A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q34145757

about

Recent advances in the genetics of schizophrenia Genomewide scans of complex human diseases: true linkage is hard to find Identification of a new candidate locus for uric acid nephrolithiasis.Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.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 11q23.3-24 and 20q12.1-11.23 A novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: altered l-serine level associated with disruption of PSAT1 gene expression DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms Genome scans and microarrays: converging on genes for schizophrenia?The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22 Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families The DISC locus in psychiatric illness A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42 GABA(A) receptors and their associated proteins: implications in the etiology and treatment of schizophrenia and related disorders.Data mining applied to linkage disequilibrium mapping Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness Association of RGS2 and RGS5 variants with schizophrenia symptom severity.Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.Two complex genotypes relevant to the kynurenine pathway and melanotropin function show association with schizophrenia and bipolar disorder Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolate.Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1 Linkage and associated studies of schizophrenia.A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.Use of closely related affected individuals for the genetic study of complex diseases in founder populations.The epidemiology of the genetic liability for schizophrenia.Genetics of schizophrenia and the new millennium: progress and pitfalls.The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia.Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters.Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.Genetic insights into schizophrenia Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission.Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia.Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.Psychosis among "healthy" siblings of schizophrenia patients.Recent advances in the genetics of schizophrenia.Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.Manic-depression genes and the new millennium: poised for discovery.

P2860

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P2860

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

http://www.wikidata.org/entity/Q34145757

description

1999 nî lūn-bûn

@nan

1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

A genomewide screen for schizo ...... multiple susceptibility loci.

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A genomewide screen for schizo ...... multiple susceptibility loci.

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A genomewide screen for schizo ...... multiple susceptibility loci.

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type

label

A genomewide screen for schizo ...... multiple susceptibility loci.

@ast

A genomewide screen for schizo ...... multiple susceptibility loci.

@en

A genomewide screen for schizo ...... multiple susceptibility loci.

@nl

prefLabel

A genomewide screen for schizo ...... multiple susceptibility loci.

@ast

A genomewide screen for schizo ...... multiple susceptibility loci.

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A genomewide screen for schizo ...... multiple susceptibility loci.

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A genomewide screen for schizo ...... multiple susceptibility loci.

@en

P2093

Arajärvi R

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Hovatta I

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Juvonen H

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Kokko-Sahin ML

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Lönnqvist J

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Mannila H

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Ollikainen V

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Peltonen L

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Suvisaari J

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Terwilliger JD

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P2860

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

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

Strategies for multilocus linkage analysis in humans

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

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

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

Easy calculations of lod scores and genetic risks on small computers

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

Probability of founder effect in a tribal population.

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

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1114-1124

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10.1086/302567

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4

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10486331

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