Results of search for 'au:"Stefánsson, Kāri"' › مکتبة رقمیه للعلوم الطبيه catalog

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	361.	Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. [electronic resource] by Went, Molly Sud, Amit Försti, Asta Halvarsson, Britt-Marie Weinhold, Niels Kimber, Scott van Duin, Mark Thorleifsson, Gudmar Holroyd, Amy Johnson, David C Li, Ni Orlando, Giulia Law, Philip J Ali, Mina Chen, Bowang Mitchell, Jonathan S Gudbjartsson, Daniel F Kuiper, Rowan Stephens, Owen W Bertsch, Uta Broderick, Peter Campo, Chiara Bandapalli, Obul R Einsele, Hermann Gregory, Walter A Gullberg, Urban Hillengass, Jens Hoffmann, Per Jackson, Graham H Jöckel, Karl-Heinz Johnsson, Ellinor Kristinsson, Sigurður Y Mellqvist, Ulf-Henrik Nahi, Hareth Easton, Douglas Pharoah, Paul Dunning, Alison Peto, Julian Canzian, Federico Swerdlow, Anthony Eeles, Rosalind A Kote-Jarai, ZSofia Muir, Kenneth Pashayan, Nora Nickel, Jolanta Nöthen, Markus M Rafnar, Thorunn Ross, Fiona M da Silva Filho, Miguel Inacio Thomsen, Hauke Turesson, Ingemar Vangsted, Annette Andersen, Niels Frost Waage, Anders Walker, Brian A Wihlborg, Anna-Karin Broyl, Annemiek Davies, Faith E Thorsteinsdottir, Unnur Langer, Christian Hansson, Markus Goldschmidt, Hartmut Kaiser, Martin Sonneveld, Pieter Stefansson, Kari Morgan, Gareth J Hemminki, Kari Nilsson, Björn Houlston, Richard S Producer: 20181231 In: Nature communications vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	362.	The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. [electronic resource] by Helgadottir, Anna Thorleifsson, Gudmar Magnusson, Kristinn P Grétarsdottir, Solveig Steinthorsdottir, Valgerdur Manolescu, Andrei Jones, Gregory T Rinkel, Gabriel J E Blankensteijn, Jan D Ronkainen, Antti Jääskeläinen, Juha E Kyo, Yoshiki Lenk, Guy M Sakalihasan, Natzi Kostulas, Konstantinos Gottsäter, Anders Flex, Andrea Stefansson, Hreinn Hansen, Torben Andersen, Gitte Weinsheimer, Shantel Borch-Johnsen, Knut Jorgensen, Torben Shah, Svati H Quyyumi, Arshed A Granger, Christopher B Reilly, Muredach P Austin, Harland Levey, Allan I Vaccarino, Viola Palsdottir, Ebba Walters, G Bragi Jonsdottir, Thorbjorg Snorradottir, Steinunn Magnusdottir, Dana Gudmundsson, Gudmundur Ferrell, Robert E Sveinbjornsdottir, Sigurlaug Hernesniemi, Juha Niemelä, Mika Limet, Raymond Andersen, Karl Sigurdsson, Gunnar Benediktsson, Rafn Verhoeven, Eric L G Teijink, Joep A W Grobbee, Diederick E Rader, Daniel J Collier, David A Pedersen, Oluf Pola, Roberto Hillert, Jan Lindblad, Bengt Valdimarsson, Einar M Magnadottir, Hulda B Wijmenga, Cisca Tromp, Gerard Baas, Annette F Ruigrok, Ynte M van Rij, Andre M Kuivaniemi, Helena Powell, Janet T Matthiasson, Stefan E Gulcher, Jeffrey R Thorgeirsson, Gudmundur Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20080226 In: Nature genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	363.	Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus. [electronic resource] by Stacey, Simon N Sulem, Patrick Zanon, Carlo Gudjonsson, Sigurjon A Thorleifsson, Gudmar Helgason, Agnar Jonasdottir, Aslaug Besenbacher, Soren Kostic, Jelena P Fackenthal, James D Huo, Dezheng Adebamowo, Clement Ogundiran, Temidayo Olson, Janet E Fredericksen, Zachary S Wang, Xianshu Look, Maxime P Sieuwerts, Anieta M Martens, John W M Pajares, Isabel Garcia-Prats, Maria D Ramon-Cajal, Jose M de Juan, Ana Panadero, Angeles Ortega, Eugenia Aben, Katja K H Vermeulen, Sita H Asadzadeh, Fatemeh van Engelenburg, K C Anton Margolin, Sara Shen, Chen-Yang Wu, Pei-Ei Försti, Asta Lenner, Per Henriksson, Roger Johansson, Robert Enquist, Kerstin Hallmans, Göran Jonsson, Thorvaldur Sigurdsson, Helgi Alexiusdottir, Kristin Gudmundsson, Julius Sigurdsson, Asgeir Frigge, Michael L Gudmundsson, Larus Kristjansson, Kristleifur Halldorsson, Bjarni V Styrkarsdottir, Unnur Gulcher, Jeffrey R Hemminki, Kari Lindblom, Annika Kiemeney, Lambertus A Mayordomo, Jose I Foekens, John A Couch, Fergus J Olopade, Olufunmilayo I Gudbjartsson, Daniel F Thorsteinsdottir, Unnur Rafnar, Thorunn Johannsson, Oskar T Stefansson, Kari Producer: 20101122 In: PLoS genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	364.	A genome-wide association study of early menopause and the combined impact of identified variants. [electronic resource] by Perry, John R B Corre, Tanguy Esko, Tõnu Chasman, Daniel I Fischer, Krista Franceschini, Nora He, Chunyan Kutalik, Zoltan Mangino, Massimo Rose, Lynda M Vernon Smith, Albert Stolk, Lisette Sulem, Patrick Weedon, Michael N Zhuang, Wei V Arnold, Alice Ashworth, Alan Bergmann, Sven Buring, Julie E Burri, Andrea Chen, Constance Cornelis, Marilyn C Couper, David J Goodarzi, Mark O Gudnason, Vilmundur Harris, Tamara Hofman, Albert Jones, Michael Kraft, Peter Launer, Lenore Laven, Joop S E Li, Guo McKnight, Barbara Masciullo, Corrado Milani, Lili Orr, Nicholas Psaty, Bruce M Ridker, Paul M Rivadeneira, Fernando Sala, Cinzia Salumets, Andres Schoemaker, Minouk Traglia, Michela Waeber, Gérard Chanock, Stephen J Demerath, Ellen W Garcia, Melissa Hankinson, Susan E Hu, Frank B Hunter, David J Lunetta, Kathryn L Metspalu, Andres Montgomery, Grant W Murabito, Joanne M Newman, Anne B Ong, Ken K Spector, Tim D Stefansson, Kari Swerdlow, Anthony J Thorsteinsdottir, Unnur Van Dam, Rob M Uitterlinden, André G Visser, Jenny A Vollenweider, Peter Toniolo, Daniela Murray, Anna Producer: 20130828 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	365.	Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. [electronic resource] by Went, Molly Sud, Amit Försti, Asta Halvarsson, Britt-Marie Weinhold, Niels Kimber, Scott van Duin, Mark Thorleifsson, Gudmar Holroyd, Amy Johnson, David C Li, Ni Orlando, Giulia Law, Philip J Ali, Mina Chen, Bowang Mitchell, Jonathan S Gudbjartsson, Daniel F Kuiper, Rowan Stephens, Owen W Bertsch, Uta Broderick, Peter Campo, Chiara Bandapalli, Obul R Einsele, Hermann Gregory, Walter A Gullberg, Urban Hillengass, Jens Hoffmann, Per Jackson, Graham H Jöckel, Karl-Heinz Johnsson, Ellinor Kristinsson, Sigurður Y Mellqvist, Ulf-Henrik Nahi, Hareth Easton, Douglas Pharoah, Paul Dunning, Alison Peto, Julian Canzian, Federico Swerdlow, Anthony Eeles, Rosalind A Kote-Jarai, Zsofia Muir, Kenneth Pashayan, Nora Nickel, Jolanta Nöthen, Markus M Rafnar, Thorunn Ross, Fiona M da Silva Filho, Miguel Inacio Thomsen, Hauke Turesson, Ingemar Vangsted, Annette Andersen, Niels Frost Waage, Anders Walker, Brian A Wihlborg, Anna-Karin Broyl, Annemiek Davies, Faith E Thorsteinsdottir, Unnur Langer, Christian Hansson, Markus Goldschmidt, Hartmut Kaiser, Martin Sonneveld, Pieter Stefansson, Kari Morgan, Gareth J Hemminki, Kari Nilsson, Björn Houlston, Richard S Publication details: Nature communications 01 2019 In: Nature communications vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	366.	Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. [electronic resource] by Gudbjartsson, Daniel F Bjornsdottir, Unnur S Halapi, Eva Helgadottir, Anna Sulem, Patrick Jonsdottir, Gudrun M Thorleifsson, Gudmar Helgadottir, Hafdis Steinthorsdottir, Valgerdur Stefansson, Hreinn Williams, Carolyn Hui, Jennie Beilby, John Warrington, Nicole M James, Alan Palmer, Lyle J Koppelman, Gerard H Heinzmann, Andrea Krueger, Marcus Boezen, H Marike Wheatley, Amanda Altmuller, Janine Shin, Hyoung Doo Uh, Soo-Taek Cheong, Hyun Sub Jonsdottir, Brynja Gislason, David Park, Choon-Sik Rasmussen, Linda M Porsbjerg, Celeste Hansen, Jakob W Backer, Vibeke Werge, Thomas Janson, Christer Jönsson, Ulla-Britt Ng, Maggie C Y Chan, Juliana So, Wing Yee Ma, Ronald Shah, Svati H Granger, Christopher B Quyyumi, Arshed A Levey, Allan I Vaccarino, Viola Reilly, Muredach P Rader, Daniel J Williams, Michael J A van Rij, Andre M Jones, Gregory T Trabetti, Elisabetta Malerba, Giovanni Pignatti, Pier Franco Boner, Attilio Pescollderungg, Lydia Girelli, Domenico Olivieri, Oliviero Martinelli, Nicola Ludviksson, Bjorn R Ludviksdottir, Dora Eyjolfsson, Gudmundur I Arnar, David Thorgeirsson, Gudmundur Deichmann, Klaus Thompson, Philip J Wjst, Matthias Hall, Ian P Postma, Dirkje S Gislason, Thorarinn Gulcher, Jeffrey Kong, Augustine Jonsdottir, Ingileif Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20090402 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	367.	Large recurrent microdeletions associated with schizophrenia. [electronic resource] by Stefansson, Hreinn Rujescu, Dan Cichon, Sven Pietiläinen, Olli P H Ingason, Andres Steinberg, Stacy Fossdal, Ragnheidur Sigurdsson, Engilbert Sigmundsson, Thordur Buizer-Voskamp, Jacobine E Hansen, Thomas Jakobsen, Klaus D Muglia, Pierandrea Francks, Clyde Matthews, Paul M Gylfason, Arnaldur Halldorsson, Bjarni V Gudbjartsson, Daniel Thorgeirsson, Thorgeir E Sigurdsson, Asgeir Jonasdottir, Adalbjorg Jonasdottir, Aslaug Bjornsson, Asgeir Mattiasdottir, Sigurborg Blondal, Thorarinn Haraldsson, Magnus Magnusdottir, Brynja B Giegling, Ina Möller, Hans-Jürgen Hartmann, Annette Shianna, Kevin V Ge, Dongliang Need, Anna C Crombie, Caroline Fraser, Gillian Walker, Nicholas Lonnqvist, Jouko Suvisaari, Jaana Tuulio-Henriksson, Annamarie Paunio, Tiina Toulopoulou, Timi Bramon, Elvira Di Forti, Marta Murray, Robin Ruggeri, Mirella Vassos, Evangelos Tosato, Sarah Walshe, Muriel Li, Tao Vasilescu, Catalina Mühleisen, Thomas W Wang, August G Ullum, Henrik Djurovic, Srdjan Melle, Ingrid Olesen, Jes Kiemeney, Lambertus A Franke, Barbara Sabatti, Chiara Freimer, Nelson B Gulcher, Jeffrey R Thorsteinsdottir, Unnur Kong, Augustine Andreassen, Ole A Ophoff, Roel A Georgi, Alexander Rietschel, Marcella Werge, Thomas Petursson, Hannes Goldstein, David B Nöthen, Markus M Peltonen, Leena Collier, David A St Clair, David Stefansson, Kari Producer: 20081021 In: Nature vol. 455 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	368.	Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. [electronic resource] by Perry, John R B Voight, Benjamin F Yengo, Loïc Amin, Najaf Dupuis, Josée Ganser, Martha Grallert, Harald Navarro, Pau Li, Man Qi, Lu Steinthorsdottir, Valgerdur Scott, Robert A Almgren, Peter Arking, Dan E Aulchenko, Yurii Balkau, Beverley Benediktsson, Rafn Bergman, Richard N Boerwinkle, Eric Bonnycastle, Lori Burtt, Noël P Campbell, Harry Charpentier, Guillaume Collins, Francis S Gieger, Christian Green, Todd Hadjadj, Samy Hattersley, Andrew T Herder, Christian Hofman, Albert Johnson, Andrew D Kottgen, Anna Kraft, Peter Labrune, Yann Langenberg, Claudia Manning, Alisa K Mohlke, Karen L Morris, Andrew P Oostra, Ben Pankow, James Petersen, Ann-Kristin Pramstaller, Peter P Prokopenko, Inga Rathmann, Wolfgang Rayner, William Roden, Michael Rudan, Igor Rybin, Denis Scott, Laura J Sigurdsson, Gunnar Sladek, Rob Thorleifsson, Gudmar Thorsteinsdottir, Unnur Tuomilehto, Jaakko Uitterlinden, Andre G Vivequin, Sidonie Weedon, Michael N Wright, Alan F Hu, Frank B Illig, Thomas Kao, Linda Meigs, James B Wilson, James F Stefansson, Kari van Duijn, Cornelia Altschuler, David Morris, Andrew D Boehnke, Michael McCarthy, Mark I Froguel, Philippe Palmer, Colin N A Wareham, Nicholas J Groop, Leif Frayling, Timothy M Cauchi, Stéphane Producer: 20120925 In: PLoS genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	369.	Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. [electronic resource] by Evangelou, Evangelos Valdes, Ana M Kerkhof, Hanneke J M Styrkarsdottir, Unnur Zhu, Yanyan Meulenbelt, Ingrid Lories, Rik J Karassa, Fotini B Tylzanowski, Przemko Bos, Steffan D Akune, Toru Arden, Nigel K Carr, Andrew Chapman, Kay Cupples, L Adrienne Dai, Jin Deloukas, Panos Doherty, Michael Doherty, Sally Engstrom, Gunnar Gonzalez, Antonio Halldorsson, Bjarni V Hammond, Christina L Hart, Deborah J Helgadottir, Hafdis Hofman, Albert Ikegawa, Shiro Ingvarsson, Thorvaldur Jiang, Qing Jonsson, Helgi Kaprio, Jaakko Kawaguchi, Hiroshi Kisand, Kalle Kloppenburg, Margreet Kujala, Urho M Lohmander, L Stefan Loughlin, John Luyten, Frank P Mabuchi, Akihiko McCaskie, Andrew Nakajima, Masahiro Nilsson, Peter M Nishida, Nao Ollier, William E R Panoutsopoulou, Kalliope van de Putte, Tom Ralston, Stuart H Rivadeneira, Fernado Saarela, Janna Schulte-Merker, Stefan Shi, Dongquan Slagboom, P Eline Sudo, Akihiro Tamm, Agu Tamm, Ann Thorleifsson, Gudmar Thorsteinsdottir, Unnur Tsezou, Aspasia Wallis, Gillian A Wilkinson, J Mark Yoshimura, Noriko Zeggini, Eleftheria Zhai, Guangju Zhang, Feng Jonsdottir, Ingileif Uitterlinden, Andre G Felson, David T van Meurs, Joyce B Stefansson, Kari Ioannidis, John P A Spector, Timothy D Producer: 20110217 In: Annals of the rheumatic diseases vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	370.	