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Hospital‐Treated Infections and Risk of Disability Worsening in Multiple Sclerosis.
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- Annals of Neurology, 2024, v. 96, n. 4, p. 694, doi. 10.1002/ana.27026
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- Article
Human genetics and genomics a decade after the release of the draft sequence of the human genome.
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- Human Genomics, 2011, v. 5, n. 6, p. 577, doi. 10.1186/1479-7364-5-6-577
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- Article
Doubly robust methods for handling confounding by cluster.
- Published in:
- 2016
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- Publication type:
- journal article
Automatic estimation of the cross-spectrum of a bivariate time series.
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- Biometrika, 1996, v. 83, n. 2, p. 419, doi. 10.1093/biomet/83.2.419
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- Article
Advancing paternal age and offspring violent offending: A sibling-comparison study.
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- Development & Psychopathology, 2012, v. 24, n. 3, p. 739, doi. 10.1017/S095457941200034X
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- Publication type:
- Article
Nontrivial Replication of Loci Detected by Multi-Trait Methods.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.627989
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- Article
Extensions of the Bartlett–Lewis model for rainfall processes.
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- Statistical Modelling: An International Journal, 2003, v. 3, n. 2, p. 79, doi. 10.1191/1471082X02st049oa
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- Article
Consistent Estimation for Non-Gaussian Non-Causal Autoregessive Processes.
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- Journal of Time Series Analysis, 1999, v. 20, n. 4, p. 417, doi. 10.1111/1467-9892.00146
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- Article
Regression standardization and attributable fraction estimation with between-within frailty models for clustered survival data.
- Published in:
- 2019
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- Publication type:
- journal article
Parametric and penalized generalized survival models.
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- 2018
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- Publication type:
- journal article
Sparse estimation of gene-gene interactions in prediction models.
- Published in:
- 2017
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- Publication type:
- journal article
Quantification of mutant–allele expression at isoform level in cancer from RNA-seq data.
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- NAR Genomics & Bioinformatics, 2022, v. 4, n. 3, p. 1, doi. 10.1093/nargab/lqac052
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- Article
Identifying and Assessing Interesting Subgroups in a Heterogeneous Population.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/462549
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- Article
Regions of homozygosity in three Southeast Asian populations.
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- Journal of Human Genetics, 2012, v. 57, n. 6, p. 400, doi. 10.1038/jhg.2012.51
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- Article
Regions of homozygosity in three Southeast Asian populations.
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- Journal of Human Genetics, 2012, v. 57, n. 2, p. 101, doi. 10.1038/jhg.2011.132
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- Article
Copy number polymorphisms in new HapMap III and Singapore populations.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 552, doi. 10.1038/jhg.2011.54
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- Article
A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals.
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- Journal of Human Genetics, 2011, v. 56, n. 7, p. 524, doi. 10.1038/jhg.2011.52
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- Article
The discovery of human genetic variations and their use as disease markers: past, present and future.
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- Journal of Human Genetics, 2010, v. 55, n. 7, p. 403, doi. 10.1038/jhg.2010.55
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- Publication type:
- Article
The pursuit of genome-wide association studies: where are we now?
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- Journal of Human Genetics, 2010, v. 55, n. 4, p. 195, doi. 10.1038/jhg.2010.19
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- Publication type:
- Article
One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins.
- Published in:
- 2016
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- Publication type:
- journal article
Filtering genes to improve sensitivity in oligonucleotide microarray data analysis.
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- Nucleic Acids Research, 2007, v. 35, n. 16, p. e102, doi. 10.1093/nar/gkm537
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- Article
Most genetic risk for autism resides with common variation.
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- Nature Genetics, 2014, v. 46, n. 8, p. 881, doi. 10.1038/ng.3039
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- Article
Likelihood ratio and score burden tests for detecting disease-associated rare variants.
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- Statistical Applications in Genetics & Molecular Biology, 2015, v. 14, n. 5, p. 481, doi. 10.1515/sagmb-2014-0089
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- Publication type:
- Article
Sparse Canonical Covariance Analysis for High-throughput Data.
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- Statistical Applications in Genetics & Molecular Biology, 2011, v. 10, n. 1, p. 1, doi. 10.2202/1544-6115.1638
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- Article
Fold-Change Estimation of Differentially Expressed Genes using Mixture Mixed-Model.
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- Statistical Applications in Genetics & Molecular Biology, 2005, v. 4, n. 1, p. 1, doi. 10.2202/1544-6115.1145
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- Article
Correction to: Resolving Zeckhauser's paradox.
