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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
Source: Nature Genetics. Unidade: IB
Subjects: 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 nov. 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 nov. 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 nov. 03 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Artigo de periodico
Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. (2018)
Zhang, Jisen; Zhang, Xingtan; Tang, Haibao; Zhang, Qing; Hua, Xiuting; Ma, Xiaokai; Zhu, Fan; Jones, Tyler; Zhu, Xinguang; Bowers, John; Wai, Ching Man; Zheng, Chunfang; Shi, Yan; Chen, Shuai; Xu, Xiuming; Yue, Jingjing; Nelson, David R; Huang, Lixian; Li, Zhen; Xu, Huimin; Van Sluys, Marie-Anne ; Souza, Gláucia Mendes
Source: Nature Genetics. Unidades: IB, IQ
Subjects: GENOMAS, CANA-DE-AÇÚCAR, GENÉTICA VEGETAL, FITOPATÓGENOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZHANG, Jisen et al. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nature Genetics, v. 50, n. 11, p. 1565–1573, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41588-018-0237-2. Acesso em: 03 nov. 2024.
APA
Zhang, J., Zhang, X., Tang, H., Zhang, Q., Hua, X., Ma, X., et al. (2018). Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nature Genetics, 50( 11), 1565–1573. doi:10.1038/s41588-018-0237-2
NLM
Zhang J, Zhang X, Tang H, Zhang Q, Hua X, Ma X, Zhu F, Jones T, Zhu X, Bowers J, Wai CM, Zheng C, Shi Y, Chen S, Xu X, Yue J, Nelson DR, Huang L, Li Z, Xu H, Van Sluys M-A, Souza GM. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. [Internet]. Nature Genetics. 2018 ; 50( 11): 1565–1573.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41588-018-0237-2
Vancouver
Zhang J, Zhang X, Tang H, Zhang Q, Hua X, Ma X, Zhu F, Jones T, Zhu X, Bowers J, Wai CM, Zheng C, Shi Y, Chen S, Xu X, Yue J, Nelson DR, Huang L, Li Z, Xu H, Van Sluys M-A, Souza GM. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. [Internet]. Nature Genetics. 2018 ; 50( 11): 1565–1573.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41588-018-0237-2
Artigo de periodico
Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L (2018)
Zhang, Jisen; Zhang, Xingtan; Tang, Haibao; Zhang, Qing; Hua, Xiuting; Ma, Xiaokai; Zhu, Fan; Jones, Tyler; Zhu, Xinguang; Bowers, John; Wai, Ching Man; Zheng, Chunfang; Shi, Yan; Chen, Shuai; Xu, Xiuming; Yue, Jingjing; Nelson, David R; Huang, Lixian; Xu, Huimin; Van Sluys, Marie-Anne ; Souza, Gláucia Mendes
Source: Nature Genetics. Unidades: IB, IQ
Subjects: GENOMAS, CANA-DE-AÇÚCAR, GENÉTICA VEGETAL, FITOPATÓGENOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZHANG, Jisen et al. Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nature Genetics, v. 50, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41588-018-0293-7. Acesso em: 03 nov. 2024.
APA
Zhang, J., Zhang, X., Tang, H., Zhang, Q., Hua, X., Ma, X., et al. (2018). Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nature Genetics, 50. doi:10.1038/s41588-018-0293-7
NLM
Zhang J, Zhang X, Tang H, Zhang Q, Hua X, Ma X, Zhu F, Jones T, Zhu X, Bowers J, Wai CM, Zheng C, Shi Y, Chen S, Xu X, Yue J, Nelson DR, Huang L, Xu H, Van Sluys M-A, Souza GM. Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L [Internet]. Nature Genetics. 2018 ; 50[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41588-018-0293-7
Vancouver
Zhang J, Zhang X, Tang H, Zhang Q, Hua X, Ma X, Zhu F, Jones T, Zhu X, Bowers J, Wai CM, Zheng C, Shi Y, Chen S, Xu X, Yue J, Nelson DR, Huang L, Xu H, Van Sluys M-A, Souza GM. Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L [Internet]. Nature Genetics. 2018 ; 50[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41588-018-0293-7
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
Source: Nature Genetics. Unidade: FM
Subjects: FIBRILAÇÃO ATRIAL, METANÁLISE, DOENÇAS CARDIOVASCULARES, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1038/ng.3843
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
Source: Nature Genetics. Unidade: FSP
Subjects: NEOPLASIAS FARÍNGEAS, GENOMAS, NEOPLASIAS OROFARÍNGEAS, INCIDÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1038/ng.3685
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
Source: Nature Genetics. Unidade: FFCLRP
Subjects: GENOMAS, ABELHAS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.138/ng.3077
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
Source: Nature Genetics. Unidade: FMRP
Subjects: GENOMAS, NEOPLASIAS, ATLAS, GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1038/ng.2764

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