PubRank

Emmanuelle Génin

Author PubWeight™ 52.29‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Estimation of the inbreeding coefficient through use of genomic data. Am J Hum Genet 2003 4.01
2 Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome. Am J Hum Genet 2007 3.42
3 Absence of association of thrombophilia polymorphisms with intrauterine growth restriction. N Engl J Med 2002 3.15
4 Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online. Hum Mutat 2007 1.93
5 Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds. Am J Hum Genet 2001 1.70
6 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
7 Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls. Am J Epidemiol 2010 1.60
8 Impact of parental relationships in maximum lod score affected sib-pair method. Genet Epidemiol 2002 1.54
9 Complex trait mapping in isolated populations: Are specific statistical methods required? Eur J Hum Genet 2005 1.30
10 Dealing with missing data in family-based association studies: a multiple imputation approach. Hum Hered 2007 1.25
11 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
12 ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease. Neurobiol Dis 2005 1.16
13 On the use of haplotype phylogeny to detect disease susceptibility loci. BMC Genet 2005 1.10
14 No replication of genetic association between candidate polymorphisms and Alzheimer's disease. Neurobiol Aging 2009 1.10
15 Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium. Carcinogenesis 2012 1.05
16 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
17 Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco. J Cyst Fibros 2008 1.00
18 Clustering of haplotypes based on phylogeny: how good a strategy for association testing? Eur J Hum Genet 2006 1.00
19 Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us? Eur J Hum Genet 2011 0.99
20 Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies. Eur J Hum Genet 2004 0.99
21 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
22 Rare and low frequency variant stratification in the UK population: description and impact on association tests. PLoS One 2012 0.91
23 High imatinib dose overcomes insufficient response associated with ABCG2 haplotype in chronic myelogenous leukemia patients. Oncotarget 2013 0.91
24 How important are rare variants in common disease? Brief Funct Genomics 2014 0.89
25 ALTree: association detection and localization of susceptibility sites using haplotype phylogenetic trees. Bioinformatics 2006 0.87
26 Impaired performance of FDR-based strategies in whole-genome association studies when SNPs are excluded prior to the analysis. Genet Epidemiol 2009 0.82
27 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
28 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
29 Genetic analysis of multiple sclerosis in Europeans: French data. J Neuroimmunol 2003 0.79
30 Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutations. Ann Hum Genet 2007 0.79
31 No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease. Neurosci Lett 2003 0.79
32 A weighted-Holm procedure accounting for allele frequencies in genomewide association studies. Genetics 2008 0.79
33 Estimating the age of CFTR mutations predominantly found in Brittany (Western France). J Cyst Fibros 2007 0.79
34 Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III. Hum Hered 2014 0.79
35 Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis. Ann Rheum Dis 2010 0.78
36 Advantage of using allele-specific copy numbers when testing for association in regions with common copy number variants. PLoS One 2013 0.77
37 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
38 Power comparison of different methods to detect genetic effects and gene-environment interactions. BMC Proc 2007 0.77
39 Molecular reclassification of Crohn's disease: a cautionary note on population stratification. PLoS One 2013 0.77
40 On the use of phylogeny-based tests to detect association between quantitative traits and haplotypes. Genet Epidemiol 2009 0.77
41 A mixture model approach to multiple testing for the genetic analysis of gene expression. BMC Proc 2007 0.76
42 A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism. Neurosci Lett 2003 0.76
43 Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans. PLoS One 2012 0.75
44 Dealing with missing phase and missing data in phylogeny-based analysis. BMC Proc 2007 0.75
45 Impact of the diagnosis definition on linkage detection. BMC Genet 2005 0.75
46 Efficiency of multiple imputation to test for association in the presence of missing data. BMC Proc 2007 0.75
47 Comparative power of family-based association strategies to detect disease-causing variants under two-locus models. Genet Epidemiol 2012 0.75
48 Editor's Note. Hum Hered 2016 0.75
49 Selecting predictive markers for pharmacogenetic traits: tagging vs. data-mining approaches. Hum Hered 2008 0.75
50 Revisiting the Polygenic Additive Liability Model through the Example of Diabetes Mellitus. Hum Hered 2016 0.75