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

2. Identification of common genetic risk variants for autism spectrum disorder

3. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.

4. An epigenetic clock for gestational age at birth based on blood methylation data

5. Genome-wide associations for birth weight and correlations with adult disease

6. Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

7. Biological insights from 108 schizophrenia-associated genetic loci

8. A polygenic resilience score moderates the genetic risk for schizophrenia

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

12. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

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

14. Genome-wide association analyses identify variants in developmental genes associated with hypospadias

15. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

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

18. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

19. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

20. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

21. Publisher Correction:Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4)

22. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

23. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

24. A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder

25. Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

26. Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

27. Genome-wide scans using archived neonatal dried blood spot samples

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

29. Discovery of the first genome-wide significant risk loci for ADHD

30. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

31. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

32. Identification of Gene Loci That Overlap Between Schizophrenia and Educational Attainment

33. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

35. RNA sequencing of archived neonatal dried blood spots

36. An epigenetic clock for gestational age at birth based on blood methylation data

37. Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

38. Biological insights from 108 schizophrenia-associated genetic loci

40. Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children

41. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

43. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

45. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

46. Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

48. Common variants associated with general and MMR vaccine-related febrile seizures

49. A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

50. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

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