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Artigo de periodico
Dynamics of the personalities of PCSK9 on missense variants (rs505151and rs562556) from elderly cohort studies in Brazil (2023)
Lopes, Vitor Galvão ; Oliveira, Victor Fernandes de ; Dati, Lívia Mendonça Munhoz ; Naslavsky, Michel ; Ferreira, Glaucio Monteiro ; Hirata, Mario Hiroyuki
Source: Journal of Biomolecular Structure and Dynamics. Unidades: IB, FCF
Subjects: LIPOPROTEÍNAS, COLESTEROL
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ABNT
LOPES, Vitor Galvão et al. Dynamics of the personalities of PCSK9 on missense variants (rs505151and rs562556) from elderly cohort studies in Brazil. Journal of Biomolecular Structure and Dynamics, v. 41, n. 24, p. 15625-15633, 2023Tradução . . Disponível em: https://doi.org/10.1080/07391102.2023.2191140. Acesso em: 03 jun. 2024.
APA
Lopes, V. G., Oliveira, V. F. de, Dati, L. M. M., Naslavsky, M., Ferreira, G. M., & Hirata, M. H. (2023). Dynamics of the personalities of PCSK9 on missense variants (rs505151and rs562556) from elderly cohort studies in Brazil. Journal of Biomolecular Structure and Dynamics, 41( 24), 15625-15633. doi:10.1080/07391102.2023.2191140
NLM
Lopes VG, Oliveira VF de, Dati LMM, Naslavsky M, Ferreira GM, Hirata MH. Dynamics of the personalities of PCSK9 on missense variants (rs505151and rs562556) from elderly cohort studies in Brazil [Internet]. Journal of Biomolecular Structure and Dynamics. 2023 ; 41( 24): 15625-15633.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1080/07391102.2023.2191140
Vancouver
Lopes VG, Oliveira VF de, Dati LMM, Naslavsky M, Ferreira GM, Hirata MH. Dynamics of the personalities of PCSK9 on missense variants (rs505151and rs562556) from elderly cohort studies in Brazil [Internet]. Journal of Biomolecular Structure and Dynamics. 2023 ; 41( 24): 15625-15633.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1080/07391102.2023.2191140
Artigo de periodico
Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample (2023)
Paradela, Regina Silva ; Justo, Alberto Fernando Oliveira ; Paes, Vítor Ribeiro; Leite, Renata E. P ; Pasqualucci, Carlos A ; Grinberg, Lea T. ; Naslavsky, Michel Satya ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: Acta Neuropathologica Communications. Unidades: FM, IB
Subjects: APOLIPOPROTEÍNAS, DOENÇAS DO SISTEMA NERVOSO, COGNIÇÃO, DEMÊNCIA
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ABNT
PARADELA, Regina Silva et al. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, v. 11, 2023Tradução . . Disponível em: https://doi.org/10.1186/s40478-023-01681-z. Acesso em: 03 jun. 2024.
APA
Paradela, R. S., Justo, A. F. O., Paes, V. R., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., et al. (2023). Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, 11. doi:10.1186/s40478-023-01681-z
NLM
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 jun. 03 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Vancouver
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 jun. 03 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Artigo de periodico
Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report (2023)
Castro, Mateus Vidigal de ; Silva, Monize V R ; Soares, Flávia B; Coria, Vivian R ; Naslavsky, Michel ; Scliar, Marilia O ; Castelli, Erick C; Oliveira, Jamille Ramos de ; Medeiros, Giuliana Xavier de ; Sasahara, Greyce Luri ; Santos, Keity S ; Cunha Neto, Edecio ; Kalil, Jorge ; Zatz, Mayana
Source: Frontiers in Medicine. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, COVID-19, CORONAVIRUS, GÊMEOS
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ABNT
CASTRO, Mateus Vidigal de et al. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, v. 10, 2023Tradução . . Disponível em: https://doi.org/10.3389/fmed.2023.1185833. Acesso em: 03 jun. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Soares, F. B., Coria, V. R., Naslavsky, M., Scliar, M. O., et al. (2023). Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, 10. doi:10.3389/fmed.2023.1185833
NLM
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
Vancouver
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
Artigo de periodico
Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study (2023)
Paradela, Regina Silva ; Itáo, Daniela Souza Farias ; Leite, Renata E.P; Pasqualucci, Carlos A; Grinberg, Lea T ; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: ournal of Stroke & Cerebrovascular Diseases. Unidades: IB, FM
Subjects: APOLIPOPROTEÍNAS, POLIMORFISMO, ARTERIOSCLEROSE, EPIDEMIOLOGIA
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ABNT
PARADELA, Regina Silva et al. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, v. 32, n. art. 107229, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229. Acesso em: 03 jun. 2024.
