Positional dependence of transcriptional inhibition by DNA torsional stress in yeast chromosomes

por Joshi, Ricky S, Piña, Benjamin, Roca, Joaquim
Publicado 2010

Topoisomerase II is required for the production of long Pol II gene transcripts in yeast

por Joshi, Ricky S., Piña, Benjamin, Roca, Joaquim
Publicado 2012

Structure and Chromosomal Organization of Yeast Genes Regulated by Topoisomerase II

por Joshi, Ricky S., Nikolaou, Christoforos, Roca, Joaquim
Publicado 2018

A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome

por Garg, Paras, Joshi, Ricky S., Watson, Corey, Sharp, Andrew J.
Publicado 2018

The DNA methylation landscape of human cancer organoids available at the American type culture collection

por Joshi, Ricky, Castro De Moura, Manuel, Piñeyro, David, Alvarez-Errico, Damiana, Arribas, Carles, Esteller, Manel
Publicado 2020

Intracellular nucleosomes constrain a DNA linking number difference of −1.26 that reconciles the Lk paradox

por Segura, Joana, Joshi, Ricky S., Díaz-Ingelmo, Ofelia, Valdés, Antonio, Dyson, Silvia, Martínez-García, Belén, Roca, Joaquim
Publicado 2018

Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans

por Quilez, Javier, Guilmatre, Audrey, Garg, Paras, Highnam, Gareth, Gymrek, Melissa, Erlich, Yaniv, Joshi, Ricky S., Mittelman, David, Sharp, Andrew J.
Publicado 2016

Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3

por Joshi, Ricky, Shvartsman, Maya, Morán, Erica, Lois, Sergi, Aranda, Jessica, Barqué, Anna, de la Cruz, Xavier, Bruguera, Miquel, Vagace, José Manuel, Gervasini, Guillermo, Sanz, Cristina, Sánchez, Mayka
Publicado 2015

Epigenetic loss of the transfer RNA-modifying enzyme TYW2 induces ribosome frameshifts in colon cancer

por Rosselló-Tortella, Margalida, Llinàs-Arias, Pere, Sakaguchi, Yuriko, Miyauchi, Kenjyo, Davalos, Veronica, Setien, Fernando, Calleja-Cervantes, Maria E., Piñeyro, David, Martínez-Gómez, Jesús, Guil, Sonia, Joshi, Ricky, Villanueva, Alberto, Suzuki, Tsutomu, Esteller, Manel
Publicado 2020

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

por Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E. L. M., de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi
Publicado 2021

Identification of rare de novo epigenetic variations in congenital disorders

por Barbosa, Mafalda, Joshi, Ricky S., Garg, Paras, Martin-Trujillo, Alejandro, Patel, Nihir, Jadhav, Bharati, Watson, Corey T., Gibson, William, Chetnik, Kelsey, Tessereau, Chloe, Mei, Hui, De Rubeis, Silvia, Reichert, Jennifer, Lopes, Fatima, Vissers, Lisenka E. L. M., Kleefstra, Tjitske, Grice, Dorothy E., Edelmann, Lisa, Soares, Gabriela, Maciel, Patricia, Brunner, Han G., Buxbaum, Joseph D., Gelb, Bruce D., Sharp, Andrew J.
Publicado 2018