Center for Applied Genomics (English Wikipedia)

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

refsWebsite

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1web.archive.org

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doi.org

Elia J, Gai X, Xie HM, et al. (June 2010). "Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes". Molecular Psychiatry. 15 (6): 637–46. doi:10.1038/mp.2009.57. PMC 2877197. PMID 19546859.
Sleiman PM, Flory J, Imielinski M, et al. (January 2010). "Variants of DENND1B associated with asthma in children". The New England Journal of Medicine. 362 (1): 36–44. doi:10.1056/NEJMoa0901867. PMID 20032318.
Wang K, Zhang H, Ma D, et al. (May 2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders". Nature. 459 (7246): 528–33. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC 2943511. PMID 19404256.
Glessner JT, Wang K, Cai G, et al. (May 2009). "Autism genome-wide copy number variation reveals ubiquitin and neuronal genes". Nature. 459 (7246): 569–73. Bibcode:2009Natur.459..569G. doi:10.1038/nature07953. PMC 2925224. PMID 19404257.
Maris JM, Mosse YP, Bradfield JP, et al. (June 2008). "Chromosome 6p22 locus associated with clinically aggressive neuroblastoma". The New England Journal of Medicine. 358 (24): 2585–93. doi:10.1056/NEJMoa0708698. PMC 2742373. PMID 18463370.
Capasso M, Devoto M, Hou C, et al. (June 2009). "Common variations in BARD1 influence susceptibility to high-risk neuroblastoma". Nature Genetics. 41 (6): 718–723. doi:10.1038/ng.374. PMC 2753610. PMID 19412175.
Diskin SJ, Hou C, Glessner JT, et al. (June 2009). "Copy number variation at 1q21.1 associated with neuroblastoma". Nature. 459 (7249): 987–91. Bibcode:2009Natur.459..987D. doi:10.1038/nature08035. PMC 2755253. PMID 19536264.
Kanetsky PA, Mitra N, Vardhanabhuti S, et al. (July 2009). "Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer". Nature Genetics. 41 (7): 811–5. doi:10.1038/ng.393. PMC 2865677. PMID 19483682.
Kugathasan S, Baldassano RN, Bradfield JP, et al. (October 2008). "Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease". Nature Genetics. 40 (10): 1211–5. doi:10.1038/ng.203. PMC 2770437. PMID 18758464.
Wang K, Zhang H, Kugathasan S, et al. (March 2009). "Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease". American Journal of Human Genetics. 84 (3): 399–405. doi:10.1016/j.ajhg.2009.01.026. PMC 2668006. PMID 19249008.
Imielinski M, Baldassano RN, Griffiths A, et al. (December 2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
Glessner JT, Reilly MP, Kim CE, et al. (June 2010). "Strong synaptic transmission impact by copy number variations in schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (23): 10584–9. Bibcode:2010PNAS..10710584G. doi:10.1073/pnas.1000274107. PMC 2890845. PMID 20489179.
Grant SF, Hakonarson H, Schwartz S (April 2010). "Can the genetics of type 1 and type 2 diabetes shed light on the genetics of latent autoimmune diabetes in adults?". Endocrine Reviews. 31 (2): 183–93. doi:10.1210/er.2009-0029. PMID 20007922.

g2conline.org

"Single Nucleotide Polymorphisms". Dolan DNA Learning Center. Archived from the original on 2011-04-08. Retrieved 2010-11-23.

harvard.edu

ui.adsabs.harvard.edu

Wang K, Zhang H, Ma D, et al. (May 2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders". Nature. 459 (7246): 528–33. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC 2943511. PMID 19404256.
Glessner JT, Wang K, Cai G, et al. (May 2009). "Autism genome-wide copy number variation reveals ubiquitin and neuronal genes". Nature. 459 (7246): 569–73. Bibcode:2009Natur.459..569G. doi:10.1038/nature07953. PMC 2925224. PMID 19404257.
Diskin SJ, Hou C, Glessner JT, et al. (June 2009). "Copy number variation at 1q21.1 associated with neuroblastoma". Nature. 459 (7249): 987–91. Bibcode:2009Natur.459..987D. doi:10.1038/nature08035. PMC 2755253. PMID 19536264.
Glessner JT, Reilly MP, Kim CE, et al. (June 2010). "Strong synaptic transmission impact by copy number variations in schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (23): 10584–9. Bibcode:2010PNAS..10710584G. doi:10.1073/pnas.1000274107. PMC 2890845. PMID 20489179.

