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Artigo de periodico
The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics (2024)
Ferrari, Rafael Rodrigues; Ricardo, Paulo Cseri ; Dias, Felipe Cordeiro ; Araujo, Natalia de Souza; Soares, Dalliane Oliveira; Zhou, Qing-Song; Zhu, Chao-Dong; Coutinho, Luiz Lehmann ; Arias, Maria Cristina ; Batista, Thiago Mafra
Source: BMC Genomics. Unidades: ESALQ, IB
Subjects: ABELHAS-SEM-FERRÃO, FILOGENIA, GENOMAS, RNA, SEQUENCIAMENTO GENÉTICO
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ABNT
FERRARI, Rafael Rodrigues et al. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics. BMC Genomics, v. 25, p. 1-15, 2024Tradução . . Disponível em: https://doi.org/10.1186/s12864-024-10502-z. Acesso em: 15 nov. 2024.
APA
Ferrari, R. R., Ricardo, P. C., Dias, F. C., Araujo, N. de S., Soares, D. O., Zhou, Q. -S., et al. (2024). The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics. BMC Genomics, 25, 1-15. doi:10.1186/s12864-024-10502-z
NLM
Ferrari RR, Ricardo PC, Dias FC, Araujo N de S, Soares DO, Zhou Q-S, Zhu C-D, Coutinho LL, Arias MC, Batista TM. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics [Internet]. BMC Genomics. 2024 ; 25 1-15.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s12864-024-10502-z
Vancouver
Ferrari RR, Ricardo PC, Dias FC, Araujo N de S, Soares DO, Zhou Q-S, Zhu C-D, Coutinho LL, Arias MC, Batista TM. The nuclear and mitochondrial genome assemblies of Tetragonisca angustula (Apidae: Meliponini), a tiny yet remarkable pollinator in the Neotropics [Internet]. BMC Genomics. 2024 ; 25 1-15.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/s12864-024-10502-z
Artigo de periodico
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries (2024)
Mazzonetto, Patricia Camacho ; Villela, Darine ; Krepischi, Ana Cristina Victorino ; Pierry, Paulo Marques ; Bonaldi, Adriano; Almeida, Luiz Gustavo Dufner de ; Paula, Marcelo Gomes de ; Bürger, Matheus Carvalho ; Oliveira, Ana Gabriela de; Fonseca, Gustavo G. G; Giugliani, Roberto ; Riegel-Giugliani, Mariluce ; Bertola, Débora Romeo ; Yamamoto, Guilherme Lopes ; Passos-Bueno, Maria Rita ; Campos, Gabriele da Silva ; Machado, Ana Claudia Dantas ; Mazzeu, Juliana Forte ; Perrone, Eduardo ; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy Mizue ; Vieira, Társis Paiva ; Steiner, Carlos Eduardo ; Gil-da-Silva-Lopes, Vera Lúcia ; Vieira, Daniela Koeller Rodrigues; Boy, Raquel ; Pina Neto, João Monteiro de ; Scapulatempo Neto, Cristovam ; Milanezi, Fernanda ; Rosenberg, Carla
Source: American Journal of Medical Genetics. Part A. Unidades: IB, BIOINFORMÁTICA, HRAC, FMRP
Subjects: CITOGENÉTICA, GENOMAS, CUIDADO PÓS-NATAL, DIAGNÓSTICO
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MAZZONETTO, Patricia Camacho et al. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, v. No 2024, n. 11, p. e63802, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63802. Acesso em: 15 nov. 2024.
APA
Mazzonetto, P. C., Villela, D., Krepischi, A. C. V., Pierry, P. M., Bonaldi, A., Almeida, L. G. D. de, et al. (2024). Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, No 2024( 11), e63802. doi:10.1002/ajmg.a.63802
NLM
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.63802
Vancouver
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.63802
Artigo de periodico
A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: testing imputation accuracy in an admixed sample from Brazil (2024)
Silva, Nayane S. B ; Bourguiba-Hachemi, Sonia ; Ciriaco, Viviane A. O; Knorst, Stefan H. Y; Carmo, Ramon T ; Masotti, Cibele ; Meyer, Diogo ; Naslavsky, Michel ; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Gourraud, Pierre-Antoine ; Limou, Sophie ; Castelli, Erick C ; Vince, Nicolas
Source: HLA. Unidades: IB, HU
Subjects: GENOMAS, ANTÍGENOS HLA, DOENÇAS AUTOIMUNES
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SILVA, Nayane S. B et al. A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: testing imputation accuracy in an admixed sample from Brazil. HLA, v. 103, n. art. 15543, 2024Tradução . . Disponível em: https://doi.org/10.1111/tan.15543. Acesso em: 15 nov. 2024.
