ReP USP - Resultado da busca

Artigo de periodico
The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry (2022)
Ali, Taccyanna M.; Linnenkamp, Bianca D. W.; Yamamoto, Guilherme L.; Honjo, Rachel S.; Menezes Filho, Hamilton Cabral de; Kim, Chong Ae ; Bertola, Debora R.
Source: American journal of medical genetics part a. Unidade: FM
Subjects: FRATURAS, ANCESTRAIS, PREVALÊNCIA, FENÓTIPOS
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ABNT
ALI, Taccyanna M. et al. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, v. 188, n. 5, p. 1545-1549, 2022Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62651. Acesso em: 05 nov. 2024.
APA
Ali, T. M., Linnenkamp, B. D. W., Yamamoto, G. L., Honjo, R. S., Menezes Filho, H. C. de, Kim, C. A., & Bertola, D. R. (2022). The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, 188( 5), 1545-1549. doi:10.1002/ajmg.a.62651
NLM
Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/ajmg.a.62651
Vancouver
Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/ajmg.a.62651
Artigo de periodico
Let's Talk About Lupus. Overview of an Innovative, High-Reach, Online Program to Fill the Education Gaps of Latin Americans Living With Lupus (2022)
Drenkard, Cristina; Fuentes-Silva, Yurilis; Seguro, Luciana Parente Costa; Reis-Neto, Edgard Torres dos; Ibanez, Soledad; Elera-Fitzcarrald, Claudia; Reategui-Sokolova, Cristina; Linhares, Fernanda Athayde; Bermudez, Witjal; Bonfa, Eloisa Silva Dutra de Oliveira
Source: Jcr-journal of clinical rheumatology. Unidade: FM
Subjects: ARTRITE, LÚPUS ERITEMATOSO SISTÊMICO, ANCESTRAIS, PREVALÊNCIA
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ABNT
DRENKARD, Cristina et al. Let's Talk About Lupus. Overview of an Innovative, High-Reach, Online Program to Fill the Education Gaps of Latin Americans Living With Lupus. Jcr-journal of clinical rheumatology, v. 28, n. 2, p. E368-E374, 2022Tradução . . Disponível em: https://doi.org/10.1097/RHU.0000000000001728. Acesso em: 05 nov. 2024.
APA
Drenkard, C., Fuentes-Silva, Y., Seguro, L. P. C., Reis-Neto, E. T. dos, Ibanez, S., Elera-Fitzcarrald, C., et al. (2022). Let's Talk About Lupus. Overview of an Innovative, High-Reach, Online Program to Fill the Education Gaps of Latin Americans Living With Lupus. Jcr-journal of clinical rheumatology, 28( 2), E368-E374. doi:10.1097/RHU.0000000000001728
NLM
Drenkard C, Fuentes-Silva Y, Seguro LPC, Reis-Neto ET dos, Ibanez S, Elera-Fitzcarrald C, Reategui-Sokolova C, Linhares FA, Bermudez W, Bonfa ESD de O. Let's Talk About Lupus. Overview of an Innovative, High-Reach, Online Program to Fill the Education Gaps of Latin Americans Living With Lupus [Internet]. Jcr-journal of clinical rheumatology. 2022 ; 28( 2): E368-E374.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/RHU.0000000000001728
Vancouver
Drenkard C, Fuentes-Silva Y, Seguro LPC, Reis-Neto ET dos, Ibanez S, Elera-Fitzcarrald C, Reategui-Sokolova C, Linhares FA, Bermudez W, Bonfa ESD de O. Let's Talk About Lupus. Overview of an Innovative, High-Reach, Online Program to Fill the Education Gaps of Latin Americans Living With Lupus [Internet]. Jcr-journal of clinical rheumatology. 2022 ; 28( 2): E368-E374.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/RHU.0000000000001728
Artigo de periodico
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women (2019)
Lawrenson, Kate; Song, Fengju; Hazelett, Dennis J.; Kar, Siddhartha P.; Tyrer, Jonathan; Phelan, Catherine M.; Corona, Rosario I.; Rodríguez-Malavé, Norma I.; Seo, Ji-Hei; Adler, Emily; Noushmehr, Houtan
Source: Gynecologic Oncology. Unidade: FMRP
Subjects: GENÉTICA DE POPULAÇÕES, ANCESTRAIS, GENOMAS, NEOPLASIAS OVARIANAS
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ABNT
LAWRENSON, Kate et al. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. Gynecologic Oncology, v. 153, n. 2, p. 343-355, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ygyno.2019.02.023. Acesso em: 05 nov. 2024.
