Czamara, Darina, De Geus, Eco J, Degenhardt, Franziska, Farmer, Anne E, Fava, Maurizio, Frank, Josef, Gainer, Vivian S, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Guipponi, Michel, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Hottenga, Jouke Jan, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohane, Isaac S, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, Macintyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, Nyholt, Dale R, O'Donovan, Michael, Oskarsson, Högni, Pedersen, Nancy, Scheftner, William A, Schulz, Andrea, Schulze, Thomas G, Shyn, Stanley I, Sigurdsson, Engilbert, Slager, Susan L, Smit, Johannes H

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How Real-World Data Can Facilitate the Development of Precision Medicine Treatment in Psychiatry von Koch, Elise, Pardiñas, Antonio F., O’Connell, Kevin S., Selvaggi, Pierluigi, Camacho Collados, José, Babic, Aleksandar, Marshall, Serena E., Van der Eycken, Erik, Angulo, Cecilia, Lu, Yi, Sullivan, Patrick F., Dale, Anders M., Molden, Espen, Posthuma, Danielle, White, Nathan, Schubert, Alexander, Djurovic, Srdjan, Heimer, Hakon, Stefánsson, Hreinn, Stefánsson, Kári, Werge, Thomas, Sønderby, Ida, O’Donovan, Michael C., Walters, James T.R., Milani, Lili, Andreassen, Ole A.

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Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm von Vicente, Vicente, Forgie, Melissa, Gretarsdottir, Solveig, Magnadottir, Hulda B, Dieplinger, Benjamin, Steinthorsdottir, Valgerdur, Wijmenga, Cisca, Corral, Javier, Palmason, Robert, Thorleifsson, Gudmar, de Graaf, Jacqueline, Stefansson, Kari, Girelli, Domenico, Rodger, Marc, van Rij, Andre M, Sakalihasan, Natzi, Stefansson, Hreinn, Aben, Katja K, Williams, Michael J A, den Heijer, Martin, Pignatti, Pier Franco, Austin, Harland, Jonasdottir, Adalbjorg, Granger, Christopher B, Gottsäter, Anders, Holm, Hilma, Collier, David A, Vaccarino, Viola, Andersen, Karl, Lindblad, Bengt, Geelkerken, Robert H, Masson, Gisli, Malerba, Giovanni, Holewijn, Suzanne, de Vries, Jean-Paul P M, Matthiasson, Stefan E, Powell, Janet T, Mouy, Magali, Becker, Lewis C, Walters, G Bragi, Martinelli, Nicola, Kostic, Jelena P, Pola, Roberto, Hansen, Torben, Rader, Daniel J, Reilly, Muredach P, Eriksson, Per, Sveinbjornsdottir, Sigurlaug, Langlois, Nicole, Haltmayer, Meinhard, Jonasdottir, Aslaug, Urbonavicius, Sigitas, Kong, Augustine, Thorsteinsdottir, Unnur, Baas, Annette F, Boll, Albert P M, Pedersen, Oluf, Ferrell, Robert E, Limet, Raymond, Kiemeney, Lambertus A, Jørgensen, Torben, Zeebregts, Clark J A M, Shah, Svati H, Kuivaniemi, Helena, Jones, Gregory T, Elmore, James R, Witte, Daniel R, van Sterkenburg, Steven M, Ruigrok, Ynte M, Sulem, Patrick, España, Francisco, Olivieri, Oliviero, Fontcuberta, Jordi, Rafnar, Thorunn, Franco-Cereceda, Anders, Kranendonk, Steef E, Magnusson, Magnus Karl, Becker, Diane M, Zafari, A Maziar, Onundarson, Pall T, Wells, Philip, Magnusson, Kristinn P, Tromp, Gerard, Gaetani, Eleonora, Grarup, Niels, Levey, Allan I, Mueller, Thomas, Folkersen, Lasse, Olafsson, Isleifur, Saemundsdottir, Jona, Carey, David J, Quyyumi, Arshed A, Defraigne, Jean-Olivier, Patel, Riyaz S, Haraldsdottir, Vilhelmina, Trabetti, Elisabetta, Thorgeirsson, Gudmundur, Grobbee, Diederick E, Valdimarsson, Einar M, Lindholt, Jes S