APA
Silva, N. S. B., Bourguiba-Hachemi, S., Ciriaco, V. A. O., Knorst, S. H. Y., Carmo, R. T., Masotti, C., et al. (2024). A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: testing imputation accuracy in an admixed sample from Brazil. HLA, 103( art. 15543). doi:10.1111/tan.15543
NLM
Silva NSB, Bourguiba-Hachemi S, Ciriaco VAO, Knorst SHY, Carmo RT, Masotti C, Meyer D, Naslavsky M, Duarte YA de O, Zatz M, Gourraud P-A, Limou S, Castelli EC, Vince N. A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: testing imputation accuracy in an admixed sample from Brazil [Internet]. HLA. 2024 ; 103( art. 15543):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/tan.15543
Vancouver
Silva NSB, Bourguiba-Hachemi S, Ciriaco VAO, Knorst SHY, Carmo RT, Masotti C, Meyer D, Naslavsky M, Duarte YA de O, Zatz M, Gourraud P-A, Limou S, Castelli EC, Vince N. A multi-ethnic reference panel to impute HLA classical and non-classical class I alleles in admixed samples: testing imputation accuracy in an admixed sample from Brazil [Internet]. HLA. 2024 ; 103( art. 15543):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/tan.15543
Artigo de periodico
Inferring balancing selection from genome-scale data (2023)
Bitarello, Bárbara D; Brandt, Débora Y C; Meyer, Diogo ; Andrés, Aida M
Source: Genome Biology and Evolution. Unidade: IB
Subjects: EVOLUÇÃO, GENOMAS, POLIMORFISMO
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ABNT
BITARELLO, Bárbara D et al. Inferring balancing selection from genome-scale data. Genome Biology and Evolution, v. 15, n. 3, 2023Tradução . . Disponível em: https://doi.org/10.1093/gbe/evad032. Acesso em: 15 nov. 2024.
APA
Bitarello, B. D., Brandt, D. Y. C., Meyer, D., & Andrés, A. M. (2023). Inferring balancing selection from genome-scale data. Genome Biology and Evolution, 15( 3). doi:10.1093/gbe/evad032
NLM
Bitarello BD, Brandt DYC, Meyer D, Andrés AM. Inferring balancing selection from genome-scale data [Internet]. Genome Biology and Evolution. 2023 ; 15( 3):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/gbe/evad032
Vancouver
Bitarello BD, Brandt DYC, Meyer D, Andrés AM. Inferring balancing selection from genome-scale data [Internet]. Genome Biology and Evolution. 2023 ; 15( 3):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/gbe/evad032
Artigo de periodico
Genomic history of coastal societies from eastern South America (2023)
Ferraz, Tiago; Tomé, Tiago; Gomes, Lisiane Müller Plumm; Villagrán, Ximena Suárez ; Nägele, Kathrin; Radzeviciute, Rita; Lemes, Renan Barbosa ; Salazar-García, Domingo C ; Santos, Verônica Wesolowski de Aguiar ; Alves, Marcony Lopes ; Bastos, Murilo; Py-Daniel, Anne Rapp ; Lima, Helena P ; Cardoso, Jéssica Mendes; Estevam, Renata da Silva; Liryo, Andersen; Guimarães, Geovan Martins; Figuti, Levy; Eggers, Sabine ; Plens, Cláudia Regina; Erler, Dionne Miranda Azevedo ; Erler, Igor da Silva; Costa, Henrique Antônio Valadares; Koole, Edward; Henriques, Gilmar; Solari, Ana; Martín, Gabriela; Silva, Sergio Francisco Serafim Monteiro da; Kipnis, Renato ; Müller, Letícia Morgana; Ferreira, Mariane Pereira ; Resende, Janine Carvalho; Chim, Eliane Nunes; Silva, Carlos Augusto; Borella, Ana Claudia; Fonseca, Diego Barros; Rosa, Cassia Santos da; Saldanha, João Darcy de Moura; Leite, Lúcio Costa; Cunha, Claudia M. S.; Viana, Sibeli Aparecida; Almeida, Fernando Ozorio de ; Klokler, Daniela Magalhães ; Fernandes, Henry Luydy Abraham; Talama, Sahra; Blasis, Paulo Antonio Dantas de ; Souza, Sheila Mendonça; Moraes, Claide de Paula ; Oliveira, Rodrigo Elias ; Hünemeier, Tábita ; Strauss, André Menezes ; Posth, Cosimo
