Diagnosis and Classification of Schizophrenia, Schizophrenia Bulletin, vol.19, issue.2, pp.199-214, 1993. ,
DOI : 10.1093/schbul/19.2.199
Symptoms, signs, and diagnosis of schizophrenia, The Lancet, vol.346, issue.8973, pp.477-481, 1995. ,
DOI : 10.1016/S0140-6736(95)91325-4
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21, American Journal of Medical Genetics, vol.56, issue.4, pp.348-351, 1999. ,
DOI : 10.1002/(SICI)1096-8628(19990820)88:4<348::AID-AJMG11>3.0.CO;2-N
Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?, The British Journal of Psychiatry, vol.164, issue.5, pp.619-624, 1994. ,
DOI : 10.1192/bjp.164.5.619
Mapping of hKCa3 to chromosome 1q21 and investigation of linkage of CAG repeat polymorphism to schizophrenia, Molecular Psychiatry, vol.4, issue.3, pp.261-266, 1999. ,
DOI : 10.1038/sj.mp.4000548
Evidence for anticipation in schizophrenia, Am J Hum Genet, vol.54, pp.864-870, 1994. ,
Schizophrenia and Affective Disorders???Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and P300 Findings in a Family, The American Journal of Human Genetics, vol.69, issue.2, pp.428-433, 2001. ,
DOI : 10.1086/321969
No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia, European Journal of Human Genetics, vol.7, issue.2, pp.247-250, 1999. ,
DOI : 10.1038/sj.ejhg.5200278
Age at onset anticipation in familial EPHE Banque de Monographies SVT 23 ,
Does the phenomenon even exist?, Schizophr Res, vol.40, pp.55-65, 1999. ,
Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia, Molecular Psychiatry, vol.3, issue.3, pp.266-269, 1998. ,
DOI : 10.1038/sj.mp.4000400
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy, Nature Genetics, vol.146, issue.2, pp.164-167, 1998. ,
DOI : 10.1016/0960-8966(93)90119-5
A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1, Human Molecular Genetics, vol.6, issue.11, pp.1855-1863, 1997. ,
DOI : 10.1093/hmg/6.11.1855
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3??? end of a transcript encoding a protein kinase family member, Cell, vol.68, issue.4, p.385, 1992. ,
DOI : 10.1016/0092-8674(92)90154-5
Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22, Science, vol.288, issue.5466, pp.678-682, 2000. ,
DOI : 10.1126/science.288.5466.678
Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion, Science, vol.271, issue.5254, pp.1423-1427, 1996. ,
DOI : 10.1126/science.271.5254.1423
Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?, Molecular Psychiatry, vol.3, issue.1, pp.32-37, 1998. ,
DOI : 10.1038/sj.mp.4000353
General method for amplifying regions of very high G+C content, Nucleic Acids Research, vol.21, pp.2953-2954, 1993. ,
The SCA12 Mutation as a Rare Cause of Spinocerebellar Ataxia, Archives of Neurology, vol.58, issue.11, pp.1833-1835, 2001. ,
DOI : 10.1001/archneur.58.11.1833
Lack of association between schizophrenia and a CAG repeat polymorphism of the hSKCa3 gene in a North Eastern US sample, Molecular Psychiatry, vol.5, issue.3 ,
DOI : 10.1038/sj.mp.4000694
Genomic scan for genes predisposing to schizophrenia, American Journal of Medical Genetics, vol.45, issue.1, pp.59-71, 1994. ,
DOI : 10.1002/ajmg.1320540111
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene., Journal of Medical Genetics, vol.29, issue.12, pp.858-860, 1992. ,
DOI : 10.1136/jmg.29.12.858
No evidence for linkage between COMT and schizophrenia in a French population, Psychiatry Research, vol.102, issue.1, pp.87-90, 2001. ,
DOI : 10.1016/S0165-1781(01)00237-2
human genes, Science, vol.282, pp.0-744, 1998. ,
