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Exercise improves health-related quality of life sleep and fatigue domains in adult high- and low-grade glioma patients.
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- Supportive Care in Cancer, 2022, v. 30, n. 2, p. 1493, doi. 10.1007/s00520-021-06566-2
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- Article
BDNF, COMT, and DRD2 polymorphisms and ability to return to work in adult patients with low- and high-grade glioma.
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- Neuro-Oncology Practice, 2019, v. 6, n. 5, p. 375, doi. 10.1093/nop/npy059
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- Article
LGG-17. DECREASED FUNCTION OF ISOPRENYLCYSTEINE CARBOXYLMETHYLTRANSFERASE RESULTS IN INCREASED SENSITIVITY TO CHEMORADIATION IN OLIGODENDROGLIOMA.
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- Neuro-Oncology, 2019, v. 21, p. ii102, doi. 10.1093/neuonc/noz036.160
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- Article
Health Related Quality of Life in Adult Low and High-Grade Glioma Patients Using the National Institutes of Health Patient Reported Outcomes Measurement Information System (PROMIS) and Neuro-QOL Assessments.
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- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00212
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- Article
Molecular ablation of tumor blood vessels inhibits therapeutic effects of radiation and bevacizumab.
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- Neuro-Oncology, 2018, v. 20, n. 10, p. 1356, doi. 10.1093/neuonc/noy055
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- Article
Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention.
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- 2017
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- journal article
Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population.
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- 2017
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- journal article
A null mutation in does not ANGPTL8 associate with either plasma glucose or type 2 diabetes in humans.
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- BMC Endocrine Disorders, 2016, v. 16, p. 1, doi. 10.1186/s12902-016-0088-8
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- Article
Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity.
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- Nature Genetics, 2015, v. 47, n. 8, p. 921, doi. 10.1038/ng.3340
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- Article
Pathways Targeted by Antidiabetes Drugs Are Enriched for Multiple Genes Associated With Type 2 Diabetes Risk.
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- Diabetes, 2015, v. 64, n. 4, p. 1470, doi. 10.2337/db14-0703
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- Article
The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease.
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- PLoS Genetics, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.pgen.1005165
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- Article
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
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- Science Translational Medicine, 2015, v. 7, n. 270, p. 1, doi. 10.1126/scitranslmed.3010134
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- Article
Clinical skills development in student-run free clinic volunteers: a multi-trait, multi-measure study.
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- BMC Medical Education, 2014, v. 14, n. 1, p. 18, doi. 10.1186/s12909-014-0250-9
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- Article
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
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- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6607, doi. 10.1093/hmg/ddu361
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- Article
Differences in vascular endothelial growth factor receptor expression and correlation with the degree of enhancement in medulloblastoma.
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- Journal of Neurosurgery, 2014, p. 121, doi. 10.3171/2014.4.PEDS13244
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- Article
Quality of life research in neuro-oncology: a quantitative comparison.
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- Journal of Neuro-Oncology, 2014, v. 116, n. 2, p. 333, doi. 10.1007/s11060-013-1299-8
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- Article
The Role of CD133+ Cells in a Recurrent Embryonal Tumor with Abundant Neuropil and True Rosettes ( ETANTR).
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- Brain Pathology, 2014, v. 24, n. 1, p. 45, doi. 10.1111/bpa.12079
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- Article
Evaluating empirical bounds on complex disease genetic architecture.
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- Nature Genetics, 2013, v. 45, n. 12, p. 1418, doi. 10.1038/ng.2804
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- Article
Validating therapeutic targets through human genetics.
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- Nature Reviews Drug Discovery, 2013, v. 12, n. 8, p. 581, doi. 10.1038/nrd4051
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- Article
Corrigendum: Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.
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- Nature, 2013, v. 495, n. 7440, p. 270, doi. 10.1038/nature12022
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- Article
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.
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- Nature, 2013, v. 493, n. 7431, p. 216, doi. 10.1038/nature11690
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- Article
An integrated map of genetic variation from 1,092 human genomes.
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- Nature, 2012, v. 491, n. 7422, p. 56, doi. 10.1038/nature11632
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- Article
Genetic Modulation of Lipid Profiles following Lifestyle Modification or Metformin Treatment: The Diabetes Prevention Program.
