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Material Type: Artigo
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Challenges and disparities in the application of personalized genomic medicine to populations with African ancestryKessler, Michael D ; Yerges-Armstrong, Laura ; Taub, Margaret A ; Shetty, Amol C ; Maloney, Kristin ; Jeng, Linda Jo Bone ; Ruczinski, Ingo ; Levin, Albert M ; Williams, L Keoki ; Beaty, Terri H ; Mathias, Rasika A ; Barnes, Kathleen C ; O'Connor, Timothy DNature communications, 2016-10, Vol.7 (1), p.12521-12521, Article 12521 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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CXCR4 and CXCR7 transduce through mTOR in human renal cancer cellsIeranò, C ; Santagata, S ; Napolitano, M ; Guardia, F ; Grimaldi, A ; Antignani, E ; Botti, G ; Consales, C ; Riccio, A ; Nanayakkara, M ; Barone, M V ; Caraglia, M ; Scala, SCell death & disease, 2014-07, Vol.5 (7), p.e1310-e1310 [Periódico revisado por pares]England: Springer Nature B.VTexto completo disponível |
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Material Type: Artigo
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Identifying tagging SNPs for African specific genetic variation from the African Diaspora GenomeJohnston, Henry Richard ; Hu, Yi-Juan ; Gao, Jingjing ; O'Connor, Timothy D ; Abecasis, Gonçalo R ; Wojcik, Genevieve L ; Gignoux, Christopher R ; Gourraud, Pierre-Antoine ; Lizee, Antoine ; Hansen, Mark ; Genuario, Rob ; Bullis, Dave ; Lawley, Cindy ; Kenny, Eimear E ; Bustamante, Carlos ; Beaty, Terri H ; Mathias, Rasika A ; Barnes, Kathleen C ; Qin, Zhaohui SScientific reports, 2017-04, Vol.7 (1), p.46398-46398, Article 46398 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohortNagar, Shashwat Deepali ; Pemu, Priscilla ; Qian, Jun ; Boerwinkle, Eric ; Cicek, Mine ; Clark, Cheryl R ; Cohn, Elizabeth ; Gebo, Kelly ; Loperena, Roxana ; Mayo, Kelsey ; Mockrin, Stephen ; Ohno-Machado, Lucila ; Ramirez, Andrea H ; Schully, Sheri ; Able, Ashley ; Green, Ashley ; Zuchner, Stephan ; Jordan, I King ; Meller, RobertScientific reports, 2022-11, Vol.12 (1), p.19797-19797, Article 19797 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Machine Learning (ML) based-method applied in recurrent pregnancy loss (RPL) patients diagnostic work-up: a potential innovation in common clinical practiceBruno, V ; D'Orazio, M ; Ticconi, C ; Abundo, P ; Riccio, S ; Martinelli, E ; Rosato, N ; Piccione, E ; Zupi, E ; Pietropolli, AScientific reports, 2020-05, Vol.10 (1), p.7970-7970, Article 7970 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndromeCOOPER, Wendy N ; LUHARIA, Anita ; SCHOFIELD, Paul N ; REIK, Wolf ; MACDONALD, Fiona ; MAHER, Eamonn R ; EVANS, Gail A ; RAZA, Hussain ; HAIRE, Antonita C ; GRUNDY, Richard ; BOWDIN, Sarah C ; RICCIO, Andrea ; SEBASTIO, Gianfranco ; BLIEK, JetEuropean journal of human genetics : EJHG, 2005-09, Vol.13 (9), p.1025-1032 [Periódico revisado por pares]Avenel, NJ: Nature PublishingTexto completo disponível |
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Material Type: Artigo
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Second family with hearing impairment linked to 19q13 and refined DFNA4 localisationMirghomizadeh, Farhad ; Bardtke, Bettina ; Devoto, Marcella ; Pfister, Markus ; Oeken, Jens ; König, Elke ; Vitale, Emilia ; Riccio, Antonio ; De Rienzo, Assunta ; Zenner, Hans Peter ; Blin, NikolausEuropean journal of human genetics : EJHG, 2002-02, Vol.10 (2), p.95-99 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |