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Journal of the American Geriatrics Society|April 21, 2023
Pragmatic evaluation of events and benefits of lipid lowering in older adults (PREVENTABLE): Trial design and rationaleJacob Joseph, Nicholas M Pajewski, Rowena J Dolor, et al.
The New England Journal of Medicine|December 28, 2020
A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19, Jens D Lundgren, Birgit Grund, et al.
Nature Genetics|April 17, 2024
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosisJonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, et al.
European Heart Journal|March 4, 2022
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapseCarolina Roselli, Mengyao Yu, Victor Nauffal, et al.
Annals of Internal Medicine|December 20, 2021
Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels : A Randomized Controlled Trial, Jens D Lundgren, Birgit Grund, et al.
Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
The New England Journal of Medicine|May 17, 2021
Comparative Effectiveness of Aspirin Dosing in Cardiovascular DiseaseW Schuyler Jones, Hillary Mulder, Lisa M Wruck, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
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