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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
Fonte: https://doi.org/10.1111/tan.15543. Unidades: IB, HU
Assuntos: GENOMAS, ANTÍGENOS HLA, DOENÇAS AUTOIMUNES
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ABNT
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. https://doi.org/10.1111/tan.15543, n. Ju 2024, 2024Tradução . . Disponível em: https://doi.org/10.1111/tan.15543. Acesso em: 19 jul. 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. https://doi.org/10.1111/tan.15543, (Ju 2024). 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]. https://doi.org/10.1111/tan.15543. 2024 ;(Ju 2024):[citado 2024 jul. 19 ] 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]. https://doi.org/10.1111/tan.15543. 2024 ;(Ju 2024):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1111/tan.15543
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
Fonte: Frontiers in Pharmacology. Unidades: EE, IB, FSP, FMRP
Assuntos: 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: 19 jul. 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 jul. 19 ] 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 jul. 19 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
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
Fonte: Scientific Reports. Unidades: IB, EE
Assuntos: 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: 19 jul. 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 jul. 19 ] 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 jul. 19 ] Available from: https://doi.org/10.1038/s41598-022-25521-7
Artigo de periodico
Health-related quality of life and associated factors: regional differences among oldest-old in Brazil (2022)
Freitas, Javanna L. G. da S; Silva, Jaíza M. M; Nóbrega, Júlia Cristina L; Simões, Raisa F. M; Medeiros, Juliana B; Alves, Ricardo O; Santos, Jair L. F; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Menezes, Tarciana N. de; Santos, Silvana
Fonte: Inquiry. Unidades: FMRP, EE, IB
Assuntos: QUALIDADE DE VIDA, IDOSOS, LONGEVIDADE
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ABNT
FREITAS, Javanna L. G. da S et al. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil. Inquiry, v. 59, 2022Tradução . . Disponível em: https://doi.org/10.1177/00469580221086922. Acesso em: 19 jul. 2024.
APA
Freitas, J. L. G. da S., Silva, J. M. M., Nóbrega, J. C. L., Simões, R. F. M., Medeiros, J. B., Alves, R. O., et al. (2022). Health-related quality of life and associated factors: regional differences among oldest-old in Brazil. Inquiry, 59. doi:10.1177/00469580221086922
NLM
Freitas JLG da S, Silva JMM, Nóbrega JCL, Simões RFM, Medeiros JB, Alves RO, Santos JLF, Duarte YA de O, Zatz M, Matheson D, Menezes TN de, Santos S. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil [Internet]. Inquiry. 2022 ; 59[citado 2024 jul. 19 ] Available from: https://doi.org/10.1177/00469580221086922
Vancouver
Freitas JLG da S, Silva JMM, Nóbrega JCL, Simões RFM, Medeiros JB, Alves RO, Santos JLF, Duarte YA de O, Zatz M, Matheson D, Menezes TN de, Santos S. Health-related quality of life and associated factors: regional differences among oldest-old in Brazil [Internet]. Inquiry. 2022 ; 59[citado 2024 jul. 19 ] Available from: https://doi.org/10.1177/00469580221086922
Artigo de periodico
Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study (2022)
Nóbrega, Júlia Cristina Leite; Medeiros, Juliana Barbosa; Freitas, Javanna Lacerda Gomes da Silva; Silva, Jaíza M. M; Simões, Raisa Fernandes Mariz; Olinda, Ricardo; Santos, Jair Licio Ferreira ; Menezes, Tarciana Nobre; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Santos, Silvana
Fonte: BMC Geriatrics. Unidades: FMRP, EE, IB
Assuntos: IDOSOS, LONGEVIDADE, MORTALIDADE
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ABNT
NÓBREGA, Júlia Cristina Leite et al. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study. BMC Geriatrics, v. 22, 2022Tradução . . Disponível em: https://doi.org/10.1186/s12877-022-02810-4. Acesso em: 19 jul. 2024.
