Using genetic variation to study human disease
- 1 November 2001
- journal article
- review article
- Published by Elsevier in Trends in Molecular Medicine
- Vol. 7 (11) , 507-512
- https://doi.org/10.1016/s1471-4914(01)02183-9
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Are Rare Variants Responsible for Susceptibility to Complex Diseases?American Journal of Human Genetics, 2001
- Genetic Susceptibility to Venous ThrombosisNew England Journal of Medicine, 2001
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphismsNature, 2001
- Initial sequencing and analysis of the human genomeNature, 2001
- Guilt by associationNature Genetics, 2000
- Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequencesNature Genetics, 2000
- Use of Unlinked Genetic Markers to Detect Population Stratification in Association StudiesAmerican Journal of Human Genetics, 1999
- The Future of Genetic Studies of Complex Human DiseasesScience, 1996
- Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanismsPharmacogenetics, 1996
- Variation in the TNF-α promoter region associated with susceptibility to cerebral malariaNature, 1994