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American College of Obstetricians and Gynecologists Committee on Genetics (2010). ACOG Committee Opinion No. 469: carrier screening for fragile X syndrome. Obstetrics and Gynecology 116, 1008–1010.
PS Appelbaum (2010). Genetic discrimination in mental disorders: the impact of GINA. Psychiatric Services 61, 338–340.
MJ Arranz , S Kapur (2008). Pharmacogenetics in psychiatry: are we ready for widespread clinical use? Schizophrenia Bulletin 34, 1130–1144.
EA Ashley , AJ Gutte , MT Wheeler , R Chen , (2010). Clinical assessment incorporating a personal genome. Lancet 375, 1525–1535.
JC Austin , WG Honer (2007). The genomic era and serious mental illness: a potential application for psychiatric genetic counseling. Psychiatric Services 58, 254–261.
MJH Baars , L Henneman , LP ten Kate (2005). Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem. Genetics in Medicine 7, 605–610.
A Bashford , P Levine (2010). The Oxford Handbook of the History of Eugenics. New York: Oxford University Press.
AS Bassett , EWC Chow , P AbdelMalik , M Gheorghiu , (2003). The schizophrenia phenotype in 22q11 deletion syndrome. American Journal of Psychiatry 160, 1580–1586.
BR Bates , JA Lynch , JL Bevan , CM Condit (2005). Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research. Social Science and Medicine 60, 331–344.
SRH Beach , GH Brody , TD Gunter , H Packer , (2010). Child maltreatment moderates the association of MAOA with symptoms of depression and antisocial personality disorder. Journal of Family Psychology 24, 12–20.
BB Biesecker , HL Peay (2003). Ethical issues in psychiatric genetics research: points to consider. Psychopharmacology (Berlin) 171, 27–35.
AL Bredenoord , HY Kroes , E Cuppen , M Parker , (2011). Disclosure of individual genetic data to research participants: the debate reconsidered. Trends in Genetics 27, 41–47.
W Burke , LE Pinsky , NA Press (2001). Categorizing tests to identify their ethical, legal, and social implications. American Journal of Medical Genetics 106, 233–240.
A Caspi , J McClay , TE Moffitt , J Mill , (2002). Role of genotype in the cycle of violence in maltreated children. Science 297, 851–854.
A Caspi , K Sugden , TE Moffitt , A Taylor , (2003). Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science 301, 386–389.
RWK Chiu , R, YWL Zheng , TY Leung , H Sun , (2011). Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. British Medical Journal 342, c7401.
LE Delisi , H Bertisch (2006). A preliminary comparison of the hopes of researchers, clinicians, and families for the future ethical use of genetic findings on schizophrenia. American Journal of Medical Genetics 141B, 110–115.
LE Duncan , MC Keller (2011). A critical review of the first 10 years of candidate gene-by-environment interaction research in psychiatry. American Journal of Psychiatry 168, 1041–1049.
CT Finn , JW Smoller (2006). Genetic counseling in psychiatry. Harvard Review of Psychiatry 14, 109–121.
CT Finn , MA Wilcox , BR Korf , D Blacker , (2005). Psychiatric genetics: a survey of psychiatrists’ knowledge, opinions, and practice patterns. Journal of Clinical Psychiatry 66, 821–830.
F Galton (1883). Inquiries into Human Faculty and its Development. London: Macmillan.
KB Garber , J Visootsak , ST Warran (2008). Fragile X syndrome. European Journal of Human Genetics 16, 666–672.
JS Goldman , JM Farmer , VM Van Deerlin , KC Wilhelmsen , (2004). Frontotemporal dementia: genetics and genetic counseling dilemmas. Neurologist 10, 227–234.
JS Goldman , SE Hahn , JW Catania , S LaRusse-Eckert , (2011). ACMG Practice Guidelines: Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors. Genetics in Medicine 13, 597–605.
