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1. Principal component analysis as an efficient method for capturing multivariate brain signatures of complex disorders-ENIGMA study in people with bipolar disorders and obesity.

3. Cell-type deconvolution of bulk-blood RNA-seq reveals biological insights into neuropsychiatric disorders

4. Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.

5. Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder.

7. Mega-analysis of association between obesity and cortical morphology in bipolar disorders: ENIGMA study in 2832 participants.

8. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

9. Diagnosis of bipolar disorders and body mass index predict clustering based on similarities in cortical thickness-ENIGMA study in 2436 individuals.

10. Powerful eQTL mapping through low-coverage RNA sequencing

11. The evolution of computational research in a data-centric world

12. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

13. A summary-statistics-based approach to examine the role of serotonin transporter promoter tandem repeat polymorphism in psychiatric phenotypes

14. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.

15. What we learn about bipolar disorder from large‐scale neuroimaging: Findings and future directions from the ENIGMA Bipolar Disorder Working Group

16. Association between body mass index and subcortical brain volumes in bipolar disorders–ENIGMA study in 2735 individuals

17. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

18. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

19. Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

20. Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

21. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.

22. Genetic and clinical analyses of psychosis spectrum symptoms in a large multiethnic youth cohort reveal significant link with ADHD.

23. Genome-wide association study identifies 48 common genetic variants associated with handedness

24. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

25. Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

26. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

27. Complement genes contribute sex-biased vulnerability in diverse disorders

28. Lithium Use during Pregnancy and the Risk of Miscarriage.

29. Complement genes contribute sex-biased vulnerability in diverse disorders.

30. Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses

31. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

32. Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

33. The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia

34. State-Dependent Functional Dysconnectivity in Youth With Psychosis Spectrum Symptoms

35. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.

36. Exploring the clinical utility of two staging models for bipolar disorder

37. Exploring the clinical utility of two staging models for bipolar disorder.

38. The association between antibodies to neurotropic pathogens and bipolar disorder : A study in the Dutch Bipolar (DB) Cohort and meta-analysis.

42. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

43. Rare coding variants in ten genes confer substantial risk for schizophrenia

44. Genetic variants associated with longitudinal changes in brain structure across the lifespan

45. Common Genetic Variation and Age of Onset of Anorexia Nervosa

46. Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI

47. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

48. Methylation age acceleration does not predict mortality in schizophrenia.

49. A Longitudinal Model of Human Neuronal Differentiation for Functional Investigation of Schizophrenia Polygenic Risk

50. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

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