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
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. A Erhardt, L Czibere, D Roeske, S Lucae, P G Unschuld, S Ripke, M Specht, M A Kohli, S Kloiber, M Ising, A Heck, H Pfister, P Zimmermann, R Lieb, B P?tz, M Uhr, P Weber, J M Deussing, M Gonik, M Bunck, M S Ke?ler, E Frank, C Hohoff, K Domschke, P Krakowitzky, W Maier, B Bandelow, C Jacob, J Deckert, S Schreiber, J Strohmaier, M N?then, S Cichon, M Rietschel, T Bettecken, M E Keck, R Landgraf, B M?ller-Myhsok, F Holsboer, E B Binder Mol Psychiatry 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 464 713-20 2010
CandiSNPer: a web tool for the identification of candidate SNPs for causal variants. Armin O Schmitt, Jens Assmus, Ralf H Bortfeldt, Gudrun A Brockmann Bioinformatics 26 969-70 2010
Rapid quantification of DNA libraries for next-generation sequencing. Bernd Buehler, Holly H Hogrefe, Graham Scott, Harini Ravi, Carlos Pab?n-Pe?a, Scott OBrien, Rachel Formosa, Scott Happe Methods 50 S15-8 2010
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains. Vardhman K Rakyan, Thomas A Down, Siarhei Maslau, Toby Andrew, Tsun-Po Yang, Huriya Beyan, Pamela Whittaker, Owen T McCann, Sarah Finer, Ana M Valdes, R David Leslie, Panogiotis Deloukas, Timothy D Spector Genome Res 20 434-9 2010
Genome-wide association studies in pharmacogenomics. Ann K Daly Nat Rev Genet 11 241-6 2010
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. Lambertus A Kiemeney, Patrick Sulem, Soren Besenbacher, Sita H Vermeulen, Asgeir Sigurdsson, Gudmar Thorleifsson, Daniel F Gudbjartsson, Simon N Stacey, Julius Gudmundsson, Carlo Zanon, Jelena Kostic, Gisli Masson, Hjordis Bjarnason, Stefan T Palsson, Oskar B Skarphedinsson, Sigurjon A Gudjonsson, J Alfred Witjes, Anne J Grotenhuis, Gerald W Verhaegh, D Timothy Bishop, Sei Chung Sak, Ananya Choudhury, Faye Elliott, Jennifer H Barrett, Carolyn D Hurst, Petra J de Verdier, Charlotta Ryk, Peter Rudnai, Eugene Gurzau, Kvetoslava Koppova, Paolo Vineis, Silvia Polidoro, Simonetta Guarrera, Carlotta Sacerdote, Marcello Campagna, Donatella Placidi, Cecilia Arici, Maurice P Zeegers, Eliane Kellen, Berta Saez Gutierrez, Jos? I Sanz-Velez, Manuel Sanchez-Zalabardo, Gabriel Valdivia, Maria D Garcia-Prats, Jan G Hengstler, Meinolf Blaszkewicz, Holger Dietrich, Roel A Ophoff, Leonard H van den Berg, Kristin Alexiusdottir, Kristleifur Kristjansson, Gudmundur Geirsson, Sigfus Nikulasson, Vigdis Petur Nat Genet 42 415-9 2010
A double hit implicates DIAPH3 as an autism risk gene. J A S Vorstman, E van Daalen, G R Jalali, E R E Schmidt, R J Pasterkamp, M de Jonge, E A M Hennekam, E Janson, W G Staal, B van der Zwaag, J P H Burbach, R S Kahn, B S Emanuel, H van Engeland, R A Ophoff Mol Psychiatry 2010
De-repression of CTGF via the miR-17-92 cluster upon differentiation of human glioblastoma spheroid cultures. A Ernst, B Campos, J Meier, F Devens, F Liesenberg, M Wolter, G Reifenberger, C Herold-Mende, P Lichter, B Radlwimmer Oncogene 29 3411-22 2010
Polydactyl inheritance in the pig. Danielle Gorbach, Benny Mote, Liviu Totir, Rohan Fernando, Max Rothschild J Hered 101 469-75
Gene-specific and global methylation patterns predict outcome in patients with acute myeloid leukemia. S Deneberg, M Gr?vdal, M Karimi, M Jansson, H Nahi, A Corbacioglu, V Gaidzik, K D?hner, C Paul, T J Ekstr?m, E Hellstr?m-Lindberg, S Lehmann Leukemia 24 932-41 2010
Dynamic changes in the human methylome during differentiation. Louise Laurent, Eleanor Wong, Guoliang Li, Tien Huynh, Aristotelis Tsirigos, Chin Thing Ong, Hwee Meng Low, Ken Wing Kin Sung, Isidore Rigoutsos, Jeanne Loring, Chia-Lin Wei Genome Res 20 320-31 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, Alice Chen-Plotkin, Li-San Wang, Neill R Graff-Radford, Dennis W Dickson, Rosa Rademakers, Bradley F Boeve, Murray Grossman, Steven E Arnold, David M A Mann, Stuart M Pickering-Brown, Harro Seelaar, Peter Heutink, John C van Swieten, Jill R Murrell, Bernardino Ghetti, Salvatore Spina, Jordan Grafman, John Hodges, Maria Grazia Spillantini, Sid Gilman, Andrew P Lieberman, Jeffrey A Kaye, Randall L Woltjer, Eileen H Bigio, Marsel Mesulam, Safa Al-Sarraj, Claire Troakes, Roger N Rosenberg, Charles L White, Isidro Ferrer, Albert Lladó, Manuela Neumann, Hans A Kretzschmar, Christine Marie Hulette, Kathleen A Welsh-Bohmer, Bruce L Miller, Ainhoa Alzualde, Adolfo Lopez de Munain, Ann C McKee, Marla Gearing, Allan I Levey, James J Lah, John Hardy, Jonathan D Rohrer, Tammaryn Lashley, Ian R A Mackenzie, Howard H Feldman, Ronald L Hamilton, Steven T Dekosky, Julie van der Zee, Samir Kumar-Singh, Christine Van Broeckhoven, Richard Nat Genet 42 234-9 2010
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
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. Annie W C Kung, Su-Mei Xiao, Stacey Cherny, Gloria H Y Li, Yi Gao, Gloria Tso, Kam S Lau, Keith D K Luk, Jian-min Liu, Bin Cui, Min-Jia Zhang, Zhen-lin Zhang, Jin-wei He, Hua Yue, Wia-bo Xia, Lian-mei Luo, Shu-li He, Douglas P Kiel, David Karasik, Yi-Hsiang Hsu, L Adrienne Cupples, Serkalem Demissie, Unnur Styrkarsdottir, Bjarni V Halldorsson, Gunnar Sigurdsson, Unnur Thorsteinsdottir, Kari Stefansson, J Brent Richards, Guangju Zhai, Nicole Soranzo, Ana Valdes, Tim D Spector, Pak C Sham Am J Hum Genet 86 229-39 2010
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