94 results on '"Zelenika, Diana"'
Search Results
2. A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14
3. Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia
4. Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13
5. Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial,
6. Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
7. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
8. Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability
9. Global Genetic Architecture of an Erythroid Quantitative Trait Locus,HMIP-2
10. Erratum to: Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms
11. Association of Genetic Variants in CDK6 and XRCC1 with the Risk of Dysplastic Nevi in Melanoma-Prone Families
12. Erratum: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
13. Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease
14. Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
15. AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
16. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
17. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
18. Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
19. Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms
20. Deciphering the 8q24.21 association for glioma
21. Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
22. Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3
23. Caution in Interpreting Results from Imputation Analysis When Linkage Disequilibrium Extends over a Large Distance: A Case Study on Venous Thrombosis
24. Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4 - the AdAPT Method
25. Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes
26. Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
27. Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
28. Serial translocation by means of circular intermediates underlies colour sidedness in cattle
29. Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein–Barr Virus Status–Defined Subgroups
30. Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project
31. High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly
32. Maternal smoking during pregnancy, genetic polymorphisms of metabolic enzymes, and childhood acute leukemia: the ESCALE Study (SFCE)
33. FCGR3A and FCGR2A Polymorphisms Do Not Affect Response and Outcome of Patients with Diffuse Large B-Cell Lymphoma Treated with Rituximab and Chemotherapy. A Study Based on 554 Patients Included in GELA (Groupe d'Etude des Lymphomes de l'Adulte) Prospective Multicentric Study LNH2003
34. Prognostic Role of Host Immune Gene Polymorphisms for Patients with Diffuse Large B-Cell Lymphoma Treated with Rituximab and Chemotherapy. A Study Based on 554 Patients Included in the GELA (Groupe d'Etude des Lymphomes de l'Adulte) Prospective Multicentric Program LNH2003,
35. A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23
36. Genome-wide association study identifies three new melanoma susceptibility loci
37. Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study
38. Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults – The GOYA Study
39. Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families
40. Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine
41. Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence
42. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
43. Chromosome 7p11.2 (EGFR) variation influences glioma risk
44. Correction: A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
45. A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1
46. Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations
47. Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD
48. A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
49. Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study
50. Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease
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