Pages that link to "Q29614875"

The following pages link to A HapMap harvest of insights into the genetics of common disease (Q29614875):

Displaying 50 items.

• Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression (Q21092443) (← links)
• The genetic signatures of noncoding RNAs (Q21092463) (← links)
• Fast association tests for genes with FAST (Q21132696) (← links)
• Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach (Q21135314) (← links)
• An Environment-Wide Association Study (EWAS) on type 2 diabetes mellitus (Q21136362) (← links)
• Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population (Q21261513) (← links)
• Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Q22066284) (← links)
• Meta-analysis in genome-wide association studies (Q24273398) (← links)
• Replication in Genome-Wide Association Studies (Q24288830) (← links)
• Complex Diseases, Complex Genes (Q24289171) (← links)
• Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases (Q24289213) (← links)
• Can Lessons Learned from Genome-Wide Research be Applied to Nutrition-Wide and Exposure-Wide Evidence? (Q24289236) (← links)
• Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765) (← links)
• Breast Cancer in the Personal Genomics Era (Q24602679) (← links)
• Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data (Q24612121) (← links)
• Genome-wide association study of bipolar disorder in European American and African American individuals (Q24628870) (← links)
• The PhenX Toolkit: get the most from your measures (Q24630562) (← links)
• Identification of Cd101 as a susceptibility gene for Novosphingobium aromaticivorans-induced liver autoimmunity (Q24633643) (← links)
• Common variants on chromosome 6p22.1 are associated with schizophrenia (Q24641881) (← links)
• Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples (Q24642868) (← links)
• Collaborative genome-wide association studies of diverse diseases: programs of the NHGRI's office of population genomics (Q24645892) (← links)
• Genetic susceptibility to Barrett's oesophagus: Lessons from early studies (Q26740556) (← links)
• Analytical Complexity in Detection of Gene Variant-by-Environment Exposure Interactions in High-Throughput Genomic and Exposomic Research (Q26774805) (← links)
• Genetic Susceptibility to Rhodococcus equi (Q26784244) (← links)
• Insights into the genetic architecture of diabetic nephropathy (Q26823352) (← links)
• The role of large pedigrees in an era of high-throughput sequencing (Q26825546) (← links)
• Annotating individual human genomes (Q26999723) (← links)
• Big data, open science and the brain: lessons learned from genomics (Q27007693) (← links)
• Epistasis and immunity: the role of genetic interactions in autoimmune diseases (Q27010680) (← links)
• CNVs: harbingers of a rare variant revolution in psychiatric genetics (Q27022289) (← links)
• Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies (Q27330547) (← links)
• Common polygenic variation contributes to risk of schizophrenia and bipolar disorder (Q28250609) (← links)
• Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays (Q28263829) (← links)
• The molecular pathology of cancer (Q28278125) (← links)
• Statistical significance in genetic association studies (Q28294975) (← links)
• A framework for interpreting genome-wide association studies of psychiatric disorders (Q28300576) (← links)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk (Q28303293) (← links)
• Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation (Q28385221) (← links)
• The power of meta-analysis in genome-wide association studies (Q28658972) (← links)
• Methodological challenges of genome-wide association analysis in Africa (Q28681049) (← links)
• Data sharing in neuroimaging research (Q28730743) (← links)
• The mystery of missing heritability: Genetic interactions create phantom heritability (Q28732355) (← links)
• Realizing the promise of population biobanks: a new model for translation (Q28741456) (← links)
• GATES: a rapid and powerful gene-based association test using extended Simes procedure (Q28741872) (← links)
• The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies (Q28742793) (← links)
• Cardiovascular genomics, personalized medicine, and the National Heart, Lung, and Blood Institute: part I: the beginning of an era (Q28744480) (← links)
• DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data (Q28748614) (← links)
• Laboratory mouse models for the human genome-wide associations (Q28748647) (← links)
• Ethical data release in genome-wide association studies in developing countries (Q28750293) (← links)
• Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies (Q28751388) (← links)