| Year |
Citation |
Score |
| 2022 |
Solís-Moruno M, Batlle-Masó L, Bonet N, Aróstegui JI, Casals F. Somatic genetic variation in healthy tissue and non-cancer diseases. European Journal of Human Genetics : Ejhg. PMID 36289407 DOI: 10.1038/s41431-022-01213-8 |
0.317 |
|
| 2022 |
Moreno-Ruiz N, Lao O, Aróstegui JI, Laayouni H, Casals F. Assessing the digenic model in rare disorders using population sequencing data. European Journal of Human Genetics : Ejhg. PMID 36192439 DOI: 10.1038/s41431-022-01191-x |
0.431 |
|
| 2022 |
Lobon I, Solís-Moruno M, Juan D, Muhaisen A, Abascal F, Esteller-Cucala P, García-Pérez R, Martí MJ, Tolosa E, Ávila J, Rahbari R, Marques-Bonet T, Casals F, Soriano E. Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes. Frontiers in Aging. 3: 851039. PMID 35821807 DOI: 10.3389/fragi.2022.851039 |
0.362 |
|
| 2021 |
Solís-Moruno M, Mensa-Vilaró A, Batlle-Masó L, Lobón I, Bonet N, Marquès-Bonet T, Aróstegui JI, Casals F. Assessment of the gene mosaicism burden in blood and its implications for immune disorders. Scientific Reports. 11: 12940. PMID 34155260 DOI: 10.1038/s41598-021-92381-y |
0.379 |
|
| 2020 |
Barrio PA, García Ó, Phillips C, Prieto L, Gusmão L, Fernández C, Casals F, Freitas JM, González-Albo MDC, Martín P, Mosquera A, Navarro-Vera I, Paredes M, Pérez JA, Pinzón A, et al. The first GHEP-ISFG collaborative exercise on forensic applications of massively parallel sequencing. Forensic Science International. Genetics. 49: 102391. PMID 32957016 DOI: 10.1016/J.Fsigen.2020.102391 |
0.356 |
|
| 2020 |
Martín-Nalda A, Fortuny C, Rey L, Bunney TD, Alsina L, Esteve-Solé A, Bull D, Anton MC, Basagaña M, Casals F, Deyá A, García-Prat M, Gimeno R, Juan M, Martinez-Banaclocha H, et al. Severe Autoinflammatory Manifestations and Antibody Deficiency Due to Novel Hypermorphic PLCG2 Mutations. Journal of Clinical Immunology. PMID 32671674 DOI: 10.1007/S10875-020-00794-7 |
0.393 |
|
| 2020 |
Batlle-Masó L, Mensa-Vilaró A, Solís-Moruno M, Marquès-Bonet T, Arostegui JI, Casals F. Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing. European Journal of Medical Genetics. 103920. PMID 32222431 DOI: 10.1016/J.Ejmg.2020.103920 |
0.425 |
|
| 2020 |
Viñas-Giménez L, Padilla N, Batlle-Masó L, Casals F, Rivière JG, Martínez-Gallo M, de la Cruz X, Colobran R. FHLdb: A Comprehensive Database on the Molecular Basis of Familial Hemophagocytic Lymphohistiocytosis. Frontiers in Immunology. 11: 107. PMID 32076423 DOI: 10.3389/Fimmu.2020.00107 |
0.497 |
|
| 2020 |
Harding T, Milot E, Moreau C, Lefebvre JF, Bournival JS, Vézina H, Laprise C, Lalueza-Fox C, Anglada R, Loewen B, Casals F, Ribot I, Labuda D. Historical human remains identification through maternal and paternal genetic signatures in a founder population with extensive genealogical record. American Journal of Physical Anthropology. PMID 32064591 DOI: 10.1002/Ajpa.24024 |
0.449 |
|
| 2019 |
Kuderna LFK, Solís-Moruno M, Batlle-Masó L, Julià E, Lizano E, Anglada R, Ramírez E, Bote A, Tormo M, Marquès-Bonet T, Fornas Ò, Casals F. Flow Sorting Enrichment and Nanopore Sequencing of Chromosome 1 From a Chinese Individual. Frontiers in Genetics. 10: 1315. PMID 31998370 DOI: 10.3389/Fgene.2019.01315 |
0.334 |
|
| 2019 |