APA
Nóbrega, J. C. L., Medeiros, J. B., Freitas, J. L. G. da S., Silva, J. M. M., Simões, R. F. M., Olinda, R., et al. (2022). Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study. BMC Geriatrics, 22. doi:10.1186/s12877-022-02810-4
NLM
Nóbrega JCL, Medeiros JB, Freitas JLG da S, Silva JMM, Simões RFM, Olinda R, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study [Internet]. BMC Geriatrics. 2022 ; 22[citado 2024 jul. 19 ] Available from: https://doi.org/10.1186/s12877-022-02810-4
Vancouver
Nóbrega JCL, Medeiros JB, Freitas JLG da S, Silva JMM, Simões RFM, Olinda R, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study [Internet]. BMC Geriatrics. 2022 ; 22[citado 2024 jul. 19 ] Available from: https://doi.org/10.1186/s12877-022-02810-4
Trabalho de evento-resumo periodico
A new HLA imputation model for admixed samples: testing imputation accuracy in Brazil (2022)
Silva, Nayane S. B; Knorst, Stefan H. Y; Carmo, Ramon T; Masotti, Cibele; Naslavsky, Michel ; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Douillard, Venceslas; Limou, Sophie; Vince, Nicolas; Castelli, Erick C
Fonte: HLA. Nome do evento: Joint 35th European Immunogenetics and Histocompatibility Conference Amsterdam, the Netherlands. Unidades: IB, EE
Assuntos: ANTÍGENOS HLA, POLIMORFISMO, GENÉTICA DE POPULAÇÕES, VARIAÇÃO GENÉTICA
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ABNT
SILVA, Nayane S. B et al. A new HLA imputation model for admixed samples: testing imputation accuracy in Brazil. HLA. Hoboken: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/tan.14606. Acesso em: 19 jul. 2024. , 2022
APA
Silva, N. S. B., Knorst, S. H. Y., Carmo, R. T., Masotti, C., Naslavsky, M., Duarte, Y. A. de O., et al. (2022). A new HLA imputation model for admixed samples: testing imputation accuracy in Brazil. HLA. Hoboken: Instituto de Biociências, Universidade de São Paulo. doi:10.1111/tan.14606
NLM
Silva NSB, Knorst SHY, Carmo RT, Masotti C, Naslavsky M, Duarte YA de O, Zatz M, Douillard V, Limou S, Vince N, Castelli EC. A new HLA imputation model for admixed samples: testing imputation accuracy in Brazil [Internet]. HLA. 2022 ; 416-550.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1111/tan.14606
Vancouver
Silva NSB, Knorst SHY, Carmo RT, Masotti C, Naslavsky M, Duarte YA de O, Zatz M, Douillard V, Limou S, Vince N, Castelli EC. A new HLA imputation model for admixed samples: testing imputation accuracy in Brazil [Internet]. HLA. 2022 ; 416-550.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1111/tan.14606
Artigo de periodico
TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil (2021)
Bride, Lais; Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Scliar, Marilia ; Pimassoni, Lucia H. S; Aguiar, Paola Sossai; Paula, Flavia de; Wang, Jaqueline; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana ; Errera, Flávia Imbroisi Valle
Fonte: PeerJ. Unidades: IB, EE, FM, BIOINFORMÁTICA
Assuntos: GENÉTICA, DIABETES MELLITUS, OBESIDADE, IDOSOS
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ABNT
BRIDE, Lais et al. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil. PeerJ, v. 9, 2021Tradução . . Disponível em: https://doi.org/10.7717/peerj.11349. Acesso em: 19 jul. 2024.