Source: Nature Ecology and Evolution. Unidades: MAE, IB
Subjects: ARQUEOLOGIA, DNA, GENOMAS
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ABNT
FERRAZ, Tiago et al. Genomic history of coastal societies from eastern South America. Nature Ecology and Evolution, n. 7, p. 1315-1330, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41559-023-02114-9. Acesso em: 15 nov. 2024.
APA
Ferraz, T., Tomé, T., Gomes, L. M. P., Villagrán, X. S., Nägele, K., Radzeviciute, R., et al. (2023). Genomic history of coastal societies from eastern South America. Nature Ecology and Evolution, ( 7), 1315-1330. doi:10.1038/s41559-023-02114-9
NLM
Ferraz T, Tomé T, Gomes LMP, Villagrán XS, Nägele K, Radzeviciute R, Lemes RB, Salazar-García DC, Santos VW de A, Alves ML, Bastos M, Py-Daniel AR, Lima HP, Cardoso JM, Estevam R da S, Liryo A, Guimarães GM, Figuti L, Eggers S, Plens CR, Erler DMA, Erler I da S, Costa HAV, Koole E, Henriques G, Solari A, Martín G, Silva SFSM da, Kipnis R, Müller LM, Ferreira MP, Resende JC, Chim EN, Silva CA, Borella AC, Fonseca DB, Rosa CS da, Saldanha JD de M, Leite LC, Cunha CMS, Viana SA, Almeida FO de, Klokler DM, Fernandes HLA, Talama S, Blasis PAD de, Souza SM, Moraes C de P, Oliveira RE, Hünemeier T, Strauss AM, Posth C. Genomic history of coastal societies from eastern South America [Internet]. Nature Ecology and Evolution. 2023 ;( 7): 1315-1330.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41559-023-02114-9
Vancouver
Ferraz T, Tomé T, Gomes LMP, Villagrán XS, Nägele K, Radzeviciute R, Lemes RB, Salazar-García DC, Santos VW de A, Alves ML, Bastos M, Py-Daniel AR, Lima HP, Cardoso JM, Estevam R da S, Liryo A, Guimarães GM, Figuti L, Eggers S, Plens CR, Erler DMA, Erler I da S, Costa HAV, Koole E, Henriques G, Solari A, Martín G, Silva SFSM da, Kipnis R, Müller LM, Ferreira MP, Resende JC, Chim EN, Silva CA, Borella AC, Fonseca DB, Rosa CS da, Saldanha JD de M, Leite LC, Cunha CMS, Viana SA, Almeida FO de, Klokler DM, Fernandes HLA, Talama S, Blasis PAD de, Souza SM, Moraes C de P, Oliveira RE, Hünemeier T, Strauss AM, Posth C. Genomic history of coastal societies from eastern South America [Internet]. Nature Ecology and Evolution. 2023 ;( 7): 1315-1330.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41559-023-02114-9
Artigo de periodico
Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing (2023)
Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Dagli-Hernandez, Carolina; Ferreira, Glaucio Monteiro ; Barbosa, Thais Kristini Almendros Afonso; Marçal, Elisangela da Silva Rodrigues; Los, Bruna ; Malaquias, Vanessa Barbosa ; Bortolin, Raul Hernandes ; Freitas, Renata Caroline Costa de ; Mori, Augusto Akira ; Hirata, Thiago Dominguez Crespo ; Nakaya, Helder Takashi Imoto ; Jannes, Cinthia Elim ; Pereira, Alexandre da Costa ; Wang, Jaqueline Yu Ting; Naslavsky, Michel ; Fajardo, Cristina Moreno ; Hirata, Rosario Dominguez Crespo
Source: Gene. Unidades: FCF, FM, IB, BIOINFORMÁTICA
Subjects: HIPERCOLESTEROLEMIA, GENOMAS, SEQUENCIAMENTO GENÉTICO
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BORGES, Jéssica Bassani et al. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing. Gene, v. 875, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147501. Acesso em: 15 nov. 2024.
