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

Results
	381.	Publisher Correction: 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 Publication details: Nature genetics Jul 2019 In: Nature genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	382.	Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. [electronic resource] by Wang, Yufei McKay, James D Rafnar, Thorunn Wang, Zhaoming Timofeeva, Maria N Broderick, Peter Zong, Xuchen Laplana, Marina Wei, Yongyue Han, Younghun Lloyd, Amy Delahaye-Sourdeix, Manon Chubb, Daniel Gaborieau, Valerie Wheeler, William Chatterjee, Nilanjan Thorleifsson, Gudmar Sulem, Patrick Liu, Geoffrey Kaaks, Rudolf Henrion, Marc Kinnersley, Ben Vallée, Maxime LeCalvez-Kelm, Florence Stevens, Victoria L Gapstur, Susan M Chen, Wei V Zaridze, David Szeszenia-Dabrowska, Neonilia Lissowska, Jolanta Rudnai, Peter Fabianova, Eleonora Mates, Dana Bencko, Vladimir Foretova, Lenka Janout, Vladimir Krokan, Hans E Gabrielsen, Maiken Elvestad Skorpen, Frank Vatten, Lars Njølstad, Inger Chen, Chu Goodman, Gary Benhamou, Simone Vooder, Tonu Välk, Kristjan Nelis, Mari Metspalu, Andres Lener, Marcin Lubiński, Jan Johansson, Mattias Vineis, Paolo Agudo, Antonio Clavel-Chapelon, Francoise Bueno-de-Mesquita, H Bas Trichopoulos, Dimitrios Khaw, Kay-Tee Johansson, Mikael Weiderpass, Elisabete Tjønneland, Anne Riboli, Elio Lathrop, Mark Scelo, Ghislaine Albanes, Demetrius Caporaso, Neil E Ye, Yuanqing Gu, Jian Wu, Xifeng Spitz, Margaret R Dienemann, Hendrik Rosenberger, Albert Su, Li Matakidou, Athena Eisen, Timothy Stefansson, Kari Risch, Angela Chanock, Stephen J Christiani, David C Hung, Rayjean J Brennan, Paul Landi, Maria Teresa Houlston, Richard S Amos, Christopher I Producer: 20140904 In: Nature genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	383.	Identification of common genetic risk variants for autism spectrum disorder. [electronic resource] by Grove, Jakob Ripke, Stephan Als, Thomas D Mattheisen, Manuel Walters, Raymond K Won, Hyejung Pallesen, Jonatan Agerbo, Esben Andreassen, Ole A Anney, Richard Awashti, Swapnil Belliveau, Rich Bettella, Francesco Buxbaum, Joseph D Bybjerg-Grauholm, Jonas Bækvad-Hansen, Marie Cerrato, Felecia Chambert, Kimberly Christensen, Jane H Churchhouse, Claire Dellenvall, Karin Demontis, Ditte De Rubeis, Silvia Devlin, Bernie Djurovic, Srdjan Dumont, Ashley L Goldstein, Jacqueline I Hansen, Christine S Hauberg, Mads Engel Hollegaard, Mads V Hope, Sigrun Howrigan, Daniel P Huang, Hailiang Hultman, Christina M Klei, Lambertus Maller, Julian Martin, Joanna Martin, Alicia R Moran, Jennifer L Nyegaard, Mette Nærland, Terje Palmer, Duncan S Palotie, Aarno Pedersen, Carsten Bøcker Pedersen, Marianne Giørtz dPoterba, Timothy Poulsen, Jesper Buchhave Pourcain, Beate St Qvist, Per Rehnström, Karola Reichenberg, Abraham Reichert, Jennifer Robinson, Elise B Roeder, Kathryn Roussos, Panos Saemundsen, Evald Sandin, Sven Satterstrom, F Kyle Davey Smith, George Stefansson, Hreinn Steinberg, Stacy Stevens, Christine R Sullivan, Patrick F Turley, Patrick Walters, G Bragi Xu, Xinyi Stefansson, Kari Geschwind, Daniel H Nordentoft, Merete Hougaard, David M Werge, Thomas Mors, Ole Mortensen, Preben Bo Neale, Benjamin M Daly, Mark J Børglum, Anders D Producer: 20190424 In: Nature genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	384.	Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. [electronic resource] by Flannick, Jason Thorleifsson, Gudmar Beer, Nicola L Jacobs, Suzanne B R Grarup, Niels Burtt, Noël P Mahajan, Anubha Fuchsberger, Christian Atzmon, Gil Benediktsson, Rafn Blangero, John Bowden, Don W Brandslund, Ivan Brosnan, Julia Burslem, Frank Chambers, John Cho, Yoon Shin Christensen, Cramer Douglas, Desirée A Duggirala, Ravindranath Dymek, Zachary Farjoun, Yossi Fennell, Timothy Fontanillas, Pierre Forsén, Tom Gabriel, Stacey Glaser, Benjamin Gudbjartsson, Daniel F Hanis, Craig Hansen, Torben Hreidarsson, Astradur B Hveem, Kristian Ingelsson, Erik Isomaa, Bo Johansson, Stefan