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Genetically Predicted Glucose-Dependent Insulinotropic Polypeptide (GIP) Levels and Cardiovascular Disease Risk Are Driven by Distinct Causal Variants in the Region.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The Y Chromosome: A Complex Locus for Genetic Analyses of Complex Human Traits.
- Published in:
- Genes, 2020, v. 11, n. 11, p. 1273, doi. 10.3390/genes11111273
- By:
- Publication type:
- Article
Mitochondrial DNA Haplogroups and Breast Cancer Risk Factors in the Avon Longitudinal Study of Parents and Children (ALSPAC).
- Published in:
- Genes, 2018, v. 9, n. 8, p. 395, doi. 10.3390/genes9080395
- By:
- Publication type:
- Article
Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications.
- Published in:
- Genes, 2018, v. 9, n. 1, p. 45, doi. 10.3390/genes9010045
- By:
- Publication type:
- Article
Supplementary to "Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications".
- Published in:
- Genes, 2018, v. 9, n. 1, p. 45, doi. 10.3390/genes9010045
- By:
- Publication type:
- Article
Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions.
- Published in:
- Annals of Human Genetics, 2016, v. 80, n. 3, p. 187, doi. 10.1111/ahg.12150
- By:
- Publication type:
- Article
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
- Published in:
- Bioinformatics, 2017, v. 33, n. 2, p. 272, doi. 10.1093/bioinformatics/btw613
- By:
- Publication type:
- Article
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.
- Published in:
- Bioinformatics, 2017, v. 33, n. 1, p. 79, doi. 10.1093/bioinformatics/btw565
- By:
- Publication type:
- Article
Nonsense Mutation in Coiled-Coil Domain Containing 151 Gene ( CCDC151) Causes Primary Ciliary Dyskinesia.
- Published in:
- Human Mutation, 2014, v. 35, n. 12, p. 1446, doi. 10.1002/humu.22698
- By:
- Publication type:
- Article
Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/923491
- By:
- Publication type:
- Article
Proxy Molecular Diagnosis from Whole-Exome Sequencing Reveals Papillon-Lefevre Syndrome Caused by a Missense Mutation in CTSC.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0121351
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- Publication type:
- Article