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Artigo de periodico
An evolutionary perspective on complex neuropsychiatric disease (2024)
McClellan, Jon M ; Zoghbi, Anthony W ; Buxbaum, Joseph D ; Cappi, Carolina ; Crowley, James J ; Flint, Jonathan ; Grice, Dorothy E ; Gulsuner, Suleyman ; Iyegbe, Conrad ; Jain, Sanjeev ; Kuo, Po-Hsiu ; Lattig, Maria Claudia ; Passos-Bueno, Maria Rita ; Purushottam, Meera ; Stein, Dan J ; Sunshine, Anna B ; Susser, Ezra S ; Walsh, Christopher A ; Wootton, Olivia ; King, Mary-Claire
Fonte: Neuron. Unidade: IB
Assuntos: NEUROPSIQUIATRIA, MUTAÇÃO GENÉTICA, DERIVA GÊNICA, ALELOS, TRANSTORNO AUTÍSTICO, ESQUIZOFRENIA
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ABNT
MCCLELLAN, Jon M et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron, v. 112, n. 1, p. 7-24, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.neuron.2023.10.037. Acesso em: 03 jul. 2024.
APA
McClellan, J. M., Zoghbi, A. W., Buxbaum, J. D., Cappi, C., Crowley, J. J., Flint, J., et al. (2024). An evolutionary perspective on complex neuropsychiatric disease. Neuron, 112( 1), 7-24. doi:10.1016/j.neuron.2023.10.037
NLM
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Vancouver
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Artigo de periodico
Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction (2023)
Alvizi, Lucas; Nani, Diogo; Brito, Luciano Abreu; Kobayashi, Gerson Shigeru ; Passos-Bueno, Maria Rita ; Mayor, Roberto
Fonte: Nature Communications. Unidade: IB
Assuntos: LÁBIO FISSURADO, EPIGÊNESE GENÉTICA, ANORMALIDADES CRANIOFACIAIS
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ABNT
ALVIZI, Lucas et al. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction. Nature Communications, v. 14, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41467-023-38526-1. Acesso em: 03 jul. 2024.
APA
Alvizi, L., Nani, D., Brito, L. A., Kobayashi, G. S., Passos-Bueno, M. R., & Mayor, R. (2023). Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction. Nature Communications, 14. doi:10.1038/s41467-023-38526-1
NLM
Alvizi L, Nani D, Brito LA, Kobayashi GS, Passos-Bueno MR, Mayor R. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction [Internet]. Nature Communications. 2023 ; 14[citado 2024 jul. 03 ] Available from: https://doi.org/10.1038/s41467-023-38526-1
Vancouver
Alvizi L, Nani D, Brito LA, Kobayashi GS, Passos-Bueno MR, Mayor R. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction [Internet]. Nature Communications. 2023 ; 14[citado 2024 jul. 03 ] Available from: https://doi.org/10.1038/s41467-023-38526-1
Artigo de periodico
Updated consensus guidelines on the management of Phelan–McDermid syndrome (2023)
Srivastava, Siddharth ; Sahin, Mustafa ; Buxbaum, Joseph D ; Berry-Kravis, Elizabeth; Soorya, Latha Valluripalli; Thurm, Audrey ; Bernstein, Jonathan A ; Asante-Otoo, Afua; Bennett Jr, William E; Betancur, Catalina ; Brickhouse, Tegwyn H; Passos-Bueno, Maria Rita
Fonte: American Journal of Medical Genetics. Part A. Unidade: IB
Assuntos: GENÉTICA MÉDICA, NEUROGENÉTICA
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ABNT
SRIVASTAVA, Siddharth et al. Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, v. 191, n. 8, p. 2015-2044, 2023Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63312. Acesso em: 03 jul. 2024.
