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Artigo de periodico
Psychiatric genetics in the diverse landscape of Latin American populations (2025)
Bruxel, Estela M; Rovaris, Diego Luiz ; Ribeiro, Alberto de Freitas ; Lima, Yago C
Fonte: Nature Genetics. Unidades: ICB, IB
Assuntos: TRANSTORNOS MENTAIS, DIVERSIDADE GENÉTICA, GENÉTICA DE POPULAÇÕES
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ABNT
BRUXEL, Estela M et al. Psychiatric genetics in the diverse landscape of Latin American populations. Nature Genetics, v. 57, p. 1074–1088, 2025Tradução . . Disponível em: https://doi.org/10.1038/s41588-025-02127-z. Acesso em: 21 out. 2025.
APA
Bruxel, E. M., Rovaris, D. L., Ribeiro, A. de F., & Lima, Y. C. (2025). Psychiatric genetics in the diverse landscape of Latin American populations. Nature Genetics, 57, 1074–1088. doi:10.1038/s41588-025-02127-z
NLM
Bruxel EM, Rovaris DL, Ribeiro A de F, Lima YC. Psychiatric genetics in the diverse landscape of Latin American populations [Internet]. Nature Genetics. 2025 ; 57 1074–1088.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-025-02127-z
Vancouver
Bruxel EM, Rovaris DL, Ribeiro A de F, Lima YC. Psychiatric genetics in the diverse landscape of Latin American populations [Internet]. Nature Genetics. 2025 ; 57 1074–1088.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-025-02127-z
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: 21 out. 2025.
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 2025 out. 21 ] 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 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Artigo de periodico
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p (2022)
Weiner, Daniel J. ; Ling, Emi ; Erdin, Serkan ; Tai, Derek J. C.; Yadav, Rachita; Grove, Jakob ; Fu, Jack M. ; Nadig, Ajay; Rovaris, Diego Luiz
Fonte: Nature Genetics. Unidade: ICB
Assunto: FISIOLOGIA
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WEINER, Daniel J. et al. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics, v. 54, p. 1630–1639, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01203-y. Acesso em: 21 out. 2025.
APA
Weiner, D. J., Ling, E., Erdin, S., Tai, D. J. C., Yadav, R., Grove, J., et al. (2022). Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics, 54, 1630–1639. doi:10.1038/s41588-022-01203-y
NLM
Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Rovaris DL. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p [Internet]. Nature Genetics. 2022 ; 54 1630–1639.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-022-01203-y
Vancouver
Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Rovaris DL. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p [Internet]. Nature Genetics. 2022 ; 54 1630–1639.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-022-01203-y
Artigo de periodico
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits (2020)
Choudhuri, Avik; Trompouki, Eirini; Abraham, Brian J.; Colli, Leandro Machado ; Kock, Kian Hong; Mallard, William; Yang, Min-Lee; Vinjamur, Divya S.; Ghamari, Alireza; Sporrij, Audrey; Hoi, Karen; Hummel, Barbara; Boatman, Sonja; Chan, Victoria; Tseng, Sierra; Nandakumar, Satish K.; Yang, Song; Lichtig, Asher; Superdock, Michael; Grimes, Seraj N.; Bowman, Teresa V.; Zhou, Yi; Takahashi, Shinichiro; Joehanes, Roby; Cantor, Alan B.; Bauer, Daniel E.; Ganesh, Santhi K.; Rinn, John; Albert, Paul S.; Bulyk, Martha L.; Chanock, Stephen J.; Young, Richard A.; Zon, Leonard I.
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: HEMOGLOBINAS, FATORES DE TRANSCRIÇÃO, EXPRESSÃO GÊNICA
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ABNT
CHOUDHURI, Avik et al. Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits. Nature Genetics, v. 52, n. 12, p. 1333-1345, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41588-020-00738-2. Acesso em: 21 out. 2025.
APA
Choudhuri, A., Trompouki, E., Abraham, B. J., Colli, L. M., Kock, K. H., Mallard, W., et al. (2020). Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits. Nature Genetics, 52( 12), 1333-1345. doi:10.1038/s41588-020-00738-2
NLM
Choudhuri A, Trompouki E, Abraham BJ, Colli LM, Kock KH, Mallard W, Yang M-L, Vinjamur DS, Ghamari A, Sporrij A, Hoi K, Hummel B, Boatman S, Chan V, Tseng S, Nandakumar SK, Yang S, Lichtig A, Superdock M, Grimes SN, Bowman TV, Zhou Y, Takahashi S, Joehanes R, Cantor AB, Bauer DE, Ganesh SK, Rinn J, Albert PS, Bulyk ML, Chanock SJ, Young RA, Zon LI. Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits [Internet]. Nature Genetics. 2020 ; 52( 12): 1333-1345.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-020-00738-2
Vancouver
Choudhuri A, Trompouki E, Abraham BJ, Colli LM, Kock KH, Mallard W, Yang M-L, Vinjamur DS, Ghamari A, Sporrij A, Hoi K, Hummel B, Boatman S, Chan V, Tseng S, Nandakumar SK, Yang S, Lichtig A, Superdock M, Grimes SN, Bowman TV, Zhou Y, Takahashi S, Joehanes R, Cantor AB, Bauer DE, Ganesh SK, Rinn J, Albert PS, Bulyk ML, Chanock SJ, Young RA, Zon LI. Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits [Internet]. Nature Genetics. 2020 ; 52( 12): 1333-1345.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-020-00738-2
Artigo de periodico
A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants (2019)
Gusev, Alexander; Lawrenson, Kate; Lin, Xianzhi; Lyra Júnior, Paulo C.; Kar, Siddhartha; Noushmehr, Houtan
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: NEOPLASIAS OVARIANAS, SEQUENCIAMENTO GENÉTICO, EXPRESSÃO GÊNICA
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ABNT
GUSEV, Alexander et al. A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants. Nature Genetics, v. 51, n. 5, p. 815-823, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41588-019-0395-x. Acesso em: 21 out. 2025.