Polyglutamine tracts in schizophrenia: gaining new insights, Molecular Psychiatry, vol.5, issue.3, pp.236-237, 2000. ,
DOI : 10.1038/sj.mp.4000675
A comprehensive genetic map of the human genome based on 5,264 microsatellites, Nature, vol.380, issue.6570, pp.152-154, 1996. ,
DOI : 10.1038/380152a0
Evidence of a Cohort Effect for Age at Onset of Schizophrenia, American Journal of Psychiatry, vol.158, issue.3, pp.489-492, 2001. ,
DOI : 10.1176/appi.ajp.158.3.489
Ethical Issues in the Treatment of Applicants to APA-Accredited Ph.D. Programs, Psychological Reports, vol.12, issue.3, pp.1323-1330, 1994. ,
DOI : 10.2466/pr0.1994.74.3c.1323
hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21, Molecular Psychiatry, vol.4, issue.3, pp.254-260, 1999. ,
DOI : 10.1038/sj.mp.4000508
Social Competence Deficits in Adolescents at Risk for Schizophrenia, The Journal of Nervous and Mental Disease, vol.182, issue.2, pp.103-108, 1994. ,
DOI : 10.1097/00005053-199402000-00007
Chromosome 1 loci in Finnish schizophrenia families, Human Molecular Genetics, vol.10, issue.15, pp.1611-1617, 2001. ,
DOI : 10.1093/hmg/10.15.1611
Anticipation in unipolar affective disorder, Journal of Affective Disorders, vol.35, issue.1-2, pp.31-40, 1995. ,
DOI : 10.1016/0165-0327(95)00035-L
Calmodulin Mediates Calcium-dependent Activation of the Intermediate Conductance KCa Channel,IKCa1, Journal of Biological Chemistry, vol.274, issue.9, pp.5746-5754, 1999. ,
DOI : 10.1074/jbc.274.9.5746
Linkage disequilibrium, J Genet Hum, vol.28, pp.105-113, 1980. ,
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family, Ann Neurol, vol.49, pp.117-121, 2001. ,
Expanded (CAG)n, (CGG)n and (GAA)n trinucleotide repeat microsatallite, and mutant purine synthesis and pigmentation genes cause schizophrenia and autism, Medical Hypotheses, vol.51, issue.3, pp.223-233, 1998. ,
DOI : 10.1016/S0306-9877(98)90080-9
Ultradian rapid cycling in prepubertal and early adolescent bipolarity is not in transmission disequilibrium with val/met COMT alleles, Biological Psychiatry, vol.47, issue.7, pp.605-609, 2000. ,
DOI : 10.1016/S0006-3223(99)00251-6
Clinical Genetics as Clues to the "Real" Genetics of Schizophrenia (A Decade of Modest Gains While Playing for Time), Schizophrenia Bulletin, vol.13, issue.1, pp.23-47, 1987. ,
DOI : 10.1093/schbul/13.1.23
Implications of a Mental Health Intervention for Elderly Mentally Ill Residents of Residential Care Facilities, The International Journal of Aging and Human Development, vol.13, issue.1, pp.229-245, 1991. ,
DOI : 10.2190/MXAQ-XKWT-BD4R-0EBT
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23, Am J Hum Genet, vol.23, issue.68, pp.3-24, 2001. ,
GENOMIC IMPRINTING: Nature and Clinical Relevance, Annual Review of Medicine, vol.48, issue.1, pp.35-44, 1997. ,
DOI : 10.1146/annurev.med.48.1.35
Pseudoautosomal gene, Psychiatric Genetics, vol.9, issue.4, pp.129-134, 1999. ,
DOI : 10.1097/00041444-199912000-00011
No evidence to support the association of the potassium channel gene hSKCa3 CAG repeat with schizophrenia or bipolar disorder in the Irish population, Molecular Psychiatry, vol.4, issue.5, pp.488-491, 1999. ,
DOI : 10.1038/sj.mp.4000560
Anticipation in schizophrenia, Schizophrenia Research, vol.35, issue.1, pp.25-32, 1999. ,
DOI : 10.1016/S0920-9964(98)00112-1
Genome scan for association and linkage, Genetic Epidemiology, vol.47, issue.6, pp.613-618, 1995. ,
DOI : 10.1002/gepi.1370120615
SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia, Brain Research Bulletin, vol.56, issue.3-4, pp.397-403, 2001. ,
