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Javier Costas
Javier Costas
Instituto de Investigación Sanitaria de Santiago de Compostela-SERGAS
Verified email at usc.es - Homepage
Title
Cited by
Cited by
Year
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
18532009
Genome Sequence of Aedes aegypti, a Major Arbovirus Vector
V Nene, JR Wortman, D Lawson, B Haas, C Kodira, Z Tu, B Loftus, Z Xi, ...
Science 316 (5832), 1718-1723, 2007
12492007
The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study
M Di Forti, D Quattrone, TP Freeman, G Tripoli, C Gayer-Anderson, ...
The Lancet Psychiatry 6 (5), 427-436, 2019
5412019
Sequencing of Culex quinquefasciatus Establishes a Platform for Mosquito Comparative Genomics
P Arensburger, K Megy, RM Waterhouse, J Abrudan, P Amedeo, B Antelo, ...
Science 330 (6000), 86-88, 2010
4992010
Comment on "current understanding of ZIP and ZnT zinc transporters in human health and diseases"
J Costas
Cellular and Molecular Life Sciences 72 (1), 197-198, 2015
247*2015
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
S Steinberg, S de Jong, OA Andreassen, T Werge, AD Børglum, O Mors, ...
Human molecular genetics 20 (20), 4076-4081, 2011
2332011
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
2062022
Mood changes after delivery: role of the serotonin transporter gene
J Sanjuan, R Martin-Santos, L Garcia-Esteve, JM Carot, R Guillamat, ...
The British Journal of Psychiatry 193 (5), 383-388, 2008
1292008
Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction
E Vilella, J Costas, J Sanjuan, M Guitart, Y De Diego, A Carracedo, ...
Journal of psychiatric research 42 (4), 278-288, 2008
1122008
Common variant at 16p11. 2 conferring risk of psychosis
S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, ...
Molecular psychiatry 19 (1), 108-114, 2014
1102014
Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non‐synonymous SNPs of 306 genes involved in …
M Gratacos, J Costas, R de Cid, M Bayes, JR Gonzalez, E Baca‐García, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009
1002009
Characterization of the intragenomic spread of the human endogenous retrovirus family HERV-W
J Costas
Molecular biology and evolution 19 (4), 526-533, 2002
912002
Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia
N Carrera, M Arrojo, J Sanjuán, R Ramos-Ríos, E Paz, JJ Suárez-Rama, ...
Biological psychiatry 71 (2), 169-177, 2012
882012
Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis
J Costas, J Sanjuán, R Ramos-Ríos, E Paz, S Agra, JL Ivorra, M Páramo, ...
Journal of Psychiatric Research 45 (1), 7-14, 2011
882011
Turnover of binding sites for transcription factors involved in early Drosophila development
J Costas, F Casares, J Vieira
Gene 310, 215-220, 2003
822003
Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women
J Costas, M Gratacòs, G Escaramís, R Martín-Santos, Y de Diego, ...
Journal of psychiatric research 44 (11), 717-724, 2010
762010
Interaction between COMT haplotypes and cannabis in schizophrenia: a case-only study in two samples from Spain
J Costas, J Sanjuán, R Ramos-Ríos, E Paz, S Agra, A Tolosa, M Páramo, ...
Schizophrenia research 127 (1-3), 22-27, 2011
752011
Evolutionary history of the human endogenous retrovirus family ERV9
J Costas, H Naveira
Molecular Biology and Evolution 17 (2), 320-330, 2000
642000
Generalized lattice graphs for 2D-visualization of biological information
H Gonzalez-Diaz, LG Perez-Montoto, A Duardo-Sanchez, E Paniagua, ...
Journal of theoretical biology 261 (1), 136-147, 2009
602009
High variability in CYP21A2 mutated alleles in Spanish 21‐hydroxylase deficiency patients, six novel mutations and a founder effect
L Loidi, C Quinteiro, S Parajes, J Barreiro, DG Lestón, ...
Clinical endocrinology 64 (3), 330-336, 2006
572006
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