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244 results on '"Nöthen, M.M."'

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1. Linking brain structure and genetic risk in large-scale data: A comparison of shared versus predominantly disorder-specific genetic risk for neuropsychiatric disorders

2. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

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

4. Genome-wide association study of pathological gambling

6. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

7. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

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

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

10. First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B

11. Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations

12. eQTL Set-Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma.

13. New insights into the genetic etiology of Alzheimer's disease and related dementias

14. Brain based BMIgap as a new tool to correlate obesity and neural alterations – a multicohort study

15. Structural alterations in psychotic disorders co-localize with serotonergic and dopaminergic neurotransmitter systems

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

19. Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients

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

21. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

22. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

23. Germline variation in the insulin-like growth factor pathway and risk of Barrett's esophagus and esophageal adenocarcinoma

24. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

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

29. Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies

30. The genetic architecture of the human cerebral cortex

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

32. Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes

33. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

34. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

35. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

37. Response to Therapeutic Sleep Deprivation: A Naturalistic Study of Clinical and Genetic Factors and Post-treatment Depressive Symptom Trajectory

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

39. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

40. Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis

41. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

42. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

43. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

44. Age at first birth in women is genetically associated with increased risk of schizophrenia

45. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

46. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

47. Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy

50. Influence of age and cognitive performance on resting-state brain networks of older adults in a population-based cohort

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