Torthaí cuardaigh - Shankaracharya,

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  1. 1
    Computational Intelligence in Early Diabetes Diagnosis: A Review

    Computational Intelligence in Early Diabetes Diagnosis: A Review de réir Shankaracharya, Odedra, Devang, Samanta, Subir, Vidyarthi, Ambarish S.

    Foilsithe / Cruthaithe 2010
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  2. 2
    Computational Intelligence-Based Diagnosis Tool for the Detection of Prediabetes and Type 2 Diabetes in India

    Computational Intelligence-Based Diagnosis Tool for the Detection of Prediabetes and Type 2 Diabetes in India de réir Shankaracharya, Odedra, Devang, Samanta, Subir, Vidyarthi, Ambarish S.

    Foilsithe / Cruthaithe 2012
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  3. 3
    Computational Intelligence in Early Diabetes Diagnosis: A Review

    Computational Intelligence in Early Diabetes Diagnosis: A Review de réir N.A. Shankaracharya, Devang Odedra, Subir Samanta, Ambarish S. Vidyarthi

    Foilsithe / Cruthaithe 2010
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  4. 4
    Java-Based Diabetes Type 2 Prediction Tool for Better Diagnosis

    Java-Based Diabetes Type 2 Prediction Tool for Better Diagnosis de réir Shankaracharya, Odedra, Devang, Mallick, Medhavi, Shukla, Prateek, Samanta, Subir, Vidyarthi, Ambarish S.

    Foilsithe / Cruthaithe 2012
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  5. 5
    Electrochemical Performance of β-Nis@Ni(OH)(2) Nanocomposite for Water Splitting Applications

    Electrochemical Performance of β-Nis@Ni(OH)(2) Nanocomposite for Water Splitting Applications de réir Jansi Rani, Balasubramanian, Dhivya, Nagasundaram, Ravi, Ganesan, Zance, Shankaracharya S., Yuvakkumar, Rathinam, Hong, Sun Ig

    Foilsithe / Cruthaithe 2019
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  6. 6
    <i>ATXN2</i> intermediate expansions in amyotrophic lateral sclerosis

    <i>ATXN2</i> intermediate expansions in amyotrophic lateral sclerosis de réir Jonathan D. Glass, Ramita Dewan, Jinhui Ding, J. Raphael Gibbs, Clifton L. Dalgard, Pamela Keagle, Shankaracharya, Alberto García‐Redondo, Bryan J. Traynor, Ruth Chia, John E. Landers

    Foilsithe / Cruthaithe 2022
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  7. 7
    Relationship Estimation from Whole-Genome Sequence Data

    Relationship Estimation from Whole-Genome Sequence Data de réir Li, Hong, Glusman, Gustavo, Hu, Hao, Shankaracharya, Caballero, Juan, Hubley, Robert, Witherspoon, David, Guthery, Stephen L., Mauldin, Denise E., Jorde, Lynn B., Hood, Leroy, Roach, Jared C., Huff, Chad D.

    Foilsithe / Cruthaithe 2014
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  8. 8
    Relationship Estimation from Whole-Genome Sequence Data

    Relationship Estimation from Whole-Genome Sequence Data de réir Hong Li, Gustavo Glusman, Hao Hu, N.A. Shankaracharya, Juan Caballero-Pérez, Robert Hubley, David J. Witherspoon, Stephen L. Guthery, Denise E. Mauldin, Lynn B. Jorde, Leroy Hood, Jared C. Roach, Chad Huff

    Foilsithe / Cruthaithe 2014
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  9. 9
    Role of Lysosomal Gene Variants in Modulating <scp><i>GBA</i></scp>‐Associated Parkinson's Disease Risk

    Role of Lysosomal Gene Variants in Modulating <scp><i>GBA</i></scp>‐Associated Parkinson's Disease Risk de réir Letizia Straniero, Valeria Rimoldi, Edoardo Monfrini, Salvatore Bonvegna, Giada Melistaccio, Julie Lake, Giulia Soldà, Massimo Aureli, Shankaracharya, Pamela Keagle, Tatiana Foroud, John E. Landers, Cornelis Blauwendraat, Anna Zecchinelli, Roberto Cilia, Alessio Di Fonzo, Gianni Pezzoli, Stefano Duga, Rosanna Asselta

    Foilsithe / Cruthaithe 2022
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  10. 10
    Role of Lysosomal Gene Variants in Modulating GBA ‐Associated Parkinson's Disease Risk

