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Blocking the EP3 receptor for PGE2 with DG-041 decreases thrombosis without impairing haemostatic competence. [electronic resource] by
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Relatedness disequilibrium regression estimates heritability without environmental bias. [electronic resource] by
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PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden. [electronic resource] by
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A direct characterization of human mutation based on microsatellites. [electronic resource] by
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- Li, Heng
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Linkage of essential hypertension to chromosome 18q. [electronic resource] by
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- Frigge, Michael L
- Kong, Augustine
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Localization of a gene for migraine without aura to chromosome 4q21. [electronic resource] by
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- Frigge, Michael L
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American journal of human genetics vol. 73
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GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs. [electronic resource] by
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Comparing migraine with and without aura to healthy controls using RNA sequencing. [electronic resource] by
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Sequences from first settlers reveal rapid evolution in Icelandic mtDNA pool. [electronic resource] by
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- Baker, Adam
- Bertranpetit, Jaume
- Arnadóttir, Lilja
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Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome. [electronic resource] by
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Genetic approaches to assessing evidence for a T helper type 1 cytokine defect in adult asthma. [electronic resource] by
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- Gislason, Thorarinn
- Gulcher, Jeffrey
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In:
American journal of respiratory and critical care medicine vol. 169
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GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture. [electronic resource] by
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- Valdimarsson, Ragnar Þór
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- Stefánsson, Sigmar K
- Másson, Gísli
- Magnússon, Gísli
- Pálmason, Vilmundur
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In:
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Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family. [electronic resource] by
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- Gulcher, Jeffrey R
- Bjornsson, Johannes
- Kong, Augustine
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A susceptibility gene for late-onset idiopathic Parkinson's disease. [electronic resource] by
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- Frigge, Michael L
- Kong, Augustine
- Gulcher, Jeffrey R
- Stefánsson, Kári
- Sveinbjörnsdóttir, Sigurlaug
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In:
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76.
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Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome. [electronic resource] by
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- Olafsdottir, Berglind Ran
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- Kong, Augustine
- Frigge, Michael L
- Jonsdottir, Guethrun M
- Hakonarson, Hakon
- Gulcher, Jeffrey
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In:
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77.
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Weighting sequence variants based on their annotation increases power of whole-genome association studies. [electronic resource] by
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- Zink, Florian
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- Oddson, Asmundur
- Másson, Gísli
- Holm, Hilma
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Sulem, Patrick
- Gudbjartsson, Daniel F
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In:
Nature genetics vol. 48
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A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas. [electronic resource] by
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- Einarsson, Gudmundur V
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- Kristjánsson, Kristleifur
- Hardarson, Sverrir
- Magnússon, Kjartan
- Gulcher, Jeffrey
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In:
International journal of cancer vol. 100
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A genome wide linkage disequilibrium screen in Parkinson's disease. [electronic resource] by
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- Hicks, Andrew
- Sawcer, Stephen
- Jonasdottir, Aslaug
- Setakis, Efrosini
- Maranian, Melanie
- Yeo, Taiwai
- Lewis, Simon
- Brayne, Carol
- Stefansson, Kari
- Compston, Alastair
- Gulcher, Jeff
- Barker, Roger A
Producer: 20060109
In:
Journal of neurology vol. 252
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80.
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Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes. [electronic resource] by
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- Viñuela, Ana
- Buil, Alfonso
- Halldorsson, Gisli H
- Thorleifsson, Gudmar
- Helgason, Hannes
- Thorsteinsdottir, Unnur
- Stefansson, Kari
- Dermitzakis, Emmanouil T
- Spector, Tim D
- Small, Kerrin S
Producer: 20170502
In:
American journal of human genetics vol. 99
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