APA
Borges, J. B., Oliveira, V. F. de, Dagli-Hernandez, C., Ferreira, G. M., Barbosa, T. K. A. A., Marçal, E. da S. R., et al. (2023). Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing. Gene, 875. doi:10.1016/j.gene.2023.147501
NLM
Borges JB, Oliveira VF de, Dagli-Hernandez C, Ferreira GM, Barbosa TKAA, Marçal E da SR, Los B, Malaquias VB, Bortolin RH, Freitas RCC de, Mori AA, Hirata TDC, Nakaya HTI, Jannes CE, Pereira A da C, Wang JYT, Naslavsky M, Fajardo CM, Hirata RDC. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing [Internet]. Gene. 2023 ; 875[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
Vancouver
Borges JB, Oliveira VF de, Dagli-Hernandez C, Ferreira GM, Barbosa TKAA, Marçal E da SR, Los B, Malaquias VB, Bortolin RH, Freitas RCC de, Mori AA, Hirata TDC, Nakaya HTI, Jannes CE, Pereira A da C, Wang JYT, Naslavsky M, Fajardo CM, Hirata RDC. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing [Internet]. Gene. 2023 ; 875[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
Artigo de periodico
Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds (2023)
Silva, Nayane Dos Santos Brito ; Souza, Andreia Da Silva ; Andrade, Heloisa De Souza ; Pereira, Raphaela Neto; Castro, Camila Ferreira Bannwart ; Vince, Nicolas ; Limou, Sophie ; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Mendes Junior, Celso Teixeira ; Castelli, Erick Da Cruz
Source: HLA: immune response genetics. Unidades: IB, EE, FFCLRP, FMRP
Subjects: GENOMAS, GENES, GENEALOGIA
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ABNT
SILVA, Nayane Dos Santos Brito et al. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds. HLA: immune response genetics, v. 101, n. 6, p. 634-646, 2023Tradução . . Disponível em: https://doi.org/10.1111/tan.15043. Acesso em: 15 nov. 2024.
APA
Silva, N. D. S. B., Souza, A. D. S., Andrade, H. D. S., Pereira, R. N., Castro, C. F. B., Vince, N., et al. (2023). Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds. HLA: immune response genetics, 101( 6), 634-646. doi:10.1111/tan.15043
NLM
Silva NDSB, Souza ADS, Andrade HDS, Pereira RN, Castro CFB, Vince N, Limou S, Naslavsky M, Zatz M, Duarte YA de O, Mendes Junior CT, Castelli EDC. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds [Internet]. HLA: immune response genetics. 2023 ; 101( 6): 634-646.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/tan.15043
Vancouver
Silva NDSB, Souza ADS, Andrade HDS, Pereira RN, Castro CFB, Vince N, Limou S, Naslavsky M, Zatz M, Duarte YA de O, Mendes Junior CT, Castelli EDC. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds [Internet]. HLA: immune response genetics. 2023 ; 101( 6): 634-646.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/tan.15043
Artigo de periodico
Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data (2023)
Bertholim-Nasciben, Luciana; Scliar, Marilia O ; Deborto, Guilherme; Thiruvahindrapuram, Bhooma; Scherer, Stephen W; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Suarez-Kurtz, Guilherme; Parra, Esteban J; Naslavsky, Michel
Source: Frontiers in Pharmacology. Unidades: EE, IB, FSP, FMRP
Subjects: SEQUENCIAMENTO GENÉTICO, IDOSOS, GENOMAS
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ABNT
BERTHOLIM-NASCIBEN, Luciana et al. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data. Frontiers in Pharmacology, v. 11, 2023Tradução . . Disponível em: https://doi.org/10.3389/fphar.2023.1178715. Acesso em: 15 nov. 2024.
