498 results on '"Moses, Eric K."'
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2. 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
3. Metabolic phenotyping of BMI to characterize cardiometabolic risk: evidence from large population-based cohorts
4. Interactions between the lipidome and genetic and environmental factors in autism
5. Association of Known Melanoma Risk Factors with Primary Melanoma of the Scalp and Neck
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. Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study
14. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
15. The transcriptional landscape of age in human peripheral blood.
16. Familial and non-familial risk factors associated with incidence of colorectal cancer in young and middle-aged persons in Western Australia
17. Western oropharyngeal and gut microbial profiles are associated with allergic conditions in Chinese immigrant children
18. 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
19. Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity
20. Endogenous factor VIII synthesis from the intron 22-inverted F8 locus may modulate the immunogenicity of replacement therapy for hemophilia A.
21. Familial and non-familial risk factors associated with colorectal cancer survival in young and middle-aged patients
22. Genomic variation associated with cardiovascular disease progression following preeclampsia: a systematic review
23. Exome array analysis suggests an increased variant burden in families with schizophrenia
24. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes
25. 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
26. Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study
27. Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22
28. Genetic Approaches in Preeclampsia
29. Differential DNA methylation of steatosis and non-alcoholic fatty liver disease in adolescence.
30. A genome-wide association study for malignant mesothelioma risk
31. Ethnic Differences in the Prevalence of Inherited Thrombophilic Polymorphisms in an Asymptomatic Australian Prenatal Population
32. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
33. Genotype × age interaction in human transcriptional ageing
34. Diverse biological activities of the vascular non-inflammatory molecules – The Vanin pantetheinases
35. Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging
36. High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes
37. Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children
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39. The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia
40. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
41. The characterization of Abelson helper integration site–1 in skeletal muscle and its links to the metabolic syndrome
42. The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
43. APOE ε2 resilience for Alzheimer's disease is mediated by plasma lipid species: Analysis of three independent cohort studies
44. C677T Methylenetetrahydrofolate Reductase Polymorphism Is Not a Risk Factor for Pre-Eclampsia/Eclampsia among Australian Women
45. Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
46. Molecular Markers of Preterm Labor in the Choriodecidua
47. Genetic variation in PARL influences mitochondrial content
48. A transcriptional profile of the decidua in preeclampsia
49. Plasma Levels of Soluble Interleukin 1 Receptor Accessory Protein Are Reduced in Obesity
50. The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
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