| scholarly article | Q13442814 |
| P50 | author | Marguerite R Irvin | Q87769958 |
| Michael A Province | Q88244370 | ||
| Donna K Arnett | Q88878357 | ||
| Ingrid B Borecki | Q89095223 | ||
| P2093 | author name string | Qunyuan Zhang | |
| P2860 | cites work | Evolutionary Rate at the Molecular Level | Q22122432 |
| Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 | ||
| Rare independent mutations in renal salt handling genes contribute to blood pressure variation | Q24627187 | ||
| Multiple rare variants in the etiology of autism spectrum disorders | Q24635522 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| Pooled association tests for rare variants in exon-resequencing studies | Q28743126 | ||
| Identification of novel putative rheumatoid arthritis susceptibility genes via analysis of rare variants | Q30976000 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| A data-adaptive sum test for disease association with multiple common or rare variants | Q33562753 | ||
| A new testing strategy to identify rare variants with either risk or protective effect on disease | Q33815362 | ||
| Testing for an unusual distribution of rare variants | Q33847792 | ||
| A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol. | Q34399014 | ||
| Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels | Q34478587 | ||
| A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression | Q35014891 | ||
| Fibrates in 2003: therapeutic action in atherogenic dyslipidaemia and future perspectives | Q35594896 | ||
| Medical sequencing at the extremes of human body mass | Q35752505 | ||
| The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment | Q36897732 | ||
| Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans. | Q37036119 | ||
| Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility | Q37699224 | ||
| Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis | Q39821504 | ||
| An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 | ||
| Adaptive tests for association analysis of rare variants | Q41898785 | ||
| Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group | Q43236071 | ||
| A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). | Q51928874 | ||
| P433 | issue | 7 | |
| P304 | page(s) | 679-685 | |
| P577 | publication date | 2011-08-04 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | A data-driven method for identifying rare variants with heterogeneous trait effects | |
| P478 | volume | 35 |
| Q40788285 | A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants. |
| Q34180858 | A comprehensive evaluation of collapsing methods using simulated and real data: excellent annotation of functionality and large sample sizes required |
| Q37031565 | A geometric framework for evaluating rare variant tests of association |
| Q34016536 | A powerful and adaptive association test for rare variants |
| Q30846312 | Adjusting family relatedness in data-driven burden test of rare variants |
| Q39382116 | Associating rare genetic variants with human diseases |
| Q57338039 | Association between SNPs in defined functional pathways and risk of early or late toxicity as well as individual radiosensitivity |
| Q35984424 | Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study |
| Q37689468 | Evaluating the impact of genotype errors on rare variant tests of association |
| Q35886146 | Rare PPARA variants and extreme response to fenofibrate in the Genetics of Lipid-Lowering Drugs and Diet Network Study. |
| Q37672566 | The next-generation sequencing revolution and its impact on genomics |
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