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. [electronic resource] by Kiemeney, Lambertus A Sulem, Patrick Besenbacher, Soren Vermeulen, Sita H Sigurdsson, Asgeir Thorleifsson, Gudmar Gudbjartsson, Daniel F Stacey, Simon N Gudmundsson, Julius Zanon, Carlo Kostic, Jelena Masson, Gisli Bjarnason, Hjordis Palsson, Stefan T Skarphedinsson, Oskar B Gudjonsson, Sigurjon A Witjes, J Alfred Grotenhuis, Anne J Verhaegh, Gerald W Bishop, D Timothy Sak, Sei Chung Choudhury, Ananya Elliott, Faye Barrett, Jennifer H Hurst, Carolyn D de Verdier, Petra J Ryk, Charlotta Rudnai, Peter Gurzau, Eugene Koppova, Kvetoslava Vineis, Paolo Polidoro, Silvia Guarrera, Simonetta Sacerdote, Carlotta Campagna, Marcello Placidi, Donatella Arici, Cecilia Zeegers, Maurice P Kellen, Eliane Gutierrez, Berta Saez Sanz-Velez, José I Sanchez-Zalabardo, Manuel Valdivia, Gabriel Garcia-Prats, Maria D Hengstler, Jan G Blaszkewicz, Meinolf Dietrich, Holger Ophoff, Roel A van den Berg, Leonard H Alexiusdottir, Kristin Kristjansson, Kristleifur Geirsson, Gudmundur Nikulasson, Sigfus Petursdottir, Vigdis Kong, Augustine Thorgeirsson, Thorgeir Mungan, N Aydin Lindblom, Annika van Es, Michael A Porru, Stefano Buntinx, Frank Golka, Klaus Mayordomo, José I Kumar, Rajiv Matullo, Giuseppe Steineck, Gunnar Kiltie, Anne E Aben, Katja K H Jonsson, Eirikur Thorsteinsdottir, Unnur Knowles, Margaret A Rafnar, Thorunn Stefansson, Kari Producer: 20100527 In: Nature genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	371.	Genetic variation at 16q24.2 is associated with small vessel stroke. [electronic resource] by Traylor, Matthew Malik, Rainer Nalls, Mike A Cotlarciuc, Ioana Radmanesh, Farid Thorleifsson, Gudmar Hanscombe, Ken B Langefeld, Carl Saleheen, Danish Rost, Natalia S Yet, Idil Spector, Tim D Bell, Jordana T Hannon, Eilis Mill, Jonathan Chauhan, Ganesh Debette, Stephanie Bis, Joshua C Longstreth, W T Ikram, M Arfan Launer, Lenore J Seshadri, Sudha Hamilton-Bruce, Monica Anne Jimenez-Conde, Jordi Cole, John W Schmidt, Reinhold Słowik, Agnieszka Lemmens, Robin Lindgren, Arne Melander, Olle Grewal, Raji P Sacco, Ralph L Rundek, Tatjana Rexrode, Kathryn Arnett, Donna K Johnson, Julie A Benavente, Oscar R Wasssertheil-Smoller, Sylvia Lee, Jin-Moo Pulit, Sara L Wong, Quenna Rich, Stephen S de Bakker, Paul I W McArdle, Patrick F Woo, Daniel Anderson, Christopher D Xu, Huichun Heitsch, Laura Fornage, Myriam Jern, Christina Stefansson, Kari Thorsteinsdottir, Unnur Gretarsdottir, Solveig Lewis, Cathryn M Sharma, Pankaj Sudlow, Cathie L M Rothwell, Peter M Boncoraglio, Giorgio B Thijs, Vincent Levi, Chris Meschia, James F Rosand, Jonathan Kittner, Steven J Mitchell, Braxton D Dichgans, Martin Worrall, Bradford B Markus, Hugh S Producer: 20170630 In: Annals of neurology vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	372.	Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. [electronic resource] by Forstner, Andreas J Awasthi, Swapnil Wolf, Christiane Maron, Eduard Erhardt, Angelika Czamara, Darina Eriksson, Elias Lavebratt, Catharina Allgulander, Christer Friedrich, Nina Becker, Jessica Hecker, Julian Rambau, Stefanie Conrad, Rupert Geiser, Franziska McMahon, Francis J Moebus, Susanne Hess, Timo Buerfent, Benedikt C Hoffmann, Per Herms, Stefan Heilmann-Heimbach, Stefanie Kockum, Ingrid Olsson, Tomas Alfredsson, Lars Weber, Heike Alpers, Georg W Arolt, Volker Fehm, Lydia Fydrich, Thomas Gerlach, Alexander L Hamm, Alfons Kircher, Tilo Pané-Farré, Christiane A Pauli, Paul Rief, Winfried Ströhle, Andreas Plag, Jens Lang, Thomas Wittchen, Hans-Ulrich Mattheisen, Manuel Meier, Sandra Metspalu, Andres Domschke, Katharina Reif, Andreas Hovatta, Iiris Lindefors, Nils Andersson, Evelyn Schalling, Martin Mbarek, Hamdi Milaneschi, Yuri