Works matching DE "GENETICS -- Risk factors"
Results: 43
Is it Useful to Classify Progressive Supranuclear Palsy and Corticobasal Degeneration as Different Disorders? No.
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- Movement Disorders Clinical Practice, 2018, v. 5, n. 2, p. 141, doi. 10.1002/mdc3.12582
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- Article
Is it Useful to Classify PSP and CBD as Different Disorders? Yes.
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- Movement Disorders Clinical Practice, 2018, v. 5, n. 2, p. 145, doi. 10.1002/mdc3.12581
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- Article
Biochemical and genetic aspects of pathogenesis of schizophrenia.
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- Journal of Evolutionary Biochemistry & Physiology, 2011, v. 47, n. 5, p. 407, doi. 10.1134/S0022093011050021
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- Article
Major psychoses with mixed psychotic and mood symptoms: are mixed psychoses associated with different neurobiological markers?
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- Acta Psychiatrica Scandinavica, 2008, v. 118, n. 3, p. 172, doi. 10.1111/j.1600-0447.2008.01230.x
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- Article
Loss of asymmetry in D<sub>2</sub> receptors of putamen in unaffected family members at increased genetic risk for schizophrenia.
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- Acta Psychiatrica Scandinavica, 2008, v. 118, n. 3, p. 200, doi. 10.1111/j.1600-0447.2008.01223.x
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- Article
Cancer risk in the relatives of patients with nasopharyngeal carcinoma-a register-based cohort study in Sweden.
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- British Journal of Cancer, 2015, v. 112, n. 11, p. 1827, doi. 10.1038/bjc.2015.140
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- Article
Cdon Mutation and Fetal Ethanol Exposure Synergize to Produce Midline Signaling Defects and Holoprosencephaly Spectrum Disorders in Mice.
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- PLoS Genetics, 2012, v. 8, n. 10, p. 1, doi. 10.1371/journal.pgen.1002999
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- Article
Long-Term Follow-Up of Intrauterine Growth Restriction: Cardiovascular Disorders.
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- Fetal Diagnosis & Therapy, 2014, v. 36, n. 2, p. 143, doi. 10.1159/000353633
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- Article
Prediction of leprosy in the Chinese population based on a weighted genetic risk score.
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- PLoS Neglected Tropical Diseases, 2018, v. 12, n. 9, p. 1, doi. 10.1371/journal.pntd.0006789
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- Article
Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk.
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- Nature Genetics, 2015, v. 47, n. 8, p. 898, doi. 10.1038/ng.3353
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- Article
Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
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- Nature Genetics, 2015, v. 47, n. 8, p. 962, doi. 10.1038/ng0815-962c
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- Article
Multi-allelic haplotype model based on genetic partition for genomic prediction and variance component estimation using SNP markers.
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- BMC Genetics, 2015, v. 16, p. 1, doi. 10.1186/s12863-015-0301-1
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- Article
Missing heritability and strategies for finding the underlying causes of complex disease.
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- 2010
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- Publication type:
- research
Genetic Risk Factors for Longitudinal Changes in Structural MRI in Former Organolead Workers.
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- Journal of Aging Research, 2011, p. 1, doi. 10.4061/2011/362189
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- Article
Poster Session PA3.
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- Alcohol & Alcoholism. Supplement, 2007, v. 42, p. i51, doi. 10.1093/alcalc/agm127
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- Article
Homozygous truncation of SIX6 causes complex microphthalmia in humans.
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- Clinical Genetics, 2013, v. 84, n. 2, p. 198, doi. 10.1111/cge.12046
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- Article
Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.
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- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 1, doi. 10.1038/ejhg.2011.27
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- Article
Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00254
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- Article
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.
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- European Journal of Clinical Investigation, 2011, v. 41, n. 9, p. 1004, doi. 10.1111/j.1365-2362.2011.02494.x
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- Article
Hereditary breast cancer: ever more pieces to the polygenic puzzle.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-12
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- Article
EVALUATION OF GENETIC RISK FACTORS FOR CHILDHOOD ASTHMA USING GENERALIZED MULTIFACTOR DIMENSIONALITY REDUCTION SOFTWARE.
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- Romanian Journal of Rheumatology / Revista Romana de Reumatologie, 2014, v. 23, n. 2, p. 148
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- Article
Discovery of genetic risk factors for disease.