APA
Paradela, R. S., Itáo, D. S. F., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., et al. (2023). Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, 32( art. 107229). doi:10.1016/j.jstrokecerebrovasdis.2023.107229
NLM
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Vancouver
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Artigo de periodico
Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study (2023)
Paradela, Regina Silva; Farias-Itao, Daniela Souza; Pasqualucci, Carlos A; Grinberg, Lea T; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie ; Leite, Renata E. P
Source: Cardiovascular Pathology. Unidades: FM, IB
Subjects: ESTUDOS TRANSVERSAIS, ARTÉRIAS CARÓTIDAS, AUTÓPSIA
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ABNT
PARADELA, Regina Silva et al. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, v. Jan./Fe, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.carpath.2022.107479. Acesso em: 03 jun. 2024.
APA
Paradela, R. S., Farias-Itao, D. S., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., Zatz, M., et al. (2023). Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, Jan./Fe. doi:10.1016/j.carpath.2022.107479
NLM
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
Vancouver
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
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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ABNT
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
Artigo de periodico-divulgacao
8 Bilhões de Homo Sapiens (2023)
Peret, Alberto Carvalho; Joly, Carlos Alfredo; Bustamante, Mercedes Maria da Cunha; Menck, Carlos Frederico Martins ; Naslavsky, Michel
Source: O Biólogo. Unidades: ICB, IB
Subjects: CRESCIMENTO POPULACIONAL, GENÉTICA DE POPULAÇÕES
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ABNT
PERET, Alberto Carvalho et al. 8 Bilhões de Homo Sapiens. O Biólogo. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://crbio01.gov.br/arquivos/revista_o_biologo_63.pdf. Acesso em: 03 jun. 2024. , 2023
APA
Peret, A. C., Joly, C. A., Bustamante, M. M. da C., Menck, C. F. M., & Naslavsky, M. (2023). 8 Bilhões de Homo Sapiens. O Biólogo. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. Recuperado de https://crbio01.gov.br/arquivos/revista_o_biologo_63.pdf
NLM
Peret AC, Joly CA, Bustamante MM da C, Menck CFM, Naslavsky M. 8 Bilhões de Homo Sapiens [Internet]. O Biólogo. 2023 ;( 63): 5-15.[citado 2024 jun. 03 ] Available from: https://crbio01.gov.br/arquivos/revista_o_biologo_63.pdf
Vancouver
Peret AC, Joly CA, Bustamante MM da C, Menck CFM, Naslavsky M. 8 Bilhões de Homo Sapiens [Internet]. O Biólogo. 2023 ;( 63): 5-15.[citado 2024 jun. 03 ] Available from: https://crbio01.gov.br/arquivos/revista_o_biologo_63.pdf
Artigo de periodico
Report on the SNP-HLA Reference Consortium (SHLARC) component (2023)
Silva, Nayane S. B; Bourguiba-Hachemi, Sonia; Douillard, Venceslas; Koskela, Satu; Degenhardt, Frauke; Clancy, Jonna; Limou, Sophie; Meyer, Diogo ; Masotti, Cibele; Knorst, Stefan; Naslavsky, Michel ; Franke, Andre; Castelli, Erick C; Gourraud, Pierre-Antoine; Vince, Nicolas
Source: HLA. Conference titles: International HLA and Immunogenetics Workshop. Unidade: IB
Subjects: IMUNOGENÉTICA, GENÔMICA
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ABNT
SILVA, Nayane S. B et al. Report on the SNP-HLA Reference Consortium (SHLARC) component. HLA, 2023Tradução . . Disponível em: https://doi.org/10.1111/tan.15293. Acesso em: 03 jun. 2024.
