Search Results - "White, Shana"

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    Harmonization of transcriptomic and methylomic analysis in environmental epidemiology studies for potential application in chemical risk assessment by Kim, Stephanie, White, Shana M., Radke, Elizabeth G., Dean, Jeffry L.

    Published in Environment international (01-06-2022)
    “…Recent efforts have posited the utility of transcriptomic-based approaches to understand chemical-related perturbations in the context of human health risk…”
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    Journal Article
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    A Biologic Combination of Lenalidomide and Rituximab for Front-Line Therapy of Indolent B-Cell Non-Hodgkin's Lymphoma by Fowler, Nathan, McLaughlin, Peter, Hagemeister, Fredrick B., Kwak, Larry, Fanale, Michelle, Neelapu, Sattva, Fayad, Luis, Pro, Barbara, Sergent, Crystal, White, Shana R.S., Samaniego, Felipe

    Published in Blood (20-11-2009)
    “…Abstract 1714▪▪This icon denotes an abstract that is clinically relevant. Poster Board I-740 Despite advances in therapy and a better understanding of the…”
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    Journal Article
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    A Quantitative Assessment of Tremor and Ataxia in Female FMR1 Premutation Carriers Using CATSYS by Narcisa, Vivien, Aguilar, Dalila, Nguyen, Danh V., Campos, Luis, Brodovsky, Jeffrey, White, Shana, Adams, Patrick, Tassone, Flora, Hagerman, Paul J., Hagerman, Randi J.

    “…The fragile X-associated tremor/ataxia syndrome (FXTAS) is a relatively common cause of balance problems leading to gait disturbances in older males (40%) with…”
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    Journal Article
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    Application and Development of Novel Methods for Pathway Analysis and Visualization of the LINCS L1000 Dataset by White, Shana

    Published 01-01-2021
    “…The LINCS L1000 dataset is a large-scale compendium that contains records of the cell line specific transcriptional effects of cellular perturbation that was…”
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    Dissertation
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    Rapid Genome Sequencing in the Critically Ill by Buchan, Jillian G, White, Shana, Joshi, Ruchi, Ashley, Euan A

    Published in Clinical chemistry (Baltimore, Md.) (01-06-2019)
    “…Solutions such as these address the accelerated processing and storage needed for the massive amounts of data generated by rGS, although these tools focus on…”
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    Journal Article
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    Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations by Lerner-Ellis, Jordan, Wang, Marina, White, Shana, Lebo, Matthew S

    Published in Journal of medical genetics (01-07-2015)
    “…The Canadian Open Genetics Repository is a collaborative effort for the collection, storage, sharing and robust analysis of variants reported by medical…”
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    Journal Article
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    Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students by White, Shana, Fisk, Dianna G., Rego, Shannon, Kohler, Jennefer N., Reuter, Chloe M., Bonner, Devon, Wheeler, Matthew T., Ormond, Kelly E., Hanson‐Kahn, Andrea K., Adams, David R., Aday, Aaron, Bacino, Carlos A., Balasubramanyam, Ashok, Barseghyan, Hayk, Batzli, Gabriel F., Bellen, Hugo J., Bernstein, Jonathan A., Bostwick, Bret L., Briere, Lauren C., Brokamp, Elly, Burrage, Lindsay C., Butte, Manish J., Chen, Shan, Clark, Gary D., Coakley, Terra R., Cogan, Joy D., Cope, Heidi, Craigen, William J., D'Souza, Precilla, Dayal, Jyoti G., Dorrani, Naghmeh, Enns, Gregory M., Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Gahl, William A., Gourdine, Jean‐Philippe F., Gropman, Andrea L., Haendel, Melissa, Johnston, Jean M., Krasnewich, Donna M., Lalani, Seema R., Lee, Brendan H., Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Majcherska, Marta M., Mamounas, Laura A., Marom, Ronit, Martin, Martin G., Martínez‐Agosto, Julian A., Marwaha, Shruti, McCormack, Colleen E., Might, Matthew, Morimoto, Marie, Mulvihill, John J., Murdock, David R., Murphy, Jennifer L., Scott Newberry, J., Nicholas, Sarah K., Novacic, Donna, Orange, Jordan S., Carl Pallais, J., Parker, Neil H., Potocki, Lorraine, Pusey, Barbara N., Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Samson, Susan L., Schoch, Kelly, Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Smith, Kevin S., Sullivan, Jennifer A., Tifft, Cynthia J., Urv, Tiina K., Vilain, Eric, Walley, Nicole M., Walsh, Chris A., Wangler, Michael F., Ward, Patricia A., Worthey, Elizabeth A., Yamamoto, Shinya, Yang, John, Yang, Yaping, Yoon, Amanda J., Yu, Guoyun, Zhao, Chunli, Zheng, Allison

    Published in Journal of genetic counseling (01-04-2019)
    “…With the wide adoption of next‐generation sequencing (NGS)‐based genetic tests, genetic counselors require increased familiarity with NGS technology, variant…”
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    Journal Article
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