A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci (Q34145757)

31 July 2017

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci (English)

1 reference

31 July 2017

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1 reference

Hovatta I

1

1 reference

31 July 2017

Varilo T

2

1 reference

31 July 2017

Suvisaari J

3

1 reference

31 July 2017

Terwilliger JD

4

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31 July 2017

Ollikainen V

5

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31 July 2017

Arajärvi R

6

1 reference

31 July 2017

Juvonen H

7

1 reference

31 July 2017

Kokko-Sahin ML

8

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31 July 2017

Väisänen L

9

1 reference

31 July 2017

Mannila H

10

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31 July 2017

Lönnqvist J

11

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31 July 2017

Peltonen L

12

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31 July 2017

language of work or name

English

0 references

publication date

1 October 1999

1 reference

American Journal of Human Genetics

31 July 2017

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31 July 2017

65

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31 July 2017

4

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31 July 2017

1114-1124

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Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A linkage study of schizophrenia to markers within Xp11 near the MAOB gene.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Screening the monoamine oxidase B gene in 100 male patients with schizophrenia: a cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Is there a paradigm shift in genetics? Lessons from the study of human diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A comprehensive genetic map of the human genome based on 5,264 microsatellites

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Easy calculations of lod scores and genetic risks on small computers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Linkage of early-onset familial breast cancer to chromosome 17q21

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A general method for isolation of high molecular weight DNA from eukaryotes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Probability of founder effect in a tribal population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Schizophrenia in a North Swedish geographical isolate, 1900-1977. Epidemiology, genetics and biochemistry

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Accuracy of register-based schizophrenia diagnoses in a genetic study.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

A comparison of clinical and research DSM-III-R diagnoses of schizophrenia in a Finnish national birth cohort. Clinical and research diagnoses of schizophrenia.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288245

Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22

28 October 2018

1 reference

12 December 2020

Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion

1 reference

12 December 2020

Genome scan of schizophrenia

1 reference

12 December 2020

Founder effect: assessment of variation in genetic contributions among founders

1 reference

12 December 2020

An international two–stage genome–wide search for schizophrenia susceptibility genes

1 reference

12 December 2020

Linkage probability and its approximate confidence interval under possible heterogeneity

1 reference

12 December 2020

The Finnish adoptive family study of schizophrenia

1 reference

12 December 2020

Search for linkage to schizophrenia on the X and Y chromosomes

1 reference

12 December 2020

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1

1 reference

12 December 2020

Genomic scan for genes predisposing to schizophrenia

1 reference

12 December 2020

Schizophrenia in the genetic isolate of Finland

1 reference

12 December 2020

Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms

1 reference

12 December 2020

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

1 reference

12 December 2020

Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred

1 reference

12 December 2020

Identifiers

DOI

10.1086/302567

1 reference

release_d7oua5d73zc3rlg5jxalb6o6fu

31 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/d7oua5d73zc3rlg5jxalb6o6fu

24 November 2022

mapped directly with Wikidata item

PMCID

1288245

1 reference

31 July 2017

1 reference