DOI : 10.1016/S0361-9230(01)00596-2
Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12, Nat Genet, vol.23, pp.391-392, 1999. ,
A Novel Long and Unstable CAG/CTG Trinucleotide Repeat on Chromosome 17q, Genomics, vol.49, issue.2, pp.321-326, 1998. ,
DOI : 10.1006/geno.1998.5266
Anticipation in Japanese families with schizophrenia, Journal of Human Genetics, vol.43, issue.4, pp.217-223, 1998. ,
DOI : 10.1007/s100380050076
No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia, Molecular Psychiatry, vol.2, issue.6, pp.478-482, 1997. ,
DOI : 10.1038/sj.mp.4000297
Possible association between schizophrenia and a CAG repeat polymorphism in the spinocerebellar ataxia type 1 (SCA1) gene on human chromosome 6p23, Psychiatric Genetics, vol.9, issue.1 ,
DOI : 10.1097/00041444-199903000-00002
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia, American Journal of Medical Genetics, vol.17, issue.2, pp.154-157, 1999. ,
DOI : 10.1002/(SICI)1096-8628(19990416)88:2<154::AID-AJMG11>3.0.CO;2-A
Polyglutamine-containing proteins in schizophrenia, Molecular Psychiatry, vol.4, issue.1, pp.53-57, 1999. ,
DOI : 10.1038/sj.mp.4000480
Molecular genetics of bipolar disorder, Neuroscience Research, vol.40, issue.2, pp.105-113, 2001. ,
DOI : 10.1016/S0168-0102(01)00221-8
NIMH genetics initiative millennium schizophrenia consortium: Linkage analysis of African-American pedigrees, American Journal of Medical Genetics, vol.153, issue.4, pp.282-289, 1998. ,
DOI : 10.1002/(SICI)1096-8628(19980710)81:4<282::AID-AJMG2>3.0.CO;2-W
Clinical heterogeneity in schizophrenia and the pattern of psychopathology in relatives: results from an epidemiologically based family study, Acta Psychiatrica Scandinavica, vol.45, issue.5, pp.294-300, 1994. ,
DOI : 10.1016/0920-9964(93)90003-2
Parametric and nonparametric linkage analysis: a unified multipoint approach, Am J Hum Genet, vol.58, pp.1347-1363, 1996. ,
Catechol-O-methyltransferase polymorphisms and schizophrenia, Psychiatric Genetics, vol.7, issue.3, 1997. ,
DOI : 10.1097/00041444-199723000-00001
Genetic dissection of complex traits, Science, vol.265, issue.5181, pp.2037-2048, 1994. ,
DOI : 10.1126/science.8091226
The affected sib-pair method using identity by state relations, Am J Hum Genet, vol.39, pp.148-150, 1986. ,
Anticipation in schizophrenia: No evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases, American Journal of Medical Genetics, vol.15, issue.4, pp.342-346, 1998. ,
DOI : 10.1002/(SICI)1096-8628(19980710)81:4<342::AID-AJMG12>3.0.CO;2-L
Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment, Genetic Epidemiology, vol.42, issue.1, pp.11-21, 1996. ,
DOI : 10.1002/(SICI)1098-2272(1996)13:1<11::AID-GEPI2>3.0.CO;2-9
A genome scan of schizophrenia, Psychiatric Genetics, vol.6, issue.3, pp.741-750, 1998. ,
DOI : 10.1097/00041444-199623000-00017
Multicenter Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5q, 6q, 10p, and 13q: Schizophrenia Linkage Collaborative Group III **The Schizophrenia Linkage Collaborative Group III includes all authors, who are listed in the following order: study coordinators (Levinson, Holmans), principal investigators of each research group (Straub, Owen, Wildenauer, Gejman, Pulver, Laurent), and additional authors from each group, with groups listed according to the number of pedigrees contributed. Participating research groups are identified in the paper as ???MCV/Ireland??? (Straub, Kendler, Walsh), ???U Wales??? (Owen, Norton, Williams), ???U Bonn??? (Wildenauer, Schwab, Lerer); ???US/Aust??? (Levinson, Mowry), ???U Chicago??? (Gejman, Sanders), ???JHU??? (Pulver, Antonarakis, Blouin), and ???CNRS??? (Laurent, DeLeuze, Mallet)., The American Journal of Human Genetics, vol.67, issue.3, pp.652-663, 2000. ,
