Websites:
The Centre for Applied Genomics
The Chromosome 7 Project
Database of Genomic Variants
McLaughlin Centre
Steve Scherer's Wiki

News:
Press Releases and Articles
Lay Reviews/Opinions/Editorials
Media/Scientific News Articles
Interviews
Video presentation and interview
Integrative research at TCAG [Video]

Contact Info:
Stephen W. Scherer
The Centre for Applied Genomics
The Hospital for Sick Children
Peter Gilgan Centre for Research and Learning
686 Bay Street, Room 13.9800
Toronto, Ontario, M5G 0A4, Canada
(416) 813-7613 (office)
(416) 813-8319 (fax)

Elaine Chang
Dr. Scherer's Assistant
Phone: (416) 813-7654 x301574
Fax: (416) 813-8319

1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]