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	1.	Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis. [electronic resource] by Rakyan, Vardhman K Beyan, Huriya Down, Thomas A Hawa, Mohammed I Maslau, Siarhei Aden, Deeqo Daunay, Antoine Busato, Florence Mein, Charles A Manfras, Burkhard Dias, Kerith-Rae M Bell, Christopher G Tost, Jörg Boehm, Bernhard O Beck, Stephan Leslie, R David Producer: 20120208 In: PLoS genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. [electronic resource] by Hunt, Karen A Smyth, Deborah J Balschun, Tobias Ban, Maria Mistry, Vanisha Ahmad, Tariq Anand, Vidya Barrett, Jeffrey C Bhaw-Rosun, Leena Bockett, Nicholas A Brand, Oliver J Brouwer, Elisabeth Concannon, Patrick Cooper, Jason D Dias, Kerith-Rae M van Diemen, Cleo C Dubois, Patrick C Edkins, Sarah Fölster-Holst, Regina Fransen, Karin Glass, David N Heap, Graham A R Hofmann, Sylvia Huizinga, Tom W J Hunt, Sarah Langford, Cordelia Lee, James Mansfield, John Marrosu, Maria Giovanna Mathew, Christopher G Mein, Charles A Müller-Quernheim, Joachim Nutland, Sarah Onengut-Gumuscu, Suna Ouwehand, Willem Pearce, Kerra Prescott, Natalie J Posthumus, Marcel D Potter, Simon Rosati, Giulio Sambrook, Jennifer Satsangi, Jack Schreiber, Stefan Shtir, Corina Simmonds, Matthew J Sudman, Marc Thompson, Susan D Toes, Rene Trynka, Gosia Vyse, Timothy J Walker, Neil M Weidinger, Stephan Zhernakova, Alexandra Zoledziewska, Magdalena Weersma, Rinse K Gough, Stephen C L Sawcer, Stephen Wijmenga, Cisca Parkes, Miles Cucca, Francesco Franke, Andre Deloukas, Panos Rich, Stephen S Todd, John A van Heel, David A Producer: 20120227 In: Nature genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. [electronic resource] by Trynka, Gosia Hunt, Karen A Bockett, Nicholas A Romanos, Jihane Mistry, Vanisha Szperl, Agata Bakker, Sjoerd F Bardella, Maria Teresa Bhaw-Rosun, Leena Castillejo, Gemma de la Concha, Emilio G de Almeida, Rodrigo Coutinho Dias, Kerith-Rae M van Diemen, Cleo C Dubois, Patrick C A Duerr, Richard H Edkins, Sarah Franke, Lude Fransen, Karin Gutierrez, Javier Heap, Graham A R Hrdlickova, Barbara Hunt, Sarah Plaza Izurieta, Leticia Izzo, Valentina Joosten, Leo A B Langford, Cordelia Mazzilli, Maria Cristina Mein, Charles A Midah, Vandana Mitrovic, Mitja Mora, Barbara Morelli, Marinita Nutland, Sarah Núñez, Concepción Onengut-Gumuscu, Suna Pearce, Kerra Platteel, Mathieu Polanco, Isabel Potter, Simon Ribes-Koninckx, Carmen Ricaño-Ponce, Isis Rich, Stephen S Rybak, Anna Santiago, José Luis Senapati, Sabyasachi Sood, Ajit Szajewska, Hania Troncone, Riccardo Varadé, Jezabel Wallace, Chris Wolters, Victorien M Zhernakova, Alexandra Thelma, B K Cukrowska, Bozena Urcelay, Elena Bilbao, Jose Ramon Mearin, M Luisa Barisani, Donatella Barrett, Jeffrey C Plagnol, Vincent Deloukas, Panos Wijmenga, Cisca van Heel, David A Producer: 20120120 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)