Resultats de la cerca - Anna C. Need

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  1. 1
    A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans

    A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans per Anna C. Need, Dalia Kasperavičiūtė, Elizabeth T. Cirulli, David B. Goldstein

    Publicat 2009
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  2. 2
    The importance of dynamic re-analysis in diagnostic whole exome sequencing

    The importance of dynamic re-analysis in diagnostic whole exome sequencing per Anna C. Need, Vandana Shashi, Kelly Schoch, Slavé Petrovski, David B. Goldstein

    Publicat 2016
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  3. 3
    Common genetic variation and performance on standardized cognitive tests

    Common genetic variation and performance on standardized cognitive tests per Elizabeth T. Cirulli, Dalia Kasperavičiūtė, Deborah K. Attix, Anna C. Need, Dongliang Ge, Greg Gibson, David B. Goldstein

    Publicat 2010
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  4. 4
    WGAViewer: Software for genomic annotation of whole genome association studies: Figure 1.

    WGAViewer: Software for genomic annotation of whole genome association studies: Figure 1. per Dongliang Ge, Kunlin Zhang, Anna C. Need, Olivier C. Martin, Jacques Fellay, Thomas Urban, Amalio Telenti, David B. Goldstein

    Publicat 2008
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  5. 5
    Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis

    Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis per Anna C. Need, Richard S.E. Keefe, Dongliang Ge, Iris Grossman, Sam Dickson, Joseph P. McEvoy, David B. Goldstein

    Publicat 2009
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  6. 6
    Temporal lobe functional activity and connectivity in young adult <i>APOE</i> ɛ4 carriers

    Temporal lobe functional activity and connectivity in young adult <i>APOE</i> ɛ4 carriers per Nancy A. Dennis, Jeffrey N. Browndyke, Jared Stokes, Anna C. Need, James R. Burke, Kathleen A. Welsh‐Bohmer, Roberto Cabeza

    Publicat 2009
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  7. 7
    Clinical application of exome sequencing in undiagnosed genetic conditions

    Clinical application of exome sequencing in undiagnosed genetic conditions per Anna C. Need, Vandana Shashi, Yuki Hitomi, Kelly Schoch, Kevin V. Shianna, Marie McDonald, Miriam H. Meisler, David B. Goldstein

    Publicat 2012
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  8. 8
    A Genomics England haplotype reference panel and imputation of UK Biobank

    A Genomics England haplotype reference panel and imputation of UK Biobank per Sinan Shi, Simone Rubinacci, Sile Hu, Loukas Moutsianas, Alexander Stuckey, Anna C. Need, Pier Francesco Palamara, Mark J. Caulfield, Jonathan Marchini, Simon Myers

    Publicat 2024
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  9. 9
    The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders

    The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders per Vandana Shashi, Allyn McConkie‐Rosell, Bruce Rosell, Kelly Schoch, Kasturi Vellore, Marie McDonald, Yong‐hui Jiang, Pingxing Xie, Anna C. Need, David B. Goldstein

    Publicat 2013
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  10. 10
    Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease

    Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease per Erin L. Heinzen, Anna C. Need, Kathleen M. Hayden, Ornit Chiba‐Falek, Allen D. Roses, Warren J. Strittmatter, James R. Burke, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, David Goldstein

    Publicat 2010
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  11. 11
    Long-Range LD Can Confound Genome Scans in Admixed Populations

    Long-Range LD Can Confound Genome Scans in Admixed Populations per Alkes L. Price, Michael E. Weale, Hon‐Cheong So, Simon Myers, Anna C. Need, Kevin V. Shianna, Dongliang Ge, Jerome I. Rotter, Esther A. Torres, Kent D. Taylor, David B. Goldstein, David Reich

    Publicat 2008
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  12. 12
    SVA: software for annotating and visualizing sequenced human genomes

    SVA: software for annotating and visualizing sequenced human genomes per Dongliang Ge, Elizabeth K. Ruzzo, Kevin V. Shianna, Min He, Kimberly Pelak, Erin L. Heinzen, Anna C. Need, Elizabeth T. Cirulli, Jessica M. Maia, Samuel P. Dickson, Mingfu Zhu, Abanish Singh, Andrew S. Allen, David B. Goldstein

    Publicat 2011
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  13. 13
    Control of Axonal Growth and Regeneration of Sensory Neurons by the p110δ PI 3-Kinase

    Control of Axonal Growth and Regeneration of Sensory Neurons by the p110δ PI 3-Kinase per Britta J. Eickholt, Aminul I. Ahmed, Meirion Davies, Evangelia A. Papakonstanti, Wayne Pearce, Michelle L. Starkey, Antonio Bilancio, Anna C. Need, Andrew J. H. Smith, Susan Hall, Frank P.T. Hamers, Karl-Peter Giese, Elizabeth J. Bradbury, Bart Vanhaesebroeck