APA
Bertholim-Nasciben, L., Scliar, M. O., Deborto, G., Thiruvahindrapuram, B., Scherer, S. W., Duarte, Y. A. de O., et al. (2023). Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data. Frontiers in Pharmacology, 11. doi:10.3389/fphar.2023.1178715
NLM
Bertholim-Nasciben L, Scliar MO, Deborto G, Thiruvahindrapuram B, Scherer SW, Duarte YA de O, Zatz M, Suarez-Kurtz G, Parra EJ, Naslavsky M. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data [Internet]. Frontiers in Pharmacology. 2023 ; 11[citado 2024 nov. 15 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
Vancouver
Bertholim-Nasciben L, Scliar MO, Deborto G, Thiruvahindrapuram B, Scherer SW, Duarte YA de O, Zatz M, Suarez-Kurtz G, Parra EJ, Naslavsky M. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data [Internet]. Frontiers in Pharmacology. 2023 ; 11[citado 2024 nov. 15 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
Artigo de periodico
Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): a steppingstone towards understanding mitochondrial function and evolution (2023)
Françoso, Elaine ; Ricardo, Paulo Cseri ; Silva, João Paulo Naldi ; Arias, Maria Cristina
Source: International Journal of Biological Macromolecules. Unidade: IB
Subjects: ABELHAS-SEM-FERRÃO, APIDAE, DNA, GENOMAS
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ABNT
FRANÇOSO, Elaine et al. Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): a steppingstone towards understanding mitochondrial function and evolution. International Journal of Biological Macromolecules, v. 242, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.124568. Acesso em: 15 nov. 2024.
APA
Françoso, E., Ricardo, P. C., Silva, J. P. N., & Arias, M. C. (2023). Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): a steppingstone towards understanding mitochondrial function and evolution. International Journal of Biological Macromolecules, 242. doi:10.1016/j.ijbiomac.2023.124568
NLM
Françoso E, Ricardo PC, Silva JPN, Arias MC. Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): a steppingstone towards understanding mitochondrial function and evolution [Internet]. International Journal of Biological Macromolecules. 2023 ; 242[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.124568
Vancouver
Françoso E, Ricardo PC, Silva JPN, Arias MC. Rapid evolution, rearrangements and whole mitogenome duplication in the Australian stingless bees Tetragonula (Hymenoptera: Apidae): a steppingstone towards understanding mitochondrial function and evolution [Internet]. International Journal of Biological Macromolecules. 2023 ; 242[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.124568
Artigo de periodico
How HLA diversity is apportioned: influence of selection and relevance to transplantation (2022)
Maróstica, André Silva; Nunes, Kelly; Castelli, Erick C; Silva, Nayane S. B; Weir, Bruce S; Goudet, Jérôme; Meyer, Diogo
Source: Royal Society of London. Philosophical Transactions B. Biological Sciences. Unidade: IB
Subjects: GENOMAS, POLIMORFISMO, ANTÍGENOS HLA, TRANSPLANTES
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ABNT
MARÓSTICA, André Silva et al. How HLA diversity is apportioned: influence of selection and relevance to transplantation. Royal Society of London. Philosophical Transactions B. Biological Sciences, 2022Tradução . . Disponível em: https://doi.org/10.1098/rstb.2020.0420. Acesso em: 15 nov. 2024.
