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Profil bibliographique

Guðmundur Einarsson

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

104Publications signalées
6331Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Genetic Associations and EpidemiologyRenal cell carcinoma treatmentMultiple and Secondary Primary CancersBladder and Urothelial Cancer TreatmentsProstate Cancer Treatment and Research

Les publications récentes

Accès ouvert 2026 preprint OpenAlex

Genome-Wide Association Analysis of Tic Disorders Reveals 6 Independent Risk Loci and Highlights Tic-Associated Cell Types and Brain Circuitry

Dongmei Yu, Nora I. Strom, Zachary F. Gerring, Apostolia Topaloudi et autres

Abstract Tourette Syndrome and other tic disorders (TD) are common, highly heritable neurodevelopmental conditions with complex genetic architectures. We conducted a genome-wide association study of 13,247 TD cases and 536,217 European ancestry controls and identified six independent genome-wide significant loci, including a …

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1 citation medRxiv
Accès ouvert 2025 article OpenAlex

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication

Guðmundur Einarsson, Hannes K. Arnason, Rósa S. Gísladóttir, Gyða Björnsdóttir et autres

Zopiclone and zolpidem are widely prescribed hypnotic medications for insomnia, sharing similar efficacy but differing in side-effect profiles, particularly concerning taste disturbances. Identifying genetic predictors of intolerance to these medications could inform personalized treatment strategies. We conducted a genome-wide association study to …

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0 citations Biological Psychiatry Global Open Science
Accès ouvert 2025 article OpenAlex

Missense variants in FRS3 affect body mass index in populations of diverse ancestries

Andrea B. Jonsdottir, Garðar Sveinbjörnsson, Rósa B. Þórólfsdóttir, Max Tamlander et autres

Obesity is associated with adverse effects on health and quality of life. Improved understanding of its underlying pathophysiology is essential for developing counteractive measures. To search for sequence variants with large effects on BMI, we perform a multi-ancestry meta-analysis of 13 genome-wide …

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3 citations Nature Communications
Accès ouvert 2024 article OpenAlex

Sequence variants associated with BMI affect disease risk through BMI itself

Guðmundur Einarsson, Gudmar Thorleifsson, Valgerður Steinthórsdóttir, Florian Zink et autres

Mendelian Randomization studies indicate that BMI contributes to various diseases, but it's unclear if this is entirely mediated by BMI itself. This study examines whether disease risk from BMI-associated sequence variants is mediated through BMI or other mechanisms, using data from Iceland …

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6 citations Nature Communications
Accès ouvert 2024 article OpenAlex

A partial loss-of-function variant in STAT6 protects against type 2 asthma

Katla Kristjánsdóttir, Gudmundur L. Norddahl, Erna V. Ivarsdottir, Gísli H. Halldórsson et autres

Background Signal transducer and activator of transcription 6 (STAT6) is central to type 2 (T2) inflammation, and common noncoding variants at the STAT6 locus associate with various T2 inflammatory traits, including diseases, and its pathway is widely targeted in asthma treatment. Objective …

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5 citations Journal of Allergy and Clinical Immunology
Accès ouvert 2024 preprint OpenAlex

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

Elise Koch, Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell et autres

Antidepressants exhibit a considerable variation in efficacy, and increasing evidence suggests that individual genetics contribute to antidepressant treatment response. Here, we combined data on antidepressant non-response measured using rating scales for depressive symptoms, questionnaires of treatment effect, and data from electronic health …

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7 citations medRxiv

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