Palomo-Díez S, Gomes C, López-Parra A, Baeza-Richer C, Cuscó I, Raffone C, García-Arumí E, Vinueza-Espinosa D, Santos C, Montes N, Rasal R, Escala O, Cuellar J, Subirá E, Casals F, et al. Genetic identification of Spanish civil war victims. The state of the art in Catalonia (Northeastern Spain) Forensic Science International: Genetics Supplement Series. 7: 419-421. DOI: 10.1016/J.Fsigss.2019.10.035 |
0.406 |
|
| 2018 |
Mattle-Greminger MP, Bilgin Sonay T, Nater A, Pybus M, Desai T, de Valles G, Casals F, Scally A, Bertranpetit J, Marques-Bonet T, van Schaik CP, Anisimova M, Krützen M. Genomes reveal marked differences in the adaptive evolution between orangutan species. Genome Biology. 19: 193. PMID 30428903 DOI: 10.1186/S13059-018-1562-6 |
0.346 |
|
| 2018 |
Mensa-Vilaró A, García-Morato MB, de la Calle-Martin O, Franco-Jarava C, Martínez-Saavedra MT, González-Granado LI, González-Roca E, Fuster JL, Alsina L, Mutchinick OM, Balderrama-Rodríguez A, Ramos E, Modesto C, Mesa-Del-Castillo P, Ortego-Centeno N, ... ... Casals F, et al. Unexpected Relevant Role of Gene Mosaicism in Primary Immunodeficiency Diseases. The Journal of Allergy and Clinical Immunology. PMID 30273710 DOI: 10.1016/J.Jaci.2018.09.009 |
0.441 |
|
| 2018 |
de Valles-Ibáñez G, Esteve-Solé A, Piquer M, González-Navarro EA, Hernandez-Rodriguez J, Laayouni H, González-Roca E, Plaza-Martin AM, Deyà-Martínez Á, Martín-Nalda A, Martínez-Gallo M, García-Prat M, Del Pino-Molina L, Cuscó I, Codina-Solà M, ... ... Casals F, et al. Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond. Frontiers in Immunology. 9: 636. PMID 29867916 DOI: 10.3389/Fimmu.2018.00636 |
0.526 |
|
| 2018 |
Schwab C, Gabrysch A, Olbrich P, Patiño V, Warnatz K, Wolff D, Hoshino A, Kobayashi M, Imai K, Takagi M, Dybedal I, Haddock JA, Sansom D, Lucena JM, Seidl M, ... ... Casals F, et al. Phenotype, penetrance, and treatment of 133 CTLA-4-insufficient individuals. The Journal of Allergy and Clinical Immunology. PMID 29729943 DOI: 10.1016/J.Jaci.2018.02.055 |
0.352 |
|
| 2017 |
Nater A, Mattle-Greminger MP, Nurcahyo A, Nowak MG, de Manuel M, Desai T, Groves C, Pybus M, Sonay TB, Roos C, Lameira AR, Wich SA, Askew J, Davila-Ross M, Fredriksson G, ... ... Casals F, et al. Morphometric, Behavioral, and Genomic Evidence for a New Orangutan Species. Current Biology : Cb. PMID 29103940 DOI: 10.1016/J.Cub.2017.09.047 |
0.362 |
|
| 2017 |
Hernandez-Rodriguez J, Arandjelovic M, Lester J, de Filippo C, Weihmann A, Meyer M, Angedakin S, Casals F, Navarro A, Vigilant L, Kühl HS, Langergraber K, Boesch C, Hughes D, Marques-Bonet T. The impact of endogenous content, replicates and pooling on genome capture from fecal samples. Molecular Ecology Resources. PMID 29058768 DOI: 10.1111/1755-0998.12728 |
0.398 |
|
| 2017 |
Casals F, Anglada R, Bonet N, Rasal R, van der Gaag KJ, Hoogenboom J, Solé-Morata N, Comas D, Calafell F. Length and repeat-sequence variation in 58 STRs and 94 SNPs in two Spanish populations. Forensic Science International. Genetics. 30: 66-70. PMID 28633070 DOI: 10.1016/J.Fsigen.2017.06.006 |
0.396 |
|
| 2017 |
Mondal M, Bergström A, Xue Y, Calafell F, Laayouni H, Casals F, Majumder PP, Tyler-Smith C, Bertranpetit J. Y-chromosomal sequences of diverse Indian populations and the ancestry of the Andamanese. Human Genetics. PMID 28444560 DOI: 10.1007/S00439-017-1800-0 |
0.388 |
|
| 2017 |
