Search Results - James Holt

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  1. 1
    Mesenteric and Retroperitoneal Cysts

    Mesenteric and Retroperitoneal Cysts by Robert J. Kurtz, Tomas M. Heimann, Asad Beck, James Holt

    Published 1986
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  2. 2
    FMLRC: Hybrid long read error correction using an FM-index

    FMLRC: Hybrid long read error correction using an FM-index by Jeremy Wang, James Holt, Leonard McMillan, Corbin D. Jones

    Published 2018
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  3. 3
    A novel multi-alignment pipeline for high-throughput sequencing data

    A novel multi-alignment pipeline for high-throughput sequencing data by Shun‐Ping Huang, James Holt, C.-Y. Kao, Leonard McMillan, Wei Wang

    Published 2014
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  4. 4
    HiPhase: jointly phasing small, structural, and tandem repeat variants from HiFi sequencing

    HiPhase: jointly phasing small, structural, and tandem repeat variants from HiFi sequencing by James Holt, Christopher T. Saunders, William J. Rowell, Zev Kronenberg, Aaron M. Wenger, Michael A. Eberle

    Published 2024
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  5. 5
    Sawfish: Improving long-read structural variant discovery and genotyping with local haplotype modeling

    Sawfish: Improving long-read structural variant discovery and genotyping with local haplotype modeling by Christopher T. Saunders, James Holt, Daniel Baker, Juniper A. Lake, Jonathan R. Belyeu, Zev Kronenberg, William J. Rowell, Michael A. Eberle

    Published 2025
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  6. 6
    Development and translation of thiometallate sulfide donors using a porcine model of coronary occlusion and reperfusion

    Development and translation of thiometallate sulfide donors using a porcine model of coronary occlusion and reperfusion by Tom Johnson, James Holt, Anna Kleyman, Shengyu Zhou, Eva Sammut, Vito Domenico Bruno, Charlotte Gaupp, Giacomo Stanzani, John Martin, Pietro Arina, Julia Deutsch, Raimondo Ascione, Mervyn Singer, Alex Dyson

    Published 2024
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  7. 7
    Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of<i>SLC12A2</i>

    Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of<i>SLC12A2</i> by Ellen F. Macnamara, Alanna E. Koehler, Precilla D’Souza, Tyra Estwick, Paul Lee, Gilbert Vézina, Harper B Fauni, Stephen R. Braddock, Erin Torti, James Holt, Prashant Sharma, May Christine V. Malicdan, Cynthia J. Tifft

    Published 2019
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  8. 8
    Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders

    Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders by Susan M. Hiatt, James M.J. Lawlor, Lori H. Handley, Ryne C. Ramaker, Brianne B. Rogers, E. Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher Plott, Jerry Jenkins, Stacy W. Gray, James Holt, Kevin M. Bowling, E. Martina Bebin, Jane Grimwood, Jeremy Schmutz, Gregory M. Cooper

    Published 2021
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  9. 9
    Epidemiological and cohort study finds no association between COVID-19 and Guillain-Barré syndrome

    Epidemiological and cohort study finds no association between COVID-19 and Guillain-Barré syndrome by Stephen Keddie, Julia Pakpoor, Christina Mousele, Menelaos Pipis, Pedro Machado, Mark Foster, Christopher J. Record, Ryan Keh, Janev Fehmi, Ross W. Paterson, Viraj Bharambe, Lisa M. Clayton, Claire Allen, Olivia Price, Jasmine Wall, Annamaria Kiss-Csenki, Devi Priya Rathnasabapathi, Ruth Geraldes, Tatyana Yermakova, Josh King‐Robson, Maya Zosmer, Sanjeev Rajakulendran, Sheetal Sumaria, Simon F. Farmer, Ross Nortley, Charles R. Marshall, Edward Newman, Niranjanan Nirmalananthan, Guru Kumar, Ashwin Pinto, James Holt, Tim Lavin, Kathryn M. Brennan, Michael S. Zandi, Dipa Jayaseelan, Jane Pritchard, Robert D. M. Hadden, Hadi Manji, Hugh J. Willison, Simon Rinaldi, Aisling Carr, Michael P. Lunn

    Published 2020
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  10. 10
    Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

    Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance by James J. Crowley, Vasyl Zhabotynsky, Wei Sun, Shun‐Ping Huang, Isa Kemal Pakatci, Yunjung Kim, Jeremy Wang, Andrew P. Morgan, John D. Calaway, David L. Aylor, Zaining Yun, Timothy A. Bell, Ryan J Buus, Mark Calaway, John P. Didion, Terry J. Gooch, Stephanie D Hansen, Nashiya N Robinson, Ginger D. Shaw, Jason S Spence, Corey R. Quackenbush, Cordelia J. Barrick, Randal J. Nonneman, Kyungsu Kim, James G. Xenakis, Yuying Xie, William Valdar, Alan Lenarcic, Wei Wang, Catherine E. Welsh, Chen-Ping Fu, Zhaojun Zhang, James Holt, Zhishan Guo, David W. Threadgill, Lisa M. Tarantino, Darla R. Miller, Fei Zou, Leonard McMillan, Patrick F. Sullivan, Fernando Pardo-Manuel de Villena

    Published 2015
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  11. 11
    <i>R2d2</i>Drives Selfish Sweeps in the House Mouse

    <i>R2d2</i>Drives Selfish Sweeps in the House Mouse by John P. Didion, Andrew P. Morgan, Liran Yadgary, Timothy A. Bell, Rachel McMullan, Lydia Ortiz de Solorzano, Janice Britton‐Davidian, Carol J. Bult, Karl J. Campbell, Riccardo Castiglia, Yung-Hao Ching, Amanda J. Chunco, James J. Crowley, Elissa J. Chesler, Daniel W. Förster, John E. French, Sofia I. Gabriel, Daniel M. Gatti, Theodore Garland, Eva B. Giagia-Athanasopoulou, Mabel D. Giménez, Sofia Grize, İslam Gündüz, Andrew Holmes, Heidi C. Hauffe, Jeremy S. Herman, James Holt, Kunjie Hua, Wesley J. Jolley, Anna K. Lindholm, María José López‐Fuster, George P. Mitsainas, María da Luz Mathias, Leonard McMillan, Maria da Graça Ramalhinho, Barbara Rehermann, Stephan P. Rosshart, Jeremy B. Searle, Meng‐Shin Shiao, Emanuela Solano, Karen L. Svenson, Patricia Thomas-Laemont, David W. Threadgill, Jacint Ventura, George M. Weinstock, Daniel Pomp, Gary A. Churchill, Fernando Pardo‐Manuel de Villena

    Published 2016
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  12. 12
    COVID-19 vaccination and Guillain-Barré syndrome: analyses using the National Immunoglobulin Database

    COVID-19 vaccination and Guillain-Barré syndrome: analyses using the National Immunoglobulin Database by Ryan Keh, Sophie Scanlon, Preeti Datta‐Nemdharry, Katherine Donegan, Sally Cavanagh, Mark Foster, David Skelland, James Palmer, Pedro Machado, Stephen Keddie, Aisling Carr, Michael P. Lunn, Hadi Manji, Tim Lavin, James B Lilleker, David Gosal, Robert D. M. Hadden, Taylor Watson-Fargie, Kathryn Brennan, Andreas C. Themistocleous, Jacquie Deeb, Ana M. Carrilho Romeiro, Puja R. Mehta, Dimitri M. Kullmann, James Miller, Amar Elsaddig, Adam Molyneux, Plamen Georgiev, Aaron Ben-Joseph, James Holt, Jacob Roelofs, Fadi Alkufri, David J. Allen, S Shields, Stephen Murphy, Harri Sivasathiaseelan, Richard Sylvester, Abdul Jabbar Omar Alsaleh, Rhys Roberts, Kannan Nithi, Lahiru Handdunnethi, Kate Wannop, Amit Batla, Anna Sadnicka, Jananee Sivaganasundaram, Tatyana Yermakova, Ravi Dasari, Graziella Quattrocchi, Harriet A. Ball, Rebecca Cooper, Daniel Whittam, Mohanned Mustafa, Gabriel Yiin, Shayan Ashjaei, Andrew J. Westwood, Michelle D'Souza, Eng Chuan Foo, Shwe Zin Tun, Khine Khine Lwin, Gorande Kanabar

