Výsledky vyhledávání - Vives, Laura

Bivalent domains enforce transcriptional memory of DNA methylated genes in cancer cells Autor Rodriguez, Jairo, Muñoz, Mar, Vives, Laura, Frangou, Costas G., Groudine, Mark, Peinado, Miguel A.

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Genome-wide tracking of unmethylated DNA Alu repeats in normal and cancer cells Autor Rodriguez, Jairo, Vives, Laura, Jordà, Mireia, Morales, Cristina, Muñoz, Mar, Vendrell, Elisenda, Peinado, Miguel A.

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Hominoid fission of chromosome 14/15 and the role of segmental duplications Autor Giannuzzi, Giuliana, Pazienza, Michele, Huddleston, John, Antonacci, Francesca, Malig, Maika, Vives, Laura, Eichler, Evan E., Ventura, Mario

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Detection of structural variants and indels within exome data Autor Karakoc, Emre, Alkan, Can, O’Roak, Brian J., Dennis, Megan, Vives, Laura, Mark, Kenneth, Rieder, Mark J., Nickerson, Debbie A., Eichler, Evan E.

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Transmission Disequilibrium of Small CNVs in Simplex Autism Autor Krumm, Niklas, O’Roak, Brian J., Karakoc, Emre, Mohajeri, Kiana, Nelson, Ben, Vives, Laura, Jacquemont, Sebastien, Munson, Jeff, Bernier, Raphe, Eichler, Evan E.

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The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2 Autor Ventura, Mario, Catacchio, Claudia R., Sajjadian, Saba, Vives, Laura, Sudmant, Peter H., Marques-Bonet, Tomas, Graves, Tina A., Wilson, Richard K., Eichler, Evan E.

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Corrigendum: The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2 Autor Ventura, Mario, Catacchio, Claudia R., Sajjadian, Saba, Vives, Laura, Sudmant, Peter H., Marques-Bonet, Tomas, Graves, Tina A., Wilson, Richard K., Eichler, Evan E.

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Accelerated exon evolution within primate segmental duplications Autor Lorente-Galdos, Belen, Bleyhl, Jonathan, Santpere, Gabriel, Vives, Laura, Ramírez, Oscar, Hernandez, Jessica, Anglada, Roger, Cooper, Gregory M, Navarro, Arcadi, Eichler, Evan E, Marques-Bonet, Tomas

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Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms Autor Campbell, Catarina D., Sampas, Nick, Tsalenko, Anya, Sudmant, Peter H., Kidd, Jeffrey M., Malig, Maika, Vu, Tiffany H., Vives, Laura, Tsang, Peter, Bruhn, Laurakay, Eichler, Evan E.

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Excess of rare, inherited truncating mutations in autism Autor Krumm, Niklas, Turner, Tychele N., Baker, Carl, Vives, Laura, Mohajeri, Kiana, Witherspoon, Kali, Raja, Archana, Coe, Bradley P., Stessman, Holly A., He, Zong-Xiao, Leal, Suzanne M., Bernier, Raphael, Eichler, Evan E.

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Estimating human mutation rate using autozygosity in a founder population Autor Campbell, Catarina D., Chong, Jessica X., Malig, Maika, Ko, Arthur, Dumont, Beth L., Han, Lide, Vives, Laura, O’Roak, Brian J., Sudmant, Peter H., Shendure, Jay, Abney, Mark, Ober, Carole, Eichler, Evan E.

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Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes Autor Girirajan, Santhosh, Brkanac, Zoran, Coe, Bradley P., Baker, Carl, Vives, Laura, Vu, Tiffany H., Shafer, Neil, Bernier, Raphael, Ferrero, Giovanni B., Silengo, Margherita, Warren, Stephen T., Moreno, Carlos S., Fichera, Marco, Romano, Corrado, Raskind, Wendy H., Eichler, Evan E.

