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About
A C Papp
Author PubWeight™ 28.01
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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