PubRank

Juan I Young

Author PubWeight™ 21.18‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Ascorbate induces ten-eleven translocation (Tet) methylcytosine dioxygenase-mediated generation of 5-hydroxymethylcytosine. J Biol Chem 2013 1.43
2 Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models. PLoS Biol 2010 1.36
3 A role for the endogenous opioid beta-endorphin in energy homeostasis. Endocrinology 2003 1.31
4 Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease. PLoS One 2010 1.18
5 Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss. Am J Hum Genet 2012 1.15
6 Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development. Hum Mol Genet 2010 1.13
7 Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice. Hum Mol Genet 2008 1.11
8 The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1. Autism Res 2012 1.10
9 Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis. Hum Mol Genet 2007 1.06
10 Ischemic preconditioning alters the epigenetic profile of the brain from ischemic intolerance to ischemic tolerance. Neurotherapeutics 2013 1.01
11 C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Ann Hum Genet 2013 0.96
12 Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome. BMC Mol Biol 2010 0.94
13 SLITRK6 mutations cause myopia and deafness in humans and mice. J Clin Invest 2013 0.93
14 Ascorbate-induced generation of 5-hydroxymethylcytosine is unaffected by varying levels of iron and 2-oxoglutarate. Biochem Biophys Res Commun 2013 0.92
15 Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome. Hum Genet 2014 0.89
16 Absence of dopamine D4 receptors results in enhanced reactivity to unconditioned, but not conditioned, fear. Eur J Neurosci 2002 0.88
17 Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes. Eur J Hum Genet 2011 0.87
18 RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome. PLoS One 2012 0.85
19 Increased splenocyte proliferative response and cytokine production in beta-endorphin-deficient mice. J Neuroimmunol 2002 0.85
20 Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome. PLoS One 2010 0.82
21 Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory. Hum Mol Genet 2013 0.81