Centre for Applied Genomics (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Centre for Applied Genomics" in English language version.

refsWebsite

Global rank English rank

17nih.gov

4^th place

11doi.org

2^nd place

9web.archive.org

1^st place

6genomecanada.ca

low place

4semanticscholar.org

11^th place

8^th place

4tcag.ca

low place

2sickkids.ca

low place

2harvard.edu

18^th place

17^th place

1oit.on.ca

low place

1mcmm.ca

low place

doi.org

Taylor MD, Liu L, Raffel C, et al. (July 2002). "Mutations in SUFU predispose to medulloblastoma". Nature Genetics. 31 (3): 306–10. doi:10.1038/ng916. PMID 12068298. S2CID 6882566.
Boocock GR, Morrison JA, Popovic M, et al. (January 2003). "Mutations in SBDS are associated with Shwachman-Diamond syndrome". Nature Genetics. 33 (1): 97–101. doi:10.1038/ng1062. PMID 12496757. S2CID 5091627.
Chan EM, Young EJ, Ianzano L, et al. (October 2003). "Mutations in NHLRC1 cause progressive myoclonus epilepsy". Nature Genetics. 35 (2): 125–7. doi:10.1038/ng1238. PMID 12958597. S2CID 32590557.
Lohi H, Young EJ, Fitzmaurice SN, et al. (January 2005). "Expanded repeat in canine epilepsy". Science. 307 (5706): 81. doi:10.1126/science.1102832. PMID 15637270. S2CID 39280939.
Mnatzakanian GN, Lohi H, Munteanu I, et al. (April 2004). "A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome". Nature Genetics. 36 (4): 339–41. doi:10.1038/ng1327. PMID 15034579.
Qu H, Bharaj B, Liu XQ, et al. (February 2005). "Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes". Nature Genetics. 37 (2): 111–2, author reply 112–3. doi:10.1038/ng0205-111. PMID 15678135.
Somerville MJ, Mervis CB, Young EJ, et al. (October 2005). "Severe expressive-language delay related to duplication of the Williams-Beuren locus". The New England Journal of Medicine. 353 (16): 1694–701. doi:10.1056/NEJMoa051962. PMC 2893213. PMID 16236740.
Scherer SW, Cheung J, MacDonald JR, et al. (May 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. Bibcode:2003Sci...300..767S. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205.
Iafrate AJ, Feuk L, Rivera MN, et al. (September 2004). "Detection of large-scale variation in the human genome". Nature Genetics. 36 (9): 949–51. doi:10.1038/ng1416. PMID 15286789.
Redon R, Ishikawa S, Fitch KR, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.
Levy S, Sutton G, Ng PC, et al. (September 2007). "The diploid genome sequence of an individual human". PLOS Biology. 5 (10): e254. doi:10.1371/journal.pbio.0050254. PMC 1964779. PMID 17803354.

genomecanada.ca

"Genome Canada Science and Technology Platforms". Archived from the original on 2008-10-19. Retrieved 2008-06-20.
"Summary of Competition III projects on the Genome Canada website". Archived from the original on 2008-10-19. Retrieved 2008-06-20.
Summary of New Technology Development projects on the Genome Canada website.[4] Archived 2009-05-23 at the Wayback Machine
Competition in Applied Genomics Research in Bioproducts or Crops (ABC) – Genome Canada website. [5] Archived 2008-10-19 at the Wayback Machine
Large-Scale Applied Research Project Competition, Genome Canada website. [6] Archived 2010-11-24 at the Wayback Machine
Advancing Technology Innovation Through Discovery Competition, Genome Canada website.[7] Archived 2010-11-13 at the Wayback Machine

harvard.edu

ui.adsabs.harvard.edu

Scherer SW, Cheung J, MacDonald JR, et al. (May 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. Bibcode:2003Sci...300..767S. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205.
Redon R, Ishikawa S, Fitch KR, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.

mcmm.ca

"McLaughlin Centre web page". Archived from the original on 2009-02-05. Retrieved 2010-03-08.

