(Q34390287)

1 August 2017

Replication of linkage studies of complex traits: an examination of variation in location estimates (English)

1 reference

1 August 2017

1 reference

5

Kendler KS

1 reference

1 August 2017

3

Neale MC

1 reference

1 August 2017

4

Eaves LJ

1 reference

1 August 2017

Roberts SB

1

1 reference

PubMed ID

10441592

1 August 2017

MacLean CJ

series ordinal

2

1 reference

PubMed ID

10441592

1 August 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

65

1 reference

1 August 2017

876-884

1 reference

1 August 2017

3

1 reference

Further evidence for the increased power of LOD scores compared with nonparametric methods

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Genomewide scan of multiple sclerosis in Finnish multiplex families

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Non-parametric analysis of chromosome 6p24-22 marker data and schizophrenia in southern African Bantu-speaking families.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Evidence for two psoriasis susceptibility loci (HLA and 17q) and two novel candidate regions (16q and 20p) by genome-wide scan

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Detecting marker-QTL linkage and estimating QTL gene effect and map location using a saturated genetic map.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Eye tracking dysfunction and schizophrenia: a critical perspective

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Complete multipoint sib-pair analysis of qualitative and quantitative traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Linkage analysis under "random" and "genetic" reduced penetrance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Cutting a Gordian knot in the linkage analysis of complex human traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Adequacy of single-locus approximations for linkage analyses of oligogenic traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

Surgical emphysema as a complication of anaesthesia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377992

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

27 October 2018

1 reference

12 December 2020

Positional cloning moves from perditional to traditional

1 reference

12 December 2020

A simple method to calculate resolving power and confidence interval of QTL map location

1 reference

12 December 2020

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis

1 reference

12 December 2020

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

12 December 2020

6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP

1 reference

12 December 2020

Evidence that a locus for familial psoriasis maps to chromosome 4q

1 reference

12 December 2020

A search for type 1 diabetes susceptibility genes in families from the United Kingdom

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1086/302528

1 reference

1 August 2017

1 reference

1 August 2017

1 reference

PubMed ID

10441592