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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and isc...
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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and isc...
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Abstract 2921: Genome-wide Association Reveals Sequence Variants on 4q25 that Af...
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Fourteen sequence variants that associate with multiple sclerosis discovered by...
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Segmental Sharing Analysis of Multiple Sclerosis Patients and Controls From the...
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High Inbreeding in the Faroe Islands Does Not Appear to Constitute a Risk Factor...
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Genetic analysis of the isolated Faroe Islands reveals SORCS3 as a potential mul...
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6
Text
1
Author
Hillert, Jan
Thorleifsson, Gudmar
4
Thorsteinsdottir, Unnur
4
Binzer, Michael
3
Binzer, Stefanie
3
Gretarsdottir, Solveig
3
Gulcher, Jeffrey
3
Holm, Hilma
3
Imrell, Kerstin
3
Kong, Augustine
3
Stefansson, Kari
3
Stenager, Egon
3
Thorgeirsson, Gudmundur
3
Baum, Larry
2
Berger, Klaus
2
Bevan, Steve
2
Carter, Shannon
2
Darbar, Dawood
2
Dichgans, Martin
2
Gieger, Christian
2
Gschwendtner, Andreas
2
Gudbjartsson, Daniel
2
Hveem, Kristian
2
Kostulas, Konstantinos
2
Kucera, Gayle
2
Kuhlenbäumer, Gregor
2
Kyvik, Kirsten
2
Løchen, Maja-Lisa
2
Njølstad, Inger
2
Nyrnes, Audhild
2
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Multiple sclerosis
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Neurology (clinical)
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Article
1
Atrial Fibrillation
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Base Sequence
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Brain Ischemia
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Cardiology and Cardiovascular Medicine
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Chromosomes
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Erfðafræði
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Faroe Islands
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Genetic Predisposition to Disease
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Genome-wide association studies
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Homeodomain Proteins
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Inbreeding
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Linkage
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MS sjúkdómur
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Pair 16
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Physiology (medical)
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Rannsóknir
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Risk factors
1
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Ovid
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Hirsla - Landspítali University Hospital research archive
1
Opin vísindi (Iceland)
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Ovid (via Crossref)
1
PubMed Central (PMC)
1
University of Southern Denmark Research Portal
1
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Norway
3
Bergen
1
Smella
1
Language
English
7
Open Polar Keyword
Iceland
4
Faroe Islands
3
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