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26 results on '"Pare, G"'

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1. Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke

2. Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

3. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

4. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)

5. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018)

6. Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events A GENIUS-CHD Study of Individual Participant Data

7. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (vol 50, pg 1412, 2018)

8. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

9. Rivaroxaban for Stroke Prevention after Embolic Stroke of Undetermined Source

10. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

11. Common coding variant in SERPINA1 increases the risk for large artery stroke

12. Evaluation of clinical and inflammatory profile in opioid addiction patients with comorbid pain: results from a multicenter investigation

13. Genetic influence on methadone treatment outcomes in patients undergoing methadone maintenance treatment for opioid addiction: a pilot study

14. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

15. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

16. Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke

17. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

18. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

21. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3)

22. Serum magnesium and calcium levels in relation to ischemic stroke Mendelian randomization study

23. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

24. Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy

25. Genetic studies of body mass index yield new insights for obesity biology

26. Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

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