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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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
Artigo de periodico
Three generation families: analysis of de novo variants in autism (2023)
Costa, Claudia I. Samogy; Campos, Gabriele da Silva; Montenegro, Eduarda Morgana da Silva; Wang, Jaqueline Yu Ting; Scliar, Marília; Monfardini, Frederico; Zachi, Elaine Cristina; Lourenço, Naila C. V ; Chan, Ada J. S; Pereira, Sergio L; Engchuan, Worrawat; Thiruvahindrapuram, Bhooma; Zarrei, Mehdi; Scherer, Stephen W; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: IP, IB, BIOINFORMÁTICA
Subjects: TRANSTORNO DO ESPECTRO AUTISTA, GENES
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COSTA, Claudia I. Samogy et al. Three generation families: analysis of de novo variants in autism. European Journal of Human Genetics, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41431-023-01398-6. Acesso em: 17 nov. 2024.
APA
Costa, C. I. S., Campos, G. da S., Montenegro, E. M. da S., Wang, J. Y. T., Scliar, M., Monfardini, F., et al. (2023). Three generation families: analysis of de novo variants in autism. European Journal of Human Genetics. doi:10.1038/s41431-023-01398-6
NLM
Costa CIS, Campos G da S, Montenegro EM da S, Wang JYT, Scliar M, Monfardini F, Zachi EC, Lourenço NCV, Chan AJS, Pereira SL, Engchuan W, Thiruvahindrapuram B, Zarrei M, Scherer SW, Passos-Bueno MR. Three generation families: analysis of de novo variants in autism [Internet]. European Journal of Human Genetics. 2023 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/s41431-023-01398-6
Vancouver
Costa CIS, Campos G da S, Montenegro EM da S, Wang JYT, Scliar M, Monfardini F, Zachi EC, Lourenço NCV, Chan AJS, Pereira SL, Engchuan W, Thiruvahindrapuram B, Zarrei M, Scherer SW, Passos-Bueno MR. Three generation families: analysis of de novo variants in autism [Internet]. European Journal of Human Genetics. 2023 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/s41431-023-01398-6
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
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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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
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
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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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.1098/rsob.210240
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
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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: 17 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. 17 ] 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. 17 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico
Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples (2021)
Castelli, Erick C ; Castro, Mateus V. de ; Naslavsky, Michel ; Scliar, Marilia O ; Silva, Nayane S. B; Andrade, Heloisa S; Souza, Andreia S; Pereira, Raphaela Neto; Castro, Camila F. B; Mendes-Júnior, Celso T ; Meyer, Diogo ; Nunes, Kelly ; Matos, Larissa R. B; Silva, Monize V. R ; Wang, Jaqueline T. W; Esposito, Joyce ; Coria, Vivian R ; Bortolin, Raul H ; Hirata, Mario Hiroyuki ; Magawa, Jhosiene Y; Cunha-Neto, Edecio ; Coelho, Verônica ; Santos, Keity S ; Marin, Maria Lucia C ; Kalil, Jorge ; Mitne Neto, Miguel ; Maciel, Rui M. B; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: medRxiv (The Preprint Server For Health Sciences). Unidades: IB, FFCLRP, FCF, FM, BIOINFORMÁTICA
Subjects: COVID-19, IMUNOLOGIA, GENES DE RESPOSTA IMUNE, HERANÇA GENÉTICA, INFECÇÕES POR CORONAVIRUS
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ABNT
CASTELLI, Erick C et al. Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples. medRxiv (The Preprint Server For Health Sciences), 2021Tradução . . Disponível em: https://doi.org/10.1101/2021.04.21.21255872. Acesso em: 17 nov. 2024.
