(Q24632864)

26

0 references

Kári Stefánsson

27

0 references

Augustine Kong

25

0 references

Solveig Gretarsdottir

1

0 references

Elisabet Einarsdottir

5

object named as

Elisabet Einarsdottir

0 references

Jeffrey Gulcher

28

object named as

Jeffrey R Gulcher

0 references

author name string

Sigurlaug Sveinbjörnsdottir

2

0 references

Hjörtur H Jonsson

3

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Finnbogi Jakobsson

4

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Uggi Agnarsson

6

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Dana Shkolny

7

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Gisli Einarsson

8

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Herdis M Gudjonsdottir

9

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Einar M Valdimarsson

10

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Olafur B Einarsson

11

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Gudmundur Thorgeirsson

12

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Radinka Hadzic

13

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Sif Jonsdottir

14

0 references

Sigridur Th Reynisdottir

15

0 references

Sigrun M Bjarnadottir

16

0 references

Thorunn Gudmundsdottir

17

0 references

Gudrun J Gudlaugsdottir

18

0 references

Ramanjit Gill

19

0 references

Klaus Lindpaintner

20

0 references

Jesus Sainz

9

0 references

Helgi H Hannesson

22

0 references

Gunnar Th Sigurdsson

23

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Michael L Frigge

American Journal of Human Genetics

24

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language of work or name

English

0 references

publication date

March 2002

0 references

published in

0 references

volume

70

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page(s)

593-603

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issue

3

0 references

cites work

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Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21

7 April 2017

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Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

7 April 2017

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Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

7 April 2017

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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

7 April 2017

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

7 April 2017

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Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

7 April 2017

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7 April 2017

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Mutation in cystatin C gene causes hereditary brain haemorrhage

7 April 2017

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7 April 2017

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7 April 2017

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Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

7 April 2017

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Protection of privacy by third-party encryption in genetic research in Iceland

27 September 2017

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Using quality measures to facilitate allele calling in high-throughput genotyping

27 September 2017

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Allele-sharing models: LOD scores and accurate linkage tests

27 September 2017

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Risk factors for stroke in Copenhagen, Denmark. I. Basic demographic and social factors

27 September 2017

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Family history of myocardial infarction as an independent risk factor for coronary heart disease

27 September 2017

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The affected-pedigree-member method of linkage analysis

27 September 2017

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Linkage strategies for genetically complex traits. II. The power of affected relative pairs

27 September 2017

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27 September 2017

Epidemiology of stroke

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27 September 2017

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Crossover counts and likelihood in multipoint linkage analysis

27 September 2017

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Parental history of cardiovascular disease and risk of stroke. A prospective follow-up of 14371 middle-aged men and women in Finland.

27 September 2017

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Parental history is an independent risk factor for coronary artery disease: the Framingham Study

30 May 2018

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Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

30 May 2018

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The Harvard Cooperative Stroke Registry: A prospective registry

30 May 2018

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Comparison of human genetic and sequence-based physical maps

30 May 2018

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28 November 2018

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A class of tests for linkage using affected pedigree members

28 November 2018

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The information contained in multiple sibling pairs

28 November 2018

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12 December 2020

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12 December 2020

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12 December 2020

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Bias in multipoint linkage analysis arising from map misspecification

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12 December 2020

The importance of family history in cerebrovascular disease

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12 December 2020

Family history as an independent risk factor for coronary artery disease

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Identifiers

DOI

10.1086/339252

1 reference

3120058

3120058

1 reference

1 reference

1 reference