Search Results - "Shuldiner, Scott"

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    Predicting eyes at risk for rapid glaucoma progression based on an initial visual field test using machine learning by Shuldiner, Scott R, Boland, Michael V, Ramulu, Pradeep Y, De Moraes, C Gustavo, Elze, Tobias, Myers, Jonathan, Pasquale, Louis, Wellik, Sarah, Yohannan, Jithin

    Published in PloS one (16-04-2021)
    “…To assess whether machine learning algorithms (MLA) can predict eyes that will undergo rapid glaucoma progression based on an initial visual field (VF) test…”
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    Journal Article
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    Utility Assessment of Follow-up Evaluation for Commotio Retinae by Zhou, Henry W., Hoyek, Sandra, Savant, Shravan V., Shuldiner, Scott R., Armstrong, Grayson W., Miller, John B., Patel, Nimesh A.

    Published in Journal of vitreoretinal diseases (Print) (12-10-2024)
    “…Purpose: To perform an outcome-and-cost analysis of follow-up visits and associated imaging in patients presenting to the Massachusetts Eye and Ear (MEE)…”
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    Differential Phosphorylation of a Regulatory Subunit of Protein Kinase CK2 by Target of Rapamycin Complex 1 Signaling and the Cdc-like Kinase Kns1 by Sanchez-Casalongue, Manuel E., Lee, Jaehoon, Diamond, Aviva, Shuldiner, Scott, Moir, Robyn D., Willis, Ian M.

    Published in The Journal of biological chemistry (13-03-2015)
    “…Transcriptional regulation of ribosome and tRNA synthesis plays a central role in determining protein synthetic capacity and is tightly controlled in response…”
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    Journal Article
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    Myocardial Fibrosis Among Antiretroviral Therapy-Treated Persons With Human Immunodeficiency Virus in South Africa by Shuldiner, Scott R, Wong, Lye-Yeng, Peterson, Tess E, Wolfson, Julian, Jermy, S, Saad, H, Lumbamba, Mbalabu A J, Singh, A, Shey, M, Meintjes, G, Ntusi, N, Ntsekhe, M, Baker, J V

    Published in Open forum infectious diseases (01-01-2021)
    “…Abstract Background Heart failure is a prominent cardiovascular disease (CVD) manifestation in sub-Sarahan Africa. Myocardial fibrosis is a central feature of…”
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    Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels by Shen, Haiqing, Damcott, Coleen, Shuldiner, Scott R, Chai, Sumbul, Yang, Rongze, Hu, Hong, Gibson, Quince, Ryan, Kathleen A, Mitchell, Braxton D, Gong, Da-Wei

    Published in Journal of human genetics (01-11-2011)
    “…We carried out a genome-wide association study of serum aspartate aminotransferase (AST) activity in 866 Amish participants of the Heredity and Phenotype…”
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    Loss of function mutation in glutamic pyruvate transaminase 2 (GPT2) causes developmental encephalopathy by Celis, Katrina, Shuldiner, Scott, Haverfield, Eden V., Cappell, Joshua, Yang, Rongze, Gong, Da-Wei, Chung, Wendy K.

    Published in Journal of inherited metabolic disease (01-09-2015)
    “…Intellectual disability is genetically heterogeneous, and it is likely that many of the responsible genes have not yet been identified. We describe three…”
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  12. 12

    Methodological challenges in mapping chinese medicine syndrome with conventional diagnosis: Implications for multi-centre trials in integrative medicine by Shuldiner, Scott R., Chung, Vincent CH, Wu, Xinyin, Ching, Jessica, Ho, Robin ST, Cheong, Pui Kuan, Wong, Wendy, Wu, Justin CY

    Published in European journal of integrative medicine (01-08-2015)
    “…Chinese medicine (CM) diagnostic instruments are increasingly developed to classify patients into different syndrome subtypes, potentially allowing for…”
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    Journal Article