Frequency and phenotype consequence of APOC3 rare variants in patients with very low triglyceride levels.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0387-1
- By:
- Publication type:
- Article
Works matching IS 17558794 AND DT 2018 AND VI 11 AND IP 3
Results: 7
1
2
Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0392-4
- By:
- Publication type:
- Article
3
Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer’s disease.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0390-6
- By:
- Publication type:
- Article
4
Integrative pathway-based survival prediction utilizing the interaction between gene expression and DNA methylation in breast cancer.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0389-z
- By:
- Publication type:
- Article
5
Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0388-0
- By:
- Publication type:
- Article
6
Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0391-5
- By:
- Publication type:
- Article
7
Pathway networks generated from human disease phenome.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0386-2
- By:
- Publication type:
- Article