PubRank

Céline Charon

Author PubWeight™ 15.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nat Genet 2006 2.95
2 Fine mapping of quantitative trait loci affecting female fertility in dairy cattle on BTA03 using a dense single-nucleotide polymorphism map. Genetics 2008 1.36
3 Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. PLoS Genet 2009 1.36
4 Two members of the Arabidopsis CLC (chloride channel) family, AtCLCe and AtCLCf, are associated with thylakoid and Golgi membranes, respectively. J Exp Bot 2007 1.13
5 Diversity and evolution of CYCLOIDEA-like TCP genes in relation to flower development in Papaveraceae. Plant Physiol 2006 0.97
6 Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. PLoS One 2012 0.91
7 Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. Am J Med Genet B Neuropsychiatr Genet 2007 0.86
8 A new phenotype linked to SPG27 and refinement of the critical region on chromosome. J Neurol 2006 0.85
9 Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genes. Neurogenetics 2007 0.82
10 Dual function of MIPS1 as a metabolic enzyme and transcriptional regulator. Nucleic Acids Res 2013 0.81
11 Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). Ann Neurol 2005 0.81
12 Multiple functions of Kip-related protein5 connect endoreduplication and cell elongation. Plant Physiol 2013 0.81
13 European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset. Am J Med Genet B Neuropsychiatr Genet 2010 0.78
14 The function of the RNA-binding protein TEL1 in moss reveals ancient regulatory mechanisms of shoot development. Plant Mol Biol 2011 0.77
15 A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3. Hum Genet 2007 0.76