Taking U out, with two nucleases?

por Mian, I Saira, Worthey, Elizabeth A, Salavati, Reza
Publicado 2006

Comparative analysis of the kinomes of three pathogenic trypanosomatids: Leishmania major, Trypanosoma brucei and Trypanosoma cruzi

por Parsons, Marilyn, Worthey, Elizabeth A, Ward, Pauline N, Mottram, Jeremy C
Publicado 2005

Development of An Individualized Risk Prediction Model for COVID-19 Using Electronic Health Record Data

por Mamidi, Tarun Karthik Kumar, Tran-Nguyen, Thi K., Melvin, Ryan L., Worthey, Elizabeth A.
Publicado 2021

Rat Strain Ontology: structured controlled vocabulary designed to facilitate access to strain data at RGD

por Nigam, Rajni, Munzenmaier, Diane H, Worthey, Elizabeth A, Dwinell, Melinda R, Shimoyama, Mary, Jacob, Howard J
Publicado 2013

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech

por Worthey, Elizabeth A, Raca, Gordana, Laffin, Jennifer J, Wilk, Brandon M, Harris, Jeremy M, Jakielski, Kathy J, Dimmock, David P, Strand, Edythe A, Shriberg, Lawrence D
Publicado 2013

Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis

por Wilk, Melissa A., Braun, Andrew T., Farrell, Philip M., Laxova, Anita, Brown, Donna M., Holt, James M., Birch, Camille L., Sosonkina, Nadiya, Wilk, Brandon M., Worthey, Elizabeth A.
Publicado 2020

Ten simple rules for using public biological data for your research

por Oza, Vishal H., Whitlock, Jordan H., Wilk, Elizabeth J., Uno-Antonison, Angelina, Wilk, Brandon, Gajapathy, Manavalan, Howton, Timothy C., Trull, Austyn, Ianov, Lara, Worthey, Elizabeth A., Lasseigne, Brittany N.
Publicado 2023

The Rat Genome Database 2009: variation, ontologies and pathways

por Dwinell, Melinda R., Worthey, Elizabeth A., Shimoyama, Mary, Bakir-Gungor, Burcu, DePons, Jeffrey, Laulederkind, Stanley, Lowry, Timothy, Nigram, Rajni, Petri, Victoria, Smith, Jennifer, Stoddard, Alexander, Twigger, Simon N., Jacob, Howard J.
Publicado 2009

Disease pathways at the Rat Genome Database Pathway Portal: genes in context—a network approach to understanding the molecular mechanisms of disease

por Petri, Victoria, Hayman, G Thomas, Tutaj, Marek, Smith, Jennifer R, Laulederkind, Stanley JF, Wang, Shur-Jen, Nigam, Rajni, De Pons, Jeff, Shimoyama, Mary, Dwinell, Melinda R, Worthey, Elizabeth A, Jacob, Howard J
Publicado 2014

Analysis of disease-associated objects at the Rat Genome Database

por Wang, Shur-Jen, Laulederkind, Stanley J. F., Hayman, G. T., Smith, Jennifer R., Petri, Victoria, Lowry, Timothy F., Nigam, Rajni, Dwinell, Melinda R., Worthey, Elizabeth A., Munzenmaier, Diane H., Shimoyama, Mary, Jacob, Howard J.
Publicado 2013

The Rat Genome Database 2013—data, tools and users

por Laulederkind, Stanley J. F., Hayman, G. Thomas, Wang, Shur-Jen, Smith, Jennifer R., Lowry, Timothy F., Nigam, Rajni, Petri, Victoria, de Pons, Jeff, Dwinell, Melinda R., Shimoyama, Mary, Munzenmaier, Diane H., Worthey, Elizabeth A., Jacob, Howard J.
Publicado 2013

The clinical measurement, measurement method and experimental condition ontologies: expansion, improvements and new applications

por Smith, Jennifer R, Park, Carissa A, Nigam, Rajni, Laulederkind, Stanley JF, Hayman, G Thomas, Wang, Shur-Jen, Lowry, Timothy F, Petri, Victoria, Pons, Jeff De, Tutaj, Marek, Liu, Weisong, Worthey, Elizabeth A, Shimoyama, Mary, Dwinell, Melinda R
Publicado 2013