Jørgensen, Torben Jørgensen, Marit Eika Kathiresan, Sekar Kong, Augustine Kooner, Jaspal Kravic, Jasmina Laakso, Markku Lee, Jong-Young Lind, Lars Lindgren, Cecilia M Linneberg, Allan Masson, Gisli Meitinger, Thomas Mohlke, Karen L Molven, Anders Morris, Andrew P Potluri, Shobha Rauramaa, Rainer Ribel-Madsen, Rasmus Richard, Ann-Marie Rolph, Tim Salomaa, Veikko Segrè, Ayellet V Skärstrand, Hanna Steinthorsdottir, Valgerdur Stringham, Heather M Sulem, Patrick Tai, E Shyong Teo, Yik Ying Teslovich, Tanya Thorsteinsdottir, Unnur Trimmer, Jeff K Tuomi, Tiinamaija Tuomilehto, Jaakko Vaziri-Sani, Fariba Voight, Benjamin F Wilson, James G Boehnke, Michael McCarthy, Mark I Njølstad, Pål R Pedersen, Oluf Groop, Leif Cox, David R Stefansson, Kari Altshuler, David Producer: 20140519 In: Nature genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	385.	Common variants at VRK2 and TCF4 conferring risk of schizophrenia. [electronic resource] by Steinberg, Stacy de Jong, Simone Andreassen, Ole A Werge, Thomas Børglum, Anders D Mors, Ole Mortensen, Preben B Gustafsson, Omar Costas, Javier Pietiläinen, Olli P H Demontis, Ditte Papiol, Sergi Huttenlocher, Johanna Mattheisen, Manuel Breuer, René Vassos, Evangelos Giegling, Ina Fraser, Gillian Walker, Nicholas Tuulio-Henriksson, Annamari Suvisaari, Jaana Lönnqvist, Jouko Paunio, Tiina Agartz, Ingrid Melle, Ingrid Djurovic, Srdjan Strengman, Eric Jürgens, Gesche Glenthøj, Birte Terenius, Lars Hougaard, David M Ørntoft, Torben Wiuf, Carsten Didriksen, Michael Hollegaard, Mads V Nordentoft, Merete van Winkel, Ruud Kenis, Gunter Abramova, Lilia Kaleda, Vasily Arrojo, Manuel Sanjuán, Julio Arango, Celso Sperling, Swetlana Rossner, Moritz Ribolsi, Michele Magni, Valentina Siracusano, Alberto Christiansen, Claus Kiemeney, Lambertus A Veldink, Jan van den Berg, Leonard Ingason, Andres Muglia, Pierandrea Murray, Robin Nöthen, Markus M Sigurdsson, Engilbert Petursson, Hannes Thorsteinsdottir, Unnur Kong, Augustine Rubino, I Alex De Hert, Marc Réthelyi, János M Bitter, István Jönsson, Erik G Golimbet, Vera Carracedo, Angel Ehrenreich, Hannelore Craddock, Nick Owen, Michael J O'Donovan, Michael C Ruggeri, Mirella Tosato, Sarah Peltonen, Leena Ophoff, Roel A Collier, David A St Clair, David Rietschel, Marcella Cichon, Sven Stefansson, Hreinn Rujescu, Dan Stefansson, Kari Producer: 20120123 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	386.	Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. [electronic resource] by Power, Robert A Tansey, Katherine E Buttenschøn, Henriette Nørmølle Cohen-Woods, Sarah Bigdeli, Tim Hall, Lynsey S Kutalik, Zoltán Lee, S Hong Ripke, Stephan Steinberg, Stacy Teumer, Alexander Viktorin, Alexander Wray, Naomi R Arolt, Volker Baune, Bernard T Boomsma, Dorret I Børglum, Anders D Byrne, Enda M Castelao, Enrique Craddock, Nick Craig, Ian W Dannlowski, Udo Deary, Ian J Degenhardt, Franziska Forstner, Andreas J Gordon, Scott D Grabe, Hans J Grove, Jakob Hamilton, Steven P Hayward, Caroline Heath, Andrew C Hocking, Lynne J Homuth, Georg Hottenga, Jouke J Kloiber, Stefan Krogh, Jesper Landén, Mikael Lang, Maren Levinson, Douglas F Lichtenstein, Paul Lucae, Susanne MacIntyre, Donald J Madden, Pamela Magnusson, Patrik K E Martin, Nicholas G McIntosh, Andrew M Middeldorp, Christel M Milaneschi, Yuri Montgomery, Grant W Mors, Ole Müller-Myhsok, Bertram Nyholt, Dale R Oskarsson, Hogni Owen, Michael J Padmanabhan, Sandosh Penninx, Brenda W J H Pergadia, Michele L Porteous, David J Potash, James B Preisig, Martin Rivera, Margarita Shi, Jianxin Shyn, Stanley I Sigurdsson, Engilbert Smit, Johannes H Smith, Blair H Stefansson, Hreinn Stefansson, Kari Strohmaier, Jana Sullivan, Patrick F Thomson, Pippa Thorgeirsson, Thorgeir E Van der Auwera, Sandra Weissman, Myrna M Breen, Gerome Lewis, Cathryn M Producer: 20170810 In: Biological psychiatry vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	387.	Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. [electronic resource] by Wang, Yufei McKay, James D Rafnar, Thorunn Wang, Zhaoming Timofeeva, Maria N Broderick, Peter Zong, Xuchen Laplana, Marina Wei, Yongyue Han, Younghun Lloyd, Amy Delahaye-Sourdeix, Manon Chubb, Daniel Gaborieau, Valerie Wheeler, William Chatterjee, Nilanjan Thorleifsson, Gudmar Sulem, Patrick Liu, Geoffrey Kaaks, Rudolf Henrion, Marc Kinnersley, Ben Vallée, Maxime Le Calvez-Kelm, Florence Stevens, Victoria L Gapstur, Susan M Chen, Wei V Zaridze, David Szeszenia-Dabrowska, Neonilia Lissowska, Jolanta Rudnai, Peter Fabianova, Eleonora Mates, Dana Bencko, Vladimir Foretova, Lenka Janout, Vladimir Krokan, Hans E Gabrielsen, Maiken Elvestad Skorpen, Frank Vatten, Lars Njølstad, Inger Chen, Chu Goodman, Gary Benhamou, Simone Vooder, Tonu Välk, Kristjan Nelis, Mari Metspalu, Andres Lener, Marcin Lubiński, Jan Johansson, Mattias Vineis, Paolo Agudo, Antonio Clavel-Chapelon, Francoise Bueno-de-Mesquita, H Bas Trichopoulos, Dimitrios Khaw, Kay-Tee Johansson, Mikael Weiderpass, Elisabete Tjønneland, Anne Riboli, Elio Lathrop, Mark Scelo, Ghislaine Albanes, Demetrius Caporaso, Neil E Ye, Yuanqing Gu, Jian Wu, Xifeng Spitz, Margaret R Dienemann, Hendrik Rosenberger, Albert Su, Li Matakidou, Athena Eisen, Timothy Stefansson, Kari Risch, Angela Chanock, Stephen J Christiani, David C Hung, Rayjean J Brennan, Paul Landi, Maria Teresa Houlston, Richard S Amos, Christopher I Publication details: Nature genetics 03 2017 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	388.	Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. [electronic resource] by Gudmundsson, Julius Sulem, Patrick Steinthorsdottir, Valgerdur Bergthorsson, Jon T Thorleifsson, Gudmar Manolescu, Andrei Rafnar, Thorunn Gudbjartsson, Daniel Agnarsson, Bjarni A Baker, Adam Sigurdsson, Asgeir Benediktsdottir, Kristrun R Jakobsdottir, Margret Blondal, Thorarinn Stacey, Simon N Helgason, Agnar Gunnarsdottir, Steinunn Olafsdottir, Adalheidur Kristinsson, Kari T Birgisdottir, Birgitta Ghosh, Shyamali Thorlacius, Steinunn Magnusdottir, Dana Stefansdottir, Gerdur Kristjansson, Kristleifur Bagger, Yu Wilensky, Robert L Reilly, Muredach P Morris, Andrew D Kimber, Charlotte H Adeyemo, Adebowale Chen, Yuanxiu Zhou, Jie So, Wing-Yee Tong, Peter C Y Ng, Maggie C Y Hansen, Torben Andersen, Gitte Borch-Johnsen, Knut Jorgensen, Torben Tres, Alejandro Fuertes, Fernando Ruiz-Echarri, Manuel Asin, Laura Saez, Berta van Boven, Erica Klaver, Siem Swinkels, Dorine W Aben, Katja K Graif, Theresa Cashy, John Suarez, Brian K van Vierssen Trip, Onco Frigge, Michael L Ober, Carole Hofker, Marten H Wijmenga, Cisca Christiansen, Claus Rader, Daniel J Palmer, Colin N A Rotimi, Charles Chan, Juliana C N Pedersen, Oluf Sigurdsson, Gunnar Benediktsson, Rafn Jonsson, Eirikur Einarsson, Gudmundur V Mayordomo, Jose I Catalona, William J Kiemeney, Lambertus A Barkardottir, Rosa B Gulcher, Jeffrey R Thorsteinsdottir, Unnur Kong, Augustine Stefansson, Kari Producer: 20070919 In: Nature genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	389.	Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. [electronic resource] by Zeggini, Eleftheria Panoutsopoulou, Kalliope Southam, Lorraine Rayner, Nigel W Day-Williams, Aaron G Lopes, Margarida C Boraska, Vesna Esko, Tonu Evangelou, Evangelos Hoffman, Albert Houwing-Duistermaat, Jeanine J Ingvarsson, Thorvaldur Jonsdottir, Ingileif Jonnson, Helgi Kerkhof, Hanneke J Kloppenburg, Margreet Bos, Steffan D Mangino, Massimo Metrustry, Sarah Slagboom, P Eline Thorleifsson, Gudmar Raine, Emma V A Ratnayake, Madhushika Ricketts, Michelle Beazley, Claude Blackburn, Hannah Bumpstead, Suzannah Elliott, Katherine S Hunt, Sarah E Potter, Simon C Shin, So-Youn Yadav, Vijay K Zhai, Guangju Sherburn, Kate Dixon, Kate Arden, Elizabeth Aslam, Nadim Battley, Phillippa-kate Carluke, Ian Doherty, Sally Gordon, Andrew Joseph, John Keen, Richard Koller, Nicola C Mitchell, Sheryl O'Neill, Fiona Paling, Ellen Reed, Mike R Rivadeneira, Fernando Swift, Diane Walker, Kirsten Watkins, Bridget Wheeler, Maggie Birrell, Fraser Ioannidis, John P A Meulenbelt, Ingrid Metspalu, Andres Rai, Ashok Salter, Donald Stefansson, Kari Stykarsdottir, Unnur Uitterlinden, André G van Meurs, Joyce B J Chapman, Kay Deloukas, Panos Ollier, William E R Wallis, Gillian A Arden, Nigel Carr, Andrew Doherty, Michael McCaskie, Andrew Willkinson, J Mark Ralston, Stuart H Valdes, Ana M Spector, Tim D Loughlin, John Producer: 20121003 In: Lancet (London, England) vol. 380 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	390.	