DOI : 10.1086/303041
Nicotinic acetylcholine receptors in health and disease, Molecular Neurobiology, vol.120, issue.Suppl. 5, pp.193-222, 1997. ,
DOI : 10.1007/BF02740634
Analysis of CAG/CTG repeat size in chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method, Biological Psychiatry, vol.44, issue.11, pp.1160-1165, 1998. ,
DOI : 10.1016/S0006-3223(97)00492-7
Detection of expanded CAG repeats in Bipolar Affective Disorder using the repeat expansion detection (RED) method, Neurobiology of Disease, vol.2, issue.1, pp.55-62, 1995. ,
DOI : 10.1006/nbdi.1995.0006
Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders?, Molecular Psychiatry, vol.3, issue.5, pp.405-410, 1998. ,
DOI : 10.1038/sj.mp.4000416
Study of anticipation in Chinese families with schizophrenia, Psychiatry and Clinical Neurosciences, vol.240, issue.2, pp.137-140, 2001. ,
DOI : 10.1002/(SICI)1096-8628(19991215)88:6<686::AID-AJMG19>3.0.CO;2-O
Association Analysis of a Functional Catechol-O-Methyltransferase Gene Polymorphism in Schizophrenic Patients in Taiwan, Neuropsychobiology, vol.43, issue.1, pp.11-14, 2001. ,
DOI : 10.1159/000054858
Karl pearson's mathematization of inheritance: From ancestral heredity to Mendelian genetics (1895???1909), Annals of Science, vol.51, issue.1, pp.35-94, 1998. ,
DOI : 10.1098/rsta.1896.0007
Anticipation is not associated with CAG repeat expansion in parent-offspring pairs of patients affected with schizophrenia, American Journal of Medical Genetics, vol.1, issue.1, pp.50-56, 1999. ,
DOI : 10.1002/(SICI)1096-8628(19990205)88:1<50::AID-AJMG9>3.0.CO;2-W
The genetic transmission of schizophrenia: Application of Mendelian latent structure analysis to eye tracking dysfunctions in schizophrenia and affective disorder, Journal of Psychiatric Research, vol.20, issue.1, pp.57-67, 1986. ,
DOI : 10.1016/0022-3956(86)90023-3
The genetic epidemiology of schizophrenia and the design of linkage studies, European Archives of Psychiatry and Clinical Neuroscience, vol.19, issue.3, pp.174-181, 1991. ,
DOI : 10.1007/BF02190760
Anticipation in bipolar affective disorder, Am J Hum Genet, vol.53, pp.385-390, 1993. ,
Anticipation in schizophrenia: A review and reconsideration, American Journal of Medical Genetics, vol.6, issue.6, pp.686-693, 1999. ,
DOI : 10.1002/(SICI)1096-8628(19991215)88:6<686::AID-AJMG19>3.0.CO;2-O
Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorder, Molecular Psychiatry, vol.4, issue.3, pp.217-219, 1999. ,
DOI : 10.1038/sj.mp.4000492
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia, Mol Psychiatry, vol.5, pp.439-442, 2000. ,
Anticipation in schizophrenia and bipolar disorder controlling for an information bias, American Journal of Medical Genetics, vol.96, issue.1, pp.61-68, 2000. ,
DOI : 10.1002/(SICI)1096-8628(20000207)96:1<61::AID-AJMG13>3.3.CO;2-N
hSKCa3, Psychiatric Genetics, vol.9, issue.2, pp.91-96, 1999. ,
DOI : 10.1097/00041444-199906000-00007
A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients, C R Acad Sci III, vol.318, pp.803-809, 1995. ,
The first generation of women psychologists and the psychology of women., American Psychologist, vol.55, issue.6, pp.616-619, 2000. ,
DOI : 10.1037/0003-066X.55.6.616