APA
Silva, N. S. B., Bourguiba-Hachemi, S., Douillard, V., Koskela, S., Degenhardt, F., Clancy, J., et al. (2023). Report on the SNP-HLA Reference Consortium (SHLARC) component. HLA. doi:10.1111/tan.15293
NLM
Silva NSB, Bourguiba-Hachemi S, Douillard V, Koskela S, Degenhardt F, Clancy J, Limou S, Meyer D, Masotti C, Knorst S, Naslavsky M, Franke A, Castelli EC, Gourraud P-A, Vince N. Report on the SNP-HLA Reference Consortium (SHLARC) component [Internet]. HLA. 2023 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1111/tan.15293
Vancouver
Silva NSB, Bourguiba-Hachemi S, Douillard V, Koskela S, Degenhardt F, Clancy J, Limou S, Meyer D, Masotti C, Knorst S, Naslavsky M, Franke A, Castelli EC, Gourraud P-A, Vince N. Report on the SNP-HLA Reference Consortium (SHLARC) component [Internet]. HLA. 2023 ;[citado 2024 jun. 03 ] Available from: https://doi.org/10.1111/tan.15293
Artigo de periodico
A systematic evaluation of normalization methods and probe replicability using infinium EPIC methylation data (2023)
Welsh, H; Batalha, C. M. P. F; Li, W; Mpye, K. L; Souza-Pinto, Nadja Cristhina de ; Naslavsky, Michel ; Parra, E. J
Source: Clinical Epigenetics. Unidades: IQ, IB
Assunto: METILAÇÃO DE DNA
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ABNT
WELSH, H et al. A systematic evaluation of normalization methods and probe replicability using infinium EPIC methylation data. Clinical Epigenetics, v. 15, p. 1-12 art. 41, 2023Tradução . . Disponível em: https://doi.org/10.1186/s13148-023-01459-z. Acesso em: 03 jun. 2024.
APA
Welsh, H., Batalha, C. M. P. F., Li, W., Mpye, K. L., Souza-Pinto, N. C. de, Naslavsky, M., & Parra, E. J. (2023). A systematic evaluation of normalization methods and probe replicability using infinium EPIC methylation data. Clinical Epigenetics, 15, 1-12 art. 41. doi:10.1186/s13148-023-01459-z
NLM
Welsh H, Batalha CMPF, Li W, Mpye KL, Souza-Pinto NC de, Naslavsky M, Parra EJ. A systematic evaluation of normalization methods and probe replicability using infinium EPIC methylation data [Internet]. Clinical Epigenetics. 2023 ; 15 1-12 art. 41.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1186/s13148-023-01459-z
Vancouver
Welsh H, Batalha CMPF, Li W, Mpye KL, Souza-Pinto NC de, Naslavsky M, Parra EJ. A systematic evaluation of normalization methods and probe replicability using infinium EPIC methylation data [Internet]. Clinical Epigenetics. 2023 ; 15 1-12 art. 41.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1186/s13148-023-01459-z
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1111/tan.15043
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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] 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: 03 jun. 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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report (2022)
Castro, Mateus Vidigal de ; Silva, Monize V R ; Soares, Flávia B; Coria, Vivian R ; Naslavsky, Michel ; Scliar, Marilia O ; Castelli, Erick C; Oliveira, Jamille Ramos de ; Medeiros, Giuliana Xavier de ; Sasahara, Greyce Luri ; Santos, Keity S ; Cunha Neto, Edecio ; Kalil, Jorge ; Zatz, Mayana
Source: Frontiers in Medicine. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, COVID-19, CORONAVIRUS, GÊMEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus Vidigal de et al. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, v. 9, 2022Tradução . . Disponível em: https://doi.org/10.3389/fmed.2022.1008585. Acesso em: 03 jun. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Soares, F. B., Coria, V. R., Naslavsky, M., Scliar, M. O., et al. (2022). Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, 9. doi:10.3389/fmed.2022.1008585
NLM
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2022 ; 9[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fmed.2022.1008585
Vancouver
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2022 ; 9[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fmed.2022.1008585
Artigo de periodico
Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair (2022)
Castro, Mateus V. de ; Santos, Keity S ; Apostolico, Juliana S; Fernandes, Edgar R; Almeida, Rafael R ; Levin, Gabriel ; Magawa, Jhosiene Y; Nunes, João Paulo S ; Bruni, Mirian; Yamamoto, Marcio M; Lima, Ariane C; Silva, Monize V. R; Matos, Larissa R. B; Coria, Vivian R; Castelli, Erick C; Scliar, Marilia O; Kuramoto, Andreia; Bruno, Fernanda R; Jacintho, Lucas C; Nunes, Kelly; Wang, Jaqueline Y. T; Coelho, Veronica P ; Mitne Neto, Miguel; Maciel, Rui M. B; Naslavsky, Michel ; Passos-Bueno, Maria Rita ; Boscardin, Silvia Beatriz ; Rosa, Daniela S ; Kalil, Jorge ; Zatz, Mayana ; Cunha-Neto, Edecio
Source: Open Biology. Unidades: FM, ICB, IB, BIOINFORMÁTICA
Subjects: COVID-19, GÊMEOS, INFECÇÕES POR CORONAVIRUS, DOENÇAS INFECCIOSAS, IMUNOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus V. de et al. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair. Open Biology, v. 12, n. 2, 2022Tradução . . Disponível em: https://doi.org/10.1098/rsob.210240. Acesso em: 03 jun. 2024.
