Canlyniadau Chwilio - Michael E. Zwick

Mireinio'r Canlyniadau
  1. 1
    Genetic Variation in Rates of Nondisjunction: Association of Two Naturally Occurring Polymorphisms in the Chromokinesin nod With Increased Rates of Nondisjunction in Drosophila melanogaster

    Genetic Variation in Rates of Nondisjunction: Association of Two Naturally Occurring Polymorphisms in the Chromokinesin nod With Increased Rates of Nondisjunction in Drosophila mel... gan Michael E. Zwick, Jennifer L. Salstrom, Charles H. Langley

    Cyhoeddwyd 1999
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  2. 2
    Haplotype Inference in Random Population Samples

    Haplotype Inference in Random Population Samples gan Shin Lin, David J. Cutler, Michael E. Zwick, Aravinda Chakravarti

    Cyhoeddwyd 2002
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  3. 3
    New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings

    New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings gan Alex Kotlar, Kristina B. Mercer, Michael E. Zwick, Jennifer G. Mullé

    Cyhoeddwyd 2015
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  4. 4
    Microarray-based mutation detection in the<i>dystrophin</i>gene

    Microarray-based mutation detection in the<i>dystrophin</i>gene gan Madhuri Hegde, Ephrem Chin, Jennifer G. Mullé, David T. Okou, Stephen T. Warren, Michael E. Zwick

    Cyhoeddwyd 2008
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  5. 5
    Structure and Complexity of a Bacterial Transcriptome

    Structure and Complexity of a Bacterial Transcriptome gan Karla D. Passalacqua, Anjana Varadarajan, Brian Ondov, David T. Okou, Michael E. Zwick, Nicholas H. Bergman

    Cyhoeddwyd 2009
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  6. 6
    Novel features of 3q29 deletion syndrome: Results from the 3q29 registry

    Novel features of 3q29 deletion syndrome: Results from the 3q29 registry gan Megan R. Glassford, Jill A. Rosenfeld, Alexa A. Freedman, Michael E. Zwick, Jennifer G. Mullé

    Cyhoeddwyd 2016
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  7. 7
    Identification of novel <i>FMR1</i> variants by massively parallel sequencing in developmentally delayed males

    Identification of novel <i>FMR1</i> variants by massively parallel sequencing in developmentally delayed males gan Stephen C. Collins, Steven M. Bray, Joshua A. Suhl, David J. Cutler, Bradford Coffee, Michael E. Zwick, Stephen T. Warren

    Cyhoeddwyd 2010
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  8. 8
    Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

    Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry gan Rebecca M. Pollak, Melissa M. Murphy, Michael P. Epstein, Michael E. Zwick, Cheryl Klaiman, Celine A. Saulnier, Jennifer G. Mullé

    Cyhoeddwyd 2019
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  9. 9
    High-Throughput Variation Detection and Genotyping Using Microarrays

    High-Throughput Variation Detection and Genotyping Using Microarrays gan David J. Cutler, Michael E. Zwick, Minerva M. Carrasquillo, Christopher T. Yohn, K Tobin, Carl Kashuk, Debra Mathews, Nila Shah, Evan E. Eichler, Janet A. Warrington, Aravinda Chakravarti

    Cyhoeddwyd 2001
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  10. 10
    Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay

    Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay gan Miao He, Lisa E. Kratz, Joshua J. Michel, Abbe N. Vallejo, Laura K. Ferris, Richard I. Kelley, Jacqueline J. Hoover, D.M. Jukic, K. Michael Gibson, Lynne A. Wolfe, Dhanya Ramachandran, Michael E. Zwick, Jerry Vockley

    Cyhoeddwyd 2011
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  11. 11
    Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease

    Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease gan Kelly Shaw, Madeline Bertha, Tatyana Hofmekler, Pankaj Chopra, Tommi Vatanen, Abhiram Srivatsa, Jarod Prince, Archana Kumar, Cary G. Sauer, Michael E. Zwick, Glen A. Satten, Aleksandar D. Kostic, Jennifer G. Mullé, Ramnik J. Xavier, Subra Kugathasan

    Cyhoeddwyd 2016
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  12. 12
    Exome Sequencing Identifies a Novel <i>FOXP3</i> Mutation in a 2‐Generation Family With Inflammatory Bowel Disease