SE Gollust , SC Hull , BS Wilfond (2002). Limitations of direct-to-consumer advertising for clinical genetic testing. Journal of the American Medical Association 288, 1762–1767.
HT Greely (2001). Informed consent and other ethical issues in human population genetics. Annual Review of Genetics 35, 785–800.
HT Greely (2011). Get ready for the flood of fetal gene screening. Nature 469, 289–291.
RC Green , S Roberts , LA Cupples , Relkin (2009). Disclosure of APOE genotype for risk of Alzheimer's disease. New England Journal of Medicine 361, 245–254.
IN Hassenfeld (2002). Doctor-patient relationships in Nazi Germany and the fate of psychiatric patients. Psychiatric Quarterly 73, 183–194.
JG Hoop , G Savla , LW Roberts , S Zisook , LB Dunn (2010). The current state of genetics training in psychiatric residency: views of 235 educators and trainees. Academic Psychiatry 34, 109–114.
S Hogarth , G Javitt , D Melzer (2008). The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues. Annual Review of Genomics and Human Genetics 9, 161–182.
I Jones , J Scourfield , F McCandless , N Craddock (2002). Attitudes towards future testing for bipolar disorder susceptibility genes: a preliminary investigation. Journal of Affective Disorders 71, 189–193.
KS Kendler (2006). ‘A gene for …’ The nature of gene action in psychiatric disorders. American Journal of Psychiatry 162, 1243–1252.
Y Kim , S Zerwas , SE Trace , PF Sullivan (2011). Schizophrenia genetics: where next? Schizophrenia Bulletin 37, 456–463.
R Klitzman (2006). Questions, complexities, and limitations in disclosing individual genetic results. American Journal of Bioethics 6, 34–36.
R Klitzman (2010 a). Exclusion of genetic information from the medical record: ethical and medical dilemmas. Journal of the American Medical Association 304, 1120–1121.
R Klitzman (2010 b). Misunderstandings concerning genetics among patients confronting genetic disease. Journal of Genetic Counseling 19, 430–446.
R Klitzman , PS Appelbaum , W Chung , MV Sauer (2008). Anticipating issues related to increasing pre-implantation genetic diagnosis use: a research agenda. Reproductive Biomedicine Online 17 (Suppl. 1), 33–42.
RE Lawrence , PS Appelbaum (2011). Genetic testing in psychiatry: a review of attitudes and beliefs. Psychiatry 74, 315–331.
M Leehey (2009). Fragile X-associated tremor/ataxia syndrome: clinical phenotype, diagnosis, and treatment. Journal of Investigative Medicine 57, 830–836.
LS Lehmann , JC Weeks , N Klar , L Biener , (2000). Disclosure of familial genetic information: perceptions of the duty to inform. American Journal of Medicine 109, 705–711.
YM Lo , KC Chan , H Sun , EZ Chen , (2010). Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Science Translational Medicine 2, 61ra91.
PO McGowan , A Sasaki , AC D'Alessio , S Dymov , (2009). Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse. Nature Neuroscience 12, 342–348.
TM Marteau , RT Croyle (1998). The new genetics: psychological responses to genetic testing. British Medical Journal 316, 693–696.
B Meiser , NA Kasparian , PB Mitchell , K Strong , (2008). Attitudes to genetic testing in families with multiple cases of bipolar disorder. Genetic Testing 12, 233–244.
J-E Meyer (1988). The fate of the mentally ill in Germany during the Third Reich. Psychological Medicine 18, 575–581.
DT Miller , MP Adam , S Aradhya , LG Biesecker , (2010). Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. American Journal of Human Genetics 86, 749–764.
KK Milner , EE Collins , GR Connors , EM Petty (1998). Attitudes of young adults to prenatal screening and genetic correction for human attributes and psychiatric conditions. American Journal of Medical Genetics 76, 111–119.
KC Murphy (2002). Schizophrenia and velo-cardio-facial syndrome. Lancet 359, 426–430.