APA
Gusev, A., Lawrenson, K., Lin, X., Lyra Júnior, P. C., Kar, S., & Noushmehr, H. (2019). A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants. Nature Genetics, 51( 5), 815-823. doi:10.1038/s41588-019-0395-x
NLM
Gusev A, Lawrenson K, Lin X, Lyra Júnior PC, Kar S, Noushmehr H. A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants [Internet]. Nature Genetics. 2019 ; 51( 5): 815-823.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-019-0395-x
Vancouver
Gusev A, Lawrenson K, Lin X, Lyra Júnior PC, Kar S, Noushmehr H. A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants [Internet]. Nature Genetics. 2019 ; 51( 5): 815-823.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/s41588-019-0395-x
Artigo de periodico
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017)
Christophersen, Ingrid E.; Rienstra, Michiel; Roselli, Carolina; Yin, Xiaoyan; Geelhoed, Bastiaan; Barnard, John; Lin, Honghuang; Arking, Dan E.; Smith, Albert V.; Albert, Christine M.; Chaffin, Mark; Tucker, Nathan R.; Li, Molong; Klarin, Derek; Bihlmeyer, Nathan A.; Low, Siew-Kee; Weeke, Peter E.; Nurasyid, Martina Müller; Smith, J. Gustav; Brody, Jennifer A.; Niemeijer, Maartje N; Dörr, Marcus; Trompet, Stella; Huffman, Jennifer; Gustafsson, Stefan; Schurmann, Claudia; Kleber, Marcus E.; Lyytikäinen, Leo-Pekka; Seppälä, Ilkka; Malik, Rainer; Horimoto, Andrea R. V; Perez, Marco; Sinisalo, Juha; Aeschbacher, Stefanie; Theriault, Sébastien; Yao, Jie; Radmanesh, Farid; Teumer, Alexander; Choi, Seung Hoan; Weng, Lu-Chen; Clauss, Sebastian; Deo, Rajat; Rader, Daniel J; Shah, Svati H; Sun, Albert; Hopewell, Jemma C.; Debette, Stephanie; Chauhan, Ganesh; Yang, Qiong; Worral, Bradford B; Paré, Guillaume; Kamatani, Yoichiro; Hagemeijer, Yanick P; Verweij, Niek; Siland, Joylene E; Kubo, Michiaki; Smith, Jonathan D; Wagoner, David R. Van; Bis, Joshua C; Perz, Siegfried; Psaty, Bruce M; Ridker, Paul M; Magnani, Jared W; Harris, Tamara B; Launer, Lenore J; Shoemaker, M. Benjamin; Padmanabhan, Sandosh; Haessler, Jeffrey; Bartz, Traci M; Waldenberger, Melanie; Lichtner, Peter; Krieger, José Eduardo; Kähönen, Mika; Risch, Lorenz; Mansur, Alfredo José; Peters, Annette; Smith, Blair H; Lind, Lars; Scott, Stuart A; Lu, Yingchang; Bottinger, Erwin B; Hernesniemi, Jussi; Lindgren, Cecilia M; Wong, Jorge A; Huang, Jie; Eskola, Markku; Morris, Andrew P; Ford, Ian; Reiner, Alex P; Delgado, Graciela; Yen, Lin Y; Chen, Yii-Der Ida; Sandhu, Roopinder; Li, Man; Boerwinkle, Eric; Eisele, Lewin; Lannfelt, Lars; Rost, Natalia; Anderson, Christopher D; Taylor, Kent D; Campbell, Archie; Magnusson, Patrick K; Porteous, David; Hoking, Lynne J; Vlachopoulou, Efthymia; Pedersen, Nancy L; Nikus, Kjell; Melander, Marju Orho; Hamsten, Anders; Heeringa, Jan; Denny, Joshua C; Kriebel, Jennifer; Darbar, Dawood; Cheh, Christopher Newton; Shaffer,Christian; Macfarlane, Peter W; Heimbach, Stefanie Heilmann; Almgren, Peter; Huang, Paul L.; Sotoodehnia, Nona; Soliman, Elsayed Z; Uitterlinden, Andre G; Hofman, Albert; Franco, Oscar H; Völker, Uwe; Jöckel, Karl-Heinz; Sinner,Moritz F; Lin, Henry J; Guo, Xiuqing; Dichgans, Martin; Ingelsson, Erik; Kooperberg, Charles; Melander, Olle; Loos, Ruth J. F; Laurikka, Jari; Conen, David; Rosand, Jonathan; Harst, Pim van der; Lokki, Marja-Liisa; Kathiresan, Sekar; Pereira, Alexandre; Jukema, J. Wouter; Hayward, Caroline; Rotter, Jerome I; März, Winfried; Lehtimäki, Terho; Stricker, Bruno H; Chung, Mina K; Felix, Stephan B; Gudnason, Vilmundur; Alonso, Alvaro; Roden, Dan M; Kääb, Stefan; Chasman, Daniel I; Heckbert, Susan R; Benjamin, Emelia J; Tanaka, Toshihiro; Lunetta, Kathryn L; Lubitz, Steven A; Ellinor, Patrick T
Fonte: Nature Genetics. Unidade: FM
Assuntos: FIBRILAÇÃO ATRIAL, METANÁLISE, DOENÇAS CARDIOVASCULARES, GENOMAS
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ABNT
CHRISTOPHERSEN, Ingrid E. et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics, v. 49, n. 6, p. 946-952, 2017Tradução . . Disponível em: https://doi.org/10.1038/ng.3843. Acesso em: 21 out. 2025.
APA
Christophersen, I. E., Rienstra, M., Roselli, C., Yin, X., Geelhoed, B., Barnard, J., et al. (2017). Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics, 49( 6), 946-952. doi:10.1038/ng.3843
NLM
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, Low S-K, Weeke PE, Nurasyid MM, Smith JG, Brody JA, Niemeijer MN, Dörr M, Trompet S, Huffman J, Gustafsson S, Schurmann C, Kleber ME, Lyytikäinen L-P, Seppälä I, Malik R, Horimoto ARV, Perez M, Sinisalo J, Aeschbacher S, Theriault S, Yao J, Radmanesh F, Teumer A, Choi SH, Weng L-C, Clauss S, Deo R, Rader DJ, Shah SH, Sun A, Hopewell JC, Debette S, Chauhan G, Yang Q, Worral BB, Paré G, Kamatani Y, Hagemeijer YP, Verweij N, Siland JE, Kubo M, Smith JD, Wagoner DRV, Bis JC, Perz S, Psaty BM, Ridker PM, Magnani JW, Harris TB, Launer LJ, Shoemaker MB, Padmanabhan S, Haessler J, Bartz TM, Waldenberger M, Lichtner P, Krieger JE, Kähönen M, Risch L, Mansur AJ, Peters A, Smith BH, Lind L, Scott SA, Lu Y, Bottinger EB, Hernesniemi J, Lindgren CM, Wong JA, Huang J, Eskola M, Morris AP, Ford I, Reiner AP, Delgado G, Yen LY, Chen Y-DI, Sandhu R, Li M, Boerwinkle E, Eisele L, Lannfelt L, Rost N, Anderson CD, Taylor KD, Campbell A, Magnusson PK, Porteous D, Hoking LJ, Vlachopoulou E, Pedersen NL, Nikus K, Melander MO, Hamsten A, Heeringa J, Denny JC, Kriebel J, Darbar D, Cheh CN, Shaffer C, Macfarlane PW, Heimbach SH, Almgren P, Huang PL, Sotoodehnia N, Soliman EZ, Uitterlinden AG, Hofman A, Franco OH, Völker U, Jöckel K-H, Sinner MF, Lin HJ, Guo X, Dichgans M, Ingelsson E, Kooperberg C, Melander O, Loos RJF, Laurikka J, Conen D, Rosand J, Harst P van der, Lokki M-L, Kathiresan S, Pereira A, Jukema JW, Hayward C, Rotter JI, März W, Lehtimäki T, Stricker BH, Chung MK, Felix SB, Gudnason V, Alonso A, Roden DM, Kääb S, Chasman DI, Heckbert SR, Benjamin EJ, Tanaka T, Lunetta KL, Lubitz SA, Ellinor PT. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation [Internet]. Nature Genetics. 2017 ; 49( 6): 946-952.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3843