    Role of Lysosomal Gene Variants in Modulating GBA ‐Associated Parkinson's Disease Risk de réir Straniero, Letizia, Rimoldi, Valeria, Monfrini, Edoardo, Bonvegna, Salvatore, Melistaccio, Giada, Lake, Julie, Soldà, Giulia, Aureli, Massimo, Shankaracharya, Keagle, Pamela, Foroud, Tatiana, Landers, John E., Blauwendraat, Cornelis, Zecchinelli, Anna, Cilia, Roberto, Di Fonzo, Alessio, Pezzoli, Gianni, Duga, Stefano, Asselta, Rosanna

    Foilsithe / Cruthaithe 2022
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  11. 11
    ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function

    ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function de réir Desiree M. Baron, Adam R. Fenton, Sara Sáez-Atiénzar, Anthony Giampetruzzi, Aparna Sreeram, Shankaracharya, Pamela Keagle, Victoria R. Doocy, Nathan J. Smith, Eric Danielson, Megan Andresano, Mary C. McCormack, Jaqueline Garcia, Valérie Bercier, Ludo Van Den Bosch, Jonathan R. Brent, Claudia Fallini, Bryan J. Traynor, Erika L.F. Holzbaur, John E. Landers

    Foilsithe / Cruthaithe 2022
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  12. 12
    Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

    Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease de réir Paul J. Hop, Dongbing Lai, Pamela Keagle, Desiree M. Baron, Brendan Kenna, Maarten Kooyman, Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I. Soto‐Beasley, Zbigniew K. Wszołek, Ryan J. Uitti, Ioannis U. Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A. Ross, Jan H. Veldink, Tatiana Foroud, Kevin Kenna, John E. Landers

    Foilsithe / Cruthaithe 2024
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  13. 13
    ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function

    ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function de réir Baron, Desiree M., Fenton, Adam R., Saez-Atienzar, Sara, Giampetruzzi, Anthony, Sreeram, Aparna, Shankaracharya, Keagle, Pamela J., Doocy, Victoria R., Smith, Nathan J., Danielson, Eric W., Andresano, Megan, McCormack, Mary C., Garcia, Jaqueline, Bercier, Valérie, Van Den Bosch, Ludo, Brent, Jonathan R., Fallini, Claudia, Traynor, Bryan J., Holzbaur, Erika L.F., Landers, John E.

    Foilsithe / Cruthaithe 2022
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  14. 14
    Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia

    Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia de réir Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, Shankaracharya, Matthew Unger, Karly M. Stallworth, Debra Cameron, Melissa Rotunno, Pepper Dawes, Megan Fowler, Pamela Keagle, Justin A. McDonough, Sivakumar Boopathy, Miguel Sena‐Esteves, Jeffrey A. Nickerson, Cathleen Lutz, William C. Skarnes, Elaine T. Lim, Dorothy P. Schafer, Francesca Massi, John E. Landers, Daryl A. Bosco

    Foilsithe / Cruthaithe 2024
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  15. 15
    A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

    A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data de réir Hu, Hao, Roach, Jared C, Coon, Hilary, Guthery, Stephen L, Voelkerding, Karl V, Margraf, Rebecca L, Durtschi, Jacob D, Tavtigian, Sean V, Shankaracharya, Wu, Wilfred, Scheet, Paul, Wang, Shuoguo, Xing, Jinchuan, Glusman, Gustavo, Hubley, Robert, Li, Hong, Garg, Vidu, Moore, Barry, Hood, Leroy, Galas, David J, Srivastava, Deepak, Reese, Martin G, Jorde, Lynn B, Yandell, Mark, Huff, Chad D

    Foilsithe / Cruthaithe 2014
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  16. 16
    A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

    A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data de réir Hao Hu, Jared C. Roach, Hilary Coon, Stephen L. Guthery, Karl V. Voelkerding, Rebecca L. Margraf, Jacob Durtschi, Sean V. Tavtigian, N.A. Shankaracharya, Wilfred Wu, Paul Scheet, Shuoguo Wang, Jinchuan Xing, Gustavo Glusman, Robert Hubley, Hong Li, Vidu Garg, Barry Moore, Leroy Hood, David J. Galas, Deepak Srivastava, Martin G. Reese, Lynn B. Jorde, Mark Yandell, Chad D. Huff

    Foilsithe / Cruthaithe 2014
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  17. 17
    Rare Mutations in <i>RINT1</i> Predispose Carriers to Breast and Lynch Syndrome–Spectrum Cancers

