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32199 publications found in the database

*2016 (534)

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

2016 Publications

Cytotoxic Cutaneous Adverse Drug Reactions during Anti-PD-1 Therapy
Goldinger, S. M. et al. Clinical Cancer Research 22(16), 4023-9, 2016, Human Transcriptome Array 2.0  PubMed

A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome
Beygo, J. et al. European Journal of Human Genetics 24(9), 1280-6, 2016, CytoScan  PubMed

Association of the IGF1 gene with fasting insulin levels
Willems, S. M. et al. European Journal of Human Genetics 24(9), 1337-43, 2016, Human Mapping 500K Array SetMapping 500K  PubMed

Immunophenotypic and Ultrastructural Analysis of Mast Cells in Hermansky-Pudlak Syndrome Type-1: A Possible Connection to Pulmonary Fibrosis
Kirshenbaum, A. S. et al. Plos One 11(7), NPG, 2016, Human Genome U133 Plus 2.0 Array  PubMed

Melanoma Lesions Independently Acquire T-cell Resistance during Metastatic Latency
Zhao, F. et al. Cancer Research 76(15), 4347-58, 2016, CytoScan  PubMed

Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43
Koyama, A. et al. Nucleic Acids Research 44(12), 5820-36, 2016, ViewRNA  PubMed

Precise Detection of IDH1/2 and BRAF Hotspot Mutations in Clinical Glioma Tissues by a Differential Calculus Analysis of High-Resolution Melting Data
Hatae, R. et al. Plos One 11(8), NPG, 2016, ExoSAP-IT  PubMed

Evaluating the contribution of genetics and familial shared environment to common disease using the UK Biobank
Munoz, M. et al. Nature Genetics 48(9), 980-3, 2016  PubMed

Transcriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type
Chiarelli, N. et al. Plos One 11(8), NPG, 2016, miRNA Array  PubMed

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