APA
Bride, L., Naslavsky, M., Yamamoto, G. L., Scliar, M., Pimassoni, L. H. S., Aguiar, P. S., et al. (2021). TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil. PeerJ, 9. doi:10.7717/peerj.11349
NLM
Bride L, Naslavsky M, Yamamoto GL, Scliar M, Pimassoni LHS, Aguiar PS, Paula F de, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M, Errera FIV. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil [Internet]. PeerJ. 2021 ; 9[citado 2024 jul. 19 ] Available from: https://doi.org/10.7717/peerj.11349
Vancouver
Bride L, Naslavsky M, Yamamoto GL, Scliar M, Pimassoni LHS, Aguiar PS, Paula F de, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M, Errera FIV. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil [Internet]. PeerJ. 2021 ; 9[citado 2024 jul. 19 ] Available from: https://doi.org/10.7717/peerj.11349
Artigo de periodico
Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study (2021)
Nóbrega, Júlia Cristina Leite; Medeiros, Juliana Barbosa; Santos, Tácila Thamires de Melo; Alves, Saionara Açucena Vieira; Freitas, Javanna Lacerda Gomes da Silva; Silva , Jaíza M. M; Simões, Raisa Fernandes Mariz; Brito, Allisson de Lima ; Weller, Mathias; Santos, Jair Licio Ferreira ; Menezes, Tarciana Nobre; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Matheson, David; Santos, Silvana
Fonte: Inquiry. Unidades: FMRP, EE, IB
Assuntos: ENVELHECIMENTO, CAPACIDADE FUNCIONAL, SAÚDE DO IDOSO, DOENÇA CRÔNICA, DESIGUALDADES SOCIAIS
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ABNT
NÓBREGA, Júlia Cristina Leite et al. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study. Inquiry, v. 58, 2021Tradução . . Disponível em: https://doi.org/10.1177/00469580211007264. Acesso em: 19 jul. 2024.
APA
Nóbrega, J. C. L., Medeiros, J. B., Santos, T. T. de M., Alves, S. A. V., Freitas, J. L. G. da S., Silva , J. M. M., et al. (2021). Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study. Inquiry, 58. doi:10.1177/00469580211007264
NLM
Nóbrega JCL, Medeiros JB, Santos TT de M, Alves SAV, Freitas JLG da S, Silva JMM, Simões RFM, Brito A de L, Weller M, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study [Internet]. Inquiry. 2021 ; 58[citado 2024 jul. 19 ] Available from: https://doi.org/10.1177/00469580211007264
Vancouver
Nóbrega JCL, Medeiros JB, Santos TT de M, Alves SAV, Freitas JLG da S, Silva JMM, Simões RFM, Brito A de L, Weller M, Santos JLF, Menezes TN, Duarte YA de O, Zatz M, Matheson D, Santos S. Socioeconomic factors and health status disparities associated with difficulty in ADLs and IADLs among long-lived populations in Brazil: a cross-sectional study [Internet]. Inquiry. 2021 ; 58[citado 2024 jul. 19 ] Available from: https://doi.org/10.1177/00469580211007264
Artigo de periodico
Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals (2021)
Naslavsky, Michel ; Scliar, Marília O; Nunes, Kelly; Wang, Jaqueline Y. T; Yamamoto, Guilherme L; Guio, Heinner; Tarazona-Santos, Eduardo; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Meyer, Diogo ; Zatz, Mayana
Fonte: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Unidades: IB, EE, BIOINFORMÁTICA, FM
Assuntos: SEQUENCIAMENTO GENÉTICO, MISCIGENAÇÃO, GENÉTICA DE POPULAÇÕES, NEOPLASIAS
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ABNT
NASLAVSKY, Michel et al. Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals. American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1002/ajmg.c.31931. Acesso em: 19 jul. 2024.
