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	261.	A sequence variant on 17q21 is associated with age at onset and severity of asthma. [electronic resource] by Halapi, Eva Gudbjartsson, Daniel F Jonsdottir, Gudrun M Bjornsdottir, Unnur S Thorleifsson, Gudmar Helgadottir, Hafdis Williams, Carolyn Koppelman, Gerard H Heinzmann, Andrea Boezen, H Marike Jonasdottir, Aslaug Blondal, Thorarinn Gudjonsson, Sigurjon A Jonasdottir, Adalbjorg Thorlacius, Theodora Henry, Amanda P Altmueller, Janine Krueger, Marcus Shin, Hyoung Doo Uh, Soo-Taek Cheong, Hyun Sub Jonsdottir, Brynja Ludviksson, Bjorn R Ludviksdottir, Dora Gislason, David Park, Choon-Sik Deichmann, Klaus Thompson, Philip J Wjst, Matthias Hall, Ian P Postma, Dirkje S Gislason, Thorarinn Kong, Augustine Jonsdottir, Ingileif Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20101101 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	262.	Identification of sequence variants influencing immunoglobulin levels. [electronic resource] by Jonsson, Stefan Sveinbjornsson, Gardar de Lapuente Portilla, Aitzkoa Lopez Swaminathan, Bhairavi Plomp, Rosina Dekkers, Gillian Ajore, Ram Ali, Mina Bentlage, Arthur E H Elmér, Evelina Eyjolfsson, Gudmundur I Gudjonsson, Sigurjon A Gullberg, Urban Gylfason, Arnaldur Halldorsson, Bjarni V Hansson, Markus Holm, Hilma Johansson, Åsa Johnsson, Ellinor Jonasdottir, Aslaug Ludviksson, Bjorn R Oddsson, Asmundur Olafsson, Isleifur Olafsson, Sigurgeir Sigurdardottir, Olof Sigurdsson, Asgeir Stefansdottir, Lilja Masson, Gisli Sulem, Patrick Wuhrer, Manfred Wihlborg, Anna-Karin Thorleifsson, Gudmar Gudbjartsson, Daniel F Thorsteinsdottir, Unnur Vidarsson, Gestur Jonsdottir, Ingileif Nilsson, Björn Stefansson, Kari Producer: 20170921 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	263.	Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls. [electronic resource] by Preuss, Michael König, Inke R Thompson, John R Erdmann, Jeanette Absher, Devin Assimes, Themistocles L Blankenberg, Stefan Boerwinkle, Eric Chen, Li Cupples, L Adrienne Hall, Alistair S Halperin, Eran Hengstenberg, Christian Holm, Hilma Laaksonen, Reijo Li, Mingyao März, Winfried McPherson, Ruth Musunuru, Kiran Nelson, Christopher P Burnett, Mary Susan Epstein, Stephen E O'Donnell, Christopher J Quertermous, Thomas Rader, Daniel J Roberts, Robert Schillert, Arne Stefansson, Kari Stewart, Alexandre F R Thorleifsson, Gudmar Voight, Benjamin F Wells, George A Ziegler, Andreas Kathiresan, Sekar Reilly, Muredach P Samani, Nilesh J Schunkert, Heribert Producer: 20110131 In: Circulation. Cardiovascular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	264.	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. [electronic resource] by Dichgans, Martin Malik, Rainer König, Inke R Rosand, Jonathan Clarke, Robert Gretarsdottir, Solveig Thorleifsson, Gudmar Mitchell, Braxton D Assimes, Themistocles L Levi, Christopher O'Donnell, Christopher J Fornage, Myriam Thorsteinsdottir, Unnur Psaty, Bruce M Hengstenberg, Christian Seshadri, Sudha Erdmann, Jeanette Bis, Joshua C Peters, Annette Boncoraglio, Giorgio B März, Winfried Meschia, James F Kathiresan, Sekar Ikram, M Arfan McPherson, Ruth Stefansson, Kari Sudlow, Cathie Reilly, Muredach P Thompson, John R Sharma, Pankaj Hopewell, Jemma C Chambers, John C Watkins, Hugh Rothwell, Peter M Roberts, Robert Markus, Hugh S Samani, Nilesh J Farrall, Martin Schunkert, Heribert Producer: 20140220 In: Stroke vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	265.	Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. [electronic resource] by Isles, Anthony R Ingason, Andrés Lowther, Chelsea Walters, James Gawlick, Micha Stöber, Gerald Rees, Elliott Martin, Joanna Little, Rosie B Potter, Harry Georgieva, Lyudmila Pizzo, Lucilla Ozaki, Norio Aleksic, Branko Kushima, Itaru Ikeda, Masashi Iwata, Nakao Levinson, Douglas F Gejman, Pablo V Shi, Jianxin Sanders, Alan R Duan, Jubao Willis, Joseph Sisodiya, Sanjay Costain, Gregory Werge, Thomas M Degenhardt, Franziska Giegling, Ina Rujescu, Dan Hreidarsson, Stefan J Saemundsen, Evald Ahn, Joo Wook Ogilvie, Caroline Girirajan, Santhosh D Stefansson, Hreinn Stefansson, Kari O'Donovan, Michael C Owen, Michael J Bassett, Anne Kirov, George Producer: 20170512 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	266.	Sequence variants associating with urinary biomarkers. [electronic resource] by Benonisdottir, Stefania Kristjansson, Ragnar P Oddsson, Asmundur Steinthorsdottir, Valgerdur Mikaelsdottir, Evgenia Kehr, Birte Jensson, Brynjar O Arnadottir, Gudny A Sulem, Gerald Sveinbjornsson, Gardar Kristmundsdottir, Snaedis Ivarsdottir, Erna V Tragante, Vinicius Gunnarsson, Bjarni Runolfsdottir, Hrafnhildur Linnet Arthur, Joseph G Deaton, Aimee M Eyjolfsson, Gudmundur I Davidsson, Olafur B Asselbergs, Folkert W Hreidarsson, Astradur B Rafnar, Thorunn Thorleifsson, Gudmar Edvardsson, Vidar Sigurdsson, Gunnar Helgadottir, Anna Halldorsson, Bjarni V Masson, Gisli Holm, Hilma Onundarson, Pall T Indridason, Olafur S Benediktsson, Rafn Palsson, Runolfur Gudbjartsson, Daniel F Olafsson, Isleifur Thorsteinsdottir, Unnur Sulem, Patrick Stefansson, Kari Producer: 20190701 In: Human molecular genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	267.	Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. [electronic resource] by Gudmundsson, Julius Sulem, Patrick Gudbjartsson, Daniel F Jonasson, Jon G Sigurdsson, Asgeir Bergthorsson, Jon T He, Huiling Blondal, Thorarinn Geller, Frank Jakobsdottir, Margret Magnusdottir, Droplaug N Matthiasdottir, Sigurborg Stacey, Simon N Skarphedinsson, Oskar B Helgadottir, Hafdis Li, Wei Nagy, Rebecca Aguillo, Esperanza Faure, Eduardo Prats, Enrique Saez, Berta Martinez, Mariano Eyjolfsson, Gudmundur I Bjornsdottir, Unnur S Holm, Hilma Kristjansson, Kristleifur Frigge, Michael L Kristvinsson, Hoskuldur Gulcher, Jeffrey R Jonsson, Thorvaldur Rafnar, Thorunn Hjartarsson, Hannes Mayordomo, Jose I de la Chapelle, Albert Hrafnkelsson, Jon Thorsteinsdottir, Unnur Kong, Augustine Stefansson, Kari Producer: 20090514 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	268.	Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. [electronic resource] by Rivadeneira, Fernando Styrkársdottir, Unnur Estrada, Karol Halldórsson, Bjarni V Hsu, Yi-Hsiang Richards, J Brent Zillikens, M Carola Kavvoura, Fotini K Amin, Najaf Aulchenko, Yurii S Cupples, L Adrienne Deloukas, Panagiotis Demissie, Serkalem Grundberg, Elin Hofman, Albert Kong, Augustine Karasik, David van Meurs, Joyce B Oostra, Ben Pastinen, Tomi Pols, Huibert A P Sigurdsson, Gunnar Soranzo, Nicole Thorleifsson, Gudmar Thorsteinsdottir, Unnur Williams, Frances M K Wilson, Scott G Zhou, Yanhua Ralston, Stuart H van Duijn, Cornelia M Spector, Timothy Kiel, Douglas P Stefansson, Kari Ioannidis, John P A Uitterlinden, André G Producer: 20091130 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	269.	Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. [electronic resource] by Zhao, Huiying Eising, Else de Vries, Boukje Vijfhuizen, Lisanne S Anttila, Verneri Winsvold, Bendik S Kurth, Tobias Stefansson, Hreinn Kallela, Mikko Malik, Rainer Stam, Anine H Ikram, M Arfan Ligthart, Lannie Freilinger, Tobias Alexander, Michael Müller-Myhsok, Bertram Schreiber, Stefan Meitinger, Thomas Aromas, Arpo Eriksson, Johan G Boomsma, Dorret I van Duijn, Cornelia M Zwart, John-Anker Quaye, Lydia Kubisch, Christian Dichgans, Martin Wessman, Maija Stefansson, Kari Chasman, Daniel I Palotie, Aarno Martin, Nicholas G Montgomery, Grant W Ferrari, Michel D Terwindt, Gisela M van den Maagdenberg, Arn M J M Nyholt, Dale R Producer: 20170310 In: Cephalalgia : an international journal of headache vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	270.	A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma. [electronic resource] by Smith, Dirk Helgason, Hannes Sulem, Patrick Bjornsdottir, Unnur Steina Lim, Ai Ching Sveinbjornsson, Gardar Hasegawa, Haruki Brown, Michael Ketchem, Randal R Gavala, Monica Garrett, Logan Jonasdottir, Adalbjorg Jonasdottir, Aslaug Sigurdsson, Asgeir Magnusson, Olafur T Eyjolfsson, Gudmundur I Olafsson, Isleifur Onundarson, Pall Torfi Sigurdardottir, Olof Gislason, David Gislason, Thorarinn Ludviksson, Bjorn Runar Ludviksdottir, Dora Boezen, H Marike Heinzmann, Andrea Krueger, Marcus Porsbjerg, Celeste Ahluwalia, Tarunveer S Waage, Johannes Backer, Vibeke Deichmann, Klaus A Koppelman, Gerard H Bønnelykke, Klaus Bisgaard, Hans Masson, Gisli Thorsteinsdottir, Unnur Gudbjartsson, Daniel F Johnston, James A Jonsdottir, Ingileif Stefansson, Kari Producer: 20170606 In: PLoS genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	271.	Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. [electronic resource] by Li, Rui Brockschmidt, Felix F Kiefer, Amy K Stefansson, Hreinn Nyholt, Dale R Song, Kijoung Vermeulen, Sita H Kanoni, Stavroula Glass, Daniel Medland, Sarah E Dimitriou, Maria Waterworth, Dawn Tung, Joyce Y Geller, Frank Heilmann, Stefanie Hillmer, Axel M Bataille, Veronique Eigelshoven, Sibylle Hanneken, Sandra Moebus, Susanne Herold, Christine den Heijer, Martin Montgomery, Grant W Deloukas, Panos Eriksson, Nicholas Heath, Andrew C Becker, Tim Sulem, Patrick Mangino, Massimo Vollenweider, Peter Spector, Tim D Dedoussis, George Martin, Nicholas G Kiemeney, Lambertus A Mooser, Vincent Stefansson, Kari Hinds, David A Nöthen, Markus M Richards, J Brent 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)
	272.	Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. [electronic resource] by Kung, Annie W C Xiao, Su-Mei Cherny, Stacey Li, Gloria H Y Gao, Yi Tso, Gloria Lau, Kam S Luk, Keith D K Liu, Jian-min Cui, Bin Zhang, Min-Jia Zhang, Zhen-lin He, Jin-wei Yue, Hua Xia, Wia-bo Luo, Lian-mei He, Shu-li Kiel, Douglas P Karasik, David Hsu, Yi-Hsiang Cupples, L Adrienne Demissie, Serkalem Styrkarsdottir, Unnur Halldorsson, Bjarni V Sigurdsson, Gunnar Thorsteinsdottir, Unnur Stefansson, Kari Richards, J Brent Zhai, Guangju Soranzo, Nicole Valdes, Ana Spector, Tim D Sham, Pak C Producer: 20100319 In: American journal of human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	273.	