Showing
1 - 14
results of
14
for search '
"deCODE genetics"
'
Skip to content
Toggle navigation
0
items
(Full)
All Fields
Title
Author
Subject
Find
Advanced
Search History
Search by Map:
Arctic
Antarctic
Reset Filters
Topic:
Genome-Wide Association Study
AND
Polymorphism
AND
Single Nucleotide
Reset Filters
Show filters (3)
Topic:
Genome-Wide Association Study
AND
Polymorphism
AND
Single Nucleotide
Search Results - Open Polar - "deCODE genetics"
Search Results
Showing
1 - 14
results of
14
for search '
"deCODE genetics"
'
, query time: 0.33s
Refine Results
Sort
Relevance
Date Descending
Date Ascending
Author
Title
List
Grid
Visual
Select Page | with selected:
Email
Export
Print
Add to Book Bag
Variant in the sequence of the LINGO1 gene confers risk of essential tremor
Get access
Get access
Weighting sequence variants based on their annotation increases power of whole-g...
Get access
Get access
Common variants near CAV1 and CAV2 are associated with primary open-angle glauco...
Get access
Get access
Association of variants at UMOD with chronic kidney disease and kidney stones-ro...
Get access
Get access
Discovery of common variants associated with low TSH levels and thyroid cancer r...
Get access
Get access
Genome-wide association and replication studies identify four variants associate...
Get access
Get access
Sequence variants affecting eosinophil numbers associate with asthma and myocard...
Get access
Get access
A study based on whole-genome sequencing yields a rare variant at 8q24 associate...
Get access
Get access
European genome-wide association study identifies SLC14A1 as a new urinary bladd...
Get access
Get access
European genome-wide association study identifies SLC14A1 as a new urinary bladd...
Get access
Get access
Identification of sequence variants influencing immunoglobulin levels.
Get access
Get access
Large-scale whole-genome sequencing of the Icelandic population.
Get access
Get access
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-...
Get access
Get access
Identification of low-frequency and rare sequence variants associated with eleva...
Get access
Get access
Select Page | with selected:
Email
Export
Print
Add to Book Bag
Search Tools:
Get RSS Feed
Back
Narrow Search
Year of Publication
From:
To:
Document Type
Article in Journal/Newspaper
14
Author
Stefansson, Kari
11
Sulem, Patrick
11
Thorsteinsdottir, Unnur
11
Gudbjartsson, Daniel F
10
Kong, Augustine
10
Thorleifsson, Gudmar
9
Masson, Gisli
7
Rafnar, Thorunn
7
Sigurdsson, Asgeir
7
Gudjonsson, Sigurjon A
5
Holm, Hilma
5
Johannsdottir, Hrefna
5
Stacey, Simon N
5
Eyjolfsson, Gudmundur I
4
Gudmundsson, Julius
4
Kiemeney, Lambertus A
4
Stefansson, Hreinn
4
Walters, G Bragi
4
Bjornsdottir, Unnur S
3
Gulcher, Jeffrey R
3
Gylfason, Arnaldur
3
Helgadottir, Hafdis Th
3
Helgason, Agnar
3
Helgason, Hannes
3
Jonasson, Jon G
3
Jonsson, Eirikur
3
Kristjansson, Kristleifur
3
Magnusson, Olafur Th
3
Mayordomo, Jose I
3
Olafsson, Isleifur
3
see all ...
Topic
Genome-Wide Association Study
Humans
14
Polymorphism
Single Nucleotide
Genetic Predisposition to Disease
11
Iceland
11
Male
8
Human
7
Female
6
Risk Factors
6
80 and over
5
Aged
5
Chromosomes
5
DNA
5
Gene Frequency
5
Genetic Variation
5
Middle Aged
5
Case-Control Studies
4
European Continental Ancestry Group
4
Genome
4
Sequence Analysis
4
Adult
3
Genetic Loci
3
Genotype
3
Risk
3
Base Sequence
2
Disease Progression
2
Homeodomain Proteins
2
Membrane Transport Proteins
2
Molecular Sequence Annotation
2
see all ...
Content Provider
Hirsla - LandspĂtali University Hospital research archive
13
The Christie School of Oncology: Christie Research Publications Repository
1
Geographic location
Kidd
2
Indel’
1
Sigrid
1
Language
English
14
Open Polar Keyword
Iceland
14
Loading...