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Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age von Deelen, Joris, Beekman, Marian, Uh, Hae-Won, Broer, Linda, Ayers, Kristin L, Tan, Qihua, Kamatani, Yoichiro, Bennet, Anna M, Tamm, Riin, Trompet, Stella, Guðbjartsson, Daníel F, Flachsbart, Friederike, Rose, Giuseppina, Viktorin, Alexander, Fischer, Krista, Nygaard, Marianne, Cordell, Heather J, Crocco, Paolina, van den Akker, Erik B, Böhringer, Stefan, Helmer, Quinta, Nelson, Christopher P, Saunders, Gary I, Alver, Maris, Andersen-Ranberg, Karen, Breen, Marie E, van der Breggen, Ruud, Caliebe, Amke, Capri, Miriam, Cevenini, Elisa, Collerton, Joanna C, Dato, Serena, Davies, Karen, Ford, Ian, Gampe, Jutta, Garagnani, Paolo, de Geus, Eco J C, Harrow, Jennifer, van Heemst, Diana, Heijmans, Bastiaan T, Heinsen, Femke-Anouska, Hottenga, Jouke-Jan, Hofman, Albert, Jeune, Bernard, Jonsson, Palmi V, Lathrop, Mark, Lechner, Doris, Martin-Ruiz, Carmen, Mcnerlan, Susan E, Mihailov, Evelin, Montesanto, Alberto, Mooijaart, Simon P, Murphy, Anne, Nohr, Ellen A, Paternoster, Lavinia, Postmus, Iris, Rivadeneira, Fernando, Ross, Owen A, Salvioli, Stefano, Sattar, Naveed, Schreiber, Stefan, Stefánsson, Hreinn, Stott, David J, Tiemeier, Henning, Uitterlinden, André G, Westendorp, Rudi G J, Willemsen, Gonneke, Samani, Nilesh J, Galan, Pilar, Sørensen, Thorkild I A, Boomsma, Dorret I, Jukema, J Wouter, Rea, Irene Maeve, Passarino, Giuseppe, de Craen, Anton J M, Christensen, Kaare, Nebel, Almut, Stefánsson, Kári, Metspalu, Andres, Magnusson, Patrik, Blanché, Hélène, Christiansen, Lene, Kirkwood, Thomas B L, van Duijn, Cornelia M, Franceschi, Claudio, Houwing-Duistermaat, Jeanine J, Slagboom, P Eline

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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Locus for severity implicates CNS resilience in progression of multiple sclerosis von Harroud, Adil, Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., Engelenburg, Hendrik J., Beecham, Ashley H., Alfredsson, Lars, Alikhani, Katayoun, Amezcua, Lilyana, Andlauer, Till F. M., Ban, Maria, Barcellos, Lisa F., Barizzone, Nadia, Berge, Tone, Berthele, Achim, Bittner, Stefan, Bos, Steffan D., Briggs, Farren B. S., Caillier, Stacy J., Calabresi, Peter A., Caputo, Domenico, Carmona-Burgos, David X., Cavalla, Paola, Celius, Elisabeth G., Cerono, Gabriel, Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., D’Alfonso, Sandra, Dardiotis, Efthimios, De Jager, Philip L., Delgado, Silvia R., Dubois, Bénédicte, Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Filippi, Massimo, Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Hamann, Jörg, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Khalil, Michael, Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Malhotra, Sunny, Manouchehrinia, Ali, Manrique, Clara P., Martinelli-Boneschi, Filippo, Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Olsson, Tomas, Oturai, Annette, Pääkkönen, Kimmo, Parnell, Grant P., Patsopoulos, Nikolaos A., Pericak-Vance, Margaret A., Piehl, Fredrik, Rubio, Justin P., Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Silva, Claudia, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vasileiou, Elena S., Vecchio, Domizia, Voortman, Margarete M., Weiner, Howard L., Wever, Dennis

