Found: 17
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A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.
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- BMC Medical Genomics, 2010, v. 3, p. 22, doi. 10.1186/1755-8794-3-22
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- Article
Intra-Familial Tests of Association between Familial Idiopathic Scoliosis and Linked Regions on 9q31.3-q34.3 and 16p12.3-q22.2.
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- Human Heredity, 2012, v. 74, n. 1, p. 36, doi. 10.1159/000343751
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- Article
Craniopharyngiomas : Radiological Differentiation of Two Types.
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- Journal of Korean Neurosurgical Society, 2016, v. 59, n. 5, p. 466, doi. 10.3340/jkns.2016.59.5.466
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- Article
Genetic Modifiers of Neurofibromatosis Type 1-Associated Café-au-Lait Macule Count Identified Using Multi-platform Analysis.
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- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004575
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- Article
A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders.
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- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02641-w
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- Article
Necessary and Sufficient Conditions for Equality of Sibling and Parent-Offspring Risk of a Disease Endophenotype in Case Families.
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- Annals of Human Genetics, 2012, v. 76, n. 1, p. 86, doi. 10.1111/j.1469-1809.2011.00685.x
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- Article
S92. PREVALENCE AND SEVERITY OF THOUGHT DISORDER IN NON-PSYCHIATRIC CONTROLS.
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- Schizophrenia Bulletin, 2019, v. 45, p. S341, doi. 10.1093/schbul/sbz020.637
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- Article
S48. HERITABILITY OF THOUGHT DISORDER IN SCHIZOPHRENIA AND BIPOLAR PATIENTS AND THEIR CLINICALLY UNAFFECTED FIRST-DEGREE BIOLOGICAL RELATIVES.
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- Schizophrenia Bulletin, 2019, v. 45, p. S324, doi. 10.1093/schbul/sbz020.593
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- Article
Exome-wide association study of treatment-resistant depression suggests novel treatment targets.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-38984-z
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- Article
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S83
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- Article
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S15
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- Article
Performance of random forests and logic regression methods using mini-exome sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S104
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- Article
Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S64
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- Article
ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available.
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- Genetic Epidemiology, 2019, v. 43, n. 1, p. 102, doi. 10.1002/gepi.22168
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- Article
Genetic associations with childhood brain growth, defined in two longitudinal cohorts.
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- Genetic Epidemiology, 2018, v. 42, n. 4, p. 405, doi. 10.1002/gepi.22122
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- Article
Cover.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1536
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- Article
Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1400
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- Article