APA
Castelli, E. C., Castro, M. V. de, Naslavsky, M., Scliar, M. O., Silva, N. S. B., Andrade, H. S., et al. (2021). Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples. medRxiv (The Preprint Server For Health Sciences). doi:10.1101/2021.04.21.21255872
NLM
Castelli EC, Castro MV de, Naslavsky M, Scliar MO, Silva NSB, Andrade HS, Souza AS, Pereira RN, Castro CFB, Mendes-Júnior CT, Meyer D, Nunes K, Matos LRB, Silva MVR, Wang JTW, Esposito J, Coria VR, Bortolin RH, Hirata MH, Magawa JY, Cunha-Neto E, Coelho V, Santos KS, Marin MLC, Kalil J, Mitne Neto M, Maciel RMB, Passos-Bueno MR, Zatz M. Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2021.04.21.21255872
Vancouver
Castelli EC, Castro MV de, Naslavsky M, Scliar MO, Silva NSB, Andrade HS, Souza AS, Pereira RN, Castro CFB, Mendes-Júnior CT, Meyer D, Nunes K, Matos LRB, Silva MVR, Wang JTW, Esposito J, Coria VR, Bortolin RH, Hirata MH, Magawa JY, Cunha-Neto E, Coelho V, Santos KS, Marin MLC, Kalil J, Mitne Neto M, Maciel RMB, Passos-Bueno MR, Zatz M. Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2021.04.21.21255872
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
Source: PeerJ. Unidades: IB, EE, FM, BIOINFORMÁTICA
Subjects: 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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.7717/peerj.11349
Artigo de periodico
HLA-G genetic diversity and evolutive aspects in worldwide populations (2021)
Castelli, Erick C ; Almeida, Bibiana S. de; Muniz , Yara C. N; Silva, Nayane S. B; Passos, Marília R. S; Souza, Andreia S; Page, Abigail E; Dyble, Mark; Smith, Daniel; Aguileta, Gabriela; Bertranpetit, Jaume; Migliano, Andrea B; Duarte, Yeda Aparecida de Oliveira ; Scliar, Marília O; Wang, Jaqueline; Passos-Bueno, Maria Rita ; Naslavsky, Michel ; Zatz, Mayana ; Mendes-Junior, Celso Teixeira; Donadi, Eduardo A
Source: Scientific Reports. Unidades: EE, BIOINFORMÁTICA, IB, FFCLRP, FMRP
Subjects: GENÉTICA DE POPULAÇÕES, VARIAÇÃO GENÉTICA, DIVERSIDADE GENÉTICA, ANTÍGENOS HLA
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ABNT
CASTELLI, Erick C et al. HLA-G genetic diversity and evolutive aspects in worldwide populations. Scientific Reports, v. 11, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-02106-4. Acesso em: 17 nov. 2024.
APA
Castelli, E. C., Almeida, B. S. de, Muniz , Y. C. N., Silva, N. S. B., Passos, M. R. S., Souza, A. S., et al. (2021). HLA-G genetic diversity and evolutive aspects in worldwide populations. Scientific Reports, 11. doi:10.1038/s41598-021-02106-4
NLM
Castelli EC, Almeida BS de, Muniz YCN, Silva NSB, Passos MRS, Souza AS, Page AE, Dyble M, Smith D, Aguileta G, Bertranpetit J, Migliano AB, Duarte YA de O, Scliar MO, Wang J, Passos-Bueno MR, Naslavsky M, Zatz M, Mendes-Junior CT, Donadi EA. HLA-G genetic diversity and evolutive aspects in worldwide populations [Internet]. Scientific Reports. 2021 ; 11[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/s41598-021-02106-4
Vancouver
Castelli EC, Almeida BS de, Muniz YCN, Silva NSB, Passos MRS, Souza AS, Page AE, Dyble M, Smith D, Aguileta G, Bertranpetit J, Migliano AB, Duarte YA de O, Scliar MO, Wang J, Passos-Bueno MR, Naslavsky M, Zatz M, Mendes-Junior CT, Donadi EA. HLA-G genetic diversity and evolutive aspects in worldwide populations [Internet]. Scientific Reports. 2021 ; 11[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/s41598-021-02106-4
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
Source: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Unidades: IB, EE, BIOINFORMÁTICA, FM
Subjects: SEQUENCIAMENTO GENÉTICO, MISCIGENAÇÃO, GENÉTICA DE POPULAÇÕES, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.c.31931
Artigo de periodico
Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2 (2021)
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, Miriam; 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 ; Neto, Miguel Mitne ; Maciel, Rui M. B ; Naslavsky, Michel ; Passos-Bueno, Maria Rita ; Boscardin, Silvia Beatriz ; Rosa, Daniela S ; Kalil, Jorge ; Zatz, Mayana ; Cunha Neto, Edecio
Source: medRxiv (The Preprint Server For Health Sciences). Unidades: FM, ICB, IB, FCF, BIOINFORMÁTICA
Subjects: COVID-19, CORONAVIRUS, INFECÇÕES POR CORONAVIRUS, GÊMEOS, IMUNOLOGIA, TRANSMISSÃO DE DOENÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus V. de et al. Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2. medRxiv (The Preprint Server For Health Sciences), 2021Tradução . . Disponível em: https://doi.org/10.1101/2021.03.26.21253645. Acesso em: 17 nov. 2024.
