| Confirmation of a dyslexia susceptibility locus on chromosome 1p34‐p36 in a set of 100 Canadian families |
|
|
|
|
|
|
|
|
|
| COMT158 polymorphism and hostility |
|
|
|
|
|
|
|
|
|
| Methylomics in psychiatry: Modulation of gene–environment interactions may be through DNA methylation |
|
|
|
|
|
|
|
|
|
| Etiology of sex differences in the prevalence of ADHD: An examination of inattention and hyperactivity–impulsivity |
|
|
|
|
|
|
|
|
|
| Linkage and association analysis at the serotonin transporter (<i>SLC6A4</i>) locus in a rigid‐compulsive subset of autism |
|
|
|
|
|
|
|
|
|
| Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample |
|
|
|
|
|
|
✓ |
✓ |
European‐American; African‐American; ethnic groups |
| Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3‐p24.2 |
|
|
|
|
|
|
|
|
|
| Association between the brain‐derived neurotrophic factor 196G/A polymorphism and eating disorders |
|
|
|
|
|
|
|
|
|
| Human personality dimensions of persistence and harm avoidance associated with DRD4 and 5‐HTTLPR polymorphisms |
|
✓ |
|
|
|
|
|
|
|
| Serotonin transporter polymorphism and depressive‐related symptoms in schizophrenia |
|
|
|
|
|
|
|
|
|
| The gamma amino butyric acid (GABA) receptor alpha‐3 subunit gene polymorphism in unipolar depressive disorder: A genetic association study |
|
|
|
|
|
|
✓ |
✓ |
German individuals of the same ethnogeographical origin |
| Polymorphism at codon 469 of the intercellular adhesion molecule‐1 gene is not associated with sporadic Alzheimer's disease |
|
|
|
|
|
|
✓ |
✓ |
Italian, Finnish, Spanish population(s) |
| Family‐based association studies of α‐adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder |
|
|
|
|
|
|
|
|
|
| Regional European differences in allele and genotype frequencies of low density lipoprotein receptor‐related protein 1 polymorphism in Alzheimer's disease |
|
|
|
|
✓ |
✓ |
|
|
comparing our results with the findings from other European populations; from Northern to Southern r |
| Ethnic difference of the BDNF 196G/A (val66met) polymorphism frequencies: The possibility to explain ethnic mental traits |
|
|
|
|
|
|
|
|
|
| Investigation of polymorphisms in the <i>CREM</i> gene in panic disorder |
|
|
|
|
|
|
|
|
|
| Lack of evidence for an association between WNT2 and RELN polymorphisms and autism |
|
|
|
|
|
|
|
|
|
| Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome |
|
|
|
|
|
|
|
|
|
| Association between the glutathione S‐transferase M1 gene deletion and female methamphetamine abusers |
|
|
|
|
|
|
|
|
|
| Family‐based association study of the serotonin‐6 receptor gene (C267T polymorphism) in schizophrenia |
|
|
|
|
|
|
|
|
|
| Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome |
|
|
|
|
|
|
|
|
|
| 102T/C SNP in the 5‐hydroxytryptamine receptor 2A (<i>HTR2A</i>) gene and schizophrenia in two southern han chinese populations: Lack of association |
|
|
|
|
|
|
|
|
|
| Association of a duplicated repeat polymorphism in the 5′‐untranslated region of the <i>DRD4</i> gene with novelty seeking |
|
|
|
|
|
|
|
|
|
| Candidate genes for nicotine dependence via linkage, epistasis, and bioinformatics |
|
|
|
|
|
|
|
|
|
| A 5‐HT<sub>2C</sub> receptor promoter polymorphism (HTR2C − 759C/T) is associated with obesity in women, and with resistance to weight loss in heterozygotes |
|
|
|
|
|
|
|
|
|
| A novel A/G SNP in the −615th position of the dopamine D4 receptor promoter region as a source of misgenotyping of the −616 C/G SNP |
|
✓ |
|
|
|
|
|
|
|
| Role of muscarinic receptors in the pathology of schizophrenia |
|
|
|
|
|
|
|
|
|
| Possible epistatic role of <i>ADH7</i> in the protection against alcoholism |
|
|
|
|
|
|
|
|
|
| Serotonergic polymorphisms and psychotic disorders in populations from North Spain |
|
|
|
|
|
|
|
|
|
| Nongenetic pathologic developments of brain‐wave patterns in monozygotic twins discordant and concordant for schizophrenia |
|
|
|
|
|
|
|
|
|
| Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation |
