| scholarly article | Q13442814 |
| P2093 | author name string | Aravinda Chakravarti | |
| Xiaofeng Zhu | |||
| Richard S Cooper | |||
| Amy Luke | |||
| Yen-Pei C Chang | |||
| Morna A Ikeda | |||
| Denise Yan | |||
| Alan Weder | |||
| P2860 | cites work | EVOLUTION IN MENDELIAN POPULATIONS | Q5418627 |
| Searching for genetic determinants in the new millennium | Q22337300 | ||
| The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models | Q24533319 | ||
| A New Statistical Method for Haplotype Reconstruction from Population Data | Q27860495 | ||
| Characterization of single-nucleotide polymorphisms in coding regions of human genes | Q28138557 | ||
| Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis | Q28138570 | ||
| Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex | Q28190352 | ||
| A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms | Q28203288 | ||
| Global patterns of linkage disequilibrium at the CD4 locus and modern human origins | Q28275689 | ||
| Linkage disequilibrium in the human genome | Q29616097 | ||
| Genetic dissection of complex traits | Q29618312 | ||
| Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci | Q33680205 | ||
| Angiotensin-converting enzyme and cardiovascular disease risk | Q33770520 | ||
| Population choice in mapping genes for complex diseases | Q33784279 | ||
| Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure | Q34020659 | ||
| Extent and distribution of linkage disequilibrium in three genomic regions | Q34043707 | ||
| Linkage disequilibrium and the search for complex disease genes | Q34066357 | ||
| The extent of linkage disequilibrium in four populations with distinct demographic histories | Q34144358 | ||
| Recombinational and mutational hotspots within the human lipoprotein lipase gene | Q34146213 | ||
| Localization of a small genomic region associated with elevated ACE | Q34146741 | ||
| Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase | Q34386645 | ||
| Ethnic-affiliation estimation by use of population-specific DNA markers | Q34421878 | ||
| Nonuniform recombination within the human beta-globin gene cluster | Q35200412 | ||
| The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes | Q35246352 | ||
| Polymorphic DNA haplotypes at the LDL receptor locus | Q35247208 | ||
| A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro | Q37365783 | ||
| Angiotensin I converting enzyme gene: regulation, polymorphism and implications in cardiovascular diseases | Q40504790 | ||
| Molecular basis of human hypertension: role of angiotensinogen | Q45118696 | ||
| Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute | Q46336499 | ||
| 'Unique' alleles in admixed populations: a strategy for determining 'hereditary' population differences of disease frequencies | Q46876879 | ||
| Sequence variation in the human angiotensin converting enzyme | Q47964948 | ||
| Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males | Q48035561 | ||
| Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. | Q52051237 | ||
| Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene. | Q52973147 | ||
| Angiotensinogen genotype and blood pressure response in the Dietary Approaches to Stop Hypertension (DASH) study. | Q55035483 | ||
| High-resolution haplotype structure in the human genome | Q56002085 | ||
| DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster | Q57162492 | ||
| Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28 | Q57232777 | ||
| Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease | Q57606857 | ||
| Haplotype tagging for the identification of common disease genes | Q59200321 | ||
| Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension | Q72036783 | ||
| Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators | Q73858290 | ||
| Prospects for whole-genome linkage disequilibrium mapping of common disease genes | Q77883184 | ||
| Linkage disequilibrium in finite populations | Q87127089 | ||
| P433 | issue | 2 | |
| P921 | main subject | linkage disequilibrium | Q2064311 |
| disequilibrium | Q5282160 | ||
| P304 | page(s) | 173-181 | |
| P577 | publication date | 2003-02-01 | |
| P1433 | published in | Genome Research | Q5533485 |
| P1476 | title | Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program | |
| P478 | volume | 13 |
| Q33240337 | A role for CETP TaqIB polymorphism in determining susceptibility to atrial fibrillation: a nested case control study |
| Q46894502 | An angiotensin converting enzyme haplotype predicts survival in patients with end stage renal disease |
| Q37194034 | Angiotensin II type 1 receptor polymorphisms and susceptibility to hypertension: a HuGE review |
| Q35448335 | Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits |
| Q37726913 | Association of angiotensinogen gene SNPs and haplotypes with risk of hypertension in eastern Indian population |
| Q43319378 | Association of the renin gene polymorphism, three angiotensinogen gene polymorphisms and the haplotypes with essential hypertension in the Mongolian population |
| Q51986656 | Context-dependency of the relation between left ventricular mass and AGT gene variants. |
| Q33410002 | Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus |
| Q51378319 | Gender-related association of AGT gene variants (M235T and T174M) with essential hypertension--a case-control study. |
| Q33879230 | Genetic and environmental risks for high blood pressure among African American mothers and daughters |
| Q47713143 | Genetic predisposition to bevacizumab-induced hypertension |
| Q36722035 | Genetics of arterial hypertension and hypotension |
| Q46509410 | Genomic evidence for recent positive selection at the human MDR1 gene locus |
| Q47722583 | Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure. |
| Q52576817 | Haplotype analysis of the estrogen receptor 1 gene in male genital and reproductive abnormalities. |
| Q53509739 | Haplotypes of the angiotensin-converting enzyme (ACE) gene are associated with coronary artery disease but not with restenosis after coronary stenting. |
| Q51910217 | Identifying haplotype block structure using an ancestor-derived model. |
| Q33998500 | Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi |
| Q54277415 | Left ventricular remodelling after acute myocardial infarction: impact of clinical, echocardiographic parameters and polymorphism of angiotensinogen gene. |
| Q33910261 | Linkage analysis of a complex disease through use of admixed populations. |
| Q35046494 | Linkage disequilibrium analysis of the renin-angiotensin system genes. |
| Q35547517 | Nutritional Genomics: Implications for Companion Animals |
| Q24792884 | Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes |
| Q57273802 | Quantitated transcript haplotypes (QTH) ofAGTR1, reduced abundance of mRNA haplotypes containing 1166C (rs5186:A>C), and relevance to metabolic syndrome traits |
| Q46100560 | Renin-angiotensin system gene polymorphisms predict the progression to renal insufficiency among Asians with lupus nephritis |
| Q45041470 | Role of two angiotensinogen polymorphisms in blood pressure variation |
| Q33307072 | Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype |
| Q34761441 | Single nucleotide polymorphisms of the angiotensin-converting enzyme (ACE) gene are associated with essential hypertension and increased ACE enzyme levels in Mexican individuals |
| Q33679056 | Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population |
| Q57316367 | The effects of polymorphisms in genes from the renin–angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels are dependent on environmental context |
| Q40588847 | Three single-nucleotide polymorphisms of the angiotensinogen gene and susceptibility to hypertension: single locus genotype vs. haplotype analysis |
| Q47399004 | X-linked insertion/deletion polymorphisms: forensic applications of a 33-markers panel |
Search more.