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Familiarity, Availability, and Use of Manipulative Devices in Mathematics at the Primary Level.
- Published in:
- School Science & Mathematics, 1988, v. 88, n. 6, p. 459, doi. 10.1111/j.1949-8594.1988.tb11838.x
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- Article
Mathematics Textbooks in Teacher Education.
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- School Science & Mathematics, 1987, v. 87, n. 7, p. 558, doi. 10.1111/j.1949-8594.1987.tb11745.x
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- Article
Automated extraction of clinical traits of multiple sclerosis in electronic medical records.
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- Journal of the American Medical Informatics Association, 2013, v. 20, n. e2, p. e334, doi. 10.1136/amiajnl-2013-001999
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- Article
ICD-9 tobacco use codes are effective identifiers of smoking status.
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- Journal of the American Medical Informatics Association, 2013, v. 20, n. 4, p. 652, doi. 10.1136/amiajnl-2012-001557
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- Article
T-cell receptor diversity in minimal change disease in the NEPTUNE study.
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- Pediatric Nephrology, 2023, v. 38, n. 4, p. 1115, doi. 10.1007/s00467-022-05696-x
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- Article
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.
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- BioData Mining, 2015, v. 8, p. 1, doi. 10.1186/s13040-015-0068-y
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- Article
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenomewide association studies.
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- BioData Mining, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1756-0381-7-6
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- Article
Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines.
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- Public Health Genomics, 2019, v. 22, n. 1/2, p. 16, doi. 10.1159/000501974
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- Article
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
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- BMC Medical Genomics, 2016, v. 9, p. 19, doi. 10.1186/s12920-016-0191-8
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- Article
Methylome-wide Analysis Reveals Epigenetic Marks Associated With Resistance to Tuberculosis in Human Immunodeficiency Virus-Infected Individuals From East Africa.
- Published in:
- 2021
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- Publication type:
- journal article
Modeling transcriptional regulation using gene regulatory networks based on multi-omics data sources.
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- BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04126-3
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- Article
magpie: A power evaluation method for differential RNA methylation analysis in N6-methyladenosine sequencing.
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- PLoS Computational Biology, 2024, v. 20, n. 2, p. 1, doi. 10.1371/journal.pcbi.1011875
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- Article
A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction.
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- Genetic Epidemiology, 2007, v. 31, n. 4, p. 306, doi. 10.1002/gepi.20211
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- Article
Leveraging Epidemiologic and Clinical Collections for Genomic Studies of Complex Traits.
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- Human Heredity, 2015, v. 79, n. 3/4, p. 137, doi. 10.1159/000381805
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- Article
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA–CLEC16A–SOCS1 gene complex.
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- Human Molecular Genetics, 2011, v. 20, n. 17, p. 3517, doi. 10.1093/hmg/ddr250
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- Article
PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection.
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- Genome Biology, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s13059-020-02121-0
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- Article
Replication of European hypertension associations in a case-control study of 9,534 African Americans.
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- PLoS ONE, 2021, v. 16, n. 11, p. 1, doi. 10.1371/journal.pone.0259962
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- Article
Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease.
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- 2022
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- Publication type:
- journal article
Genetic variants and functional pathways associated with resilience to Alzheimer's disease.
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- 2020
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- Publication type:
- journal article
Sex differences in the genetic predictors of Alzheimer's pathology.
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- 2019
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- Publication type:
- journal article
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.
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- BMC Bioinformatics, 2015, v. 16, p. 1, doi. 10.1186/s12859-015-0760-4
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- Article
Higher CSF Ferritin Heavy-Chain (Fth1) and Transferrin Predict Better Neurocognitive Performance in People with HIV.
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- Molecular Neurobiology, 2021, v. 58, n. 10, p. 4842, doi. 10.1007/s12035-021-02433-7
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- Article
Sex-specific genetic predictors of Alzheimer's disease biomarkers.
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- Acta Neuropathologica, 2018, v. 136, n. 6, p. 857, doi. 10.1007/s00401-018-1881-4
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- Article
The myth of the community fix: Inequality and the politics of youth punishment.
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- Law & Society Review, 2023, v. 57, n. 3, p. 411, doi. 10.1111/lasr.12667
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- Article
A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data.
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- Journal of the American Medical Informatics Association, 2012, v. 19, n. 2, p. 289, doi. 10.1136/amiajnl-2011-000652
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- Article
eMERGEing progress in genomics--the first seven years.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Article
eMERGEing progress in genomics---the first seven years.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Article
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
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- 2016
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- Publication type:
- journal article
Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists.
