| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/9781118445112.STAT05400.PUB2 |
| P50 | author | Paola Sebastiani | Q7132103 |
| P2093 | author name string | Lyle J. Palmer | |
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | Q21061203 | ||
| The Sequence of the Human Genome | Q22065842 | ||
| Genome-Wide Association Studies in Alzheimer Disease | Q22253050 | ||
| Replication in Genome-Wide Association Studies | Q24288830 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Complement factor H polymorphism in age-related macular degeneration | Q24553334 | ||
| Five years of GWAS discovery | Q24610574 | ||
| Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia | Q24621301 | ||
| A haplotype map of the human genome | Q24679827 | ||
| Rare-variant association analysis: study designs and statistical tests | Q26852733 | ||
| The structure of haplotype blocks in the human genome | Q27860500 | ||
| The International HapMap Project | Q27860695 | ||
| Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| A genome-wide association study identifies novel risk loci for type 2 diabetes | Q28287727 | ||
| The Human Genome Project: big science transforms biology and medicine | Q28657810 | ||
| A new multipoint method for genome-wide association studies by imputation of genotypes | Q29547209 | ||
| Estimation of the multiple testing burden for genomewide association studies of nearly all common variants | Q29614917 | ||
| Fast and accurate genotype imputation in genome-wide association studies through pre-phasing | Q29614942 | ||
| Genetic dissection of complex traits | Q29618312 | ||
| Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease | Q29619085 | ||
| Computational neuroanatomy of speech production. | Q30360356 | ||
| From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. | Q30374131 | ||
| Learning Bayesian Networks from Correlated Data | Q31090735 | ||
| A reference panel of 64,976 haplotypes for genotype imputation | Q33553419 | ||
| Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster | Q33706399 | ||
| Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans | Q34475541 | ||
| Coming of age: ten years of next-generation sequencing technologies | Q34526801 | ||
| A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene | Q34651283 | ||
| A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. | Q34674466 | ||
| Naïve Bayesian Classifier and Genetic Risk Score for Genetic Risk Prediction of a Categorical Trait: Not so Different after all! | Q35788654 | ||
| Minimal haplotype tagging | Q35814348 | ||
| Risk estimation and risk prediction using machine-learning methods. | Q36203499 | ||
| Genome-wide association studies and the genetic dissection of complex traits | Q37537247 | ||
| Family-based designs for genome-wide association studies | Q37883023 | ||
| Genetic Risk Scores | Q39302536 | ||
| A genome-wide scalable SNP genotyping assay using microarray technology | Q46111789 | ||
| Array of hope | Q47606760 | ||
| P304 | page(s) | 1-6 | |
| P577 | publication date | 2017-11-15 | |
| P1476 | title | Human Genome Project |
Search more.