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18 results on '"Banasik, Karina"'

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1. Homozygosity for a stop-gain variant in CCDC201causes primary ovarian insufficiency

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

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

4. Variants at the Interleukin 1 Gene Locus and Pericarditis

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

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

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

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

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

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

11. Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis

12. SMIM1absence is associated with reduced energy expenditure and excess weight

13. Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data

14. Intervening on the storage time of RBC units and its effects on adverse recipient outcomes using real-world data

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

16. Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease

17. The FOXO3A rs2802292 G-Allele Associates with Improved Peripheral and Hepatic Insulin Sensitivity and Increased Skeletal Muscle-FOXO3A mRNA Expression in Twins

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

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