Búsqueda | Portal de Búsqueda de la BVS Enfermería

1.

Establishing a blockchain-enabled Indigenous data sovereignty framework for genomic data.

Mackey, Tim K; Calac, Alec J; Chenna Keshava, B S; Yracheta, Joseph; Tsosie, Krystal S; Fox, Keolu.

Cell ; 185(15): 2626-2631, 2022 07 21.

Artículo en Inglés | MEDLINE | ID: mdl-35868267

2.

Paths and timings of the peopling of Polynesia inferred from genomic networks.

Ioannidis, Alexander G; Blanco-Portillo, Javier; Sandoval, Karla; Hagelberg, Erika; Barberena-Jonas, Carmina; Hill, Adrian V S; Rodríguez-Rodríguez, Juan Esteban; Fox, Keolu; Robson, Kathryn; Haoa-Cardinali, Sonia; Quinto-Cortés, Consuelo D; Miquel-Poblete, Juan Francisco; Auckland, Kathryn; Parks, Tom; Sofro, Abdul Salam M; Ávila-Arcos, María C; Sockell, Alexandra; Homburger, Julian R; Eng, Celeste; Huntsman, Scott; Burchard, Esteban G; Gignoux, Christopher R; Verdugo, Ricardo A; Moraga, Mauricio; Bustamante, Carlos D; Mentzer, Alexander J; Moreno-Estrada, Andrés.

Nature ; 597(7877): 522-526, 2021 09.

Artículo en Inglés | MEDLINE | ID: mdl-34552258

3.

Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data.

Hudson, Maui; Garrison, Nanibaa' A; Sterling, Rogena; Caron, Nadine R; Fox, Keolu; Yracheta, Joseph; Anderson, Jane; Wilcox, Phil; Arbour, Laura; Brown, Alex; Taualii, Maile; Kukutai, Tahu; Haring, Rodney; Te Aika, Ben; Baynam, Gareth S; Dearden, Peter K; Chagné, David; Malhi, Ripan S; Garba, Ibrahim; Tiffin, Nicki; Bolnick, Deborah; Stott, Matthew; Rolleston, Anna K; Ballantyne, Leah L; Lovett, Ray; David-Chavez, Dominique; Martinez, Andrew; Sporle, Andrew; Walter, Maggie; Reading, Jeff; Carroll, Stephanie Russo.

Nat Rev Genet ; 21(6): 377-384, 2020 06.

Artículo en Inglés | MEDLINE | ID: mdl-32251390

4.

ABO Genetic Variation in Neanderthals and Denisovans.

Villanea, Fernando A; Huerta-Sanchez, Emilia; Fox, Keolu.

Mol Biol Evol ; 38(8): 3373-3382, 2021 07 29.

Artículo en Inglés | MEDLINE | ID: mdl-33892510

5.

Why community consultation matters in genomic research benefit-sharing models.

LeBaron von Baeyer, Sarah; Crocker, Rebecca; Rakotoarivony, Rindra; Ranaivoarisoa, Jean Freddy; Spiral, Germain Jules; Castel, Stephane; Farnum, Andrew; Vance, Holly; Collins, Noah; Fox, Keolu; Wasik, Kaja.

Genome Res ; 34(1): 1-6, 2024 Feb 07.

Artículo en Inglés | MEDLINE | ID: mdl-38296591

6.

Genomics data: the broken promise is to Indigenous people.

Tsosie, Krystal S; Fox, Keolu; Yracheta, Joseph M.

Nature ; 591(7851): 529, 2021 03.

Artículo en Inglés | MEDLINE | ID: mdl-33742179

7.

Changing the wrapping won't fix genetic-racism package.

Jackson, Latifa; Tsosie, Krystal S; Fox, Keolu.

Nature ; 597(7877): 475, 2021 09.

Artículo en Inglés | MEDLINE | ID: mdl-34548642

8.

Ancient-DNA researchers write their own rules.

Tsosie, Krystal S; Bader, Alyssa C; Fox, Keolu; Bolnick, Deborah A; Garrison, Nanibaa' A; Smith, Rick W A.

Nature ; 600(7887): 37, 2021 12.

Artículo en Inglés | MEDLINE | ID: mdl-34848867

9.

Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.

