At Illumina, we enjoy seeing how researchers are successfully using our products for a wide range of genetic analysis applications. We are proud to share this list of publications from the growing community of Illumina customers, collaborators, and internal scientists. If we missed one, please send the citation to publications@illumina.com.

Title Authors Source Year
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, Patrick L M Huygen, Ghazanfar Ali, Lies H Hoefsloot, Joris A Veltman, Frans P M Cremers, Sulman Basit, Muhammad Ansar, Cor W R J Cremers, Henricus P M Kunst, Wasim Ahmad, Ronald J C Admiraal, Suzanne M Leal, Hannie Kremer Am J Hum Genet 86 138-47 2010
The genetic map of Artemisia annua L. identifies loci affecting yield of the antimalarial drug artemisinin. Ian A Graham, Katrin Besser, Susan Blumer, Caroline A Branigan, Tomasz Czechowski, Luisa Elias, Inna Guterman, David Harvey, Peter G Isaac, Awais M Khan, Tony R Larson, Yi Li, Tanya Pawson, Teresa Penfield, Anne M Rae, Deborah A Rathbone, Sonja Reid, Joe Ross, Margaret F Smallwood, Vincent Segura, Theresa Townsend, Darshna Vyas, Thilo Winzer, Dianna Bowles Science 327 328-31 2010
Impact of reduced marker set estimation of genomic relationship matrices on genomic selection for feed efficiency in Angus cattle. Megan M Rolf, Jeremy F Taylor, Robert D Schnabel, Stephanie D McKay, Matthew C McClure, Sally L Northcutt, Monty S Kerley, Robert L Weaber BMC Genet 11 24 2010
Identification of a novel cerebral malaria susceptibility locus (Berr5) on mouse chromosome 19. J Berghout, G Min-Oo, M Tam, S Gauthier, M M Stevenson, P Gros Genes Immun 11 310-8 2010
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Obesity (Silver Spring) 18 803-8 2010
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. Barry A Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Athanasios Covanis, Joseph M Dooley, Olivier Dulac, Martina Durner, Orvar Eeg-Olofsson, Martha Feucht, Mogens Laue Friis, Renzo Guerrini, Marianne Juel Kjeldsen, Rima Nabbout, Lina Nashef, Thomas Sander, Auli Sirén, Elaine Wirrell, Paul McKeigue, Robert Robinson, R Mark Gardiner, Kate V Everett Epilepsy Res 87 247-55 2009
T (brachyury) gene duplication confers major susceptibility to familial chordoma. Xiaohong R Yang, David Ng, David A Alcorta, Norbert J Liebsch, Eamonn Sheridan, Sufeng Li, Alisa M Goldstein, Dilys M Parry, Michael J Kelley Nat Genet 41 1176-8 2009
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate. Brett T Chiquet, Syed S Hashmi, Robin Henry, Amber Burt, John B Mulliken, Samuel Stal, Molly Bray, Susan H Blanton, Jacqueline T Hecht Eur J Hum Genet 17 195-204 2009