A high-density screen for linkage in multiple sclerosis (Q34021149)

30 July 2017

title

A high-density screen for linkage in multiple sclerosis (English)

1 reference

Margaret A. Pericak-Vance

30 July 2017

0 references

17

Margaret A Pericak-Vance

0 references

Eric Lander

10

Eric S Lander

1 reference

30 July 2017

25

Kjell-Morten Myhr

1 reference

30 July 2017

5

Alastair Compston

1 reference

30 July 2017

24

Anne Spurkland

1 reference

30 July 2017

7

Mark J Daly

1 reference

30 July 2017

12

David A Hafler

1 reference

30 July 2017

1

Stephen Sawcer

1 reference

30 July 2017

35

Jonathan L Haines

1 reference

30 July 2017

8

Philip L De Jager

1 reference

30 July 2017

31

Lisa F Barcellos

1 reference

30 July 2017

33

Jorge R Oksenberg

1 reference

30 July 2017

32

Stephen L Hauser

1 reference

30 July 2017

23

Hanne F Harbo

1 reference

30 July 2017

11

John D Rioux

1 reference

International Multiple Sclerosis Genetics Consortium

30 July 2017

36

International Multiple Sclerosis Genetics Consortium

1 reference

30 July 2017

21

Annette Oturai

1 reference

30 July 2017

13

Adrian Ivinson

1 reference

30 July 2017

Graeme Andrew Stewart

29

Graeme Stewart

1 reference

30 July 2017

16

Silke Schmidt

1 reference

30 July 2017

4

Tai Wai Yeo

1 reference

30 July 2017

9

Emily Walsh

1 reference

30 July 2017

14

Jacqueline Rimmler

1 reference

30 July 2017

34

Shannon J Kenealy

1 reference

30 July 2017

3

Mel Maranian

1 reference

30 July 2017

22

Lars P Ryder

1 reference

30 July 2017

Maria Ban

2

1 reference

30 July 2017

Andrew Kirby

6

1 reference

30 July 2017

Simon G Gregory

15

1 reference

30 July 2017

Eva Akesson

18

1 reference

30 July 2017

Jan Hillert

19

1 reference

30 July 2017

Pameli Datta

20

1 reference

30 July 2017

Mikko Laaksonen

26

1 reference

30 July 2017

David Booth

27

1 reference

30 July 2017

Robert Heard

28

1 reference

30 July 2017

Robin Lincoln

30

1 reference

30 July 2017

language of work or name

English

0 references

publication date

29 July 2005

1 reference

American Journal of Human Genetics

30 July 2017

published in

1 reference

30 July 2017

volume

77

1 reference

30 July 2017

issue

3

1 reference

30 July 2017

page(s)

454-467

1 reference

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A note on exact tests of Hardy-Weinberg equilibrium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Complement factor H variant increases the risk of age-related macular degeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Genome-wide association studies: theoretical and practical concerns

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Timing of birth and risk of multiple sclerosis: population based 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=1226210

A second-generation genomic screen for multiple sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Haploview: analysis and visualization of LD and haplotype 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=1226210

Twin concordance and sibling recurrence rates in multiple sclerosis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A bias-ed assessment of the use of SNPs in human complex traits

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A high-resolution recombination map of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Comprehensive human genome amplification using multiple displacement amplification

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Disease steps in multiple sclerosis: a longitudinal study comparing disease steps and EDSS to evaluate disease progression

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

PedCheck: a program for identification of genotype incompatibilities in 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=1226210

Genomewide scan of multiple sclerosis in Finnish multiplex families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Allele-sharing models: LOD scores and accurate linkage tests

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

The epidemiology of multiple sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Risks of multiple sclerosis in relatives of patients in Flanders, Belgium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

The future of genetic studies of complex 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=1226210

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Parametric and nonparametric linkage analysis: a unified multipoint approach

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

The British Isles survey of multiple sclerosis in twins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Molecular and statistical approaches to the detection and correction of errors in genotype databases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Complete multipoint sib-pair analysis of qualitative and quantitative traits

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

HL-A antigens and multiple sclerosis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Multiple sclerosis: updated risks for relatives

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Linkage strategies for genetically complex traits. I. Multilocus models

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

HLA class II-associated genetic susceptibility in multiple sclerosis: a critical 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=1226210

B-lymphocyte alloantigens associated with multiple sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Multiple sclerosis among immigrants in Greater London

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A meta-analysis of whole genome linkage screens in multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A whole genome screen for linkage in Turkish multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Pedigree disequilibrium tests for multilocus haplotypes.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A genome screen for multiple sclerosis in Italian families.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Offspring recurrence rates and clinical characteristics of conjugal multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

HLA-DR, -DQA1 and -DQB1 associations in Australian multiple sclerosis patients

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Age-adjusted recurrence risks for relatives of patients with multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A class of tests for linkage using affected pedigree members

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

An Icelandic example of the impact of population structure on association studies

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

The impact of genotyping error on family-based analysis of quantitative traits

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

A full genome search in multiple sclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226210

Genetic basis for clinical expression in multiple sclerosis

29 October 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Parent-of-origin effect in multiple sclerosis: observations in half-siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Ordered subset analysis in genetic linkage mapping of complex traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

B-cell alloantigen Ag 7a in multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Diagnostic criteria for multiple sclerosis research involving multiply affected families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

GRR: graphical representation of relationship errors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

A genome screen for multiple sclerosis in Sardinian multiplex families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16080120

12 December 2020

Identifiers

DOI

10.1086/444547

1 reference

30 July 2017

1 reference

30 July 2017

1 reference