These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
244 related articles for article (PubMed ID: 37526719)
1. Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry. Jordan E; Kinnamon DD; Haas GJ; Hofmeyer M; Kransdorf E; Ewald GA; Morris AA; Owens A; Lowes B; Stoller D; Tang WHW; Garg S; Trachtenberg BH; Shah P; Pamboukian SV; Sweitzer NK; Wheeler MT; Wilcox JE; Katz S; Pan S; Jimenez J; Fishbein DP; Smart F; Wang J; Gottlieb SS; Judge DP; Moore CK; Mead JO; Hurst N; Cao J; Huggins GS; Cowan J; Ni H; Rehm HL; Jarvik GP; Vatta M; Burke W; Hershberger RE; JAMA; 2023 Aug; 330(5):432-441. PubMed ID: 37526719 [TBL] [Abstract][Full Text] [Related]
2. Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study. Hofmeyer M; Haas GJ; Jordan E; Cao J; Kransdorf E; Ewald GA; Morris AA; Owens A; Lowes B; Stoller D; Wilson Tang WH; Garg S; Trachtenberg BH; Shah P; Pamboukian SV; Sweitzer NK; Wheeler MT; Wilcox JE; Katz S; Pan S; Jimenez J; Smart F; Wang J; Gottlieb SS; Judge DP; Moore CK; Huggins GS; Kinnamon DD; Ni H; Hershberger RE; Circulation; 2023 Sep; 148(11):872-881. PubMed ID: 37641966 [TBL] [Abstract][Full Text] [Related]
3. Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals. Myers VD; Gerhard GS; McNamara DM; Tomar D; Madesh M; Kaniper S; Ramsey FV; Fisher SG; Ingersoll RG; Kasch-Semenza L; Wang J; Hanley-Yanez K; Lemster B; Schwisow JA; Ambardekar AV; Degann SH; Bristow MR; Sheppard R; Alexis JD; Tilley DG; Kontos CD; McClung JM; Taylor AL; Yancy CW; Khalili K; Seidman JG; Seidman CE; McTiernan CF; Cheung JY; Feldman AM JAMA Cardiol; 2018 Oct; 3(10):929-938. PubMed ID: 30140897 [TBL] [Abstract][Full Text] [Related]
4. Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy. Huggins GS; Kinnamon DD; Haas GJ; Jordan E; Hofmeyer M; Kransdorf E; Ewald GA; Morris AA; Owens A; Lowes B; Stoller D; Tang WHW; Garg S; Trachtenberg BH; Shah P; Pamboukian SV; Sweitzer NK; Wheeler MT; Wilcox JE; Katz S; Pan S; Jimenez J; Aaronson KD; Fishbein DP; Smart F; Wang J; Gottlieb SS; Judge DP; Moore CK; Mead JO; Ni H; Burke W; Hershberger RE; JAMA; 2022 Feb; 327(5):454-463. PubMed ID: 35103767 [TBL] [Abstract][Full Text] [Related]
5. Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study. Kinnamon DD; Morales A; Bowen DJ; Burke W; Hershberger RE; Circ Cardiovasc Genet; 2017 Dec; 10(6):. PubMed ID: 29237686 [TBL] [Abstract][Full Text] [Related]
6. Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants. Pottinger TD; Puckelwartz MJ; Pesce LL; Robinson A; Kearns S; Pacheco JA; Rasmussen-Torvik LJ; Smith ME; Chisholm R; McNally EM J Am Heart Assoc; 2020 Feb; 9(3):e013808. PubMed ID: 32009526 [TBL] [Abstract][Full Text] [Related]
7. Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study. Morales A; Kinnamon DD; Jordan E; Platt J; Vatta M; Dorschner MO; Starkey CA; Mead JO; Ai T; Burke W; Gastier-Foster J; Jarvik GP; Rehm HL; Nickerson DA; Hershberger RE; ; Circ Genom Precis Med; 2020 Apr; 13(2):e002480. PubMed ID: 32160020 [TBL] [Abstract][Full Text] [Related]
8. TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study. Trachtenberg BH; Jimenez J; Morris AA; Kransdorf E; Owens A; Fishbein DP; Jordan E; Kinnamon DD; Mead JO; Huggins GS; Hershberger RE; Genet Med; 2022 Jul; 24(7):1495-1502. PubMed ID: 35438637 [TBL] [Abstract][Full Text] [Related]
9. Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality. Patel AP; Dron JS; Wang M; Pirruccello JP; Ng K; Natarajan P; Lebo M; Ellinor PT; Aragam KG; Khera AV JAMA Cardiol; 2022 Jul; 7(7):723-732. PubMed ID: 35544052 [TBL] [Abstract][Full Text] [Related]