APA
Naslavsky, M., Scliar, M. O., Nunes, K., Wang, J. Y. T., Yamamoto, G. L., Guio, H., et al. (2021). Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals. American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. doi:10.1002/ajmg.c.31931
NLM
Naslavsky M, Scliar MO, Nunes K, Wang JYT, Yamamoto GL, Guio H, Tarazona-Santos E, Duarte YA de O, Passos-Bueno MR, Meyer D, Zatz M. Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals [Internet]. American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. 2021 ;[citado 2024 jul. 19 ] Available from: https://doi.org/10.1002/ajmg.c.31931
Vancouver
Naslavsky M, Scliar MO, Nunes K, Wang JYT, Yamamoto GL, Guio H, Tarazona-Santos E, Duarte YA de O, Passos-Bueno MR, Meyer D, Zatz M. Biased pathogenic assertions of loss of function variants challenge molecular diagnosis of admixed individuals [Internet]. American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. 2021 ;[citado 2024 jul. 19 ] Available from: https://doi.org/10.1002/ajmg.c.31931
Artigo de periodico
Structural variation of the malaria-associated human glycophorin A-B-E region (2020)
Louzada, Sandra; Algady, Walid; Weyell, Eleanor; Zuccherato, Luciana W; Brajer, Paulina; Almalki, Faisal; Scliar, Marilia O; Naslavsky, Michel ; Yamamoto, Guilherme L; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana ; Yang, Fengtang; Hollox, Edward J
Fonte: BMC Genomics. Unidades: IB, EE
Assuntos: VARIAÇÃO GENÉTICA, PLASMODIUM FALCIPARUM, MALÁRIA
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ABNT
LOUZADA, Sandra et al. Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics, v. 21, n. artigo 446, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12864-020-06849-8. Acesso em: 19 jul. 2024.
APA
Louzada, S., Algady, W., Weyell, E., Zuccherato, L. W., Brajer, P., Almalki, F., et al. (2020). Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics, 21( artigo 446). doi:10.1186/s12864-020-06849-8
NLM
Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky M, Yamamoto GL, Duarte YA de O, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Structural variation of the malaria-associated human glycophorin A-B-E region [Internet]. BMC Genomics. 2020 ; 21( artigo 446):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1186/s12864-020-06849-8
Vancouver
Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky M, Yamamoto GL, Duarte YA de O, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Structural variation of the malaria-associated human glycophorin A-B-E region [Internet]. BMC Genomics. 2020 ; 21( artigo 446):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1186/s12864-020-06849-8
Artigo de periodico
Quantitative evaluation of brain volume among elderly individuals in São Paulo, Brazil: a population-based study (2019)
Rodrigues, Mariana Athaniel Silva ; Rodrigues, Thiago Pereira ; Zatz, Mayana ; Lebrão, Maria Lúcia ; Duarte, Yeda Aparecida de Oliveira ; Naslavsky, Michel ; Nascimento, Felipe Barjud Pereira do; Amaro Junior, Edson
Fonte: Radiologia Brasileira. Unidades: IB, FSP, EE
Assuntos: ENVELHECIMENTO, IDOSOS, RESSONÂNCIA MAGNÉTICA, NEUROIMAGEM
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ABNT
RODRIGUES, Mariana Athaniel Silva et al. Quantitative evaluation of brain volume among elderly individuals in São Paulo, Brazil: a population-based study. Radiologia Brasileira, v. 52, n. 5, 2019Tradução . . Disponível em: https://doi.org/10.1590/0100-3984.2018.0074. Acesso em: 19 jul. 2024.
