Kết quả tìm kiếm - Anna C. Need
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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 Bằng Anna C. Need, Dalia Kasperavičiūtė, Elizabeth T. Cirulli, David B. Goldstein
Được phát hành 2009Artigo -
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The importance of dynamic re-analysis in diagnostic whole exome sequencing Bằng Anna C. Need, Vandana Shashi, Kelly Schoch, Slavé Petrovski, David B. Goldstein
Được phát hành 2016Carta -
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The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders Bằng Vandana Shashi, Allyn McConkie‐Rosell, Bruce Rosell, Kelly Schoch, Kasturi Vellore, Marie McDonald, Yong‐hui Jiang, Pingxing Xie, Anna C. Need, David B. Goldstein
Được phát hành 2013Artigo -
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Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Bằng 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
Được phát hành 2010Artigo -
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SVA: software for annotating and visualizing sequenced human genomes Bằng 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
Được phát hành 2011Artigo -
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Control of Axonal Growth and Regeneration of Sensory Neurons by the p110δ PI 3-Kinase Bằng 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
Được phát hành 2007Artigo -
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Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes Bằng 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
Được phát hành 2012Artigo -
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Failure to replicate effect of kibra on human memory in two large cohorts of European origin Bằng 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
Được phát hành 2008Artigo -
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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB Bằng 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
Được phát hành 2009Artigo -
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A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci Bằng 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
Được phát hành 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 Bằng 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
Được phát hành 2012Artigo -
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Copy Number Variation of KIR Genes Influences HIV-1 Control Bằng 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
Được phát hành 2011Artigo -
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Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios Bằng 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
Được phát hành 2015Artigo
Công cụ tìm kiếm:
Các môn học liên quan
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