APA
Castro, M. V. de, Santos, K. S., Apostolico, J. S., Fernandes, E. R., Almeida, R. R., Levin, G., et al. (2021). Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2. medRxiv (The Preprint Server For Health Sciences). doi:10.1101/2021.03.26.21253645
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, Neto MM, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha Neto E. Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2 [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2021.03.26.21253645
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, Neto MM, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha Neto E. Monozygotic twins discordant for severe clinical recurrence of COVID-19 show drastically distinct T cell responses to SARS-Cov-2 [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2021.03.26.21253645
Artigo de periodico
Noninvasive prenatal paternity determination using microhaplotypes: a pilot study (2020)
Wang, Jaqueline Yu Ting; Whittle, Martin R. ; Puga, Renato David ; Yambartsev, Anatoli ; Fujita, André ; Nakaya, Helder Takashi Imoto
Source: BMC Medical Genomics. Unidades: IME, FCF, BIOINFORMÁTICA
Subjects: DIAGNÓSTICO PRÉ-NATAL, PATERNIDADE, BIOINFORMÁTICA, HAPLOTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WANG, Jaqueline Yu Ting et al. Noninvasive prenatal paternity determination using microhaplotypes: a pilot study. BMC Medical Genomics, v. 13, n. art. 157, p. 1-8, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12920-020-00806-w. Acesso em: 17 nov. 2024.
APA
Wang, J. Y. T., Whittle, M. R., Puga, R. D., Yambartsev, A., Fujita, A., & Nakaya, H. T. I. (2020). Noninvasive prenatal paternity determination using microhaplotypes: a pilot study. BMC Medical Genomics, 13( art. 157), 1-8. doi:10.1186/s12920-020-00806-w
NLM
Wang JYT, Whittle MR, Puga RD, Yambartsev A, Fujita A, Nakaya HTI. Noninvasive prenatal paternity determination using microhaplotypes: a pilot study [Internet]. BMC Medical Genomics. 2020 ; 13( art. 157): 1-8.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1186/s12920-020-00806-w
Vancouver
Wang JYT, Whittle MR, Puga RD, Yambartsev A, Fujita A, Nakaya HTI. Noninvasive prenatal paternity determination using microhaplotypes: a pilot study [Internet]. BMC Medical Genomics. 2020 ; 13( art. 157): 1-8.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1186/s12920-020-00806-w
Artigo de periodico
Variants in the Kisspeptin-GnRH Pathway Modulate the hormonal profile and reproductive outcomes (2020)
Trevisan, Camila Martins; Naslavsky, Michel ; Monfardini, Frederico; Wang, Jaqueline; Zatz, Mayana ; Peluso, Carla; Pellegrino, Renata; Mafra, Fernanda; Hakonarson, Hakon; Ferreira, Frederico Moraes; Nakaya, Helder Takashi Imoto ; Christofolini, Denise Maria; Montagna, Erik; Crandall, Keith A; Barbosa, Caio Parente; Bianco, Bianca
Source: DNA and Cell Biology. Unidades: IB, FM, FCF, BIOINFORMÁTICA
Subjects: GENES, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TREVISAN, Camila Martins et al. Variants in the Kisspeptin-GnRH Pathway Modulate the hormonal profile and reproductive outcomes. DNA and Cell Biology, v. 39, n. 6, p. 1012–1022, 2020Tradução . . Disponível em: https://doi.org/10.1089/dna.2019.5165. Acesso em: 17 nov. 2024.
