Published in N Engl J Med on July 04, 2002
Prothrombin gene G20210A mutation and obstetric complications. Obstet Gynecol (2010) 1.34
Thrombophilia and pregnancy. Reprod Biol Endocrinol (2003) 1.16
Incidence of deep vein thrombosis related to peripherally inserted central catheters in children and adolescents. CMAJ (2007) 1.08
Innate immunity, coagulation and placenta-related adverse pregnancy outcomes. Thromb Res (2009) 0.92
Drinking water contaminants, gene polymorphisms, and fetal growth. Environ Health Perspect (2004) 0.89
Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation. J Mol Diagn (2003) 0.83
Individual risk assessment of adverse pregnancy outcome by multivariate regression analysis may serve as basis for drug intervention studies: retrospective analysis of 426 high-risk patients including ethical aspects. Arch Gynecol Obstet (2013) 0.81
Thrombophilia polymorphisms and intrauterine growth restriction. N Engl J Med (2002) 0.81
Clotting and hemorrhage in the placenta--a delicate balance. N Engl J Med (2002) 0.80
Analysis of Case-Parent Trios Using a Loglinear Model with Adjustment for Transmission Ratio Distortion. Front Genet (2016) 0.77
Effects of maternal 5,10-methylenetetrahydrofolate reductase C677T and A1298C Polymorphisms and tobacco smoking on infant birth weight in a Japanese population. J Epidemiol (2012) 0.76
Impact of smoking during pregnancy on functional coagulation testing. Am J Perinatol (2011) 0.75
The cost-benefit ratio of screening pregnant women for thrombophilia. Blood Transfus (2007) 0.75
Thrombophilia polymorphisms and intrauterine growth restriction. N Engl J Med (2002) 0.75
Ethnic differences in the association of thrombophilic polymorphisms with obstetric complications in Slovak and Roma (Gypsy) populations. Genet Test Mol Biomarkers (2014) 0.75
The Obstetric Medicine Listserv: review of controversies surrounding thrombophilia testing. Obstet Med (2012) 0.75
The role of proteoglycans in contributing to placental thrombosis and fetal growth restriction. J Pregnancy (2011) 0.75
Factor V Leiden, Prothrombin and MTHFR Mutation in Patients with Preeclamsia, Intrauterine Growth Restriction and Placental Abruption. Open Access Maced J Med Sci (2015) 0.75
Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate. Iran J Public Health (2014) 0.75
The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein. Reprod Biol Endocrinol (2004) 0.75
Estimation of the inbreeding coefficient through use of genomic data. Am J Hum Genet (2003) 4.01
Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome. Am J Hum Genet (2007) 3.42
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema. J Allergy Clin Immunol (2004) 3.30
A combined analysis of North American case-control studies of residential radon and lung cancer. J Toxicol Environ Health A (2006) 2.78
2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol (2010) 2.75
Residential radon and risk of lung cancer: a combined analysis of 7 North American case-control studies. Epidemiology (2005) 2.56
Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations. Am J Epidemiol (2002) 2.56
Response to combination antiretroviral therapy: variation by age. AIDS (2008) 2.28
Unexpected relationship between plasma homocysteine and intrauterine growth restriction. Clin Chem (2003) 2.14
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online. Hum Mutat (2007) 1.93
Early percutaneous tracheotomy versus prolonged intubation of mechanically ventilated patients after cardiac surgery: a randomized trial. Ann Intern Med (2011) 1.89
Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. Ann Allergy Asthma Immunol (2008) 1.76
Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds. Am J Hum Genet (2001) 1.70
Long-term observational study of sporadic inclusion body myositis. Brain (2011) 1.69
Robustness of case-control studies of genetic factors to population stratification: magnitude of bias and type I error. Cancer Epidemiol Biomarkers Prev (2004) 1.68
Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls. Am J Epidemiol (2010) 1.60
Impact of parental relationships in maximum lod score affected sib-pair method. Genet Epidemiol (2002) 1.54
Generation of kinins during preparation and storage of whole blood-derived platelet concentrates. Transfusion (2007) 1.49
Imported malaria in HIV-infected patients enrolled in the ANRS CO4 FHDH study. J Acquir Immune Defic Syndr (2008) 1.46
Correlation of anti-signal recognition particle autoantibody levels with creatine kinase activity in patients with necrotizing myopathy. Arthritis Rheum (2011) 1.36
Kaposi sarcoma incidence and survival among HIV-infected homosexual men after HIV seroconversion. J Natl Cancer Inst (2010) 1.31
