PubRank

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Author PubWeight™ 51.60‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An efficient procedure for genotyping single nucleotide polymorphisms. Nucleic Acids Res 2001 4.77
2 Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective study. Lancet 2001 2.44
3 The use of long PCR to confirm three common alleles at the CYP2A6 locus and the relationship between genotype and smoking habit. Ann Hum Genet 2000 1.71
4 The immunolocalization of protein gene product 9.5 using rabbit polyclonal and mouse monoclonal antibodies. Br J Exp Pathol 1988 1.67
5 Birthweight, vitamin D receptor genotype and the programming of osteoporosis. Paediatr Perinat Epidemiol 2001 1.61
6 Insulin-like growth factor II (IGF-II). Int J Biochem Cell Biol 1998 1.40
7 Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males. Hum Mol Genet 2001 1.23
8 Complete amino acid sequence of the neurone-specific gamma isozyme of enolase (NSE) from human brain and comparison with the non-neuronal alpha form (NNE). Eur J Biochem 1988 1.21
9 Comparison of three methods for single nucleotide polymorphism typing for DNA bank studies: sequence-specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE). Hum Mutat 1999 1.19
10 Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred. J Lipid Res 1999 1.17
11 Structure of human muscle (beta) enolase mRNA and protein deduced from a genomic clone. Nucleic Acids Res 1989 1.04
12 Microarray analysis of nicotine-induced changes in gene expression in endothelial cells. Physiol Genomics 2001 1.03
13 High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresis. Clin Chem 1995 1.02
14 Effect on plasma lipid levels of different classes of mutations in the low-density lipoprotein receptor gene in patients with familial hypercholesterolemia. Arterioscler Thromb 1994 1.01
15 Molecular cloning of cDNA coding for human PGP 9.5 protein. A novel cytoplasmic marker for neurones and neuroendocrine cells. FEBS Lett 1987 1.00
16 Single-strand conformation polymorphism analysis with high throughput modifications, and its use in mutation detection in familial hypercholesterolemia. International Federation of Clinical Chemistry Scientific Division: Committee on Molecular Biology Techniques. Clin Chem 1997 0.98
17 Universal primer quantitative fluorescent multiplex (UPQFM) PCR: a method to detect major and minor rearrangements of the low density lipoprotein receptor gene. J Med Genet 2000 0.98
18 Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhage. Stroke 2001 0.96
19 Apal polymorphism in insulin-like growth factor II (IGF2) gene and weight in middle-aged males. Int J Obes Relat Metab Disord 1997 0.95
20 Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probands. Hum Genet 1998 0.93
21 Associations of IGF2 ApaI RFLP and INS VNTR class I allele size with obesity. Eur J Hum Genet 2000 0.92
22 PGP9.5, a ubiquitin C-terminal hydrolase; pattern of mRNA and protein expression during neural development in the mouse. Brain Res Dev Brain Res 1995 0.91
23 Candidate-gene studies of the atherogenic lipoprotein phenotype: a sib-pair linkage analysis of DZ women twins. Am J Hum Genet 1998 0.91
24 Rate of progression of cognitive decline in Alzheimer's disease: effect of butyrylcholinesterase K gene variation. J Neurol Neurosurg Psychiatry 2005 0.91
25 Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies. Diabetologia 2011 0.88
26 Higher resolution microplate array diagonal gel electrophoresis: application to a multiallelic minisatellite. Hum Mutat 2000 0.87
27 Localisation of neurone-specific enolase (ENO2) to 12p13. Cytogenet Cell Genet 1990 0.85
28 Analysis of the association of a heat shock protein70-1 gene promoter polymorphism with myocardial infarction and coronary risk traits. Dis Markers 1998 0.85
29 Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor gene. J Med Genet 1995 0.85
30 Rapid methods for population-scale analysis for gene polymorphisms: the ACE gene as an example. Br Heart J 1995 0.85
31 SNP genotyping by combination of 192-well MADGE, ARMS and computerized gel image analysis. Biotechniques 2000 0.83
32 A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling. Am J Cardiol 1998 0.81
33 Elimination of dumbbell bands and enhancement of resolution in MADGE using delayed start electrophoresis. Biotechniques 2000 0.81
34 Measuring serum neurone-specific enolase. Lancet 1982 0.81
35 Molecular structure of the human muscle-specific enolase gene (ENO3). Biochem J 1991 0.81
36 Levels of immunoreactive aldolase C, creatine kinase-BB, neuronal and non-neuronal enolase, and 14-3-3 protein in circulating human blood cells. Clin Chim Acta 1984 0.80
37 Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland. J Med Genet 1998 0.80
38 A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation. Hum Mutat 1997 0.78
39 The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14. Ann Hum Genet 1991 0.78
40 Denaturing gradient gel electrophoretic analysis of codons 3456-3553 of the apolipoprotein-B gene in 106 type 11a hyperlipoproteinaemic individuals. Ann Clin Biochem 1998 0.78
41 PCR induction of a TaqI restriction site at any CpG dinucleotide using two mismatched primers (CpG-PCR). Genome Res 1996 0.77
42 Handling of large (300 x 400 mm), thin (0.4 mm) polyacrylamide gels and recovery as dried gels. Biotechniques 1994 0.77
43 A differential molecular clock in enolase isoprotein evolution. J Mol Evol 1993 0.76
44 Gene-environment interaction in the determination of levels of plasma fibrinogen. Thromb Haemost 1999 0.76
45 Molecular biology of the human enolase gene family: nerve (gamma), muscle (beta) and general (alpha) isoforms. Biochem Soc Trans 1990 0.76
46 Estimation of the age of the ancestral arginine3500-->glutamine mutation in human apoB-100. Genomics 1997 0.76
47 Patterns of DNA methylation of the parathyroid hormone-related protein gene in human lung carcinoma. Eur J Cancer 1995 0.76
48 Methylation patterns in the human muscle-specific enolase gene (ENO3). Biochem J 1993 0.75
49 Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindreds. Ann Hum Genet 1997 0.75
50 High throughput modifications of single-strand conformation polymorphism analysis : mutation detection in familial hypercholesterolemia. Methods Mol Med 1996 0.75
51 DNA sequence comparison between human and marsupial genes encoding PGP9.5--a neurone-specific ubiquitin C-terminal hydrolase. Biochem Soc Trans 1992 0.75
52 Use of the single strand conformation polymorphism method for rapid screening for mutations in the low density lipoprotein receptor gene in patients with familial hypercholesterolemia: effect on plasma lipid levels of different classes of mutations. Z Gastroenterol 1996 0.75
53 CpG-PCR combined with sample pooling and mutant enrichment for CpG mutation screening in population studies. Clin Chem 1998 0.75
54 Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemia. Clin Genet 1998 0.75
55 Characterisation of an epitope specific to the neuron-specific isoform of human enolase recognised by a monoclonal antibody raised against a synthetic peptide corresponding to the C-terminus of beta/A4-protein. Biochim Biophys Acta 1993 0.75
56 Mapping of antigenic sites in human neuron-specific enolase by expression subcloning. Clin Chem 1994 0.75
57 Tools for molecular genetic epidemiology: a comparison of MADGE methodology with other systems. Biotechnol Genet Eng Rev 2000 0.75
58 Single-strand conformation polymorphism analysis with high throughput modifications, and its use in mutation detection in familial hypercholesterolemia. The IFCC Scientific Division: Committee on Molecular Biology Techniques. J Int Fed Clin Chem 1997 0.75
59 Simplified detection of a mutation causing familial hypercholesterolaemia throughout Britain: evidence for an origin in a common distant ancestor. Ann Clin Biochem 1998 0.75
60 Rapid testing for three mutations causing familial defective apolipoprotein B100 in 562 patients with familial hypercholesterolaemia. Atherosclerosis 1996 0.75
61 W64R mutation in beta-3-adrenergic receptor gene and weight in a large population sample. Int J Obes Relat Metab Disord 1998 0.75