APA
Castro, M. V. de, Santos, K. S., Apostolico, J. S., Fernandes, E. R., Almeida, R. R., Levin, G., et al. (2022). Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair. Open Biology, 12( 2). doi:10.1098/rsob.210240
NLM
Castro MV de, Santos KS, Apostolico JS, Fernandes ER, Almeida RR, Levin G, Magawa JY, Nunes JPS, Bruni M, Yamamoto MM, Lima AC, Silva MVR, Matos LRB, Coria VR, Castelli EC, Scliar MO, Kuramoto A, Bruno FR, Jacintho LC, Nunes K, Wang JYT, Coelho VP, Mitne Neto M, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha-Neto E. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair [Internet]. Open Biology. 2022 ; 12( 2):[citado 2024 jun. 03 ] Available from: https://doi.org/10.1098/rsob.210240
Vancouver
Castro MV de, Santos KS, Apostolico JS, Fernandes ER, Almeida RR, Levin G, Magawa JY, Nunes JPS, Bruni M, Yamamoto MM, Lima AC, Silva MVR, Matos LRB, Coria VR, Castelli EC, Scliar MO, Kuramoto A, Bruno FR, Jacintho LC, Nunes K, Wang JYT, Coelho VP, Mitne Neto M, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha-Neto E. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair [Internet]. Open Biology. 2022 ; 12( 2):[citado 2024 jun. 03 ] Available from: https://doi.org/10.1098/rsob.210240
Artigo de periodico
Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics (2022)
Palmeira, Ondina; Matos, Larissa R. B; Naslavsky, Michel ; Bueno, Heloisa Maria Siqueira ; Soler, Júlia Maria Pavan ; Setubal, João Carlos ; Zatz, Mayana
Source: iScience. Unidades: IB, IQ, IME, BIOINFORMÁTICA
Subjects: BIOTA INTESTINAL, BEBÊS, RNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALMEIRA, Ondina et al. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics. iScience, v. 25, n. 3, p. 1-18 art. 103861, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.isci.2022.103861. Acesso em: 03 jun. 2024.
APA
Palmeira, O., Matos, L. R. B., Naslavsky, M., Bueno, H. M. S., Soler, J. M. P., Setubal, J. C., & Zatz, M. (2022). Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics. iScience, 25( 3), 1-18 art. 103861. doi:10.1016/j.isci.2022.103861
NLM
Palmeira O, Matos LRB, Naslavsky M, Bueno HMS, Soler JMP, Setubal JC, Zatz M. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics [Internet]. iScience. 2022 ; 25( 3): 1-18 art. 103861.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.isci.2022.103861
Vancouver
Palmeira O, Matos LRB, Naslavsky M, Bueno HMS, Soler JMP, Setubal JC, Zatz M. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics [Internet]. iScience. 2022 ; 25( 3): 1-18 art. 103861.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.isci.2022.103861
Artigo de periodico
Global and local ancestry modulate APOE association with Alzheimer’s neuropathology and cognitive outcomes in an admixed sample (2022)
Naslavsky, Michel ; Suemoto, Claudia Kimie ; Brito, Luciano Abreu; Scliar, Marília Oliveira ; Ferretti-Rebustini, Renata Eloah de Lucena ; Rodriguez, Roberta Diehl; Leite, Renata Elaine Paraizo ; Araujo, Nathalia Matta; Borda, Victor; Tarazona-Santos, Eduardo; Jacob Filho, Wilson ; Pasqualucci, Carlos Augusto ; Nitrini, Ricardo ; Yaffe, Kristine; Zatz, Mayana ; Grinberg, Lea T.