Emde, Anne-Katrin; Phipps-Green, Amanda; Cadzow, Murray; Gallagher, C Scott; Major, Tanya J; Merriman, Marilyn E; Topless, Ruth K; Takei, Riku; Dalbeth, Nicola; Murphy, Rinki; Stamp, Lisa K; de Zoysa, Janak; Wilcox, Philip L; Fox, Keolu; Wasik, Kaja A; Merriman, Tony R; Castel, Stephane E.

BMC Genomics ; 22(1): 666, 2021 Nov 01.

Artículo en Inglés | MEDLINE | ID: mdl-34719381

10.

Use ancient remains more wisely.

Fox, Keolu; Hawks, John.

Nature ; 572(7771): 581-583, 2019 08.

Artículo en Inglés | MEDLINE | ID: mdl-31462783

11.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.

Polfus, Linda M; Khajuria, Rajiv K; Schick, Ursula M; Pankratz, Nathan; Pazoki, Raha; Brody, Jennifer A; Chen, Ming-Huei; Auer, Paul L; Floyd, James S; Huang, Jie; Lange, Leslie; van Rooij, Frank J A; Gibbs, Richard A; Metcalf, Ginger; Muzny, Donna; Veeraraghavan, Narayanan; Walter, Klaudia; Chen, Lu; Yanek, Lisa; Becker, Lewis C; Peloso, Gina M; Wakabayashi, Aoi; Kals, Mart; Metspalu, Andres; Esko, Tõnu; Fox, Keolu; Wallace, Robert; Franceschini, Nora; Matijevic, Nena; Rice, Kenneth M; Bartz, Traci M; Lyytikäinen, Leo-Pekka; Kähönen, Mika; Lehtimäki, Terho; Raitakari, Olli T; Li-Gao, Ruifang; Mook-Kanamori, Dennis O; Lettre, Guillaume; van Duijn, Cornelia M; Franco, Oscar H; Rich, Stephen S; Rivadeneira, Fernando; Hofman, Albert; Uitterlinden, André G; Wilson, James G; Psaty, Bruce M; Soranzo, Nicole; Dehghan, Abbas; Boerwinkle, Eric; Zhang, Xiaoling.

Am J Hum Genet ; 99(2): 481-8, 2016 08 04.

Artículo en Inglés | MEDLINE | ID: mdl-27486782

12.

The "All of Us" Program and Indigenous Peoples. Reply.

Fox, Keolu.

N Engl J Med ; 383(19): 1892-1893, 2020 11 05.

Artículo en Inglés | MEDLINE | ID: mdl-33211940

13.

The Illusion of Inclusion - The "All of Us" Research Program and Indigenous Peoples' DNA.

Fox, Keolu.

N Engl J Med ; 383(5): 411-413, 2020 Jul 30.

Artículo en Inglés | MEDLINE | ID: mdl-32726527

14.

Corrigendum to: ABO Genetic Variation in Neanderthals and Denisovans.

Villanea, Fernando A; Huerta-Sanchez, Emilia; Fox, Keolu.

Mol Biol Evol ; 38(12): 5835, 2021 Dec 09.

Artículo en Inglés | MEDLINE | ID: mdl-34622284

15.

Chaco Canyon Dig Unearths Ethical Concerns.

Claw, Katrina G; Lippert, Dorothy; Bardill, Jessica; Cordova, Anna; Fox, Keolu; Yracheta, Joseph M; Bader, Alyssa C; Bolnick, Deborah A; Malhi, Ripan S; TallBear, Kimberly; Garrison, Nanibaa' A.

Hum Biol ; 89(3): 177-180, 2017 07.

Artículo en Inglés | MEDLINE | ID: mdl-29745246

16.

Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.

Fox, Keolu; Johnsen, Jill M; Coe, Bradley P; Frazar, Chris D; Reiner, Alexander P; Eichler, Evan E; Nickerson, Deborah A.

Transfusion ; 56(11): 2744-2749, 2016 11.

Artículo en Inglés | MEDLINE | ID: mdl-27580710

17.

Global increases in both common and rare copy number load associated with autism.

Girirajan, Santhosh; Johnson, Rebecca L; Tassone, Flora; Balciuniene, Jorune; Katiyar, Neerja; Fox, Keolu; Baker, Carl; Srikanth, Abhinaya; Yeoh, Kian Hui; Khoo, Su Jen; Nauth, Therese B; Hansen, Robin; Ritchie, Marylyn; Hertz-Picciotto, Irva; Eichler, Evan E; Pessah, Isaac N; Selleck, Scott B.