    Publicat 2007
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  14. 14
    Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes

    Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes per Mingfu Zhu, Anna C. Need, Yujun Han, Dongliang Ge, Jessica M. Maia, Qianqian Zhu, Erin L. Heinzen, Elizabeth T. Cirulli, Kimberly Pelak, Min He, Elizabeth K. Ruzzo, Curtis Gumbs, Abanish Singh, Sheng Feng, Kevin V. Shianna, David B. Goldstein

    Publicat 2012
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  15. 15
    Failure to replicate effect of kibra on human memory in two large cohorts of European origin

    Failure to replicate effect of kibra on human memory in two large cohorts of European origin per Anna C. Need, Deborah K. Attix, Jill M. McEvoy, Elizabeth T. Cirulli, Kristen N. Linney, Ana Patricia Wagoner, Curtis Gumbs, Ina Giegling, Hans‐Jürgen Möller, Clyde Francks, Pierandrea Muglia, Allen D. Roses, Greg Gibson, Michael E. Weale, Dan Rujescu, David B. Goldstein

    Publicat 2008
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  16. 16
    A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

    A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB per Anna C. Need, Deborah K. Attix, Jill M. McEvoy, Elizabeth T. Cirulli, Kristen L. Linney, Priscilla Hunt, Dongliang Ge, Erin L. Heinzen, Jessica M. Maia, Kevin V. Shianna, Michael E. Weale, Lynn Cherkas, Gail Clement, Tim D. Spector, Greg Gibson, David B. Goldstein

    Publicat 2009
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  17. 17
    A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci

    A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci per Sreekumar Pillai, Dongliang Ge, Guohua Zhu, Xiangyang Kong, Kevin V. Shianna, Anna C. Need, Sheng Feng, Craig P. Hersh, Per Bakke, Amund Gulsvik, Andreas Ruppert, Karin C. Lødrup Carlsen, Allen D. Roses, W. J. Anderson, Stephen I. Rennard, David A. Lomas, Edwin K. Silverman, David B. Goldstein

    Publicat 2009
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  18. 18
    Exome Sequencing Followed by Large-Scale Genotyping Suggests a Limited Role for Moderately Rare Risk Factors of Strong Effect in Schizophrenia

    Exome Sequencing Followed by Large-Scale Genotyping Suggests a Limited Role for Moderately Rare Risk Factors of Strong Effect in Schizophrenia per Anna C. Need, Joseph P. McEvoy, Massimo Gennarelli, Erin L. Heinzen, Dongliang Ge, Jessica M. Maia, Kevin V. Shianna, Min He, Elizabeth T. Cirulli, Curtis Gumbs, Qian Zhao, C. Ryan Campbell, Linda K. Hong, Peter B. Rosenquist, Anu Putkonen, Tero Hallikainen, Eila Repo‐Tiihonen, Jari Tiihonen, Deborah L. Levy, Herbert Y. Meltzer, David B. Goldstein

    Publicat 2012
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  19. 19
    Copy Number Variation of KIR Genes Influences HIV-1 Control

    Copy Number Variation of KIR Genes Influences HIV-1 Control per Kimberly Pelak, Anna C. Need, Jacques Fellay, Kevin V. Shianna, Sheng Feng, Thomas Urban, Dongliang Ge, Andrea De Luca, Javier Martínez‐Picado, Steven M. Wolinsky, Jeremy Martinson, Beth D. Jamieson, Jay H. Bream, Maureen P. Martin, Persephone Borrow, Norman L. Letvin, Andrew J. McMichael, Barton F. Haynes, Amalio Telenti, Mary Carrington, David B. Goldstein, Galit Alter

    Publicat 2011
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  20. 20
    Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

    Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios per Xiaolin Zhu, Slavé Petrovski, Pingxing Xie, Elizabeth K. Ruzzo, Yifan Lu, K. Melodi McSweeney, Bruria Ben‐Zeev, Andreea Nissenkorn, Yair Anikster, Danit Oz-Levi, Ryan S. Dhindsa, Yuki Hitomi, Kelly Schoch, Rebecca C. Spillmann, Gali Heimer, Dina Marek‐Yagel, Michal Tzadok, Yujun Han, Gordon Worley, Jennifer Goldstein, Yong‐hui Jiang, Doron Lancet, Elon Pras, Vandana Shashi, Duncan McHale, Anna C. Need, David B. Goldstein

    Publicat 2015
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