    Exome Sequencing Identifies a Novel <i>FOXP3</i> Mutation in a 2‐Generation Family With Inflammatory Bowel Disease gan David T. Okou, Kajari Mondal, William A. Faubion, Lisa Kobrynski, Lee A. Denson, Jennifer G. Mullé, Dhanya Ramachandran, Yuning Xiong, Phyllis A. Svingen, Viren Patel, Promita Bose, Jon Waters, Sampath Prahalad, David J. Cutler, Michael E. Zwick, Subra Kugathasan

    Cyhoeddwyd 2014
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  13. 13
    Genomic characterization of the<i>Bacillus cereus</i>sensu lato species: Backdrop to the evolution of<i>Bacillus anthracis</i>

    Genomic characterization of the<i>Bacillus cereus</i>sensu lato species: Backdrop to the evolution of<i>Bacillus anthracis</i> gan Michael E. Zwick, Sandeep J. Joseph, Xavier Didelot, Peter E. Chen, Kimberly A. Bishop‐Lilly, Andrew C. Stewart, Kristin M. Willner, Nichole Nolan, Shannon M. Lentz, Maureen K. Thomason, Shanmuga Sozhamannan, Alfred Mateczun, Lei Du, Timothy D. Read

    Cyhoeddwyd 2012
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  14. 14
    Genomic characterization of the Yersinia genus

    Genomic characterization of the Yersinia genus gan Peter E. Chen, Christopher L. Cook, Andrew C. Stewart, Niranjan Nagarajan, Dan Sommer, Mihai Pop, Brendan Thomason, Maureen P Kiley Thomason, Shannon M. Lentz, Nichole Nolan, Shanmuga Sozhamannan, Alexander Sulakvelidze, Alfred Mateczun, Lei Du, Michael E. Zwick, Timothy D. Read

    Cyhoeddwyd 2010
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  15. 15
    Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis

    Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis gan Suresh Venkateswaran, Jarod Prince, David J. Cutler, Urko M. Marigorta, David T. Okou, Sampath Prahalad, David Mack, Brendan Boyle, Sonia Thomas, Anne M. Griffiths, Cary G. Sauer, Neal S. LeLeiko, David J. Keljo, James Markowitz, Susan S. Baker, Joel R. Rosh, Marian Pfefferkorn, Melvin B. Heyman, Ashish Patel, Anthony Otley, Robert N. Baldassano, Joshua D. Noe, Paul A. Rufo, Maria Oliva‐Hemker, Sonia M. Davis, Michael E. Zwick, Greg Gibson, Lee A. Denson, Jeffrey S. Hyams, Subra Kugathasan

    Cyhoeddwyd 2018
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  16. 16
    Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn’s Disease

    Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn’s Disease gan Lee A. Denson, Ingrid Jurickova, Rebekah Karns, Kelly Shaw, David J. Cutler, David T. Okou, Anne Dodd, Kathryn Quinn, Kajari Mondal, Bruce J. Aronow, Yael Haberman, Aaron Linn, Adam Price, Ramona Bezold, Kathleen D. Lake, Kimberly Jackson, Thomas D. Walters, Anne M. Griffiths, Robert N. Baldassano, Joshua D. Noe, Jeffrey S. Hyams, Wallace Crandall, Barbara S. Kirschner, Melvin B. Heyman, Scott B. Snapper, Stephen L. Guthery, Marla C. Dubinsky, Neal S. LeLeiko, Anthony Otley, Ramnik J. Xavier, Christine Stevens, Mark J. Daly, Michael E. Zwick, Subra Kugathasan

    Cyhoeddwyd 2018
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  17. 17
    Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care

    Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care gan Rossana Sanchez Russo, Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell, Grace Carlock, Joseph F. Cubells, Michael T. Epstein, Roberto España, Katrina Goines, Ryan M. Guest, Cheryl Klaiman, Sookyong Koh, Elizabeth J. Leslie, Longchuan Li, Derek M. Novacek, Celine A. Saulnier, Esra Sefik, Sarah Shultz, Elaine F. Walker, Stormi P. White, Hallie Averbach, Gary J. Bassell, Shanthi Cambala, Tamara Caspary, David J. Cutler, Paul A. Dawson, Michael P. Epstein, H. Richard Johnston, Bryan C. Mak, Tamika Malone, Trenell J. Mosley, Ava Papetti, Rebecca M. Pollak, Ryan H. Purcell, Nikisha Sisodoya, Steven A. Sloan, Stephen T. Warren, David Weinshenker, Zhexing Wen, Michael E. Zwick, Jennifer G. Mullé

