Ferran Casals
Ferran Casals
Verified email at upf.edu
Title
Cited by
Cited by
Year
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
74452010
Great ape genetic diversity and population history
J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ...
Nature 499 (7459), 471-475, 2013
7052013
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
5742011
Variation in genome-wide mutation rates within and between human families
DF Conrad, JEM Keebler, MA DePristo, SJ Lindsay, Y Zhang, F Casals, ...
Nature genetics 43 (7), 712, 2011
5742011
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts
P Awadalla, J Gauthier, RA Myers, F Casals, FF Hamdan, AR Griffing, ...
The American Journal of Human Genetics 87 (3), 316-324, 2010
2572010
Morphometric, behavioral, and genomic evidence for a new orangutan species
A Nater, MP Mattle-Greminger, A Nurcahyo, MG Nowak, M De Manuel, ...
Current Biology 27 (22), 3487-3498. e10, 2017
1962017
How malleable is the eukaryotic genome? Extreme rate of chromosomal rearrangement in the genus Drosophila
JM Ranz, F Casals, A Ruiz
Genome research 11 (2), 230-239, 2001
1912001
A Natural History of FUT2 Polymorphism in Humans
A Ferrer-Admetlla, M Sikora, H Laayouni, A Esteve, F Roubinet, ...
Molecular biology and evolution 26 (9), 1993-2003, 2009
1872009
Balancing selection is the main force shaping the evolution of innate immunity genes
A Ferrer-Admetlla, E Bosch, M Sikora, T Marquès-Bonet, ...
The Journal of Immunology 181 (2), 1315-1322, 2008
1872008
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects
C Schwab, A Gabrysch, P Olbrich, V Patiño, K Warnatz, D Wolff, ...
Journal of Allergy and Clinical Immunology 142 (6), 1932-1946, 2018
1792018
Chimpanzee genomic diversity reveals ancient admixture with bonobos
M De Manuel, M Kuhlwilm, P Frandsen, VC Sousa, T Desai, ...
Science 354 (6311), 477-481, 2016
1782016
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia
ME Samuels, J Majewski, N Alirezaie, I Fernandez, F Casals, N Patey, ...
Journal of medical genetics 50 (5), 324-329, 2013
1042013
Genomic analysis of Andamanese provides insights into ancient human migration into Asia and adaptation
M Mondal, F Casals, T Xu, GM Dall'Olio, M Pybus, MG Netea, D Comas, ...
Nature Genetics 48 (9), 1066-1070, 2016
1002016
The Foldback-like Transposon Galileo Is Involved in the Generation of Two Different Natural Chromosomal Inversions of Drosophila buzzatii
F Casals, M Cáceres, A Ruiz
Molecular biology and evolution 20 (5), 674-685, 2003
992003
A population genetic approach to mapping neurological disorder genes using deep resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan, J Keebler, AR Boyko, ...
PLoS Genet 7 (2), e1001318, 2011
842011
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans
F Casals, A Hodgkinson, J Hussin, Y Idaghdour, V Bruat, T de Maillard, ...
PLoS Genet 9 (9), e1003815, 2013
782013
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data
C Morcillo-Suarez, J Alegre, R Sangros, E Gazave, R De Cid, R Milne, ...
Bioinformatics 24 (14), 1643-1644, 2008
742008
Evaluating the genetics of common variable immunodeficiency: monogenetic model and beyond
G de Valles-Ibáñez, A Esteve-Solé, M Piquer, EA González-Navarro, ...
Frontiers in Immunology 9, 636, 2018
682018
Extreme selective sweeps independently targeted the X chromosomes of the great apes
K Nam, K Munch, A Hobolth, JY Dutheil, KR Veeramah, AE Woerner, ...
Proceedings of the National Academy of Sciences 112 (20), 6413-6418, 2015
592015
Rare allelic forms of PRDM9 associated with childhood leukemogenesis
J Hussin, D Sinnett, F Casals, Y Idaghdour, V Bruat, V Saillour, J Healy, ...
Genome research 23 (3), 419-430, 2013
532013
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