APA
Rodrigues, M. A. S., Rodrigues, T. P., Zatz, M., Lebrão, M. L., Duarte, Y. A. de O., Naslavsky, M., et al. (2019). Quantitative evaluation of brain volume among elderly individuals in São Paulo, Brazil: a population-based study. Radiologia Brasileira, 52( 5). doi:10.1590/0100-3984.2018.0074
NLM
Rodrigues MAS, Rodrigues TP, Zatz M, Lebrão ML, Duarte YA de O, Naslavsky M, Nascimento FBP do, Amaro Junior E. Quantitative evaluation of brain volume among elderly individuals in São Paulo, Brazil: a population-based study [Internet]. Radiologia Brasileira. 2019 ; 52( 5):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1590/0100-3984.2018.0074
Vancouver
Rodrigues MAS, Rodrigues TP, Zatz M, Lebrão ML, Duarte YA de O, Naslavsky M, Nascimento FBP do, Amaro Junior E. Quantitative evaluation of brain volume among elderly individuals in São Paulo, Brazil: a population-based study [Internet]. Radiologia Brasileira. 2019 ; 52( 5):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1590/0100-3984.2018.0074
Artigo de periodico
Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes (2019)
Scliar, Marilia O; Anna, Hanaisa P, Sant; L Santolalla, Meddly; Leal , Thiago P; Araújo , Nathalia M; Alvim , Isabela; Borda , Victor; Magalhães , Wagner C. S; Gouveia , Mateus H; Lyra, Ricardo; Machado , Moara; Michelin , Lucas; Rodrigues, Maíra R; Araújo, Gilderlanio S; Kehdy , Fernanda S. G; Zolini , Camila; Peixoto, Sérgio Viana; Luizon , Marcelo; Lobo , Francisco; Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Duarte, Yeda Aparecida de Oliveira ; Hansen , Matthew E. B; Norris , Shane A; Gilman , Robert H; Guio, Heinner; Hsing , Ann W; Mbulaiteye, Sam M ; Mensah, James; Dutil, Julie; Yeager, Meredith; Yeboah, Edward; Tishkoff, Sarah A; Choudhury, Ananyo; Ramsay, Michele; Passos-Bueno, Maria Rita ; Zatz, Mayana ; O’Connor, Timothy D; Pereira, Alexandre C; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo
Fonte: BioRxiv. Unidades: IB, EE, FM
Assuntos: FENÓTIPOS, MUTAÇÃO GENÉTICA, VARIAÇÃO GENÉTICA, GENOMAS
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ABNT
SCLIAR, Marilia O et al. Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes. BioRxiv, 2019Tradução . . Disponível em: https://doi.org/10.1101/827311. Acesso em: 19 jul. 2024.
APA
Scliar, M. O., Anna, H. P., L Santolalla, M., Leal , T. P., Araújo , N. M., Alvim , I., et al. (2019). Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes. BioRxiv. doi:10.1101/827311
NLM
Scliar MO, Anna HP, L Santolalla M, Leal TP, Araújo NM, Alvim I, Borda V, Magalhães WCS, Gouveia MH, Lyra R, Machado M, Michelin L, Rodrigues MR, Araújo GS, Kehdy FSG, Zolini C, Peixoto SV, Luizon M, Lobo F, Naslavsky M, Yamamoto GL, Duarte YA de O, Hansen MEB, Norris SA, Gilman RH, Guio H, Hsing AW, Mbulaiteye SM, Mensah J, Dutil J, Yeager M, Yeboah E, Tishkoff SA, Choudhury A, Ramsay M, Passos-Bueno MR, Zatz M, O’Connor TD, Pereira AC, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E. Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes [Internet]. BioRxiv. 2019 ;[citado 2024 jul. 19 ] Available from: https://doi.org/10.1101/827311
Vancouver
Scliar MO, Anna HP, L Santolalla M, Leal TP, Araújo NM, Alvim I, Borda V, Magalhães WCS, Gouveia MH, Lyra R, Machado M, Michelin L, Rodrigues MR, Araújo GS, Kehdy FSG, Zolini C, Peixoto SV, Luizon M, Lobo F, Naslavsky M, Yamamoto GL, Duarte YA de O, Hansen MEB, Norris SA, Gilman RH, Guio H, Hsing AW, Mbulaiteye SM, Mensah J, Dutil J, Yeager M, Yeboah E, Tishkoff SA, Choudhury A, Ramsay M, Passos-Bueno MR, Zatz M, O’Connor TD, Pereira AC, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E. Admixture/fine-mapping in Brazilians reveals a West African associated potential regulatory variant (rs114066381) with a strong female-specific effect on body mass- and fat mass-indexes [Internet]. BioRxiv. 2019 ;[citado 2024 jul. 19 ] Available from: https://doi.org/10.1101/827311
Trabalho de evento-resumo
Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation (2019)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Scliar, M. O; Wang, J; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Abstracts. Nome do evento: ASHG Annual Meeting. Unidades: EE, IB, BIOINFORMÁTICA, FM
Assuntos: GENÉTICA, IDOSOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. 2019, Anais.. Houston: Escola de Enfermagem, Universidade de São Paulo, 2019. Disponível em: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf. Acesso em: 19 jul. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Scliar, M. O., Wang, J., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2019). Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. In Abstracts. Houston: Escola de Enfermagem, Universidade de São Paulo. Recuperado de https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
NLM
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 jul. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Vancouver
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 jul. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Trabalho de evento-resumo
Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? (2018)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Ezquina, Suzana ; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Abstracts. Nome do evento: ASHI Annual Meeting. Unidades: EE, IB, FM, BIOINFORMÁTICA
Assuntos: NEOPLASIAS, IDOSOS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? 2018, Anais.. Baltimore: Escola de Enfermagem, Universidade de São Paulo, 2018. . Acesso em: 19 jul. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Ezquina, S., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2018). Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? In Abstracts. Baltimore: Escola de Enfermagem, Universidade de São Paulo.