Common variants conferring risk of schizophrenia. [electronic resource] by Stefansson, Hreinn Ophoff, Roel A Steinberg, Stacy Andreassen, Ole A Cichon, Sven Rujescu, Dan Werge, Thomas Pietiläinen, Olli P H Mors, Ole Mortensen, Preben B Sigurdsson, Engilbert Gustafsson, Omar Nyegaard, Mette Tuulio-Henriksson, Annamari Ingason, Andres Hansen, Thomas Suvisaari, Jaana Lonnqvist, Jouko Paunio, Tiina Børglum, Anders D Hartmann, Annette Fink-Jensen, Anders Nordentoft, Merete Hougaard, David Norgaard-Pedersen, Bent Böttcher, Yvonne Olesen, Jes Breuer, René Möller, Hans-Jürgen Giegling, Ina Rasmussen, Henrik B Timm, Sally Mattheisen, Manuel Bitter, István Réthelyi, János M Magnusdottir, Brynja B Sigmundsson, Thordur Olason, Pall Masson, Gisli Gulcher, Jeffrey R Haraldsson, Magnus Fossdal, Ragnheidur Thorgeirsson, Thorgeir E Thorsteinsdottir, Unnur Ruggeri, Mirella Tosato, Sarah Franke, Barbara Strengman, Eric Kiemeney, Lambertus A Melle, Ingrid Djurovic, Srdjan Abramova, Lilia Kaleda, Vasily Sanjuan, Julio de Frutos, Rosa Bramon, Elvira Vassos, Evangelos Fraser, Gillian Ettinger, Ulrich Picchioni, Marco Walker, Nicholas Toulopoulou, Timi Need, Anna C Ge, Dongliang Yoon, Joeng Lim Shianna, Kevin V Freimer, Nelson B Cantor, Rita M Murray, Robin Kong, Augustine Golimbet, Vera Carracedo, Angel Arango, Celso Costas, Javier Jönsson, Erik G Terenius, Lars Agartz, Ingrid Petursson, Hannes Nöthen, Markus M Rietschel, Marcella Matthews, Paul M Muglia, Pierandrea Peltonen, Leena St Clair, David Goldstein, David B Stefansson, Kari Collier, David A Producer: 20090918 In: Nature vol. 460 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	391.	Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. [electronic resource] by Rafnar, Thorunn Sulem, Patrick Stacey, Simon N Geller, Frank Gudmundsson, Julius Sigurdsson, Asgeir Jakobsdottir, Margret Helgadottir, Hafdis Thorlacius, Steinunn Aben, Katja K H Blöndal, Thorarinn Thorgeirsson, Thorgeir E Thorleifsson, Gudmar Kristjansson, Kristleifur Thorisdottir, Kristin Ragnarsson, Rafn Sigurgeirsson, Bardur Skuladottir, Halla Gudbjartsson, Tomas Isaksson, Helgi J Einarsson, Gudmundur V Benediktsdottir, Kristrun R Agnarsson, Bjarni A Olafsson, Karl Salvarsdottir, Anna Bjarnason, Hjordis Asgeirsdottir, Margret Kristinsson, Kari T Matthiasdottir, Sigurborg Sveinsdottir, Steinunn G Polidoro, Silvia Höiom, Veronica Botella-Estrada, Rafael Hemminki, Kari Rudnai, Peter Bishop, D Timothy Campagna, Marcello Kellen, Eliane Zeegers, Maurice P de Verdier, Petra Ferrer, Ana Isla, Dolores Vidal, Maria Jesus Andres, Raquel Saez, Berta Juberias, Pablo Banzo, Javier Navarrete, Sebastian Tres, Alejandro Kan, Donghui Lindblom, Annika Gurzau, Eugene Koppova, Kvetoslava de Vegt, Femmie Schalken, Jack A van der Heijden, Henricus F M Smit, Hans J Termeer, René A Oosterwijk, Egbert van Hooij, Onno Nagore, Eduardo Porru, Stefano Steineck, Gunnar Hansson, Johan Buntinx, Frank Catalona, William J Matullo, Giuseppe Vineis, Paolo Kiltie, Anne E Mayordomo, José I Kumar, Rajiv Kiemeney, Lambertus A Frigge, Michael L Jonsson, Thorvaldur Saemundsson, Hafsteinn Barkardottir, Rosa B Jonsson, Eirikur Jonsson, Steinn Olafsson, Jon H Gulcher, Jeffrey R Masson, Gisli Gudbjartsson, Daniel F Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20090213 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	392.	Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. [electronic resource] by Lunetta, Kathryn L Day, Felix R Sulem, Patrick Ruth, Katherine S Tung, Joyce Y Hinds, David A Esko, Tõnu Elks, Cathy E Altmaier, Elisabeth He, Chunyan Huffman, Jennifer E Mihailov, Evelin Porcu, Eleonora Robino, Antonietta Rose, Lynda M Schick, Ursula M Stolk, Lisette Teumer, Alexander Thompson, Deborah J Traglia, Michela Wang, Carol A Yerges-Armstrong, Laura M Antoniou, Antonis C Barbieri, Caterina Coviello, Andrea D Cucca, Francesco Demerath, Ellen W Dunning, Alison M Gandin, Ilaria Grove, Megan L Gudbjartsson, Daniel F Hocking, Lynne J Hofman, Albert Huang, Jinyan Jackson, Rebecca D Karasik, David Kriebel, Jennifer Lange, Ethan M Lange, Leslie A Langenberg, Claudia Li, Xin Luan, Jian'an Mägi, Reedik Morrison, Alanna C Padmanabhan, Sandosh Pirie, Ailith Polasek, Ozren Porteous, David Reiner, Alex P Rivadeneira, Fernando Rudan, Igor Sala, Cinzia F Schlessinger, David Scott, Robert A Stöckl, Doris Visser, Jenny A Völker, Uwe Vozzi, Diego Wilson, James G Zygmunt, Marek Boerwinkle, Eric Buring, Julie E Crisponi, Laura Easton, Douglas F Hayward, Caroline Hu, Frank B Liu, Simin Metspalu, Andres Pennell, Craig E Ridker, Paul M Strauch, Konstantin Streeten, Elizabeth A Toniolo, Daniela Uitterlinden, André G Ulivi, Sheila Völzke, Henry Wareham, Nicholas J Wellons, Melissa Franceschini, Nora Chasman, Daniel I Thorsteinsdottir, Unnur Murray, Anna Stefansson, Kari Murabito, Joanne M Ong, Ken K Perry, John R B Producer: 20160325 In: Nature communications vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	393.	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. [electronic resource] by Bellenguez, Céline Bevan, Steve Gschwendtner, Andreas Spencer, Chris C A Burgess, Annette I Pirinen, Matti Jackson, Caroline A Traylor, Matthew Strange, Amy Su, Zhan Band, Gavin Syme, Paul D Malik, Rainer Pera, Joanna Norrving, Bo Lemmens, Robin Freeman, Colin Schanz, Renata James, Tom Poole, Deborah Murphy, Lee Segal, Helen Cortellini, Lynelle Cheng, Yu-Ching Woo, Daniel Nalls, Michael A Müller-Myhsok, Bertram Meisinger, Christa Seedorf, Udo Ross-Adams, Helen Boonen, Steven Wloch-Kopec, Dorota Valant, Valerie Slark, Julia Furie, Karen Delavaran, Hossein Langford, Cordelia Deloukas, Panos Edkins, Sarah Hunt, Sarah Gray, Emma Dronov, Serge Peltonen, Leena Gretarsdottir, Solveig Thorleifsson, Gudmar Thorsteinsdottir, Unnur Stefansson, Kari Boncoraglio, Giorgio B Parati, Eugenio A Attia, John Holliday, Elizabeth Levi, Chris Franzosi, Maria-Grazia Goel, Anuj Helgadottir, Anna Blackwell, Jenefer M Bramon, Elvira Brown, Matthew A Casas, Juan P Corvin, Aiden Duncanson, Audrey Jankowski, Janusz Mathew, Christopher G Palmer, Colin N A Plomin, Robert Rautanen, Anna Sawcer, Stephen J Trembath, Richard C Viswanathan, Ananth C Wood, Nicholas W Worrall, Bradford B Kittner, Steven J Mitchell, Braxton D Kissela, Brett Meschia, James F Thijs, Vincent Lindgren, Arne Macleod, Mary Joan Slowik, Agnieszka Walters, Matthew Rosand, Jonathan Sharma, Pankaj Farrall, Martin Sudlow, Cathie L M Rothwell, Peter M Dichgans, Martin Donnelly, Peter Markus, Hugh S Producer: 20120420 In: Nature genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	394.	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. [electronic resource] by Traylor, Matthew Farrall, Martin Holliday, Elizabeth G Sudlow, Cathie Hopewell, Jemma C Cheng, Yu-Ching Fornage, Myriam Ikram, M Arfan Malik, Rainer Bevan, Steve Thorsteinsdottir, Unnur Nalls, Mike A Longstreth, Wt Wiggins, Kerri L Yadav, Sunaina Parati, Eugenio A Destefano, Anita L Worrall, Bradford B Kittner, Steven J Khan, Muhammad Saleem Reiner, Alex P Helgadottir, Anna Achterberg, Sefanja Fernandez-Cadenas, Israel Abboud, Sherine Schmidt, Reinhold Walters, Matthew Chen, Wei-Min Ringelstein, E Bernd O'Donnell, Martin Ho, Weang Kee Pera, Joanna Lemmens, Robin Norrving, Bo Higgins, Peter Benn, Marianne Sale, Michele Kuhlenbäumer, Gregor Doney, Alexander S F Vicente, Astrid M Delavaran, Hossein Algra, Ale Davies, Gail Oliveira, Sofia A Palmer, Colin N A Deary, Ian Schmidt, Helena Pandolfo, Massimo Montaner, Joan Carty, Cara de Bakker, Paul