An international two???stage genome???wide search for schizophrenia susceptibility genes, Nature Genetics, vol.52, issue.3, pp.321-324, 1995. ,
DOI : 10.1038/ng1195-321
Detection of polyglutamine expansion in a new acidic protein: a candidate for childhood onset schizophrenia?, Molecular Psychiatry, vol.4, issue.1, pp.58-63, 1999. ,
DOI : 10.1038/sj.mp.4000448
CAG repeat expansions and schizophrenia: association with disease in females and with early age-at-onset, Human Molecular Genetics, vol.4, issue.10, pp.1957-1961, 1995. ,
DOI : 10.1093/hmg/4.10.1957
Anticipating more anticipation, The Lancet, vol.347, issue.9009, p.1132, 1996. ,
DOI : 10.1016/S0140-6736(96)90605-4
Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophrenia, The British Journal of Psychiatry, vol.170, issue.3, pp.278-280, 1997. ,
DOI : 10.1192/bjp.170.3.278
Sequential tests for the detection of linkage Amer, J. Hum. Gen, vol.7, pp.277-318, 1955. ,
A lecture on heredity and insanity, Lancet, vol.1, pp.1251-1259, 1911. ,
Prospects for research on schizophrenia. IV. Genetic and environmental factors. Parallels in medicine, Neurosci Res Program Bull, vol.10, pp.403-406, 1972. ,
Diagnostic Interview for Genetic Studies, Archives of General Psychiatry, vol.51, issue.11, pp.849-859, 1994. ,
DOI : 10.1001/archpsyc.1994.03950110009002
Anticipation in Swedish families with bipolar affective disorder., Journal of Medical Genetics, vol.31, issue.9, pp.686-689, 1994. ,
DOI : 10.1136/jmg.31.9.686
The Molecular Genetics of Schizophrenia, Annals of Medicine, vol.4, issue.6, pp.541-546, 1996. ,
DOI : 10.3109/07853899608999118
Candidate-gene association studies of schizophrenia, Am J Hum Genet, vol.65, pp.587-592, 1999. ,
Anticipation, imprinting, trinucleotide repeat expansions and psychoses, Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol.25, issue.1, pp.167-192, 2001. ,
DOI : 10.1016/S0278-5846(00)00152-4
A CAG trinucleotide repeat expansion and familial schizophrenia, Psychiatry Research, vol.94, issue.3, pp.257-262, 2000. ,
DOI : 10.1016/S0165-1781(00)00156-6
Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells?, Molecular Psychiatry, vol.5, issue.3, pp.234-236, 2000. ,
DOI : 10.1038/sj.mp.4000673
Schizophrenia: An Epigenetic Puzzle?, Schizophrenia Bulletin, vol.25, issue.4, pp.639-655, 1999. ,
DOI : 10.1093/oxfordjournals.schbul.a033408
THE PROBLEM OF ANTICIPATION IN PEDIGREES OF DYSTROPHIA MYOTONICA, Annals of Eugenics, vol.13, issue.1, pp.125-132, 1948. ,
DOI : 10.1111/j.1469-1809.1947.tb02384.x
Anticipating incoming events: an impaired cognitive process in schizophrenia, Cognition, vol.81, issue.3, pp.209-225, 2001. ,
DOI : 10.1016/S0010-0277(01)00133-0
URL : https://hal.archives-ouvertes.fr/hal-00655457
Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13.1: Part 1, American Journal of Medical Genetics, vol.26, issue.1, pp.36-43, 1994. ,
DOI : 10.1002/ajmg.1320540108
Human genes containing polymorphic trinucleotide repeats, Nature Genetics, vol.10, issue.3, pp.186-191, 1992. ,
DOI : 10.1016/0027-5107(91)90021-F
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs, Am J Hum Genet, vol.46, pp.242-253, 1990. ,
An association of CAG repeats at the KCNN3 locus with symptom dimensions of schizophrenia, Biological Psychiatry, vol.51, issue.10, pp.788-794, 2002. ,
DOI : 10.1016/S0006-3223(01)01348-8
hSKCa3, Psychiatric Genetics, vol.9, issue.4, pp.169-175, 1999. ,
DOI : 10.1097/00041444-199912000-00001