Spataro N, Roca-Umbert A, Cervera-Carles L, Vallès M, Anglada R, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Kulisevsky J, Casals F, Clarimón J, Bosch E. Detection of genomic rearrangements from targeted resequencing data in Parkinson's disease patients. Movement Disorders : Official Journal of the Movement Disorder Society. 32: 165-169. PMID 28124432 DOI: 10.1002/Mds.26845 |
0.349 |
|
| 2016 |
Cagan A, Theunert C, Laayouni H, Santpere G, Pybus M, Casals F, Prüfer K, Navarro A, Marques-Bonet T, Bertranpetit J, Andrés AM. Natural Selection in the Great Apes. Molecular Biology and Evolution. PMID 27795229 DOI: 10.1093/Molbev/Msw215 |
0.371 |
|
| 2016 |
de Manuel M, Kuhlwilm M, Frandsen P, Sousa VC, Desai T, Prado-Martinez J, Hernandez-Rodriguez J, Dupanloup I, Lao O, Hallast P, Schmidt JM, Heredia-Genestar JM, Benazzo A, Barbujani G, Peter BM, ... ... Casals F, et al. Chimpanzee genomic diversity reveals ancient admixture with bonobos. Science (New York, N.Y.). 354: 477-481. PMID 27789843 DOI: 10.1126/Science.Aag2602 |
0.439 |
|
| 2016 |
Calafell F, Anglada R, Bonet N, González-Ruiz M, Prats-Muñoz G, Rasal R, Lalueza-Fox C, Bertranpetit J, Malgosa A, Casals F. An assessment of a massively parallel sequencing approach for the identification of individuals from mass graves of the Spanish Civil War (1936-1939). Electrophoresis. PMID 27489250 DOI: 10.1002/Elps.201600180 |
0.34 |
|
| 2016 |
Mondal M, Casals F, Xu T, Dall'Olio GM, Pybus M, Netea MG, Comas D, Laayouni H, Li Q, Majumder PP, Bertranpetit J. Genomic analysis of Andamanese provides insights into ancient human migration into Asia and adaptation. Nature Genetics. PMID 27455350 DOI: 10.1038/Ng.3621 |
0.461 |
|
| 2016 |
de Valles-Ibáñez G, Hernandez-Rodriguez J, Prado-Martinez J, Luisi P, Marquès-Bonet T, Casals F. Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes. Genome Biology and Evolution. 8: 871-7. PMID 26912403 DOI: 10.1093/Gbe/Evw040 |
0.488 |
|
| 2015 |
Spataro N, Calafell F, Cervera-Carles L, Casals F, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Kulisevsky J, Lleó A, Navarro A, Clarimón J, Bosch E. Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease. Human Molecular Genetics. 24: 2023-34. PMID 25504046 DOI: 10.1093/Hmg/Ddu616 |
0.353 |
|
| 2014 |
Juyal G, Mondal M, Luisi P, Laayouni H, Sood A, Midha V, Heutink P, Bertranpetit J, Thelma BK, Casals F. Population and genomic lessons from genetic analysis of two Indian populations. Human Genetics. 133: 1273-87. PMID 24980708 DOI: 10.1007/S00439-014-1462-0 |
0.483 |
|
| 2013 |
Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, de Maillard T, Grenier JC, Grenier JC, Gbeha E, Hamdan FF, Girard S, Spinella JF, Larivière M, Saillour V, Healy J, et al. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. Plos Genetics. 9: e1003815. PMID 24086152 DOI: 10.1371/Journal.Pgen.1003815 |
0.768 |
|
| 2013 |
Hodgkinson A, Casals F, Idaghdour Y, Grenier JC, Hernandez RD, Awadalla P. Selective constraint, background selection, and mutation accumulation variability within and between human populations. Bmc Genomics. 14: 495. PMID 23875710 DOI: 10.1186/1471-2164-14-495 |
0.792 |
|
| 2013 |
Prado-Martinez J, Sudmant PH, Kidd JM, Li H, Kelley JL, Lorente-Galdos B, Veeramah KR, Woerner AE, O'Connor TD, Santpere G, Cagan A, Theunert C, Casals F, Laayouni H, Munch K, et al. Great ape genetic diversity and population history. Nature. 499: 471-5. PMID 23823723 DOI: 10.1038/Nature12228 |
