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32199 publications found in the database

*2011 (1784)

*Starting in 2010, coverage has been refocused on core journals.

2011 Publications

Soybean Homologs of MPK4 Negatively Regulate Defense Responses and Positively Regulate Growth and Development
Liu, J. Z. et al. Plant Physiology 157(3), 1363-78, 2011, Soybean Genome Array  PubMed

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function
Paciorkowski, A. R. et al. European Journal of Human Genetics 9(12), 1238-45, 2011  PubMed

Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study
Wineinger, N. E. et al. European Journal of Human Genetics 9(12), 1271-5, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Drosophila Duplication Hotspots Are Associated with Late-Replicating Regions of the Genome
Cardoso-Moreira, M. et al. Plos Genetics 7(11), NPG, 2011, Drosophila Tiling 1.0R Array  PubMed

Evidence-Based Annotation of Gene Function in Shewanella oneidensis MR-1 Using Genome-Wide Fitness Profiling across 121 Conditions
Deutschbauer, A. et al. Plos Genetics 7(11), NPG, 2011  PubMed

Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia
Shen, Y. et al. Blood 118(20), 5593-603, 2011, Human Genome U133 Plus 2.0 Array  PubMed

Minimal genotype-phenotype correlation for small deletions within distal 1p36
Buck, A. et al. American Journal of Medical Genetics Part a 155A(12), 3164-9, 2011  PubMed

Newly recognized recessive syndrome characterized by dysmorphic features, hypogonadotropic hypogonadism, severe microcephaly, and sensorineural hearing loss maps to 3p21.3
Jenkinson, E. M. et al. American Journal of Medical Genetics Part a 155A(12), 2910-5, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Severe neonatal-onset panniculitis in a female infant with Prader-Willi syndrome
Sakthivel, M. et al. American Journal of Medical Genetics Part a 155A(12), 3087-9, 2011, Genome-Wide Human SNP Array 6.0  PubMed

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