Hum Mol Genet ; 22(14): 2870-80, 2013 Jul 15.

Artículo en Inglés | MEDLINE | ID: mdl-23535821

18.

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Auer, Paul L; Johnsen, Jill M; Johnson, Andrew D; Logsdon, Benjamin A; Lange, Leslie A; Nalls, Michael A; Zhang, Guosheng; Franceschini, Nora; Fox, Keolu; Lange, Ethan M; Rich, Stephen S; O'Donnell, Christopher J; Jackson, Rebecca D; Wallace, Robert B; Chen, Zhao; Graubert, Timothy A; Wilson, James G; Tang, Hua; Lettre, Guillaume; Reiner, Alex P; Ganesh, Santhi K; Li, Yun.

Am J Hum Genet ; 91(5): 794-808, 2012 Nov 02.

Artículo en Inglés | MEDLINE | ID: mdl-23103231

19.

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.

Johnsen, Jill M; Auer, Paul L; Morrison, Alanna C; Jiao, Shuo; Wei, Peng; Haessler, Jeffrey; Fox, Keolu; McGee, Sean R; Smith, Joshua D; Carlson, Christopher S; Smith, Nicholas; Boerwinkle, Eric; Kooperberg, Charles; Nickerson, Deborah A; Rich, Stephen S; Green, David; Peters, Ulrike; Cushman, Mary; Reiner, Alex P.

Blood ; 122(4): 590-7, 2013 Jul 25.

Artículo en Inglés | MEDLINE | ID: mdl-23690449

20.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.

Polfus, Linda M; Khajuria, Rajiv K; Schick, Ursula M; Pankratz, Nathan; Pazoki, Raha; Brody, Jennifer A; Chen, Ming-Huei; Auer, Paul L; Floyd, James S; Huang, Jie; Lange, Leslie; van Rooij, Frank J A; Gibbs, Richard A; Metcalf, Ginger; Muzny, Donna; Veeraraghavan, Narayanan; Walter, Klaudia; Chen, Lu; Yanek, Lisa; Becker, Lewis C; Peloso, Gina M; Wakabayashi, Aoi; Kals, Mart; Metspalu, Andres; Esko, Tõnu; Fox, Keolu; Wallace, Robert; Franceschini, Nora; Matijevic, Nena; Rice, Kenneth M; Bartz, Traci M; Lyytikäinen, Leo-Pekka; Kähönen, Mika; Lehtimäki, Terho; Raitakari, Olli T; Li-Gao, Ruifang; Mook-Kanamori, Dennis O; Lettre, Guillaume; van Duijn, Cornelia M; Franco, Oscar H; Rich, Stephen S; Rivadeneira, Fernando; Hofman, Albert; Uitterlinden, André G; Wilson, James G; Psaty, Bruce M; Soranzo, Nicole; Dehghan, Abbas; Boerwinkle, Eric; Zhang, Xiaoling.

Am J Hum Genet ; 99(3): 785, 2016 09 01.

Artículo en Inglés | MEDLINE | ID: mdl-27588453

Portal de Búsqueda de la BVS Enfermería

Información y Conocimiento para la Salud

Configurar filtros

Su selección (0)

Formato de exportación:

Exportar:

Establishing a blockchain-enabled Indigenous data sovereignty framework for genomic data.

Paths and timings of the peopling of Polynesia inferred from genomic networks.

Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data.

ABO Genetic Variation in Neanderthals and Denisovans.

Why community consultation matters in genomic research benefit-sharing models.

Genomics data: the broken promise is to Indigenous people.

Changing the wrapping won't fix genetic-racism package.

Ancient-DNA researchers write their own rules.

Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.

Use ancient remains more wisely.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.

The "All of Us" Program and Indigenous Peoples. Reply.

The Illusion of Inclusion - The "All of Us" Research Program and Indigenous Peoples' DNA.

Corrigendum to: ABO Genetic Variation in Neanderthals and Denisovans.

Chaco Canyon Dig Unearths Ethical Concerns.

Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.

Global increases in both common and rare copy number load associated with autism.

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.