1 - 25 of
144
results
for author:"Estivill X."
in Literature Citations
| Functional variants of the serotonin receptor type 3A and B gene are associated with eating disorders. Hammer C., Kapeller J., Endele M., Fischer C., Hebebrand J., Hinney A., Friedel S., Gratacos M., Estivill X., Fichter M. et al. Pharmacogenet. Genomics 19:790-799(2009) · Mapped (8) |
| Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder. Ribases M., Bosch R., Hervas A., Ramos-Quiroga J.A., Sanchez-Mora C., Bielsa A., Gastaminza X., Guijarro-Domingo S., Nogueira M., Gomez-Barros N. et al. Biol. Psychiatry 66:926-934(2009) · Mapped (20) |
| Association between leptin receptor (LEPR) and brain-derived neurotrophic factor (BDNF) gene variants and obesity: a case-control study. Marti A., Santos J.L., Gratacos M., Moreno-Aliaga M.J., Maiz A., Martinez J.A., Estivill X. Nutr Neurosci 12:183-188(2009) · Mapped (10) |
| A brain-derived neurotrophic factor haplotype is associated with therapeutic response in obsessive-compulsive disorder. Real E., Gratacos M., Soria V., Escaramis G., Alonso P., Segalas C., Bayes M., de Cid R., Menchon J.M., Estivill X. Biol. Psychiatry 66:674-680(2009) · Mapped (6) |
| Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia. Rodriguez-Santiago B., Brunet A., Sobrino B., Serra-Juhe C., Flores R., Armengol L., Vilella E., Gabau E., Guitart M., Guillamat R. et al. Mol. Psychiatry 0:0-0(2009) · Mapped (6) |
| Allele variants in functional MicroRNA target sites of the neurotrophin-3 receptor gene (NTRK3) as susceptibility factors for anxiety disorders. Muinos-Gimeno M., Guidi M., Kagerbauer B., Martin-Santos R., Navines R., Alonso P., Menchon J.M., Gratacos M., Estivill X., Espinosa-Parrilla Y. Hum. Mutat. 30:1062-1071(2009) · Mapped (6) |
| GSTM1 polymorphisms modify the effect of maternal smoking during pregnancy on cognitive functioning in preschoolers. Morales E., Sunyer J., Julvez J., Castro-Giner F., Estivill X., Torrent M., De Cid R. Int J Epidemiol 38:690-697(2009) · Mapped (10) |
| Joint effect of obesity and TNFA variability on asthma: two international cohort studies. Castro-Giner F., Kogevinas M., Imboden M., de Cid R., Jarvis D., Machler M., Berger W., Burney P., Franklin K.A., Gonzalez J.R. et al. Eur. Respir. J. 33:1003-1009(2009) · Mapped (9) |
| Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. de Cid R., Riveira-Munoz E., Zeeuwen P.L., Robarge J., Liao W., Dannhauser E.N., Giardina E., Stuart P.E., Nair R., Helms C. et al. Nat. Genet. 41:211-215(2009) · Mapped (373) |
| Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment. Gratacos M., Costas J., de Cid R., Bayes M., Gonzalez J.R., Baca-Garcia E., de Diego Y., Fernandez-Aranda F., Fernandez-Piqueras J., Guitart M. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:808-816(2009) · Mapped (1,287) |
| Influence of glutathione S-transferase polymorphisms on cognitive functioning effects induced by p,p'-DDT among preschoolers. Morales E., Sunyer J., Castro-Giner F., Estivill X., Julvez J., Ribas-Fito N., Torrent M., Grimalt J.O., de Cid R. Environ. Health Perspect. 116:1581-1585(2008) · Mapped (13) |
| Are MYO1C and MYO1F associated with hearing loss? Zadro C., Alemanno M.S., Bellacchio E., Ficarella R., Donaudy F., Melchionda S., Zelante L., Rabionet R., Hilgert N., Estivill X. et al. Biochim. Biophys. Acta 1792:27-32(2009) · Mapped (4) |
| Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome. Ortiz-Abalia J., Sahun I., Altafaj X., Andreu N., Estivill X., Dierssen M., Fillat C. Am. J. Hum. Genet. 83:479-488(2008) · Mapped (7) |
| DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. Canzonetta C., Mulligan C., Deutsch S., Ruf S., O'Doherty A., Lyle R., Borel C., Lin-Marq N., Delom F., Groet J. et al. Am. J. Hum. Genet. 83:388-400(2008) · Mapped (20) |
| Genetic susceptibility to obsessive-compulsive hoarding: the contribution of neurotrophic tyrosine kinase receptor type 3 gene. Alonso P., Gratacos M., Menchon J.M., Segalas C., Gonzalez J.R., Labad J., Bayes M., Real E., de Cid R., Pertusa A. et al. Genes Brain Behav. 7:778-785(2008) · Mapped (6) |
| TNFA -308G>A in two international population-based cohorts and risk of asthma. Castro-Giner F., Kogevinas M., Machler M., de Cid R., Van Steen K., Imboden M., Schindler C., Berger W., Gonzalez J.R., Franklin K.A. et al. Eur. Respir. J. 32:350-361(2008) · Mapped (22) |
| Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. Mercader J.M., Saus E., Aguera Z., Bayes M., Boni C., Carreras A., Cellini E., de Cid R., Dierssen M., Escaramis G. et al. Hum. Mol. Genet. 17:1234-1244(2008) · Mapped (45) |
| Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. Sole X., Hernandez P., de Heredia M.L., Armengol L., Rodriguez-Santiago B., Gomez L., Maxwell C.A., Aguilo F., Condom E., Abril J. et al. BMC Genomics 9:12-12(2008) · Mapped (8) |
| Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: Interaction of its intracellular domain with Myt1l. Llorens F., Gil V., Iraola S., Carim-Todd L., Marti E., Estivill X., Soriano E., Del Rio J.A., Sumoy L. Dev. Neurobiol. 68:521-541(2008) · UniProtKB (1) |
| BDNF variability in opioid addicts and response to methadone treatment: preliminary findings. de Cid R., Fonseca F., Gratacos M., Gutierrez F., Martin-Santos R., Estivill X., Torrens M. Genes Brain Behav. 7:515-522(2008) · Mapped (6) |
| Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder. Ribases M., Hervas A., Ramos-Quiroga J.A., Bosch R., Bielsa A., Gastaminza X., Fernandez-Anguiano M., Nogueira M., Gomez-Barros N., Valero S. et al. Biol. Psychiatry 63:935-945(2008) · Mapped (18) |
| MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene. Ballana E., Mercader J.M., Fischel-Ghodsian N., Estivill X. BMC Med. Genet. 8:81-81(2007) · Mapped (4) |
| Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. Witsch-Baumgartner M., Schwentner I., Gruber M., Benlian P., Bertranpetit J., Bieth E., Chevy F., Clusellas N., Estivill X., Gasparini G. et al. J. Med. Genet. 45:200-209(2008) · Mapped (4) |
| Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB. Ribases M., Ramos-Quiroga J.A., Hervas A., Bosch R., Bielsa A., Gastaminza X., Artigas J., Rodriguez-Ben S., Estivill X., Casas M. et al. Mol. Psychiatry 14:71-85(2009) · Mapped (13) |
| An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss. Guipponi M., Toh M.-Y., Tan J., Park D., Hanson K., Ballana E., Kwong D., Cannon P.Z.F., Wu Q., Gout A. et al. Hum. Mutat. 29:130-141(2008) · UniProtKB (4) |