Complex trait mapping in isolated populations: Are specific statistical methods required? Eur J Hum Genet (2005) 1.30
Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study. Hum Mutat (2011) 1.25
Plasminogen alleles influence susceptibility to invasive aspergillosis. PLoS Genet (2008) 1.25
Dealing with missing data in family-based association studies: a multiple imputation approach. Hum Hered (2007) 1.25
Periostin, a member of a novel family of vitamin K-dependent proteins, is expressed by mesenchymal stromal cells. J Biol Chem (2008) 1.24
Hierarchical cluster and survival analyses of antisynthetase syndrome: phenotype and outcome are correlated with anti-tRNA synthetase antibody specificity. Autoimmun Rev (2012) 1.22
ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease. Neurobiol Dis (2005) 1.16
Impact of late presentation on the risk of death among HIV-infected people in France (2003-2009). J Acquir Immune Defic Syndr (2013) 1.14
On the use of haplotype phylogeny to detect disease susceptibility loci. BMC Genet (2005) 1.10
No replication of genetic association between candidate polymorphisms and Alzheimer's disease. Neurobiol Aging (2009) 1.10
Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium. Carcinogenesis (2012) 1.05
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? Eur J Hum Genet (2006) 1.02
Comparative impact of antiretroviral drugs on markers of inflammation and immune activation during the first two years of effective therapy for HIV-1 infection: an observational study. BMC Infect Dis (2014) 1.02
An overview of the North American residential radon and lung cancer case-control studies. J Toxicol Environ Health A (2006) 1.02
The spectrum of malignancies in HIV-infected patients in 2006 in France: the ONCOVIH study. Int J Cancer (2011) 1.00
Clustering of haplotypes based on phylogeny: how good a strategy for association testing? Eur J Hum Genet (2006) 1.00
Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco. J Cyst Fibros (2008) 1.00
Acute hepatitis C in HIV-infected patients: rare spontaneous clearance correlates with weak memory CD4 T-cell responses to hepatitis C virus. AIDS (2009) 1.00
Impact of HIV infection on severity of imported malaria is restricted to patients with CD4 cell counts < 350 cells/microl. AIDS (2009) 0.99
Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us? Eur J Hum Genet (2011) 0.99
Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies. Eur J Hum Genet (2004) 0.99
Raltegravir as functional monotherapy leads to virological failure and drug resistance in highly treatment-experienced HIV-infected patients. Scand J Infect Dis (2010) 0.97
Xenobiotic-metabolizing genes and small-for-gestational-age births: interaction with maternal smoking. Epidemiology (2006) 0.96
Cohort Profile: French hospital database on HIV (FHDH-ANRS CO4). Int J Epidemiol (2014) 0.96
Nosocomial infections in adult cardiogenic shock patients supported by venoarterial extracorporeal membrane oxygenation. Clin Infect Dis (2012) 0.96
Family history of hematopoietic and other cancers in children with acute lymphoblastic leukemia. Cancer Detect Prev (2004) 0.94
Assessment of occupational exposure to human immunodeficiency virus and hepatitis C virus in a referral hospital in Burundi, Central Africa. Infect Control Hosp Epidemiol (2003) 0.92
Evaluation of rapid progressors in HIV infection as an extreme phenotype. J Acquir Immune Defic Syndr (2014) 0.92
Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy. Proc Natl Acad Sci U S A (2012) 0.91
Rare and low frequency variant stratification in the UK population: description and impact on association tests. PLoS One (2012) 0.91
Proangiogenic effects of protease-activated receptor 2 are tumor necrosis factor-alpha and consecutively Tie2 dependent. Arterioscler Thromb Vasc Biol (2006) 0.91
High imatinib dose overcomes insufficient response associated with ABCG2 haplotype in chronic myelogenous leukemia patients. Oncotarget (2013) 0.91
How important are rare variants in common disease? Brief Funct Genomics (2014) 0.89
An exploratory study on the CHRNA3-CHRNA5-CHRNB4 cluster, smoking, and Parkinson's disease. Neurodegener Dis (2011) 0.88
Forced-air warming: a source of airborne contamination in the operating room? Orthop Rev (Pavia) (2009) 0.88
Tissue factor pathway inhibitor (TFPI) interferes with endothelial cell migration by inhibition of both the Erk pathway and focal adhesion proteins. Thromb Haemost (2008) 0.88
ALTree: association detection and localization of susceptibility sites using haplotype phylogenetic trees. Bioinformatics (2006) 0.87
Symptomatic illness and low CD4 cell count at HIV seroconversion as markers of severe primary HIV infection. PLoS One (2013) 0.87
