484 results on '"Moses, Eric K."'
Search Results
102. [81-OR]
103. MACROD2 gene associated with autistic-like traits in a general population sample
104. Genome-Wide Genetic and Transcriptomic Investigation of Variation in Antibody Response to Dietary Antigens
105. Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns
106. Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease
107. A genome-wide association study for malignant mesothelioma risk
108. Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1
109. Genetic Architecture of Carotid Artery Intima-Media Thickness in Mexican Americans
110. OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits
111. OP006. A preeclampsia genome-wide linkage scan in norwegian families
112. A Genome-Wide Integrative Genomic Study Localizes Genetic Factors Influencing Antibodies against Epstein-Barr Virus Nuclear Antigen 1 (EBNA-1)
113. Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans
114. Genome-Wide Association Study of Autistic-Like Traits in a General Population Study of Young Adults
115. GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
116. Genotype×age interaction in human transcriptional ageing
117. Corrigendum to “Diverse biological activities of the vascular non-inflammatory molecules – The Vanin pantetheinases” [Biochem. Biophys. Res. Commun. 417 (2012) 653–658]
118. Diverse biological activities of the vascular non-inflammatory molecules – The Vanin pantetheinases
119. Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos
120. Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging
121. Novel Associations of Nonstructural Loci with Paraoxonase Activity
122. High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes
123. The antihypertensive MTHFRgene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia
124. The Entire Primary Sequence of Factor VIII Is Synthesized As Two Polypeptide Chains in Hemophilia A Patients with the Intron-22-Inversion
125. Inherited thrombophilias and adverse pregnancy outcomes: a case-control study in an Australian population
126. Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease
127. [278-POS]: A genetic connection between preeclampsia and chronic hypertension in Norwegian families
128. [81-OR]: Genome-wide transcriptome directed pathway analysis of maternal preeclampsia susceptibility genes
129. No Evidence of Cis-Acting SNPs In Immune Response Genes Previously Associated with Factor VIII Inhibitors: The San Antonio Family Heart Study
130. Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
131. Genetic and Molecular Functional Characterization of Variants within TNFSF13B, a Positional Candidate Preeclampsia Susceptibility Gene on 13q
132. Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes
133. Inherited Thrombophilia Polymorphisms and Pregnancy Outcomes in Nulliparous Women
134. Chemerin, A Novel Adipokine in the Regulation of Angiogenesis
135. Genetic Variation at the FTO Locus Influences RBL2 Gene Expression
136. Genetic variation in PARL influences mitochondrial content
137. A critical assessment of the factors affecting reporter gene assays for promoter SNP function: a reassessment of −308 TNF polymorphism function using a novel integrated reporter system
138. Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
139. Heritability of Commonly Measured Blood Cell Phenotypes in the San Antonio Family Heart Study.
140. Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes
141. Genotype × Adiposity Interaction Linkage Analyses Reveal a Locus on Chromosome 1 for Lipoprotein-Associated Phospholipase A2, a Marker of Inflammation and Oxidative Stress
142. Ethnic Differences in the Prevalence of Inherited Thrombophilic Polymorphisms in an Asymptomatic Australian Prenatal Population
143. The −56T HLA-G Promoter Polymorphism is Not Associated with Pre-eclampsia/Eclampsia in Australian and New Zealand Women
144. An emerging role for comprehensive proteome analysis in human pregnancy research
145. Proteomic approaches in endometriosis research
146. Association of the TNF2 Allele with Eclampsia
147. Thrombomodulin Ala455Val Dimorphism Is Not Associated with Pre-Eclampsia in Australian and New Zealand Women
148. The Ark: a customizable web-based data management tool for health and medical research.
149. C677T Methylenetetrahydrofolate Reductase Polymorphism Is Not a Risk Factor for Pre-Eclampsia/Eclampsia among Australian Women
150. Prothrombin G20210A Mutation: Is It Associated with Pre-Eclampsia?
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