The Hospital for Sick Children

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

Publications (2007)
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  1. Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Redon R, Bird CP, de Grassi A, Lee C, Tyler-Smith, Carter NC, Scherer SW, Tavar S, Deloukas P, Hurles, ME and Dermitzakis 2007 ET Relative impact of nucleotide and copy number variation on gene expression phenotypes Science Feb 9 [PMID: 17289997]
  2. The Autism Genome Project Consortium 2007 Mapping autism risk lock using generic linkage and chromosomal rearrangements Nature Genetics Feb 18 [PMID: 17322880]
  3. Parker-Katiraee L, Carson AR, Yamada T, Abu-Amero SN, Moore GE, Kaneda M, Perry GH, Stone AC, Lee C, Meguro-Horike M, Sasaki H, Kobayashi K, Nakabayashi, K and Scherer SW Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution PLos Genetics Mar 12 [PMID: 17480121]
  4. Harvey CG, Menon SD, Stachowiak B, Noor A, Proctor A, Mensah AK, Mnatzakanian GN, Alfred SE, Guo R, Scherer SW, Kennedy JL, Roberts W, Srivistava AK, Minassian BA, Vincent JB, Sequence variants within exon 1 of MECP2 occur in females with mental retardation American Journal of Medical Genetics Apr 5 [PMID: 17171659]
  5. Okamura K, Wei J and Scherer SW Evolutionary implications of the symmetry of complementary DNA strands BMC Genomics Jun 11 [PMID: 17562011]
  6. Mensah AK, De Luca V, Stachowiak B, Noor A, Windpassinger C, Lam ST, Kennedy JL, Scherer SW, Lo IF, Vincent JB Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong Kong Schizophrenia Research Jul 16; [PMID: 17644315]
  7. Zogopoulos G, Ha KC, Naqib F, Moore S, Kim H, Montpetit A, Robidoux F, Laflamme P, Cotterchio M, Greenwood C, Scherer SW, Zanke B, Hudson TJ, Bader GD, Gallinger S Germ-line DNA copy number variation frequencies in a large North American population Human Genetics July 19 [PMID: 17638019]
  8. Scherer, S.W., Lee, C., Birney, E., Altshuler, D.M., Eichler, E.E., Carter, N.P., Hurles, M.E., Feuk, L. Challenges and standards in integrating surveys of structural variation. Nature Genetics. July; [PMID: 17597783] (ISI: 0; GS: 9).
  9. Levy, S., Sutton, G., Ng, P.C., Feuk, L., Halpern, A.L., Walenz, B.P., Axelrod, N., Huang, J., Kirkness, E.F., Denisov, G., Lin, Y., MacDonald, J.R., Pang, A.W., Shago, M., Stockwell, T.B., Tsiamouri, A., Bafna, V., Bansal, V., Kravitz, S.A., Busam, D.A., Beeson, K.Y., McIntosh, T.C., Remington, K.A., Abril, J.F., Gill, J., Borman, J., Rogers, Y.H., Frazier, M.E., Scherer, S.W., Strausberg, R.L., Venter, J.C. 2007. The diploid genome sequence of an individual human. PLoS Biol. Sep 4. [PMID - in process] [PMID: 17803354] (ISI: 0; GS: 6).
  10. Pinto, D., Marshall, C., Feuk, L., Scherer, S.W. 2007. Copy-number variation in control population cohorts. Human Molecular Genetics 16, R168-173 [PubMed - in process] [PMID: 17911159] (ISI: 0; GS: 0)
  11. Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer S.W. 2007. Contribution of SHANK3 mutations to autism spectrum disorder. American Journal of Human Genetics Dec;81(6):1289-97. Epub 2007 Oct 16. [PMID: 17999366] (ISI: 0; GS: 0)
1988 - 1995  |   1996  |   1997  |   1998  |   1999  |   2000  |   2001  |   2002  |   2003  |   2004  |   2005  |   2006  |   2007 2008  |   2009  |   2010  |