<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(1)</volume><submitter>Melinyte-Ankudavice K</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Careful interpretation of the relation between phenotype changes of the heart and gene variants detected in dilated cardiomyopathy (DCM) is important for patient care and monitoring.&lt;h4>Objective&lt;/h4>We sought to assess the association between cardiac-related genes and whole-heart myocardial mechanics or morphometrics in nonischemic dilated cardiomyopathy (NIDCM).&lt;h4>Methods&lt;/h4>It was a prospective study consisting of patients with NIDCM. All patients were referred for genetic testing and a genetic analysis was performed using Illumina NextSeq 550 and a commercial gene capture panel of 233 genes (Systems Genomics, Cardiac-GeneSGKit®). It was analyzed whether there are significant differences in clinical, two-dimensional (2D) echocardiographic, and magnetic resonance ima</pubmed_abstract><journal>BMC cardiovascular disorders</journal><pagination>224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11044472</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association of uncertain significance genetic variants with myocardial mechanics and morphometrics in patients with nonischemic dilated cardiomyopathy.</pubmed_title><pmcid>PMC11044472</pmcid><pubmed_authors>Melinyte-Ankudavice K</pubmed_authors><pubmed_authors>Krikstolaitis R</pubmed_authors><pubmed_authors>Galnaitiene G</pubmed_authors><pubmed_authors>Mizariene V</pubmed_authors><pubmed_authors>Sukys M</pubmed_authors><pubmed_authors>Sakalyte G</pubmed_authors><pubmed_authors>Jurkevicius R</pubmed_authors><pubmed_authors>Ereminiene E</pubmed_authors><pubmed_authors>Krilavicius T</pubmed_authors><pubmed_authors>Kasputyte G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of uncertain significance genetic variants with myocardial mechanics and morphometrics in patients with nonischemic dilated cardiomyopathy.</name><description>&lt;h4>Background&lt;/h4>Careful interpretation of the relation between phenotype changes of the heart and gene variants detected in dilated cardiomyopathy (DCM) is important for patient care and monitoring.&lt;h4>Objective&lt;/h4>We sought to assess the association between cardiac-related genes and whole-heart myocardial mechanics or morphometrics in nonischemic dilated cardiomyopathy (NIDCM).&lt;h4>Methods&lt;/h4>It was a prospective study consisting of patients with NIDCM. All patients were referred for genetic testing and a genetic analysis was performed using Illumina NextSeq 550 and a commercial gene capture panel of 233 genes (Systems Genomics, Cardiac-GeneSGKit®). It was analyzed whether there are significant differences in clinical, two-dimensional (2D) echocardiographic, and magnetic resonance ima</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-02T02:13:20.95Z</modification><creation>2026-04-13T03:12:44.401Z</creation></dates><accession>S-EPMC11044472</accession><cross_references><pubmed>38664609</pubmed><doi>10.1186/s12872-024-03888-x</doi></cross_references></HashMap>