|
|
|
|
|
|
|
|
|
| No evidence of association or linkage disequilibrium between polymorphisms in the 5′ upstream and coding regions of the dopamine D4 receptor gene and schizophrenia in a Portuguese population |
|
|
|
|
|
|
|
|
|
| Association study of cannabinoid receptor gene (<i>CNR1</i>) alleles and anorexia nervosa: Differences between restricting and bingeing/purging subtypes |
|
|
|
|
|
|
|
|
|
| Genetic mapping using haplotype and model‐free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31‐33 |
|
|
|
|
|
|
|
|
|
| <i>CALCYON</i>gene variation, schizophrenia, and cocaine dependence |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐American (EA); African‐American (AA) |
| An investigation into sub‐telomeric deletions of chromosome 22 and pervasive developmental disorders |
|
|
|
|
|
|
|
|
|
| Multiple missense mutations in the diazepam binding inhibitor (<i>DBI</i>) gene identified in schizophrenia but lack of disease association |
|
|
|
|
|
|
|
|
|
| Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: A family based association study |
|
|
|
|
|
|
|
|
|
| Haplotypes of the monoamine oxidase genes and the risk for substance use disorders |
|
|
|
|
|
✓ |
|
|
adult males of European ancestry |
| The gender effect in juvenile Huntington disease patients of Italian origin |
|
|
|
|
|
|
✓ |
✓ |
Italian origin |
| <i>Notch4</i> gene polymorphisms are not associated with autism in Japanese population |
|
|
|
|
|
|
✓ |
|
Japanese population |
| Association of adverse childhood experiences, age of menarche, and adult reproductive behavior: Does the androgen receptor gene play a role? |
|
|
|
|
|
|
|
|
|
| Is the <i>WKL1</i> gene associated with schizophrenia? |
|
|
|
|
|
|
✓ |
✓ |
Israeli Jewish; Ashkenazi; non-Ashkenazi Jews |
| A dyslexia susceptibility locus (<i>DYX7</i>) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5 |
|
|
|
|
|
|
|
|
|
| Association and transmission analysis of the FMR1 IVS10 + 14C‐T variant in autism |
|
|
|
|
|
|
✓ |
✓ |
East Asian individuals |
| TNXB locus may be a candidate gene predisposing to schizophrenia |
|
|
|
|
|
|
|
|
|
| No association between the <i>APOE</i> gene and autism |
|
|
|
|
|
|
|
|
|
| No association between the insulin degrading enzyme gene and Alzheimer's disease in a Japanese population |
|
|
|
|
|
|
|
|
|
| Confirming <i>RGS4</i> as a susceptibility gene for schizophrenia |
|
✓ |
|
|
|
|
✓ |
✓ |
"ethnically diverse"; "Irish sample" |
| Polymorphisms in the dopamine D5 receptor (<i>DRD5</i>) gene and ADHD |
|
|
|
|
|
|
|
|
|
| Association of tryptophan 2,3 dioxygenase gene polymorphism with autism |
|
|
|
|
|
|
|
|
|
| Association between the TPH gene A218C polymorphism and suicidal behavior: A meta‐analysis |
|
|
|
|
|
|
|
|
|
| Variation in the urokinase‐plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD |
|
|
|
|
|
|
|
|
|
| No association between a neuronal nitric oxide synthase (<i>NOS1</i>) gene polymorphism on chromosome 12q24 and bipolar disorder |
|
|
|
|
|
|
|
|
|
| Nature and nurture: Interaction and coaction |
|
|
|
|
|
|
|
|
|
| Role of dopamine D3 receptor (DRD3) and dopamine transporter (DAT) polymorphism in cognitive dysfunctions and therapeutic response to atypical antipsychotics in patients with schizophrenia |
|
|
|
|
|
|
|
|
|
| Personality traits in young female apolipoprotein E (apoE) ε4 and non‐ε4 carriers |
|
|
|
|
|
|
|
|
|
| Mutation screen of the glutamate decarboxylase‐67 gene and haplotype association to unipolar depression |
|
|
|
|
|
✓ |
|
|
European‐American (EA) |
| Re‐Screening serotonin receptors for genetic variants identifies population and molecular genetic complexity |
|
✓ |
|
|
|
|
✓ |
✓ |
African-American |
| Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia |
|
|
|
|
|
|
|
|
|
| An indirect test of the new mutation hypothesis associating advanced paternal age with the etiology of schizophrenia |
|
|
|
|
|
|
|
|
|
