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FOREST LITTER PRODUCTION, CHEMISTRY, AND DECOMPOSITION FOLLOWING TWO YEARS OF FREE-AIR CO[sub 2]....
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- Ecology, 2001, v. 82, n. 2, p. 470, doi. 10.2307/2679873
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- Article
Single-nucleus DNA sequencing reveals hidden somatic loss-of-heterozygosity in Cerebral Cavernous Malformations.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-42908-w
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- Article
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
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- Nature Communications, 2023, n. 1, p. 1, doi. 10.1038/s41467-023-39539-6
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- Article
Family-based association tests for rare variants with censored traits.
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- PLoS ONE, 2019, v. 14, n. 1, p. 1, doi. 10.1371/journal.pone.0210870
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- Article
Correction: Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics.
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- 2018
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- Correction Notice
Robust estimation and testing of haplotype effects in case-control studies.
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- Genetic Epidemiology, 2008, v. 32, n. 1, p. 29, doi. 10.1002/gepi.20259
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- Article
Inference on haplotype/disease association using parent-affected-child data: the projection conditional on parental haplotypes method.
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- Genetic Epidemiology, 2007, v. 31, n. 3, p. 211, doi. 10.1002/gepi.20203
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- Article
Summary of contributions to GAW15 Group 13: candidate gene association studies.
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- Genetic Epidemiology, 2007, v. 31, n. S1, p. S110, doi. 10.1002/gepi.20287
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- Article
Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring.
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- Genetic Epidemiology, 2006, v. 30, n. 3, p. 248, doi. 10.1002/gepi.20141
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- Publication type:
- Article
Fast and Robust Association Tests for Untyped SNPs in Case-Control Studies.
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- Human Heredity, 2010, v. 70, n. 3, p. 167, doi. 10.1159/000308456
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- Article
Statistical Models for Haplotype Sharing in Case-Parent Trio Data.
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- Human Heredity, 2007, v. 64, n. 1, p. 35, doi. 10.1159/000101421
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- Article
Evaluating Chromatin Accessibility Differences Across Multiple Primate Species Using a Joint Modeling Approach.
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- Genome Biology & Evolution, 2019, v. 11, n. 10, p. 3035, doi. 10.1093/gbe/evz218
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- Article
Secondary analysis of case-control association studies: Insights on weighting-based inference motivate a new specification test.
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- 2020
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- journal article
Joint Models for Toxicology Studies with Dose-Dependent Number of Implantations.
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- Risk Analysis: An International Journal, 2002, v. 22, n. 6, p. 1165, doi. 10.1111/1539-6924.00280
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- Article
Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy.
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- Annals of Neurology, 2015, v. 78, n. 2, p. 323, doi. 10.1002/ana.24457
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- Article
Testing for risk and protective trends in genetic analyses of HIV acquisition.
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- 2015
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- journal article
Locally-efficient robust estimation of haplotype-disease association in family-based studies.
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- Biometrika, 2005, v. 92, n. 3, p. 559, doi. 10.1093/biomet/92.3.559
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- Publication type:
- Article
Ancestry adjustment improves genome-wide estimates of regional intolerance.
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- Genetics, 2022, v. 221, n. 2, p. 1, doi. 10.1093/genetics/iyac050
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- Publication type:
- Article
Mapping eQTL by leveraging multiple tissues and DNA methylation.
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- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1856-9
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- Publication type:
- Article
Exploiting expression patterns across multiple tissues to map expression quantitative trait loci.
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- BMC Bioinformatics, 2016, v. 17, p. 1, doi. 10.1186/s12859-016-1123-5
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- Article
The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.
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- PLoS Genetics, 2015, v. 11, n. 9, p. 1, doi. 10.1371/journal.pgen.1005492
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- Article
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes.
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- PLoS Genetics, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pgen.1003709
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- Publication type:
- Article
Focused goodness of fit tests for gene set analyses.
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- Briefings in Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1093/bib/bbab472
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- Publication type:
- Article
Human genome-wide measurement of drug-responsive regulatory activity.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07607-x
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- Publication type:
- Article
A Regression-based Association Test for Case-control Studies that Uses Inferred Ancestral Haplotype Similarity.