Coding variants in [electronic resource] by Thorolfsdottir, Rosa B Sveinbjornsson, Gardar Sulem, Patrick Nielsen, Jonas B Jonsson, Stefan Halldorsson, Gisli H Melsted, Pall Ivarsdottir, Erna V Davidsson, Olafur B Kristjansson, Ragnar P Thorleifsson, Gudmar Helgadottir, Anna Gretarsdottir, Solveig Norddahl, Gudmundur Rajamani, Sridharan Torfason, Bjarni Valgardsson, Atli S Sverrisson, Jon T Tragante, Vinicius Holmen, Oddgeir L Asselbergs, Folkert W Roden, Dan M Darbar, Dawood Pedersen, Terje R Sabatine, Marc S Willer, Cristen J Løchen, Maja-Lisa Halldorsson, Bjarni V Jonsdottir, Ingileif Hveem, Kristian Arnar, David O Thorsteinsdottir, Unnur Gudbjartsson, Daniel F Holm, Hilma Stefansson, Kari Publication details: Communications biology 2018 In: Communications biology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	274.	Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition. [electronic resource] by Small, Kerrin S Todorčević, Marijana Civelek, Mete El-Sayed Moustafa, Julia S Wang, Xiao Simon, Michelle M Fernandez-Tajes, Juan Mahajan, Anubha Horikoshi, Momoko Hugill, Alison Glastonbury, Craig A Quaye, Lydia Neville, Matt J Sethi, Siddharth Yon, Marianne Pan, Calvin Che, Nam Vinuela, Ana Tsai, Pei-Chien Nag, Abhishek Buil, Alfonso Thorleifsson, Gudmar Raghavan, Avanthi Ding, Qiurong Morris, Andrew P Bell, Jordana T Thorsteinsdottir, Unnur Stefansson, Kari Laakso, Markku Dahlman, Ingrid Arner, Peter Gloyn, Anna L Musunuru, Kiran Lusis, Aldons J Cox, Roger D Karpe, Fredrik McCarthy, Mark I Publication details: Nature genetics 09 2018 In: Nature genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	275.	GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. [electronic resource] by Rongve, Arvid Witoelar, Aree Ruiz, Agustín Athanasiu, Lavinia Abdelnour, Carla Clarimon, Jordi Heilmann-Heimbach, Stefanie Hernández, Isabel Moreno-Grau, Sonia de Rojas, Itziar Morenas-Rodríguez, Estrella Fladby, Tormod Sando, Sigrid B Bråthen, Geir Blanc, Frédéric Bousiges, Olivier Lemstra, Afina W van Steenoven, Inger Londos, Elisabet Almdahl, Ina S Pålhaugen, Lene Eriksen, Jon A Djurovic, Srdjan Stordal, Eystein Saltvedt, Ingvild Ulstein, Ingun D Bettella, Francesco Desikan, Rahul S Idland, Ane-Victoria Toft, Mathias Pihlstrøm, Lasse Snaedal, Jon Tárraga, Lluís Boada, Mercè Lleó, Alberto Stefánsson, Hreinn Stefánsson, Kári Ramírez, Alfredo Aarsland, Dag Andreassen, Ole A Producer: 20201013 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	276.	Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture. [electronic resource] by Richards, J Brent Kavvoura, Fotini K Rivadeneira, Fernando Styrkársdóttir, Unnur Estrada, Karol Halldórsson, Bjarni V Hsu, Yi-Hsiang Zillikens, M Carola Wilson, Scott G Mullin, Benjamin H Amin, Najaf Aulchenko, Yurii S Cupples, L Adrienne Deloukas, Panagiotis Demissie, Serkalem Hofman, Albert Kong, Augustine Karasik, David van Meurs, Joyce B Oostra, Ben A Pols, Huibert A P Sigurdsson, Gunnar Thorsteinsdottir, Unnur Soranzo, Nicole Williams, Frances M K Zhou, Yanhua Ralston, Stuart H Thorleifsson, Gudmar van Duijn, Cornelia M Kiel, Douglas P Stefansson, Kari Uitterlinden, André G Ioannidis, John P A Spector, Tim D Producer: 20091102 In: Annals of internal medicine vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	277.	