Profil bibliographique

Daniel Gudbjartsson

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

27Publications signalées

0Citations signalées

3Affiliations récentes

Institutions déclarées

deCODE Genetics (Iceland)University of Iceland Amgen (Germany)

Domaines associés

High Altitude and HypoxiaNeuroscience of respiration and sleepAutoimmune Neurological Disorders and Treatmentsinterferon and immune responsesThyroid Disorders and Treatments

Publications récentes

Accès ouvert 2026 articleOpenAlex

Sex-stratified polygenic scores for 47 inflammation and vascular stress biomarkers provide a resource for profiling chronic disease risk

Joseph Dowsett, Bertram Kjerulff, Jakob Hjorth von Stemann, Mette Skou Bentsen et autres

0 citationsScientific Reports

Accès ouvert 2026 articleOpenAlex

Combining genome-wide polygenic scores with registry data for colorectal cancer risk-based screening

Anne Krogh Nøhr, Marie Giehm Overby, Mads Munk Nielsen, Emil-August Torp et autres

0 citationsVBN Forskningsportal (Aalborg Universitet)

Accès ouvert 2026 preprintOpenAlex

Sequence variants affecting fetal globin expression pointing to potential drug targets

Magnus Magnusson, Gudjon Oskarsson, Sarnaver Mwende, Katla Kristjánsdóttir et autres

0 citationsResearch Square

Accès ouvert 2026 preprintOpenAlex

GWAS of amiodarone-induced thyroid dysfunction: Applications for genotype-guided risk stratification

Soren A. Rand, Johan Skov Bundgaard, Vinicius Tragante, Sölvi Rögnvaldsson et autres

0 citationsmedRxiv

Accès ouvert 2024 articleOpenAlex

SMIM1 absence is associated with reduced energy expenditure and excess weight

Luca Stefanucci, Camous Moslemi, Ana R. Tomé, Sam Virtue et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 7: Figure S4. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 5: Table S2. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 2: Table S1. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 6: Supplementary Information. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Ö. Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 9: Table S4. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Ö. Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 5: Table S2. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

Accès ouvert 2017 articleOpenAlex

Additional file 3: Figure S2. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Brynjar Jensson, Sif Hansdóttir, Gudny A. Arnadottir, Gerald Sulem et autres

0 citationsFigshare

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