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Your search keyword '"Banasik, Karina"' showing total 36 results

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36 results on '"Banasik, Karina"'

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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. 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

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

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

32. Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: an IMI-DIRECT study

35. Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank

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