nih.gov

pubmed.ncbi.nlm.nih.gov

Taylor MD, Liu L, Raffel C, et al. (July 2002). "Mutations in SUFU predispose to medulloblastoma". Nature Genetics. 31 (3): 306–10. doi:10.1038/ng916. PMID 12068298. S2CID 6882566.
Boocock GR, Morrison JA, Popovic M, et al. (January 2003). "Mutations in SBDS are associated with Shwachman-Diamond syndrome". Nature Genetics. 33 (1): 97–101. doi:10.1038/ng1062. PMID 12496757. S2CID 5091627.
Chan EM, Young EJ, Ianzano L, et al. (October 2003). "Mutations in NHLRC1 cause progressive myoclonus epilepsy". Nature Genetics. 35 (2): 125–7. doi:10.1038/ng1238. PMID 12958597. S2CID 32590557.
Lohi H, Young EJ, Fitzmaurice SN, et al. (January 2005). "Expanded repeat in canine epilepsy". Science. 307 (5706): 81. doi:10.1126/science.1102832. PMID 15637270. S2CID 39280939.
Mnatzakanian GN, Lohi H, Munteanu I, et al. (April 2004). "A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome". Nature Genetics. 36 (4): 339–41. doi:10.1038/ng1327. PMID 15034579.
Qu H, Bharaj B, Liu XQ, et al. (February 2005). "Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes". Nature Genetics. 37 (2): 111–2, author reply 112–3. doi:10.1038/ng0205-111. PMID 15678135.
Somerville MJ, Mervis CB, Young EJ, et al. (October 2005). "Severe expressive-language delay related to duplication of the Williams-Beuren locus". The New England Journal of Medicine. 353 (16): 1694–701. doi:10.1056/NEJMoa051962. PMC 2893213. PMID 16236740.
Scherer SW, Cheung J, MacDonald JR, et al. (May 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. Bibcode:2003Sci...300..767S. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205.
Iafrate AJ, Feuk L, Rivera MN, et al. (September 2004). "Detection of large-scale variation in the human genome". Nature Genetics. 36 (9): 949–51. doi:10.1038/ng1416. PMID 15286789.
Redon R, Ishikawa S, Fitch KR, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.
Levy S, Sutton G, Ng PC, et al. (September 2007). "The diploid genome sequence of an individual human". PLOS Biology. 5 (10): e254. doi:10.1371/journal.pbio.0050254. PMC 1964779. PMID 17803354.

ncbi.nlm.nih.gov

PubMed search for publications authored by these individuals during calendar year 2008, excluding Brudno, who was added in 2009 [2]^{[citation needed]}
PubMed search for publications authored by these individuals, 2002 through present, excluding Drs. Brudno and Beyene who were added more recently [3]^{[citation needed]}
Somerville MJ, Mervis CB, Young EJ, et al. (October 2005). "Severe expressive-language delay related to duplication of the Williams-Beuren locus". The New England Journal of Medicine. 353 (16): 1694–701. doi:10.1056/NEJMoa051962. PMC 2893213. PMID 16236740.
Scherer SW, Cheung J, MacDonald JR, et al. (May 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. Bibcode:2003Sci...300..767S. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205.
Redon R, Ishikawa S, Fitch KR, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.
Levy S, Sutton G, Ng PC, et al. (September 2007). "The diploid genome sequence of an individual human". PLOS Biology. 5 (10): e254. doi:10.1371/journal.pbio.0050254. PMC 1964779. PMID 17803354.

oit.on.ca

Integrative Genomics for Health Research news item (Ontario Innovation Trust website) [1] Archived 2011-07-06 at the Wayback Machine

semanticscholar.org

api.semanticscholar.org

Taylor MD, Liu L, Raffel C, et al. (July 2002). "Mutations in SUFU predispose to medulloblastoma". Nature Genetics. 31 (3): 306–10. doi:10.1038/ng916. PMID 12068298. S2CID 6882566.
Boocock GR, Morrison JA, Popovic M, et al. (January 2003). "Mutations in SBDS are associated with Shwachman-Diamond syndrome". Nature Genetics. 33 (1): 97–101. doi:10.1038/ng1062. PMID 12496757. S2CID 5091627.
Chan EM, Young EJ, Ianzano L, et al. (October 2003). "Mutations in NHLRC1 cause progressive myoclonus epilepsy". Nature Genetics. 35 (2): 125–7. doi:10.1038/ng1238. PMID 12958597. S2CID 32590557.
Lohi H, Young EJ, Fitzmaurice SN, et al. (January 2005). "Expanded repeat in canine epilepsy". Science. 307 (5706): 81. doi:10.1126/science.1102832. PMID 15637270. S2CID 39280939.

sickkids.ca

tcag.ca

The Centre for Applied Genomics has moved - news item, TCAG website, October 229, 2013
"Databases section of the TCAG website". Archived from the original on 2008-05-08. Retrieved 2008-06-20.
Steve Scherer biographical web page

dgv.tcag.ca

Database of Genomic Variants

web.archive.org

"Genome Canada Science and Technology Platforms". Archived from the original on 2008-10-19. Retrieved 2008-06-20.
Integrative Genomics for Health Research news item (Ontario Innovation Trust website) [1] Archived 2011-07-06 at the Wayback Machine
"Summary of Competition III projects on the Genome Canada website". Archived from the original on 2008-10-19. Retrieved 2008-06-20.
Summary of New Technology Development projects on the Genome Canada website.[4] Archived 2009-05-23 at the Wayback Machine
Competition in Applied Genomics Research in Bioproducts or Crops (ABC) – Genome Canada website. [5] Archived 2008-10-19 at the Wayback Machine
Large-Scale Applied Research Project Competition, Genome Canada website. [6] Archived 2010-11-24 at the Wayback Machine
Advancing Technology Innovation Through Discovery Competition, Genome Canada website.[7] Archived 2010-11-13 at the Wayback Machine
"Databases section of the TCAG website". Archived from the original on 2008-05-08. Retrieved 2008-06-20.
"McLaughlin Centre web page". Archived from the original on 2009-02-05. Retrieved 2010-03-08.