161 results on '"Rujescu, D"'
Search Results
2. Erratum: GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium
3. GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
4. Association of norepinephrine transporter methylation with in vivo NET expression and hyperactivity–impulsivity symptoms in ADHD measured with PET
5. A novel Alzheimer disease locus located near the gene encoding tau protein.
6. Correction: Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years
7. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia
8. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia
9. High loading of polygenic risk in cases with chronic schizophrenia
10. Genome-wide autozygosity is associated with lower general cognitive ability
11. A genome-wide association study of anorexia nervosa
12. Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
13. Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci
14. Common variant at 16p11.2 conferring risk of psychosis
15. Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients
16. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
17. Meta-analysis of genome-wide association studies for personality
18. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia
19. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
20. Expanding the range of ZNF804A variants conferring risk of psychosis
21. Copy number variations of chromosome 16p13.1 region associated with schizophrenia
22. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha
23. Population-based linkage analysis of schizophrenia and bipolar case–control cohorts identifies a potential susceptibility locus on 19q13
24. Genome-wide association study of alcohol dependence: significant findings in African- and European-Americans including novel risk loci
25. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2
26. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
27. Plexin B3 is genetically associated with verbal performance and white matter volume in human brain
28. Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples
29. M129V variation in the prion protein may influence cognitive performance
30. Association of anger-related traits with SNPs in the TPH gene
31. Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years
32. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2
33. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells
34. A human specific haplotype in Plexin B3 is associated with verbal performance and brain white matter volume
35. No association of alcohol dependence with a NMDA-receptor 2B gene variant
36. Erratum: Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients
37. Association of norepinephrine transporter methylation with in vivo NET expression and hyperactivity–impulsivity symptoms in ADHD measured with PET
38. Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOEstatus in a community-based cohort prospectively followed over 17 years
39. Genome-wide autozygosity is associated with lower general cognitive ability
40. Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients
41. Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
42. Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci
43. Meta-analysis of genome-wide association studies for personality
44. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha
45. Population-based linkage analysis of schizophrenia and bipolar case–control cohorts identifies a potential susceptibility locus on 19q13
46. Plexin B3 is genetically associated with verbal performance and white matter volume in human brain
47. Correction: Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOEstatus in a community-based cohort prospectively followed over 17 years
48. Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia
49. Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia
50. Mitochondrial DNA abundance in blood is associated with Alzheimer's disease- and dementia-risk.
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