APA
Srivastava, S., Sahin, M., Buxbaum, J. D., Berry-Kravis, E., Soorya, L. V., Thurm, A., et al. (2023). Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, 191( 8), 2015-2044. doi:10.1002/ajmg.a.63312
NLM
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Vancouver
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Artigo de periodico
Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature (2022)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Freire, Bruna Lucheze; Homma, Thais Kataoka; Honjo, Rachel Sayuri ; Yamamoto, Guilherme Lopes ; Passos-Bueno, Maria Rita ; Koiffmann, Celia Priszkulnik ; Kim, Chong Ae ; Vianna-Morgante, Angela M ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino
Fonte: Journal of Autism and Developmental Disorders. Unidades: IB, FM
Assuntos: MICROCEFALIA, REVISÃO SISTEMÁTICA
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ABNT
TOLEZANO, Giovanna Cantini et al. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10803-022-05853-z. Acesso em: 03 jul. 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Freire, B. L., Homma, T. K., Honjo, R. S., et al. (2022). Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders. doi:10.1007/s10803-022-05853-z
NLM
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Artigo de periodico-carta/editorial
FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? (2022)
Girardi, Ana Cristina De Sanctis ; Takahashi, Vanessa Naomi Van Opstal ; Vadasz, Estêvão ; Costa, Claudia Ismania Samogi ; Zachi, Elaine Cristina; Vianna-Morgante, Angela M ; Passos-Bueno, Maria Rita
Fonte: American Journal of Medical Genetics. Part A. Unidades: IB, IP
Assuntos: TRANSTORNO AUTÍSTICO, CRIANÇAS AUTISTAS
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ABNT
GIRARDI, Ana Cristina De Sanctis et al. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed?. American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/ajmg.a.62624. Acesso em: 03 jul. 2024. , 2022
APA
Girardi, A. C. D. S., Takahashi, V. N. V. O., Vadasz, E., Costa, C. I. S., Zachi, E. C., Vianna-Morgante, A. M., & Passos-Bueno, M. R. (2022). FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/ajmg.a.62624
NLM
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Vancouver
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Artigo de periodico
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022)
Fu, Jack M; Satterstrom, F. Kyle; Peng, Minshi; Passos-Bueno, Maria Rita
Fonte: Nature Genetics. Unidade: IB
Assuntos: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, GENOMAS
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ABNT
FU, Jack M et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, v. 54, p. 1320–1331, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01104-0. Acesso em: 03 jul. 2024.
APA
Fu, J. M., Satterstrom, F. K., Peng, M., & Passos-Bueno, M. R. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54, 1320–1331. doi:10.1038/s41588-022-01104-0
NLM
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Vancouver
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Fonte: Human Mutation. Unidades: HRACF, HRAC, IB
Assuntos: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
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ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 03 jul. 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/humu.24349
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
Fonte: medRxiv (The Preprint Server For Health Sciences). Unidades: IB, FFCLRP, FCF, FM, BIOINFORMÁTICA
Assuntos: 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: 03 jul. 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 jul. 03 ] 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 jul. 03 ] Available from: https://doi.org/10.1101/2021.04.21.21255872
Artigo de periodico
Congenital limb deficiency: genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms (2021)
Rocha, Letícia Alves da ; Pires, Lucas Vieira Lacerda ; Yamamoto, Guilherme Lopes ; Ceroni, José Ricardo Magliocco; Honjo, Rachel Sayuri; França Bisneto, Edgard de Novaes; Oliveira, Luiz Antônio Nunes; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino ; Passos-Bueno, Maria Rita ; Kim, Chong Ae ; Bertola, Débora Romeo
Fonte: Clinical Genetics. Unidades: IB, FM
Assuntos: GENÉTICA MÉDICA, DOENÇAS CONGÊNITAS, DOENÇAS GENÉTICAS
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ABNT
ROCHA, Letícia Alves da et al. Congenital limb deficiency: genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms. Clinical Genetics, v. 100, n. 5, p. 615-623, 2021Tradução . . Disponível em: https://doi.org/10.1111/cge.14041. Acesso em: 03 jul. 2024.
