DCDC2 (Portuguese Wikipedia)
Analysis of information sources in references of the Wikipedia article "DCDC2" in Portuguese language version.
Last modified:
Ref.Un. Ref.Website
Global rank
Portuguese rank
10th place
284th place
1,390th place
948th place
1st place
1st place
cell.com (Global: 2,821st place; Portuguese: 1,658th place)
download.cell.com
- Schumacher, J.; Anthoni H.; Dadouh F.; et al. (janeiro de 2006). «Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.» (PDF). The American Journal of Human Genetics. 78 (1): 52–62. PMC 1380223
. PMID 16385449. doi:10.1086/498992. Arquivado do original (PDF) em 15 de maio de 2013
doi.org (Global: 2nd place; Portuguese: 4th place)
dx.doi.org
- Van Den Eynde BJ, Gaugler B, Probst-Kepper M, Michaux L, Devuyst O, Lorge F, Weynants P, Boon T (janeiro de 2000). «A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription». J Exp Med. 190 (12): 1793–800. PMC 2195717. PMID 10601354. doi:10.1084/jem.190.12.1793
- Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O (janeiro de 2000). «Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain». DNA Res. 6 (5): 329–36. PMID 10574461. doi:10.1093/dnares/6.5.329
- Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC (junho de 2010). «Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample». Eur. J. Hum. Genet. 18 (6): 668–73. PMC 2987340. PMID 20068590. doi:10.1038/ejhg.2009.237
- Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (novembro de 2005). «DCDC2 is associated with reading disability and modulates neuronal development in the brain». Proc. Natl. Acad. Sci. U.S.A. 102 (47): 17053–8. PMC 1278934. PMID 16278297. doi:10.1073/pnas.0508591102. Resumo divulgativo – Sciencedaily
- Schumacher, J.; Anthoni H.; Dadouh F.; et al. (janeiro de 2006). «Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.» (PDF). The American Journal of Human Genetics. 78 (1): 52–62. PMC 1380223. PMID 16385449. doi:10.1086/498992. Arquivado do original (PDF) em 15 de maio de 2013
- Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR (fevereiro de 2012). «DCDC2 genetic variants and susceptibility to developmental dyslexia». Psychiatr. Genet. 22 (1): 25–30. PMC 3232293. PMID 21881542. doi:10.1097/YPG.0b013e32834acdb2
nih.gov (Global: 5th place; Portuguese: 6th place)
ncbi.nlm.nih.gov
- «Human PubMed Reference:»
- Van Den Eynde BJ, Gaugler B, Probst-Kepper M, Michaux L, Devuyst O, Lorge F, Weynants P, Boon T (janeiro de 2000). «A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription». J Exp Med. 190 (12): 1793–800. PMC 2195717. PMID 10601354. doi:10.1084/jem.190.12.1793
- Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O (janeiro de 2000). «Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain». DNA Res. 6 (5): 329–36. PMID 10574461. doi:10.1093/dnares/6.5.329
- «Entrez Gene: DCDC2 doublecortin domain containing 2»
- Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC (junho de 2010). «Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample». Eur. J. Hum. Genet. 18 (6): 668–73. PMC 2987340. PMID 20068590. doi:10.1038/ejhg.2009.237
- Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (novembro de 2005). «DCDC2 is associated with reading disability and modulates neuronal development in the brain». Proc. Natl. Acad. Sci. U.S.A. 102 (47): 17053–8. PMC 1278934. PMID 16278297. doi:10.1073/pnas.0508591102. Resumo divulgativo – Sciencedaily
- Schumacher, J.; Anthoni H.; Dadouh F.; et al. (janeiro de 2006). «Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.» (PDF). The American Journal of Human Genetics. 78 (1): 52–62. PMC 1380223. PMID 16385449. doi:10.1086/498992. Arquivado do original (PDF) em 15 de maio de 2013
- Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR (fevereiro de 2012). «DCDC2 genetic variants and susceptibility to developmental dyslexia». Psychiatr. Genet. 22 (1): 25–30. PMC 3232293. PMID 21881542. doi:10.1097/YPG.0b013e32834acdb2
ox.ac.uk (Global: 541st place; Portuguese: 790th place)
ora.ox.ac.uk
- The DCDC2 deletion is not a risk factor for dyslexia | Peer reviewed| Date of acceptance: 2017-06-13| https://ora.ox.ac.uk/objects/uuid:812610e3-4d0e-41a9-8c73-6109e677f5ee
sciencedaily.com (Global: 1,390th place; Portuguese: 948th place)
- Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (novembro de 2005). «DCDC2 is associated with reading disability and modulates neuronal development in the brain». Proc. Natl. Acad. Sci. U.S.A. 102 (47): 17053–8. PMC 1278934. PMID 16278297. doi:10.1073/pnas.0508591102. Resumo divulgativo – Sciencedaily
web.archive.org (Global: 1st place; Portuguese: 1st place)
- Schumacher, J.; Anthoni H.; Dadouh F.; et al. (janeiro de 2006). «Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.» (PDF). The American Journal of Human Genetics. 78 (1): 52–62. PMC 1380223. PMID 16385449. doi:10.1086/498992. Arquivado do original (PDF) em 15 de maio de 2013