APA
Maróstica, A. S., Nunes, K., Castelli, E. C., Silva, N. S. B., Weir, B. S., Goudet, J., & Meyer, D. (2022). How HLA diversity is apportioned: influence of selection and relevance to transplantation. Royal Society of London. Philosophical Transactions B. Biological Sciences. doi:10.1098/rstb.2020.0420
NLM
Maróstica AS, Nunes K, Castelli EC, Silva NSB, Weir BS, Goudet J, Meyer D. How HLA diversity is apportioned: influence of selection and relevance to transplantation [Internet]. Royal Society of London. Philosophical Transactions B. Biological Sciences. 2022 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rstb.2020.0420
Vancouver
Maróstica AS, Nunes K, Castelli EC, Silva NSB, Weir BS, Goudet J, Meyer D. How HLA diversity is apportioned: influence of selection and relevance to transplantation [Internet]. Royal Society of London. Philosophical Transactions B. Biological Sciences. 2022 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rstb.2020.0420
Artigo de periodico
Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population (2022)
Escher, Luciana Maia; Naslavsky, Michel ; Scliar, Marília O; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Nunes, Kelly
Source: Scientific Reports. Unidades: IB, EE
Subjects: MISCIGENAÇÃO, GENEALOGIA, GENOMAS
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ABNT
ESCHER, Luciana Maia et al. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. Scientific Reports, v. 12, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-25521-7. Acesso em: 15 nov. 2024.
APA
Escher, L. M., Naslavsky, M., Scliar, M. O., Duarte, Y. A. de O., Zatz, M., & Nunes, K. (2022). Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. Scientific Reports, 12. doi:10.1038/s41598-022-25521-7
NLM
Escher LM, Naslavsky M, Scliar MO, Duarte YA de O, Zatz M, Nunes K. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population [Internet]. Scientific Reports. 2022 ; 12[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-022-25521-7
Vancouver
Escher LM, Naslavsky M, Scliar MO, Duarte YA de O, Zatz M, Nunes K. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population [Internet]. Scientific Reports. 2022 ; 12[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41598-022-25521-7
Artigo de periodico
Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1831, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29575-z. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1831). doi:10.1038/s41467-022-29575-z
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1004, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-28648-3. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1004). doi:10.1038/s41467-022-28648-3
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022)
Fu, Jack M; Satterstrom, F. Kyle; Peng, Minshi; Passos-Bueno, Maria Rita
Source: Nature Genetics. Unidade: IB
Subjects: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FU, Jack M et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, v. 54, p. 1320–1331, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01104-0. Acesso em: 15 nov. 2024.
APA
Fu, J. M., Satterstrom, F. K., Peng, M., & Passos-Bueno, M. R. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54, 1320–1331. doi:10.1038/s41588-022-01104-0
NLM
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Vancouver
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Artigo de periodico
Prediction of eye, hair and skin colour in Latin Americans (2021)
Palmal, Sagnik; Adhikari, Kaustubh; Mendoza-Revilla, Javier; Fuentes-Guajardo, Macarena; Cerqueira, Caio Cesar Silva de; Bonfant, Betty; Chacón-Duque, Juan Camilo; Sohail, Anood; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Jaramillo, Claudia; Arias, William; Lozano, Rodrigo Barquera; Everardo-Martínez, Paola; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Hünemeier, Tábita ; Ramallo, Virginia; Parolin, Maria-Laura; Gonzalez-José, Rolando; Schüler-Faccini, Lavinia; Bortolini, Maria-Cátira; Acuña-Alonzo, Victor; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Balding, David; Faux, Pierre; Ruiz-Linares, Andrés
Source: Forensic Science International: Genetics. Unidade: IB
Subjects: MISCIGENAÇÃO, PELE, OLHO, CABELO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALMAL, Sagnik et al. Prediction of eye, hair and skin colour in Latin Americans. Forensic Science International: Genetics, v. 53, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.fsigen.2021.102517. Acesso em: 15 nov. 2024.