APA
Rocha, L. A. da, Pires, L. V. L., Yamamoto, G. L., Ceroni, J. R. M., Honjo, R. S., França Bisneto, E. de N., et al. (2021). Congenital limb deficiency: genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms. Clinical Genetics, 100( 5), 615-623. doi:10.1111/cge.14041
NLM
Rocha LA da, Pires LVL, Yamamoto GL, Ceroni JRM, Honjo RS, França Bisneto E de N, Oliveira LAN, Rosenberg C, Krepischi ACV, Passos-Bueno MR, Kim CA, Bertola DR. Congenital limb deficiency: genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms [Internet]. Clinical Genetics. 2021 ; 100( 5): 615-623.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cge.14041
Vancouver
Rocha LA da, Pires LVL, Yamamoto GL, Ceroni JRM, Honjo RS, França Bisneto E de N, Oliveira LAN, Rosenberg C, Krepischi ACV, Passos-Bueno MR, Kim CA, Bertola DR. Congenital limb deficiency: genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms [Internet]. Clinical Genetics. 2021 ; 100( 5): 615-623.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cge.14041
Artigo de periodico
COVID-19 in twins: what can we learn from them? (2021)
Castro, Mateus V de ; Silva, Monize V R ; Naslavsky, Michel ; Santos, Keity S ; Magawa, Jhosiene Y; Cunha Neto, Edecio ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: medRxiv (The Preprint Server For Health Sciences). Unidades: IB, FM
Assuntos: GÊMEOS, COVID-19, IMUNOLOGIA, INFECÇÕES POR CORONAVIRUS
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ABNT
CASTRO, Mateus V de et al. COVID-19 in twins: what can we learn from them?. medRxiv (The Preprint Server For Health Sciences), 2021Tradução . . Disponível em: https://doi.org/10.1101/2021.09.29.21263145. Acesso em: 03 jul. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Naslavsky, M., Santos, K. S., Magawa, J. Y., Cunha Neto, E., et al. (2021). COVID-19 in twins: what can we learn from them? medRxiv (The Preprint Server For Health Sciences). doi:10.1101/2021.09.29.21263145
NLM
Castro MV de, Silva MVR, Naslavsky M, Santos KS, Magawa JY, Cunha Neto E, Passos-Bueno MR, Zatz M. COVID-19 in twins: what can we learn from them? [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1101/2021.09.29.21263145
Vancouver
Castro MV de, Silva MVR, Naslavsky M, Santos KS, Magawa JY, Cunha Neto E, Passos-Bueno MR, Zatz M. COVID-19 in twins: what can we learn from them? [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1101/2021.09.29.21263145
Artigo de periodico
Men are the main COVID-19 transmitters: lessons from couples (2021)
Silva, Monize V. R ; Castro, Mateus V. de ; Passos-Bueno, Maria Rita ; Otto, Paulo A ; Naslavsky, Michel ; Zatz, Mayana
Fonte: medRxiv (The Preprint Server For Health Sciences). Unidades: IB, FCF
Assuntos: COVID-19, CORONAVIRUS, INFECÇÕES POR CORONAVIRUS, TRANSMISSÃO DE DOENÇAS
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ABNT
SILVA, Monize V. R et al. Men are the main COVID-19 transmitters: lessons from couples. medRxiv (The Preprint Server For Health Sciences), 2021Tradução . . Disponível em: https://doi.org/10.1101/2021.08.18.21262187. Acesso em: 03 jul. 2024.
APA
Silva, M. V. R., Castro, M. V. de, Passos-Bueno, M. R., Otto, P. A., Naslavsky, M., & Zatz, M. (2021). Men are the main COVID-19 transmitters: lessons from couples. medRxiv (The Preprint Server For Health Sciences). doi:10.1101/2021.08.18.21262187
NLM
Silva MVR, Castro MV de, Passos-Bueno MR, Otto PA, Naslavsky M, Zatz M. Men are the main COVID-19 transmitters: lessons from couples [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1101/2021.08.18.21262187
Vancouver
Silva MVR, Castro MV de, Passos-Bueno MR, Otto PA, Naslavsky M, Zatz M. Men are the main COVID-19 transmitters: lessons from couples [Internet]. medRxiv (The Preprint Server For Health Sciences). 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.1101/2021.08.18.21262187
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: 03 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. 03 ] 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. 03 ] 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
Fonte: medRxiv (The Preprint Server For Health Sciences). Unidades: FM, ICB, IB, FCF, BIOINFORMÁTICA
Assuntos: 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: 03 jul. 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 jul. 03 ] 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 jul. 03 ] Available from: https://doi.org/10.1101/2021.03.26.21253645
Artigo de periodico
Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects (2021)
Mansur, Fernanda ; Silva, André Luiz Teles e ; Santos-Gomes, Ana Karolyne ; Magdalon, Juliana ; Souza, Janaina Sena de ; Griesi-Oliveira, Karina ; Passos-Bueno, Maria Rita ; Sertié, Andréa Laurato
Fonte: Research Square. Unidade: IB
Assunto: TRANSTORNO DO ESPECTRO AUTISTA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MANSUR, Fernanda et al. Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects. Research Square, 2021Tradução . . Disponível em: https://doi.org/10.21203/rs.3.rs-297808/v1. Acesso em: 03 jul. 2024.