    Rare Mutations in <i>RINT1</i> Predispose Carriers to Breast and Lynch Syndrome–Spectrum Cancers de réir Daniel J. Park, Kayoko Tao, Florence Le Calvez‐Kelm, Tú Nguyen‐Dumont, Nivonirina Robinot, Fleur Hammet, Fabrice Odefrey, Helen Tsimiklis, Zhi L. Teo, Louise B. Thingholm, Erin L. Young, Catherine Voegele, Andrew Lonie, Bernard J. Pope, Terrell C. Roane, Russell Bell, Hao Hu, N.A. Shankaracharya, Chad Huff, Jonathan J. Ellis, Jun Li, Igor V. Makunin, Esther M. John, Irene L. Andrulis, Mary Beth Terry, Mary B. Daly, Saundra S. Buys, Carrie Snyder, Henry T. Lynch, Peter Devilee, Graham G. Giles, John L. Hopper, Bing Feng, Fabienne Lesueur, Sean V. Tavtigian, Melissa C. Southey, David E. Goldgar

    Foilsithe / Cruthaithe 2014
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  18. 18
    Rare mutations in RINT1 predispose carriers to breast and Lynch Syndrome-spectrum cancers

    Rare mutations in RINT1 predispose carriers to breast and Lynch Syndrome-spectrum cancers de réir Park, Daniel J., Tao, Kayoko, Le Calvez-Kelm, Florence, Nguyen-Dumont, Tu, Robinot, Nivonirina, Hammet, Fleur, Odefrey, Fabrice, Tsimiklis, Helen, Teo, Zhi L., Thingholm, Louise B., Young, Erin L., Voegele, Catherine, Lonie, Andrew, Pope, Bernard J., Roane, Terrell C., Bell, Russell, Hu, Hao, Shankaracharya, Huff, Chad D., Ellis, Jonathan, Li, Jun, Makunin, Igor V., John, Esther M., Andrulis, Irene L., Terry, Mary B., Daly, Mary, Buys, Saundra S., Snyder, Carrie, Lynch, Henry T., Devilee, Peter, Giles, Graham G., Hopper, John L., Feng, Bing J., Lesueur, Fabienne, Tavtigian, Sean V., Southey, Melissa C., Goldgar, David E.

    Foilsithe / Cruthaithe 2014
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  19. 19
    CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis

    CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis de réir Carol Dobson‐Stone, Marianne Hallupp, Hamideh Shahheydari, Audrey Ragagnin, Zac Chatterton, Francine Carew‐Jones, Claire E. Shepherd, Holly Stefen, Esmeralda Parić, Thomas Fath, Elizabeth M. Thompson, Peter Blumbergs, Cathy L. Short, Colin D. Field, Peter K. Panegyres, Jane Hecker, Garth A. Nicholson, Alex D. Shaw, Janice M. Fullerton, Agnes A. Luty, Peter R. Schofield, William S. Brooks, Neil Rajan, Mark F. Bennett, Melanie Bahlo, N.A. Shankaracharya, John E. Landers, Olivier Piguet, John R. Hodges, Glenda M. Halliday, Simon Topp, Bradley Smith, Christopher E. Shaw, Emily P. McCann, Jennifer A. Fifita, Kelly L. Williams, Julie D. Atkin, Ian P. Blair, John B. Kwok

    Foilsithe / Cruthaithe 2020
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  20. 20
    CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis

    CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis de réir Dobson-Stone, Carol, Hallupp, Marianne, Shahheydari, Hamideh, Ragagnin, Audrey M G, Chatterton, Zac, Carew-Jones, Francine, Shepherd, Claire E, Stefen, Holly, Paric, Esmeralda, Fath, Thomas, Thompson, Elizabeth M, Blumbergs, Peter, Short, Cathy L, Field, Colin D, Panegyres, Peter K, Hecker, Jane, Nicholson, Garth, Shaw, Alex D, Fullerton, Janice M, Luty, Agnes A, Schofield, Peter R, Brooks, William S, Rajan, Neil, Bennett, Mark F, Bahlo, Melanie, Shankaracharya, Landers, John E, Piguet, Olivier, Hodges, John R, Halliday, Glenda M, Topp, Simon D, Smith, Bradley N, Shaw, Christopher E, McCann, Emily, Fifita, Jennifer A, Williams, Kelly L, Atkin, Julie D, Blair, Ian P, Kwok, John B

    Foilsithe / Cruthaithe 2020
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