    Cyhoeddwyd 2021
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  18. 18
    Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome

    Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome gan Austin L. Brown, Adam J. de Smith, Vincent U. Gant, Wenjian Yang, Michael E. Scheurer, Kyle M. Walsh, Jonathan M. Chernus, Noah A. Kallsen, Stephen Peyton, Gareth E. Davies, Erik A. Ehli, Naomi J. Winick, Nyla A. Heerema, Andrew J. Carroll, Michael J. Borowitz, Brent L. Wood, William L. Carroll, Elizabeth A. Raetz, Eleanor Feingold, Meenakshi Devidas, Lisa F. Barcellos, Helen M. Hansen, Libby M. Morimoto, Alice Y. Kang, I. Smirnov, Jasmine Healy, Caroline Laverdière, Daniel Sinnett, Jeffrey W. Taub, Jillian M. Birch, Pamela Thompson, Logan G. Spector, Maria S. Pombo‐de‐Oliveira, Andrew T. DeWan, Charles G. Mullighan, Stephen P. Hunger, Ching‐Hon Pui, Mignon L. Loh, Michael E. Zwick, Catherine Metayer, Xiaomei Ma, Beth A. Mueller, Stephanie L. Sherman, Joseph L. Wiemels, Mary V. Relling, Jun J. Yang, Philip J. Lupo, Karen R. Rabin

    Cyhoeddwyd 2019
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  19. 19
    Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans

    Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans gan Chengrui Huang, Talin Haritunians, David T. Okou, David J. Cutler, Michael E. Zwick, Kent D. Taylor, Lisa W. Datta, Joseph Maranville, Zhenqiu Liu, Shannon Ellis, Pankaj Chopra, J. Steven Alexander, Robert N. Baldassano, Raymond K. Cross, Themistocles Dassopoulos, Tanvi Dhere, Richard H. Duerr, John S. Hanson, Jason K. Hou, Sunny Z. Hussain, Kim L. Isaacs, Kelly Kachelries, Howard A. Kader, Michael D. Kappelman, Jeffrey A. Katz, Richárd Kellermayer, Barbara S. Kirschner, John F. Kuemmerle, Archana Kumar, John H. Kwon, Mark Lazarev, Peter Mannon, Dedrick E. Moulton, B. O. Osuntokun, Ashish Patel, John D. Rioux, Jerome I. Rotter, Shehzad A. Saeed, Ellen Scherl, Mark S. Silverberg, Ann L. Silverman, Stephan R. Targan, John F. Valentine, Ming‐Hsi Wang, Claire L. Simpson, S. Louis Bridges, Robert P. Kimberly, Stephen S. Rich, Judy H. Cho, Anna Di Rienzo, Linda Kao, Dermot McGovern, Steven R. Brant, Subra Kugathasan

    Cyhoeddwyd 2015
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  20. 20
    Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease

    Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease gan Steven R. Brant, David T. Okou, Claire L. Simpson, David J. Cutler, Talin Haritunians, Jonathan P. Bradfield, Pankaj Chopra, Jarod Prince, Ferdouse Begum, Archana Kumar, Chengrui Huang, Suresh Venkateswaran, Lisa W. Datta, Zhi Wei, Kelly Thomas, Lisa J. Herrinton, Jan-Micheal A. Klapproth, Antonio Quiros, Jenifer Seminerio, Zhenqiu Liu, J. Steven Alexander, Robert N. Baldassano, Sharon Dudley‐Brown, Raymond K. Cross, Themistocles Dassopoulos, Lee A. Denson, Tanvi Dhere, Gerald W. Dryden, John S. Hanson, Jason K. Hou, Sunny Z. Hussain, Jeffrey S. Hyams, Kim L. Isaacs, Howard A. Kader, Michael D. Kappelman, Jeffry Katz, Richárd Kellermayer, Barbara S. Kirschner, John F. Kuemmerle, John H. Kwon, Mark Lazarev, Ellen Li, David R. Mack, Peter Mannon, Dedrick E. Moulton, Rodney D. Newberry, B. O. Osuntokun, Ashish Patel, Shehzad A. Saeed, Stephan R. Targan, John F. Valentine, Ming‐Hsi Wang, Martin Zonca, John D. Rioux, Richard H. Duerr, Mark S. Silverberg, Judy H. Cho, Hákon Hákonarson, Michael E. Zwick, Dermot McGovern, Subra Kugathasan

    Cyhoeddwyd 2016
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