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Genome-wide meta-analysis identifies new susceptibility loci for migraine von Anttila, Verneri, Winsvold, Bendik S, Gormley, Padhraig, Kurth, Tobias, Bettella, Francesco, McMahon, George, Kallela, Mikko, Malik, Rainer, de Vries, Boukje, Terwindt, Gisela, Medland, Sarah E, Todt, Unda, McArdle, Wendy L, Quaye, Lydia, Koiranen, Markku, Ikram, M Arfan, Lehtimäki, Terho, Stam, Anine H, Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M, Palta, Priit, Hamalainen, Eija, Schürks, Markus, Rose, Lynda M, Buring, Julie E, Ridker, Paul M, Steinberg, Stacy, Stefansson, Hreinn, Jakobsson, Finnbogi, Lawlor, Debbie A, Evans, David M, Ring, Susan M, Färkkilä, Markus, Artto, Ville, Kaunisto, Mari A, Freilinger, Tobias, Schoenen, Jean, Frants, Rune R, Pelzer, Nadine, Weller, Claudia M, Zielman, Ronald, Heath, Andrew C, Madden, Pamela A F, Montgomery, Grant W, Martin, Nicholas G, Borck, Guntram, Göbel, Hartmut, Heinze, Axel, Heinze-Kuhn, Katja, Williams, Frances M K, Hartikainen, Anna-Liisa, Pouta, Anneli, van den Ende, Joyce, Uitterlinden, Andre G, Hofman, Albert, Amin, Najaf, Hottenga, Jouke-Jan, Vink, Jacqueline M, Heikkilä, Kauko, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Wichmann, Heinz Erich, Aromaa, Arpo, Eriksson, Johan G, Traynor, Bryan J, Trabzuni, Daniah, Rossin, Elizabeth, Lage, Kasper, Jacobs, Suzanne B R, Gibbs, J Raphael, Birney, Ewan, Kaprio, Jaakko, Penninx, Brenda W, Boomsma, Dorret I, van Duijn, Cornelia, Raitakari, Olli, Jarvelin, Marjo-Riitta, Zwart, John-Anker, Cherkas, Lynn, Strachan, David P, Kubisch, Christian, Ferrari, Michel D, van den Maagdenberg, Arn M J M, Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Daly, Mark J

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Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci von Tromp, Gerard, Gretarsdottir, Solveig, Baas, Annette F, Giusti, Betti, Strauss, Ewa, van‘t Hof, Femke N.G, Webb, Thomas R, Erdman, Robert, Ritchie, Marylyn D, Elmore, James R, Verma, Anurag, Pendergrass, Sarah, Kullo, Iftikhar J, Peissig, Peggy L, Verma, Shefali S, Malinowski, Jennifer, Rasmussen-Torvik, Laura J, Borthwick, Kenneth M, Smelser, Diane T, Crosslin, David R, de Andrade, Mariza, Ryer, Evan J, McCarty, Catherine A, Böttinger, Erwin P, Pacheco, Jennifer A, Carrell, David S, Franklin, David P, Phillips, Victoria L, Williams, Michael J.A, Wei, Wenhua, Blair, Ross, Hill, Andrew A, Vasudevan, Thodor M, Lewis, David R, Thomson, Ian A, Krysa, Jo, Hill, Geraldine B, Roake, Justin, Merriman, Tony R, Oszkinis, Grzegorz, Galora, Silvia, Saracini, Claudia, Abbate, Rosanna, Pulli, Raffaele, Saratzis, Athanasios, Verissimo, Ana R, Bumpstead, Suzannah, Badger, Stephen A, Clough, Rachel E, Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A, Futers, T Simon, Romaine, Simon P.R, Griffin, Kathryn J, Bailey, Marc A, Smith, Alberto, van Bockxmeer, Frank M, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D, Teijink, Joep A.W, de Graaf, Jacqueline, Kiemeney, Lambertus A, Lindholt, Jes S, Hughes, Anne, Bradley, Declan T, Stirrups, Kathleen, Golledge, Jonathan, Norman, Paul E, Powell, Janet T, Humphries, Steve E, Goodall, Alison H, Nelson, Christopher P, Sakalihasan, Natzi, Courtois, Audrey, Ferrell, Robert E, Eriksson, Per, Folkersen, Lasse, Franco-Cereceda, Anders, Eicher, John D, Johnson, Andrew D, Betsholtz, Christer, Ruusalepp, Arno, Franzén, Oscar, Schadt, Eric E, Lipovich, Leonard, Verhoeven, Eric L, Zeebregts, Clark J, Geelkerken, Robert H, van Sambeek, Marc R, van Sterkenburg, Steven M, de Vries, Jean-Paul, Stefansson, Kari, de Bakker, Paul I.W, Deloukas, Panos, Harrison, Seamus C, van Rij, Andre M, Samani, Nilesh J, Bown, Matthew J

