The postgenomic era and complex disease

Pharmacogenomics

Volumn 7, Issue 3, 2006, Pages 341-343

  Witkowski, J A ^a  

^a Howard Hughes Medical Institute Cold Spring Harbor Laboratory Cold Spring Harbor   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN;

ALKAPTONURIA; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHRONIC FATIGUE SYNDROME; CYSTIC FIBROSIS; DIAGNOSTIC ACCURACY; DUCHENNE MUSCULAR DYSTROPHY; EDITORIAL; GENE EXPRESSION; GENE MUTATION; GENOMICS; HEREDITY; HUMAN; HUNTINGTON CHOREA; PATHOGENESIS; PHARMACOGENOMICS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SICKLE CELL ANEMIA; THALASSEMIA;

FATIGUE SYNDROME, CHRONIC; HUMANS; PHARMACOGENETICS;

EID: 33646024935     PISSN: 14622416     EISSN: 17448042     Source Type: Journal    
DOI: 10.2217/14622416.7.3.341     Document Type: Editorial

References (14)

1. Vernon SD, Reeves WC: The challenge of integrating disparate high-content data: epidemiological, clinical and laboratory data collected during an in-hospital study of chronic fatigue syndrome. Pharmacogenomics 7(3), 345-354 (2006).
2. Garrod AE: Inborn Errors of Metabolism (reprinted by Oxford University Press, 1963) Oxford, UK (1909).
3. Bateson W, Saunders ER: Report I. In: Reports to the Evolution Committee of the Royal Society. Harrison, London, UK, 1-160 (1902).
4. Garrod AE: The croonian lectures of the royal college of physicians. Lancet ii, 1-7, 73-79, 142-148, 214-220 (1908).
5. Pauling L: The molecular basis of genetics. Am. J. Psychiaty 113(6), 492-495 (1956).
6. Itano HA, Neel JV: A new inherited abnormality of human hemoglobin. Proc. Natl Acad. Sci. USA 36 (11), 613-617 (1950).
7. Ingram VM: Gene mutations in human hemoglobin: the chemical difference between normal and sickle cell haemoglobin. Nature 180(4581), 326-328 (1957).
8. Tjio TH, Levan A: The chromosome number of man. Hereditas 42, 1 (1956).
9. Lejeune J: Mongolism, regressive trisomy. Ann. Genet. 2,1-38 (1960).
10. McKusick VA: Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders. 12th Edition. The Johns Hopkins University Press, Baltimore, MD, USA (1998).
11. Botstein D, White RL, Skolnick M, Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32(3), 314-331 (1980).
12. Bishop DT, Cannon LA, Quigley AC, Skolnick MH: Strategies for efficient linkage analysis: example of Huntington's disease pedigrees. Genet. Epidemiol. (Suppl.1), 217-222 (1986).
13. Davis AE 3rd: C1 inhibitor and hereditary angioneurotic edema. Annu. Rev. Immunol. 6, 595-628 (1988).
14. Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nature Genet. 11(3), 241-247 (1995).