Vancouver
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, Low S-K, Weeke PE, Nurasyid MM, Smith JG, Brody JA, Niemeijer MN, Dörr M, Trompet S, Huffman J, Gustafsson S, Schurmann C, Kleber ME, Lyytikäinen L-P, Seppälä I, Malik R, Horimoto ARV, Perez M, Sinisalo J, Aeschbacher S, Theriault S, Yao J, Radmanesh F, Teumer A, Choi SH, Weng L-C, Clauss S, Deo R, Rader DJ, Shah SH, Sun A, Hopewell JC, Debette S, Chauhan G, Yang Q, Worral BB, Paré G, Kamatani Y, Hagemeijer YP, Verweij N, Siland JE, Kubo M, Smith JD, Wagoner DRV, Bis JC, Perz S, Psaty BM, Ridker PM, Magnani JW, Harris TB, Launer LJ, Shoemaker MB, Padmanabhan S, Haessler J, Bartz TM, Waldenberger M, Lichtner P, Krieger JE, Kähönen M, Risch L, Mansur AJ, Peters A, Smith BH, Lind L, Scott SA, Lu Y, Bottinger EB, Hernesniemi J, Lindgren CM, Wong JA, Huang J, Eskola M, Morris AP, Ford I, Reiner AP, Delgado G, Yen LY, Chen Y-DI, Sandhu R, Li M, Boerwinkle E, Eisele L, Lannfelt L, Rost N, Anderson CD, Taylor KD, Campbell A, Magnusson PK, Porteous D, Hoking LJ, Vlachopoulou E, Pedersen NL, Nikus K, Melander MO, Hamsten A, Heeringa J, Denny JC, Kriebel J, Darbar D, Cheh CN, Shaffer C, Macfarlane PW, Heimbach SH, Almgren P, Huang PL, Sotoodehnia N, Soliman EZ, Uitterlinden AG, Hofman A, Franco OH, Völker U, Jöckel K-H, Sinner MF, Lin HJ, Guo X, Dichgans M, Ingelsson E, Kooperberg C, Melander O, Loos RJF, Laurikka J, Conen D, Rosand J, Harst P van der, Lokki M-L, Kathiresan S, Pereira A, Jukema JW, Hayward C, Rotter JI, März W, Lehtimäki T, Stricker BH, Chung MK, Felix SB, Gudnason V, Alonso A, Roden DM, Kääb S, Chasman DI, Heckbert SR, Benjamin EJ, Tanaka T, Lunetta KL, Lubitz SA, Ellinor PT. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation [Internet]. Nature Genetics. 2017 ; 49( 6): 946-952.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3843
Artigo de periodico
Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax (2016)
Hupalo, Daniel N; Luo, Zunping; Melnikov, Alexandre; Sutton, Patrick L; Rogov, Peter; Escalante, Ananias; Vallejo, Andrés F; Herrera, Sócrates; Arévalo-Herrera, Myriam; Fan, Qi; Wang, Ying; Cui, Liwang; Lucas, Carmen M; Durand, Salomon; Sanchez, Juan F; Baldeviano, G Christian; Lescano, Andres G; Laman, Moses; Barnadas, Celine; Barry, Alyssa; Mueller, Ivo; Kazura, James W; Eapen, Alex; Kanagaraj, Deena; Valecha, Neena; Ferreira, Marcelo Urbano ; Roobsoong, Wanlapa; Nguitragool, Wang; Sattabonkot, Jetsumon; Gamboa, Dionicia; Kosek, Margaret; Vinetz, Joseph M; González-Cerón, Lilia; Birren, Bruce W; Neafsey, Daniel E; Carlton, Jane M
Fonte: Nature Genetics. Unidade: ICB
Assuntos: PARASITOLOGIA, GENÔMICA, PLASMODIUM, MALÁRIA, PLASMODIUM FALCIPARUM
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ABNT
HUPALO, Daniel N et al. Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax. Nature Genetics, v. 48, n. 8, p. 953-958, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3588. Acesso em: 21 out. 2025.
APA
Hupalo, D. N., Luo, Z., Melnikov, A., Sutton, P. L., Rogov, P., Escalante, A., et al. (2016). Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax. Nature Genetics, 48( 8), 953-958. doi:10.1038/ng.3588
NLM
Hupalo DN, Luo Z, Melnikov A, Sutton PL, Rogov P, Escalante A, Vallejo AF, Herrera S, Arévalo-Herrera M, Fan Q, Wang Y, Cui L, Lucas CM, Durand S, Sanchez JF, Baldeviano GC, Lescano AG, Laman M, Barnadas C, Barry A, Mueller I, Kazura JW, Eapen A, Kanagaraj D, Valecha N, Ferreira MU, Roobsoong W, Nguitragool W, Sattabonkot J, Gamboa D, Kosek M, Vinetz JM, González-Cerón L, Birren BW, Neafsey DE, Carlton JM. Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax [Internet]. Nature Genetics. 2016 ; 48( 8): 953-958.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3588
Vancouver
Hupalo DN, Luo Z, Melnikov A, Sutton PL, Rogov P, Escalante A, Vallejo AF, Herrera S, Arévalo-Herrera M, Fan Q, Wang Y, Cui L, Lucas CM, Durand S, Sanchez JF, Baldeviano GC, Lescano AG, Laman M, Barnadas C, Barry A, Mueller I, Kazura JW, Eapen A, Kanagaraj D, Valecha N, Ferreira MU, Roobsoong W, Nguitragool W, Sattabonkot J, Gamboa D, Kosek M, Vinetz JM, González-Cerón L, Birren BW, Neafsey DE, Carlton JM. Population genomics studies identify signatures of global dispersal and drug resistance in Plasmodium vivax [Internet]. Nature Genetics. 2016 ; 48( 8): 953-958.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3588
Artigo de periodico
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer (2016)
Lesseur, Corina; Diergaarde, Brenda; Olshan, Andrew F; Wünsch Filho, Victor ; Ness, Andrew R; Liu, Geoffrey; Lacko, Martin; Eluf Neto, José; Franceschi, Silvia; Lagiou, Pagona; Macfarlane, Gary J; Richiardi, Lorenzo; Boccia, Stefania; Polesel, Jerry; Kjaerheim, Kristina; Zaridze, David; Johansson, Mattias; Menezes, Ana M; Curado, Maria Paula; Robinson, Max; Ahrens, Wolfgang; Canova, Cristina; Znaor, Ariana; Castellsagué, Xavier; Conway, David I; Holcátová, Ivana; Mates, Dana; Vilensky, Marta; Healy, Claire M; Szeszenia-Dąbrowska, Neonila; Fabiánová, Eleonóra; Lissowska, Jolanta; Grandis, Jennifer R; Weissler, Mark C; Tajara, Eloiza H; Nunes, Fabio D; Carvalho, Marcos B. de; Thomas, Steve; Hung, Rayjean J; Peters, Wilbert H M; Herrero, Rolando; Cadoni, Gabriella; Bueno-de-Mesquita, H Bas; Steffen, Annika; Agudo, Antonio; Shangina, Oxana; Xiao, Xiangjun; Gaborieau, Valérie; Chabrier, Amélie; Anantharaman, Devasena; Boffetta, Paolo; Amos, Christopher I; McKay, James D; Brennan, Paul
Fonte: Nature Genetics. Unidade: FSP
Assuntos: NEOPLASIAS FARÍNGEAS, GENOMAS, NEOPLASIAS OROFARÍNGEAS, INCIDÊNCIA
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ABNT
LESSEUR, Corina et al. Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Nature Genetics, v. 48, n. 12, p. 1544-1550, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3685. Acesso em: 21 out. 2025.