| Interleukin‐1β (<i>IL‐1β</i>) gene and increased risk for the depressive symptom‐dimension in schizophrenia spectrum disorders |
|
|
|
|
|
|
|
|
|
| No evidence of linkage or association between the norepinephrine transporter (NET) gene <i>MnlI</i> polymorphism and adult ADHD |
|
|
|
|
|
|
|
|
|
| Co‐occurrence of ADHD and low IQ has genetic origins |
|
|
|
|
|
|
|
|
|
| Effects of dopamine receptor D4 variation on alcohol and tobacco use and on novelty seeking: Multivariate linkage and association analysis |
|
|
|
|
|
|
|
|
|
| Association between brain‐derived neurotrophic factor 196 G/A polymorphism and personality traits in healthy subjects |
|
|
|
|
|
|
✓ |
✓ |
Japanese healthy subjects |
| Linkage disequilibrium analysis of polymorphisms in the gene for myelin oligodendrocyte glycoprotein in Tourette's syndrome patients from a Chinese sample |
|
|
|
|
|
|
✓ |
✓ |
Chinese |
| Ethnicity‐independent genetic basis of functional psychoses: A genotype‐to‐phenotype approach |
|
|
|
|
|
|
✓ |
✓ |
Afro-American; non-Afro-American; US-American ethnicities |
| Combined family trio and case‐control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa |
|
|
|
|
✓ |
✓ |
|
|
European population; combined European sample; European patients |
| Association between interleukin 1‐β promoter (−511) polymorphism and depressive symptoms in Alzheimer's disease |
|
|
|
|
|
|
|
|
|
| The 1239G/C polymorphism in exon 5 of <i>BACE1</i> gene may be associated with sporadic Alzheimer's disease in Chinese Hans |
|
✓ |
|
|
|
|
|
|
|
| Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database |
|
|
|
|
|
|
✓ |
✓ |
Afrikaner population; Afrikaners |
| No association between allelic variants of HOXA1/HOXB1 and autism |
|
|
|
|
|
|
✓ |
✓ |
Irish families |
| Dinucleotide repeat polymorphism in interferon‐γ gene is not associated with sporadic Alzheimer's disease |
|
|
|
|
|
|
|
|
|
| Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia |
|
|
|
|
|
|
|
|
|
| Polymorphism Screening of PIP5K2A: A Candidate Gene for Chromosome 10p‐Linked Psychiatric Disorders |
|
|
|
|
|
|
|
|
|
| Meta‐analysis of the association between the catecholamine‐<i>O</i>‐methyl‐transferase gene and obsessive‐compulsive disorder |
|
|
|
|
|
|
|
|
|
| Polymorphism analysis of <i>HOPA</i>: A candidate gene for schizophrenia |
|
|
|
|
|
|
|
|
|
| Candidate gene analysis of the human metabotropic glutamate receptor type 4 (<i>GRM4</i>) in patients with juvenile myoclonic epilepsy |
|
|
|
|
|
|
|
|
|
| Association study of a brain‐derived neurotrophic‐factor genetic polymorphism and major depressive disorders, symptomatology, and antidepressant response |
|
|
|
|
|
|
|
|
|
| Influence of <i>CLOCK</i> gene polymorphism on circadian mood fluctuation and illness recurrence in bipolar depression |
|
|
|
|
|
|
|
|
|
| Comparison of polymorphisms in the α7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects |
|
|
|
|
|
|
|
|
|
| Genome‐wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early‐onset, major depression |
|
|
|
|
|
|
|
|
|
| Author Index |
|
|
|
|
|
|
|
|
|
| Abstracts for the XIth World Congress of Psychiatric Genetics |
|
|
|
|
|
|
|
|
|
| Clinical features of boys with fragile X premutations and intermediate alleles |
|
|
|
|
|
|
|
|
|
| Association of the C766T polymorphism of the low‐density lipoprotein receptor‐related protein gene with Alzheimer's disease |
|
|
|
|
|
|
|
|
|
| Report from the 4th International Meeting of the Attention Deficit Hyperactivity Disorder Molecular Genetics Network |
|
|
|
|
|
|
|
|
|
| CAG‐Repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: A meta‐analysis of association studies |
|
|
|
|
|
|
|
|
|
| Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (<i>SSTR5</i>) gene in patients with autism |
|
|
|
|
|
|
|
|
|
| Genome scan of the fifty‐six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21 |
|
|
|
|
|
|
|
|
|
| Genetic dissection of psychopathological symptoms: Insomnia in mood disorders and <i>CLOCK</i> gene polymorphism |
