F Annesi

Author PubWeight™ 25.11‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Expression of two Xenopus laevis ribosomal protein genes in injected frog oocytes. A specific splicing block interferes with the L1 RNA maturation. J Mol Biol 1984 2.03
2 Isolation and nucleotide sequences of cDNAs for Xenopus laevis ribosomal protein S8: similarities in the 5' and 3' untranslated regions of mRNAs for various r-proteins. Gene 1988 1.93
3 The parkin gene is not involved in late-onset Parkinson's disease. Neurology 2001 1.51
4 A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1. Neurology 2000 1.45
5 Splicing of Xenopus laevis ribosomal protein RNAs is inhibited in vivo by antisera to ribonucleoproteins containing U1 small nuclear RNA. J Mol Biol 1984 1.23
6 The fragile X premutation presenting as postprandial hypotension. Neurology 2004 0.95
7 Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjögren syndrome. Ann Neurol 2000 0.95
8 Molecular systematics and evolutionary biogeography of the genus Talpa (Soricomorpha: Talpidae). Mol Phylogenet Evol 2010 0.89
9 Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene. Ann Neurol 1998 0.88
10 Sequence of the gene coding for ribosomal protein S8 of Xenopus laevis. Gene 1993 0.88
11 DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. Clin Genet 2009 0.87
12 SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases. Clin Genet 2007 0.84
13 Association of tau gene polymorphism with Parkinson's disease. Neurol Sci 2003 0.83
14 Structure of Xenopus laevis ribosomal protein L32 and its expression during development. Nucleic Acids Res 1990 0.82
15 Zebrafish 5S rRNA genes map to the long arms of chromosome 3. Chromosome Res 2000 0.82
16 The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease. Mov Disord 2000 0.81
17 NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy. Neurosci Lett 2003 0.81
18 Human ribosomal protein L4: cloning and sequencing of the cDNA and primary structure of the protein. Biochim Biophys Acta 1993 0.81
19 Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet 2008 0.80
20 The parkin gene is not a major susceptibility locus for typical late-onset Parkinson's disease. Neurol Sci 2001 0.80
21 Cytogenetic studies in Sparus auratus (Pisces, Perciformes): molecular organization of 5S rDNA and chromosomal mapping of 5S and 45S ribosomal genes and of telomeric repeats. Hereditas 2003 0.80
22 LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease. Clin Genet 2007 0.78
23 Contact zones between chromosomal races of Mus musculus domesticus. 3. Molecular and chromosomal evidence of restricted gene flow between the CD race (2n = 22) and the ACR race (2n = 24). Heredity (Edinb) 2002 0.78
24 Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet 2007 0.77
25 Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancy. Hum Genet 2010 0.76
26 Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet 2007 0.75
27 Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease. Neurology 2002 0.75
28 Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease. Hum Genet 2010 0.75
29 Gene dosage influences the age at onset of SCA2 in a family from southern Italy. Clin Genet 2007 0.75
30 Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet 2007 0.75
31 A procedure for cloning genomic DNA fragments with increasing thermoresistance. Gene 1998 0.75
32 Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. Hum Genet 2009 0.75
33 Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease. Hum Genet 2010 0.75