Ohcanbohtosat - Vives, Laura

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Accelerated exon evolution within primate segmental duplications Dahkki 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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Excess of rare, inherited truncating mutations in autism Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Estimating human mutation rate using autozygosity in a founder population Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Discovery and genotyping of structural variation from long-read haploid genome sequence data Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations Dahkki 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.

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta

Role of targeted therapies in rheumatic patients on COVID-19 outcomes: results from the COVIDSER study Dahkki 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

Viečča ollesdeavstta Viečča ollesdeavstta Viečča ollesdeavstta