APA
Trevisan, C. M., Naslavsky, M., Monfardini, F., Wang, J., Zatz, M., Peluso, C., et al. (2020). Variants in the Kisspeptin-GnRH Pathway Modulate the hormonal profile and reproductive outcomes. DNA and Cell Biology, 39( 6), 1012–1022. doi:10.1089/dna.2019.5165
NLM
Trevisan CM, Naslavsky M, Monfardini F, Wang J, Zatz M, Peluso C, Pellegrino R, Mafra F, Hakonarson H, Ferreira FM, Nakaya HTI, Christofolini DM, Montagna E, Crandall KA, Barbosa CP, Bianco B. Variants in the Kisspeptin-GnRH Pathway Modulate the hormonal profile and reproductive outcomes [Internet]. DNA and Cell Biology. 2020 ; 39( 6): 1012–1022.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1089/dna.2019.5165
Vancouver
Trevisan CM, Naslavsky M, Monfardini F, Wang J, Zatz M, Peluso C, Pellegrino R, Mafra F, Hakonarson H, Ferreira FM, Nakaya HTI, Christofolini DM, Montagna E, Crandall KA, Barbosa CP, Bianco B. Variants in the Kisspeptin-GnRH Pathway Modulate the hormonal profile and reproductive outcomes [Internet]. DNA and Cell Biology. 2020 ; 39( 6): 1012–1022.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1089/dna.2019.5165
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) (2020)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly
Source: BioRxiv (The Preprint Server for Biology). Unidades: IB, BIOINFORMÁTICA
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO
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 the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), p. 1-29, 2020Tradução . . Disponível em: https://doi.org/10.1101/2020.09.15.298026. Acesso em: 17 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., & Nunes, K. (2020). Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), 1-29. doi:10.1101/2020.09.15.298026
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Artigo de periodico
Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate (2019)
Alvizi, Lucas ; Brito, Luciano Abreu; Bischain, Bárbara; Silva, Camila Bassi Fernandes da; Ramos, Sofia Ligia Guimaraes; Kobayashi, Gerson Shigeru; Wang, Jaqueline; Passos-Bueno, Maria Rita
Source: BioRxiv. Unidades: IB, BIOINFORMÁTICA
Subjects: MALFORMAÇÕES, FISSURA LÁBIOPALATINA, EXPRESSÃO GÊNICA, METILAÇÃO DE DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVIZI, Lucas et al. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate. BioRxiv, 2019Tradução . . Disponível em: https://doi.org/10.1101/850016. Acesso em: 17 nov. 2024.
APA
Alvizi, L., Brito, L. A., Bischain, B., Silva, C. B. F. da, Ramos, S. L. G., Kobayashi, G. S., et al. (2019). Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate. BioRxiv. doi:10.1101/850016
NLM
Alvizi L, Brito LA, Bischain B, Silva CBF da, Ramos SLG, Kobayashi GS, Wang J, Passos-Bueno MR. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate [Internet]. BioRxiv. 2019 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/850016
Vancouver
Alvizi L, Brito LA, Bischain B, Silva CBF da, Ramos SLG, Kobayashi GS, Wang J, Passos-Bueno MR. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate [Internet]. BioRxiv. 2019 ;[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/850016
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
Source: Abstracts. Conference titles: ASHG Annual Meeting. Unidades: EE, IB, BIOINFORMÁTICA, FM
Subjects: 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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Dissertação (Mestrado)
Determinação pré-natal não invasiva de paternidade utilizando micro-haplótipos (2017)
Wang, Jaqueline Yu Ting; Fujita, André (Orientador) ; Nakaya, Helder Takashi Imoto (Orientador)
Unidade: BIOINFORMÁTICA
Subjects: BIOINFORMÁTICA, POLIMORFISMO, DIAGNÓSTICO PRÉ-NATAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WANG, Jaqueline Yu Ting. Determinação pré-natal não invasiva de paternidade utilizando micro-haplótipos. 2017. Dissertação (Mestrado) – Universidade de São Paulo, São Paulo, 2017. Disponível em: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-08012018-143011/. Acesso em: 17 nov. 2024.
APA
Wang, J. Y. T. (2017). Determinação pré-natal não invasiva de paternidade utilizando micro-haplótipos (Dissertação (Mestrado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/95/95131/tde-08012018-143011/
NLM
Wang JYT. Determinação pré-natal não invasiva de paternidade utilizando micro-haplótipos [Internet]. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-08012018-143011/
Vancouver
Wang JYT. Determinação pré-natal não invasiva de paternidade utilizando micro-haplótipos [Internet]. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-08012018-143011/

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