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	161.	A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation. [electronic resource] by Gudbjartsson, Daniel F Holm, Hilma Sulem, Patrick Masson, Gisli Oddsson, Asmundur Magnusson, Olafur Th Saemundsdottir, Jona Helgadottir, Hafdis Th Helgason, Hannes Johannsdottir, Hrefna Gretarsdottir, Solveig Gudjonsson, Sigurjon A Njølstad, Inger Løchen, Maja-Lisa Baum, Larry Ma, Ronald C W Sigfusson, Gunnlaugur Kong, Augustine Thorgeirsson, Guðmundur Sverrisson, Jon Th Thorsteinsdottir, Unnur Stefansson, Kari Arnar, David O Producer: 20180306 In: European heart journal vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	162.	Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. [electronic resource] by Zengini, Eleni Hatzikotoulas, Konstantinos Tachmazidou, Ioanna Steinberg, Julia Hartwig, Fernando P Southam, Lorraine Hackinger, Sophie Boer, Cindy G Styrkarsdottir, Unnur Gilly, Arthur Suveges, Daniel Killian, Britt Ingvarsson, Thorvaldur Jonsson, Helgi Babis, George C McCaskie, Andrew Uitterlinden, Andre G van Meurs, Joyce B J Thorsteinsdottir, Unnur Stefansson, Kari Davey Smith, George Wilkinson, Jeremy M Zeggini, Eleftheria Producer: 20190508 In: Nature genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury. [electronic resource] by Cirulli, Elizabeth T Nicoletti, Paola Abramson, Karen Andrade, Raul J Bjornsson, Einar S Chalasani, Naga Fontana, Robert J Hallberg, Pär Li, Yi Ju Lucena, M Isabel Long, Nanye Molokhia, Mariam Nelson, Matthew R Odin, Joseph A Pirmohamed, Munir Rafnar, Thorunn Serrano, Jose Stefánsson, Kári Stolz, Andrew Daly, Ann K Aithal, Guruprasad P Watkins, Paul B Producer: 20190513 In: Gastroenterology vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. [electronic resource] by Hammerschlag, Anke R Stringer, Sven de Leeuw, Christiaan A Sniekers, Suzanne Taskesen, Erdogan Watanabe, Kyoko Blanken, Tessa F Dekker, Kim Te Lindert, Bart H W Wassing, Rick Jonsdottir, Ingileif Thorleifsson, Gudmar Stefansson, Hreinn Gislason, Thorarinn Berger, Klaus Schormair, Barbara Wellmann, Juergen Winkelmann, Juliane Stefansson, Kari Oexle, Konrad Van Someren, Eus J W Posthuma, Danielle Producer: 20171102 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	165.	The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects. [electronic resource] by Choquet, Hélène Cavalcanti-Proença, Christine Lecoeur, Cécile Dina, Christian Cauchi, Stéphane Vaxillaire, Martine Hadjadj, Samy Horber, Fritz Potoczna, Natasha Charpentier, Guillaume Ruiz, Juan Hercberg, Serge Maimaitiming, Suliya Roussel, Ronan Boenhnke, Michael Jackson, Anne U Patsch, Wolfgang Krempler, Franz Voight, Benjamin F Altshuler, David Groop, Leif Thorleifsson, Gudmar Steinthorsdottir, Valgerdur Stefansson, Kari Balkau, Beverley Froguel, Philippe Meyre, David Producer: 20090813 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder. [electronic resource] by Curran, Sarah Bolton, Patrick Rozsnyai, Kinga Chiocchetti, Andreas Klauck, Sabine M Duketis, Eftichia Poustka, Fritz Schlitt, Sabine Freitag, Christine M Lee, Irene Muglia, Pierandrea Poot, Martin Staal, Wouter de Jonge, Maretha V Ophoff, Roel A Lewis, Cathryn Skuse, David Mandy, Will Vassos, Evangelos Fossdal, Ragnheidur Magnusson, Páll Hreidarsson, Stefan Saemundsen, Evald Stefansson, Hreinn Stefansson, Kari Collier, David Producer: 20120203 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 156B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. [electronic resource] by Sigurdsson, Snaevar Alexandersson, Kristjan F Sulem, Patrick Feenstra, Bjarke Gudmundsdottir, Steinunn Halldorsson, Gisli H Olafsson, Sigurgeir Sigurdsson, Asgeir Rafnar, Thorunn Thorgeirsson, Thorgeir Sørensen, Erik Nordholm-Carstensen, Andreas Burcharth, Jakob Andersen, Jens Jørgensen, Henrik Stig Possfelt-Møller, Emma Ullum, Henrik Thorleifsson, Gudmar Masson, Gisli Thorsteinsdottir, Unnur Melbye, Mads Gudbjartsson, Daniel F Stefansson, Tryggvi Jonsdottir, Ingileif Stefansson, Kari Producer: 20181218 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	168.	Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. [electronic resource] by Kristjansson, Ragnar P Oddsson, Asmundur Helgason, Hannes Sveinbjornsson, Gardar Arnadottir, Gudny A Jensson, Brynjar O Jonasdottir, Aslaug Jonasdottir, Adalbjorg Bragi Walters, G Sulem, Gerald Oskarsdottir, Arna Benonisdottir, Stefania Davidsson, Olafur B Masson, Gisli Magnusson, Olafur Th Holm, Hilma Sigurdardottir, Olof Jonsdottir, Ingileif Eyjolfsson, Gudmundur I Olafsson, Isleifur Gudbjartsson, Daniel F Thorsteinsdottir, Unnur Sulem, Patrick Stefansson, Kari Producer: 20160615 In: Nature communications vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	169.	A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin. [electronic resource] by Oskarsson, Gudjon R Kristjansson, Ragnar P Lee, Amy L Sveinbjornsson, Gardar Magnusson, Magnus K Ivarsdottir, Erna V Benonisdottir, Stefania Oddsson, Asmundur Davidsson, Olafur B Saemundsdottir, Jona Halldorsson, Gisli H Arthur, Joseph Arnadottir, Gudny A Masson, Gisli Jensson, Brynjar O Holm, Hilma Olafsson, Isleifur Onundarson, Pall T Gudbjartsson, Daniel F Norddahl, Gudmundur L Thorsteinsdottir, Unnur Sulem, Patrick 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)
	170.	Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death. [electronic resource] by Sveinbjornsson, Gardar Olafsdottir, Eva F Thorolfsdottir, Rosa B Davidsson, Olafur B Helgadottir, Anna Jonasdottir, Adalbjorg Jonasdottir, Aslaug Bjornsson, Eythor Jensson, Brynjar O Arnadottir, Gudny A Kristinsdottir, Hallfridur Stephensen, Sigurdur S Oskarsson, Gylfi Gudbjartsson, Tomas Sigurdsson, Emil L Andersen, Karl Danielsen, Ragnar Arnar, David O Jonsdottir, Ingileif Thorsteinsdottir, Unnur Sulem, Patrick Thorgeirsson, Gudmundur Gudbjartsson, Daniel F Holm, Hilma Stefansson, Kari Producer: 20190926 In: Circulation. Genomic and precision medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. [electronic resource] by Lo, Min-Tzu Hinds, David A Tung, Joyce Y Franz, Carol Fan, Chun-Chieh Wang, Yunpeng Smeland, Olav B Schork, Andrew Holland, Dominic Kauppi, Karolina Sanyal, Nilotpal Escott-Price, Valentina Smith, Daniel J O'Donovan, Michael Stefansson, Hreinn Bjornsdottir, Gyda Thorgeirsson, Thorgeir E Stefansson, Kari McEvoy, Linda K Dale, Anders M Andreassen, Ole A Chen, Chi-Hua Producer: 20170907 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	172.	Profile of common prostate cancer risk variants in an unscreened Romanian population. [electronic resource] by Iordache, Paul D Mates, Dana Gunnarsson, Bjarni Eggertsson, Hannes P Sulem, Patrick Guðmundsson, Júlíus Benónísdóttir, Stefania Csiki, Irma Eva Rascu, Stefan Radavoi, Daniel Ursu, Radu Staicu, Catalin Calota, Violeta Voinoiu, Angelica Jinga, Mariana Rosoga, Gabriel Danau, Razvan Sima, Sorin Cristian Badescu, Daniel Suciu, Nicoleta Radoi, Viorica Manolescu, Andrei Rafnar, Thorunn Halldórsson, Bjarni V Jinga, Viorel Stefánsson, Kári Producer: 20191010 In: Journal of cellular and molecular medicine vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	173.	Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation. [electronic resource] by Bjornsdottir, Gyda Benonisdottir, Stefania Sveinbjornsson, Gardar Styrkarsdottir, Unnur Thorleifsson, Gudmar Walters, G Bragi Bjornsson, Aron Olafsson, Ingvar H Ulfarsson, Elfar Vikingsson, Arnor Hansdottir, Ragnheidur Karlsson, Karl O Rafnar, Thorunn Jonsdottir, Ingileif Frigge, Michael L Kong, Augustine Oddsson, Asmundur Masson, Gisli Magnusson, Olafur T Gudbjartsson, Tomas Stefansson, Hreinn Sulem, Patrick Gudbjartsson, Daniel Thorsteinsdottir, Unnur Thorgeirsson, Thorgeir E Stefansson, Kari Producer: 20181109 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA. [electronic resource] by Jensson, Brynjar O Hansdottir, Sif Arnadottir, Gudny A Sulem, Gerald Kristjansson, Ragnar P Oddsson, Asmundur Benonisdottir, Stefania Jonsson, Hakon Helgason, Agnar Saemundsdottir, Jona Magnusson, Olafur T Masson, Gisli Thorisson, Gudmundur A Jonasdottir, Adalbjorg Jonasdottir, Aslaug Sigurdsson, Asgeir