Anticipatory saccades during smooth pursuit eye movements and familial transmission of schizophrenia, Biological Psychiatry, vol.44, issue.8, pp.690-697, 1998. ,
DOI : 10.1016/S0006-3223(98)00052-3
Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder, Molecular Psychiatry, vol.6, issue.6, pp.694-700, 2000. ,
DOI : 10.1038/sj.mp.4000924
Association analysis of CAG repeats at theKCNN3 locus in Indian patients with bipolar disorder and schizophrenia, American Journal of Medical Genetics, vol.10, issue.6, pp.744-748, 2000. ,
DOI : 10.1002/1096-8628(20001204)96:6<744::AID-AJMG9>3.0.CO;2-Z
Schizophrenia, The Lancet, vol.353, issue.9162, pp.1425-1430, 1999. ,
DOI : 10.1016/S0140-6736(98)07549-7
URL : https://hal.archives-ouvertes.fr/hal-00633986
A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involved, Psychiatry Research, vol.72, issue.2, pp.141-144, 1997. ,
DOI : 10.1016/S0165-1781(97)00070-X
A genome-wide search for schizophrenia susceptibility genes, American Journal of Medical Genetics, vol.60, issue.5, pp.364-376, 1998. ,
DOI : 10.1002/(SICI)1096-8628(19980907)81:5<364::AID-AJMG4>3.0.CO;2-T
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib???pair linkage analysis, Nature Genetics, vol.10, issue.3, pp.325-327, 1995. ,
DOI : 10.1038/ng1195-325
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis, Molecular Psychiatry, vol.2, issue.2, pp.156-160, 1997. ,
DOI : 10.1038/sj.mp.4000263
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6, Molecular Psychiatry, vol.5, issue.6, pp.638-649, 2000. ,
DOI : 10.1038/sj.mp.4000791
Obstetric Complications and Twin Studies of Schizophrenia: Clarifications and Affirmations, Schizophrenia Bulletin, vol.3, issue.3, pp.351-354, 1977. ,
DOI : 10.1093/schbul/3.3.351
Direct detection of novel expanded trinucleotide repeats in the human genome, Nature Genetics, vol.12, issue.2, pp.135-139, 1993. ,
DOI : 10.1038/ng1192-186
A Triplet Repeat on 17q Accounts for Most Expansions Detected by the Repeat-Expansion???Detection Technique, The American Journal of Human Genetics, vol.62, issue.6, pp.1548-1551, 1998. ,
DOI : 10.1086/301876
Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred, American Journal of Medical Genetics, vol.15, issue.5, pp.546-548, 1997. ,
DOI : 10.1002/(SICI)1096-8628(19970919)74:5<546::AID-AJMG19>3.0.CO;2-C
TDT Clarification, The American Journal of Human Genetics, vol.64, issue.2, p.668, 1999. ,
DOI : 10.1086/302265
European multicentre association study of schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms, American Journal of Medical Genetics, vol.19, issue.1, pp.24-28, 1998. ,
DOI : 10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N
Nonparametric test for doubly interval-censored failure time data Lifetime Data, Anal, vol.7, pp.363-375, 2001. ,
Short CAG repeats within the hSKCa3 gene associated with schizophrenia, NeuroReport, vol.9, issue.16, pp.3595-3599, 1998. ,
DOI : 10.1097/00001756-199811160-00010
The age of onset of schizophrenia and the theory of anticipation, Psychiatry Research, vol.93, issue.2, pp.125-134, 2000. ,
DOI : 10.1016/S0165-1781(00)00103-7
A potential vulnerability locus for schizophrenia on chromosome 6p24???22: evidence for genetic heterogeneity, Nature Genetics, vol.51, issue.3, pp.287-293, 1995. ,
DOI : 10.1038/ng1195-287
Support for a possible schizophrenia vulnerability locus in region 5q22???31 in Irish families, Molecular Psychiatry, vol.2, issue.2, pp.148-155, 1997. ,
DOI : 10.1038/sj.mp.4000258
The linear arrangement of six sex-linked factors in Drosophila, as shown by their mode of association, Journal of Experimental Zoology, vol.3, issue.1, pp.43-59, 1913. ,
