TitleDateAuthorsDOI
New sequencing technologies2013-11-01Gut, IG (2013). New sequencing technologies. Clinical & Translational Oncology, 15(11), 879-881. DOI: 10.1007/s12094-013-1073-6https://doi.org/10.1007/s12094-013-1073-6
Target prediction for an open access set of compounds active against Mycobacterium tuberculosis2013-10-01Martínez-Jiménez, F; Papadatos, G; Yang, L; Wallace, IM; Kumar, V; Pieper, U; Sali, A; Brown, JR; Overington, JP; Marti-Renom, MA (2013). Target prediction for an open access set of compounds active against Mycobacterium tuberculosis. Plos Computational Biology, 9(10), e1003253-. DOI: 10.1371/journal.pcbi.1003253https://doi.org/10.1371/journal.pcbi.1003253
Transcriptome and genome sequencing uncovers functional variation in humans2013-09-26Lappalainen, T; Sammeth, M; Friedländer, MR; 't Hoen, PAC; Monlong, J; Rivas, MA; Gonzàlez-Porta, M; Kurbatova, N; Griebel, T; Ferreira, PG; Barann, M (2013). Transcriptome and genome sequencing uncovers functional variation in humans. Nature, 501(7468), 506-511. DOI: 10.1038/nature12531https://doi.org/10.1038/nature12531
Whole-Genome Bisulfite Sequencing of Two Distinct Interconvertible DNA Methylomes of Mouse Embryonic Stem Cells2013-09-05Habibi, E; Brinkman, AB; Arand, J; Kroeze, LI; Kerstens, HHD; Matarese, F; Lepikhov, K; Gut, M; Brun-Heath, I; Hubner, NC; Benedetti, R; Altucci, L; J (2013). Whole-Genome Bisulfite Sequencing of Two Distinct Interconvertible DNA Methylomes of Mouse Embryonic Stem Cells. Cell Stem Cell, 13(3), 360-369. DOI: 10.1016/j.stem.2013.06.002https://doi.org/10.1016/j.stem.2013.06.002
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs2013-09-01Lee, SH; Ripke, S; Neale, BM; Faraone, SV; Purcell, SM; Perlis, RH; Mowry, BJ; Thapar, A; Goddard, ME; Witte, JS; Absher, D; Agartz, I; Akil, H; Amin, (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45(9), 984-+. DOI: 10.1038/ng.2711https://doi.org/10.1038/ng.2711
Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC2013-09-01Toma, C; Hervás, A; Balmaña, N; Salgado, M; Maristany, M; Vilella, E; Aguilera, F; Orejuela, C; Cusco, I; Gallastegui, F; Pérez-Jurado, LA; Caballero- (2013). Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC. World Journal Of Biological Psychiatry, 14(7), 516-527. DOI: 10.3109/15622975.2011.602719https://doi.org/10.3109/15622975.2011.602719
Genome sequence of Plesiomonas shigelloides strain 302-73 (serotype O1)2013-08-01Piqué, N; Aquilini, E; Alioto, T; Miñana-Galbis, D; Tomás, JM (2013). Genome sequence of Plesiomonas shigelloides strain 302-73 (serotype O1). Genome Announcements, 1(4), e00404-13-. DOI: 10.1128/genomeA.00404-13https://doi.org/10.1128/genomeA.00404-13
Great ape genetic diversity and population history2013-07-25Prado-Martinez, J; Sudmant, PH; Kidd, JM; Li, H; Kelley, JL; Lorente-Galdos, B; Veeramah, KR; Woerner, AE; O'Connor, TD; Santpere, G; Cagan, A; Theune (2013). Great ape genetic diversity and population history. Nature, 499(7459), 471-475. DOI: 10.1038/nature12228https://doi.org/10.1038/nature12228
A novel family of soluble minimal scaffolds provides structural insight into the catalytic domains of integral membrane metallopeptidases2013-07-19López-Pelegrín, M; Cerdà-Costa, N; Martínez-Jiménez, F; Cintas-Pedrola, A; Canals, A; Peinado, JR; Marti-Renom, MA; López-Otín, C; Arolas, JL; Gomis-R (2013). A novel family of soluble minimal scaffolds provides structural insight into the catalytic domains of integral membrane metallopeptidases. Journal Of Biological Chemistry, 288(29), 21279-21294. DOI: 10.1074/jbc.M113.476580https://doi.org/10.1074/jbc.M113.476580
Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification2013-07-02Bezerra, AR; Simoes, J; Lee, W; Rung, J; Weil, T; Gut, IG; Gut, M; Bayés, M; Rizzetto, L; Cavalieri, D; Giovannini, G; Bozza, S; Romani, L; Kapushesky (2013). Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification. Proceedings Of The National Academy Of Sciences Of The United States Of America, 110(27), 11079-11084. DOI: 10.1073/pnas.1302094110https://doi.org/10.1073/pnas.1302094110