I W Kostulas, Konstantinos Ferro, Jose M van Zuydam, Natalie R Valdimarsson, Einar Nordestgaard, Børge G Lindgren, Arne Thijs, Vincent Slowik, Agnieszka Saleheen, Danish Paré, Guillaume Berger, Klaus Thorleifsson, Gudmar Hofman, Albert Mosley, Thomas H Mitchell, Braxton D Furie, Karen Clarke, Robert Levi, Christopher Seshadri, Sudha Gschwendtner, Andreas Boncoraglio, Giorgio B Sharma, Pankaj Bis, Joshua C Gretarsdottir, Solveig Psaty, Bruce M Rothwell, Peter M Rosand, Jonathan Meschia, James F Stefansson, Kari Dichgans, Martin Markus, Hugh S Producer: 20121231 In: The Lancet. Neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	395.	A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis. [electronic resource] by Rivas, Manuel A Graham, Daniel Sulem, Patrick Stevens, Christine Desch, A Nicole Goyette, Philippe Gudbjartsson, Daniel Jonsdottir, Ingileif Thorsteinsdottir, Unnur Degenhardt, Frauke Mucha, Sören Kurki, Mitja I Li, Dalin D'Amato, Mauro Annese, Vito Vermeire, Severine Weersma, Rinse K Halfvarson, Jonas Paavola-Sakki, Paulina Lappalainen, Maarit Lek, Monkol Cummings, Beryl Tukiainen, Taru Haritunians, Talin Halme, Leena Koskinen, Lotta L E Ananthakrishnan, Ashwin N Luo, Yang Heap, Graham A Visschedijk, Marijn C MacArthur, Daniel G Neale, Benjamin M Ahmad, Tariq Anderson, Carl A Brant, Steven R Duerr, Richard H Silverberg, Mark S Cho, Judy H Palotie, Aarno Saavalainen, Päivi Kontula, Kimmo Färkkilä, Martti McGovern, Dermot P B Franke, Andre Stefansson, Kari Rioux, John D Xavier, Ramnik J Daly, Mark J Barrett, J de Lane, K Edwards, C Hart, A Hawkey, C Jostins, L Kennedy, N Lamb, C Lee, J Lees, C Mansfield, J Mathew, C Mowatt, C Newman, B Nimmo, E Parkes, M Pollard, M Prescott, N Randall, J Rice, D Satsangi, J Simmons, A Tremelling, M Uhlig, H Wilson, D Abraham, C Achkar, J P Bitton, A Boucher, G Croitoru, K Fleshner, P Glas, J Kugathasan, S Limbergen, J V Milgrom, R Proctor, D Regueiro, M Schumm, P L Sharma, Y Stempak, J M Targan, S R Wang, M H Producer: 20180903 In: Nature communications vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	396.	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. [electronic resource] by Demontis, Ditte Walters, Raymond K Martin, Joanna Mattheisen, Manuel Als, Thomas D Agerbo, Esben Baldursson, Gísli Belliveau, Rich Bybjerg-Grauholm, Jonas Bækvad-Hansen, Marie Cerrato, Felecia Chambert, Kimberly Churchhouse, Claire Dumont, Ashley Eriksson, Nicholas Gandal, Michael Goldstein, Jacqueline I Grasby, Katrina L Grove, Jakob Gudmundsson, Olafur O Hansen, Christine S Hauberg, Mads Engel Hollegaard, Mads V Howrigan, Daniel P Huang, Hailiang Maller, Julian B Martin, Alicia R Martin, Nicholas G Moran, Jennifer Pallesen, Jonatan Palmer, Duncan S Pedersen, Carsten Bøcker Pedersen, Marianne Giørtz Poterba, Timothy Poulsen, Jesper Buchhave Ripke, Stephan Robinson, Elise B Satterstrom, F Kyle Stefansson, Hreinn Stevens, Christine Turley, Patrick Walters, G Bragi Won, Hyejung Wright, Margaret J Andreassen, Ole A Asherson, Philip Burton, Christie L Boomsma, Dorret I Cormand, Bru Dalsgaard, Søren Franke, Barbara Gelernter, Joel Geschwind, Daniel Hakonarson, Hakon Haavik, Jan Kranzler, Henry R Kuntsi, Jonna Langley, Kate Lesch, Klaus-Peter Middeldorp, Christel Reif, Andreas Rohde, Luis Augusto Roussos, Panos Schachar, Russell Sklar, Pamela Sonuga-Barke, Edmund J S Sullivan, Patrick F Thapar, Anita Tung, Joyce Y Waldman, Irwin D Medland, Sarah E Stefansson, Kari Nordentoft, Merete Hougaard, David M Werge, Thomas Mors, Ole Mortensen, Preben Bo Daly, Mark J Faraone, Stephen V Børglum, Anders D Neale, Benjamin M Producer: 20190424 In: Nature genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	397.	