    Published 2022
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  13. 13
    Oral fingolimod for chronic inflammatory demyelinating polyradiculoneuropathy (FORCIDP Trial): a double-blind, multicentre, randomised controlled trial

    Oral fingolimod for chronic inflammatory demyelinating polyradiculoneuropathy (FORCIDP Trial): a double-blind, multicentre, randomised controlled trial by Richard AC Hughes, Marinos C. Dalakas, Ingemar S. J. Merkies, Norman Latov, Jean‐Marc Léger, Eduardo Nobile‐Orazio, Gen Sobue, Angela Genge, David R. Cornblath, Martin Merschhemke, Carolyn M. Ervin, Catherine Agoropoulou, Hans‐Peter Hartung, Timothy Day, Judith Spies, L. Jackson Roberts, Philip Van Damme, P Y Van den Bergh, Alain Maertens De Noordhout, Annie Dionne, Sandrine Larue, Rami Massie, Michel Melanson, William Camu, de Sèze, Gwendal Le Masson, Jean Pouget, Jens Schmidt, Vasilios Κ. Kimiskidis, Joab Chapman, Vivian E. Drory, Raffaella Fazio, Francesca Gallia, Susumu Kusunoki, Masahiro Mori, Masahiro Iijima, Tomoko Okamoto, Masayuki Baba, Catharina G. Faber, Ivo N. van Schaik, Waldemar Fryze, Ewa Motta, Krzysztof Selmaj, Carlos Casasnovas, A. Guerrero Sola, Isabel Illa, James Holt, James Miller, Michael P. Lunn, Thomas H. Brannagan, M. Brown, J Kelemen, Stanley Iyadurai, Kourosh Rezania, Khema R. Sharma, Rup Tandan, Mark Gudesblatt, V. Lawson, Anthony A. Amato

    Published 2018
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  14. 14
    The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

    The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change by Heidi L. Rehm, Joseph T. Alaimo, Swaroop Aradhya, Pınar Bayrak‐Toydemir, Hunter Best, Rhonda Brandon, Jillian G. Buchan, Elizabeth Chao, Elaine Chen, Jacob Clifford, Ana S.A. Cohen, Laura K. Conlin, Soma Das, Kyle Davis, Daniela del Gaudio, Florencia Del Viso, Christina DiVincenzo, Marcia Eisenberg, Lucia Guidugli, Monia Hammer, Steven M. Harrison, Kathryn E. Hatchell, Lindsay Havens Dyer, Lily Hoang, James Holt, Vaidehi Jobanputra, Izabela Karbassi, Hutton M. Kearney, Melissa Kelly, Jacob M. Kelly, Michelle L. Kluge, Timothy Komala, Paul Kruszka, Lynette Lau, Matthew S. Lebo, Christian R. Marshall, Dianalee McKnight, Kirsty McWalter, Yan Meng, Narasimhan Nagan, Christian S. Neckelmann, Nir Neerman, Zhiyv Niu, Vitoria Paolillo, Sarah A Paolucci, Denise Perry, Tina Pesaran, Kelly Radtke, Kristen Rasmussen, Kyle Retterer, Carol Saunders, Elizabeth Spiteri, Christine M. Stanley, Anna Szuto, Ryan J. Taft, Isabelle Thiffault, Brittany C. Thomas, Amanda Thomas‐Wilson, Erin Thorpe, Timothy Tidwell, Meghan C. Towne, Hana Zouk, Christian Marshall, Linyan Meng, Vaidehi Jobanputra, Ryan J. Taft, Euan A. Ashley, Ghunwa Nakouzi, Wei Shen, Stephen F. Kingsmore, Heidi L. Rehm

    Published 2023
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  15. 15
    Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD

    Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD by Andrea Cortese, Maike F. Dohrn, Riccardo Currò, Sara Negri, Petra Laššuthová, Chiara Pisciotta, Stefano Tozza, Abdullah Al‐Ajmi, Changyoung Feng, Pedro José Tomaselli, Gorka Fernández‐Eulate, S. Haddad, Matilde Laurà, Alexander M. Rossor, Elisa Vegezzi, Stefano Facchini, James N. Sleigh, Adriana Rebelo, Danique Beijer, Jacquelyn Raposo, Mario Saporta, Barbora Lauerová, Helena F. Pernice, Pascal Achenbach, Ulrike Schöne, Tayir Alon, Marcus Deschauer, Isabell Cordts, Carolin D. Obermaier, Natalie Winter, Peter D. Creigh, Janet E. Sowden, Tyler Rehbein, Stefania Magri, Alessandro Bertini, Paola Saveri, Paolo Ripellino, Jingyu Huang, Aleksandra Nadaj-Pakleza, Alison Ross, James Holt, Kathryn M. Brennan, Rivka Sukenik‐Halevy, Varoona Bizaoui, Yeşim Parman, Esra Battaloğlu, Arman Çakar, Hadil Alrohaif, Simon Hammans, Kishore R. Kumar, Marina Kennerson, Hülya Kayserili, Defne A. Amado, Katrin Hahn, Paola Valentino, Francesca Cavalcanti, Carlo Gaetano, Franco Taroni, Geir J. Braathen, Henry Houlden, Tanya Stojkovic, Stojan Peric, Alessandra Bolino, Stefano C. Previtali, Yi‐Chung Lee, A. Nazlı Başak, Sherifa A. Hamed, Ricardo Rojas‐García, Tanya Stojkovic, Wilson Marques, Teresa Sevilla, Beate Schlotter‐Weigel, Fiore Manganelli, Ruxu Zhang, David N. Herrmann, Steven S. Scherer, Pavel Seeman, Davide Pareyson, Mary M. Reilly, Michael E. Shy, Stephan Züchner

    Published 2025
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  16. 16
    CSF Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barré Syndrome

    CSF Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barré Syndrome by Helle Al-Hakem, Alex Y. Doets, Amro Stino, Sasha Živković, Henning Andersen, Hugh J. Willison, David R. Cornblath, Kenneth C. Gorson, Zhahirul Islam, Quazi Deen Mohammad, Søren H. Sindrup, Susumu Kusunoki, Amy Davidson, Carlos Casasnovas, Kathleen Bateman, James Miller, Bianca van den Berg, Christine Verboon, Joyce Roodbol, Sonja E. Leonhard, Samuel Arends, Linda W.G. Luijten, Luana Benedetti, Satoshi Kuwabara, Peter Van den Bergh, Soledad Monges, Girolama Alessandra Marfia, Nortina Shahrizaila, Giuliana Galassi, Yann Péréon, J. Bürmann, Krista Kuitwaard, R. P. Kleyweg, Cintia Marchesoni, María J. Sedano Tous, Luís Querol, L. Aguilar, Yuzhong Wang, Eduardo Nobile‐Orazio, Simon Rinaldi, Angelo Schenone, J. Marín Pardo, Frédérique H Vermeij, Waqar Waheed, Helmar C. Lehmann, Volkan Granit, Beth Stein, Guido Cavaletti, Gerardo Gutiérrez‐Gutiérrez, Fábio Barroso, Leo H. Visser, Hans Katzberg, Efthimios Dardiotis, Shahram Attarian, Anneke J. van der Kooi, Filip Eftimov, Paul W. Wirtz, Johnny P.A. Samijn, H. Jacobus Gilhuis, Robert D. M. Hadden, James Holt, Kazim A. Sheikh, Noah Kolb, Summer Karafiath, Michal Vytopil, Giovanni Antonini, Thomas E. Feasby, Catharina G. Faber, H. A. Kramers, Mark Busby, Rhys Roberts, Nicholas J. Silvestri, Raffaella Fazio, Gert W. van Dijk, Marcel P.J. Garssen, Jan J.G.M. Verschuuren, Thomas Harbo, Bart C. Jacobs, Richard AC Hughes, H.‐P. Hartung, L.C. de Koning, Melissa R. Mandarakas, M. van Woerkom, Ricardo Reisin, Stephen W. Reddel, Sung‐Tsang Hsieh, Jean Addington, Senda Ajroud‐Driss, Lucas Alessandro, Umesh A. Badrising, G. Balloy, I.R. Bella, T. E. Bertoríni, R. Bhavaraju-Sanka, Mariangela Bianco, Thomas H. Brannagan, Kirsty Brennan, Chiara Briani, S. Butterworth, Chi‐Chao Chao

    Published 2023
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