36 results on '"Banasik, Karina"'
Search Results
2. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency
3. Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage
4. Determinants of plasma levels of proglucagon and the metabolic impact of glucagon receptor signalling: a UK Biobank study
5. Uncovering the heritable components of multimorbidities and disease trajectories using a nationwide cohort
6. Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors
7. GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
8. Lifestyle and demographic associations with 47 inflammatory and vascular stress biomarkers in 9876 blood donors
9. A genome-wide association study of social trust in 33,882 Danish blood donors
10. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
11. Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination
12. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
13. Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
14. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target
15. Symptoms of attention deficit hyperactivity disorder are associated with Hidradenitis suppurativa in Danish blood donors
16. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
17. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
18. Identification of biomarkers for glycaemic deterioration in type 2 diabetes
19. DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals
20. Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models
21. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
22. Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
23. Author Correction: Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models
24. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
25. A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
26. Chronic inflammation markers and cytokine-specific autoantibodies in Danish blood donors with restless legs syndrome
27. Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
28. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
29. Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease
30. A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy
31. Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients
32. Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: an IMI-DIRECT study
33. Disease trajectory browser for exploring temporal, population-wide disease progression patterns in 7.2 million Danish patients
34. The governance structure for data access in the DIRECT consortium: an innovative medicines initiative (IMI) project
35. Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank
36. Blood parameters in a population of blood donors are not affected by hidradenitis suppurativa
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