The Statistical and Data Management Core will provide support to most aspects of this program project. This includes software and hardware support for all data collection and entering aspects, genetic analysis aspects, and database searches.
| Jaijo, Teresa; Oshima, Aki; Aller, Elena et al. (2012) Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I. Mol Vis 18:1719-26 |
| Malm, Eva; Ponjavic, Vesna; Möller, Claes et al. (2011) Alteration of rod and cone function in children with Usher syndrome. Eur J Ophthalmol 21:30-8 |
| Hmani-Aifa, Mounira; Benzina, Zeineb; Zulfiqar, Fareeha et al. (2009) Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. Eur J Hum Genet 17:474-82 |
| Tamayo, M L; Lopez, G; Gelvez, N et al. (2008) Genetic counseling in Usher syndrome: linkage and mutational analysis of 10 Colombian families. Genet Couns 19:15-27 |
| Oshima, A; Jaijo, T; Aller, E et al. (2008) Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I. Hum Mutat 29:E37-46 |
| Gopalarao, Deepika; Kimberling, William J; Jesteadt, Walt et al. (2008) Is hearing loss due to mutations in the Connexin 26 gene progressive? Int J Audiol 47:11-20 |
| Cremers, Frans P M; Kimberling, William J; Kulm, Maigi et al. (2007) Development of a genotyping microarray for Usher syndrome. J Med Genet 44:153-60 |
| Yang, Yan-Jun; Wang, Yan-Bo; Lei, Shu-Feng et al. (2007) AHSG gene polymorphisms are associated with bone mineral density in Caucasian nuclear families. Eur J Epidemiol 22:527-32 |
| Chen, Xiang-Ding; Shen, Hui; Recker, Robert R et al. (2006) Linkage exclusion mapping with bone size in 79 Caucasian pedigrees. J Bone Miner Metab 24:337-43 |
| Chen, Xiang-Ding; Shen, Hui; Lei, Shu-Feng et al. (2006) Exclusion mapping of chromosomes 1, 4, 6 and 14 with bone mineral density in 79 Caucasian pedigrees. Bone 38:450-5 |
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