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Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CGS Sharing GJB2/GJB6 genetic test information with family members.
Journal of Genetic Counseling
; in press:
.
Palmer CGS, Hsieh HJ, Reed EF, Lonnqvist J, Peltonen L, Woodward JA, Sinsheimer JS HLA-B maternal-fetal genotype matching increases risk for schizophrenia.
American Journal of Human Genetics
2006; 79:
710-715.
Palmer CGS, Hadley DW Evaluating the impact of genetic counseling and testing with signal detection methods.
Journal of Genetic Counseling
2005; 14:
17-27.
Palmer CGS, Martinez A, Sininger Y, Shapiro N, Grody W, Schimmenti LA Prelingual siblings of children with GJB2 hearing loss: Issues to consider.
Archives of Otolaryngology Head and Neck Surgery
2005; 131:
1020-1022.
Kraft P, Palmer CGS, Woodward JA, Turunen JA, Minassian S, Paunio T, Lonnqvist J, Peltonen L, Sinsheimer JS RHD maternal-fetal genotype incompatibility and schizophrenia: Extending the MFG test to include multiple siblings and birth order.
European Journal of Human Genetics
2004; 12:
192-198.
Hadley DW, Jenkins JF, Dimond E, de Carvalho M, Kirsch I, Palmer CGS Colon cancer screening practices following genetic counseling and testing for hereditary non-polyposis colorectal cancer.
Journal of Clinical Oncology
2004; 22:
39-44.
Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CGS Commentary: Genetic testing as part of the early hearing detection and intervention (EHDI) process.
Genetics in Medicine
2004; 6:
521-525.
Gasperoni TL, Ekelund J, Huttunen M, Palmer CGS, Tuulio-Henriksson A, Lonnqvist J, Kaprio J, Koskenvuo M, Peltonen L, Cannon TD Genetic linkage and association between chromosome 1q and working memory function in schizophrenia.
American Journal of Medical Genetics (Neuropsychiatric Genetics)
2003; 116:
8-16.
Palmer CGS, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Schimmenti LA Genetic testing and the early hearing detection and intervention process.
The Volta Review
2003; 103:
371-390.
Palmer CGS Risk perception: Another look at the 'White Male' effect.
Health, Risk & Society
2003; 5:
71-83.
Sinsheimer JS, Palmer CGS, Woodward JA The maternal-fetal genotype incompatibility test: Detecting genotype combinations that increase risk for disease.
Genetic Epidemiology
2003; 24:
1-13.
Martinez A, Linden J, Schimmenti LA, Palmer CGS Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness.
Genetics in Medicine
2003; 5:
106-112.
Palmer CGS, Turunen J, Sinsheimer JS, Minassian S, Paunio T, Lonnqvist J, Peltonen L, Woodward JA RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility.
American Journal of Human Genetics
2002; 71:
1312-1319.
Palmer CGS, Carlstrom LK, Woodward JA Risk perception and ethnicity.
Risk, Decision, and Policy
2001; 6:
187-206.
Palmer CGS, Bailey JN, Ramsey C, Cantwell, D, Sinsheimer JS, Del'Homme M, McGough J, Woodward JA, Asarnow R, Asarnow J, Nelson S, Smalley SL No evidence of linkage or linkage disequilibrium between DAT1 and attention deficit hyperactivity disorder in a large sample.
Psychiatric Genetics
1999; 9:
157-160.
Smalley SL, Bailey JN, Palmer CGS, Cantwell DP, McGough JJ, Del'Homme MA, Asarnow JR, Woodward JA, Ramsey C, Nelson SF Evidence that the dopamine D4 receptor is a susceptibility gene in attention deficit hyperactivity disorder.
Molecular Psychiatry
1998; 3:
427-430.
Smalley SL, Woodward JA, Palmer CGS A general statistical model for detecting complex trait loci using affected relative pairs in a genome search..
American Journal of Human Genetics
1996; 58:
844-860.
Palmer CGS Risk perception: An empirical study of the relationship between worldview and the risk construct.
Risk Analysis
1996; 16:
717-723.
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