The pathway ontology – updates and applications

por Petri, Victoria, Jayaraman, Pushkala, Tutaj, Marek, Hayman, G Thomas, Smith, Jennifer R, De Pons, Jeff, Laulederkind, Stanley JF, Lowry, Timothy F, Nigam, Rajni, Wang, Shur-Jen, Shimoyama, Mary, Dwinell, Melinda R, Munzenmaier, Diane H, Worthey, Elizabeth A, Jacob, Howard J
Publicado 2014

VarSight: prioritizing clinically reported variants with binary classification algorithms

por Holt, James M., Wilk, Brandon, Birch, Camille L., Brown, Donna M., Gajapathy, Manavalan, Moss, Alexander C., Sosonkina, Nadiya, Wilk, Melissa A., Anderson, Julie A., Harris, Jeremy M., Kelly, Jacob M., Shaterferdosian, Fariba, Uno-Antonison, Angelina E., Weborg, Arthur, Worthey, Elizabeth A.
Publicado 2019

Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease

por Marshall, Christian R., Chowdhury, Shimul, Taft, Ryan J., Lebo, Mathew S., Buchan, Jillian G., Harrison, Steven M., Rowsey, Ross, Klee, Eric W., Liu, Pengfei, Worthey, Elizabeth A., Jobanputra, Vaidehi, Dimmock, David, Kearney, Hutton M., Bick, David, Kulkarni, Shashikant, Taylor, Stacie L., Belmont, John W., Stavropoulos, Dimitri J., Lennon, Niall J.
Publicado 2020

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

por Cochran, J. Nicholas, McKinley, Emily C., Cochran, Meagan, Amaral, Michelle D., Moyers, Bryan A., Lasseigne, Brittany N., Gray, David E., Lawlor, James M.J., Prokop, Jeremy W., Geier, Ethan G., Holt, James M., Thompson, Michelle L., Newberry, J. Scott, Yokoyama, Jennifer S., Worthey, Elizabeth A., Geldmacher, David S., Love, Marissa Natelson, Cooper, Gregory M., Myers, Richard M., Roberson, Erik D.
Publicado 2019

Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project

por Stenton, Sarah L., O’Leary, Melanie, Lemire, Gabrielle, VanNoy, Grace E., DiTroia, Stephanie, Ganesh, Vijay S., Groopman, Emily, O’Heir, Emily, Mangilog, Brian, Osei-Owusu, Ikeoluwa, Pais, Lynn S., Serrano, Jillian, Singer-Berk, Moriel, Weisburd, Ben, Wilson, Michael, Austin-Tse, Christina, Abdelhakim, Marwa, Althagafi, Azza, Babbi, Giulia, Bellazzi, Riccardo, Bovo, Samuele, Carta, Maria Giulia, Casadio, Rita, Coenen, Pieter-Jan, De Paoli, Federica, Floris, Matteo, Gajapathy, Manavalan, Hoehndorf, Robert, Jacobsen, Julius O.B., Joseph, Thomas, Kamandula, Akash, Katsonis, Panagiotis, Kint, Cyrielle, Lichtarge, Olivier, Limongelli, Ivan, Lu, Yulan, Magni, Paolo, Mamidi, Tarun Karthik Kumar, Martelli, Pier Luigi, Mulargia, Marta, Nicora, Giovanna, Nykamp, Keith, Pejaver, Vikas, Peng, Yisu, Pham, Thi Hong Cam, Podda, Maurizio S., Rao, Aditya, Rizzo, Ettore, Saipradeep, Vangala G, Savojardo, Castrense, Schols, Peter, Shen, Yang, Sivadasan, Naveen, Smedley, Damian, Soru, Dorian, Srinivasan, Rajgopal, Sun, Yuanfei, Sunderam, Uma, Tan, Wuwei, Tiwari, Naina, Wang, Xiao, Wang, Yaqiong, Williams, Amanda, Worthey, Elizabeth A., Yin, Rujie, You, Yuning, Zeiberg, Daniel, Zucca, Susanna, Bakolitsa, Constantina, Brenner, Steven E., Fullerton, Stephanie M, Radivojac, Predrag, Rehm, Heidi L., O’Donnell-Luria, Anne
Publicado 2023