0.467 |
|
| 2013 |
Samuels ME, Majewski J, Alirezaie N, Fernandez I, Casals F, Patey N, Decaluwe H, Gosselin I, Haddad E, Hodgkinson A, Idaghdour Y, Marchand V, Michaud JL, Rodrigue MA, Desjardins S, et al. Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia. Journal of Medical Genetics. 50: 324-9. PMID 23423984 DOI: 10.1136/Jmedgenet-2012-101483 |
0.787 |
|
| 2013 |
Cagliani R, Guerini FR, Rubio-Acero R, Baglio F, Forni D, Agliardi C, Griffanti L, Fumagalli M, Pozzoli U, Riva S, Calabrese E, Sikora M, Casals F, Comi GP, Bresolin N, et al. Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease. Human Mutation. 34: 743-53. PMID 23420636 DOI: 10.1002/Humu.22301 |
0.329 |
|
| 2013 |
Hussin J, Sinnett D, Casals F, Idaghdour Y, Bruat V, Saillour V, Healy J, Grenier JC, de Malliard T, Busche S, Spinella JF, Larivière M, Gibson G, Andersson A, Holmfeldt L, et al. Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Research. 23: 419-30. PMID 23222848 DOI: 10.1101/Gr.144188.112 |
0.781 |
|
| 2012 |
Casals F, Bertranpetit J. Genetics. Human genetic variation, shared and private. Science (New York, N.Y.). 337: 39-40. PMID 22767915 DOI: 10.1126/Science.1224528 |
0.477 |
|
| 2012 |
Casals F, Idaghdour Y, Hussin J, Awadalla P. Next-generation sequencing approaches for genetic mapping of complex diseases. Journal of Neuroimmunology. 248: 10-22. PMID 22285396 DOI: 10.1016/J.Jneuroim.2011.12.017 |
0.765 |
|
| 2011 |
Sikora M, Laayouni H, Menendez C, Mayor A, Bardaji A, Sigauque B, Netea MG, Casals F, Bertranpetit J. A targeted association study of immunity genes and networks suggests novel associations with placental malaria infection. Plos One. 6: e24996. PMID 21949827 DOI: 10.1371/Journal.Pone.0024996 |
0.354 |
|
| 2011 |
Casals F, Sikora M, Laayouni H, Montanucci L, Muntasell A, Lazarus R, Calafell F, Awadalla P, Netea MG, Bertranpetit J. Genetic adaptation of the antibacterial human innate immunity network. Bmc Evolutionary Biology. 11: 202. PMID 21745391 DOI: 10.1186/1471-2148-11-202 |
0.621 |
|
| 2011 |
Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, et al. Variation in genome-wide mutation rates within and between human families. Nature Genetics. 43: 712-4. PMID 21666693 DOI: 10.1038/Ng.862 |
0.738 |
|
| 2011 |
Laayouni H, Montanucci L, Sikora M, Melé M, Dall'Olio GM, Lorente-Galdos B, McGee KM, Graffelman J, Awadalla P, Bosch E, Comas D, Navarro A, Calafell F, Casals F, Bertranpetit J. Similarity in recombination rate estimates highly correlates with genetic differentiation in humans. Plos One. 6: e17913. PMID 21464928 DOI: 10.1371/Journal.Pone.0017913 |
0.69 |
|
| 2011 |
Myers RA, Casals F, Gauthier J, Hamdan FF, Keebler J, Boyko AR, Bustamante CD, Piton AM, Spiegelman D, Henrion E, Zilversmit M, Hussin J, Quinlan J, Yang Y, Lafrenière RG, et al. A population genetic approach to mapping neurological disorder genes using deep resequencing. Plos Genetics. 7: e1001318. PMID 21383861 DOI: 10.1371/Journal.Pgen.1001318 |
0.705 |
|
| 2011 |
Marigorta UM, Lao O, Casals F, Calafell F, Morcillo-Suárez C, Faria R, Bosch E, Serra F, Bertranpetit J, Dopazo H, Navarro A. Recent human evolution has shaped geographical differences in susceptibility to disease. Bmc Genomics. 12: 55. PMID 21261943 DOI: 10.1186/1471-2164-12-55 |
