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188 results on '"Nöthen, Markus M."'

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1. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

2. The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression

3. Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder

4. Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder

5. Effects of urban living environments on mental health in adults

6. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

7. Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

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

9. New insights into the genetic etiology of Alzheimer’s disease and related dementias

10. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

11. Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history

12. Genome-wide interaction study with major depression identifies novel variants associated with cognitive function

13. A saturated map of common genetic variants associated with human height

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

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

16. Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study

17. Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning

18. Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

19. Search for AL amyloidosis risk factors using Mendelian randomization

20. Search for AL amyloidosis risk factors using Mendelian randomization

21. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

22. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

23. Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

24. Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition

25. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

26. “The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment

27. Epigenome-wide association study of alcohol use disorder in five brain regions

28. Cortical surface area alterations shaped by genetic load for neuroticism

29. Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1

30. Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

31. HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

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

33. Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

34. Genome-wide association study identifies 30 loci associated with bipolar disorder

35. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

36. A longitudinal approach to biological psychiatric research: The PsyCourse study

37. First genotype-phenotype study reveals HLA-DQß1 insertion heterogeneity in high-resolution manometry achalasia subtypes

38. First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypes

40. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

41. Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

42. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

43. Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap

44. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

45. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

46. El estudio Andalusian Bipolar Family(ABiF): protocolo y descripción de la muestra

47. Shared genetic etiology between alcohol dependence and major depressive disorder

48. Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata

49. The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults

50. Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment

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