(Q28754746)

8

0 references

Samuli Ripatti

11

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Aarno Palotie

15

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Leena Peltonen-Palotie

16

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Shaun Purcell

12

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Tiina Paunio

5

Tiina Paunio

0 references

Teppo Varilo

Teppo Varilo

3

0 references

Andrew Collins

Andrew Collins

13

0 references

Mark Joseph Daly

14

Mark J Daly

0 references

Nancy Pedersen

6

Nancy L Pedersen

0 references

author name string

Eveliina Jakkula

1

0 references

Karola Rehnström

2

0 references

Olli P H Pietiläinen

4

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Ulf deFaire

7

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Juha Saharinen

9

0 references

Nelson Freimer

American Journal of Human Genetics

10

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language of work or name

English

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publication date

December 2008

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published in

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volume

83

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issue

6

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page(s)

787-94

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cites work

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

1 reference

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Correlation between genetic and geographic structure in Europe

16 March 2017

1 reference

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Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle

16 March 2017

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

16 March 2017

1 reference

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PLINK: a tool set for whole-genome association and population-based linkage analyses

16 March 2017

1 reference

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Population structure and eigenanalysis

16 March 2017

1 reference

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Regional differences among the Finns: a Y-chromosomal perspective

16 March 2017

1 reference

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Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

16 March 2017

1 reference

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Worldwide human relationships inferred from genome-wide patterns of variation

16 March 2017

1 reference

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

1 reference

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Genomic control for association studies

7 April 2017

1 reference

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Genotype, haplotype and copy-number variation in worldwide human populations

7 April 2017

1 reference

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Analysis and application of European genetic substructure using 300 K SNP information

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668058

Discerning the ancestry of European Americans in genetic association studies

3 June 2018

1 reference

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Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

3 June 2018

1 reference

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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

3 June 2018

1 reference

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Quantification of homozygosity in consanguineous individuals with autosomal recessive disease

3 June 2018

1 reference

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The Finnish Disease Heritage III: the individual diseases

3 June 2018

1 reference

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Finnish Disease Heritage II: population prehistory and genetic roots of Finns

3 June 2018

1 reference

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The Swedish Twin Registry in the third millennium

3 June 2018

1 reference

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The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis

3 June 2018

1 reference

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Use of population isolates for mapping complex traits

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668058

Molecular genetics of the Finnish disease heritage.

3 June 2018

1 reference

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The longitudinal study of the northern Finland birth cohort of 1966.

3 June 2018

1 reference

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3 June 2018

Inbreeding in Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668058

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668058

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668058

Increasing prevalence of multiple sclerosis in Finland

27 November 2018

1 reference

12 December 2020

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

1 reference

12 December 2020

Dissecting a population genome for targeted screening of disease mutations

1 reference

12 December 2020

Schizophrenia in the genetic isolate of Finland

1 reference

12 December 2020

Linkage disequilibrium in finite populations

1 reference

12 December 2020

10.1016/J.AJHG.2008.11.005

Identifiers

DOI

1 reference

release_ewhp7kqz7fh2po3qkanjjwzybe

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ewhp7kqz7fh2po3qkanjjwzybe

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

19061986

1 reference