nih.gov

pubmed.ncbi.nlm.nih.gov

Elia J, Gai X, Xie HM, et al. (June 2010). "Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes". Molecular Psychiatry. 15 (6): 637–46. doi:10.1038/mp.2009.57. PMC 2877197. PMID 19546859.
Sleiman PM, Flory J, Imielinski M, et al. (January 2010). "Variants of DENND1B associated with asthma in children". The New England Journal of Medicine. 362 (1): 36–44. doi:10.1056/NEJMoa0901867. PMID 20032318.
Wang K, Zhang H, Ma D, et al. (May 2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders". Nature. 459 (7246): 528–33. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC 2943511. PMID 19404256.
Glessner JT, Wang K, Cai G, et al. (May 2009). "Autism genome-wide copy number variation reveals ubiquitin and neuronal genes". Nature. 459 (7246): 569–73. Bibcode:2009Natur.459..569G. doi:10.1038/nature07953. PMC 2925224. PMID 19404257.
Maris JM, Mosse YP, Bradfield JP, et al. (June 2008). "Chromosome 6p22 locus associated with clinically aggressive neuroblastoma". The New England Journal of Medicine. 358 (24): 2585–93. doi:10.1056/NEJMoa0708698. PMC 2742373. PMID 18463370.
Capasso M, Devoto M, Hou C, et al. (June 2009). "Common variations in BARD1 influence susceptibility to high-risk neuroblastoma". Nature Genetics. 41 (6): 718–723. doi:10.1038/ng.374. PMC 2753610. PMID 19412175.
Diskin SJ, Hou C, Glessner JT, et al. (June 2009). "Copy number variation at 1q21.1 associated with neuroblastoma". Nature. 459 (7249): 987–91. Bibcode:2009Natur.459..987D. doi:10.1038/nature08035. PMC 2755253. PMID 19536264.
Kanetsky PA, Mitra N, Vardhanabhuti S, et al. (July 2009). "Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer". Nature Genetics. 41 (7): 811–5. doi:10.1038/ng.393. PMC 2865677. PMID 19483682.
Kugathasan S, Baldassano RN, Bradfield JP, et al. (October 2008). "Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease". Nature Genetics. 40 (10): 1211–5. doi:10.1038/ng.203. PMC 2770437. PMID 18758464.
Wang K, Zhang H, Kugathasan S, et al. (March 2009). "Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease". American Journal of Human Genetics. 84 (3): 399–405. doi:10.1016/j.ajhg.2009.01.026. PMC 2668006. PMID 19249008.
Imielinski M, Baldassano RN, Griffiths A, et al. (December 2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
Glessner JT, Reilly MP, Kim CE, et al. (June 2010). "Strong synaptic transmission impact by copy number variations in schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (23): 10584–9. Bibcode:2010PNAS..10710584G. doi:10.1073/pnas.1000274107. PMC 2890845. PMID 20489179.
Grant SF, Hakonarson H, Schwartz S (April 2010). "Can the genetics of type 1 and type 2 diabetes shed light on the genetics of latent autoimmune diabetes in adults?". Endocrine Reviews. 31 (2): 183–93. doi:10.1210/er.2009-0029. PMID 20007922.

ncbi.nlm.nih.gov

Elia J, Gai X, Xie HM, et al. (June 2010). "Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes". Molecular Psychiatry. 15 (6): 637–46. doi:10.1038/mp.2009.57. PMC 2877197. PMID 19546859.
Wang K, Zhang H, Ma D, et al. (May 2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders". Nature. 459 (7246): 528–33. Bibcode:2009Natur.459..528W. doi:10.1038/nature07999. PMC 2943511. PMID 19404256.
Glessner JT, Wang K, Cai G, et al. (May 2009). "Autism genome-wide copy number variation reveals ubiquitin and neuronal genes". Nature. 459 (7246): 569–73. Bibcode:2009Natur.459..569G. doi:10.1038/nature07953. PMC 2925224. PMID 19404257.
Maris JM, Mosse YP, Bradfield JP, et al. (June 2008). "Chromosome 6p22 locus associated with clinically aggressive neuroblastoma". The New England Journal of Medicine. 358 (24): 2585–93. doi:10.1056/NEJMoa0708698. PMC 2742373. PMID 18463370.
Capasso M, Devoto M, Hou C, et al. (June 2009). "Common variations in BARD1 influence susceptibility to high-risk neuroblastoma". Nature Genetics. 41 (6): 718–723. doi:10.1038/ng.374. PMC 2753610. PMID 19412175.
Diskin SJ, Hou C, Glessner JT, et al. (June 2009). "Copy number variation at 1q21.1 associated with neuroblastoma". Nature. 459 (7249): 987–91. Bibcode:2009Natur.459..987D. doi:10.1038/nature08035. PMC 2755253. PMID 19536264.
Kanetsky PA, Mitra N, Vardhanabhuti S, et al. (July 2009). "Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer". Nature Genetics. 41 (7): 811–5. doi:10.1038/ng.393. PMC 2865677. PMID 19483682.
Kugathasan S, Baldassano RN, Bradfield JP, et al. (October 2008). "Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease". Nature Genetics. 40 (10): 1211–5. doi:10.1038/ng.203. PMC 2770437. PMID 18758464.
Wang K, Zhang H, Kugathasan S, et al. (March 2009). "Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease". American Journal of Human Genetics. 84 (3): 399–405. doi:10.1016/j.ajhg.2009.01.026. PMC 2668006. PMID 19249008.
Imielinski M, Baldassano RN, Griffiths A, et al. (December 2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
Glessner JT, Reilly MP, Kim CE, et al. (June 2010). "Strong synaptic transmission impact by copy number variations in schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 107 (23): 10584–9. Bibcode:2010PNAS..10710584G. doi:10.1073/pnas.1000274107. PMC 2890845. PMID 20489179.

web.archive.org

"Single Nucleotide Polymorphisms". Dolan DNA Learning Center. Archived from the original on 2011-04-08. Retrieved 2010-11-23.