9 Result(s)
within
Roser Corominas
English
-
Article
Open AccessAuthor Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
-
Article
Open AccessMolecular genetics of cocaine use disorders in humans
Drug addiction, one of the major health problems worldwide, is characterized by the loss of control in drug intake, craving, and withdrawal. At the individual level, drugs of abuse produce serious consequences...
-
Article
Open AccessMutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia
Episodic ataxia is an autosomal dominant ion channel disorder characterized by episodes of imbalance and incoordination. The disease is genetically heterogeneous and is classified as episodic ataxia type 2 (EA...
-
Protocol
Comprehensive Analyses of Tissue-Specific Networks with Implications to Psychiatric Diseases
Recent advances in genome sequencing and “omics” technologies are opening new opportunities for improving diagnosis and treatment of human diseases. The precision medicine initiative in particular aims at deve...
-
Article
Open AccessProtein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
Increased risk for autism spectrum disorders (ASD) is attributed to hundreds of genetic loci. The convergence of ASD variants have been investigated using various approaches, including protein interactions extrac...
-
Article
Erratum: Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
Nature 471, 499–501 (2011) In Figure 3 of this Letter, there were labelling errors on the x-axis in which the 05C48386 and 05C43079 cell-line labels were both duplicated. The labels should have corresponded to...
-
Article
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
Based on genome-wide analysis of copy number variants in two large schizophrenia cohorts, Vacic et al. report a significant association between duplications within a region of chromosome 7 and schizophrenia. Usin...
-
Article
Open AccessTwo-stage case-control association study of dopamine-related genes and migraine
We previously reported risk haplotypes for two genes related with serotonin and dopamine metabolism: MAOA in migraine without aura and DDC in migraine with aura. Herein we investigate the contribution to migraine...
-
Article
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
We sought to map the disease-causing gene in a large Spanish kindred with familial hemiplegic migraine (FHM). Patients were classified according to the ICHD-II criteria. After ruling out linkage to known migra...