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- Annals of Human Genetics, 2009, v. 73, n. 5, p. 520, doi. 10.1111/j.1469-1809.2009.00536.x
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- Article
Leveraging Prior Information to Detect Causal Variants via Multi-Variant Regression.
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- PLoS Computational Biology, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pcbi.1003093
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- Publication type:
- Article
Bayesian hierarchical model to estimate DNA methylation conservation in colorectal tumors.
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- Bioinformatics, 2022, v. 38, n. 1, p. 22, doi. 10.1093/bioinformatics/btab637
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- Publication type:
- Article
Bayesian estimation of genetic regulatory effects in high-throughput reporter assays.
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- Bioinformatics, 2020, v. 36, n. 2, p. 331, doi. 10.1093/bioinformatics/btz545
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- Publication type:
- Article
Robust Regression Analysis of Copy Number Variation Data based on a Univariate Score.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0086272
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- Article
Prevalences of type 2 diabetes, the insulin resistance syndrome, and coronary heart disease in an elderly, biethnic population.
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- 1998
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- Publication type:
- journal article
De novo mutations in epileptic encephalopathies.
- Published in:
- Nature, 2013, v. 501, n. 7466, p. 217, doi. 10.1038/nature12439
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- Publication type:
- Article
Robust analysis of secondary phenotypes in case-control genetic association studies.
- Published in:
- 2016
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- Publication type:
- journal article
Estimating Crude or Common Odds Ratios in Case-Control Studies with Informatively Missing Exposure Data.
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- American Journal of Epidemiology, 2002, v. 155, n. 3, p. 274, doi. 10.1093/aje/155.3.274
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- Publication type:
- Article
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
- Published in:
- 2017
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- Publication type:
- journal article
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting.
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- BMC Infectious Diseases, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2334-14-83
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- Publication type:
- Article
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting.
- Published in:
- 2014
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- Publication type:
- journal article
Transversions have larger regulatory effects than transitions.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3785-4
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- Publication type:
- Article
Genetic variation in HTR2A influences serotonin transporter binding potential as measured using PET and [<sup>11</sup>C]DASB.
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- International Journal of Neuropsychopharmacology, 2010, v. 13, n. 6, p. 715, doi. 10.1017/S1461145709991027
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- Publication type:
- Article
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics.
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- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0181604
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- Publication type:
- Article
High-throughput interpretation of gene structure changes in human and nonhuman resequencing data, using ACE.
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- Bioinformatics, 2017, v. 33, n. 10, p. 1437, doi. 10.1093/bioinformatics/btw799
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- Publication type:
- Article
SVA: software for annotating and visualizing sequenced human genomes.
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- Bioinformatics, 2011, v. 27, n. 14, p. 1998, doi. 10.1093/bioinformatics/btr317
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- Article
Controls on microbial CO[sub 2] production: a comparison of surface and subsurface soil horizons.
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- Global Change Biology, 2003, v. 9, n. 9, p. 1322, doi. 10.1046/j.1365-2486.2003.00663.x
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- Publication type:
- Article
A weighted accumulation test for associating rare genetic variation with quantitative phenotypes.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S6
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- Publication type:
- Article
Genome-wide association analysis of rheumatoid arthritis data via haplotype sharing.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S30
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- Publication type:
- Article
Effect of population stratification on the identification of significant single-nucleotide polymorphisms in genome-wide association studies.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S13
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- Publication type:
- Article
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.
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- PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007281
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- Publication type:
- Article
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations.
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- PLoS Genetics, 2017, v. 13, n. 11, p. 1, doi. 10.1371/journal.pgen.1007104
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- Publication type:
- Article
Incorporating external information to improve sparse signal detection in rare‐variant gene‐set‐based analyses.
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- Genetic Epidemiology, 2020, v. 44, n. 4, p. 330, doi. 10.1002/gepi.22283
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- Publication type:
- Article
Leveraging population information in family-based rare variant association analyses of quantitative traits.
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- Genetic Epidemiology, 2017, v. 41, n. 2, p. 98, doi. 10.1002/gepi.22022
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- Publication type:
- Article
Testing the Effect of Rare Compound-Heterozygous and Recessive Mutations in Case-Parent Sequencing Studies.
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- Genetic Epidemiology, 2015, v. 39, n. 3, p. 166, doi. 10.1002/gepi.21885
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- Publication type:
- Article