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Artigo de periodico
Heritability and sex-specific genetic efects of self-reported physical activity in a brazilian highly admixed population (2020)
Leite, Jean Michel Rocha Sampaio ; Soler, Júlia Maria Pavan ; Horimoto, Andréa Roseli Vançan Russo ; Alvim, Rafael O; Pereira, Alexandre da Costa
Fonte: Human Heredity. Unidades: IME, IB, FM, FSP
Assuntos: SEDENTARISMO, ATIVIDADE FÍSICA, HERANÇA GENÉTICA, BIOESTATÍSTICA, REGRESSÃO LINEAR
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ABNT
LEITE, Jean Michel Rocha Sampaio et al. Heritability and sex-specific genetic efects of self-reported physical activity in a brazilian highly admixed population. Human Heredity, v. 84, n. 3, p. 151-157, 2020Tradução . . Disponível em: https://doi.org/10.1159/000506007. Acesso em: 20 out. 2025.
APA
Leite, J. M. R. S., Soler, J. M. P., Horimoto, A. R. V. R., Alvim, R. O., & Pereira, A. da C. (2020). Heritability and sex-specific genetic efects of self-reported physical activity in a brazilian highly admixed population. Human Heredity, 84( 3), 151-157. doi:10.1159/000506007
NLM
Leite J M R S, Soler JMP, Horimoto A R V R, Alvim R O, Pereira A da C. Heritability and sex-specific genetic efects of self-reported physical activity in a brazilian highly admixed population [Internet]. Human Heredity. 2020 ; 84( 3): 151-157.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000506007
Vancouver
Leite J M R S, Soler JMP, Horimoto A R V R, Alvim R O, Pereira A da C. Heritability and sex-specific genetic efects of self-reported physical activity in a brazilian highly admixed population [Internet]. Human Heredity. 2020 ; 84( 3): 151-157.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000506007
Artigo de periodico
Global individual ancestry using principal components for family data (2015)
Andrade, Mariza de; Ray, Debashree; Pereira, Alexandre C; Soler, Júlia Maria Pavan
Fonte: Human Heredity. Unidade: IME
Assuntos: BIOESTATÍSTICA, GENÉTICA ESTATÍSTICA, ESTATÍSTICA APLICADA, MAPEAMENTO GENÉTICO
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ABNT
ANDRADE, Mariza de et al. Global individual ancestry using principal components for family data. Human Heredity, v. 80, n. 1, p. 11 , 2015Tradução . . Disponível em: https://doi.org/10.1159/000381908. Acesso em: 20 out. 2025.
APA
Andrade, M. de, Ray, D., Pereira, A. C., & Soler, J. M. P. (2015). Global individual ancestry using principal components for family data. Human Heredity, 80( 1), 11 . doi:10.1159/000381908
NLM
Andrade M de, Ray D, Pereira AC, Soler JMP. Global individual ancestry using principal components for family data [Internet]. Human Heredity. 2015 ; 80( 1): 11 .[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000381908
Vancouver
Andrade M de, Ray D, Pereira AC, Soler JMP. Global individual ancestry using principal components for family data [Internet]. Human Heredity. 2015 ; 80( 1): 11 .[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000381908
Artigo de periodico
Genetic analysis of age-at-onset for cardiovascular risk factors in brazilian family study (2009)
Giolo, Suely Ruiz; Pereira, Alexandre Costa; Andrade, Mariza de; Oliveira, Camila Maciel de; Krieger, José Eduardo; Soler, Júlia Maria Pavan
Fonte: Human Heredity. Unidades: FM, IME
Assuntos: HEREDITARIEDADE, ANÁLISE DE SOBREVIVÊNCIA
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ABNT
GIOLO, Suely Ruiz et al. Genetic analysis of age-at-onset for cardiovascular risk factors in brazilian family study. Human Heredity, v. 68, n. 2, p. 131-138, 2009Tradução . . Disponível em: https://doi.org/10.1159/000218111. Acesso em: 20 out. 2025.
