檢索結果 - Anna C. Need
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The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders 由 Vandana Shashi, Allyn McConkie‐Rosell, Bruce Rosell, Kelly Schoch, Kasturi Vellore, Marie McDonald, Yong‐hui Jiang, Pingxing Xie, Anna C. Need, David B. Goldstein
出版 2013Artigo -
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SVA: software for annotating and visualizing sequenced human genomes 由 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
出版 2011Artigo -
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Control of Axonal Growth and Regeneration of Sensory Neurons by the p110δ PI 3-Kinase 由 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
出版 2007Artigo -
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Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes 由 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
出版 2012Artigo -
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Failure to replicate effect of kibra on human memory in two large cohorts of European origin 由 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
出版 2008Artigo -
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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB 由 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
出版 2009Artigo -
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A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci 由 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
出版 2009Artigo -
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Exome Sequencing Followed by Large-Scale Genotyping Suggests a Limited Role for Moderately Rare Risk Factors of Strong Effect in Schizophrenia 由 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
出版 2012Artigo -
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Copy Number Variation of KIR Genes Influences HIV-1 Control 由 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
出版 2011Artigo -
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Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios 由 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
出版 2015Artigo
相關主題
Biology
Genetics
Gene
Medicine
Genome
Genotype
Computational biology
Single-nucleotide polymorphism
Internal medicine
Phenotype
Genome-wide association study
Disease
Neuroscience
Exome sequencing
Allele
Bioinformatics
Mutation
Exome
Genetic association
Pathology
Population
Psychiatry
Psychology
Computer science
Copy-number variation
Environmental health
Schizophrenia (object-oriented programming)
Candidate gene
Cognition
Genomics