Chromosome 1 loci in Finnish schizophrenia families

Human Molecular Genetics

Volumn 10, Issue 15, 2001, Pages 1611-1617

  Ekelund, Jesper ^a   Hovatta, Iiris ^a   Parker, Alex ^b   Paunio, Tiina ^a   Varilo, Teppo ^a   Martin, Rory ^b   Suhonen, Johanna ^a   Ellonen, Pekka ^a   Chan, Gayun ^b   Sinsheimer, Janet S ^c,d   Sobel, Eric ^c   Juvonen, Hannu ^a   Arajärvi, Ritva ^a   Partonen, Timo ^a   Suvisaari, Jaana ^a   Lönnqvist, Jouko ^a   Meyer, Joanne ^b   Peltonen, Leena ^a,c  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b MILLENNIUM PHARMACEUTICALS INC   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISRUPTER IN SCHIZOPHRENIA PROTEIN; GENE PRODUCT; MICROSATELLITE DNA; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CENTROMERE; CHROMOSOME 1Q; CONTROLLED STUDY; FEMALE; FINLAND; GAMETE; GENE ISOLATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MARKER GENE; PRIORITY JOURNAL; PSYCHIATRIC DIAGNOSIS; SCHIZOPHRENIA;

EID: 0035878561     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.15.1611     Document Type: Article

References (33)

1. The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study
2. A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
3. Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
4. A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2
5. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
6. 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 20q12.1-11.23
7. Association within a family of a balanced autosomal translocation with major mental illness
8. Disease gene mapping in isolated human populations: The example of Finland
9. The Finnish population structure. A genetic and genealogical study
10. Hereditary diseases in Finland; rare flora in rare soul
11. Molecular genetics of the Finnish disease heritage
12. A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2
13. The renin-angiotensin-system in essential hypertension: Evidence for involvement of the angiotensin receptor type-1 gene in Finnish patients
14. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
15. Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: Evidence for a locus on 2q
16. Disruption of two novel genes by a translocation co-segregating with schizophrenia
17. Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set
18. Replication of linkage studies of complex traits: An examination of variation in location estimates
19. Schizophrenia in the genetic isolate of Finland
20. Concordance for sex and the pseudoautosomal gene hypothesis revisited: No evidence of increased sex concordance in a nationwide Finnish sample of siblings with paternally derived schizophrenia
21. A general method for isolation of high molecular weight DNA from eukaryotes
22. A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system
23. On the diagnosis of schizophrenic psychoses in clinical practice
24. A comparison of clinical and research DSM-III-R diagnoses of schizophrenia in a Finnish national birth cohort. Clinical and research diagnoses of schizophrenia
25. Accuracy of register-based schizophrenia diagnoses in a genetic study
26. The Roscommon Family Study. IV. Affective illness, anxiety disorders, and alcoholism in relatives
27. Linkage analysis in nuclear families. 2: Relationship between affected sib-pair tests and lod score analysis
28. Comparison of nonparametric statistics for detection of linkage in nuclear families: Single-marker evaluation
29. Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis
30. Linkage analysis, model-based
31. Gamete-competition models
32. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics