Published in J Thromb Haemost on October 01, 2011
Customized Choice of Oral P2Y12 Receptor Blocker (PRU-MATRIX) | NCT01477775
Pharmacogenetics and cardiovascular disease--implications for personalized medicine. Pharmacol Rev (2013) 1.04
Influence of the paraoxonase-1 Q192R genetic variant on clopidogrel responsiveness and recurrent cardiovascular events: a systematic review and meta-analysis. J Thromb Haemost (2012) 0.91
Personalized antiplatelet therapy with P2Y12 receptor inhibitors: benefits and pitfalls. Postepy Kardiol Interwencyjnej (2015) 0.84
Paraoxonase 1 gene polymorphism does not affect clopidogrel response variability but is associated with clinical outcome after PCI. PLoS One (2013) 0.83
Pharmacogenomics of anti-platelet and anti-coagulation therapy. Curr Cardiol Rep (2013) 0.81
Interplay between genetic and clinical variables affecting platelet reactivity and cardiac adverse events in patients undergoing percutaneous coronary intervention. PLoS One (2014) 0.80
Association of PON1, P2Y12 and COX1 with Recurrent Ischemic Events in Patients with Extracranial or Intracranial Stenting. PLoS One (2016) 0.77
Complete sequence of pSC101. Nucleic Acids Res (1984) 2.22
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients. J Med Genet (2007) 2.21
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nat Genet (1999) 2.05
Meeting report ESC forum on drug eluting stents, European Heart House, Nice, 27-28 September 2007. EuroIntervention (2009) 1.94
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease. N Engl J Med (2000) 1.94
Computational evidence in favor of a two-state, two-mode model of the retinal chromophore photoisomerization. Proc Natl Acad Sci U S A (2000) 1.92
Potyvirus proteins: a wealth of functions. Virus Res (2001) 1.85
Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost (1998) 1.71
Circulating levels of allopregnanolone in humans: gender, age, and endocrine influences. J Clin Endocrinol Metab (1998) 1.63
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma. Thromb Haemost (1996) 1.51
Activated protein C resistance: a comparison between two clotting assays and their relationship to the presence of the factor V Leiden mutation. Br J Haematol (1996) 1.39
Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis. Blood (1995) 1.39
Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels? J Thromb Haemost (2005) 1.38
Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH. Thromb Haemost (1995) 1.36
Two TaqI RFLPs in the human von Willebrand factor gene. Nucleic Acids Res (1987) 1.33
Potyviral HC-Pro: a multifunctional protein. J Gen Virol (1996) 1.26
PvuII RFLP inside the human estrogen receptor gene. Nucleic Acids Res (1987) 1.22
Complete sequence of an IS element present in pSC101. Nucleic Acids Res (1981) 1.22
Coronary artery remodelling is related to plaque composition. Heart (2005) 1.18
Thyroid abnormalities during lithium treatment. Acta Psychiatr Scand (1991) 1.18
Neonatal screening for congenital adrenal hyperplasia. Arch Dis Child (1983) 1.17
Serum allopregnanolone levels in pregnant women: changes during pregnancy, at delivery, and in hypertensive patients. J Clin Endocrinol Metab (2000) 1.16
Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate. Hum Mutat (2004) 1.15
Glansectomy with split-thickness skin graft for the treatment of penile carcinoma. Int J Impot Res (2009) 1.09
Preferential maternal derivation in inv dup(15): analysis of eight new cases. Hum Genet (1981) 1.08
Spectral versus visual EEG analysis in mild hepatic encephalopathy. Clin Neurophysiol (1999) 1.08
Gene deletion in an Italian haemophilia B subject. J Med Genet (1985) 1.05
Gene expression from viral RNA genomes. Plant Mol Biol (1996) 1.05
A heminested polymerase chain reaction for the detection of Brazilian rabies isolates from vampire bats and herbivores. Mem Inst Oswaldo Cruz (2002) 1.04
The frequency of oligonucleotides in mammalian genic regions. Comput Appl Biosci (1989) 1.03
Allopregnanolone concentrations and premenstrual syndrome. Eur J Endocrinol (2000) 0.99
Narcolepsy-cataplexy associated with precocious puberty. Neurology (2006) 0.99
Construction in vitro of hybrid plasmids carrying all the EcoRI fragments from lambdarifd18 DNA. Eur J Biochem (1979) 0.99
Combined surgery and chemotherapy for the treatment of primary gastrointestinal intermediate- or high-grade non-Hodgkin's lymphomas. Br J Cancer (1989) 0.99
Systemic and splanchnic hemodynamic changes after liver transplantation for cirrhosis: a long-term prospective study. Hepatology (1999) 0.99
Study of the PVRL1 gene in Italian nonsyndromic cleft lip patients with or without cleft palate. Ann Hum Genet (2006) 0.98
Influence of canine brain decomposition on laboratory diagnosis of rabies. Rev Soc Bras Med Trop (1999) 0.98
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost (1993) 0.98
Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions. J Mol Biol (1988) 0.97
Enhanced superoxide production with no change of the antioxidant activity in gingival fluid of patients with chronic adult periodontitis. Free Radic Res Commun (1991) 0.97
Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study. BMJ (2001) 0.96
[Occupational mortality in Italy during 1992, assessed through record-linkage between pension records and death certificates]. Med Lav (2005) 0.96
Visual control of hand-reaching movement: activity in parietal area 7m. Eur J Neurosci (1997) 0.96
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet (1993) 0.95
Changes of serum allopregnanolone levels in the first 2 years of life and during pubertal development. Pediatr Res (1999) 0.95
Esophageal leiomyomatosis in children: report of a case and review of the literature. Eur J Pediatr Surg (1998) 0.94
Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet (1982) 0.94
Self-preventive oral behavior in an Italian university student population. J Clin Periodontol (2001) 0.94
Atypical deletions generated by mutated IS102 elements. Mol Gen Genet (1984) 0.93
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII. J Thromb Haemost (2006) 0.93
Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay. Thromb Haemost (1993) 0.93
Clinical picture and management of congenital factor VII deficiency. Haemophilia (2004) 0.93
A new approach to DNA polymerase kinetics. J Mol Biol (1979) 0.93
Protein S deficiency: a database of mutations--summary of the first update. Thromb Haemost (2000) 0.92
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects. Arterioscler Thromb Vasc Biol (1997) 0.92
A double-blind study of L-sulpiride versus amitriptyline in lithium-maintained bipolar depressives. Acta Psychiatr Scand (1993) 0.91
Long-term low-dose dehydroepiandrosterone replacement therapy in aging males with partial androgen deficiency. Aging Male (2004) 0.91
Sublocalization of the human protein C gene on chromosome 2q13-q14. Hum Genet (1989) 0.91
Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma. Leukemia (1995) 0.91
Gene-gene and gene - clinical factors interaction in acute myocardial infarction: a new detailed risk chart. Curr Pharm Des (2010) 0.90
Neonatal screening for cystic fibrosis by dried blood spot trypsin assay. Results in 47 127 newborn infants from a homogeneous population. Acta Paediatr Scand (1984) 0.90
Thrombosis in inherited factor VII deficiency. J Thromb Haemost (2003) 0.90
Tibolone, transdermal estradiol or oral estrogen-progestin therapies: effects on circulating allopregnanolone, cortisol and dehydroepiandrosterone levels. Gynecol Endocrinol (2005) 0.89
Current concepts on antiplatelet therapy: focus on the novel thienopyridine and non-thienopyridine agents. Adv Hematol (2010) 0.89
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol (1997) 0.89
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene. Blood (1998) 0.89
Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation. J Thromb Haemost (2005) 0.89
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Hum Genet (1993) 0.89
Resistance to activated protein C in healthy women taking oral contraceptives. Br J Haematol (1995) 0.89
Luteinising hormone-releasing hormone nasal spray as therapy for undescended testicle. Arch Dis Child (1978) 0.89
Site-specific deletions in the recombinant plasmid pSC101 containing the redB-ori region of phage lambda. Gene (1981) 0.88
Molecular characteristics of a non-deletion alpha-thalassaemia of the Po River Delta. Eur J Biochem (1981) 0.88
Relationships among the secretion of ACTH, GH, and cortisol during the insulin-induced hypoglycemia test in the normal and obese child. J Clin Endocrinol Metab (1975) 0.88
Hypophyso-gonadal function in the cryptorchid child: differences between unilateral and bilateral cryptorchids. Acta Endocrinol (Copenh) (1976) 0.87
RNA-based therapeutic approaches for coagulation factor deficiencies. J Thromb Haemost (2011) 0.87
Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V. Br J Haematol (1997) 0.87
The use of dopamine agonists in the treatment of schizophrenia. Neuropharmacology (1981) 0.87
Hormonal replacement therapy affects calcitonin gene-related peptide and atrial natriuretic peptide secretion in postmenopausal women. Eur J Endocrinol (1997) 0.87
Displacement of T lymphocytes with the 'Helper/Inducer' phenotype from peripheral blood to lymphoid organs in untreated patients with Hodgkin's disease. Scand J Haematol (1983) 0.87
Pulmonary function abnormalities in children with Henoch-Schönlein purpura. Eur Respir J (1999) 0.87
Measurement of oxidative stress in human liver by EPR spin-probe technique. Free Radic Res (2000) 0.86
Incidence rates of surgically treated idiopathic carpal tunnel syndrome in blue- and white-collar workers and housewives in Tuscany, Italy. Occup Environ Med (2009) 0.86
The course of thyroid abnormalities during lithium treatment: a two-year follow-up study. Acta Psychiatr Scand (1992) 0.86
Risk of venous thromboembolism and stroke associated with oral contraceptives. Role of congenital thrombophilias. Recenti Prog Med (1996) 0.86
The accuracy of DNA replication. Biochimie (1978) 0.86
Menopause and the central nervous system: intervention options. Maturitas (1999) 0.86
One year clinical follow up of paclitaxel eluting stents for acute myocardial infarction compared with sirolimus eluting stents. Heart (2005) 0.86
Potyvirus helper component-proteinase self-interaction in the yeast two-hybrid system and delineation of the interaction domain involved. Virology (1999) 0.86
ESC Forum on Drug Eluting Stents European Heart House, Nice, 27-28 September 2007. Eur Heart J (2008) 0.85
Duplex Doppler findings in splenic arteriovenous fistula. J Clin Ultrasound (1998) 0.85
Neuropeptides, neurotransmitters, neurosteroids, and the onset of puberty. Ann N Y Acad Sci (2000) 0.85
Effect of obesity on the hypothalamo-pituitary-gonadal function in childhood. Acta Paediatr Scand (1977) 0.85
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family. Blood (2000) 0.85
Effect of long-term GH administration on pituitary-thyroid function in idiopathic hypopituitarism. Acta Paediatr Scand (1979) 0.85
Protein A reactivity of IgM- and IgD-bearing lymphocytes from some patients with chronic lymphocytic leukemia. Clin Immunol Immunopathol (1981) 0.85
Multiple brain metastases from "lymphoepithelioma-like" thymic carcinoma: a combined stereotactic-radiosurgical approach. Surg Neurol (2001) 0.84