APA
Lesseur, C., Diergaarde, B., Olshan, A. F., Wünsch Filho, V., Ness, A. R., Liu, G., et al. (2016). Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Nature Genetics, 48( 12), 1544-1550. doi:10.1038/ng.3685
NLM
Lesseur C, Diergaarde B, Olshan AF, Wünsch Filho V, Ness AR, Liu G, Lacko M, Eluf Neto J, Franceschi S, Lagiou P, Macfarlane GJ, Richiardi L, Boccia S, Polesel J, Kjaerheim K, Zaridze D, Johansson M, Menezes AM, Curado MP, Robinson M, Ahrens W, Canova C, Znaor A, Castellsagué X, Conway DI, Holcátová I, Mates D, Vilensky M, Healy CM, Szeszenia-Dąbrowska N, Fabiánová E, Lissowska J, Grandis JR, Weissler MC, Tajara EH, Nunes FD, Carvalho MB de, Thomas S, Hung RJ, Peters WHM, Herrero R, Cadoni G, Bueno-de-Mesquita HB, Steffen A, Agudo A, Shangina O, Xiao X, Gaborieau V, Chabrier A, Anantharaman D, Boffetta P, Amos CI, McKay JD, Brennan P. Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer [Internet]. Nature Genetics. 2016 ;48( 12): 1544-1550.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3685
Vancouver
Lesseur C, Diergaarde B, Olshan AF, Wünsch Filho V, Ness AR, Liu G, Lacko M, Eluf Neto J, Franceschi S, Lagiou P, Macfarlane GJ, Richiardi L, Boccia S, Polesel J, Kjaerheim K, Zaridze D, Johansson M, Menezes AM, Curado MP, Robinson M, Ahrens W, Canova C, Znaor A, Castellsagué X, Conway DI, Holcátová I, Mates D, Vilensky M, Healy CM, Szeszenia-Dąbrowska N, Fabiánová E, Lissowska J, Grandis JR, Weissler MC, Tajara EH, Nunes FD, Carvalho MB de, Thomas S, Hung RJ, Peters WHM, Herrero R, Cadoni G, Bueno-de-Mesquita HB, Steffen A, Agudo A, Shangina O, Xiao X, Gaborieau V, Chabrier A, Anantharaman D, Boffetta P, Amos CI, McKay JD, Brennan P. Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer [Internet]. Nature Genetics. 2016 ;48( 12): 1544-1550.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3685
Artigo de periodico
Genomic analysis of local variation and recent evolution in Plasmodium vivax (2016)
Pearson, Richard D.; Amato, Roberto; Auburn, Sarah; Miotto, Olivo; Almagro-Garcia, Jacob; Amaratunga, Chanaki; Suon, Seila; Mao, Sivanna; Noviyanti, Rintis; Trimarsanto, Hidayat; Marfurt, Jutta; Anstey, Nicholas M.; William, Timothy; Boni, Maciej F.; Dolecek, Christiane; Tran, Hien Tinh; White, Nicholas J; Michon, Pascal; Siba, Peter; Tavul, Livingstone; Harrison, Gabrielle; Barry, Alyssa; Mueller, Ivo; Ferreira, Marcelo Urbano ; Karunaweera, Nadira; Randrianarivelojosia, Milijaona; Gao, Qi; Hubbart, Christina; Hart, Lee; Jeffery, Ben; Drury, Eleanor; Mead, Daniel; Kekre, Mihir; Campino, Susana; Manske, Magnus; Cornelius, Victoria J; Mac Innis, Bronwyn; Rockett, Kirk A; Miles, Alistair; Rayner, Julian; Fairhurst, Rick M; Nosten, Francois; Price, Ric N; Kwiatkowski, Dominic P
Fonte: Nature Genetics. Unidade: ICB
Assuntos: PARASITOLOGIA, GENÔMICA, PLASMODIUM, MALÁRIA, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEARSON, Richard D. et al. Genomic analysis of local variation and recent evolution in Plasmodium vivax. Nature Genetics, v. 48, n. 8, p. 959-964, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3599. Acesso em: 21 out. 2025.
APA
Pearson, R. D., Amato, R., Auburn, S., Miotto, O., Almagro-Garcia, J., Amaratunga, C., et al. (2016). Genomic analysis of local variation and recent evolution in Plasmodium vivax. Nature Genetics, 48( 8), 959-964. doi:10.1038/ng.3599
NLM
Pearson RD, Amato R, Auburn S, Miotto O, Almagro-Garcia J, Amaratunga C, Suon S, Mao S, Noviyanti R, Trimarsanto H, Marfurt J, Anstey NM, William T, Boni MF, Dolecek C, Tran HT, White NJ, Michon P, Siba P, Tavul L, Harrison G, Barry A, Mueller I, Ferreira MU, Karunaweera N, Randrianarivelojosia M, Gao Q, Hubbart C, Hart L, Jeffery B, Drury E, Mead D, Kekre M, Campino S, Manske M, Cornelius VJ, Mac Innis B, Rockett KA, Miles A, Rayner J, Fairhurst RM, Nosten F, Price RN, Kwiatkowski DP. Genomic analysis of local variation and recent evolution in Plasmodium vivax [Internet]. Nature Genetics. 2016 ; 48( 8): 959-964.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3599
Vancouver
Pearson RD, Amato R, Auburn S, Miotto O, Almagro-Garcia J, Amaratunga C, Suon S, Mao S, Noviyanti R, Trimarsanto H, Marfurt J, Anstey NM, William T, Boni MF, Dolecek C, Tran HT, White NJ, Michon P, Siba P, Tavul L, Harrison G, Barry A, Mueller I, Ferreira MU, Karunaweera N, Randrianarivelojosia M, Gao Q, Hubbart C, Hart L, Jeffery B, Drury E, Mead D, Kekre M, Campino S, Manske M, Cornelius VJ, Mac Innis B, Rockett KA, Miles A, Rayner J, Fairhurst RM, Nosten F, Price RN, Kwiatkowski DP. Genomic analysis of local variation and recent evolution in Plasmodium vivax [Internet]. Nature Genetics. 2016 ; 48( 8): 959-964.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3599
Artigo de periodico
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery (2016)