DOI : 10.1002/jez.1400140104
Further evidence for anticipation in schizophrenia, Psychiatry Research, vol.59, issue.1-2, pp.25-33, 1995. ,
DOI : 10.1016/0165-1781(95)02778-5
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias, Nature, vol.378, issue.6555, pp.403-406, 1995. ,
DOI : 10.1038/378403a0
Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan, Molecular Psychiatry, vol.4, issue.3, pp.271-273, 1999. ,
DOI : 10.1038/sj.mp.4000482
Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder, Psychiatry Research, vol.101, issue.3, pp.203-207, 2001. ,
DOI : 10.1016/S0165-1781(01)00229-3
Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR, Genomics, vol.14, issue.4, pp.1104-1106, 1992. ,
DOI : 10.1016/S0888-7543(05)80138-7
Genetic basis of schizophrenia: trinucleotide repeats an update, Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol.25, issue.6, pp.1187-1201, 2001. ,
DOI : 10.1016/S0278-5846(01)00186-5
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome, Cell, vol.65, issue.5, pp.905-914, 1991. ,
DOI : 10.1016/0092-8674(91)90397-H
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome, Cell, vol.65, issue.5, pp.905-914, 1991. ,
DOI : 10.1016/0092-8674(91)90397-H
No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins, Human Genetics, vol.103, issue.1, pp.41-47, 1998. ,
DOI : 10.1007/s004390050780
Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression, American Journal of Medical Genetics, vol.15, issue.1, pp.79-82, 1999. ,
DOI : 10.1002/(SICI)1096-8628(19990205)88:1<79::AID-AJMG14>3.0.CO;2-N
The unstable trinucleotide repeat story EPHE Banque de Monographies SVT 32 ,
An Unstable Trinucleotide-Repeat Region on Chromosome 13 Implicated in Spinocerebellar Ataxia: A Common Expansion Locus, The American Journal of Human Genetics, vol.66, issue.3, pp.819-829, 2000. ,
DOI : 10.1086/302803
Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype, Journal of Neurology, Neurosurgery & Psychiatry, vol.68, issue.5, pp.672-675, 2000. ,
DOI : 10.1136/jnnp.68.5.672
A second-generation linkage map of the human genome, Nature, vol.359, issue.6398, pp.794-801, 1992. ,
DOI : 10.1038/359794a0
Progress with Proteome Projects: Why all Proteins Expressed by a Genome Should be Identified and How To Do It, Biotechnology and Genetic Engineering Reviews, vol.13, issue.1, pp.19-50, 1996. ,
DOI : 10.1080/02648725.1996.10647923
Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene, The Lancet, vol.347, issue.9011, pp.1294-1296, 1996. ,
DOI : 10.1016/S0140-6736(96)90939-3
A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia, Molecular Psychiatry, vol.3, issue.2, pp.141-149, 1998. ,
DOI : 10.1038/sj.mp.4000376
A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs, Human Molecular Genetics, vol.8, issue.9, pp.1729-1739, 1999. ,
DOI : 10.1093/hmg/8.9.1729
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios, Molecular Psychiatry, vol.4, issue.3, pp.267-270, 1999. ,
DOI : 10.1038/sj.mp.4000495
Clinicopathology of spinocerebellar degeneration: Its correlation to the unstable CAG repeat of the affected gene, Pathology International, vol.86, issue.Suppl. 2, pp.1-15, 1997. ,
DOI : 10.1111/j.1440-1827.1997.tb04429.x
CAG repeat sequences in bipolar affective disorder: No evidence for association in a french population, American Journal of Medical Genetics, vol.15, issue.4, pp.338-341, 1998. ,
DOI : 10.1002/(SICI)1096-8628(19980710)81:4<338::AID-AJMG11>3.0.CO;2-M