APA
Giolo, S. R., Pereira, A. C., Andrade, M. de, Oliveira, C. M. de, Krieger, J. E., & Soler, J. M. P. (2009). Genetic analysis of age-at-onset for cardiovascular risk factors in brazilian family study. Human Heredity, 68( 2), 131-138. doi:10.1159/000218111
NLM
Giolo SR, Pereira AC, Andrade M de, Oliveira CM de, Krieger JE, Soler JMP. Genetic analysis of age-at-onset for cardiovascular risk factors in brazilian family study [Internet]. Human Heredity. 2009 ; 68( 2): 131-138.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000218111
Vancouver
Giolo SR, Pereira AC, Andrade M de, Oliveira CM de, Krieger JE, Soler JMP. Genetic analysis of age-at-onset for cardiovascular risk factors in brazilian family study [Internet]. Human Heredity. 2009 ; 68( 2): 131-138.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000218111
Artigo de periodico
The Phylogeography of African Brazilians (2008)
Gonçalves, Vanessa F.; Carvalho, Cláudia M. B.; Bortolini, Maria Cátira; Bydlowski, Sérgio P.; Pena, Sérgio D. J.
Fonte: Human Heredity. Unidade: FM
Assuntos: CROMOSSOMO Y, FILOGENIA
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ABNT
GONÇALVES, Vanessa F. et al. The Phylogeography of African Brazilians. Human Heredity, v. 65, n. 1, p. 23-32, 2008Tradução . . Disponível em: https://doi.org/10.1159/000106059. Acesso em: 20 out. 2025.
APA
Gonçalves, V. F., Carvalho, C. M. B., Bortolini, M. C., Bydlowski, S. P., & Pena, S. D. J. (2008). The Phylogeography of African Brazilians. Human Heredity, 65( 1), 23-32. doi:10.1159/000106059
NLM
Gonçalves VF, Carvalho CMB, Bortolini MC, Bydlowski SP, Pena SDJ. The Phylogeography of African Brazilians [Internet]. Human Heredity. 2008 ; 65( 1): 23-32.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000106059
Vancouver
Gonçalves VF, Carvalho CMB, Bortolini MC, Bydlowski SP, Pena SDJ. The Phylogeography of African Brazilians [Internet]. Human Heredity. 2008 ; 65( 1): 23-32.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000106059
Artigo de periodico
Color and genomic ancestry in brazilians: a study with forensic microsatellites (2006)
Pimenta, Juliana R.; Zuccherato, Luciana W; Debes, Adriana A.; Maselli, Luciana; Soares, Rosângela P.; Moura Neto, Rodrigo S.; Rocha, Jorge; Bydlowski, Sergio Paulo; Pena, Sérgio D. J.
Fonte: Human Heredity. Unidade: FM
Assuntos: MARCADOR MOLECULAR, BIOMARCADORES, GENOMAS, BRASILEIROS
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ABNT
PIMENTA, Juliana R. et al. Color and genomic ancestry in brazilians: a study with forensic microsatellites. Human Heredity, v. 62, p. 190-195, 2006Tradução . . Acesso em: 20 out. 2025.
APA
Pimenta, J. R., Zuccherato, L. W., Debes, A. A., Maselli, L., Soares, R. P., Moura Neto, R. S., et al. (2006). Color and genomic ancestry in brazilians: a study with forensic microsatellites. Human Heredity, 62, 190-195.