|
|
|
|
|
|
|
|
|
| D2 and D4 dopamine receptor gene polymorphisms and personality traits in a young Korean population |
|
|
|
|
|
|
✓ |
✓ |
Koreans |
| Association between human μ‐opioid receptor gene polymorphism, pain tolerance, and opioid addiction |
|
|
|
|
|
|
✓ |
✓ |
African‐American |
| Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia‐Pacific region |
|
✓ |
|
|
|
|
✓ |
✓ |
Australian, Indian Fijian, Indigenous Fijian, Brahmin populations; phrase 'Australian Caucasian pedi |
| Association of a haplotype in the serotonin 5‐HT4 receptor gene (<i>HTR4</i>) with Japanese schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Japanese |
| The association of the D2S2944 124 bp allele with recurrent early onset major depressive disorder in women |
|
|
|
|
|
|
|
|
|
| A psychometrically derived impulsive trait related to a polymorphism in the serotonin transporter gene‐linked polymorphic region (5‐HTTLPR) in a japanese nonclinical population: Assessment by the barr |
|
|
|
|
|
|
✓ |
✓ |
Japanese |
| Linkage disequilibrium and haplotype analysis between serotonin receptor 1B gene variations and subtypes of alcoholism |
|
|
|
|
|
|
✓ |
✓ |
Finnish; American Indian |
| Children at familial risk for Tourette's disorder: Child and parent diagnoses |
|
|
|
|
|
|
|
|
|
| Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP‐17 family |
|
|
|
|
|
|
|
|
|
| Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding |
|
|
|
|
|
|
|
|
|
| Multipoint and single point non‐parametric linkage analysis with imperfect data |
|
|
|
|
|
|
|
|
|
| Linkage and association between serotonin 2A receptor gene polymorphisms and bipolar I disorder |
|
|
|
|
|
|
|
|
|
| Association of the 480 bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD |
|
|
|
|
|
|
✓ |
✓ |
Irish |
| Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7 |
|
|
|
|
|
|
|
|
|
| DNA stability and schizophrenia in twins |
|
|
|
|
|
|
|
|
|
| Association between depressed mood in the elderly and a <i>5‐HTR2A</i> gene variant |
|
|
|
|
|
|
✓ |
✓ |
Swedish |
| Beta‐1‐adrenergic receptor gene in major depression: Influence on antidepressant treatment response |
|
|
|
|
|
|
|
|
|
| Is the α‐2A adrenergic receptor gene (<i>ADRA2A</i>) associated with attention‐deficit/hyperactivity disorder? |
|
|
|
|
|
|
|
|
|
| Aggressive behavior in schizophrenia is associated with the low enzyme activity COMT polymorphism: A replication study |
|
|
|
|
|
|
|
|
|
| Initial genome‐wide scan for linkage with schizophrenia in the Japanese schizophrenia sib‐pair linkage group (JSSLG) families |
|
|
|
|
|
|
|
|
|
| Relationship between catechol‐<i>O</i>‐methyltransferase polymorphism and treatment‐resistant schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Japanese population |
| No evidence of molecular heterosis at the dopamine D2 receptor gene locus for smoking in schizophrenia |
|
|
|
|
|
|
|
|
|
| Apolipoprotein E Pittsburgh variant is not associated with the risk of late‐onset Alzheimer's disease in a Spanish population |
|
|
|
|
|
|
|
|
|
| Etiology of the comorbidity between RD and ADHD: Exploration of the non‐random mating hypothesis |
|
|
|
|
|
|
|
|
|
| Family‐based association study of markers on chromosome 22 in schizophrenia using African‐American, European‐American, and Chinese families |
|
|
|
|
|
|
✓ |
✓ |
African-American; European-American; Chinese |
| Mutation screening of the <i>Homer</i> gene family and association analysis in schizophrenia |
|
|
|
|
|
|
|
|
|
| <i>NURR1</i> promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits |
|
|
|
|
|
|
|
|
|
| Haplotypes at the OPRM1 locus are associated with susceptibility to substance dependence in European‐Americans |
|
|
|
|
✓ |
✓ |
|
|
European‐American (EA) |
| Monoamine oxidase B polymorphism, cigarette smoking and risk of Parkinson's disease: A study in an Asian population |
|
✓ |
|
|
|
|
|
|
|