Source: Molecular Psychiatry. Unidades: IB, FM, EE
Subjects: ANCESTRAIS, DOENÇA DE ALZHEIMER, DEMÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Global and local ancestry modulate APOE association with Alzheimer’s neuropathology and cognitive outcomes in an admixed sample. Molecular Psychiatry, v. 27, p. 4800–4808, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41380-022-01729-x. Acesso em: 03 jun. 2024.
APA
Naslavsky, M., Suemoto, C. K., Brito, L. A., Scliar, M. O., Ferretti-Rebustini, R. E. de L., Rodriguez, R. D., et al. (2022). Global and local ancestry modulate APOE association with Alzheimer’s neuropathology and cognitive outcomes in an admixed sample. Molecular Psychiatry, 27, 4800–4808. doi:10.1038/s41380-022-01729-x
NLM
Naslavsky M, Suemoto CK, Brito LA, Scliar MO, Ferretti-Rebustini RE de L, Rodriguez RD, Leite REP, Araujo NM, Borda V, Tarazona-Santos E, Jacob Filho W, Pasqualucci CA, Nitrini R, Yaffe K, Zatz M, Grinberg LT. Global and local ancestry modulate APOE association with Alzheimer’s neuropathology and cognitive outcomes in an admixed sample [Internet]. Molecular Psychiatry. 2022 ; 27 4800–4808.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1038/s41380-022-01729-x
Vancouver
Naslavsky M, Suemoto CK, Brito LA, Scliar MO, Ferretti-Rebustini RE de L, Rodriguez RD, Leite REP, Araujo NM, Borda V, Tarazona-Santos E, Jacob Filho W, Pasqualucci CA, Nitrini R, Yaffe K, Zatz M, Grinberg LT. Global and local ancestry modulate APOE association with Alzheimer’s neuropathology and cognitive outcomes in an admixed sample [Internet]. Molecular Psychiatry. 2022 ; 27 4800–4808.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1038/s41380-022-01729-x
Artigo de periodico
MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil (2022)
Castelli, Erick C ; Castro, Mateus Vidigal de ; Naslavsky, Michel ; Scliar, Marilia O ; Silva, Nayane S. B; Pereira, Raphaela Neto ; Ciriaco, Viviane A. O; Castro, Camila F. B; Mendes Junior, Celso Teixeira ; Silveira, Etiele de S ; Oliveira, Iuri M. de; Antonio, Eduardo C; Vieira, Gustavo F ; Meyer, Diogo ; Nunes, Kelly ; Matos, Larissa R. B; Bortolin, Raul Hernandes ; Hirata, Mario Hiroyuki
Unidades: IB, FFCLRP, FCF
Subjects: COVID-19, IDOSOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTELLI, Erick C et al. MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil. v. 13, p. 1-15 art. 975918, 2022Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2022.975918. Acesso em: 03 jun. 2024.
