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A compendium of inborn errors of metabolism mapped onto the human metabolic network

Molecular bioSystems, 2012-01, Vol.8 (10), p.2545-2558

2012

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Microgels and apparatus for PAGE of nucleic acids in one or two dimensions

BioTechniques, 2018-07, Vol.65 (1), p.15-19

2018

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Large-scale whole-genome sequencing of the Icelandic population

Nature genetics, 2015-05, Vol.47 (5), p.435

2015

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Ethical issues in precision medicine

Annals of clinical biochemistry, 2019-11, Vol.56 (6), p.628-629

2019

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Molecular genetics of inherited retinal degenerations in Icelandic patients

Clinical genetics, 2021-08, Vol.100 (2), p.156-167

2021

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Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

European journal of human genetics : EJHG, 2020-12, Vol.28 (12), p.1656-1661

2020

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Membrane transporters in a human genome-scale metabolic knowledgebase and their implications for disease

Frontiers in physiology, 2014, Vol.5, p.91-91

2014

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Northern lights assay: a versatile method for comprehensive detection of DNA damage

Nucleic acids research, 2018-11, Vol.46 (20), p.e118

2018

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Genome-scale network analysis of imprinted human metabolic genes

Epigenetics, 2009-01, Vol.4 (1), p.43-46

2009

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Encapsidation Determinants Located Downstream of the Major Splice Donor in the Maedi-Visna Virus Leader Region

Journal of Virology, 2006-12, Vol.80 (23), p.11743-11755

2006

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HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination

Genome Research, 2009-04, Vol.19 (4), p.581-589

2009

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Iceland—Genetic Counseling Services

Journal of genetic counseling, 2013-12, Vol.22 (6), p.907-910

2013

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Variability of ethics education in laboratory medicine training programs: Results of an international survey

Clinica chimica acta, 2015-03, Vol.442, p.115-118

2015

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Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information

Journal of community genetics, 2016-07, Vol.7 (3), p.229-235

2016

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Importance of the efficiency of double-stranded DNA formation in cDNA synthesis for the imprecision of microarray expression analysis

Clinical chemistry (Baltimore, Md.), 2013-04, Vol.59 (4), p.667-674

2013

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Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genome

Gene, 2012-01, Vol.492 (1), p.104-109

2012

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The use of genealogy databases for risk assessment in genetic health service: a systematic review

Journal of community genetics, 2013-01, Vol.4 (1), p.1-7

2013

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A rapid real-time qRT-PCR assay for ovine β-actin mRNA

Journal of biotechnology, 2005-05, Vol.117 (2), p.173-182

2005

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Two-dimensional strandness-dependent electrophoresis

Nature protocols, 2007-01, Vol.1 (6), p.3011-3018

2007

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A community-driven global reconstruction of human metabolism

Nature biotechnology, 2013-05, Vol.31 (5), p.419

2013

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The distribution of a germline methylation marker suggests a regional mechanism of LINE-1 silencing by the piRNA-PIWI system

BMC genetics, 2012-04, Vol.13, p.31

2012

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Two-dimensional strandness-dependent electrophoresis: A method to characterize single-stranded DNA, double-stranded DNA, and RNA–DNA hybrids in complex samples

Analytical biochemistry, 2006-03, Vol.350 (1), p.120-127

2006

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Positive association between DNA strand breaks in peripheral blood mononuclear cells and polyunsaturated fatty acids in red blood cells from women

Nutrition and cancer, 2007-01, Vol.59 (1), p.21-28

2007

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Quantitative assays for maedi-visna virus genetic sequences and mRNA’s based on RT-PCR with real-time FRET measurements

Virology (New York, N.Y.), 2003-03, Vol.307 (1), p.135-142

2003

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A compendium of inborn errors of metabolism mapped onto the human metabolic network

Microgels and apparatus for PAGE of nucleic acids in one or two dimensions

Large-scale whole-genome sequencing of the Icelandic population

Ethical issues in precision medicine

Molecular genetics of inherited retinal degenerations in Icelandic patients

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

Membrane transporters in a human genome-scale metabolic knowledgebase and their implications for disease

Northern lights assay: a versatile method for comprehensive detection of DNA damage

Genome-scale network analysis of imprinted human metabolic genes

Encapsidation Determinants Located Downstream of the Major Splice Donor in the Maedi-Visna Virus Leader Region

HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination

Iceland—Genetic Counseling Services

Variability of ethics education in laboratory medicine training programs: Results of an international survey

Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information

Importance of the efficiency of double-stranded DNA formation in cDNA synthesis for the imprecision of microarray expression analysis

Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genome

The use of genealogy databases for risk assessment in genetic health service: a systematic review

A rapid real-time qRT-PCR assay for ovine β-actin mRNA

Two-dimensional strandness-dependent electrophoresis

A community-driven global reconstruction of human metabolism

The distribution of a germline methylation marker suggests a regional mechanism of LINE-1 silencing by the piRNA-PIWI system

Two-dimensional strandness-dependent electrophoresis: A method to characterize single-stranded DNA, double-stranded DNA, and RNA–DNA hybrids in complex samples

Positive association between DNA strand breaks in peripheral blood mononuclear cells and polyunsaturated fatty acids in red blood cells from women

Quantitative assays for maedi-visna virus genetic sequences and mRNA’s based on RT-PCR with real-time FRET measurements

Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene

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