Scott, Eric M.; Halees, A.; Itan, Y.; Spencer, E. G.; He,Y.; Azab, M. A.; Gabriel, S. B.; Belkadi, A.; Boisson, B.; Abel, L.; Clark, A. G.; Consortium, Greater Middle East Variome; Alkuraya, F. S.; Casanova, J. L.; Gleeson, J. G.; Rahim, S. A.; Abdel-Hadi, S.; Abdel-Salam, G.; Abdel-Salam, E.; Abdou, M.; Abhytankar, A.; Adimi, P.; Ahmad, J.; Akcakus, M.; Aksu, G.; Hajjar, S. A.; Juamaah, S. A.; Muhsen, S. A.; Sannaa, N. A.; Tameni, S. A.; Al-Aama, J.; Al-Allawi, N.; Al-Baradie, R.; Al-Gazali, L.; Al-Hashem, A.; Al-Herz, W.; Al-Jeaid, D.; Al-Tawari, A.; Alangari, A.; Alcais, A.; AlFawaz, T.; Alsum, Z.; Ammar-Khodja, A.; Amouian, S.; Ammar-Khodja, A.; Arikan, C.; Aryani, O.; Aslanger, A.; Aydogmus, C.; Aytekin, C.; Azam, M.; Bansagi, B.; Barbouche, M. R.; Bastaki, L.; Ben-Omran, T.; Bindu, P. S.; Blancas, L.; Boisson-Dupuis, S.; Bonnet, D.; Stambouli, O. B.; Bousfiha, A.; Boussafara, L.; Boutros, J.; Bustamante, J.; Caksen, H.; Camcioglu, Y.; Catherinot, E.; Celik, F. C.; Ciancanelli, M.; Cipe, F. E.; Clark, G.; Cobat, A.; Comu, S.; Condie, A.; Condino-Neto, A.; Desai, M.; Dobyns, W.; Dogu, F.; Domaia, M.; Egritas, O.; Azbaoui, S. E.; Baghdadi, J. E.; Ruby, M. E.; El-Harouni, A.; Elfeky,R. A.; Elghazali, G.; Faqeih, E.; Fenerci, E.; Fieschi, C.; Funda, C.; Gamal, I.; Gelik, U.; Genel, F.; Gezdirici, A.; Girisha, K. M.; Goldstein, A.; Grattan-Smith, P.; Gupta, N.; Hahn, J.; Hatipoglu, N.; Hennekam, R.; Houshmand, M.; Ichai, P.; Ikinciogullari, A.; Ismail, S.; Jalas, C.; Jouanguy, E.; Kabra, M.; Kalkan, G.; Kara, M.; Karaca, N.; Karaer, K.; Kariminejad, A.; Kayserili, H.; Keser-Emiroglu, M.; Kilic, S. S.; Kissani, N.; Kokron, C.; Koul, R.; Kutukculer, N.; Lanternier, F.; Mahdaviani, A.; Mahlaoui, N.; Mansour, L.; Mansouri, D.; Margari, L.; Valente, E. M.; Marzouki, N.; Masri, A.; Megahed, A.; Megahed, H.; Mekki, N.; Mesdaghi, M.; Mikati, M.; Mojahedi, F.; Mulley, J.; Nampoothiri, S.; Navarrete, C.; Omar, T.; Oraby, A.; Pandaluz, A.; Parvaneh, N.; Patiroglu, T.; Koc, Z. P.; Pellier, I.; Picard, C.; Puel, A.; Raas-Rothschild, A.; Rajab, A.; Raoult, D.; Reisli, I.; Rezaei, N.; Sabri, A.; Sahin, Y.; Saleem, L.; Salem, F.; AlSediq, N. S.; Sanal, O.; Sanger, T.; Shakankiry, H.; Shang, L.; Shehata, N.; Shembesh, N.; Shkalim, V.; Softah, A.; Sogaty, S.; Soliman, N.; Sonmez Aunaci, F.; Sztriha, L.; Taibi-Berrah, L.; Temtamy, S.; Tonekaboni, H.; Trauner, D.; Tuysuz, B.; Varan, A.; Vogt, G.; Walsh, C.; Woods, G.; Yesil, G.; Yildiran, A.; Yildiz, B.; Yuksel, A.; Zaki, M.; Zhang, S. Y.
Fonte: Nature Genetics. Unidade: ICB
Assuntos: VARIAÇÃO GENÉTICA, GENÉTICA, GENÉTICA DE POPULAÇÕES, IMUNOLOGIA, ALELOS
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ABNT
SCOTT, Eric M. et al. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, v. 48, n. 9, p. 1071-1076, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3592. Acesso em: 21 out. 2025.
APA
Scott, E. M., Halees, A., Itan, Y., Spencer, E. G., He, Y., Azab, M. A., et al. (2016). Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, 48( 9), 1071-1076. doi:10.1038/ng.3592
NLM
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3592
Vancouver
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3592
Artigo de periodico
Identification of six new susceptibility loci for invasive epithelial ovarian cancer (2015)
Kuchenbaecker, Karoline B.; Coetzee, Simon G.; Noushmehr, Houtan
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: NEOPLASIAS EPITELIAIS E GLANDULARES (GENÉTICA), NEOPLASIAS OVARIANAS (GENÉTICA), POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KUCHENBAECKER, Karoline B. e COETZEE, Simon G. e NOUSHMEHR, Houtan. Identification of six new susceptibility loci for invasive epithelial ovarian cancer. Nature Genetics, v. 47, n. 2, p. 164–171, 2015Tradução . . Disponível em: https://doi.org/10.1038/ng.3185. Acesso em: 21 out. 2025.
APA
Kuchenbaecker, K. B., Coetzee, S. G., & Noushmehr, H. (2015). Identification of six new susceptibility loci for invasive epithelial ovarian cancer. Nature Genetics, 47( 2), 164–171. doi:10.1038/ng.3185
NLM
Kuchenbaecker KB, Coetzee SG, Noushmehr H. Identification of six new susceptibility loci for invasive epithelial ovarian cancer [Internet]. Nature Genetics. 2015 ; 47( 2): 164–171.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3185
Vancouver
Kuchenbaecker KB, Coetzee SG, Noushmehr H. Identification of six new susceptibility loci for invasive epithelial ovarian cancer [Internet]. Nature Genetics. 2015 ; 47( 2): 164–171.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.3185
Artigo de periodico
A worldwide survey of genome sequence variation provides insight into the evolutionary history of the honeybee Apis mellifera (2014)
Wallberg, Andreas; Han, Fan; Wellhagen, Gustaf; Dahle, Bjørn; Kawata, Masakado; Haddad, Nizar; Simoes, Zila Luz Paulino; Allsopp, Mike H; Kandemir, Irfan; De la Rúa, Pilar; Pirk, Christian W; Webster, Matthew T
Fonte: Nature Genetics. Unidade: FFCLRP
Assuntos: GENOMAS, ABELHAS, SEQUENCIAMENTO GENÉTICO
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ABNT
WALLBERG, Andreas et al. A worldwide survey of genome sequence variation provides insight into the evolutionary history of the honeybee Apis mellifera. Nature Genetics, v. 46, n. 10, p. 1081-1088, 2014Tradução . . Disponível em: https://doi.org/10.138/ng.3077. Acesso em: 21 out. 2025.
