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2. The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study

3. Psychological distress and suicidal ideation in Sicilian Medical Students: The SMS-ME project

4. The association of jumping to conclusions and facial emotion recognition with genetic liability and outcome of psychosis

5. The Role of Social Deprivation and Cannabis Use in Explaining Variation in the Incidence of Psychotic Disorders: Findings From the EU-GEI Study

6. Metabolic Syndrome in people treated with Antipsychotics (RISKMet): A multimethod study protocol investigating genetic, behavioural, and environmental risk factors

7. The effect of polygenic risk score and childhood adversity experiences on transdiagnostic symptom dimensions at first-episode psychosis: evidence for an affective pathway to psychosis

8. The relationship of symptom dimensions with premorbid adjustment and cognitive characteristics at first episode psychosis: Findings from the EU-GEI study

9. Variation of subclinical psychosis across 16 sites in Europe and Brazil: findings from the multi-national EU-GEI study.

11. The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study

12. Methylomic signature of current cannabis use in two first-episode psychosis cohorts

14. The association between reasons for first using cannabis, later pattern of use, and risk of first-episode psychosis: the EU-GEI case–control study.

15. Cannabis use as a potential mediator between childhood adversity and first-episode psychosis: results from the EU-GEI case–control study.

16. IL RICONOSCIMENTO DELLE EMOZIONI FACCIALI NEI DISTURBI PSICOTICI: UNO STUDIO SUI MECCANISMI GENETICI ED EPIGENETICI

17. Lifestyles and Quality of Life of People with Mental Illness During the COVID-19 Pandemic

18. Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: the EU-GEI study

19. Child maltreatment, migration and risk of first-episode psychosis: results from the multinational EU-GEI study

20. Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study

21. Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: The EU-GEI study

22. The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study

23. Child maltreatment, migration and risk of first-episode psychosis: results from the multinational EU-GEI study

24. Childhood Maltreatment, Educational Attainment, and IQ: Findings From a Multicentric Case-control Study of First-episode Psychosis (EU-GEI)

25. Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study.

26. Perceived major experiences of discrimination, ethnic group, and risk of psychosis in a six-country case-control study

27. Childhood Maltreatment, Educational Attainment, and IQ: Findings From a Multicentric Case-control Study of First-episode Psychosis (EU-GEI)

28. Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case-Control Study

29. Migration history and risk of psychosis: results from the multinational EU-GEI study

31. Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: the EU-GEI study.

32. Premorbid Adjustment and IQ in Patients With First-Episode Psychosis: A Multisite Case-Control Study of Their Relationship With Cannabis Use

33. Facial Emotion Recognition in Psychosis and Associations With Polygenic Risk for Schizophrenia: Findings From the Multi-Center EU-GEI Case–Control Study

34. The EUropean Network of National Schizophrenia Networks Studying Gene-Environment Interactions (EU-GEI)

35. Use of multiple polygenic risk scores for distinguishing schizophrenia-spectrum disorder and affective psychosis categories in a first-episode sample; the EU-GEI study

36. The continuity of effect of schizophrenia polygenic risk score and patterns of cannabis use on transdiagnostic symptom dimensions at first-episode psychosis: findings from the EU-GEI study

37. First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data.

38. Perceived major experiences of discrimination, ethnic group, and risk of psychosis in a six-country case−control study.

39. Jumping to conclusions, general intelligence, and psychosis liability: findings from the multi-centre EU-GEI case-control study

40. Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: the EU-GEI study

41. Pre-training inter-rater reliability of clinical instruments in an international psychosis research project

42. Pre-training inter-rater reliability of clinical instruments in an international psychosis research project

43. The relationship of symptom dimensions with premorbid adjustment and cognitive characteristics at first episode psychosis: Findings from the EU-GEI study

44. Association of extent of cannabis use and psychotic like intoxication experiences in a multi-national sample of first episode psychosis patients and controls

45. IS THE ERA OF CANDIDATE GENES X CANNABIS USE REALLY DEAD?

46. DOES POLYGENIC RISK SCORE FOR SCHIZOPHRENIA IMPACT ON JUMPING TO CONCLUSIONS? PRELIMINARY FINDINGS FROM THE EU-GEI CASE-CONTROL STUDY

47. Transdiagnostic dimensions of psychopathology at first episode psychosis: findings from the multinational EU-GEI study

48. Use of multiple Polygenic Risk Scores for distinguishing Schizophrenia-spectrum disorder and Affective psychosis categories; the EUGEI study

49. Pre-training inter-rater reliability of clinical instruments in an international psychosis research project

50. Perceived major experiences of discrimination, ethnic group, and risk of psychosis in a six-country case−control study

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