Many sequence variants affecting diversity of adult human height. [electronic resource] by Gudbjartsson, Daniel F Walters, G Bragi Thorleifsson, Gudmar Stefansson, Hreinn Halldorsson, Bjarni V Zusmanovich, Pasha Sulem, Patrick Thorlacius, Steinunn Gylfason, Arnaldur Steinberg, Stacy Helgadottir, Anna Ingason, Andres Steinthorsdottir, Valgerdur Olafsdottir, Elinborg J Olafsdottir, Gudridur H Jonsson, Thorvaldur Borch-Johnsen, Knut Hansen, Torben Andersen, Gitte Jorgensen, Torben Pedersen, Oluf Aben, Katja K Witjes, J Alfred Swinkels, Dorine W den Heijer, Martin Franke, Barbara Verbeek, Andre L M Becker, Diane M Yanek, Lisa R Becker, Lewis C Tryggvadottir, Laufey Rafnar, Thorunn Gulcher, Jeffrey Kiemeney, Lambertus A Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20080522 In: Nature genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	278.	Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. [electronic resource] by Nyholt, Dale R Anttila, Verneri Winsvold, Bendik S Kurth, Tobias Stefansson, Hreinn Kallela, Mikko Malik, Rainer Vries, Boukje de Terwindt, Gisela M Ikram, M Arfan Stam, Anine H Ligthart, Lannie Freilinger, Tobias Alexander, Michael Muller-Myhsok, Bertram Schreiber, Stefan Meitinger, Thomas Aromaa, Arpo Eriksson, Johan G Kaprio, Jaakko Boomsma, Dorret I Duijn, Cornelia van Raitakari, Olli Järvelin, Marjo-Riitta Zwart, John-Anker Quaye, Lydia Strachan, David P Kubisch, Christian Ferrari, Michel D van den Maagdenberg, Arn M J M Dichgans, Martin Wessman, Maija Smith, George Davey Stefansson, Kari Chasman, Daniel I Palotie, Aarno Producer: 20160113 In: Cephalalgia : an international journal of headache vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	279.	A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. [electronic resource] by Helgason, Hannes Sulem, Patrick Duvvari, Maheswara R Luo, Hongrong Thorleifsson, Gudmar Stefansson, Hreinn Jonsdottir, Ingileif Masson, Gisli Gudbjartsson, Daniel F Walters, G Bragi Magnusson, Olafur Th Kong, Augustine Rafnar, Thorunn Kiemeney, Lambertus A Schoenmaker-Koller, Frederieke E Zhao, Ling Boon, Camiel J F Song, Yaojun Fauser, Sascha Pei, Michelle Ristau, Tina Patel, Shirrina Liakopoulos, Sandra van de Ven, Johannes P H Hoyng, Carel B Ferreyra, Henry Duan, Yaou Bernstein, Paul S Geirsdottir, Asbjorg Helgadottir, Gudleif Stefansson, Einar den Hollander, Anneke I Zhang, Kang Jonasson, Fridbert Sigurdsson, Haraldur Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20140108 In: Nature genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	280.	A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. [electronic resource] by Praetorius, Christian Grill, Christine Stacey, Simon N Metcalf, Alexander M Gorkin, David U Robinson, Kathleen C Van Otterloo, Eric Kim, Reuben S Q Bergsteinsdottir, Kristin Ogmundsdottir, Margret H Magnusdottir, Erna Mishra, Pravin J Davis, Sean R Guo, Theresa Zaidi, M Raza Helgason, Agnar S Sigurdsson, Martin I Meltzer, Paul S Merlino, Glenn Petit, Valerie Larue, Lionel Loftus, Stacie K Adams, David R Sobhiafshar, Ulduz Emre, N C Tolga Pavan, William J Cornell, Robert Smith, Aaron G McCallion, Andrew S Fisher, David E Stefansson, Kari Sturm, Richard A Steingrimsson, Eirikur Producer: 20140210 In: Cell vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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