MicroRNAs in β-Cell Biology, Insulin Resistance, Diabetes and Its Complications

por Fernandez-Valverde, Selene L., Taft, Ryan J., Mattick, John S.
Publicado 2011

The relationship between transcription initiation RNAs and CCCTC-binding factor (CTCF) localization

por Taft, Ryan J, Hawkins, Peter G, Mattick, John S, Morris, Kevin V
Publicado 2011

Estimating the burden and economic impact of pediatric genetic disease

por Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Publicado 2018

Correction: Estimating the burden and economic impact of pediatric genetic disease

por Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.
Publicado 2019

Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases

por Bick, David, Jones, Marilyn, Taylor, Stacie L, Taft, Ryan J, Belmont, John
Publicado 2019

Diverse RNA interference strategies in early-branching metazoans

por Calcino, Andrew D., Fernandez-Valverde, Selene L., Taft, Ryan J., Degnan, Bernard M.
Publicado 2018

Systematic interrogation of the Conus marmoreus venom duct transcriptome with ConoSorter reveals 158 novel conotoxins and 13 new gene superfamilies

por Lavergne, Vincent, Dutertre, Sébastien, Jin, Ai-hua, Lewis, Richard J, Taft, Ryan J, Alewood, Paul F
Publicado 2013

Information compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interest

por Hudson, Nicholas J, Porto-Neto, Laercio R, Kijas, James, McWilliam, Sean, Taft, Ryan J, Reverter, Antonio
Publicado 2014

The diagnostic trajectory of infants and children with clinical features of genetic disease

por Schroeder, Brock E., Gonzaludo, Nina, Everson, Katie, Than, Kyi-Sin, Sullivan, Jeff, Taft, Ryan J., Belmont, John W.
Publicado 2021

Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data

por Chen, Xiao, Shen, Fei, Gonzaludo, Nina, Malhotra, Alka, Rogert, Cande, Taft, Ryan J., Bentley, David R., Eberle, Michael A.
Publicado 2021

Publisher Correction: Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data

por Chen, Xiao, Shen, Fei, Gonzaludo, Nina, Malhotra, Alka, Rogert, Cande, Taft, Ryan J., Bentley, David R., Eberle, Michael A.
Publicado 2022

Identification of miR-29b targets using 3-cyanovinylcarbazole containing mimics

por Choudhary, Anupma, Vanichkina, Darya P., Ender, Christine, Crawford, Joanna, Baillie, Gregory J., Calcino, Andrew D., Ru, Kelin, Taft, Ryan J.
Publicado 2018

Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III–related leukodystrophy and Feingold syndrome

por Muirhead, Kayla J., Clause, Amanda R., Schlachetzki, Zinayida, Dubbs, Holly, Perry, Denise L., Hagelstrom, R. Tanner, Taft, Ryan J., Vanderver, Adeline
Publicado 2021

Identification of nuclear-enriched miRNAs during mouse granulopoiesis

por Wong, Justin JL, Ritchie, William, Gao, Dadi, Lau, Katherine A, Gonzalez, Maria, Choudhary, Anupma, Taft, Ryan J, Rasko, John EJ, Holst, Jeff
Publicado 2014

Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient

por Miller, David K., Menezes, Minal J., Simons, Cas, Riley, Lisa G., Cooper, Sandra T., Grimmond, Sean M., Thorburn, David R., Christodoulou, John, Taft, Ryan J.
Publicado 2014

Genome-wide discovery of human splicing branchpoints

por Mercer, Tim R., Clark, Michael B., Andersen, Stacey B., Brunck, Marion E., Haerty, Wilfried, Crawford, Joanna, Taft, Ryan J., Nielsen, Lars K., Dinger, Marcel E., Mattick, John S.
Publicado 2015

Human iPSC-Derived Cerebellar Neurons from a Patient with Ataxia-Telangiectasia Reveal Disrupted Gene Regulatory Networks

por Nayler, Sam P., Powell, Joseph E., Vanichkina, Darya P., Korn, Othmar, Wells, Christine A., Kanjhan, Refik, Sun, Jian, Taft, Ryan J., Lavin, Martin F., Wolvetang, Ernst J.
Publicado 2017

DNA methylation regulates discrimination of enhancers from promoters through a H3K4me1-H3K4me3 seesaw mechanism

por Sharifi-Zarchi, Ali, Gerovska, Daniela, Adachi, Kenjiro, Totonchi, Mehdi, Pezeshk, Hamid, Taft, Ryan J., Schöler, Hans R., Chitsaz, Hamidreza, Sadeghi, Mehdi, Baharvand, Hossein, Araúzo-Bravo, Marcos J.
Publicado 2017

Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

por Clause, Amanda R., Taylor, Julie P., Rajkumar, Revathi, Bluske, Krista, Bennett, Maren, Amendola, Laura M., Bentley, David R., Taft, Ryan J., Perry, Denise L., Coffey, Alison J.
Publicado 2023

Expression of Transposable Elements in Neural Tissues during Xenopus Development

por Faunes, Fernando, Sanchez, Natalia, Moreno, Mauricio, Olivares, Gonzalo H., Lee-Liu, Dasfne, Almonacid, Leonardo, Slater, Alex W., Norambuena, Tomas, Taft, Ryan J., Mattick, John S., Melo, Francisco, Larrain, Juan
Publicado 2011