| scholarly article | Q13442814 |
| P50 | author | Carmen Marsit | Q37378932 |
| P2093 | author name string | Jia Chen | |
| Ke Hao | |||
| Luca Lambertini | |||
| Shouneng Peng | |||
| Antonio F Di Narzo | |||
| Maya A Deyssenroth | |||
| P2860 | cites work | Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 |
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease | Q22251067 | ||
| Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease | Q22251082 | ||
| Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder | Q22252418 | ||
| Genetic studies of body mass index yield new insights for obesity biology | Q22305005 | ||
| Biological insights from 108 schizophrenia-associated genetic loci | Q24561833 | ||
| The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | Q24568334 | ||
| Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 | ||
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | Q24630394 | ||
| Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks | Q24633890 | ||
| Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes | Q28272915 | ||
| A large-scale, consortium-based genomewide association study of asthma | Q28293885 | ||
| The Genotype-Tissue Expression (GTEx) project | Q28657968 | ||
| Bayesian test for colocalisation between pairs of genetic association studies using summary statistics | Q28660129 | ||
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis | Q29416987 | ||
| Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease | Q29417023 | ||
| A mega-analysis of genome-wide association studies for major depressive disorder | Q29417093 | ||
| Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 | Q29417143 | ||
| Genetics of gene expression and its effect on disease | Q29614591 | ||
| Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma | Q29614903 | ||
| Quality control and quality assurance in genotypic data for genome-wide association studies | Q30498925 | ||
| Improved integrative framework combining association data with gene expression features to prioritize Crohn's disease genes | Q30942462 | ||
| A reference panel of 64,976 haplotypes for genotype imputation | Q33553419 | ||
| Asthma-associated polymorphisms in 17q21 influence cord blood ORMDL3 and GSDMA gene expression and IL-17 secretion | Q33890722 | ||
| Placental FKBP5 genetic and epigenetic variation is associated with infant neurobehavioral outcomes in the RICHS cohort | Q34035506 | ||
| Defining the role of common variation in the genomic and biological architecture of adult human height | Q34441746 | ||
| Lung eQTLs to help reveal the molecular underpinnings of asthma | Q34499419 | ||
| Meta-eQTL: a tool set for flexible eQTL meta-analysis | Q34676543 | ||
| Learning gene networks under SNP perturbations using eQTL datasets | Q35105560 | ||
| Placental adaptive responses and fetal programming | Q36392502 | ||
| Toward a comprehensive set of asthma susceptibility genes | Q36565021 | ||
| Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. | Q37408201 | ||
| The obstetric origins of health for a lifetime | Q38115935 | ||
| Placental programming of chronic diseases, cancer and lifespan: a review. | Q38126668 | ||
| Prenatal exposure to famine and the development of hyperglycemia and type 2 diabetes in adulthood across consecutive generations: a population-based cohort study of families in Suihua, China | Q38786012 | ||
| Next-generation genotype imputation service and methods | Q40603492 | ||
| Cardiometabolic risk loci share downstream cis- and trans-gene regulation across tissues and diseases. | Q40615674 | ||
| The correlation between sampling site and gene expression in the term human placenta | Q42477322 | ||
| The placental origins of sudden cardiac death | Q43650403 | ||
| Human genetics: GTEx pilot quantifies eQTL variation across tissues and individuals | Q85382935 | ||
| P433 | issue | 17 | |
| P921 | main subject | quantitative trait locus | Q853421 |
| P304 | page(s) | 3432-3441 | |
| P577 | publication date | 2017-09-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Expression quantitative trait loci (eQTLs) in human placentas suggest developmental origins of complex diseases. | |
| P478 | volume | 26 |
| Q50421130 | Epigenetics as a mechanism linking developmental exposures to long-term toxicity. |
| Q47171958 | Genetic Pleiotropy between Nicotine Dependence and Respiratory Outcomes |
| Q61453599 | Genetic regulation of the placental transcriptome underlies birth weight and risk of childhood obesity |
| Q60053983 | Genetic variants influence on the placenta regulatory landscape |
| Q90583148 | Integrating -Omics Approaches into Human Population-Based Studies of Prenatal and Early-Life Exposures |
| Q64109834 | Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors |
| Q98158680 | Neonatal genetics of gene expression reveal potential origins of autoimmune and allergic disease risk |
| Q89708646 | Palmitate induces apoptotic cell death and inflammasome activation in human placental macrophages |
| Q92903824 | Sex modifies placental gene expression in response to metabolic and inflammatory stress |
| Q64910140 | The Effect of Genetic Variation on the Placental Transcriptome in Humans. |
| Q93064046 | Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration |
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