APA
Palmal, S., Adhikari, K., Mendoza-Revilla, J., Fuentes-Guajardo, M., Cerqueira, C. C. S. de, Bonfant, B., et al. (2021). Prediction of eye, hair and skin colour in Latin Americans. Forensic Science International: Genetics, 53. doi:10.1016/j.fsigen.2021.102517
NLM
Palmal S, Adhikari K, Mendoza-Revilla J, Fuentes-Guajardo M, Cerqueira CCS de, Bonfant B, Chacón-Duque JC, Sohail A, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Lozano RB, Everardo-Martínez P, Gómez-Valdés J, Villamil-Ramírez H, Hünemeier T, Ramallo V, Parolin M-L, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Faux P, Ruiz-Linares A. Prediction of eye, hair and skin colour in Latin Americans [Internet]. Forensic Science International: Genetics. 2021 ; 53[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102517
Vancouver
Palmal S, Adhikari K, Mendoza-Revilla J, Fuentes-Guajardo M, Cerqueira CCS de, Bonfant B, Chacón-Duque JC, Sohail A, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Lozano RB, Everardo-Martínez P, Gómez-Valdés J, Villamil-Ramírez H, Hünemeier T, Ramallo V, Parolin M-L, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Faux P, Ruiz-Linares A. Prediction of eye, hair and skin colour in Latin Americans [Internet]. Forensic Science International: Genetics. 2021 ; 53[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102517
Artigo de periodico
Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing (2021)
Villela, Darine; Barros, Juliana Sobral de; Costa, Silvia Souza da; Aguiar, Talita F. M; Campagnari, Francine; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Annals of human genetics. Unidade: IB
Subjects: GENOMAS, ANORMALIDADES CROMOSSÔMICAS, SEQUÊNCIA DO DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, v. 85, n. Ja 2021, p. 18-26, 2021Tradução . . Disponível em: https://doi.org/10.1111/ahg.12402. Acesso em: 15 nov. 2024.
APA
Villela, D., Barros, J. S. de, Costa, S. S. da, Aguiar, T. F. M., Campagnari, F., Vianna-Morgante, A. M., et al. (2021). Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, 85( Ja 2021), 18-26. doi:10.1111/ahg.12402
NLM
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/ahg.12402
Vancouver
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/ahg.12402
Parte de monografia/livro
The human mitocondrial DNA (2021)
Mingroni Netto, Regina Celia
Source: Human genome structure, function and clinical considerations. Unidade: IB
Subjects: DNA MITOCONDRIAL, GENOMAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia. The human mitocondrial DNA. Human genome structure, function and clinical considerations. Tradução . Cham: Instituto de Biociências, Universidade de São Paulo, 2021. p. 301-329. Disponível em: https://doi.org/10.1007/978-3-030-73151-9_10. Acesso em: 15 nov. 2024.
APA
Mingroni Netto, R. C. (2021). The human mitocondrial DNA. In Human genome structure, function and clinical considerations (p. 301-329). Cham: Instituto de Biociências, Universidade de São Paulo. doi:10.1007/978-3-030-73151-9_10
NLM
Mingroni Netto RC. The human mitocondrial DNA [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 301-329.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_10
Vancouver
Mingroni Netto RC. The human mitocondrial DNA [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 301-329.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_10
Parte de monografia/livro
Protein-coding genes (2021)
Haddad, Luciana Amaral
Source: Human genome structure, function and clinical considerations. Unidade: IB
Subjects: PROTEÍNAS, GENOMAS, GENES, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HADDAD, Luciana Amaral. Protein-coding genes. Human genome structure, function and clinical considerations. Tradução . Cham: Instituto de Biociências, Universidade de São Paulo, 2021. p. 93-138. Disponível em: https://doi.org/10.1007/978-3-030-73151-9_4. Acesso em: 15 nov. 2024.
