Bartoloni L, Blouin JL, Maiti AK, et al. Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia. Genomics. 2001;72(1):21-33. doi:10.1006/geno.2000.6462
Xu Y, Stange-Thomann N, Weber G, et al. Pathogen discovery from human tissue by sequence-based computational subtraction. Genomics. 2003;81(3):329-35.
Klockars T, Holmberg V, Savukoski M, Lander ES, Peltonen L. Transcript identification on the CLN5 region on chromosome 13q22. Hum Genet. 1999;105(1-2):51-6.
Lehesjoki AE, Koskiniemi M, Norio R, et al. Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. Hum Mol Genet. 1993;2(8):1229-34.
Bell CJ, Budarf ML, Nieuwenhuijsen BW, et al. Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers. Hum Mol Genet. 1995;4(1):59-69.
Laitinen T, Kauppi P, Ignatius J, et al. Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population. Hum Mol Genet. 1997;6(12):2069-76.
Ober C, Cox NJ, Abney M, et al. Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma. Hum Mol Genet. 1998;7(9):1393-8.
Williams N, Kocher K, Lander ES, Daly MJ, Rioux JD. Using a genome-wide scan and meta-analysis to identify a novel IBD locus and confirm previously identified IBD loci. Inflamm Bowel Dis. 2002;8(6):375-81.
Lander ES. Genomics: launching a revolution in medicine. J Law Med Ethics. 2000;28(4 Suppl):3-14.
Pettersson A, Wilson D, Daniels T, et al. Thyroiditis in the BB rat is associated with lymphopenia but occurs independently of diabetes. J Autoimmun. 1995;8(4):493-505.