A C Papp

Author PubWeight™ 28.01‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation. Hum Mol Genet 1993 1.67
2 The I1307K polymorphism of the APC gene in colorectal cancer. Gastroenterology 1999 1.43
3 A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient. Nat Genet 1993 1.15
4 Spectrum of small mutations in the dystrophin coding region. Am J Hum Genet 1995 1.15
5 Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy. Clin Pharmacol Ther 2011 1.15
6 Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosis. Hum Pathol 2001 0.99
7 Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion. Neurology 1997 0.96
8 Dopamine transporter DAT and receptor DRD2 variants affect risk of lethal cocaine abuse: a gene-gene-environment interaction. Transl Psychiatry 2013 0.94
9 Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome. Hum Genet 2001 0.90
10 Profiling solute carrier transporters in the human blood-brain barrier. Clin Pharmacol Ther 2013 0.89
11 Stimulation of endothelial cell prostacyclin formation by interleukin-2. Lymphokine Res 1986 0.87
12 Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides. Clin Chem 1990 0.86
13 Interaction between lymphocytes and platelets in the synthesis of prostacyclin. J Clin Invest 1987 0.86
14 Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection. Am J Med Genet 1994 0.86
15 Evaluation of celiac disease biopsies for adenovirus 12 DNA using a multiplex polymerase chain reaction. Mod Pathol 1993 0.86
16 Optimization of DNA extraction from formalin-fixed tissue and its clinical application in Duchenne muscular dystrophy. Am J Clin Pathol 1992 0.85
17 Southern transfer protocol for confirmation of Huntington disease. Clin Chem 1996 0.83
18 Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCR. Transplantation 1994 0.82
19 Serum prostacyclin binding defects in thrombotic thrombocytopenic purpura. J Clin Invest 1985 0.82
20 A molecular protocol for diagnosing myotonic dystrophy. Clin Chem 1995 0.81
21 Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysis. Hum Mutat 1993 0.81
22 ARIC hemostasis study--II. Organizational plan and feasibility study. Thromb Haemost 1990 0.80
23 Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing. Hum Mutat 1995 0.80
24 Production of eicosanoids by deendothelialized rabbit aorta: interaction between platelets and vascular wall in the synthesis of prostacyclin. Thromb Res 1986 0.80
25 Germline mosaicism at the fragile X locus. Am J Med Genet 1995 0.78
26 Nonsense mutations in a Becker muscular dystrophy and an intermediate patient. Hum Mutat 1996 0.78
27 Reduction of serum prostacyclin stability in ischemic stroke. Stroke 1985 0.78
28 A HindIII/BglII dystrophin gene polymorphism in the African-American population. Hum Genet 1992 0.78
29 Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16. Hum Mol Genet 1994 0.76
30 A novel splice site mutation in a Becker muscular dystrophy patient. J Med Genet 1996 0.75
31 Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy. Muscle Nerve 1992 0.75
32 Bovine aorta endothelial cell incubation with interleukin 2: morphological changes correlate with enhanced vascular permeability. Scanning Microsc 1988 0.75
33 Binding of prostacyclin by plasma glycoproteins. Prostaglandins 1985 0.75
34 Interaction between platelets and lymphocytes in biosynthesis of prostacyclin. Methods Enzymol 1990 0.75
35 Stimulation of de novo synthesis of prostaglandin G/H synthase in endothelial cells. Adv Prostaglandin Thromboxane Leukot Res 1989 0.75
36 Detection of an exon 53 polymorphism in the dystrophin gene. Hum Genet 1993 0.75