NLM
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 jul. 19 ]
Vancouver
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 jul. 19 ]
Artigo de periodico
Exomic variants of an elderly cohort of Brazilians in the ABraOM database (2017)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes; Almeida, Tatiana Ferreira de; Ezquina, Suzana A. M; Sunaga, Daniele Yumi; Pho, Nam; Bozoklian, Daniel; Sandberg, Tatiana Orli Milkewitz; Brito, Luciano Abreu; Lazar, Monize; Bernardo, Danilo Vicensotto; Amaro Jr., Edson; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lúcia; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Human Mutation. Unidades: IB, FM, EE
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES, ENVELHECIMENTO, ESTUDOS DE COORTES, ESTUDOS LONGITUDINAIS, SAÚDE DO IDOSO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Exomic variants of an elderly cohort of Brazilians in the ABraOM database. Human Mutation, p. 1-13, 2017Tradução . . Disponível em: https://doi.org/10.1002/humu.23220. Acesso em: 19 jul. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Almeida, T. F. de, Ezquina, S. A. M., Sunaga, D. Y., Pho, N., et al. (2017). Exomic variants of an elderly cohort of Brazilians in the ABraOM database. Human Mutation, 1-13. doi:10.1002/humu.23220
NLM
Naslavsky M, Yamamoto GL, Almeida TF de, Ezquina SAM, Sunaga DY, Pho N, Bozoklian D, Sandberg TOM, Brito LA, Lazar M, Bernardo DV, Amaro Jr. E, Duarte YA de O, Lebrão ML, Passos-Bueno MR, Zatz M. Exomic variants of an elderly cohort of Brazilians in the ABraOM database [Internet]. Human Mutation. 2017 ; 1-13.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1002/humu.23220
Vancouver
Naslavsky M, Yamamoto GL, Almeida TF de, Ezquina SAM, Sunaga DY, Pho N, Bozoklian D, Sandberg TOM, Brito LA, Lazar M, Bernardo DV, Amaro Jr. E, Duarte YA de O, Lebrão ML, Passos-Bueno MR, Zatz M. Exomic variants of an elderly cohort of Brazilians in the ABraOM database [Internet]. Human Mutation. 2017 ; 1-13.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1002/humu.23220
Artigo de periodico
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility (2015)
Toledo, Rodrigo A.; Hatakana, Roxanne; Lourenço Jr, Delmar M.; Lindsey, Susan C.; Camacho, Cleber P.; Almeida, Marcio; Lima Jr, José V.; Sekiya, Tomoko; Garralda, Elena; Naslavsky, Michel ; Yamamoto, Guilherme L.; Lazar, Monize; Meirelles, Osorio; Sobreira, Tiago J. P.; Lebrao, Maria Lucia; Duarte, Yeda Aparecida de Oliveira ; Blangero, John; Zatz, Mayana ; Cerutti, Janete M.; Maciel, Rui M. B.; Toledo, Sergio P. A.
Fonte: Endocrine - Related Cancer. Unidades: FSP, EE, IB, FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA, PROTO-ONCOGENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Rodrigo A. et al. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility. Endocrine - Related Cancer, v. 22, n. 2, 2015Tradução . . Disponível em: https://doi.org/10.1530/ERC-14-0491. Acesso em: 19 jul. 2024.
