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.
643 related articles for article (PubMed ID: 32160020)
21. Specifications of the ACMG/AMP Variant Classification Guidelines for Germline Hatton JN; Frone MN; Cox HC; Crowley SB; Hiraki S; Yokoyama NN; Abul-Husn NS; Amatruda JF; Anderson MJ; Bofill-De Ros X; Carr AG; Chao EC; Chen KS; Gu S; Higgs C; Machado J; Ritter D; Schultz KA; Soper ER; Wu MK; Mester JL; Kim J; Foulkes WD; Witkowski L; Stewart DR Hum Mutat; 2023; 2023():. PubMed ID: 38084291 [TBL] [Abstract][Full Text] [Related]
22. Good performance of the criteria of American College of Medical Genetics and Genomics/Association for Molecular Pathology in prediction of pathogenicity of genetic variants causing thoracic aortic aneurysms and dissections. Ponińska JK; Bilińska ZT; Truszkowska G; Michalak E; Podgórska A; Stępień-Wojno M; Chmielewski P; Lutyńska A; Płoski R J Transl Med; 2022 Jan; 20(1):42. PubMed ID: 35078481 [TBL] [Abstract][Full Text] [Related]
23. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing. Carnevale A; Rosas-Madrigal S; Rosendo-Gutiérrez R; López-Mora E; Romero-Hidalgo S; Avila-Vazzini N; Jacobo-Albavera L; Domínguez-Pérez M; Vargas-Alarcón G; Pérez-Villatoro F; Navarrete-Martínez JI; Villarreal-Molina MT Mol Genet Genomic Med; 2020 Nov; 8(11):e1504. PubMed ID: 32969603 [TBL] [Abstract][Full Text] [Related]
24. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel. Ross JE; Zhang BM; Lee K; Mohan S; Branchford BR; Bray P; Dugan SN; Freson K; Heller PG; Kahr WHA; Lambert MP; Luchtman-Jones L; Luo M; Perez Botero J; Rondina MT; Ryan G; Westbury S; Bergmeier W; Di Paola J Blood Adv; 2021 Jan; 5(2):414-431. PubMed ID: 33496739 [TBL] [Abstract][Full Text] [Related]
25. Clinical Interpretation of Sequence Variants. Zhang J; Yao Y; He H; Shen J Curr Protoc Hum Genet; 2020 Jun; 106(1):e98. PubMed ID: 32176464 [TBL] [Abstract][Full Text] [Related]
26. Effectiveness of the Kinnamon DD; Jordan E; 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; Aaronson KD; Fishbein DP; Smart F; Wang J; Gottlieb SS; Judge DP; Moore CK; Mead JO; Huggins GS; Ni H; Burke W; Hershberger RE; Circulation; 2023 Apr; 147(17):1281-1290. PubMed ID: 36938756 [TBL] [Abstract][Full Text] [Related]
27. Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel. Burdon KP; Graham P; Hadler J; Hulleman JD; Pasutto F; Boese EA; Craig JE; Fingert JH; Hewitt AW; Siggs OM; Whisenhunt K; Young TL; Mackey DA; Dubowsky A; Souzeau E Hum Mutat; 2022 Dec; 43(12):2170-2186. PubMed ID: 36217948 [TBL] [Abstract][Full Text] [Related]
29. Implications of Genetic Testing in Dilated Cardiomyopathy. Verdonschot JAJ; Hazebroek MR; Krapels IPC; Henkens MTHM; Raafs A; Wang P; Merken JJ; Claes GRF; Vanhoutte EK; van den Wijngaard A; Heymans SRB; Brunner HG Circ Genom Precis Med; 2020 Oct; 13(5):476-487. PubMed ID: 32880476 [TBL] [Abstract][Full Text] [Related]
30. Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants. Lee K; Krempely K; Roberts ME; Anderson MJ; Carneiro F; Chao E; Dixon K; Figueiredo J; Ghosh R; Huntsman D; Kaurah P; Kesserwan C; Landrith T; Li S; Mensenkamp AR; Oliveira C; Pardo C; Pesaran T; Richardson M; Slavin TP; Spurdle AB; Trapp M; Witkowski L; Yi CS; Zhang L; Plon SE; Schrader KA; Karam R Hum Mutat; 2018 Nov; 39(11):1553-1568. PubMed ID: 30311375 [TBL] [Abstract][Full Text] [Related]
31. Evaluating ClinGen variant curation expert panels' application of PVS1 code. Wang X; Li H; Luo H; Zou Y; Li H; Qin Y; Song J Eur J Med Genet; 2024 Feb; 67():104909. PubMed ID: 38199457 [TBL] [Abstract][Full Text] [Related]
32. A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy. Horvat C; Johnson R; Lam L; Munro J; Mazzarotto F; Roberts AM; Herman DS; Parfenov M; Haghighi A; McDonough B; DePalma SR; Keogh AM; Macdonald PS; Hayward CS; Roberts A; Barton PJR; Felkin LE; Giannoulatou E; Cook SA; Seidman JG; Seidman CE; Fatkin D Genet Med; 2019 Jan; 21(1):133-143. PubMed ID: 29892087 [TBL] [Abstract][Full Text] [Related]
34. Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup. Walker LC; Hoya M; Wiggins GAR; Lindy A; Vincent LM; Parsons MT; Canson DM; Bis-Brewer D; Cass A; Tchourbanov A; Zimmermann H; Byrne AB; Pesaran T; Karam R; Harrison SM; Spurdle AB; Am J Hum Genet; 2023 Jul; 110(7):1046-1067. PubMed ID: 37352859 [TBL] [Abstract][Full Text] [Related]
35. Genetics and genomics of dilated cardiomyopathy and systolic heart failure. Tayal U; Prasad S; Cook SA Genome Med; 2017 Feb; 9(1):20. PubMed ID: 28228157 [TBL] [Abstract][Full Text] [Related]
36. Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy. Mazzarotto F; Tayal U; Buchan RJ; Midwinter W; Wilk A; Whiffin N; Govind R; Mazaika E; de Marvao A; Dawes TJW; Felkin LE; Ahmad M; Theotokis PI; Edwards E; Ing AY; Thomson KL; Chan LLH; Sim D; Baksi AJ; Pantazis A; Roberts AM; Watkins H; Funke B; O'Regan DP; Olivotto I; Barton PJR; Prasad SK; Cook SA; Ware JS; Walsh R Circulation; 2020 Feb; 141(5):387-398. PubMed ID: 31983221 [TBL] [Abstract][Full Text] [Related]
37. Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy. Zhao Y; Feng Y; Zhang YM; Ding XX; Song YZ; Zhang AM; Liu L; Zhang H; Ding JH; Xia XS Int J Mol Med; 2015 Dec; 36(6):1479-86. PubMed ID: 26458567 [TBL] [Abstract][Full Text] [Related]
38. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512 [TBL] [Abstract][Full Text] [Related]
39. Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Minoche AE; Horvat C; Johnson R; Gayevskiy V; Morton SU; Drew AP; Woo K; Statham AL; Lundie B; Bagnall RD; Ingles J; Semsarian C; Seidman JG; Seidman CE; Dinger ME; Cowley MJ; Fatkin D Genet Med; 2019 Mar; 21(3):650-662. PubMed ID: 29961767 [TBL] [Abstract][Full Text] [Related]
40. Genetic testing for dilated cardiomyopathy in clinical practice. Lakdawala NK; Funke BH; Baxter S; Cirino AL; Roberts AE; Judge DP; Johnson N; Mendelsohn NJ; Morel C; Care M; Chung WK; Jones C; Psychogios A; Duffy E; Rehm HL; White E; Seidman JG; Seidman CE; Ho CY J Card Fail; 2012 Apr; 18(4):296-303. PubMed ID: 22464770 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]