| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1039248903 |
| P356 | DOI | 10.1038/325806A0 |
| P698 | PubMed publication ID | 3547139 |
| P2093 | author name string | Anderson S | |
| Detera-Wadleigh SD | |||
| Gershon ES | |||
| Berrettini WH | |||
| Goldin LR | |||
| Boorman D | |||
| P2860 | cites work | Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 |
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| The assessment of affective disorders in children and adolescents by semistructured interview. Test-retest reliability of the schedule for affective disorders and schizophrenia for school-age children, present episode version | Q34198901 | ||
| Bipolar affective disorders linked to DNA markers on chromosome 11 | Q39461777 | ||
| Morbidity risks of schizophrenia and affective disorders among first degree relatives of patients with schizophrenia, mania, depression and surgical conditions | Q41477110 | ||
| The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences | Q48406236 | ||
| Psychiatric disorders in the relatives of probands with affective disorders. The Yale University--National Institute of Mental Health Collaborative Study. | Q52093345 | ||
| A Family Study of Schizoaffective, Bipolar I, Bipolar II, Unipolar, and Normal Control Probands | Q63869312 | ||
| Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12 | Q69848389 | ||
| Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques | Q69848405 | ||
| Clinical findings in patients with anorexia nervosa and affective illness in their relatives | Q70664693 | ||
| P433 | issue | 6107 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | preproinsulin | Q7240673 |
| P1104 | number of pages | 3 | |
| P304 | page(s) | 806-808 | |
| P577 | publication date | 1987-02-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Close linkage of c-Harvey-ras-1 and the insulin gene to affective disorder is ruled out in three North American pedigrees | |
| P478 | volume | 325 |
| Q73423727 | A chromosome 18 genetic linkage study in three large Belgian pedigrees with bipolar disorder |
| Q35199576 | A controlled study of Tourette syndrome. V. Depression and mania |
| Q57655483 | A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26 |
| Q38562217 | A systematic evaluation of linkage studies in bipolar disorder |
| Q33675777 | A weak association between TH and DRD2 genes and bipolar affective disorder in a Spanish sample |
| Q36307331 | Advances and retreats in the molecular genetics of major mental illness |
| Q35882725 | Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q |
| Q35613746 | An overview of the genetics of psychotic mood disorders |
| Q40769909 | Approaches to the genetics of affective disorders |
| Q41851240 | Assessing the effect of multiple linkage tests in complex diseases. |
| Q52038666 | Behavioural disorders: lessons in linkage. |
| Q41479712 | Bipolar disorder: from families to genes |
| Q42904898 | Blue genes |
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| Q37802850 | Complexity and accountability: The witches’ brew of psychiatric genetics |
| Q42656223 | Confirmation of the relationship of HLA (chromosome 6) genes to depression and manic depression. II. The Ontario follow-up and analysis of 117 kindreds |
| Q37218496 | Current perspectives on the genetics of unipolar depression |
| Q35197573 | Detection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseases |
| Q44137047 | Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4. |
| Q34626051 | Endophenotypes in bipolar disorder |
| Q35197797 | Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36. |
| Q52064668 | Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders. |
| Q35245926 | Feature article: Recombinant DNA technology, genetic tests, and public policy |
| Q60923137 | From the neo-Kraepelinian framework to the new mechanical philosophy of psychiatry: regaining common sense |
| Q37906324 | Genetic factors in child psychiatric disorders--I. A review of research strategies |
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| Q41635355 | Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree |
| Q52391664 | Genetic linkage analysis of manic depression in Iceland. |
| Q37917304 | Genetic linkage and complex diseases, with special reference to psychiatric disorders |
| Q33408823 | Genomic landscape of a three-generation pedigree segregating affective disorder |
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| Q68289500 | H-ras-1 polymorphism in leukemia |
| Q41225785 | Inherited mental disorders |
| Q67783688 | Linkage Analysis of Affective Disorder Using DNA Markers on Chromosomes 11 and X |
| Q33681873 | Linkage analysis of manic depression in an Irish family using H-ras 1 and INS DNA markers |
| Q60627366 | Linkage findings in bipolar disorder |
| Q68426782 | Linkage of c-Harvey-ras-1 and INS DNA markers to unipolar depression and alcoholism is ruled out in 18 families |
| Q57016508 | Linkage of mood disorders with D2, D3 and TH genes: a multicenter study |
| Q57403467 | Linkage studies in bipolar affective disorder with markers on chromosome 21 |
| Q39582283 | Molecular genetics and heterogeneity in manic depression |
| Q34072352 | Molecular genetics of common diseases |
| Q35236130 | Molecular linkage studies of bipolar disorder |
| Q52067248 | New linkage findings in affective disorders. |
| Q68309203 | No Evidence for a Susceptibility Locus Predisposing to Manic Depression in the Region of the Dopamine (D2) Receptor Gene |
| Q69899822 | Polymorphic DNA marker on X chromosome and manic depression |
| Q39470852 | Polymorphic DNA markers and mental disease |
| Q28214642 | Post-genomic era and gene discovery for psychiatric diseases: there is a new art of the trade? The example of the HUMTH01 microsatellite in the Tyrosine Hydroxylase gene |
| Q52071948 | Power of the affected-sib-pair method for heterogeneous disorders. |
| Q34511287 | Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish |
| Q36382197 | Relevance of Early Age-of-Onset in Genetic Studies of Bipolar Affective Disorder |
| Q44385134 | Sampling strategies for linkage studies. |
| Q33991084 | Schizophrenia: genetic tools for unraveling the nature of a complex disorder |
| Q35436486 | Should be biologic marker be sensitive and specific? |
| Q35197804 | Simulation of Mendelism revisited: the recessive gene for attending medical school. |
| Q35868361 | Specificity of effect in psychiatric research |
| Q28585685 | Targeted Disruption of the Tyrosine Hydroxylase Locus Results in Severe Catecholamine Depletion and Perinatal Lethality in Mice |
| Q37113993 | The expression of folate sensitive fragile sites in patients with bipolar disorder. |
| Q42624472 | The genetics of Alzheimer disease--a teasing problem |
| Q40729004 | The genetics of bipolar disorder. |
| Q52056032 | The impact of phenotypic variation on genetic analysis: application to X-linkage in manic-depressive illness. |
| Q39468306 | The neurobiology of aging: does it predispose to depression? |
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