de Geus, Eco J C Boomsma, Dorret I Penninx, Brenda W J H Thorgeirsson, Thorgeir E Steinberg, Stacy Stefansson, Kari Stefansson, Hreinn Müller-Myhsok, Bertram Hansen, Thomas Folkmann Børglum, Anders D Werge, Thomas Mortensen, Preben Bo Nordentoft, Merete Hougaard, David M Hultman, Christina M Sullivan, Patrick F Nöthen, Markus M Woldbye, David P D Mors, Ole Binder, Elisabeth B Rück, Christian Ripke, Stephan Deckert, Jürgen Schumacher, Johannes Producer: 20220127 In: Molecular psychiatry vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	373.	Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. [electronic resource] by Gudmundsson, Julius Sulem, Patrick Rafnar, Thorunn Bergthorsson, Jon T Manolescu, Andrei Gudbjartsson, Daniel Agnarsson, Bjarni A Sigurdsson, Asgeir Benediktsdottir, Kristrun R Blondal, Thorarinn Jakobsdottir, Margret Stacey, Simon N Kostic, Jelena Kristinsson, Kari T Birgisdottir, Birgitta Ghosh, Shyamali Magnusdottir, Droplaug N Thorlacius, Steinunn Thorleifsson, Gudmar Zheng, S Lilly Sun, Jielin Chang, Bao-Li Elmore, J Bradford Breyer, Joan P McReynolds, Kate M Bradley, Kevin M Yaspan, Brian L Wiklund, Fredrik Stattin, Par Lindström, Sara Adami, Hans-Olov McDonnell, Shannon K Schaid, Daniel J Cunningham, Julie M Wang, Liang Cerhan, James R St Sauver, Jennifer L Isaacs, Sara D Wiley, Kathleen E Partin, Alan W Walsh, Patrick C Polo, Sonia Ruiz-Echarri, Manuel Navarrete, Sebastian Fuertes, Fernando Saez, Berta Godino, Javier Weijerman, Philip C Swinkels, Dorine W Aben, Katja K Witjes, J Alfred Suarez, Brian K Helfand, Brian T Frigge, Michael L Kristjansson, Kristleifur Ober, Carole Jonsson, Eirikur Einarsson, Gudmundur V Xu, Jianfeng Gronberg, Henrik Smith, Jeffrey R Thibodeau, Stephen N Isaacs, William B Catalona, William J Mayordomo, Jose I Kiemeney, Lambertus A Barkardottir, Rosa B Gulcher, Jeffrey R Thorsteinsdottir, Unnur Kong, Augustine Stefansson, Kari Producer: 20080402 In: Nature genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	374.	European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. [electronic resource] by Rafnar, Thorunn Vermeulen, Sita H Sulem, Patrick Thorleifsson, Gudmar Aben, Katja K Witjes, J Alfred Grotenhuis, Anne J Verhaegh, Gerald W Hulsbergen-van de Kaa, Christina A Besenbacher, Soren Gudbjartsson, Daniel Stacey, Simon N Gudmundsson, Julius Johannsdottir, Hrefna Bjarnason, Hjordis Zanon, Carlo Helgadottir, Hafdis Jonasson, Jon Gunnlaugur Tryggvadottir, Laufey Jonsson, Eirikur Geirsson, Gudmundur Nikulasson, Sigfus Petursdottir, Vigdis Bishop, D Timothy Chung-Sak, Sei Choudhury, Ananya Elliott, Faye Barrett, Jennifer H Knowles, Margaret A de Verdier, Petra J Ryk, Charlotta Lindblom, Annika Rudnai, Peter Gurzau, Eugene Koppova, Kvetoslava Vineis, Paolo Polidoro, Silvia Guarrera, Simonetta Sacerdote, Carlotta Panadero, Angeles Sanz-Velez, José I Sanchez, Manuel Valdivia, Gabriel Garcia-Prats, Maria D Hengstler, Jan G Selinski, Silvia Gerullis, Holger Ovsiannikov, Daniel Khezri, Abdolaziz Aminsharifi, Alireza Malekzadeh, Mahyar van den Berg, Leonard H Ophoff, Roel A Veldink, Jan H Zeegers, Maurice P Kellen, Eliane Fostinelli, Jacopo Andreoli, Daniele Arici, Cecilia Porru, Stefano Buntinx, Frank Ghaderi, Abbas Golka, Klaus Mayordomo, José I Matullo, Giuseppe Kumar, Rajiv Steineck, Gunnar Kiltie, Anne E Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari Kiemeney, Lambertus A Producer: 20120131 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	375.	Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. [electronic resource] by Cichon, Sven Mühleisen, Thomas W Degenhardt, Franziska A Mattheisen, Manuel Miró, Xavier Strohmaier, Jana Steffens, Michael Meesters, Christian Herms, Stefan Weingarten, Moritz Priebe, Lutz Haenisch, Britta Alexander, Michael Vollmer, Jennifer Breuer, René Schmäl, Christine Tessmann, Peter Moebus, Susanne Wichmann, H-Erich Schreiber, Stefan Müller-Myhsok, Bertram Lucae, Susanne Jamain, Stéphane Leboyer, Marion Bellivier, Frank Etain, Bruno Henry, Chantal Kahn, Jean-Pierre Heath, Simon Hamshere, Marian O'Donovan, Michael C Owen, Michael J Craddock, Nick Schwarz, Markus Vedder, Helmut Kammerer-Ciernioch, Jutta Reif, Andreas Sasse, Johanna Bauer, Michael Hautzinger, Martin Wright, Adam Mitchell, Philip B Schofield, Peter R Montgomery, Grant W Medland, Sarah E Gordon, Scott D Martin, Nicholas G Gustafsson, Omar Andreassen, Ole Djurovic, Srdjan Sigurdsson, Engilbert Steinberg, Stacy Stefansson, Hreinn Stefansson, Kari Kapur-Pojskic, Lejla Oruc, Liliana Rivas, Fabio Mayoral, Fermín Chuchalin, Alexander Babadjanova, Gulja Tiganov, Alexander S Pantelejeva, Galina Abramova, Lilia I Grigoroiu-Serbanescu, Maria Diaconu, Carmen C Czerski, Piotr M Hauser, Joanna Zimmer, Andreas Lathrop, Mark Schulze, Thomas G Wienker, Thomas F Schumacher, Johannes Maier, Wolfgang Propping, Peter Rietschel, Marcella Nöthen, Markus M Producer: 20110516 In: American journal of human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	376.	A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus. [electronic resource] by 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 Producer: 20140908 In: Journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	377.	Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer. [electronic resource] by 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 Producer: 20150603 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	378.	Loss of Cardioprotective Effects at the [electronic resource] by Saleheen, Danish Zhao, Wei Young, Robin Nelson, Christopher P Ho, WeangKee Ferguson, Jane F Rasheed, Asif Ou, Kristy Nurnberg, Sylvia T Bauer, Robert C Goel, Anuj Do, Ron Stewart, Alexandre F R Hartiala, Jaana Zhang, Weihua Thorleifsson, Gudmar Strawbridge, Rona J Sinisalo, Juha Kanoni, Stavroula Sedaghat, Sanaz Marouli, Eirini Kristiansson, Kati Hua Zhao, Jing Scott, Robert Gauguier, Dominique Shah, Svati H Smith, Albert Vernon van Zuydam, Natalie Cox, Amanda J Willenborg, Christina Kessler, Thorsten Zeng, Lingyao Province, Michael A Ganna, Andrea Lind, Lars Pedersen, Nancy L White, Charles C Joensuu, Anni Edi Kleber, Marcus Hall, Alistair S März, Winfried Salomaa, Veikko O'Donnell, Christopher Ingelsson, Erik Feitosa, Mary F Erdmann, Jeanette Bowden, Donald W Palmer, Colin N A Gudnason, Vilmundur Faire, Ulf De Zalloua, Pierre Wareham, Nicholas Thompson, John R Kuulasmaa, Kari Dedoussis, George Perola, Markus Dehghan, Abbas Chambers, John C Kooner, Jaspal Allayee, Hooman Deloukas, Panos McPherson, Ruth Stefansson, Kari Schunkert, Heribert Kathiresan, Sekar Farrall, Martin Marcel Frossard, Philippe Rader, Daniel J Samani, Nilesh J Reilly, Muredach P Producer: 20170829 In: Circulation vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	379.	