APA
Haddad, L. A. (2021). Protein-coding genes. In Human genome structure, function and clinical considerations (p. 93-138). Cham: Instituto de Biociências, Universidade de São Paulo. doi:10.1007/978-3-030-73151-9_4
NLM
Haddad LA. Protein-coding genes [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 93-138.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_4
Vancouver
Haddad LA. Protein-coding genes [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 93-138.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_4
Monografia/livro-ed/org
Human genome structure, function and clinical considerations (2021)
Haddad, Luciana Amaral (Editor)
Unidade: IB
Subjects: GENOMAS, DNA, GENES, CROMOSSOMOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
Human genome structure, function and clinical considerations. . Cham: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/978-3-030-73151-9. Acesso em: 15 nov. 2024. , 2021
APA
Human genome structure, function and clinical considerations. (2021). Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo. doi:10.1007/978-3-030-73151-9
NLM
Human genome structure, function and clinical considerations [Internet]. 2021 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9
Vancouver
Human genome structure, function and clinical considerations [Internet]. 2021 ;[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/978-3-030-73151-9
Artigo de periodico
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation (2021)
Bonfante, Betty; Faux, Pierr; Navarro, Nicolas; Mendoza-Revilla, Javier; Dubied, Morgane; Montillot, Charlotte; Wentworth, Emma; Poloni, Lauriane; Varón-González, Ceferino; Jones, Philip; Xiong, Ziyi; Fuentes-Guajardo, Macarena; Palmal, Sagnik; Chacón-Duque, Juan Camilo; Hurtado, Malena; Villegas, Valeria; Granja, Vanessa; Jaramillo, Claudia; Arias, William; Barquera, Rodrigo; Everardo-Martínez, Paola; Sánchez-Quinto, Mirsha; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Cerqueira, Caio C. Silva de; Hünemeier, Tábita ; Ramallo, Virginia; Liu, Fan; Weinberg, Seth M; Shaffer, John R; Stergiakouli, Evie; Howe, Laurence J; Hysi, Pirro G; Spector, Timothy D; Gonzalez-José, Rolando; Schüler-Faccini, Lavinia; Bortolini, Maria-Cátira; Acuña-Alonzo, Victor; Canizales-Quinteros, Samuel; Gallo, Carla; Poletti, Giovanni; Bedoya, Gabriel; Rothhammer, Francisco; Thauvin-Robinet, Christel; Faivre, Laurence; Costedoat, Caroline; Balding, David; Cox, Timothy; Kayser, Manfred; Duplomb, Laurence; Yalcin, Binnaz; Cotney, Justin; Adhikari, Kaustubh; Ruiz-Linares, Andrés
Source: Science Advances. Unidade: IB
Subjects: PELE, GENOMAS, GENEALOGIA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONFANTE, Betty et al. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Science Advances, v. 7, n. 6, 2021Tradução . . Disponível em: https://doi.org/10.1126/sciadv.abc6160. Acesso em: 15 nov. 2024.
APA
Bonfante, B., Faux, P., Navarro, N., Mendoza-Revilla, J., Dubied, M., Montillot, C., et al. (2021). A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Science Advances, 7( 6). doi:10.1126/sciadv.abc6160
NLM
Bonfante B, Faux P, Navarro N, Mendoza-Revilla J, Dubied M, Montillot C, Wentworth E, Poloni L, Varón-González C, Jones P, Xiong Z, Fuentes-Guajardo M, Palmal S, Chacón-Duque JC, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Barquera R, Everardo-Martínez P, Sánchez-Quinto M, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Liu F, Weinberg SM, Shaffer JR, Stergiakouli E, Howe LJ, Hysi PG, Spector TD, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Thauvin-Robinet C, Faivre L, Costedoat C, Balding D, Cox T, Kayser M, Duplomb L, Yalcin B, Cotney J, Adhikari K, Ruiz-Linares A. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation [Internet]. Science Advances. 2021 ; 7( 6):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciadv.abc6160
Vancouver
Bonfante B, Faux P, Navarro N, Mendoza-Revilla J, Dubied M, Montillot C, Wentworth E, Poloni L, Varón-González C, Jones P, Xiong Z, Fuentes-Guajardo M, Palmal S, Chacón-Duque JC, Hurtado M, Villegas V, Granja V, Jaramillo C, Arias W, Barquera R, Everardo-Martínez P, Sánchez-Quinto M, Gómez-Valdés J, Villamil-Ramírez H, Cerqueira CCS de, Hünemeier T, Ramallo V, Liu F, Weinberg SM, Shaffer JR, Stergiakouli E, Howe LJ, Hysi PG, Spector TD, Gonzalez-José R, Schüler-Faccini L, Bortolini M-C, Acuña-Alonzo V, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Thauvin-Robinet C, Faivre L, Costedoat C, Balding D, Cox T, Kayser M, Duplomb L, Yalcin B, Cotney J, Adhikari K, Ruiz-Linares A. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation [Internet]. Science Advances. 2021 ; 7( 6):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1126/sciadv.abc6160

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