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- Database: The Journal of Biological Databases & Curation, 2013, v. 2013, p. 1, doi. 10.1093/database/bat056
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- Article
Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease.
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- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12255
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- Article
Editorial: The Importance of Diversity in Precision Medicine Research.
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- 2020
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- Publication type:
- Editorial
Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 413, doi. 10.1002/ajmg.b.32530
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- Article
A Small Number of Candidate Gene SNPs Reveal Continental Ancestry in African Americans.
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- Annals of Human Genetics, 2013, v. 77, n. 1, p. 56, doi. 10.1111/j.1469-1809.2012.00738.x
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- Article
Structural characterization of rare missense variants within known neurodegenerative disease proteins: Genetics/omics and systems biology.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046405
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- Article
Mapping Alzheimer disease–associated regions in the African American population: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046072
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- Article
Using linkage analysis to identify novel gene‐gene interactions in Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043435
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- Article
Sex differences in genetic predictors of resilience to Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043259
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- Article
Comparative trans‐ethnic meta‐analysis of whole exome sequencing variation for Alzheimer's disease (AD) in 18,402 individuals of the Alzheimer's Disease Sequencing Project (ADSP): Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041583
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- Article
Tissue‐specific genetically regulated expression in late‐onset Alzheimer's disease implicates risk genes within known and 30 novel loci: Genetics: Genetics and omics of AD II.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.039475
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- Article
P4‐114: EQTL ANALYSIS IDENTIFIES ANCESTRY SPECIFIC REGULATORY EFFECTS OF ALZHEIMER DISEASE ASSOCIATED VARIANTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1319, doi. 10.1016/j.jalz.2019.06.3775
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- Article
P4‐097: RARE VARIANTS IN FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE IDENTIFIED FROM LARGE SCALE WHOLE GENOME SEQUENCING.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1312, doi. 10.1016/j.jalz.2019.06.3757
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- Article
P4‐094: EXOME‐WIDE ANALYSIS IDENTIFIES NOVEL SEX‐SPECIFIC CANDIDATE GENES FOR ALZHEIMER DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1310, doi. 10.1016/j.jalz.2019.06.3754
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- Article
P3‐129: SOMATIC LOSS OF Y CHROMOSOME IN THE ADGC COHORTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P980, doi. 10.1016/j.jalz.2019.06.3157
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- Publication type:
- Article
O3‐13‐04: GENETIC VARIANTS IN ALZHEIMER'S DISEASE‐ASSOCIATED REGIONS HAVE DIFFERENT EFFECTS ON RNA EDITING RATES IN AFRICAN‐AMERICAN AND NON‐HISPANIC WHITE POPULATIONS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P920, doi. 10.1016/j.jalz.2019.06.4699
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- Article
P2‐108: WHOLE‐GENOME SEQUENCING IN NON‐HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE‐ONSET ALZHEIMER'S DISEASE RISK.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P710, doi. 10.1016/j.jalz.2018.06.794
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- Article
O2‐01‐05: MULTI‐ETHNIC ALZHEIMER'S DISEASE RELATED CHANGES OF RNA EDITING AFFECT IMMUNE REGULATION, ENDOCYTOSIS, AND AMYLOID PRECURSOR PROTEIN CATABOLISM.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P609, doi. 10.1016/j.jalz.2018.06.2643
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- Article
P1‐156: GENE‐BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P336, doi. 10.1016/j.jalz.2018.06.160
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- Article
P1‐144: TRANSCRIPTOMIC ANALYSIS OF WHOLE BLOOD IN AFRICAN AMERICAN AND NON‐HISPANIC WHITE ALZHEIMER DISEASE CASES AND CONTROLS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P331, doi. 10.1016/j.jalz.2018.06.147
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- Article
P1‐139: THE CONTRIBUTION OF SEX‐SPECIFIC ASSOCIATIONS IN GENETIC STUDIES OF ALZHEIMER'S DISEASE PATHOLOGY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P327, doi. 10.1016/j.jalz.2018.06.142
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- Publication type:
- Article
THE RELEVANCE OF APOE4 TO ALZHEIMER’S DISEASE IN THE PRESENCE OF LOCAL ANCESTRY DIFFERENCES.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P650, doi. 10.1016/j.jalz.2017.06.763
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- Publication type:
- Article