Publications:
A selected list of publications:
Boudreault Patrick, Baldwin Erin E, Fox Michelle, Dutton Loriel, Tullis Leeelle, Linden Joyce, Kobayashi Yoko, Zhou Jin, Sinsheimer Janet S, Sininger Yvonne, Grody Wayne W, Palmer Christina G S
Deaf adults' reasons for genetic testing depend on cultural
affiliation: results from a prospective, longitudinal genetic
counseling and testing study
Journal of deaf studies and deaf education,
2010; 15(3):
209-27.
Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody WW, Palmer CGS
Deaf adults' reasons for genetic testing depend on cultural affiliation: Results from a prospective, longitudinal genetic counseling and testing study,
Journal of Deaf Studies and Deaf Education,
2010; 15:
209-227.
Palmer CGS
Evidence for maternal-fetal genotype incompatibility as a risk factos for schizophrenia,
Journal of Biomedicine and Biotechnology,
2010;
article 576318.
Enns EE, Boudreault P, Palmer CGS
Examining the relationship between genetic counselors' attitudes toward deaf people and the genetic counseling session,
Journal of Genetic Counseling,
2010; 19:
161-173.
Childs E, Palmer CGS, Lange K, Sinsheimer JS
Modeling maternal-offspring gene-gene interactions: The extended -MFG test,
Genetic Epidemiology,
2010; 34:
512-521.
Palmer CGS, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody WW, Schimmenti LA
A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants,
American Journal of Medical Genetics,
2009; 149A:
1169-1182.
Palmer CGS, Lueddeke, JT, Zhou J
Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child,
Genetics in Medicine,
2009; 11:
248-255.
Schimmenti Lisa A, Martinez Ariadna, Telatar Milhan, Lai Chih-Hung, Shapiro Nina, Fox Michelle, Warman Berta, McCarra Matthew, Crandall Barbara, Sininger Yvonne, Grody Wayne W, Palmer Christina G S
Infant hearing loss and connexin testing in a diverse population
Genetics in medicine : official journal of the American College of Medical Genetics,
2008; 10(7):
517-24.
Palmer CGS, Mallery E, Turunen JA, Hsieh HJ, Peltonen L, Lonnqvist, J. Woodward JA, Sinsheimer JS
Effect of Rhesus D incompatibility on schizophrenia depends on offspring sex,
Schizophrenia Research,
2008; 104:
135-145.
Palmer CGS, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA
Ethnic differences in parental perceptions of genetic testing for infants with hearing loss,
Journal of Genetic Counseling,
2008; 17:
129-138.
Schimmenti LA, Martinez A, Teletar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CGS
Infant hearing loss and connexin testing in a diverse population,
Genetics in Medicine,
2008; 10:
517-524.
Peay HL, Veach PM, Palmer CGS, Rosen-Sheidley B, Gettig E, Austin JC
Psychiatric disorders in clinical genetics I: Addressing family histories of psychiatric illness,
Journal of Genetic Counseling,
2008; 17:
6-17.
Austin JC, Palmer CGS, Rosen-Sheidley B, Veach PM, Gettig E, Peay HL
Psychiatric disorders in clinical genetics II: Individualizing recurrence risks,
Journal of Genetic Counseling,
2008; 17:
18-29.
Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CGS
Sharing GJB2/GJB6 genetic test information with family members,
Journal of Genetic Counseling,
2007; 16:
313-324.
Hsieh HJ, Palmer CGS, Sinsheimer JS
Allowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects,
Human Heredity,
2006; 62:
165-174.
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.
Minassian SL, Palmer CGS, Turunen JA, Paunio T, Lonnqvist J, Peltonen L, Woodward JA, Sinsheimer JS
Incorporating serotypes into family based association studies using the MFG test,
Annals of Human Genetics,
2006; 70:
541-553.
Hsieh HJ, Palmer CGS, Harney S, Newton JL, Wordsworth P, Brown MA, Sinsheimer JS
The v-MFG test: Investigating maternal, offspring, and maternal-fetal genetic incompatibility effects on disease and viability,
Genetic Epidemiology,
2006; 30:
333-347.
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.
Minassian SL, Palmer CGS, Sinsheimer JS
An exact maternal-fetal genotype incompatibility (MFG) test,
Genetic Epidemiology,
2004; 27:
.
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.
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.
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.
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.
Gasperoni Timothy L, Ekelund Jesper, Huttunen Matti, Palmer Christina G S, Tuulio-Henriksson Annamari, Lönnqvist Jouko, Kaprio Jaakko, Peltonen Leena, Cannon Tyrone D
Genetic linkage and association between chromosome 1q and working
memory function in schizophrenia
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics,
2003; 116B(1):
8-16.
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AK, MacPhie IL, Newbury DF, Palmer CGS, Woodward JA, Del'Homme M, Cantwell D, Nelson SF, Monaco AP, Smalley SL
A genome-wide scan for loci involved in attention-deficit/hyperactivity disorder (ADHA),
American Journal of Human Genetics,
2002; 70:
1183-1196.
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.
Fisher Simon E, Francks Clyde, McCracken James T, McGough James J, Marlow Angela J, MacPhie I Laurence, Newbury Dianne F, Crawford Lori R, Palmer Christina G S, Woodward J Arthur, Del'Homme Melissa, Cantwell Dennis P, Nelson Stanley F, Monaco Anthony P, Smalley Susan L
A genomewide scan for loci involved in attention-deficit/hyperactivity
disorder
American journal of human genetics,
2002; 70(5):
1183-96.
Palmer CGS, Carlstrom LK, Woodward JA
Risk perception and ethnicity,
Risk, Decision, and Policy,
2001; 6:
187-206.
Carlstrom LK, Woodward JA, Palmer CGS
Evaluating the simplified conjoint expected risk model: Comparing the use of objective and subjective information,
Risk Analysis,
2000; 20:
385-392.
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.