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations Autor O’Roak, Brian J., Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J., Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P., Ng, Sarah B., Baker, Carl, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Fisher, Simon E., Shendure, Jay, Eichler, Evan E.

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Discovery and genotyping of structural variation from long-read haploid genome sequence data Autor Huddleston, John, Chaisson, Mark J.P., Steinberg, Karyn Meltz, Warren, Wes, Hoekzema, Kendra, Gordon, David, Graves-Lindsay, Tina A., Munson, Katherine M., Kronenberg, Zev N., Vives, Laura, Peluso, Paul, Boitano, Matthew, Chin, Chen-Shin, Korlach, Jonas, Wilson, Richard K., Eichler, Evan E.

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Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data Autor Huddleston, John, Chaisson, Mark J.P., Steinberg, Karyn Meltz, Warren, Wes, Hoekzema, Kendra, Gordon, David, Graves-Lindsay, Tina A., Munson, Katherine M., Kronenberg, Zev N., Vives, Laura, Peluso, Paul, Boitano, Matthew, Chin, Chen-Shin, Korlach, Jonas, Wilson, Richard K., Eichler, Evan E.

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A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk Autor Antonacci, Francesca, Kidd, Jeffrey M., Marques-Bonet, Tomas, Teague, Brian, Ventura, Mario, Girirajan, Santhosh, Alkan, Can, Campbell, Catarina D., Vives, Laura, Malig, Maika, Rosenfeld, Jill A., Ballif, Blake C., Shaffer, Lisa G., Graves, Tina A., Wilson, Richard K., Schwartz, David C., Eichler, Evan E.

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Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability Autor Antonacci, Francesca, Dennis, Megan Y., Huddleston, John, Sudmant, Peter H., Steinberg, Karyn Meltz, Rosenfeld, Jill A., Miroballo, Mattia, Graves, Tina A., Vives, Laura, Malig, Maika, Denman, Laura, Raja, Archana, Stuart, Andrew, Tang, Joyce, Munson, Brenton, Shaffer, Lisa G., Amemiya, Chris T., Wilson, Richard K., Eichler, Evan E.

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Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism Autor Steinberg, Karyn Meltz, Antonacci, Francesca, Sudmant, Peter H., Kidd, Jeffrey M., Campbell, Catarina D., Vives, Laura, Malig, Maika, Scheinfeldt, Laura, Beggs, William, Ibrahim, Muntaser, Lema, Godfrey, Nyambo, Thomas B., Omar, Sabah A., Bodo, Jean-Marie, Froment, Alain, Donnelly, Michael P., Kidd, Kenneth K., Tishkoff, Sarah A., Eichler, Evan E.

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations Autor O’Roak, Brian J., Vives, Laura, Girirajan, Santhosh, Karakoc, Emre, Krumm, Nik, Coe, Bradley P., Levy, Roie, Ko, Arthur, Lee, Choli, Smith, Joshua D., Turner, Emily H., Stanaway, Ian B., Vernot, Benjamin, Malig, Maika, Baker, Carl, Reilly, Beau, Akey, Joshua M., Borenstein, Elhanan, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Shendure, Jay, Eichler, Evan E.

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Role of targeted therapies in rheumatic patients on COVID-19 outcomes: results from the COVIDSER study Autor Álvaro Gracia, Jose María, Sanchez-Piedra, Carlos, Manero, Javier, Ruiz-Lucea, María Ester, López-Vives, Laura, Bohorquez, Cristina, Martinez-Barrio, Julia, Bonilla, Gema, Vela, Paloma, García-Villanueva, María Jesús, Navío-Marco, María Teresa, Pavía, Marina, Galindo, María, Erausquin, Celia, Gonzalez-Gay, Miguel A, Rua-Figueroa, Inigo, Pego-Reigosa, Jose M, Castrejon, Isabel, Sanchez-Costa, Jesús T, González-Dávila, Enrique, Diaz-Gonzalez, Federico

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