NLM
Pimenta JR, Zuccherato LW, Debes AA, Maselli L, Soares RP, Moura Neto RS, Rocha J, Bydlowski SP, Pena SDJ. Color and genomic ancestry in brazilians: a study with forensic microsatellites. Human Heredity. 2006 ; 62 190-195.[citado 2025 out. 20 ]
Vancouver
Pimenta JR, Zuccherato LW, Debes AA, Maselli L, Soares RP, Moura Neto RS, Rocha J, Bydlowski SP, Pena SDJ. Color and genomic ancestry in brazilians: a study with forensic microsatellites. Human Heredity. 2006 ; 62 190-195.[citado 2025 out. 20 ]
Artigo de periodico
The split of the Arara population: comparison of genetic Drift and founder effect (2001)
Ribeiro-dos-Santos, Andrea K. C.; Guerreiro, João Farias; Santos, Sidney Emanuel Batista dos; Zago, Marco Antônio
Fonte: Human Heredity. Unidade: FMRP
Assuntos: GENÉTICA DE POPULAÇÕES, DNA
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ABNT
RIBEIRO-DOS-SANTOS, Andrea K. C. et al. The split of the Arara population: comparison of genetic Drift and founder effect. Human Heredity, v. 51, p. 79-84, 2001Tradução . . Acesso em: 20 out. 2025.
APA
Ribeiro-dos-Santos, A. K. C., Guerreiro, J. F., Santos, S. E. B. dos, & Zago, M. A. (2001). The split of the Arara population: comparison of genetic Drift and founder effect. Human Heredity, 51, 79-84.
NLM
Ribeiro-dos-Santos AKC, Guerreiro JF, Santos SEB dos, Zago MA. The split of the Arara population: comparison of genetic Drift and founder effect. Human Heredity. 2001 ; 51 79-84.[citado 2025 out. 20 ]
Vancouver
Ribeiro-dos-Santos AKC, Guerreiro JF, Santos SEB dos, Zago MA. The split of the Arara population: comparison of genetic Drift and founder effect. Human Heredity. 2001 ; 51 79-84.[citado 2025 out. 20 ]
Artigo de periodico
Heterogeneous ethinic distribution of the 844ins68 in the cystathionine 'beta'-synthase gene (1998)
Franco, Rendrik França; Elion, Jacques; Lavinha, João; Krishnamoorthy, Ragajopal; Tavella, Marli Haydee; Zago, Marco Antônio
Fonte: Human Heredity. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
FRANCO, Rendrik França et al. Heterogeneous ethinic distribution of the 844ins68 in the cystathionine 'beta'-synthase gene. Human Heredity, v. 48, p. 338-342, 1998Tradução . . Acesso em: 20 out. 2025.
APA
Franco, R. F., Elion, J., Lavinha, J., Krishnamoorthy, R., Tavella, M. H., & Zago, M. A. (1998). Heterogeneous ethinic distribution of the 844ins68 in the cystathionine 'beta'-synthase gene. Human Heredity, 48, 338-342.
NLM
Franco RF, Elion J, Lavinha J, Krishnamoorthy R, Tavella MH, Zago MA. Heterogeneous ethinic distribution of the 844ins68 in the cystathionine 'beta'-synthase gene. Human Heredity. 1998 ; 48 338-342.[citado 2025 out. 20 ]
Vancouver
Franco RF, Elion J, Lavinha J, Krishnamoorthy R, Tavella MH, Zago MA. Heterogeneous ethinic distribution of the 844ins68 in the cystathionine 'beta'-synthase gene. Human Heredity. 1998 ; 48 338-342.[citado 2025 out. 20 ]
Artigo de periodico
Interpopulational and intrapopulational genetic diversity of amerindians as revealed by six variable number of tandem repeats (1996)
Zago, M A; Silva Junior, W. A.; Tavella, M H; Santos, S. E. B.; Guerreiro, J F; Figueiredo, Mauro Silvério
Fonte: Human Heredity. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
ZAGO, M A et al. Interpopulational and intrapopulational genetic diversity of amerindians as revealed by six variable number of tandem repeats. Human Heredity, v. 46, p. 274-89, 1996Tradução . . Acesso em: 20 out. 2025.
APA
Zago, M. A., Silva Junior, W. A., Tavella, M. H., Santos, S. E. B., Guerreiro, J. F., & Figueiredo, M. S. (1996). Interpopulational and intrapopulational genetic diversity of amerindians as revealed by six variable number of tandem repeats. Human Heredity, 46, 274-89.