APA
Lawrenson, K., Song, F., Hazelett, D. J., Kar, S. P., Tyrer, J., Phelan, C. M., et al. (2019). Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. Gynecologic Oncology, 153( 2), 343-355. doi:10.1016/j.ygyno.2019.02.023
NLM
Lawrenson K, Song F, Hazelett DJ, Kar SP, Tyrer J, Phelan CM, Corona RI, Rodríguez-Malavé NI, Seo J-H, Adler E, Noushmehr H. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women [Internet]. Gynecologic Oncology. 2019 ; 153( 2): 343-355.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ygyno.2019.02.023
Vancouver
Lawrenson K, Song F, Hazelett DJ, Kar SP, Tyrer J, Phelan CM, Corona RI, Rodríguez-Malavé NI, Seo J-H, Adler E, Noushmehr H. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women [Internet]. Gynecologic Oncology. 2019 ; 153( 2): 343-355.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ygyno.2019.02.023
Artigo de periodico
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018)
Feitosa, Mary F.; Krieger, Jose E.
Source: PLOS ONE. Unidade: FM
Subjects: GENÔMICA, HIPERTENSÃO, DOENÇAS GENÉTICAS, ANCESTRAIS
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ABNT
FEITOSA, Mary F. e KRIEGER, Jose E. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLOS ONE, v. 13, n. 6, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0198166. Acesso em: 05 nov. 2024.
APA
Feitosa, M. F., & Krieger, J. E. (2018). Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLOS ONE, 13( 6). doi:10.1371/journal.pone.0198166
NLM
Feitosa MF, Krieger JE. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries [Internet]. PLOS ONE. 2018 ; 13( 6):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1371/journal.pone.0198166
Vancouver
Feitosa MF, Krieger JE. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries [Internet]. PLOS ONE. 2018 ; 13( 6):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1371/journal.pone.0198166
Artigo de periodico
Extended HLA-G genetic diversity and ancestry composition in a Brazilian admixed population sample: implications for HLA-G transcriptional control and for case-control association studies (2018)
Oliveira, Maria Luiza Guimarães de; Castelli, Luciana Caricati Veiga; Marcorin, Letícia; Debortoli, Guilherme; Pereira, Alison Luis Eburneo; Fracasso, Nádia Carolina de Aguiar; Silva, Guilherme do Valle; Souza, Andréia S.; Massaro, Juliana Doblas; Simões, Aguinaldo Luiz; Sabbagh, Audrey; Donadi, Eduardo Antônio; Castelli, Erick C.; Mendes Júnior, Celso Teixeira
Source: Human Immunology. Unidades: FMRP, FFCLRP
Subjects: ANTÍGENOS, LEUCÓCITOS, ANCESTRAIS, BRASIL REPÚBLICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Maria Luiza Guimarães de et al. Extended HLA-G genetic diversity and ancestry composition in a Brazilian admixed population sample: implications for HLA-G transcriptional control and for case-control association studies. Human Immunology, v. 79, n. 11, p. 790-799, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.humimm.2018.08.005. Acesso em: 05 nov. 2024.
APA
Oliveira, M. L. G. de, Castelli, L. C. V., Marcorin, L., Debortoli, G., Pereira, A. L. E., Fracasso, N. C. de A., et al. (2018). Extended HLA-G genetic diversity and ancestry composition in a Brazilian admixed population sample: implications for HLA-G transcriptional control and for case-control association studies. Human Immunology, 79( 11), 790-799. doi:10.1016/j.humimm.2018.08.005
NLM
Oliveira MLG de, Castelli LCV, Marcorin L, Debortoli G, Pereira ALE, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Donadi EA, Castelli EC, Mendes Júnior CT. Extended HLA-G genetic diversity and ancestry composition in a Brazilian admixed population sample: implications for HLA-G transcriptional control and for case-control association studies [Internet]. Human Immunology. 2018 ; 79( 11): 790-799.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.humimm.2018.08.005
Vancouver
Oliveira MLG de, Castelli LCV, Marcorin L, Debortoli G, Pereira ALE, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Donadi EA, Castelli EC, Mendes Júnior CT. Extended HLA-G genetic diversity and ancestry composition in a Brazilian admixed population sample: implications for HLA-G transcriptional control and for case-control association studies [Internet]. Human Immunology. 2018 ; 79( 11): 790-799.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.humimm.2018.08.005
Artigo de periodico
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population (2012)
Brito, Luciano A.; Bassi, Camila F. S.; Masotti, Cibele; Malcher, Carolina; Rocha, Kátia M.; Schlesinger, David; Bueno, Daniela F.; Cruz, Lucas A.; Barbara, Ligia K.; Bertola, Débora R.; Meyer, Diogo ; Franco, Diogo; Alonso, Nivaldo; Passos-Bueno, Maria Rita
Source: American journal of medical genetics part. A. Unidades: IB, FM
Subjects: DOENÇAS HEREDITÁRIAS, FATORES DE RISCO, EXPRESSÃO GÊNICA, GENÉTICA MÉDICA, ANCESTRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRITO, Luciano A. et al. IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population. American journal of medical genetics part. A, v. 158A, n. 9, p. 2170\20132175, 2012Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35526/pdf. Acesso em: 05 nov. 2024.