APA
Mansur, F., Silva, A. L. T. e, Santos-Gomes, A. K., Magdalon, J., Souza, J. S. de, Griesi-Oliveira, K., et al. (2021). Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects. Research Square. doi:10.21203/rs.3.rs-297808/v1
NLM
Mansur F, Silva ALT e, Santos-Gomes AK, Magdalon J, Souza JS de, Griesi-Oliveira K, Passos-Bueno MR, Sertié AL. Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects [Internet]. Research Square. 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.21203/rs.3.rs-297808/v1
Vancouver
Mansur F, Silva ALT e, Santos-Gomes AK, Magdalon J, Souza JS de, Griesi-Oliveira K, Passos-Bueno MR, Sertié AL. Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects [Internet]. Research Square. 2021 ;[citado 2024 jul. 03 ] Available from: https://doi.org/10.21203/rs.3.rs-297808/v1
Artigo de periodico
Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil (2020)
Bertola, Débora R; Castro, Matheus A. A; Yamamoto, Guilherme Lopes ; Honjo, Rachel Sayuri ; Ceroni, José Ricardo; Buscarilli, Michele M; Freitas, Amanda B; Malaquias, Alexsandra C; Pereira, Alexandre C; Jorge, Alexander A. L; Passos-Bueno, Maria Rita ; Kim, Chong A
Fonte: American journal of medical genetics. Part C, Seminars in medical genetics. Unidades: IB, FM
Assuntos: MUTAÇÃO GENÉTICA, ANOMALIA CRANIOFACIAL, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLA, Débora R et al. Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil. American journal of medical genetics. Part C, Seminars in medical genetics, v. 184, n. 4, p. 896-911, 2020Tradução . . Disponível em: https://doi.org/10.1002/ajmg.c.31851. Acesso em: 03 jul. 2024.
APA
Bertola, D. R., Castro, M. A. A., Yamamoto, G. L., Honjo, R. S., Ceroni, J. R., Buscarilli, M. M., et al. (2020). Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil. American journal of medical genetics. Part C, Seminars in medical genetics, 184( 4), 896-911. doi:10.1002/ajmg.c.31851
NLM
Bertola DR, Castro MAA, Yamamoto GL, Honjo RS, Ceroni JR, Buscarilli MM, Freitas AB, Malaquias AC, Pereira AC, Jorge AAL, Passos-Bueno MR, Kim CA. Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil [Internet]. American journal of medical genetics. Part C, Seminars in medical genetics. 2020 ; 184( 4): 896-911.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.c.31851
Vancouver
Bertola DR, Castro MAA, Yamamoto GL, Honjo RS, Ceroni JR, Buscarilli MM, Freitas AB, Malaquias AC, Pereira AC, Jorge AAL, Passos-Bueno MR, Kim CA. Phenotype-genotype analysis of 242 individuals with RASopathies: 18-year experience of a tertiary center in Brazil [Internet]. American journal of medical genetics. Part C, Seminars in medical genetics. 2020 ; 184( 4): 896-911.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.c.31851
Artigo de periodico
Meta-analyses support previous and novel autism candidate genes: outcomes of an unexplored Brazilian cohort (2020)
Montenegro, Eduarda Morgana da Silva; Costa, Claudia Samogy; Campos, Gabriele; Scliar, Marília; Almeida, Tatiana Ferreira de; Zachi, Elaine Cristina; Silva, Isabela Maya Wahys; Chan, Ada J. S; Zarrei, Mehd; Lourenço, Naila C. V; Yamamoto, Guilherme Lopes ; Scherer, Stephen; Passos-Bueno, Maria Rita
Fonte: Autism Research (Online). Unidades: IB, IP, FM
Assuntos: TRANSTORNO AUTÍSTICO, GENÉTICA, GENOMAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTENEGRO, Eduarda Morgana da Silva et al. Meta-analyses support previous and novel autism candidate genes: outcomes of an unexplored Brazilian cohort. Autism Research (Online), v. 13, n. 2, p. 199-206, 2020Tradução . . Disponível em: https://doi.org/10.1002/aur.2238. Acesso em: 03 jul. 2024.
