Found: 11
Select item for more details and to access through your institution.
Genome-Wide Association Studies and the Problem of Relatedness Among Advanced Intercross Lines and Other Highly Recombinant Populations.
- Published in:
- Genetics, 2010, v. 185, n. 3, p. 1033, doi. 10.1534/genetics.110.116863
- By:
- Publication type:
- Article
The ExAC browser: displaying reference data information from over 60 000 exomes.
- Published in:
- Nucleic Acids Research, 2017, v. 45, n. D1, p. D840, doi. 10.1093/nar/gkw971
- By:
- Publication type:
- Article
Contribution of retrotransposition to developmental disorders.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12520-y
- By:
- Publication type:
- Article
Replication of long-bone length QTL in the F<sub>9</sub>-F<sub>10</sub> LG,SM advanced intercross.
- Published in:
- Mammalian Genome, 2009, v. 20, n. 4, p. 224, doi. 10.1007/s00335-009-9174-9
- By:
- Publication type:
- Article
Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 6, p. 1, doi. 10.1371/journal.pgen.1006121
- By:
- Publication type:
- Article
Patterns and rates of exonic de novo mutations in autism spectrum disorders.
- Published in:
- Nature, 2012, v. 485, n. 7397, p. 242, doi. 10.1038/nature11011
- By:
- Publication type:
- Article
The contribution of X-linked coding variation to severe developmental disorders.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20852-3
- By:
- Publication type:
- Article
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00725-6
- By:
- Publication type:
- Article
Quantifying prion disease penetrance using large population control cohorts.
- Published in:
- Science Translational Medicine, 2016, v. 8, n. 322, p. 1, doi. 10.1126/scitranslmed.aad5169
- By:
- Publication type:
- Article
A framework for the interpretation of de novo mutation in human disease.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
- By:
- Publication type:
- Article
The Evaluation of Tools Used to Predict the Impact of Missense Variants Is Hindered by Two Types of Circularity.
- Published in:
- Human Mutation, 2015, v. 36, n. 5, p. 513, doi. 10.1002/humu.22768
- By:
- Publication type:
- Article