Web sites:
The Centre for Applied Genomics
The Chromosome 7 Project
Database of Genomic Variants

News:
Press Releases and Articles
Lay Reviews/Opinions/Editorials
Media/Scientific News Articles
Interviews
Dr. Scherer's Innovation Profile - TRRA - IGLOO

Contact Info:
Stephen W. Scherer
The Centre for Applied Genomics
The Hospital for Sick Children
14th Floor, Toronto Medical Discovery Tower/MaRS Discovery District
101 College St., Toronto, Ontario, M5G 1L7, Canada
(416) 813-7613 (office)
(416) 813-8319 (fax)

Jenny Kaderali,
Dr. Scherer's Assistant
Phone: (416) 813-7654 x1574     Fax: (416) 813-8319

141. Nakabayashi, K., Fernandez, B.A., Teshima, I., Shuman, C., Proud, V.K., Curry, C.J., Chitayat, D., Grebe, T., Ming, J., Oshimura, M., Meguro, M., Mitsuya, K., Deb-Rinker, P., Herbrick, J.A., Weksberg, R. and Scherer S.W. 2002. Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome. Genomics 79, 186-96. [PMID: 11829489]
142. Hellman, A., Zlotorynski, E., Scherer, S.W., Cheung, J., 2, Vincent, J.B., 2, Smith, D., Trakhtenbrot, D. and Kerem. B. 2002. A role for common fragile site induction in amplification of human oncogenes. Cancer Cell 1, 89-97. [PMID: 12086891]
143. Chun, K., Teebi, A.S., Jung, J.H., Kennedy, S., Laframboise, R., Meschino, W.S., Nakabayashi, K., Scherer, S.W., Ray, P.N. and Teshima, I. 2002. Genetic analysis of patients with the Saethre-Chotzen Phenotype. American Journal of Medical Genetics 110, 136-143. [PMID: 12116251]
144. Lettice, L.A., Horikoshi, T., Heaney, S.J.H., van Baren M.J., van der Linde, H.C., Breedveld, G., Joosse, M., Akarsu, N., Oostra, B.A., Endo, N., Shibata, M., Suzuki, M., Takahashi, E., Shinka, T., Nakahori, Y., Ayusawa, D., Nakabayashi, K., Scherer, S.W., Heutink, P., Hill, R. and Noji, S. 2002. Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly. Proc. Natl. Acad. Sciences U.S.A. 11, 7548-7553. [PMID:12032320]
145. Taylor, M.D., Liu, L., Raffel, C., Hui, C-C., Mainprize, T.G., Zhang, X., Agatep, R., Chiappa, S., Gao, L., Lowrance, A., Hao, A., Goldstein, A.M., Stavrou, T., Scherer, S.W., Dura, W.T., Wainwright, B., Squire, J.A., Rutka, J.T. and Hogg, D. 2002. Mutations in SUFU predispose to medulloblastoma. Nature Genetics 3, 306-310. [PMID: 12068298]
146. Nakabayashi, K., Bentley, L., Hitchins, M.P., Mitsuya, K., Meguro, M., Minagawa, S., Bamforth, J.S., Stanier, P.S., Preece, M., Weksberg, R., Oshimura, M., Moore, G.E. and Scherer, S.W. 2002. Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32. Human Molecular Genetics 11, 1743-1756. [PMID: 12095916]
147. Estivill, X., Cheung, J., Pujana, M.A., Nakabayashi, K., Scherer, S.W., Tsui, L.C. 2002. Chromosomal regions containing high-density and ambiguous-mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome. Human Molecular Genetics 11, 1987-1995. [PMID: 12165560]
148. Scherer, S.W. and Cheung, J. 2002. Discovery of the human genome sequence in the public and private databases. Current Biology 20, R808-811. [PMID: 11676931]
149. Vincent, J.B., Petek, E., Thevarkunnel, S., Kolozsvari, D., Cheung, J., Patel, M. and Scherer, S.W. 2002. The RAY1-ST7 tumour suppressor locus on chromosome 7q31 represents a complex multi-transcript system. Genomics 80, 283-94. [PMID: 12213198]