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351 results on '"Ophoff, R"'

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1. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

3. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

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

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

8. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

9. A genome-wide association study of anorexia nervosa

11. Common variant at 16p11.2 conferring risk of psychosis

12. Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

13. High educational performance is a distinctive feature of bipolar disorder: a study on cognition in bipolar disorder, schizophrenia patients, relatives and controls

14. A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides

16. Genome-wide association study of obsessive-compulsive disorder

17. Genome-wide association study of Tourette's syndrome

18. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

19. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

21. Expanding the range of ZNF804A variants conferring risk of psychosis

22. Copy number variations of chromosome 16p13.1 region associated with schizophrenia

25. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x)

26. Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches

30. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

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

32. No association between anti-thyroidperoxidase antibodies and bipolar disorder: A study in the Dutch Bipolar Cohort and a meta-analysis

33. Genetic architecture of subcortical brain structures in 38,854 individuals worldwide

38. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

41. Genetic architecture of subcortical brain structures in 38,851 individuals

42. Erratum: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

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

45. Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

47. Improving genetic prediction by leveraging genetic correlations among human diseases and traits

48. An amino acid motif in HLA-DRb1 distinguishes patients with uveitis in juvenile idiopathic arthritis

49. Analysis of shared heritability in common disorders of the brain

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