APA
Wallberg, A., Han, F., Wellhagen, G., Dahle, B., Kawata, M., Haddad, N., et al. (2014). A worldwide survey of genome sequence variation provides insight into the evolutionary history of the honeybee Apis mellifera. Nature Genetics, 46( 10), 1081-1088. doi:10.138/ng.3077
NLM
Wallberg A, Han F, Wellhagen G, Dahle B, Kawata M, Haddad N, Simoes ZLP, Allsopp MH, Kandemir I, De la Rúa P, Pirk CW, Webster MT. A worldwide survey of genome sequence variation provides insight into the evolutionary history of the honeybee Apis mellifera [Internet]. Nature Genetics. 2014 ; 46( 10): 1081-1088.[citado 2025 out. 21 ] Available from: https://doi.org/10.138/ng.3077
Vancouver
Wallberg A, Han F, Wellhagen G, Dahle B, Kawata M, Haddad N, Simoes ZLP, Allsopp MH, Kandemir I, De la Rúa P, Pirk CW, Webster MT. A worldwide survey of genome sequence variation provides insight into the evolutionary history of the honeybee Apis mellifera [Internet]. Nature Genetics. 2014 ; 46( 10): 1081-1088.[citado 2025 out. 21 ] Available from: https://doi.org/10.138/ng.3077
Artigo de periodico
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice (2013)
Keller, Annika; Westenberger, Ana; Sobrido, Maria J; Zatz, Mayana
Fonte: Nature Genetics. Unidade: IB
Assuntos: MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
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ABNT
KELLER, Annika et al. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nature Genetics, v. 45, n. 9, p. 2013. online, 2013Tradução . . Disponível em: https://doi.org/10.1038/ng.2723. Acesso em: 21 out. 2025.
APA
Keller, A., Westenberger, A., Sobrido, M. J., & Zatz, M. (2013). Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nature Genetics, 45( 9), 2013. online. doi:10.1038/ng.2723
NLM
Keller A, Westenberger A, Sobrido MJ, Zatz M. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice [Internet]. Nature Genetics. 2013 ; 45( 9): 2013. online.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2723
Vancouver
Keller A, Westenberger A, Sobrido MJ, Zatz M. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice [Internet]. Nature Genetics. 2013 ; 45( 9): 2013. online.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2723
Artigo de periodico
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer (2013)
Noushmehr, Houtan
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: NEOPLASIAS OVARIANAS, INTERAÇÃO GENÓTIPO-AMBIENTE, POLIMORFISMO, FATORES DE RISCO, ESTUDOS DE CASOS E CONTROLES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOUSHMEHR, Houtan. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. Nature Genetics, v. 45, n. 4, p. 362-370, 2013Tradução . . Disponível em: https://doi.org/10.1038/ng.2564. Acesso em: 21 out. 2025.
APA
Noushmehr, H. (2013). GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. Nature Genetics, 45( 4), 362-370. doi:10.1038/ng.2564
NLM
Noushmehr H. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer [Internet]. Nature Genetics. 2013 ; 45( 4): 362-370.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2564
Vancouver
Noushmehr H. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer [Internet]. Nature Genetics. 2013 ; 45( 4): 362-370.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2564
Artigo de periodico
The cancer genome atlas pan-cancer analysis project (2013)
Weinstein, John N.; Collison, Eric A.; Mills, Gordon B.; Shaw, Kenna R. Mills; Ozenberger, Brad A.; Ellrott, Kyle; Shmulevich, Ilya; Sander, Chris; Stuart, Joshua M.; Noushmehr, Houtan
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: GENOMAS, NEOPLASIAS, ATLAS, GENÉTICA MOLECULAR
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ABNT
WEINSTEIN, John N. et al. The cancer genome atlas pan-cancer analysis project. Nature Genetics, v. 45, n. 10, p. 1113-1120, 2013Tradução . . Disponível em: https://doi.org/10.1038/ng.2764. Acesso em: 21 out. 2025.
APA
Weinstein, J. N., Collison, E. A., Mills, G. B., Shaw, K. R. M., Ozenberger, B. A., Ellrott, K., et al. (2013). The cancer genome atlas pan-cancer analysis project. Nature Genetics, 45( 10), 1113-1120. doi:10.1038/ng.2764
NLM
Weinstein JN, Collison EA, Mills GB, Shaw KRM, Ozenberger BA, Ellrott K, Shmulevich I, Sander C, Stuart JM, Noushmehr H. The cancer genome atlas pan-cancer analysis project [Internet]. Nature Genetics. 2013 ; 45( 10): 1113-1120.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2764
Vancouver
Weinstein JN, Collison EA, Mills GB, Shaw KRM, Ozenberger BA, Ellrott K, Shmulevich I, Sander C, Stuart JM, Noushmehr H. The cancer genome atlas pan-cancer analysis project [Internet]. Nature Genetics. 2013 ; 45( 10): 1113-1120.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.2764
Artigo de periodico
SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas (2009)
Bass, Adam J; Watanabe, Hideo; Mermel, Craig H; Yu, Soyoung; Perner, Sven; Verhaak, Roel G; Kim, So Young; Wardwell, Leslie; Tamayo, Pablo; Gat-Viks, Irit; Ramos, Alex H; Woo, Michele S; Weir, Barbara A; Getz, Gad; Beroukhim, Rameen; O'Kelly, Michael; Dutt, Amit; Rozenblatt-Rosen, Orit; Dziunycz, Piotr; Komisarof, Justin; Chirieac, Lucian R; LaFargue, Christopher J; Scheblel, Veit; Wilbertz, Theresia; Ma, Changqing; Rao, Shilpa; Nakagawa, Hiroshi; Stairs, Douglas; Lin Lin; Giordano, Thomas J; Wagner, Patrick; Minna, John D; Gazdar, Adi F; Zhu, Chang Qi; Brose, Marcia S; Cecconello, Ivan; Ribeiro Junior, Ulysses; Marie, Suely Kazue Nagahashi; Dahl, Olav; Shivdasani, Ramesh A; Tsao, Ming-Sound; Rubin, Mark A; Wong, Kwok; Regev, Aviv; Hahn, William C; Rustgi, Anil K; Meyerson, Matthew
Fonte: Nature Genetics. Unidade: FM
Assuntos: ONCOGENES, NEOPLASIAS PULMONARES, NEOPLASIAS ESOFÁGICAS, CARCINOMA DE CÉLULAS ESCAMOSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASS, Adam J et al. SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas. Nature Genetics, v. 41, n. 11, p. 1238-1244, 2009Tradução . . Disponível em: https://doi.org/10.1038/ng.465. Acesso em: 21 out. 2025.