APA
Brito, L. A., Bassi, C. F. S., Masotti, C., Malcher, C., Rocha, K. M., Schlesinger, D., et al. (2012). IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population. American journal of medical genetics part. A, 158A( 9), 2170\20132175. doi:10.1002/ajmg.a.35526
NLM
Brito LA, Bassi CFS, Masotti C, Malcher C, Rocha KM, Schlesinger D, Bueno DF, Cruz LA, Barbara LK, Bertola DR, Meyer D, Franco D, Alonso N, Passos-Bueno MR. IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population [Internet]. American journal of medical genetics part. A. 2012 ; 158A( 9): 2170\20132175.[citado 2024 nov. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35526/pdf
Vancouver
Brito LA, Bassi CFS, Masotti C, Malcher C, Rocha KM, Schlesinger D, Bueno DF, Cruz LA, Barbara LK, Bertola DR, Meyer D, Franco D, Alonso N, Passos-Bueno MR. IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population [Internet]. American journal of medical genetics part. A. 2012 ; 158A( 9): 2170\20132175.[citado 2024 nov. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35526/pdf
Trabalho de evento-resumo periodico
Is the contribution of African ancestry to the gene pool of neuromyelitis optica patients different from those with multiple sclerosis? (2011)
Brum, Doralina Guimarães; Luizon, Marcelo Rizzatti; Lana-Peixoto, Marco Aurélio; Ferreira, Maria Lúcia; Gabbai, Alberto A.; Oliveira, Enedina; Bichuetti, Denis; Diniz, Denise S.; Maciel, Ramon Kaimen; Frota, Elizabeth Regina Comini; Rocha, Cristiane Franklin; Santos, Antônio Carlos dos; Donadi, Eduardo Antônio; Barreira, Amilton Antunes; Mendes Júnior, Celso Teixeira; Simoes, Aguinaldo Luiz
Source: Neurology. Conference titles: Annual Meeting of Neurology. Unidades: FMRP, FFCLRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, HERANÇA GENÉTICA (ANÁLISE), ANCESTRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRUM, Doralina Guimarães et al. Is the contribution of African ancestry to the gene pool of neuromyelitis optica patients different from those with multiple sclerosis?. Neurology. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2011
APA
Brum, D. G., Luizon, M. R., Lana-Peixoto, M. A., Ferreira, M. L., Gabbai, A. A., Oliveira, E., et al. (2011). Is the contribution of African ancestry to the gene pool of neuromyelitis optica patients different from those with multiple sclerosis? Neurology. Philadelphia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Brum DG, Luizon MR, Lana-Peixoto MA, Ferreira ML, Gabbai AA, Oliveira E, Bichuetti D, Diniz DS, Maciel RK, Frota ERC, Rocha CF, Santos AC dos, Donadi EA, Barreira AA, Mendes Júnior CT, Simoes AL. Is the contribution of African ancestry to the gene pool of neuromyelitis optica patients different from those with multiple sclerosis? Neurology. 2011 ; 76 A538.[citado 2024 nov. 05 ]
Vancouver
Brum DG, Luizon MR, Lana-Peixoto MA, Ferreira ML, Gabbai AA, Oliveira E, Bichuetti D, Diniz DS, Maciel RK, Frota ERC, Rocha CF, Santos AC dos, Donadi EA, Barreira AA, Mendes Júnior CT, Simoes AL. Is the contribution of African ancestry to the gene pool of neuromyelitis optica patients different from those with multiple sclerosis? Neurology. 2011 ; 76 A538.[citado 2024 nov. 05 ]

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