J Murphy , J Scott , D Kaufman , G Geller , (2008). Public expectations for return of results from large-cohort genetic research. American Journal of Bioethics 8, 36–43.
MR Munafo , C Currant , G Lewis , J Flint (2009). Gene×environment interactions at the serotonin transporter locus. Biological Psychiatry 65, 211–219.
C Netzer , N Biller-Andorno (2004). Pharmacogenetic testing, informed consent and the problem of secondary information. Bioethics 18, 344–360.
T Nieminen , M Kähönen , LE Viiri , P Grönroos , (2008). Pharmacogenetics of apolipoprotein E gene during lipid-lowering therapy: lipid levels and prevention of coronary heart disease. Pharmacogenomics 9, 1475–1486.
R Ottman , S Hirose , S Jain , H Lerche , (2010). Genetic testing in the epilepsies – Report of the ILAE Genetics Commission. Epilepsia 51, 655–670.
B Pasche , D Absher (2011). Whole-genome sequencing a step closer to personalized medicine. Journal of the American Medical Association 305, 1596–1597.
J Phelan (2005). Geneticization of deviant behavior and consequences for stigma: the case of mental illness. Journal of Health and Social Behavior 46, 307–322.
R Plomin , OS Davis (2009). The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. Journal of Child Psychology and Psychiatry, and Allied Disciplines 50, 63–71.
HS Richardson (2008). Incidental findings and ancillary-care obligations. Journal of Law, Medicine and Ethics 36, 256–270.
MA Rothstein (2010). Is deidentification sufficient to protect health privacy in research? American Journal of Bioethics 10, 3–11.
GWC Tam , R Redon , NP Carter , SGN Grant (2009). The role of DNA copy number variation in schizophrenia. Biological Psychiatry 66, 1005–1012.
BA Tarini , D Singer , SJ Clark , MM Davis (2009). Parents’ interest in predictive genetic testing for their children when a disease has no treatment. Pediatrics 124, e432–e438.
EF Torrey , R Yolken (2010). Psychiatric genocide: Nazi attempts to eradicate schizophrenia. Schizophrenia Bulletin 36, 26–32.
CL Trippitelli , KR Jamison , MF Folstein , JJ Bartko , (1998). Pilot study on patients’ and spouses’ attitudes toward potential genetic testing for bipolar disorder. American Journal of Psychiatry 155, 899–904.
E Vassos , DA Collier , S Holden , C Patch , (2010). Penetrance for copy number variants associated with schizophrenia. Human Molecular Genetics 19, 3477–3481.
PB Verghese , JM Castellano , DM Holtzman (2011). Apolipoprotein E in Alzheimer's disease and other neurological disorders. Lancet Neurology 10, 241–252.
T Walsh , JM McClellan , SE McCarthy , AM Addington , (2008). Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320, 539–543.
IC Weaver , N Cervoni , FA Champagne , AC D'Alessio , (2004). Epigenetic programming by maternal behavior. Nature Neuroscience 7, 847–854.
D Wendler , E Emanuel (2002). The debate over research on stored biological samples: what do sources think? Archives of Internal Medicine 162, 1457–1462.
K Wilhelm , B Meiser , PB Mitchell , AW Finch , (2009). Issues concerning feedback about genetic testing and risk of depression. British Journal of Psychiatry 194, 404–410.
JG Winner , D Goebert , C Matsu , DA Mrazek (2010). Training in psychiatric genomics during residency: a new challenge. Academic Psychiatry 34, 115–118.
SM Wolf , FP Lawrenz , CA Nelson , JP Kahn , (2008). Managing incidental findings in human subjects research: analysis and recommendations. Journal of Law, Medicine and Ethics 36, 219–248.
CD Zick , CJ Mathews , JS Roberts , R Cook-Deegan , (2005). Genetic testing for Alzheimer's disease and its impact on insurance purchasing behavior. Health Affairs (Millwood) 24, 483–490.