APA
Bass, A. J., Watanabe, H., Mermel, C. H., Yu, S., Perner, S., Verhaak, R. G., et al. (2009). SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas. Nature Genetics, 41( 11), 1238-1244. doi:10.1038/ng.465
NLM
Bass AJ, Watanabe H, Mermel CH, Yu S, Perner S, Verhaak RG, Kim SY, Wardwell L, Tamayo P, Gat-Viks I, Ramos AH, Woo MS, Weir BA, Getz G, Beroukhim R, O'Kelly M, Dutt A, Rozenblatt-Rosen O, Dziunycz P, Komisarof J, Chirieac LR, LaFargue CJ, Scheblel V, Wilbertz T, Ma C, Rao S, Nakagawa H, Stairs D, Lin Lin, Giordano TJ, Wagner P, Minna JD, Gazdar AF, Zhu CQ, Brose MS, Cecconello I, Ribeiro Junior U, Marie SKN, Dahl O, Shivdasani RA, Tsao M-S, Rubin MA, Wong K, Regev A, Hahn WC, Rustgi AK, Meyerson M. SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas [Internet]. Nature Genetics. 2009 ; 41( 11): 1238-1244.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.465
Vancouver
Bass AJ, Watanabe H, Mermel CH, Yu S, Perner S, Verhaak RG, Kim SY, Wardwell L, Tamayo P, Gat-Viks I, Ramos AH, Woo MS, Weir BA, Getz G, Beroukhim R, O'Kelly M, Dutt A, Rozenblatt-Rosen O, Dziunycz P, Komisarof J, Chirieac LR, LaFargue CJ, Scheblel V, Wilbertz T, Ma C, Rao S, Nakagawa H, Stairs D, Lin Lin, Giordano TJ, Wagner P, Minna JD, Gazdar AF, Zhu CQ, Brose MS, Cecconello I, Ribeiro Junior U, Marie SKN, Dahl O, Shivdasani RA, Tsao M-S, Rubin MA, Wong K, Regev A, Hahn WC, Rustgi AK, Meyerson M. SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas [Internet]. Nature Genetics. 2009 ; 41( 11): 1238-1244.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.465
Artigo de periodico
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma (2009)
Northcott, Paul A.; Nakahara, Yukiko; Wu, Xiaochong; Freuk, Lars; Ellison, David W.; Croul, Sid; Mack, Stephen; Kongkham, Paul N.; Peacock, John; Dubuc, Adrian; Ra, Young-Shin; Zilberberg, Karen; Mcleod, Jessica; Scherer, Stephen W.; Rao, J. Sunil; Eberhart, Charles G.; Grajkowska, Wiesia; Gillespie, Yancey; Lach, Boleslaw; Grundy, Richard; Pollack, Ian F.; Hamilton, Ronald L.; Meter, Timothy Van; Carlotti Júnior, Carlos Gilberto; Boop, Frederick; Bigner, Darrell; Gilbertson, Richard J.; Rutka, James T.; Taylor, Michael D.
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: NEOPLASIAS CEREBRAIS, CRIANÇAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NORTHCOTT, Paul A. et al. Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma. Nature Genetics, v. 41, n. 4, p. 465-472, 2009Tradução . . Disponível em: https://doi.org/10.1038/ng.336. Acesso em: 21 out. 2025.
APA
Northcott, P. A., Nakahara, Y., Wu, X., Freuk, L., Ellison, D. W., Croul, S., et al. (2009). Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma. Nature Genetics, 41( 4), 465-472. doi:10.1038/ng.336
NLM
Northcott PA, Nakahara Y, Wu X, Freuk L, Ellison DW, Croul S, Mack S, Kongkham PN, Peacock J, Dubuc A, Ra Y-S, Zilberberg K, Mcleod J, Scherer SW, Rao JS, Eberhart CG, Grajkowska W, Gillespie Y, Lach B, Grundy R, Pollack IF, Hamilton RL, Meter TV, Carlotti Júnior CG, Boop F, Bigner D, Gilbertson RJ, Rutka JT, Taylor MD. Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma [Internet]. Nature Genetics. 2009 ; 41( 4): 465-472.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.336
Vancouver
Northcott PA, Nakahara Y, Wu X, Freuk L, Ellison DW, Croul S, Mack S, Kongkham PN, Peacock J, Dubuc A, Ra Y-S, Zilberberg K, Mcleod J, Scherer SW, Rao JS, Eberhart CG, Grajkowska W, Gillespie Y, Lach B, Grundy R, Pollack IF, Hamilton RL, Meter TV, Carlotti Júnior CG, Boop F, Bigner D, Gilbertson RJ, Rutka JT, Taylor MD. Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma [Internet]. Nature Genetics. 2009 ; 41( 4): 465-472.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.336
Artigo de periodico
Multiple ADH genes are associated with upper aerodigestive cancers (2008)
Hashibe, Mia; McKay, James D.; Curado, Maria Paula; Oliveira, Jose Carlos; Koifman, Sergio; Koifman, Rosalina; Zaridze, David; Shangina, Oxana; Wünsch Filho, Victor ; Eluf Neto, José; Levi, Jose Eduardo; Matos, Elena; Lagiou, Pagona; Lagiou, Areti; Benhamou, Simone; Bouchardy, Christine; Szesznia-Dabrowska, Neonilia; Menezes, Ana; Dall`Agnol, Marinel Mór; Merletti, Franco; Richiardi, Lorenzo; Fernandez, Leticia; Lence, Juan; Talamini, Renato; Barzan, Luigi; Mates, Dana; Mates, Ioan Nicolae; Kjaerheim, Kristina; Macfarlane, Gary J.; Macfarlane, Tatiana V.; Simonato, Lorenzo; Canova, Cristina; Holcátová, Ivana; Agudo, Antonio; Castellsagué, Xavier; Lowry, Ray; Janout, Vladimir; Kollarova, Helena; Conway, David I.; McKinney, Patricia A.; Znaor, Ariana; Fabianova, Eleonara; Bencko, Vladimir; Lissowska, Jolanta; Chabrier, Amelie; Hung, Rayean J.; Gaborieau, Valerie; Boffetta, Paolo; Brennan, Paul
Fonte: Nature Genetics. Unidade: FM
Assuntos: FATORES DE RISCO, ALCOOLISMO, NEOPLASIAS DO SISTEMA DIGESTÓRIO, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HASHIBE, Mia et al. Multiple ADH genes are associated with upper aerodigestive cancers. Nature Genetics, v. 40, n. 6, p. 707-709, 2008Tradução . . Disponível em: https://doi.org/10.1038/ng.151. Acesso em: 21 out. 2025.