APA
Montenegro, E. M. da S., Costa, C. S., Campos, G., Scliar, M., Almeida, T. F. de, Zachi, E. C., et al. (2020). Meta-analyses support previous and novel autism candidate genes: outcomes of an unexplored Brazilian cohort. Autism Research (Online), 13( 2), 199-206. doi:10.1002/aur.2238
NLM
Montenegro EM da S, Costa CS, Campos G, Scliar M, Almeida TF de, Zachi EC, Silva IMW, Chan AJS, Zarrei M, Lourenço NCV, Yamamoto GL, Scherer S, Passos-Bueno MR. Meta-analyses support previous and novel autism candidate genes: outcomes of an unexplored Brazilian cohort [Internet]. Autism Research (Online). 2020 ; 13( 2): 199-206.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/aur.2238
Vancouver
Montenegro EM da S, Costa CS, Campos G, Scliar M, Almeida TF de, Zachi EC, Silva IMW, Chan AJS, Zarrei M, Lourenço NCV, Yamamoto GL, Scherer S, Passos-Bueno MR. Meta-analyses support previous and novel autism candidate genes: outcomes of an unexplored Brazilian cohort [Internet]. Autism Research (Online). 2020 ; 13( 2): 199-206.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/aur.2238
Artigo de periodico
Recapitulation of neural crest specification and EMT via induction from neural plate border-like cells (2020)
Kobayashi, Gerson Shigeru ; Musso, Camila Manso; Moreira, Danielle de Paula; Pontillo-Guimarães, Giovanna; Hsia, Gabriella Shih Ping; Caires-Júnior, Luiz Carlos; Goulart, Ernesto ; Passos-Bueno, Maria Rita
Fonte: Stem Cell Reports. Unidade: IB
Assuntos: CÉLULAS-TRONCO, BIOLOGIA CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOBAYASHI, Gerson Shigeru et al. Recapitulation of neural crest specification and EMT via induction from neural plate border-like cells. Stem Cell Reports, v. 15, n. 3, p. Se 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.stemcr.2020.07.023. Acesso em: 03 jul. 2024.
APA
Kobayashi, G. S., Musso, C. M., Moreira, D. de P., Pontillo-Guimarães, G., Hsia, G. S. P., Caires-Júnior, L. C., et al. (2020). Recapitulation of neural crest specification and EMT via induction from neural plate border-like cells. Stem Cell Reports, 15( 3), Se 2020. doi:10.1016/j.stemcr.2020.07.023
NLM
Kobayashi GS, Musso CM, Moreira D de P, Pontillo-Guimarães G, Hsia GSP, Caires-Júnior LC, Goulart E, Passos-Bueno MR. Recapitulation of neural crest specification and EMT via induction from neural plate border-like cells [Internet]. Stem Cell Reports. 2020 ; 15( 3): Se 2020.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.stemcr.2020.07.023
Vancouver
Kobayashi GS, Musso CM, Moreira D de P, Pontillo-Guimarães G, Hsia GSP, Caires-Júnior LC, Goulart E, Passos-Bueno MR. Recapitulation of neural crest specification and EMT via induction from neural plate border-like cells [Internet]. Stem Cell Reports. 2020 ; 15( 3): Se 2020.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.stemcr.2020.07.023
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
Fonte: BioRxiv. Unidades: IB, BIOINFORMÁTICA
Assuntos: 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: 03 jul. 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 jul. 03 ] 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 jul. 03 ] Available from: https://doi.org/10.1101/850016
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 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. 03 ] 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. 03 ] 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: 03 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. 03 ] 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. 03 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf

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