Treatment of acute HCV infection in HIV-positive patients: experience from a multicentre European cohort. Antivir Ther (2010) 0.86
Glanzmann thrombasthenia in an Oldenbourg filly. Vet Clin Pathol (2007) 0.86
A comparison of urinary and sexual outcomes in women experiencing vaginal and Caesarean births. J Obstet Gynaecol Can (2005) 0.86
Injection Drug Use and Hepatitis C as Risk Factors for Mortality in HIV-Infected Individuals: The Antiretroviral Therapy Cohort Collaboration. J Acquir Immune Defic Syndr (2015) 0.85
Analysis of Scutellaria lateriflora and its adulterants Teucrium canadense and Teucrium chamaedrys by LC-UV/MS, TLC, and digital photomicroscopy. J AOAC Int (2003) 0.85
Antisynthetase syndrome with anti-Jo1 antibodies in 48 patients: pulmonary involvement predicts disease-modifying antirheumatic drug use. J Rheumatol (2012) 0.84
Protease inhibitors exposure is not related to lung cancer risk in HIV smoker patients: a nested case-control study. AIDS (2015) 0.83
VEGF increases the fibrinolytic activity of endothelial cells within fibrin matrices: involvement of VEGFR-2, tissue type plasminogen activator and matrix metalloproteinases. Thromb Res (2007) 0.82
[Cancer and HIV infection]. Med Sci (Paris) (2010) 0.82
c-Met activation in medulloblastoma induces tissue factor expression and activity: effects on cell migration. Carcinogenesis (2009) 0.82
Impaired performance of FDR-based strategies in whole-genome association studies when SNPs are excluded prior to the analysis. Genet Epidemiol (2009) 0.82
Cardiac tamponade in a patient with moderate hemophilia A and factor VIII Inhibitors. Can J Cardiol (2006) 0.82
On the use of sibling recurrence risks to select environmental factors liable to interact with genetic risk factors. Eur J Hum Genet (2010) 0.81
Role of genotype G hepatitis B virus mixed infection on the progression of hepatic fibrosis in HIV positive patients over 5 years of follow-up. J Clin Virol (2013) 0.80
Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data. BMC Genomics (2012) 0.80
Lack of TGF-β production by hepatitis C virus-specific T cells during HCV acute phase is associated with HCV clearance in HIV coinfection. J Hepatol (2012) 0.79
No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease. Neurosci Lett (2003) 0.79
Hepatic steatosis in HIV-HCV coinfected patients receiving antiretroviral therapy is associated with HCV-related factors but not antiretrovirals. BMC Res Notes (2012) 0.79
A weighted-Holm procedure accounting for allele frequencies in genomewide association studies. Genetics (2008) 0.79
Genetic analysis of multiple sclerosis in Europeans: French data. J Neuroimmunol (2003) 0.79
Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutations. Ann Hum Genet (2007) 0.79
Computation of the optical trapping force using an FDTD based technique. Opt Express (2005) 0.79
The effect of computer-assisted evaluation of labor on cesarean rates. J Healthc Qual (2004) 0.79
Estimating the age of CFTR mutations predominantly found in Brittany (Western France). J Cyst Fibros (2007) 0.79
Clinical effects of preoperative radiation therapy on anorectal function after proctectomy and colonic J-pouch-anal anastomosis. Dis Colon Rectum (2002) 0.79
Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III. Hum Hered (2014) 0.79
Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis. Ann Rheum Dis (2010) 0.78
Levels of intracellular HIV-DNA in patients with suppressive antiretroviral therapy. AIDS (2015) 0.78
Oxidative tyrosylation of high density lipoproteins impairs cholesterol efflux from mouse J774 macrophages: role of scavenger receptors, classes A and B. J Cell Sci (2003) 0.78
Tissue factor mediates the HGF/Met-induced anti-apoptotic pathway in DAOY medulloblastoma cells. J Neurooncol (2009) 0.78
Cortactin activation by FVIIa/tissue factor and PAR2 promotes endothelial cell migration. Am J Physiol Regul Integr Comp Physiol (2010) 0.78
Thrombophilic polymorphisms and intrauterine growth restriction. Epidemiology (2005) 0.77
Perinatal reference intervals for plasma homocysteine and factors influencing its concentration. Clin Chem (2002) 0.77
Genome-scan for bipolar disorder with sib-pair families in the Sardinian population: a new susceptibility locus on chromosome 1p22-p21? Am J Med Genet B Neuropsychiatr Genet (2010) 0.77
Power comparison of different methods to detect genetic effects and gene-environment interactions. BMC Proc (2007) 0.77
Molecular reclassification of Crohn's disease: a cautionary note on population stratification. PLoS One (2013) 0.77
On the use of phylogeny-based tests to detect association between quantitative traits and haplotypes. Genet Epidemiol (2009) 0.77