APA
Hashibe, M., McKay, J. D., Curado, M. P., Oliveira, J. C., Koifman, S., Koifman, R., et al. (2008). Multiple ADH genes are associated with upper aerodigestive cancers. Nature Genetics, 40( 6), 707-709. doi:10.1038/ng.151
NLM
Hashibe M, McKay JD, Curado MP, Oliveira JC, Koifman S, Koifman R, Zaridze D, Shangina O, Wünsch Filho V, Eluf Neto J, Levi JE, Matos E, Lagiou P, Lagiou A, Benhamou S, Bouchardy C, Szesznia-Dabrowska N, Menezes A, Dall`Agnol MM, Merletti F, Richiardi L, Fernandez L, Lence J, Talamini R, Barzan L, Mates D, Mates IN, Kjaerheim K, Macfarlane GJ, Macfarlane TV, Simonato L, Canova C, Holcátová I, Agudo A, Castellsagué X, Lowry R, Janout V, Kollarova H, Conway DI, McKinney PA, Znaor A, Fabianova E, Bencko V, Lissowska J, Chabrier A, Hung RJ, Gaborieau V, Boffetta P, Brennan P. Multiple ADH genes are associated with upper aerodigestive cancers [Internet]. Nature Genetics. 2008 ; 40( 6): 707-709.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.151
Vancouver
Hashibe M, McKay JD, Curado MP, Oliveira JC, Koifman S, Koifman R, Zaridze D, Shangina O, Wünsch Filho V, Eluf Neto J, Levi JE, Matos E, Lagiou P, Lagiou A, Benhamou S, Bouchardy C, Szesznia-Dabrowska N, Menezes A, Dall`Agnol MM, Merletti F, Richiardi L, Fernandez L, Lence J, Talamini R, Barzan L, Mates D, Mates IN, Kjaerheim K, Macfarlane GJ, Macfarlane TV, Simonato L, Canova C, Holcátová I, Agudo A, Castellsagué X, Lowry R, Janout V, Kollarova H, Conway DI, McKinney PA, Znaor A, Fabianova E, Bencko V, Lissowska J, Chabrier A, Hung RJ, Gaborieau V, Boffetta P, Brennan P. Multiple ADH genes are associated with upper aerodigestive cancers [Internet]. Nature Genetics. 2008 ; 40( 6): 707-709.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng.151
Artigo de periodico
Comparative genomic analysis of three Leishmania species that cause diverse human disease (2007)
Peacock, Christopher S.; Seeger, Kathy; Harris, David; Muphy, Lee; Ruiz, Jeronimo C.; Quail, Michael A.; Peters, N.; Adlem, Ellen; Tivey, Adrian; Aslett, Martin; Kerhornou, Arnaud; Ivens, Alasdair; Fraser, A.; Rajandream, Marie-Adele; Carver, Tim; Norbertczak, Halina; Chillingworth, Tracey; Hance, Z.; Jagels, Kay; Moule, Sharon; Ormond, Doug; Rutter, Simon; Squares, Rob; Whitehead, Sally; Rabbinowitsch, Ester; Arrowsmith, Claire; White, Brian; Thurston, Scott; Bringaud, Fréderic; Baldauf, Sandra L.; Faulconbridge, Adam; Jeffares, Daniel; Depledge, Daniel P.; Oyola, Samuel O.; Hilley, James D.; Brito, Loislene O.; Barrell, Barclay; Cruz, Ângela Kaysel; Mottram, Jeremy C.; Smith, Deborah F.; Berriman, Matthew
Fonte: Nature Genetics. Unidade: FMRP
Assuntos: LEISHMANIA, GENOMAS (ANÁLISE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEACOCK, Christopher S. et al. Comparative genomic analysis of three Leishmania species that cause diverse human disease. Nature Genetics, v. 39, n. 7, p. 839-847, 2007Tradução . . Disponível em: https://doi.org/10.1038/ng2053. Acesso em: 21 out. 2025.
APA
Peacock, C. S., Seeger, K., Harris, D., Muphy, L., Ruiz, J. C., Quail, M. A., et al. (2007). Comparative genomic analysis of three Leishmania species that cause diverse human disease. Nature Genetics, 39( 7), 839-847. doi:10.1038/ng2053
NLM
Peacock CS, Seeger K, Harris D, Muphy L, Ruiz JC, Quail MA, Peters N, Adlem E, Tivey A, Aslett M, Kerhornou A, Ivens A, Fraser A, Rajandream M-A, Carver T, Norbertczak H, Chillingworth T, Hance Z, Jagels K, Moule S, Ormond D, Rutter S, Squares R, Whitehead S, Rabbinowitsch E, Arrowsmith C, White B, Thurston S, Bringaud F, Baldauf SL, Faulconbridge A, Jeffares D, Depledge DP, Oyola SO, Hilley JD, Brito LO, Barrell B, Cruz ÂK, Mottram JC, Smith DF, Berriman M. Comparative genomic analysis of three Leishmania species that cause diverse human disease [Internet]. Nature Genetics. 2007 ; 39( 7): 839-847.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng2053
Vancouver
Peacock CS, Seeger K, Harris D, Muphy L, Ruiz JC, Quail MA, Peters N, Adlem E, Tivey A, Aslett M, Kerhornou A, Ivens A, Fraser A, Rajandream M-A, Carver T, Norbertczak H, Chillingworth T, Hance Z, Jagels K, Moule S, Ormond D, Rutter S, Squares R, Whitehead S, Rabbinowitsch E, Arrowsmith C, White B, Thurston S, Bringaud F, Baldauf SL, Faulconbridge A, Jeffares D, Depledge DP, Oyola SO, Hilley JD, Brito LO, Barrell B, Cruz ÂK, Mottram JC, Smith DF, Berriman M. Comparative genomic analysis of three Leishmania species that cause diverse human disease [Internet]. Nature Genetics. 2007 ; 39( 7): 839-847.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng2053
Artigo de periodico
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability (2006)
Shaw-Smith, Charles; Pittman, Alan M.; Willatt, Lionel; Martin, Howard; Rickman, Lisa; Gribble, Susan; Curley, Rebecca; Cumming, Sally; Dunn, Carolyn; Kalaitzopoulos, Dimitrios; Porter, Keith R.; Prigmore, Elena; Krepischi, Ana Cristina Victorino ; Varela, Monica Castro; Koiffmann, Celia Priszkulnik ; Lees, Andrew J.; Rosenberg, Carla ; Firth, Helen V.; Silva, Rohan de; Carter, Nigel P.
Fonte: Nature Genetics. Unidade: IB
Assuntos: ANORMALIDADES CROMOSSÔMICAS, MALFORMAÇÕES, GENÉTICA MÉDICA, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHAW-SMITH, Charles et al. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics, v. 38, n. 9, p. 1032-1037, 2006Tradução . . Disponível em: https://doi.org/10.1038/ng1858. Acesso em: 21 out. 2025.
APA
Shaw-Smith, C., Pittman, A. M., Willatt, L., Martin, H., Rickman, L., Gribble, S., et al. (2006). Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics, 38( 9), 1032-1037. doi:10.1038/ng1858
NLM
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter KR, Prigmore E, Krepischi ACV, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, Silva R de, Carter NP. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability [Internet]. Nature Genetics. 2006 ; 38( 9): 1032-1037.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng1858
Vancouver
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter KR, Prigmore E, Krepischi ACV, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, Silva R de, Carter NP. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability [Internet]. Nature Genetics. 2006 ; 38( 9): 1032-1037.[citado 2025 out. 21 ] Available from: https://doi.org/10.1038/ng1858

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