Citations for
1DRD4, PTNS
Novelty seeking traits and D4 dopamine receptors.
Swift G, Larsen B, Hawi Z, Gill M.
Am J Med Genet 96(2):222-3. No abstract available. 2000
2DFNA17, MHA, MYH9, PTNS
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.
Lalwani AK, Goldstein JA, Kelley MJ, Luxford W, Castelein CM, Mhatre AN.
Am J Hum Genet 67(5):1121-8. 2000
3FTNS, MYH9, PTNS
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13.
Cusano R, Gangarossa S, Forabosco P, Caridi G, Ghiggeri GM, Russo G, Iolascon A, Ravazzolo R, Seri M.
Eur J Hum Genet 8(11):895-9. 2000
4DRD4, PTNS
Association between novelty seeking and dopamine receptor D4 (DRD4) exon III polymorphism in Japanese subjects.
Tomitaka M, et al.
Am J Med Genet 88(5):469-471 1999
5DRD4, PTNS
Human novelty-seeking personality traits and dopamine D4 receptor polymorphisms : a twin and genetic association study.
Pogue-Geile M, Ferrell R, Deka R, Debski T, Manuck S.
Am J Med Genet 81(1):44-8. 1998
6DRD3, DRD4, HTR2C, PTNS, PTNS2, PTNS3
5-HT2C (HTR2C) serotonin receptor gene polymorphism associated with the human personality trait of reward dependence : interaction with dopamine D4 receptor (D4DR) and dopamine D3 receptor (D3DR) polymorphisms.
Ebstein RP, et al.
Am J med Genet 74 : 65-72. 1997
7DRD4, PTNS
Mapping genes for human personality.
Cloninger CR, et al.
Nat Genet 12 : 3-4. 1996
8DRD4, PTNS
Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking.
Ebstein RP, et al.
Nat Genet 12 : 78-80. 1996
9DRD4, PTNS
Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking.
Benjamin J, et al.
Nat Genet 12 : 81-84. 1996