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1. Longitudinal metabolite and protein trajectories prior to diabetes mellitus diagnosis in Danish blood donors: a nested case–control study

2. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.

3. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

4. Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage

7. Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors

8. GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

9. Lifestyle and demographic associations with 47 inflammatory and vascular stress biomarkers in 9876 blood donors

10. A genome-wide association study of social trust in 33,882 Danish blood donors

11. Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

12. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

13. Developmental language disorder – heritability and genetic correlations with other disorders affecting language

14. Impact of CCR5Δ32 on the risk of infection, Staphylococcus aureus carriage, and plasma concentrations of chemokines in Danish blood donors

15. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

16. Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

17. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

18. Symptoms of attention deficit hyperactivity disorder are associated with Hidradenitis suppurativa in Danish blood donors

19. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

20. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

21. Identification of biomarkers for glycaemic deterioration in type 2 diabetes

22. DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals

23. Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

24. Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism

25. Complex effects of sequence variants on lipid levels and coronary artery disease

29. Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study

30. Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study

31. Author Correction: Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

32. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

33. A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

35. Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

36. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

37. Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease

38. Inflammatory and endothelial host responses in community-acquired pneumonia: exploring the relationships with HbA1c, admission plasma glucose, and glycaemic gap—a cross-sectional study

40. Inflammatory and endothelial host responses in community-acquired pneumonia:exploring the relationships with HbA1c, admission plasma glucose, and glycaemic gap—a cross-sectional study

41. Clonal hematopoiesis and COVID-19 hospitalization in Danish adults

42. Variants at the Interleukin 1 Gene Locus and Pericarditis

43. Finding Ophthalmic Risk and Evaluating the Value of Eye exams and their predictive Reliability (FOREVER)—A cohort study in a Danish high street optician setting:Design and methodology

44. Multi‐omics analysis reveals drivers of loss of β‐cell function after newly diagnosed autoimmune type 1 diabetes: An INNODIA multicenter study.

45. Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

46. A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

48. Herpes Simplex Virus Type 1 infection is associated with suicidal behavior and first registered psychiatric diagnosis in a healthy population

49. Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration

50. Large-scale study of Toxoplasma and Cytomegalovirus shows an association between infection and serious psychiatric disorders

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