APA
Toledo, R. A., Hatakana, R., Lourenço Jr, D. M., Lindsey, S. C., Camacho, C. P., Almeida, M., et al. (2015). Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility. Endocrine - Related Cancer, 22( 2). doi:10.1530/ERC-14-0491
NLM
Toledo RA, Hatakana R, Lourenço Jr DM, Lindsey SC, Camacho CP, Almeida M, Lima Jr JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrao ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RMB, Toledo SPA. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/ERC-14-0491
Vancouver
Toledo RA, Hatakana R, Lourenço Jr DM, Lindsey SC, Camacho CP, Almeida M, Lima Jr JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrao ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RMB, Toledo SPA. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/ERC-14-0491
Artigo de periodico
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations (2014)
Longuini, Viviane Cristina; Lourenço Júnior, Delmar M; Sekiya, Tomoko; Meirelles, Osorio; Goncalves, Tatiana D.; Coutinho, Flavia L.; Francisco, Guilherme; Osaki, Luciana H.; Chammas, Roger; Alves, Venâncio Avancini Ferreira; Siqueira, Sheila A. C.; Schlesinger, David; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lucia; Gama, Patrícia ; Lee, Misu; Molatore, Sara; Pereira, Maria Adelaide A.; Jallad, Raquel S.; Bronstein, Marcello D.; Cunha-Neto, Malebranche B.; Liberman, Bernardo; Fragoso, Maria Candida B. V.; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo A.
Fonte: European Journal of Endocrinology. Unidades: FM, IB, EE, FSP, ICB
Assuntos: MUTAÇÃO GENÉTICA, GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LONGUINI, Viviane Cristina et al. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, n. Ju 2014, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0130. Acesso em: 19 jul. 2024.
APA
Longuini, V. C., Lourenço Júnior, D. M., Sekiya, T., Meirelles, O., Goncalves, T. D., Coutinho, F. L., et al. (2014). Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, ( Ju 2014). doi:10.1530/EJE-14-0130
NLM
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/EJE-14-0130
Vancouver
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/EJE-14-0130
Artigo de periodico
p27 variant and corticotropinoma susceptibility: a genetic and in vitro study (2014)
Sekiya, Tomoko; Bronstein, Marcello Delano ; Benfini, Katiuscia; Longuini, Viviane Cristina; Jallad, Raquel Soares; Machado, Marcio Cardoso; Gonçalves, Tatiana Denk; Osaki, Luciana Harumi; Higashi, Leonardo; Viana Junior, Jose; Kater, Claudio; Lee, Misu; Molatore, Sara; Francisco, Guilherme; Chammas, Roger ; Naslavsky, Michel ; Schlesinger, David; Gama, Patrícia ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lúcia ; Zatz, Mayana ; Meirelles, Osorio; Liberman, Bernardo; Fragoso, Maria Candida Barisson Villares ; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo de Almeida; Zatz, Mayana
Fonte: Endocrine-Related Cancer. Unidades: ICB, FM, EE, IB, FSP
Assuntos: BIOLOGIA CELULAR, GENÉTICA, MUTAÇÃO GENÉTICA, RATOS, POLIMORFISMO, GENÓTIPOS, NEOPLASIAS DA TIREOIDE, ADENOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SEKIYA, Tomoko et al. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, v. 21, n. 3, p. 395-404, 2014Tradução . . Disponível em: https://doi.org/10.1530/ERC-13-0486. Acesso em: 19 jul. 2024.
APA
Sekiya, T., Bronstein, M. D., Benfini, K., Longuini, V. C., Jallad, R. S., Machado, M. C., et al. (2014). p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, 21( 3), 395-404. doi:10.1530/ERC-13-0486
NLM
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/ERC-13-0486
Vancouver
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 jul. 19 ] Available from: https://doi.org/10.1530/ERC-13-0486

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