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- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002895
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- Article
Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0041730
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- Article
Analysis of case–control association studies with known risk variants.
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- Bioinformatics, 2012, v. 28, n. 13, p. 1729, doi. 10.1093/bioinformatics/bts259
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- Article
Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation.
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- PLoS Computational Biology, 2012, v. 8, n. 7, p. 1, doi. 10.1371/journal.pcbi.1002604
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- Article
Risk and Return for the Clinician-Investigator.
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- Science Translational Medicine, 2012, v. 4, n. 135, p. 1, doi. 10.1126/scitranslmed.3004110
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- Article
African Ancestry and Its Correlation to Type 2 Diabetes in African Americans: A Genetic Admixture Analysis in Three U.S. Population Cohorts.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032840
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- Article
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
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- Nature Genetics, 2011, v. 43, n. 8, p. 801, doi. 10.1038/ng.871
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- Article
Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism.
- Published in:
- 2011
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- Publication type:
- journal article
A framework for variation discovery and genotyping using next-generation DNA sequencing data.
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- Nature Genetics, 2011, v. 43, n. 5, p. 491, doi. 10.1038/ng.806
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- Article
Updated Genetic Score Based on 34 Confirmed Type 2 Diabetes Loci Is Associated With Diabetes Incidence and Regression to Normoglycemia in the Diabetes Prevention Program.
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- Diabetes, 2011, v. 60, n. 4, p. 1340, doi. 10.2337/db10-1119
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- Article
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
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- Nature Genetics, 2011, v. 43, n. 4, p. 333, doi. 10.1038/ng.784
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- Article
Testing for an Unusual Distribution of Rare Variants.
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- PLoS Genetics, 2011, v. 7, n. 3, p. 1, doi. 10.1371/journal.pgen.1001322
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- Article
Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population.
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- Human Molecular Genetics, 2011, v. 20, n. 4, p. 827, doi. 10.1093/hmg/ddq510
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- Article
Common Variants in 40 Genes Assessed for Diabetes Incidence and Response to Metformin and Lifestyle Intervention in the Diabetes Prevention Program.
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- Diabetes, 2010, v. 59, n. 10, p. 2672, doi. 10.2337/db10-0543
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- Article
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
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- Nature Genetics, 2010, v. 42, n. 10, p. 851, doi. 10.1038/ng.659
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- Article
Integrating common and rare genetic variation in diverse human populations.
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- Nature, 2010, v. 467, n. 7311, p. 52, doi. 10.1038/nature09298
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- Article
A large study of androgen receptor germline variants and their relation to sex hormone levels and prostate cancer risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.
- Published in:
- 2010
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- Publication type:
- journal article
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 309, doi. 10.1038/ejhg.2009.180
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- Article
Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.
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- Nature Genetics, 2009, v. 41, n. 12, p. 1341, doi. 10.1038/ng.490
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- Article
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.
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- Nature Genetics, 2009, v. 41, n. 11, p. 1182, doi. 10.1038/ng.467
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- Article
Tissue-specific alternative splicing of TCF7L2.
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- Human Molecular Genetics, 2009, v. 18, n. 20, p. 3795, doi. 10.1093/hmg/ddp321
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- Article
Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations.
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- American Journal of Epidemiology, 2009, v. 170, n. 5, p. 537, doi. 10.1093/aje/kwp145
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- Article
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
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- Nature Genetics, 2009, v. 41, n. 8, p. 931, doi. 10.1038/ng.415
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- Publication type:
- Article
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects.
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- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2495, doi. 10.1093/hmg/ddp169
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- Article
Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions.
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- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000534
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- Article
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
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- Nature Genetics, 2009, v. 41, n. 1, p. 82, doi. 10.1038/ng.288
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- Article
Genetic Analysis of Human Traits In Vitro: Drug Response and Gene Expression in Lymphoblastoid Cell Lines.
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- PLoS Genetics, 2008, v. 4, n. 11, p. 1, doi. 10.1371/journal.pgen.1000287
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- Article
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
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- Nature Genetics, 2008, v. 40, n. 10, p. 1253, doi. 10.1038/ng.237
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- Article