Year |
Citation |
Score |
2019 |
Nutile T, Ruggiero D, Herzig A, Tirozzi A, Nappo S, Sorice R, Marangio F, Bellenguez C, Leutenegger A, Ciullo M. Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy. Scientific Reports. 9: 4059-4059. PMID 30858532 DOI: 10.1038/S41598-019-41022-6 |
0.458 |
|
2018 |
Herzig AF, Nutile T, Ruggiero D, Ciullo M, Perdry H, Leutenegger A. Detecting the dominance component of heritability in isolated and outbred human populations. Scientific Reports. 8: 1-14. PMID 30575761 DOI: 10.1038/S41598-018-36050-7 |
0.423 |
|
2018 |
Herzig AF, Nutile T, Babron M, Ciullo M, Bellenguez C, Leutenegger A. Strategies for phasing and imputation in a population isolate. Genetic Epidemiology. 42: 201-213. PMID 29319195 DOI: 10.1002/Gepi.22109 |
0.418 |
|
2015 |
Gazal S, Sahbatou M, Babron M, Génin E, Leutenegger A. High level of inbreeding in final phase of 1000 Genomes Project. Scientific Reports. 5: 17453-17453. PMID 26625947 DOI: 10.1038/Srep17453 |
0.443 |
|
2015 |
Jalkh N, Sahbatou M, Chouery E, Megarbane A, Leutenegger A, Serre J. Genome-wide inbreeding estimation within Lebanese communities using SNP arrays European Journal of Human Genetics. 23: 1364-1369. PMID 25424710 DOI: 10.1038/Ejhg.2014.246 |
0.361 |
|
2014 |
Gazal S, Sahbatou M, Perdry H, Letort S, Génin E, Leutenegger A. Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III. Human Heredity. 77: 49-62. PMID 25060269 DOI: 10.1159/000358224 |
0.396 |
|
2012 |
Génin E, Sahbatou M, Gazal S, Babron M, Perdry H, Leutenegger A. Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed? Human Heredity. 74: 142-152. PMID 23594492 DOI: 10.1159/000346790 |
0.384 |
|
2012 |
Sorice R, Ruggiero D, Nutile T, Aversano M, Husemoen L, Linneberg A, Bourgain C, Leutenegger A, Ciullo M. Genetic and Environmental Factors Influencing the Placental Growth Factor (PGF) Variation in Two Populations Plos One. 7. PMID 22916133 DOI: 10.1371/Journal.Pone.0042537 |
0.366 |
|
2011 |
Leutenegger A, Sahbatou M, Gazal S, Cann H, Génin E. Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us? European Journal of Human Genetics. 19: 583-587. PMID 21364699 DOI: 10.1038/Ejhg.2010.205 |
0.447 |
|
2011 |
Ruggiero D, Dalmasso C, Nutile T, Sorice R, Dionisi L, Aversano M, Bröet P, Leutenegger A, Bourgain C, Ciullo M. Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms Plos One. 6. PMID 21347390 DOI: 10.1371/Journal.Pone.0016982 |
0.387 |
|
2007 |
Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger A, Nelson I, Babron M, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G. A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3 Human Genetics. 122: 261-273. PMID 17605047 DOI: 10.1007/S00439-007-0396-1 |
0.306 |
|
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