NLM
Zago MA, Silva Junior WA, Tavella MH, Santos SEB, Guerreiro JF, Figueiredo MS. Interpopulational and intrapopulational genetic diversity of amerindians as revealed by six variable number of tandem repeats. Human Heredity. 1996 ;46 274-89.[citado 2025 out. 20 ]
Vancouver
Zago MA, Silva Junior WA, Tavella MH, Santos SEB, Guerreiro JF, Figueiredo MS. Interpopulational and intrapopulational genetic diversity of amerindians as revealed by six variable number of tandem repeats. Human Heredity. 1996 ;46 274-89.[citado 2025 out. 20 ]
Artigo de periodico
Genetic epidemiology of the mitsuda reaction in leprosy (1996)
Feitosa, M F; Krieger, Henrique; Borecki, I; Rao, D C
Fonte: Human Heredity. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
FEITOSA, M F et al. Genetic epidemiology of the mitsuda reaction in leprosy. Human Heredity, v. 46, p. 32-5, 1996Tradução . . Acesso em: 20 out. 2025.
APA
Feitosa, M. F., Krieger, H., Borecki, I., & Rao, D. C. (1996). Genetic epidemiology of the mitsuda reaction in leprosy. Human Heredity, 46, 32-5.
NLM
Feitosa MF, Krieger H, Borecki I, Rao DC. Genetic epidemiology of the mitsuda reaction in leprosy. Human Heredity. 1996 ;46 32-5.[citado 2025 out. 20 ]
Vancouver
Feitosa MF, Krieger H, Borecki I, Rao DC. Genetic epidemiology of the mitsuda reaction in leprosy. Human Heredity. 1996 ;46 32-5.[citado 2025 out. 20 ]
Artigo de periodico
Beta-globin gene cluster haplotypes of amerindian populations from the brazilian amazon region (1994)
Guerreiro, J F; Figueiredo, Mauro Silvério; Zago, M A
Fonte: Human Heredity. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
GUERREIRO, J F e FIGUEIREDO, Mauro Silvério e ZAGO, M A. Beta-globin gene cluster haplotypes of amerindian populations from the brazilian amazon region. Human Heredity, v. 44, p. 142-9, 1994Tradução . . Acesso em: 20 out. 2025.
APA
Guerreiro, J. F., Figueiredo, M. S., & Zago, M. A. (1994). Beta-globin gene cluster haplotypes of amerindian populations from the brazilian amazon region. Human Heredity, 44, 142-9.
NLM
Guerreiro JF, Figueiredo MS, Zago MA. Beta-globin gene cluster haplotypes of amerindian populations from the brazilian amazon region. Human Heredity. 1994 ;44 142-9.[citado 2025 out. 20 ]
Vancouver
Guerreiro JF, Figueiredo MS, Zago MA. Beta-globin gene cluster haplotypes of amerindian populations from the brazilian amazon region. Human Heredity. 1994 ;44 142-9.[citado 2025 out. 20 ]
Artigo de periodico
Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies (1991)
Rabbi-Bortolini, E; Colletto, G M D D; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Rapaport, D; Zatz, Mayana
Fonte: Human Heredity. Unidades: ICB, IB
Assunto: GENÉTICA MÉDICA
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ABNT
RABBI-BORTOLINI, E et al. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity, v. no/dec. 1991, n. 6 , p. 370-8, 1991Tradução . . Acesso em: 20 out. 2025.
APA
Rabbi-Bortolini, E., Colletto, G. M. D. D., Passos-Bueno, M. R., Vainzof, M., Rapaport, D., & Zatz, M. (1991). Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity, no/dec. 1991( 6 ), 370-8.