APA
Castelli, E. C., Castro, M. V. de, Naslavsky, M., Scliar, M. O., Silva, N. S. B., Pereira, R. N., et al. (2022). MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil, 13, 1-15 art. 975918. doi:10.3389/fimmu.2022.975918
NLM
Castelli EC, Castro MV de, Naslavsky M, Scliar MO, Silva NSB, Pereira RN, Ciriaco VAO, Castro CFB, Mendes Junior CT, Silveira E de S, Oliveira IM de, Antonio EC, Vieira GF, Meyer D, Nunes K, Matos LRB, Bortolin RH, Hirata MH. MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil [Internet]. 2022 ; 13 1-15 art. 975918.[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fimmu.2022.975918
Vancouver
Castelli EC, Castro MV de, Naslavsky M, Scliar MO, Silva NSB, Pereira RN, Ciriaco VAO, Castro CFB, Mendes Junior CT, Silveira E de S, Oliveira IM de, Antonio EC, Vieira GF, Meyer D, Nunes K, Matos LRB, Bortolin RH, Hirata MH. MUC22, HLA-A, and HLA-DOB variants and COVID-19 in resilient super-agers from Brazil [Internet]. 2022 ; 13 1-15 art. 975918.[citado 2024 jun. 03 ] Available from: https://doi.org/10.3389/fimmu.2022.975918
Artigo de periodico-carta/editorial
Open access: Brazilian scientists denied waivers and discounts [Carta] (2022)
Kowaltowski, Alicia Juliana ; Naslavsky, Michel ; Zatz, Mayana
Source: Nature. Unidades: IQ, IB
Subjects: PRODUÇÃO CIENTÍFICA, PESQUISA CIENTÍFICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOWALTOWSKI, Alicia Juliana e NASLAVSKY, Michel e ZATZ, Mayana. Open access: Brazilian scientists denied waivers and discounts [Carta]. Nature. London: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/d41586-022-00864-3. Acesso em: 03 jun. 2024. , 2022
APA
Kowaltowski, A. J., Naslavsky, M., & Zatz, M. (2022). Open access: Brazilian scientists denied waivers and discounts [Carta]. Nature. London: Instituto de Química, Universidade de São Paulo. doi:10.1038/d41586-022-00864-3
NLM
Kowaltowski AJ, Naslavsky M, Zatz M. Open access: Brazilian scientists denied waivers and discounts [Carta] [Internet]. Nature. 2022 ; 603 793.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1038/d41586-022-00864-3
Vancouver
Kowaltowski AJ, Naslavsky M, Zatz M. Open access: Brazilian scientists denied waivers and discounts [Carta] [Internet]. Nature. 2022 ; 603 793.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1038/d41586-022-00864-3
Artigo de jornal-dep/entr
Queda no custo de sequenciamento do DNA e melhora na capacidade de interpretar os dados aproximam os testes genéticos da prática clínica [Depoimento] (2022)
Naslavsky, Michel ; Passos-Bueno, Maria Rita
Source: Revista Pesquisa FAPESP. Unidade: IB
Subjects: DOENÇAS RARAS, NEOPLASIAS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel e PASSOS-BUENO, Maria Rita. Queda no custo de sequenciamento do DNA e melhora na capacidade de interpretar os dados aproximam os testes genéticos da prática clínica [Depoimento]. Revista Pesquisa FAPESP. Sâo Paulo: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://revistapesquisa.fapesp.br/queda-no-custo-de-sequenciamento-do-dna-e-melhora-na-capacidade-de-interpretar-os-dados-aproximam-os-testes-geneticos-da-pratica-clinica/. Acesso em: 03 jun. 2024. , 2022
APA
Naslavsky, M., & Passos-Bueno, M. R. (2022). Queda no custo de sequenciamento do DNA e melhora na capacidade de interpretar os dados aproximam os testes genéticos da prática clínica [Depoimento]. Revista Pesquisa FAPESP. Sâo Paulo: Instituto de Biociências, Universidade de São Paulo. Recuperado de https://revistapesquisa.fapesp.br/queda-no-custo-de-sequenciamento-do-dna-e-melhora-na-capacidade-de-interpretar-os-dados-aproximam-os-testes-geneticos-da-pratica-clinica/
NLM
Naslavsky M, Passos-Bueno MR. Queda no custo de sequenciamento do DNA e melhora na capacidade de interpretar os dados aproximam os testes genéticos da prática clínica [Depoimento] [Internet]. Revista Pesquisa FAPESP. 2022 ; 42-47.[citado 2024 jun. 03 ] Available from: https://revistapesquisa.fapesp.br/queda-no-custo-de-sequenciamento-do-dna-e-melhora-na-capacidade-de-interpretar-os-dados-aproximam-os-testes-geneticos-da-pratica-clinica/
Vancouver
Naslavsky M, Passos-Bueno MR. Queda no custo de sequenciamento do DNA e melhora na capacidade de interpretar os dados aproximam os testes genéticos da prática clínica [Depoimento] [Internet]. Revista Pesquisa FAPESP. 2022 ; 42-47.[citado 2024 jun. 03 ] Available from: https://revistapesquisa.fapesp.br/queda-no-custo-de-sequenciamento-do-dna-e-melhora-na-capacidade-de-interpretar-os-dados-aproximam-os-testes-geneticos-da-pratica-clinica/

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