Andrew S. McCallion

Johns Hopkins University, Baltimore, MD 
Cell Biology, Molecular Biology, Neuroscience Biology
"Andrew McCallion"
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Fufa TD, Harris ML, Watkins-Chow DE, et al. (2015) Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes. Human Molecular Genetics. 24: 5433-50
Lee D, Gorkin DU, Baker M, et al. (2015) A method to predict the impact of regulatory variants from DNA sequence. Nature Genetics
Fischer A, Wolman M, Granato M, et al. (2015) Carbamate nerve agent prophylatics exhibit distinct toxicological effects in the zebrafish embryo model. Neurotoxicology and Teratology. 50: 1-10
Xiang Y, Stine ZE, Xia J, et al. (2015) Targeted inhibition of tumor-specific glutaminase diminishes cell-autonomous tumorigenesis. The Journal of Clinical Investigation. 125: 2293-306
Jiang Q, Arnold S, Heanue T, et al. (2015) Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. American Journal of Human Genetics. 96: 581-96
Liu Y, Pham X, Zhang L, et al. (2014) Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling. G3 (Bethesda, Md.). 5: 61-72
Maragh S, Miller RA, Bessling SL, et al. (2014) Rbm24a and Rbm24b are required for normal somitogenesis. Plos One. 9: e105460
Praetorius C, Grill C, Stacey SN, et al. (2013) A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell. 155: 1022-33
Pol SU, Lang JK, O'Bara MA, et al. (2013) Sox10-MCS5 enhancer dynamically tracks human oligodendrocyte progenitor fate. Experimental Neurology. 247: 694-702
Doyle AJ, Doyle JJ, Bessling SL, et al. (2012) Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm. Nature Genetics. 44: 1249-54
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