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- 2020
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- Correction Notice
Resolving Zeckhauser's paradox.
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- Theory & Decision, 2020, v. 88, n. 4, p. 595, doi. 10.1007/s11238-019-09740-5
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- Article
The transcriptome‐wide landscape of molecular subtype‐specific mRNA expression profiles in acute myeloid leukemia.
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- American Journal of Hematology, 2021, v. 96, n. 5, p. 580, doi. 10.1002/ajh.26141
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- Article
Isoform-level quantification for single-cell RNA sequencing.
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- Bioinformatics, 2022, v. 38, n. 5, p. 1287, doi. 10.1093/bioinformatics/btab807
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- Publication type:
- Article
Model-based estimation of the attributable fraction for cross-sectional, case-control and cohort studies using the R package AF.
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- European Journal of Epidemiology, 2016, v. 31, n. 6, p. 575, doi. 10.1007/s10654-016-0137-7
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- Article
Bounds on sufficient-cause interaction.
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- European Journal of Epidemiology, 2014, v. 29, n. 11, p. 813, doi. 10.1007/s10654-014-9953-9
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- Article
Discovery of druggable cancer-specific pathways with application in acute myeloid leukemia.
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- GigaScience, 2022, v. 11, p. 1, doi. 10.1093/gigascience/giac091
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- Article
Operator Dependent Choice of Prostate Cancer Biopsy Has Limited Impact on a Gene Signature Analysis for the Highly Expressed Genes IGFBP3 and F3 in Prostate Cancer Epithelial Cells.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109610
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- Article
Is the Association between General Cognitive Ability and Violent Crime Caused by Family-Level Confounders?
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041783
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- Article
How Many Genetic Variants Remain to Be Discovered?
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- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0007969
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- Article
Annotated regions of significance of SELDI-TOF-MS spectra for detecting protein biomarkers.
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- Proteomics, 2006, v. 6, n. 23, p. 6124, doi. 10.1002/pmic.200600505
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- Article
On the relationship between the heritability and the attributable fraction.
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- Human Genetics, 2019, v. 138, n. 4, p. 425, doi. 10.1007/s00439-019-02006-8
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- Article
Revisiting Mendelian disorders through exome sequencing.
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- Human Genetics, 2011, v. 129, n. 4, p. 351, doi. 10.1007/s00439-011-0964-2
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- Article
Regions of homozygosity and their impact on complex diseases and traits.
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- Human Genetics, 2011, v. 129, n. 1, p. 1, doi. 10.1007/s00439-010-0920-6
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- Article
Strategies and issues in the detection of pathway enrichment in genome-wide association studies.
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- Human Genetics, 2009, v. 126, n. 2, p. 289, doi. 10.1007/s00439-009-0676-z
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- Article
Correlation between leukocyte phenotypes and prognosis of amyotrophic lateral sclerosis.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.74065
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- Article
Disease trajectories and mortality among women diagnosed with breast cancer.
- Published in:
- 2019
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- Publication type:
- journal article
A clinical model for identifying the short-term risk of breast cancer.
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- 2017
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- Publication type:
- journal article
Epistemic confidence in the observed confidence interval.
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- Scandinavian Journal of Statistics, 2023, v. 50, n. 4, p. 1859, doi. 10.1111/sjos.12654
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- Publication type:
- Article
Quasi-likelihood Estimation of Non-invertible Moving Average Processes.
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- Scandinavian Journal of Statistics, 2000, v. 27, n. 4, p. 689, doi. 10.1111/1467-9469.00216
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- Article
Large-scale non-targeted metabolomic profiling in three human population-based studies.
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- Metabolomics, 2016, v. 12, n. 1, p. N.PAG, doi. 10.1007/s11306-015-0893-5
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- Publication type:
- Article
Network enrichment analysis: extension of gene-set enrichment analysis to gene networks.
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- BMC Bioinformatics, 2012, v. 13, n. 1, p. 226, doi. 10.1186/1471-2105-13-226
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- Publication type:
- Article
Super-sparse principal component analyses forhigh-throughput genomic data.
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- BMC Bioinformatics, 2010, v. 11, p. 296, doi. 10.1186/1471-2105-11-296
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- Publication type:
- Article
Identification of recurrent regions of copynumbervariants across multiple individuals.
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- BMC Bioinformatics, 2010, v. 11, p. 147, doi. 10.1186/1471-2105-11-147
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- Publication type:
- Article
Normalization of oligonucleotide arrays based on the least-variant set of genes.
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- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-140
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- Publication type:
- Article