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1. A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals

2. Genetic contribution to the comorbidity between attention-deficit/hyperactivity disorder and substance use disorders

3. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

4. Fine-mapping genomic loci refines bipolar disorder risk genes

5. Molecular mechanisms underlying variations in lung function: a systems genetics analysis

6. Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

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

10. Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2)

11. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

12. Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes

14. Protein-altering germline mutations implicate novel genes related to lung cancer development

15. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

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

17. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

18. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

19. Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

20. Genomic Relationships, Novel Loci, And Pleiotropic Mechanisms Across Eight Psychiatric Disorders

23. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

24. 48. A Polygenic Score for Course of Illness in ADHD

25. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

26. F5EPIGENETIC SIGNATURE FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER: IDENTIFICATION OF MIR-23A-5P, MIR-26B-5P, MIR-185-5P AND MIR-191-5P AS A POTENTIAL BIOMARKER IN PERIPHERAL BLOOD MONONUCLEAR CELLS

27. Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk

32. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

33. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

34. Genetic studies of body mass index yield new insights for obesity biology

35. New genetic loci link adipose and insulin biology to body fat distribution

42. Whole-genome sequence-based analysis of thyroid function

43. The UK10K project identifies rare variants in health and disease

44. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

45. Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

46. A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

47. A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

48. A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample

49. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

50. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

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