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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 2 |
2021 | 3 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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7 results
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Page 1
Cardiovascular Characteristics of Patients with Genetic Variation in Desmoplakin (DSP).
Cardiogenetics. 2022 Mar;12(1):24-36. doi: 10.3390/cardiogenetics12010003. Epub 2022 Jan 6.
Cardiogenetics. 2022.
PMID: 35083019
Free PMC article.
A Novel Human Biospecimen Repository for Clinical and Molecular Investigation of Thoracic Aortopathy.
Vujakovich CE, Landis BJ.
Vujakovich CE, et al.
Cardiogenetics. 2021 Sep;11(3):148-163. doi: 10.3390/cardiogenetics11030017. Epub 2021 Sep 18.
Cardiogenetics. 2021.
PMID: 34912529
Free PMC article.
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Human SMAD4 Genomic Variants Identified in Individuals with Heritable and Early-Onset Thoracic Aortic Disease.
Bhave SA, Guo DC, Angelov S, Bamshad MJ, Nickerson DA, Milewicz D, Wallingford MC.
Bhave SA, et al.
Cardiogenetics. 2021 Sep;11(3):132-138. doi: 10.3390/cardiogenetics11030015. Epub 2021 Aug 18.
Cardiogenetics. 2021.
PMID: 36158166
Free PMC article.
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Sex Differences in Fatty Acid Metabolism and Blood Pressure Response to Dietary Salt in Humans.
Ishimwe JA, Ferguson JF, Kirabo A.
Ishimwe JA, et al.
Cardiogenetics. 2023 Mar;13(1):33-46. doi: 10.3390/cardiogenetics13010005. Epub 2023 Mar 3.
Cardiogenetics. 2023.
PMID: 38605973
Free PMC article.
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Biventricular Strain Imaging with Cardiac MRI in Genotyped and Histology Validated Amyloid Cardiomyopathy.
Reddy A, Singh V, Karthikeyan B, Jiang L, Kristo S, Kattel S, Amuthan R, Pokharel S, Sharma UC.
Reddy A, et al.
Cardiogenetics. 2021 Sep;11(3):98-110. doi: 10.3390/cardiogenetics11030011. Epub 2021 Jun 30.
Cardiogenetics. 2021.
PMID: 34336147
Free PMC article.
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LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype.
Cheng J, Norstrand DW, Medeiros-Domingo A, Tester DJ, Valdivia CR, Tan BH, Vatta M, Makielski JC, Ackerman MJ.
Cheng J, et al.
Cardiogenetics. 2011 Oct 25;1(1):136. doi: 10.4081/cardiogenetics.2011.e13.
Cardiogenetics. 2011.
PMID: 24319568
Free PMC article.
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Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant.
Wells QS, Ausborn NL, Funke BH, Pfotenhauer JP, Fredi JL, Baxter S, Disalvo TD, Hong CC.
Wells QS, et al.
Cardiogenetics. 2011 Aug 22;1(1):e10. doi: 10.4081/cardiogenetics.2011.e10.
Cardiogenetics. 2011.
PMID: 24062880
Free PMC article.
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