Traços complexos (Portuguese Wikipedia)
Analysis of information sources in references of the Wikipedia article "Traços complexos" in Portuguese language version.
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doi.org
dx.doi.org
- Fisher, R. A. (1919). «XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance.». Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163
- Gibson G (janeiro de 2012). «Rare and common variants: twenty arguments». Nature Reviews. Genetics. 13 (2): 135–45. PMC 4408201
. PMID 22251874. doi:10.1038/nrg3118 - Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (outubro de 2009). «Finding the missing heritability of complex diseases». Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. PMC 2831613. PMID 19812666. doi:10.1038/nature08494
- Shi H, Kichaev G, Pasaniuc B (julho de 2016). «Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data». American Journal of Human Genetics. 99 (1): 139–53. PMC 5005444. PMID 27346688. doi:10.1016/j.ajhg.2016.05.013
- Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (junho de 2015). «Excess of rare, inherited truncating mutations in autism». Nature Genetics. 47 (6): 582–8. PMC 4449286. PMID 25961944. doi:10.1038/ng.3303
- Boyle EA, Li YI, Pritchard JK (junho de 2017). «An Expanded View of Complex Traits: From Polygenic to Omnigenic». Cell. 169 (7): 1177–1186. PMC 5536862. PMID 28622505. doi:10.1016/j.cell.2017.05.038
harvard.edu
ui.adsabs.harvard.edu
- Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (outubro de 2009). «Finding the missing heritability of complex diseases». Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. PMC 2831613. PMID 19812666. doi:10.1038/nature08494
nih.gov
ncbi.nlm.nih.gov
- Gibson G (janeiro de 2012). «Rare and common variants: twenty arguments». Nature Reviews. Genetics. 13 (2): 135–45. PMC 4408201. PMID 22251874. doi:10.1038/nrg3118
- Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (outubro de 2009). «Finding the missing heritability of complex diseases». Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. PMC 2831613. PMID 19812666. doi:10.1038/nature08494
- Shi H, Kichaev G, Pasaniuc B (julho de 2016). «Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data». American Journal of Human Genetics. 99 (1): 139–53. PMC 5005444. PMID 27346688. doi:10.1016/j.ajhg.2016.05.013
- Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (junho de 2015). «Excess of rare, inherited truncating mutations in autism». Nature Genetics. 47 (6): 582–8. PMC 4449286. PMID 25961944. doi:10.1038/ng.3303
- Boyle EA, Li YI, Pritchard JK (junho de 2017). «An Expanded View of Complex Traits: From Polygenic to Omnigenic». Cell. 169 (7): 1177–1186. PMC 5536862. PMID 28622505. doi:10.1016/j.cell.2017.05.038
worldcat.org
- Griffiths, Anthony J F; Wessler, Susan R; Carroll, Sean B; Doebley, John F (12 de janeiro de 2015). Introduction to genetic analysis Eleventh ed. New York, NY: [s.n.] ISBN 978-1-4641-0948-5. OCLC 900650999
zenodo.org
- Fisher, R. A. (1919). «XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance.». Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163