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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci von Lee, Mei Chin, Igo, Robert P, Haripriya, Aravind, Orr, Andrew C, Nakano, Satoko, Mori, Kazuhiko, Kang, Jae H, Nelson, Sarah, Manabe, Shin-ichi, Lamari, Hasnaa, Bikbov, Mukharram, Zenteno, Juan C, Jonas, Jost B, Perera, Shamira A, George, Ronnie, Vijaya, Lingam, Do, Tan, Edward, Deepak P, de Juan Marcos, Lourdes, Pakravan, Mohammad, Bedard, Karen, Greer, Wenda L, Chen, Xueyi, Huang, Lulin, Sang, Jinghong, Jia, Hongyan, Jia, Liyun, Berner, Daniel, Mossböck, Georg, Welge-Luessen, Ulrich-Christoph, Chatzikyriakidou, Anthi, Anastasopoulos, Eleftherios, Porporato, Natalia, Saravanan, Vijayan, Shivkumar, Chandrashekaran, Yazdani, Shahin, Lavia, Carlo, Dallorto, Laura, Salvi, Erika, Manunta, Paolo, Mori, Yosai, Higashide, Tomomi, Chihara, Etsuo, Yanagi, Masahide, Kiuchi, Yoshiaki, Chuman, Hideki, Yoshimura, Nagahisa, Ikeda, Yoko, Park, Kyu Hyung, Ahn, Jeeyun, Rafei, Abderrahman, Chong, Yaan Fun, Ng, Xiao Yu, Goh, Shuang Ru, Ugbede, Idakwo, Suwan, Yanin, Supakontanasan, Wasu, Okeke, Suhanya, Asimadu, Ifeoma, Castro, Vania, Dervan, Edward, Silke, Eoin, Cuello, Osvaldo, Zompa, Tamara, Souzeau, Emmanuelle, Mitchell, Paul, Crowston, Jonathan G, Aljasim, Leyla Ali, Chowbay, Balram, Foo, Jia Nee, Xie, Zhicheng, Cheong, Augustine W O, Chen, Xiao Yin, Peh, Su Qin, Husain, Rahat, Salas, Antonio, Sakuntabhai, Anavaj, Herms, Stefan, Moebus, Susanne, Ziskind, Ari, Carmichael, Trevor R, Álvarez, Lydia, Rodríguez-Calvo, Pedro P, Tamcelik, Nevbahar, Aktas, Dilek, Kasım, Burcu, Challa, Pratap, Chaya, Craig J, Crandall, Alan, Zangwill, Linda M, den Hollander, Anneke I, Fingert, John H, Shingleton, Bradford J, Pericak-Vance, Margaret A, Raychaudhuri, Soumya, Haines, Jonathan L, Jonasson, Fridbert, Milea, Dan, Micheal, Shazia, Pasutto, Francesca

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm von Bradley, Declan T, Hughes, Anne E, Badger, Stephen A, Jones, Gregory T, Harrison, Seamus C, Wright, Benjamin J, Bumpstead, Suzannah, Baas, Annette F, Grétarsdóttir, Sólveig, Burnand, Kevin, Child, Anne H, Clough, Rachel E, Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A, Ariëns, Robert A.S, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M, van Bockxmeer, Frank M, Waltham, Matthew, Matthíasson, Stefán E, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D, Teijink, Joep A.W, Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A, Wild, John B, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E, Potter, Simon, Lindholt, Jes S, Golledge, Jonathan, Norman, Paul E, van Rij, Andre, Powell, Janet T, Eriksson, Per, Stefánsson, Kári, Thompson, John R, Humphries, Steve E, Sayers, Robert D, Deloukas, Panos, Samani, Nilesh J, Bown, Matthew J

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

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