Jonsdottir, Ingileif Petursdottir, Vigdis Kristinsson, Jon R Gudbjartsson, Daniel F Thorsteinsdottir, Unnur Arngrimsson, Reynir Sulem, Patrick Gudmundsson, Gunnar Stefansson, Kari Producer: 20171129 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. [electronic resource] by Reynisdottir, Inga Thorleifsson, Gudmar Benediktsson, Rafn Sigurdsson, Gunnar Emilsson, Valur Einarsdottir, Anna Sigurlin Hjorleifsdottir, Eyrun Edda Orlygsdottir, Gudbjorg Th Bjornsdottir, Gudrun Thora Saemundsdottir, Jona Halldorsson, Skarphedinn Hrafnkelsdottir, Soffia Sigurjonsdottir, Steinunn Bjorg Steinsdottir, Svana Martin, Mitchell Kochan, Jarema P Rhees, Brian K Grant, Struan F A Frigge, Michael L Kong, Augustine Gudnason, Vilmundur Stefansson, Kari Gulcher, Jeffrey R Producer: 20030924 In: American journal of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	176.	Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial. [electronic resource] by Hakonarson, Hakon Thorvaldsson, Sverrir Helgadottir, Anna Gudbjartsson, Daniel Zink, Florian Andresdottir, Margret Manolescu, Andrei Arnar, David O Andersen, Karl Sigurdsson, Axel Thorgeirsson, Gestur Jonsson, Asgeir Agnarsson, Uggi Bjornsdottir, Halldora Gottskalksson, Gizur Einarsson, Atli Gudmundsdottir, Hrefna Adalsteinsdottir, Asdis E Gudmundsson, Kolbeinn Kristjansson, Kristleifur Hardarson, Thordur Kristinsson, Arni Topol, Eric J Gulcher, Jeffrey Kong, Augustine Gurney, Mark Thorgeirsson, Gudmundur Stefansson, Kari Producer: 20050516 In: JAMA vol. 293 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	Genetic determinants of hair, eye and skin pigmentation in Europeans. [electronic resource] by Sulem, Patrick Gudbjartsson, Daniel F Stacey, Simon N Helgason, Agnar Rafnar, Thorunn Magnusson, Kristinn P Manolescu, Andrei Karason, Ari Palsson, Arnar Thorleifsson, Gudmar Jakobsdottir, Margret Steinberg, Stacy Pálsson, Snaebjörn Jonasson, Fridbert Sigurgeirsson, Bardur Thorisdottir, Kristin Ragnarsson, Rafn Benediktsdottir, Kristrun R Aben, Katja K Kiemeney, Lambertus A Olafsson, Jon H Gulcher, Jeffrey Kong, Augie Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20071211 In: Nature genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	Association between microdeletion and microduplication at 16p11.2 and autism. [electronic resource] by Weiss, Lauren A Shen, Yiping Korn, Joshua M Arking, Dan E Miller, David T Fossdal, Ragnheidur Saemundsen, Evald Stefansson, Hreinn Ferreira, Manuel A R Green, Todd Platt, Orah S Ruderfer, Douglas M Walsh, Christopher A Altshuler, David Chakravarti, Aravinda Tanzi, Rudolph E Stefansson, Kari Santangelo, Susan L Gusella, James F Sklar, Pamela Wu, Bai-Lin Daly, Mark J Producer: 20080219 In: The New England journal of medicine vol. 358 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	Variant of TREM2 associated with the risk of Alzheimer's disease. [electronic resource] by Jonsson, Thorlakur Stefansson, Hreinn Steinberg, Stacy Jonsdottir, Ingileif Jonsson, Palmi V Snaedal, Jon Bjornsson, Sigurbjorn Huttenlocher, Johanna Levey, Allan I Lah, James J Rujescu, Dan Hampel, Harald Giegling, Ina Andreassen, Ole A Engedal, Knut Ulstein, Ingun Djurovic, Srdjan Ibrahim-Verbaas, Carla Hofman, Albert Ikram, M Arfan van Duijn, Cornelia M Thorsteinsdottir, Unnur Kong, Augustine Stefansson, Kari Producer: 20130117 In: The New England journal of medicine vol. 368 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	180.	Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. [electronic resource] by Thorleifsson, Gudmar Holm, Hilma Edvardsson, Vidar Walters, G Bragi Styrkarsdottir, Unnur Gudbjartsson, Daniel F Sulem, Patrick Halldorsson, Bjarni V de Vegt, Femmie d'Ancona, Frank C H den Heijer, Martin Franzson, Leifur Christiansen, Claus Alexandersen, Peter Rafnar, Thorunn Kristjansson, Kristleifur Sigurdsson, Gunnar Kiemeney, Lambertus A Bodvarsson, Magnus Indridason, Olafur S Palsson, Runolfur Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari Producer: 20090909 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 517 results.