Your search returned 8 results.

Results
	1.	Using ancestry-informative markers to identify fine structure across 15 populations of European origin. [electronic resource] by Huckins, Laura M Boraska, Vesna Franklin, Christopher S Floyd, James A B Southam, Lorraine Sullivan, Patrick F Bulik, Cynthia M Collier, David A Tyler-Smith, Chris Zeggini, Eleftheria Tachmazidou, Ioanna Producer: 20150611 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability. [electronic resource] by Grozeva, Detelina Carss, Keren Spasic-Boskovic, Olivera Parker, Michael J Archer, Hayley Firth, Helen V Park, Soo-Mi Canham, Natalie Holder, Susan E Wilson, Meredith Hackett, Anna Field, Michael Floyd, James A B Hurles, Matthew Raymond, F Lucy Producer: 20140530 In: American journal of human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. [electronic resource] by Williamson, Kathleen A Rainger, Joe Floyd, James A B Ansari, Morad Meynert, Alison Aldridge, Kishan V Rainger, Jacqueline K Anderson, Carl A Moore, Anthony T Hurles, Matthew E Clarke, Angus van Heyningen, Veronica Verloes, Alain Taylor, Martin S Wilkie, Andrew O M Fitzpatrick, David R Producer: 20140331 In: American journal of human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. [electronic resource] by Grozeva, Detelina Carss, Keren Spasic-Boskovic, Olivera Tejada, Maria-Isabel Gecz, Jozef Shaw, Marie Corbett, Mark Haan, Eric Thompson, Elizabeth Friend, Kathryn Hussain, Zaamin Hackett, Anna Field, Michael Renieri, Alessandra Stevenson, Roger Schwartz, Charles Floyd, James A B Bentham, Jamie Cosgrove, Catherine Keavney, Bernard Bhattacharya, Shoumo Hurles, Matthew Raymond, F Lucy Producer: 20160819 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. [electronic resource] by Mells, George F Floyd, James A B Morley, Katherine I Cordell, Heather J Franklin, Christopher S Shin, So-Youn Heneghan, Michael A Neuberger, James M Donaldson, Peter T Day, Darren B Ducker, Samantha J Muriithi, Agnes W Wheater, Elizabeth F Hammond, Christopher J Dawwas, Muhammad F Jones, David E Peltonen, Leena Alexander, Graeme J Sandford, Richard N Anderson, Carl A Producer: 20110509 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. [electronic resource] by Cordell, Heather J Han, Younghun Mells, George F Li, Yafang Hirschfield, Gideon M Greene, Casey S Xie, Gang Juran, Brian D Zhu, Dakai Qian, David C Floyd, James A B Morley, Katherine I Prati, Daniele Lleo, Ana Cusi, Daniele Gershwin, M Eric Anderson, Carl A Lazaridis, Konstantinos N Invernizzi, Pietro Seldin, Michael F Sandford, Richard N Amos, Christopher I Siminovitch, Katherine A Producer: 20160524 In: Nature communications vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. [electronic resource] by Rainger, Joe Pehlivan, Davut Johansson, Stefan Bengani, Hemant Sanchez-Pulido, Luis Williamson, Kathleen A Ture, Mehmet Barker, Heather Rosendahl, Karen Spranger, Jürgen Horn, Denise Meynert, Alison Floyd, James A B Prescott, Trine Anderson, Carl A Rainger, Jacqueline K Karaca, Ender Gonzaga-Jauregui, Claudia Jhangiani, Shalini Muzny, Donna M Seawright, Anne Soares, Dinesh C Kharbanda, Mira Murday, Victoria Finch, Andrew Gibbs, Richard A van Heyningen, Veronica Taylor, Martin S Yakut, Tahsin Knappskog, Per M Hurles, Matthew E Ponting, Chris P Lupski, James R Houge, Gunnar FitzPatrick, David R Producer: 20140729 In: American journal of human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. [electronic resource] by Anderson, Carl A Boucher, Gabrielle Lees, Charlie W Franke, Andre D'Amato, Mauro Taylor, Kent D Lee, James C Goyette, Philippe Imielinski, Marcin Latiano, Anna Lagacé, Caroline Scott, Regan Amininejad, Leila Bumpstead, Suzannah Baidoo, Leonard Baldassano, Robert N Barclay, Murray Bayless, Theodore M Brand, Stephan Büning, Carsten Colombel, Jean-Frédéric Denson, Lee A De Vos, Martine Dubinsky, Marla Edwards, Cathryn Ellinghaus, David Fehrmann, Rudolf S N Floyd, James A B Florin, Timothy Franchimont, Denis Franke, Lude Georges, Michel Glas, Jürgen Glazer, Nicole L Guthery, Stephen L Haritunians, Talin Hayward, Nicholas K Hugot, Jean-Pierre Jobin, Gilles Laukens, Debby Lawrance, Ian Lémann, Marc Levine, Arie Libioulle, Cecile Louis, Edouard McGovern, Dermot P Milla, Monica Montgomery, Grant W Morley, Katherine I Mowat, Craig Ng, Aylwin Newman, William Ophoff, Roel A Papi, Laura Palmieri, Orazio Peyrin-Biroulet, Laurent Panés, Julián Phillips, Anne Prescott, Natalie J Proctor, Deborah D Roberts, Rebecca Russell, Richard Rutgeerts, Paul Sanderson, Jeremy Sans, Miquel Schumm, Philip Seibold, Frank Sharma, Yashoda Simms, Lisa A Seielstad, Mark Steinhart, A Hillary Targan, Stephan R van den Berg, Leonard H Vatn, Morten Verspaget, Hein Walters, Thomas Wijmenga, Cisca Wilson, David C Westra, Harm-Jan Xavier, Ramnik J Zhao, Zhen Z Ponsioen, Cyriel Y Andersen, Vibeke Torkvist, Leif Gazouli, Maria Anagnou, Nicholas P Karlsen, Tom H Kupcinskas, Limas Sventoraityte, Jurgita Mansfield, John C Kugathasan, Subra Silverberg, Mark S Halfvarson, Jonas Rotter, Jerome I Mathew, Christopher G Griffiths, Anne M Gearry, Richard Ahmad, Tariq Brant, Steven R Chamaillard, Mathias Satsangi, Jack Cho, Judy H Schreiber, Stefan Daly, Mark J Barrett, Jeffrey C Parkes, Miles Annese, Vito Hakonarson, Hakon Radford-Smith, Graham Duerr, Richard H Vermeire, Séverine Weersma, Rinse K Rioux, John D Producer: 20110419 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)