The impact of low-frequency and rare variants on lipid levels. [electronic resource] by Surakka, Ida Horikoshi, Momoko Mägi, Reedik Sarin, Antti-Pekka Mahajan, Anubha Lagou, Vasiliki Marullo, Letizia Ferreira, Teresa Miraglio, Benjamin Timonen, Sanna Kettunen, Johannes Pirinen, Matti Karjalainen, Juha Thorleifsson, Gudmar Hägg, Sara Hottenga, Jouke-Jan Isaacs, Aaron Ladenvall, Claes Beekman, Marian Esko, Tõnu Ried, Janina S Nelson, Christopher P Willenborg, Christina Gustafsson, Stefan Westra, Harm-Jan Blades, Matthew de Craen, Anton J M de Geus, Eco J Deelen, Joris Grallert, Harald Hamsten, Anders Havulinna, Aki S Hengstenberg, Christian Houwing-Duistermaat, Jeanine J Hyppönen, Elina Karssen, Lennart C Lehtimäki, Terho Lyssenko, Valeriya Magnusson, Patrik K E Mihailov, Evelin Müller-Nurasyid, Martina Mpindi, John-Patrick Pedersen, Nancy L Penninx, Brenda W J H Perola, Markus Pers, Tune H Peters, Annette Rung, Johan Smit, Johannes H Steinthorsdottir, Valgerdur Tobin, Martin D Tsernikova, Natalia van Leeuwen, Elisabeth M Viikari, Jorma S Willems, Sara M Willemsen, Gonneke Schunkert, Heribert Erdmann, Jeanette Samani, Nilesh J Kaprio, Jaakko Lind, Lars Gieger, Christian Metspalu, Andres Slagboom, P Eline Groop, Leif van Duijn, Cornelia M Eriksson, Johan G Jula, Antti Salomaa, Veikko Boomsma, Dorret I Power, Christine Raitakari, Olli T Ingelsson, Erik Järvelin, Marjo-Riitta Thorsteinsdottir, Unnur Franke, Lude Ikonen, Elina Kallioniemi, Olli Pietiäinen, Vilja Lindgren, Cecilia M Stefansson, Kari Palotie, Aarno McCarthy, Mark I Morris, Andrew P Prokopenko, Inga Ripatti, Samuli Producer: 20150807 In: Nature genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	398.	Rare coding variants and X-linked loci associated with age at menarche. [electronic resource] by Lunetta, Kathryn L Day, Felix R Sulem, Patrick Ruth, Katherine S Tung, Joyce Y Hinds, David A Esko, Tõnu Elks, Cathy E Altmaier, Elisabeth He, Chunyan Huffman, Jennifer E Mihailov, Evelin Porcu, Eleonora Robino, Antonietta Rose, Lynda M Schick, Ursula M Stolk, Lisette Teumer, Alexander Thompson, Deborah J Traglia, Michela Wang, Carol A Yerges-Armstrong, Laura M Antoniou, Antonis C Barbieri, Caterina Coviello, Andrea D Cucca, Francesco Demerath, Ellen W Dunning, Alison M Gandin, Ilaria Grove, Megan L Gudbjartsson, Daniel F Hocking, Lynne J Hofman, Albert Huang, Jinyan Jackson, Rebecca D Karasik, David Kriebel, Jennifer Lange, Ethan M Lange, Leslie A Langenberg, Claudia Li, Xin Luan, Jian'an Mägi, Reedik Morrison, Alanna C Padmanabhan, Sandosh Pirie, Ailith Polasek, Ozren Porteous, David Reiner, Alex P Rivadeneira, Fernando Rudan, Igor Sala, Cinzia F Schlessinger, David Scott, Robert A Stöckl, Doris Visser, Jenny A Völker, Uwe Vozzi, Diego Wilson, James G Zygmunt, Marek Boerwinkle, Eric Buring, Julie E Crisponi, Laura Easton, Douglas F Hayward, Caroline Hu, Frank B Liu, Simin Metspalu, Andres Pennell, Craig E Ridker, Paul M Strauch, Konstantin Streeten, Elizabeth A Toniolo, Daniela Uitterlinden, André G Ulivi, Sheila Völzke, Henry Wareham, Nicholas J Wellons, Melissa Franceschini, Nora Chasman, Daniel I Thorsteinsdottir, Unnur Murray, Anna Stefansson, Kari Murabito, Joanne M Ong, Ken K Perry, John R B Producer: 20160412 In: Nature communications vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	399.	Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. [electronic resource] by Yu, Dongmei Sul, Jae Hoon Tsetsos, Fotis Nawaz, Muhammad S Huang, Alden Y Zelaya, Ivette Illmann, Cornelia Osiecki, Lisa Darrow, Sabrina M Hirschtritt, Matthew E Greenberg, Erica Muller-Vahl, Kirsten R Stuhrmann, Manfred Dion, Yves Rouleau, Guy Aschauer, Harald Stamenkovic, Mara Schlögelhofer, Monika Sandor, Paul Barr, Cathy L Grados, Marco Singer, Harvey S Nöthen, Markus M Hebebrand, Johannes Hinney, Anke King, Robert A Fernandez, Thomas V Barta, Csaba Tarnok, Zsanett Nagy, Peter Depienne, Christel Worbe, Yulia Hartmann, Andreas Budman, Cathy L Rizzo, Renata Lyon, Gholson J McMahon, William M Batterson, James R Cath, Danielle C Malaty, Irene A Okun, Michael S Berlin, Cheston Woods, Douglas W Lee, Paul C Jankovic, Joseph Robertson, Mary M Gilbert, Donald L Brown, Lawrence W Coffey, Barbara J Dietrich, Andrea Hoekstra, Pieter J Kuperman, Samuel Zinner, Samuel H Luðvigsson, Pétur Sæmundsen, Evald Thorarensen, Ólafur Atzmon, Gil Barzilai, Nir Wagner, Michael Moessner, Rainald Ophoff, Roel Pato, Carlos N Pato, Michele T Knowles, James A Roffman, Joshua L Smoller, Jordan W Buckner, Randy L Willsey, A Jeremy Tischfield, Jay A Heiman, Gary A Stefansson, Hreinn Stefansson, Kári Posthuma, Danielle Cox, Nancy J Pauls, David L Freimer, Nelson B Neale, Benjamin M Davis, Lea K Paschou, Peristera Coppola, Giovanni Mathews, Carol A Scharf, Jeremiah M Producer: 20191217 In: The American journal of psychiatry vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	400.	Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. [electronic resource] by Helgadottir, Anna Gretarsdottir, Solveig Thorleifsson, Gudmar Holm, Hilma Patel, Riyaz S Gudnason, Thorarinn Jones, Gregory T van Rij, Andre M Eapen, Danny J Baas, Annette F Tregouet, David-Alexandre Morange, Pierre-Emmanuel Emmerich, Joseph Lindblad, Bengt Gottsäter, Anders Kiemeny, Lambertus A Lindholt, Jes S Sakalihasan, Natzi Ferrell, Robert E Carey, David J Elmore, James R Tsao, Philip S Grarup, Niels Jørgensen, Torben Witte, Daniel R Hansen, Torben Pedersen, Oluf Pola, Roberto Gaetani, Eleonora Magnadottir, Hulda B Wijmenga, Cisca Tromp, Gerard Ronkainen, Antti Ruigrok, Ynte M Blankensteijn, Jan D Mueller, Thomas Wells, Philip S Corral, Javier Soria, Jose Manuel Souto, Juan Carlos Peden, John F Jalilzadeh, Shapour Mayosi, Bongani M Keavney, Bernard Strawbridge, Rona J Sabater-Lleal, Maria Gertow, Karl Baldassarre, Damiano Nyyssönen, Kristiina Rauramaa, Rainer Smit, Andries J Mannarino, Elmo Giral, Philippe Tremoli, Elena de Faire, Ulf Humphries, Steve E Hamsten, Anders Haraldsdottir, Vilhelmina Olafsson, Isleifur Magnusson, Magnus K Samani, Nilesh J Levey, Allan I Markus, Hugh S Kostulas, Konstantinos Dichgans, Martin Berger, Klaus Kuhlenbäumer, Gregor Ringelstein, E Bernd Stoll, Monika Seedorf, Udo Rothwell, Peter M Powell, Janet T Kuivaniemi, Helena Onundarson, Pall T Valdimarsson, Einar Matthiasson, Stefan E Gudbjartsson, Daniel F Thorgeirsson, Guðmundur Quyyumi, Arshed A Watkins, Hugh Farrall, Martin Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20121016 In: Journal of the American College of Cardiology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. [electronic resource] by

Helgadottir, Anna
Gretarsdottir, Solveig
Thorleifsson, Gudmar
Holm, Hilma
Patel, Riyaz S
Gudnason, Thorarinn
Jones, Gregory T
van Rij, Andre M
Eapen, Danny J
Baas, Annette F
Tregouet, David-Alexandre
Morange, Pierre-Emmanuel
Emmerich, Joseph
Lindblad, Bengt
Gottsäter, Anders
Kiemeny, Lambertus A
Lindholt, Jes S
Sakalihasan, Natzi
Ferrell, Robert E
Carey, David J
Elmore, James R
Tsao, Philip S
Grarup, Niels
Jørgensen, Torben
Witte, Daniel R
Hansen, Torben
Pedersen, Oluf
Pola, Roberto
Gaetani, Eleonora
Magnadottir, Hulda B
Wijmenga, Cisca
Tromp, Gerard
Ronkainen, Antti
Ruigrok, Ynte M
Blankensteijn, Jan D
Mueller, Thomas
Wells, Philip S
Corral, Javier
Soria, Jose Manuel
Souto, Juan Carlos
Peden, John F
Jalilzadeh, Shapour
Mayosi, Bongani M
Keavney, Bernard
Strawbridge, Rona J
Sabater-Lleal, Maria
Gertow, Karl
Baldassarre, Damiano
Nyyssönen, Kristiina
Rauramaa, Rainer
Smit, Andries J
Mannarino, Elmo
Giral, Philippe
Tremoli, Elena
de Faire, Ulf
Humphries, Steve E
Hamsten, Anders
Haraldsdottir, Vilhelmina
Olafsson, Isleifur
Magnusson, Magnus K
Samani, Nilesh J
Levey, Allan I
Markus, Hugh S
Kostulas, Konstantinos
Dichgans, Martin
Berger, Klaus
Kuhlenbäumer, Gregor
Ringelstein, E Bernd
Stoll, Monika
Seedorf, Udo
Rothwell, Peter M
Powell, Janet T
Kuivaniemi, Helena
Onundarson, Pall T
Valdimarsson, Einar
Matthiasson, Stefan E
Gudbjartsson, Daniel F
Thorgeirsson, Guðmundur
Quyyumi, Arshed A
Watkins, Hugh
Farrall, Martin
Thorsteinsdottir, Unnur
Stefansson, Kari

Producer: 20121016 In: Journal of the American College of Cardiology vol. 60

Online resources:

Available from publisher's website

Availability: No items available.

Refine your search

Availability

Authors

Topics

Languages

Your search returned 517 results.