A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. [electronic resource] by Evangelou, Evangelos Kerkhof, Hanneke J Styrkarsdottir, Unnur Ntzani, Evangelia E Bos, Steffan D Esko, Tonu Evans, Daniel S Metrustry, Sarah Panoutsopoulou, Kalliope Ramos, Yolande F M Thorleifsson, Gudmar Tsilidis, Konstantinos K Arden, Nigel Aslam, Nadim Bellamy, Nicholas Birrell, Fraser Blanco, Francisco J Carr, Andrew Chapman, Kay Day-Williams, Aaron G Deloukas, Panos Doherty, Michael Engström, Gunnar Helgadottir, Hafdis T Hofman, Albert Ingvarsson, Thorvaldur Jonsson, Helgi Keis, Aime Keurentjes, J Christiaan Kloppenburg, Margreet Lind, Penelope A McCaskie, Andrew Martin, Nicholas G Milani, Lili Montgomery, Grant W Nelissen, Rob G H H Nevitt, Michael C Nilsson, Peter M Ollier, William Er Parimi, Neeta Rai, Ashok Ralston, Stuart H Reed, Mike R Riancho, Jose A Rivadeneira, Fernando Rodriguez-Fontenla, Cristina Southam, Lorraine Thorsteinsdottir, Unnur Tsezou, Aspasia Wallis, Gillian A Wilkinson, J Mark Gonzalez, Antonio Lane, Nancy E Lohmander, L Stefan Loughlin, John Metspalu, Andres Uitterlinden, Andre G Jonsdottir, Ingileif Stefansson, Kari Slagboom, P Eline Zeggini, Eleftheria Meulenbelt, Ingrid Ioannidis, John Pa Spector, Tim D van Meurs, Joyce B J Valdes, Ana M Producer: 20141230 In: Annals of the rheumatic diseases vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	380.	Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. [electronic resource] by 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 Producer: 20190510 In: Nature genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. [electronic resource] by

Cichon, Sven
Mühleisen, Thomas W
Degenhardt, Franziska A
Mattheisen, Manuel
Miró, Xavier
Strohmaier, Jana
Steffens, Michael
Meesters, Christian
Herms, Stefan
Weingarten, Moritz
Priebe, Lutz
Haenisch, Britta
Alexander, Michael
Vollmer, Jennifer
Breuer, René
Schmäl, Christine
Tessmann, Peter
Moebus, Susanne
Wichmann, H-Erich
Schreiber, Stefan
Müller-Myhsok, Bertram
Lucae, Susanne
Jamain, Stéphane
Leboyer, Marion
Bellivier, Frank
Etain, Bruno
Henry, Chantal
Kahn, Jean-Pierre
Heath, Simon
Hamshere, Marian
O'Donovan, Michael C
Owen, Michael J
Craddock, Nick
Schwarz, Markus
Vedder, Helmut
Kammerer-Ciernioch, Jutta
Reif, Andreas
Sasse, Johanna
Bauer, Michael
Hautzinger, Martin
Wright, Adam
Mitchell, Philip B
Schofield, Peter R
Montgomery, Grant W
Medland, Sarah E
Gordon, Scott D
Martin, Nicholas G
Gustafsson, Omar
Andreassen, Ole
Djurovic, Srdjan
Sigurdsson, Engilbert
Steinberg, Stacy
Stefansson, Hreinn
Stefansson, Kari
Kapur-Pojskic, Lejla
Oruc, Liliana
Rivas, Fabio
Mayoral, Fermín
Chuchalin, Alexander
Babadjanova, Gulja
Tiganov, Alexander S
Pantelejeva, Galina
Abramova, Lilia I
Grigoroiu-Serbanescu, Maria
Diaconu, Carmen C
Czerski, Piotr M
Hauser, Joanna
Zimmer, Andreas
Lathrop, Mark
Schulze, Thomas G
Wienker, Thomas F
Schumacher, Johannes
Maier, Wolfgang
Propping, Peter
Rietschel, Marcella
Nöthen, Markus M

Producer: 20110516 In: American journal of human genetics vol. 88

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