NLM
Rabbi-Bortolini E, Colletto GMDD, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity. 1991 ; no/dec. 1991( 6 ): 370-8.[citado 2025 out. 20 ]
Vancouver
Rabbi-Bortolini E, Colletto GMDD, Passos-Bueno MR, Vainzof M, Rapaport D, Zatz M. Estimate of the intrafamilial correlation for serum creatine kinase (ck) and pyruvate kinase (pk) in females at risk for duchenne (dmd) and becker (dmb) muscular dystrophies. Human Heredity. 1991 ; no/dec. 1991( 6 ): 370-8.[citado 2025 out. 20 ]
Artigo de periodico
Association between the acid phosphatase 1 and adenosine deaminase systems in a brazilian sample (1991)
Engracia, V; Mestriner, Moacyr Antonio; Cabello, P H; Krieger, Henrique
Fonte: Human Heredity. Unidades: FMRP, ICB
Assunto: PARASITOLOGIA
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ABNT
ENGRACIA, V et al. Association between the acid phosphatase 1 and adenosine deaminase systems in a brazilian sample. Human Heredity, v. 41, n. 3, p. 147-150, 1991Tradução . . Acesso em: 20 out. 2025.
APA
Engracia, V., Mestriner, M. A., Cabello, P. H., & Krieger, H. (1991). Association between the acid phosphatase 1 and adenosine deaminase systems in a brazilian sample. Human Heredity, 41( 3), 147-150.
NLM
Engracia V, Mestriner MA, Cabello PH, Krieger H. Association between the acid phosphatase 1 and adenosine deaminase systems in a brazilian sample. Human Heredity. 1991 ; 41( 3): 147-150.[citado 2025 out. 20 ]
Vancouver
Engracia V, Mestriner MA, Cabello PH, Krieger H. Association between the acid phosphatase 1 and adenosine deaminase systems in a brazilian sample. Human Heredity. 1991 ; 41( 3): 147-150.[citado 2025 out. 20 ]
Artigo de periodico
Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy (1989)
Passos-Bueno, Maria Rita ; Otto, Paulo A ; Zatz, Mayana
Fonte: Human Heredity. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, GENÉTICA
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ABNT
PASSOS-BUENO, Maria Rita e OTTO, Paulo A e ZATZ, Mayana. Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy. Human Heredity, v. 39, n. 4 , p. 202-11, 1989Tradução . . Acesso em: 20 out. 2025.
APA
Passos-Bueno, M. R., Otto, P. A., & Zatz, M. (1989). Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy. Human Heredity, 39( 4 ), 202-11.
NLM
Passos-Bueno MR, Otto PA, Zatz M. Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy. Human Heredity. 1989 ;39( 4 ): 202-11.[citado 2025 out. 20 ]
Vancouver
Passos-Bueno MR, Otto PA, Zatz M. Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy. Human Heredity. 1989 ;39( 4 ): 202-11.[citado 2025 out. 20 ]
Artigo de periodico
A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome (1982)
Cavalli, Iglenir João; Sbalqueiro, Ives J.; Wajntal, Anita; Freire-Maia, Newton
Fonte: Human Heredity. Unidade: IB
Assuntos: CROMOSSOMOS HUMANOS (ANORMALIDADES), DOENÇAS GENÉTICAS, MALFORMAÇÕES
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ABNT
CAVALLI, Iglenir João et al. A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome. Human Heredity, v. 32, p. 149-151, 1982Tradução . . Disponível em: https://doi.org/10.1159/000153279. Acesso em: 20 out. 2025.
APA
Cavalli, I. J., Sbalqueiro, I. J., Wajntal, A., & Freire-Maia, N. (1982). A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome. Human Heredity, 32, 149-151. doi:10.1159/000153279
NLM
Cavalli IJ, Sbalqueiro IJ, Wajntal A, Freire-Maia N. A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome [Internet]. Human Heredity. 1982 ; 32 149-151.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000153279
Vancouver
Cavalli IJ, Sbalqueiro IJ, Wajntal A, Freire-Maia N. A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome [Internet]. Human Heredity. 1982 ; 32 149-151.[citado 2025 out. 20 ] Available from: https://doi.org/10.1159/000153279

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