0.499 |
|
| 2010 |
Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR, Côté M, Henrion E, Spiegelman D, Tarabeux J, Piton A, Yang Y, Boyko A, Bustamante C, Xiong L, et al. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. American Journal of Human Genetics. 87: 316-24. PMID 20797689 DOI: 10.1016/J.Ajhg.2010.07.019 |
0.76 |
|
| 2010 |
Vallès X, Roca A, Lozano F, Morais L, Suárez B, Casals F, Mandomando I, Sigaúque B, Nhalungo D, Esquinas C, Quintó L, Alonso PL, Torres A. Serotype-specific pneumococcal disease may be influenced by mannose-binding lectin deficiency. The European Respiratory Journal. 36: 856-63. PMID 20150204 DOI: 10.1183/09031936.00171409 |
0.325 |
|
| 2009 |
Vallès X, Sarrias MR, Casals F, Farnós M, Piñer R, Suárez B, Morais L, Mandomando I, Sigaúque B, Roca A, Alonso PL, Torres A, Thielens NM, Lozano F. Genetic and structural analysis of MBL2 and MASP2 polymorphisms in south-eastern African children. Tissue Antigens. 74: 298-307. PMID 19775369 DOI: 10.1111/J.1399-0039.2009.01328.X |
0.458 |
|
| 2009 |
Bosch E, Laayouni H, Morcillo-Suarez C, Casals F, Moreno-Estrada A, Ferrer-Admetlla A, Gardner M, Rosa A, Navarro A, Comas D, Graffelman J, Calafell F, Bertranpetit J. Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD. Bmc Genomics. 10: 338. PMID 19638193 DOI: 10.1186/1471-2164-10-338 |
0.408 |
|
| 2009 |
Moreno-Estrada A, Tang K, Sikora M, Marquès-Bonet T, Casals F, Navarro A, Calafell F, Bertranpetit J, Stoneking M, Bosch E. Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations. Molecular Biology and Evolution. 26: 2285-97. PMID 19578157 DOI: 10.1093/Molbev/Msp134 |
0.436 |
|
| 2009 |
Ferrer-Admetlla A, Sikora M, Laayouni H, Esteve A, Roubinet F, Blancher A, Calafell F, Bertranpetit J, Casals F. A natural history of FUT2 polymorphism in humans. Molecular Biology and Evolution. 26: 1993-2003. PMID 19487333 DOI: 10.1093/Molbev/Msp108 |
0.489 |
|
| 2009 |
Sikora M, Ferrer-Admetlla A, Laayouni H, Menendez C, Mayor A, Bardaji A, Sigauque B, Mandomando I, Alonso PL, Bertranpetit J, Casals F. A variant in the gene FUT9 is associated with susceptibility to placental malaria infection. Human Molecular Genetics. 18: 3136-44. PMID 19460885 DOI: 10.1093/Hmg/Ddp240 |
0.312 |
|
| 2009 |
Casals F, Ferrer-Admetlla A, Sikora M, Ramírez-Soriano A, Marquès-Bonet T, Despiau S, Roubinet F, Calafell F, Bertranpetit J, Blancher A. Human pseudogenes of the ABO family show a complex evolutionary dynamics and loss of function. Glycobiology. 19: 583-91. PMID 19218399 DOI: 10.1093/Glycob/Cwp017 |
0.482 |
|
| 2008 |
Ferrer-Admetlla A, Bosch E, Sikora M, Marquès-Bonet T, RamÃrez-Soriano A, Muntasell A, Navarro A, Lazarus R, Calafell F, Bertranpetit J, Casals F. Balancing selection is the main force shaping the evolution of innate immunity genes. Journal of Immunology (Baltimore, Md. : 1950). 181: 1315-22. PMID 18606686 DOI: 10.4049/Jimmunol.181.2.1315 |
0.405 |
|
| 2008 |
Casals F, Ferrer-Admetlla A, Chillarón J, Torrents D, Palacín M, Bertranpetit J. Is there selection for the pace of successive inactivation of the arpAT gene in primates? Journal of Molecular Evolution. 67: 23-8. PMID 18566733 DOI: 10.1007/S00239-008-9120-6 |
0.437 |
|
| 2008 |
