191 results on '"Moses, Eric K."'
Search Results
2. A lipidomic based metabolic age score captures cardiometabolic risk independent of chronological age
3. Development and validation of a plasmalogen score as an independent modifiable marker of metabolic health: population based observational studies and a placebo-controlled cross-over study
4. Interactions between the lipidome and genetic and environmental factors in autism
5. Metabolic phenotyping of BMI to characterize cardiometabolic risk: evidence from large population-based cohorts
6. Potential Role for Immune-Related Genes in Autism Spectrum Disorders: Evidence from Genome-Wide Association Meta-Analysis of Autistic Traits
7. A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia
8. Cascade testing for elevated lipoprotein(a) in relatives of probands with high lipoprotein(a)
9. A Methylome and Transcriptome Analysis of Normal Human Scar Cells Reveals a Role for FOXF2 in Scar Maintenance
10. Cascade testing for elevated lipoprotein(a) in relatives of probands with familial hypercholesterolaemia and elevated lipoprotein(a)
11. Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
12. Evaluation of epigenetic age calculators between preeclampsia and normotensive pregnancies in an Australian cohort
13. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
14. Familial and non-familial risk factors associated with incidence of colorectal cancer in young and middle-aged persons in Western Australia
15. Western oropharyngeal and gut microbial profiles are associated with allergic conditions in Chinese immigrant children
16. Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity
17. Familial and non-familial risk factors associated with colorectal cancer survival in young and middle-aged patients
18. Exome array analysis suggests an increased variant burden in families with schizophrenia
19. Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts
20. Genomic variation associated with cardiovascular disease progression following preeclampsia: a systematic review.
21. Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study
22. Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22
23. Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children
24. Ethnic Differences in the Prevalence of Inherited Thrombophilic Polymorphisms in an Asymptomatic Australian Prenatal Population
25. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
26. Identifying genetic risk loci associated with cardiovascular disease progression following preeclampsia: A genome-wide association study.
27. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
28. The characterization of Abelson helper integration site–1 in skeletal muscle and its links to the metabolic syndrome
29. The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
30. C677T Methylenetetrahydrofolate Reductase Polymorphism Is Not a Risk Factor for Pre-Eclampsia/Eclampsia among Australian Women
31. Endogenous factor VIII synthesis from the intron 22--inverted F8 locus may modulate the immunogenicity of replacement therapy for hemophilia A
32. Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
33. Molecular Markers of Preterm Labor in the Choriodecidua
34. Genetic variation in PARL influences mitochondrial content
35. A transcriptional profile of the decidua in preeclampsia
36. The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
37. Genetic association of preeclampsia to the inflammatory response gene SEPS1
38. A Chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study
39. Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase [A.sub.2], a marker of inflammation and oxidative stress
40. Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease
41. ADAM28 is elevated in humans with the metabolic syndrome and is a novel sheddase of human tumour necrosis factor-α
42. Inherited thrombophilias and adverse pregnancy outcomes: a case–control study in an Australian population
43. The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells
44. Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study
45. Genetic Variation at the FTO Locus Influences RBL2 Gene Expression
46. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population
47. Genetic determinants of mitochondrial content
48. Identification and sequencing of the groE operon and flanking genes of Lawsonia intracellularis: use in phylogeny
49. 5β-Dihydroprogesterone and steroid 5β–reductase decrease in association with human parturition at term
50. Genetic organization of the duplicated vap region of the Dichelobacter nodosus genome
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