Accès ouvert
2026
preprint
OpenAlex
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 …
us, dk, de, se, au, fi, no, gb, gr, il, it, ch, ca, hu, al, nl, kr, is, pl, es, ie, fr, ec, qa, pt, Afrique du Sud
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Accès ouvert
2026
preprint
OpenAlex
Adalheidur E. Larusdottir, Unnur D. Teitsdottir, Vinicius Tragante, Frosti Pálsson et autres
is, de, fi, ee, dk, no, gb, au, us
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2025
article
OpenAlex
Elise Koch, Tuuli Puusepp, Guðmundur Einarsson, Brittany L. Mitchell et autres
no, ee, is, au, se, gb, dk
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Accès ouvert
2025
article
OpenAlex
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 …
is, no
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2025
article
OpenAlex
Elise Koch, Alexey Shadrin, Kevin S. O’Connell, Maris Alver et autres
no, ee, is, de, gb, se, au, dk
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Accès ouvert
2025
article
OpenAlex
Elise Koch, Sophie E. Smart, Guðmundur Einarsson, Anders Kämpe et autres
no, gb, is, fi, se, ee, us, dk, de, it
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Accès ouvert
2025
preprint
OpenAlex
Elise Koch, Sophie E. Smart, Guðmundur Einarsson, Anders Kämpe et autres
While information from real-world data (RWD) can be utilized to identify factors able to aid treatment choice, guidelines for the use of RWD are lacking. The aim of this narrative review and expert opinion is to summarize and evaluate definitions of treatment …
Accès ouvert
2025
article
OpenAlex
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 …
is, fi, dk, us
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Accès ouvert
2024
preprint
OpenAlex
Elise Koch, Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell et autres
no, us, au, lk, ee, se, gb, is, de
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Accès ouvert
2024
article
OpenAlex
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 …
is
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Accès ouvert
2024
article
OpenAlex
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 …
is, dk
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Accès ouvert
2024
preprint
OpenAlex
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 …
no, ee, is, au, se, gb, ca
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