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- Journal of the Royal Society of New Zealand, 2018, v. 48, n. 2/3, p. 191, doi. 10.1080/03036758.2017.1392324
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- Article
Machine learning algorithm-based risk prediction model of coronary artery disease.
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- Molecular Biology Reports, 2018, v. 45, n. 5, p. 901, doi. 10.1007/s11033-018-4236-2
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- Article
The c.−190 C>A transversion in promoter region of protamine1 gene as a genetic risk factor for idiopathic oligozoospermia.
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- Molecular Biology Reports, 2016, v. 43, n. 8, p. 795, doi. 10.1007/s11033-016-4017-8
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- Article
Use of allele scores as instrumental variables for Mendelian randomization.
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- International Journal of Epidemiology, 2013, v. 42, n. 4, p. 1134, doi. 10.1093/ije/dyt093
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- Article
Genetic susceptibility to lung cancer—light at the end of the tunnel?
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- Carcinogenesis, 2013, v. 34, n. 3, p. 487, doi. 10.1093/carcin/bgt016
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- Article
Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information.
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- Public Health Genomics, 2016, v. 19, n. 5, p. 307, doi. 10.1159/000448913
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- Article
Applying a Theory-Based Framework to Understand Public Knowledge of Genetic Risk Factors: A Case for the Distinction between How-To Knowledge and Principles Knowledge.
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- Public Health Genomics, 2011, v. 14, n. 4/5, p. 259, doi. 10.1159/000294149
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- Article
Non-Replication of Genome-Wide Based Associations between Common Variants in INSIG2 and PFKP and Obesity in Studies of 18,014 Danes.
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- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002872
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- Article
Do Late Bubbles Correspond to Early Hepatopulmonary Syndrome?
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- Annals of Hepatology: Official Journal of the Mexican Association of Hepatology, 2017, v. 16, n. 4, p. 476, doi. 10.5604/01.3001.0010.0268
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- Article
Thrombotic Thrombocytopenic Purpura in Black People: Impact of Ethnicity on Survival and Genetic Risk Factors.
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- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0156679
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- Article
Epidemiology of Parkinson's disease.
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- Journal of Neural Transmission, 2017, v. 124, n. 8, p. 901, doi. 10.1007/s00702-017-1686-y
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- Article
Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis.
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- 2018
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- Publication type:
- journal article
Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions.
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- Human Genetics, 2017, v. 136, n. 1, p. 75, doi. 10.1007/s00439-016-1737-8
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- Publication type:
- Article
Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders.
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- Human Genetics, 2014, v. 133, n. 2, p. 173, doi. 10.1007/s00439-013-1370-8
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- Article
Genetic risk factors for inhibitors in haemophilia A.
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- European Journal of Haematology, 2015, v. 94, p. 7, doi. 10.1111/ejh.12495
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- Article
A common haplotype of the C-C chemokine receptor 2 gene and HLA-DRB1*0301 are independent genetic risk factors for Löfgren’s syndrome.
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- Journal of Internal Medicine, 2008, v. 264, n. 5, p. 433, doi. 10.1111/j.1365-2796.2008.01984.x
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- Article
Holistic management of osteoarthritis.
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- Practice Nursing, 2008, v. 19, n. 6, p. 298, doi. 10.12968/pnur.2008.19.6.30276
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- Article
Setting the stage.
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- Diabetes, Obesity & Metabolism, 2009, v. 11, p. 1, doi. 10.1111/j.1463-1326.2008.00996.x
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- Publication type:
- Article
Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies.
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- Diabetes, Obesity & Metabolism, 2009, v. 11, p. 101, doi. 10.1111/j.1463-1326.2008.01010.x
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- Article
Results of the MHC Fine Mapping Workshop.
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- Diabetes, Obesity & Metabolism, 2009, v. 11, p. 108, doi. 10.1111/j.1463-1326.2008.01011.x
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- Publication type:
- Article
Genetic variants of eNOS gene may modify the susceptibility to idiopathic male infertility.
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- Biomarkers, 2013, v. 18, n. 5, p. 412, doi. 10.3109/1354750X.2013.805245
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- Article
Straight talk with...Daniel Levy.
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- Nature Medicine, 2013, v. 19, n. 10, p. 1197, doi. 10.1038/nm1013-1197
- Publication type:
- Article