Daniel D Kinnamon
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Explore the profile of Daniel D Kinnamon including associated specialties, affiliations and a list of published articles.
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35
Citations
615
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Recent Articles
1.
Kransdorf E, Jain R, Mead J, Haas G, Hofmeyer M, Ewald G, et al.
medRxiv
. 2025 Mar;
PMID: 40034776
Background: Peripartum cardiomyopathy (PPCM) presents substantial risk of maternal mortality, but underlying cause remains unsettled. Methods: We compared the prevalence of dilated cardiomyopathy (DCM)-relevant genetic variants in 452 female patients...
2.
Jordan E, Ni H, Parker P, Kinnamon D, Owens A, Lowes B, et al.
medRxiv
. 2024 Dec;
PMID: 39649582
Background: Clinical genetic evaluation of dilated cardiomyopathy (DCM) is implemented variably or not at all. Identifying needs and barriers to genetic evaluations will enable strategies to enhance precision medicine care....
3.
Bidirectional Risk Modulator and Modifier Variant of Dilated and Hypertrophic Cardiomyopathy in BAG3
Park J, Levin M, Zhang D, Reza N, Mead J, Carruth E, et al.
JAMA Cardiol
. 2024 Nov;
9(12):1124-1133.
PMID: 39535783
Importance: The genetic factors that modulate the reduced penetrance and variable expressivity of heritable dilated cardiomyopathy (DCM) are largely unknown. BAG3 genetic variants have been implicated in both DCM and...
4.
Dratch L, Kinnamon D, Harrington E, Goldman J, Fong J, Jones T, et al.
Amyotroph Lateral Scler Frontotemporal Degener
. 2024 Jun;
25(7-8):797-799.
PMID: 38902980
No abstract available.
5.
Hofmeyer M, Haas G, Jordan E, Cao J, Kransdorf E, Ewald G, et al.
Circulation
. 2023 Aug;
148(11):872-881.
PMID: 37641966
Background: Dilated cardiomyopathy (DCM) can lead to advanced disease, defined herein as necessitating a durable left ventricular assist device or a heart transplant (LVAD/HT). DCM is known to have a...
6.
Jordan E, Kinnamon D, Haas G, Hofmeyer M, Kransdorf E, Ewald G, et al.
JAMA
. 2023 Aug;
330(5):432-441.
PMID: 37526719
Importance: Black patients with dilated cardiomyopathy (DCM) have increased familial risk and worse outcomes than White patients, but most DCM genetic data are from White patients. Objective: To compare the...
7.
Wilcox J, Beussink-Nelson L, Cao J, Kumar R, Jordan E, Ni H, et al.
medRxiv
. 2023 Jul;
PMID: 37398079
Aims: Among genetically at-risk first-degree relatives (FDRs) of probands with dilated cardiomyopathy (DCM), the ability to detect changes in left ventricular (LV) mechanics with normal LV size and ejection fraction...
8.
Ni H, Jordan E, Kinnamon D, Cao J, Haas G, Hofmeyer M, et al.
J Am Coll Cardiol
. 2023 May;
81(21):2059-2071.
PMID: 37225358
Background: Cardiovascular screening is recommended for first-degree relatives (FDRs) of patients with dilated cardiomyopathy (DCM), but the yield of FDR screening is uncertain for DCM patients without known familial DCM,...
9.
Kinnamon D, Jordan E, Haas G, Hofmeyer M, Kransdorf E, Ewald G, et al.
Circulation
. 2023 Mar;
147(17):1281-1290.
PMID: 36938756
Background: Managing disease risk among first-degree relatives of probands diagnosed with a heritable disease is central to precision medicine. A critical component is often clinical screening, which is particularly important...
10.
Ni H, Jordan E, Cao J, Kinnamon D, Gottlieb S, Hofmeyer M, et al.
JAMA Cardiol
. 2022 Nov;
8(1):33-42.
PMID: 36383367
Importance: Cardiovascular disease contributes outsized mortality in patients from underrepresented racial and ethnic groups. Understanding levels of trust in medical researchers and knowledge of genome sequencing may help identify barriers...