M Benjamin Shoemaker
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Explore the profile of M Benjamin Shoemaker including associated specialties, affiliations and a list of published articles.
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101
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3360
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Recent Articles
1.
Choi S, Jurgens S, Xiao L, Hill M, Haggerty C, Sveinbjornsson G, et al.
Nat Genet
. 2025 Mar;
57(3):548-562.
PMID: 40050430
Atrial fibrillation (AF) is a prevalent and morbid abnormality of the heart rhythm with a strong genetic component. Here, we meta-analyzed genome and exome sequencing data from 36 studies that...
2.
Roselli C, Surakka I, S Olesen M, Sveinbjornsson G, Marston N, Choi S, et al.
Nat Genet
. 2025 Mar;
57(3):539-547.
PMID: 40050429
Atrial fibrillation (AF) is the most common heart rhythm abnormality and is a leading cause of heart failure and stroke. This large-scale meta-analysis of genome-wide association studies increased the power...
3.
Gigli M, Stolfo D, Barbati G, Graw S, Chen S, Merlo M, et al.
JAMA Cardiol
. 2025 Feb;
PMID: 39937464
Importance: Filamin C truncating variants (FLNCtv) are a rare cause of cardiomyopathy with heterogeneous phenotypic presentations. Despite a high incidence of life-threatening ventricular arrhythmias and sudden cardiac death (SCD), reliable...
4.
Weng L, Ramo J, Jurgens S, Khurshid S, Chaffin M, Hall A, et al.
Nat Genet
. 2025 Jan;
57(1):53-64.
PMID: 39747593
To broaden our understanding of bradyarrhythmias and conduction disease, we performed common variant genome-wide association analyses in up to 1.3 million individuals and rare variant burden testing in 460,000 individuals...
5.
Asaeikheybari G, El-Harasis M, Gupta A, Shoemaker M, Barnard J, Hunter J, et al.
Circ Arrhythm Electrophysiol
. 2024 Dec;
17(12):e012679.
PMID: 39624901
Background: Atrial fibrillation (AF) recurrence is common after catheter ablation. Pulmonary vein (PV) isolation is the cornerstone of AF ablation, but PV remodeling has been associated with the risk of...
6.
Virk Z, El-Harasis M, Yoneda Z, Anderson K, Sun L, Quintana J, et al.
JACC Clin Electrophysiol
. 2024 Oct;
10(11):2445-2457.
PMID: 39453294
Background: TTN encodes a sarcomeric protein called titin. Pathogenic rare variants in TTN are the most common finding in patients with atrial fibrillation (AF) and positive genetic testing. Objectives: This...
7.
Hawkes G, Beaumont R, Li Z, Mandla R, Li X, Albert C, et al.
Nat Commun
. 2024 Oct;
15(1):8549.
PMID: 39362880
The role of rare non-coding variation in complex human phenotypes is still largely unknown. To elucidate the impact of rare variants in regulatory elements, we performed a whole-genome sequencing association...
8.
El-Harasis M, Yoneda Z, Anderson K, Ye F, Quintana J, Martinez-Parachini J, et al.
JACC Clin Electrophysiol
. 2024 Sep;
10(11):2359-2370.
PMID: 39243256
Background: Patients with rare, pathogenic cardiomyopathy (CM) and arrhythmia variants can present with atrial fibrillation (AF). The efficacy of AF ablation in these patients is unknown. Objective: This study tested...
9.
Lancaster M, Chen H, Shoemaker M, Fleming M, Strickland T, Baker J, et al.
Nat Commun
. 2024 Aug;
15(1):7507.
PMID: 39209900
Rare genetic diseases are typically studied in referral populations, resulting in underdiagnosis and biased assessment of penetrance and phenotype. To address this, we develop a generalizable method of genotype inference...
10.
Kany S, Jurgens S, Ramo J, Christophersen I, Rienstra M, Chung M, et al.
Eur Heart J
. 2024 Jul;
45(34):3111-3123.
PMID: 39028637
Atrial fibrillation (AF) is a globally prevalent cardiac arrhythmia with significant genetic underpinnings, as highlighted by recent large-scale genetic studies. A prominent clinical and genetic overlap exists between AF, heritable...