Morcillo-Suarez C, Alegre J, Sangros R, Gazave E, de Cid R, Milne R, Amigo J, Ferrer-Admetlla A, Moreno-Estrada A, Gardner M, Casals F, Pérez-Lezaun A, Comas D, Bosch E, Calafell F, et al. SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data. Bioinformatics (Oxford, England). 24: 1643-4. PMID 18515823 DOI: 10.1093/Bioinformatics/Btn241 |
0.357 |
|
| 2008 |
Sikora M, Ferrer-Admetlla A, Mayor A, Bertranpetit J, Casals F. Evolutionary analysis of genes of two pathways involved in placental malaria infection. Human Genetics. 123: 343-57. PMID 18317811 DOI: 10.1007/S00439-008-0483-Y |
0.399 |
|
| 2008 |
Moreno-Estrada A, Casals F, Ramírez-Soriano A, Oliva B, Calafell F, Bertranpetit J, Bosch E. Signatures of selection in the human olfactory receptor OR5I1 gene. Molecular Biology and Evolution. 25: 144-54. PMID 17981927 DOI: 10.1093/Molbev/Msm240 |
0.388 |
|
| 2008 |
Rosa A, Casals F, Ferrer-Admetlla A, Gardner M, Bertranpetit J, Comas D. WORLDWIDE GENETIC VARIATION IN THE REELIN GENE: IMPLICATIONS FOR GENETIC ASSOCIATION STUDIES Schizophrenia Research. 102: 189. DOI: 10.1016/S0920-9964(08)70574-7 |
0.419 |
|
| 2008 |
Rosa A, Casals F, Ferrer-Admetlla A, Bertranpetit J, Comas D. 173 – Analysis of genetic structure and geographical variation across the reelin gene: implications for association studies Schizophrenia Research. 98: 104. DOI: 10.1016/J.Schres.2007.12.240 |
0.402 |
|
| 2007 |
Casals F, Navarro A. Chromosomal evolution: inversions: the chicken or the egg? Heredity. 99: 479-80. PMID 17895906 DOI: 10.1038/Sj.Hdy.6801046 |
0.36 |
|
| 2007 |
Gardner M, Williamson S, Casals F, Bosch E, Navarro A, Calafell F, Bertranpetit J, Comas D. Extreme individual marker F(ST )values do not imply population-specific selection in humans: the NRG1 example. Human Genetics. 121: 759-62. PMID 17457614 DOI: 10.1007/S00439-007-0364-9 |
0.378 |
|
| 2005 |
González J, Nefedov M, Bosdet I, Casals F, Calvete O, Delprat A, Shin H, Chiu R, Mathewson C, Wye N, Hoskins RA, Schein JE, de Jong P, Ruiz A. A BAC-based physical map of the Drosophila buzzatii genome. Genome Research. 15: 885-92. PMID 15930498 DOI: 10.1101/Gr.3263105 |
0.359 |
|
| 2004 |
González J, Casals F, Ruiz A. Duplicative and conservative transpositions of larval serum protein 1 genes in the genus Drosophila. Genetics. 168: 253-64. PMID 15454541 DOI: 10.1534/Genetics.103.025916 |
0.354 |
|
| 2003 |
Negre B, Ranz JM, Casals F, Cáceres M, Ruiz A. A new split of the Hox gene complex in Drosophila: relocation and evolution of the gene labial. Molecular Biology and Evolution. 20: 2042-54. PMID 12949134 DOI: 10.1093/Molbev/Msg238 |
0.379 |
|
| 2003 |
Ranz JM, González J, Casals F, Ruiz A. Low occurrence of gene transposition events during the evolution of the genus Drosophila. Evolution; International Journal of Organic Evolution. 57: 1325-35. PMID 12894940 DOI: 10.1111/J.0014-3820.2003.Tb00340.X |
0.383 |
|
| 2003 |
Casals F, Cáceres M, Ruiz A. The foldback-like transposon Galileo is involved in the generation of two different natural chromosomal inversions of Drosophila buzzatii. Molecular Biology and Evolution. 20: 674-85. PMID 12679549 DOI: 10.1093/Molbev/Msg070 |
0.33 |
|
| 2001 |
Ranz JM, Casals F, Ruiz A. How malleable is the eukaryotic genome? Extreme rate of chromosomal rearrangement in the genus Drosophila. Genome Research. 11: 230-9. PMID 11157786 DOI: 10.1101/Gr.162901 |
0.347 |
|
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