The genome-wide patterns of variation expose significant substructure in a founder population (Q28754746)

8

0 references

Samuli Ripatti

11

0 references

Aarno Palotie

15

0 references

Leena Peltonen-Palotie

16

0 references

Shaun Purcell

12

0 references

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

0 references

Ulf deFaire

7

0 references

Juha Saharinen

9

0 references

Nelson Freimer

American Journal of Human Genetics

10

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language of work or name

English

0 references

publication date

December 2008

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language of work

0 references

volume

83

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issue

6

0 references

page(s)

787-94

0 references

cites work

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Correlation between genetic and geographic structure in Europe

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

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

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Worldwide human relationships inferred from genome-wide patterns of variation

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

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Genomic control for association studies

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

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

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Discerning the ancestry of European Americans in genetic association studies

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Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

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

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

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The Swedish Twin Registry in the third millennium

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

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Use of population isolates for mapping complex traits

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Inbreeding in Finland

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

27 November 2018

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Increasing prevalence of multiple sclerosis in Finland

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12 December 2020

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

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Dissecting a population genome for targeted screening of disease mutations

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Schizophrenia in the genetic isolate of Finland

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Linkage disequilibrium in finite populations

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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