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p162013-07-01Cordell, HJ; Bentham, J; Topf, A; Zelenika, D; Heath, S; Mamasoula, C; Cosgrove, C; Blue, G; Granados-Riveron, J; Setchfield, K; Thornborough, C; Brec (2013). Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Nature Genetics, 45(7), 822-U151. DOI: 10.1038/ng.2637https://doi.org/10.1038/ng.2637
Neutral Theory Predicts the Relative Abundance and Diversity of Genetic Elements in a Broad Array of Eukaryotic Genomes2013-06-14Serra, FCO; Becher, V; Dopazo, H (2013). Neutral Theory Predicts the Relative Abundance and Diversity of Genetic Elements in a Broad Array of Eukaryotic Genomes. Plos One, 8(6), e63915-9. DOI: 10.1371/journal.pone.0063915https://doi.org/10.1371/journal.pone.0063915
Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD2013-06-01Sánchez-Mora, C; Cormand, B; Ramos-Quiroga, JA; Hervás, A; Bosch, R; Palomar, G; Nogueira, M; Gómez-Barros, N; Richarte, V; Corrales, M; Garcia-Martin (2013). Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD. European Neuropsychopharmacology, 23(6), 426-435. DOI: 10.1016/j.euroneuro.2012.07.014https://doi.org/10.1016/j.euroneuro.2012.07.014
Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor2013-06-01Llorens, F; Hummel, M; Pantano, L; Pastor, X; Vivancos, A; Castillo, E; Mattlin, H; Ferrer, A; Ingham, M; Noguera, M; Kofler, R; Dohm, JC; Pluvinet, R (2013). Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor. Bmc Genomics, 14(1), 371-. DOI: 10.1186/1471-2164-14-371https://doi.org/10.1186/1471-2164-14-371
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild2013-05-31Prado-Martinez, J; Hernando-Herraez, I; Lorente-Galdos, B; Dabad, M; Ramirez, O; Baeza-Delgado, C; Morcillo-Suarez, C; Alkan, C; Hormozdiari, F; Raine (2013). The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild. Bmc Genomics, 14(1), 363-. DOI: 10.1186/1471-2164-14-363https://doi.org/10.1186/1471-2164-14-363
DNA sequencing - spanning the generations2013-05-25McGinn, S; Gut, IG (2013). DNA sequencing - spanning the generations. New Biotechnology, 30(4), 366-372. DOI: 10.1016/j.nbt.2012.11.012https://doi.org/10.1016/j.nbt.2012.11.012
PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data2013-05-21Escaramís, G; Tornador, C; Bassaganyas, L; Rabionet, R; Tubio, JMC; Martínez-Fundichely, A; Cáceres, M; Gut, M; Ossowski, S; Estivill, X (2013). PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data. Plos One, 8(5), e63377-. DOI: 10.1371/journal.pone.0063377https://doi.org/10.1371/journal.pone.0063377
Using tertiary structure for the computation of highly accurate multiple RNA Coffee package2013-05-01Kemena, C; Bussotti, G; Capriotti, E; Marti-Renom, MA; Notredame, C (2013). Using tertiary structure for the computation of highly accurate multiple RNA Coffee package. Bioinformatics, 29(9), 1112-1119. DOI: 10.1093/bioinformatics/btt096https://doi.org/10.1093/bioinformatics/btt096
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene2013-05-01Melià, MJ; Kubota, A; Ortolano, S; Vílchez, JJ; Gámez, J; Tanji, K; Bonilla, E; Palenzuela, L; Fernández-Cadenas, I; Pristoupilová, A; García-Arumí, E (2013). Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene. Brain, 136(5), 1508-1517. DOI: 10.1093/brain/awt074https://doi.org/10.1093/brain/awt074
Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP22013-04-01Toma, C; Hervás, A; Torrico, B; Balmaña, N; Salgado, M; Maristany, M; Vilella, E; Martínez-Leal, R; Planelles, MI; Cuscó, I; del Campo, M; Pérez-Jurad (2013). Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2. Psychiatric Genetics, 23(2), 82-85. DOI: 10.1097/YPG.0b013e32835d6fc6https://doi.org/10.1097/YPG.0b013e32835d6fc6