Association Between ECG Abnormalities and Fatal Cardiovascular Disease Among Patients With and Without Severe Mental Illness

Christoffer Polcwiartek , Brett D Atwater , Kristian Kragholm , Daniel J Friedman
Journal of the American Heart Association 10 ( 2) 1 -11

2021
Genome-wide association study of cardiac troponin I in the general population.

Nay Aung , Jonathon LeFaive , Wei Zhou , Sarah A Gagliano Taliun
Human Molecular Genetics

2021
Reply to the Editor--Regarding the Role of Advanced Interatrial Block Pattern as a Predictor of Atrial Fibrillation.

Jonas B Nielsen , Claus Graff , Jesper H Svendsen , Anders G Holst
Heart Rhythm 13 ( 3)

2016
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

Morten S Olesen , Bo H Bentzen , Jonas B Nielsen , Annette B Steffensen
BMC Medical Genetics 13 ( 1) 24 -24

67
2012
Cardiac symptoms before sudden cardiac death caused by coronary artery disease: a nationwide study among young Danish people

Reza Jabbari , Bjarke Risgaard , Anders G Holst , Jonas B Nielsen
Heart 99 ( 13) 938 -943

17
2013
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

Manuel A Ferreira , Judith M Vonk , Hansjörg Baurecht , Ingo Marenholz
Nature Genetics 49 ( 12) 1752 -1757

395
2017
High prevalence of genetic variants previously associated with LQT syndrome in new exome data

Lena Refsgaard , Anders G Holst , Golnaz Sadjadieh , Stig Haunsø
European Journal of Human Genetics 20 ( 8) 905 -908

112
2012
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.

Charlotte Andreasen , Jonas B Nielsen , Lena Refsgaard , Anders G Holst
European Journal of Human Genetics 21 ( 9) 918 -928

182
2013
Brugada syndrome risk loci seem protective against atrial fibrillation

Laura Andreasen , Jonas B Nielsen , Stine Darkner , Ingrid E Christophersen
European Journal of Human Genetics 22 ( 12) 1357 -1361

7
2014
Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

David Ray , Deborah A Lawlor , Martin K Rutter , Michael N Weedon
bioRxiv 454561

2
2018
Mitochondrial genome-wide association study of migraine - the HUNT Study.

Sigrid Børte , John-Anker Zwart , Anne Heidi Skogholt , Maiken Elvestad Gabrielsen
Cephalalgia 40 ( 6) 625 -634

3
2020
2020
New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome.

Ren-Qiang Yang , Javad Jabbari , Xiao-Shu Cheng , Reza Jabbari
BMC Genetics 15 ( 1) 74 -74

10
2014
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

George Hindy , Daniel J Tyrrell , Alexi Vasbinder , Changli Wei
The Journal of clinical investigation 132 ( 24)

2
2022
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Krishna G Aragam , Tao Jiang , Anuj Goel , Stavroula Kanoni
Nature Genetics 54 ( 12) 1803 -1815

34
2022
Multi-ancestry GWAS deciphers genetic architecture of abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Tanmoy Roychowdhury , Derek Klarin , Michael G Levin , Joshua M Spin
Medrxiv 2022 -05

2
2022
Implantable loop recorder detection of atrial fibrillation to prevent stroke (The LOOP Study): a randomised controlled trial

Jesper H Svendsen , Søren Z Diederichsen , Søren Højberg , Derk W Krieger
The Lancet 398 ( 10310) 1507 -1516

171
2021
Genome-wide association study of liver fat, iron, and extracellular fluid fraction in the UK Biobank

Colm O’Dushlaine , Mary Germino , Niek Verweij , Jonas B Nielsen
medRxiv 2021 -10

2
2021
Genetic diversity fuels gene discovery for tobacco and alcohol use

Gretchen RB Saunders , Xingyan Wang , Fang Chen , Seon-Kyeong Jang
Nature 612 ( 7941) 720 -724

148
2022