| Association between Val<sup>108/158</sup>met polymorphism of the<i>COMT</i>gene and schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
ethnicity; population |
| Genome wide scan using homozygosity mapping and linkage analyses of a single pedigree with affective disorder suggests oligogenic inheritance |
|
|
|
|
|
|
|
|
|
| Association of mitochondrial complex I subunit gene <i>NDUFV2</i> at 18p11 with bipolar disorder |
|
|
|
|
|
|
|
|
|
| Association analysis of MAOA and COMT with neuroticism assessed by peers |
|
|
|
|
|
|
|
|
|
| Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia |
|
|
|
|
|
|
|
|
|
| Genetic approaches to polydipsia in schizophrenia: A preliminary report of a family study and an association study of an angiotensin‐converting enzyme gene polymorphism |
|
|
|
|
|
|
|
|
|
| Association of <i>HFE</i> mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with <i>APOE</i> |
|
|
|
|
|
|
|
|
|
| CHIP: Defining a dimension of the vulnerability to attention deficit hyperactivity disorder (ADHD) using sibling and individual data of children in a community‐based sample |
|
|
|
|
|
|
|
|
|
| HLA‐DRB genotyping in Gilles de la Tourette patients and their parents |
|
|
|
|
|
|
|
|
|
| Genetics of recurrent early‐onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies |
|
|
|
|
|
|
|
|
|
| <i>N</i>‐methyl‐<scp>d</scp>‐aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case‐control analyses |
|
|
|
|
|
|
|
|
|
| No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21‐q22 and autism |
|
|
|
|
|
|
|
|
|
| Study of <i>MECP2</i> gene in Rett syndrome variants and autistic girls |
|
|
|
|
|
|
|
|
|
| Evaluation of the genes for the adrenergic receptors α2A and α1C and Gilles de la Tourette Syndrome |
|
|
|
|
|
|
|
|
|
| Dopamine D2 receptor gene Ser311Cys variant and schizophrenia: association study and meta‐analysis |
|
|
|
|
|
|
|
|
|
| Association of the dopamine beta hydroxylase gene with attention deficit hyperactivity disorder: Genetic analysis of the Milwaukee longitudinal study |
|
✓ |
|
|
|
|
|
|
|
| Family‐based and case–control study of catechol‐<i>O</i>‐methyltransferase in schizophrenia among Palestinian Arabs |
|
|
|
|
|
|
✓ |
✓ |
Palestinian Arab; ethnically akin; ethnically matched control group |
| Wolfram syndrome and suicide: Evidence for a role of WFS1 in suicidal and impulsive behavior |
|
|
|
|
|
|
|
|
|
| Specific BACE1 genotypes provide additional risk for late‐onset alzheimer disease in APOE ε4 carriers |
|
|
|
|
|
|
|
|
|
| 5HTTLPR polymorphism in schizophrenic patients: Further support for association with violent suicide attempts |
|
✓ |
|
|
|
|
✓ |
✓ |
ethnically matched controls |
| Genetic heterogeneity in a very large bipolar affective disorder pedigree from Quebec |
|
|
|
|
|
|
|
|
|
| Severe myoclonus‐dystonia syndrome associated with a novel epsilon‐sarcoglycan gene truncating mutation |
|
|
|
|
|
|
|
|
|
| Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X |
|
|
|
|
|
|
|
|
|
| Depression in Alzheimer's disease: The effect of serotonin receptor gene variation |
|
|
|
|
|
|
|
|
|
| Apolipoprotein E in schizophrenia: A French association study and meta‐analysis |
|
✓ |
|
|
|
|
|
|
|
| Reduced expression of the muscarinic 1 receptor cortical subtype in schizophrenia |
|
|
|
|
|
|
|
|
|
| Editor's note |
|
|
|
|
|
|
|
|
|
| Elucidating the role of genetic factors in smoking behavior and nicotine dependence |
|
|
|
|
|
|
|
|
|
| White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging |
|
|
|
|
|
|
|
|
|
| <i>NOTCH4</i> and the frontal lobe in schizophrenia |
|
|
|
|
|
|
|
|
|
| Association between the <i>CCK‐A</i> receptor gene and panic disorder |
|
|
|
|
|
|
|
|
|
| Association between the cortisol response to opioid blockade and the Asn40Asp polymorphism at the μ‐opioid receptor locus (OPRM1) |
|
|
|
|
|
✓ |
|
|
European Americans |
| Enhanced production of amyloid precursor protein mRNA by peripheral mononuclear blood cell in Alzheimer's disease |
|
|
|
|
|
|
|
|
|