10. Native American genetic ancestry and pigmentation allele contributions to skin color in a Caribbean population. Ang KC; Canfield VA; Foster TC; Harbaugh TD; Early KA; Harter RL; Reid KP; Leong SL; Kawasawa Y; Liu D; Hawley JW; Cheng KC Elife; 2023 Jun; 12():. PubMed ID: 37294081 [TBL] [Abstract][Full Text] [Related]
11. Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. Liu C; Zeinomar N; Chung WK; Kiryluk K; Gharavi AG; Hripcsak G; Crew KD; Shang N; Khan A; Fasel D; Manolio TA; Jarvik GP; Rowley R; Justice AE; Rahm AK; Fullerton SM; Smoller JW; Larson EB; Crane PK; Dikilitas O; Wiesner GL; Bick AG; Terry MB; Weng C JAMA Netw Open; 2021 Aug; 4(8):e2119084. PubMed ID: 34347061 [TBL] [Abstract][Full Text] [Related]
13. Genetic ancestry and lower extremity peripheral artery disease in the Multi-Ethnic Study of Atherosclerosis. Allison MA; Peralta CA; Wassel CL; Aboyans V; Arnett DK; Cushman M; Eng J; Ix J; Rich SS; Criqui MH Vasc Med; 2010 Oct; 15(5):351-9. PubMed ID: 20926494 [TBL] [Abstract][Full Text] [Related]
14. Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals. Chalazan B; Mol D; Darbar FA; Ornelas-Loredo A; Al-Azzam B; Chen Y; Tofovic D; Sridhar A; Alzahrani Z; Ellinor P; Darbar D JAMA Cardiol; 2021 Jul; 6(7):811-819. PubMed ID: 33950154 [TBL] [Abstract][Full Text] [Related]
15. Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants. Haggerty CM; Damrauer SM; Levin MG; Birtwell D; Carey DJ; Golden AM; Hartzel DN; Hu Y; Judy R; Kelly MA; Kember RL; Lester Kirchner H; Leader JB; Liang L; McDermott-Roe C; Babu A; Morley M; Nealy Z; Person TN; Pulenthiran A; Small A; Smelser DT; Stahl RC; Sturm AC; Williams H; Baras A; Margulies KB; Cappola TP; Dewey FE; Verma A; Zhang X; Correa A; Hall ME; Wilson JG; Ritchie MD; Rader DJ; Murray MF; Fornwalt BK; Arany Z Circulation; 2019 Jul; 140(1):42-54. PubMed ID: 31216868 [TBL] [Abstract][Full Text] [Related]
16. Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry. Damrauer SM; Chaudhary K; Cho JH; Liang LW; Argulian E; Chan L; Dobbyn A; Guerraty MA; Judy R; Kay J; Kember RL; Levin MG; Saha A; Van Vleck T; Verma SS; Weaver J; Abul-Husn NS; Baras A; Chirinos JA; Drachman B; Kenny EE; Loos RJF; Narula J; Overton J; Reid J; Ritchie M; Sirugo G; Nadkarni G; Rader DJ; Do R JAMA; 2019 Dec; 322(22):2191-2202. PubMed ID: 31821430 [TBL] [Abstract][Full Text] [Related]
17. High-proportion spliced-in titin truncating variants in African and European ancestry in the All of Us Research Program. Shetty NS; Pampana A; Patel N; Li P; Arora G; Arora P Nat Cardiovasc Res; 2024 Feb; 3(2):140-144. PubMed ID: 39196186 [TBL] [Abstract][Full Text] [Related]
18. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. Norton N; Li D; Rampersaud E; Morales A; Martin ER; Zuchner S; Guo S; Gonzalez M; Hedges DJ; Robertson PD; Krumm N; Nickerson DA; Hershberger RE; Circ Cardiovasc Genet; 2013 Apr; 6(2):144-53. PubMed ID: 23418287 [TBL] [Abstract][Full Text] [Related]
19. Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs. Al-Shafai KN; Al-Hashemi M; Manickam C; Musa R; Selvaraj S; Syed N; Vempalli F; Ali M; Yacoub M; Estivill X Mol Genet Genomic Med; 2021 Jul; 9(7):e1709. PubMed ID: 34137518 [TBL] [Abstract][Full Text] [Related]
20. Prevalence and Reclassification of Genetic Variants in South African Populations with Breast Cancer. Osler TS; Brandenburg JT; Schoeman M; Chen WC; Urban MF; Mathew CG Genes Chromosomes Cancer; 2024 Sep; 63(9):e23275. PubMed ID: 39324485 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]