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2010
J. R. Pimenta and Pena, S. D. J., Efficient human paternity testing with a panel of 40 short insertion-deletion polymorphisms, vol. 9, pp. 601-607, 2010.
American Association of Blood Banks (AABB) (2006). Annual Report Summary for Testing in 2006. Available at [http://www.gep-isfg.org/documentos/AABB%202006.pdf]. Accessed March 1, 2010.   Ayres KL (2005). The expected performance of single nucleotide polymorphism loci in paternity testing. Forensic Sci. Int. 154: 167-172. http://dx.doi.org/10.1016/j.forsciint.2004.10.004 PMid:16182962   Bastos-Rodrigues L, Pimenta JR and Pena SD (2006). The genetic structure of human populations studied through short insertion-deletion polymorphisms. Ann. Hum. Genet. 70: 658-665. http://dx.doi.org/10.1111/j.1469-1809.2006.00287.x PMid:16907710   Børsting C, Rockenbauer E and Morling N (2009). Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standard. Forensic Sci. Int. Genet. 4: 34-42. http://dx.doi.org/10.1016/j.fsigen.2009.04.004 PMid:19948332   Budowle B, Moretti TR, Baumstark AL, Defenbaugh DA, et al. (1999). Population data on the thirteen CODIS core short tandem repeat loci in African Americans, U.S. Caucasians, Hispanics, Bahamians, Jamaicans, and Trinidadians. J. Forensic Sci. 44: 1277-1286. PMid:10582369   Butler JM (2005). Forensic DNA Typing: Biology, Technology and Genetics of STR Markers. 2nd edn. Elsevier Academic Press, Amsterdam.   Cifuentes LO, Martinez EH, Acuna MP and Jonquera HG (2006). Probability of exclusion in paternity testing: time to reassess. J. Forensic Sci. 51: 349-350. http://dx.doi.org/10.1111/j.1556-4029.2006.00064.x PMid:16566769   Gjertson DW, Brenner CH, Baur MP, Carracedo A, et al. (2007). ISFG: Recommendations on biostatistics in paternity testing. Forensic Sci. Int. Genet. 1: 223-231. http://dx.doi.org/10.1016/j.fsigen.2007.06.006 PMid:19083766   Guo SW and Thompson EA (1992). Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics 48: 361-372. http://dx.doi.org/10.2307/2532296 PMid:1637966   Inagaki S, Yamamoto Y, Doi Y, Takata T, et al. (2004). A new 39-plex analysis method for SNPs including 15 blood group loci. Forensic Sci. Int. 144: 45-57. http://dx.doi.org/10.1016/j.forsciint.2004.03.005 PMid:15240020   Jeffreys AJ and Pena SDJ (1993). A Brief Introduction to Human DNA Fingerprinting. In: DNA Fingerprinting: State of the Science (Pena SDJ, Chakraborty R, Epplen JT and Jeffreys AJ, eds.). Birkhãuser Verlag, Basel, 1-20. http://dx.doi.org/10.1007/978-3-0348-8583-6_1   Klintschar M and Neuhuber F (1998). A study on the short tandem repeat system ACTBP2 (SE33) in an Austrian population sample. Int. J. Legal Med. 111: 46-48. http://dx.doi.org/10.1007/s004140050111 PMid:9457540   Krawczak M (1999). Informativity assessment for biallelic single nucleotide polymorphisms. Electrophoresis 20: 1676-1681. http://dx.doi.org/10.1002/(SICI)1522-2683(19990101)20:8<1676::AID-ELPS1676>3.0.CO;2-D   Leopoldino AM and Pena SD (2003). The mutational spectrum of human autosomal tetranucleotide microsatellites. Hum. Mutat. 21: 71-79. http://dx.doi.org/10.1002/humu.10153 PMid:12497633   Mansfield ES, Robertson JM, Vainer M, Isenberg AR, et al. (1998). Analysis of multiplexed short tandem repeat (STR) systems using capillary array electrophoresis. Electrophoresis 19: 101-107. http://dx.doi.org/10.1002/elps.1150190118 PMid:9511870   Nachman MW and Crowell SL (2000). Estimate of the mutation rate per nucleotide in humans. Genetics 156: 297-304. PMid:10978293 PMCid:1461236   Pena SDJ (1999). Single-tube single-colour multiplex PCR amplification of ten polymorphic microsatellites (ALF10): a new powerful tool for DNA profiling. Pure Appl. Chem. 71: 1683-1690. http://dx.doi.org/10.1351/pac199971091683   Pena SD, Bastos-Rodrigues L, Pimenta JR and Bydlowski SP (2009). DNA tests probe the genomic ancestry of Brazilians. Braz. J. Med. Biol. Res. 42: 870-876. http://dx.doi.org/10.1590/S0100-879X2009005000026 PMid:19738982   Phillips C, Fondevila M, Garcia-Magarinos M, Rodriguez A, et al. (2008). Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci. Int. Genet. 2: 198-204. http://dx.doi.org/10.1016/j.fsigen.2008.02.002 PMid:19083821   Saitou N and Ueda S (1994). Evolutionary rates of insertion and deletion in noncoding nucleotide sequences of primates. Mol. Biol. Evol. 11: 504-512. PMid:8015443   Weber JL, David D, Heil J, Fan Y, et al. (2002). Human diallelic insertion/deletion polymorphisms. Am. J. Hum. Genet. 71: 854-862. http://dx.doi.org/10.1086/342727 PMid:12205564 PMCid:378541