226 related articles for article (PubMed ID: 26040335)
21. Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.
Marian AJ; van Rooij E; Roberts R
J Am Coll Cardiol; 2016 Dec; 68(25):2831-2849. PubMed ID: 28007145
[TBL] [Abstract][Full Text] [Related]
22. Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy.
Mazzarotto F; Olivotto I; Walsh R
Cardiovasc Drugs Ther; 2020 Apr; 34(2):241-253. PubMed ID: 32080787
[TBL] [Abstract][Full Text] [Related]
23. An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data.
Jun G; Wing MK; Abecasis GR; Kang HM
Genome Res; 2015 Jun; 25(6):918-25. PubMed ID: 25883319
[TBL] [Abstract][Full Text] [Related]
24. Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy.
Lopes LR; Murphy C; Syrris P; Dalageorgou C; McKenna WJ; Elliott PM; Plagnol V
Eur J Med Genet; 2015 Nov; 58(11):611-6. PubMed ID: 26455666
[TBL] [Abstract][Full Text] [Related]
25. Progress in detecting genetic alterations and their association with human disease.
Schwartz CE; Chen CF
J Mol Biol; 2013 Nov; 425(21):3914-8. PubMed ID: 23876707
[TBL] [Abstract][Full Text] [Related]
26. Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.
Punetha J; Hoffman EP
Circ Cardiovasc Genet; 2013 Aug; 6(4):427-34. PubMed ID: 23852418
[No Abstract] [Full Text] [Related]
27. [Genomic studies of hereditary cardiomyopathies].
Stepanov VA; Puzyrev KV
Genetika; 1998 Mar; 34(3):325-34. PubMed ID: 9589860
[TBL] [Abstract][Full Text] [Related]
28. Sequencing your genome: what does it mean?
Marian AJ
Methodist Debakey Cardiovasc J; 2014; 10(1):3-6. PubMed ID: 24932355
[TBL] [Abstract][Full Text] [Related]
29. Next-generation sequencing of pharmacogenes: a critical analysis focusing on schizophrenia treatment.
Drögemöller BI; Wright GE; Niehaus DJ; Emsley R; Warnich L
Pharmacogenet Genomics; 2013 Dec; 23(12):666-74. PubMed ID: 24141736
[TBL] [Abstract][Full Text] [Related]
30. Impacts of variation in the human genome on gene regulation.
Haraksingh RR; Snyder MP
J Mol Biol; 2013 Nov; 425(21):3970-7. PubMed ID: 23871684
[TBL] [Abstract][Full Text] [Related]
31. Cancer whole-genome sequencing: present and future.
Nakagawa H; Wardell CP; Furuta M; Taniguchi H; Fujimoto A
Oncogene; 2015 Dec; 34(49):5943-50. PubMed ID: 25823020
[TBL] [Abstract][Full Text] [Related]
32. Whole-exome/genome sequencing and genomics.
Grody WW; Thompson BH; Hudgins L
Pediatrics; 2013 Dec; 132(Suppl 3):S211-5. PubMed ID: 24298129
[TBL] [Abstract][Full Text] [Related]
33. Exome and genome sequencing: a revolution for the discovery and diagnosis of monogenic disorders.
Stranneheim H; Wedell A
J Intern Med; 2016 Jan; 279(1):3-15. PubMed ID: 26250718
[TBL] [Abstract][Full Text] [Related]
34. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
Teekakirikul P; Kelly MA; Rehm HL; Lakdawala NK; Funke BH
J Mol Diagn; 2013 Mar; 15(2):158-70. PubMed ID: 23274168
[TBL] [Abstract][Full Text] [Related]
35. Genomic medicine and risk prediction across the disease spectrum.
Kotze MJ; Lückhoff HK; Peeters AV; Baatjes K; Schoeman M; van der Merwe L; Grant KA; Fisher LR; van der Merwe N; Pretorius J; van Velden DP; Myburgh EJ; Pienaar FM; van Rensburg SJ; Yako YY; September AV; Moremi KE; Cronje FJ; Tiffin N; Bouwens CS; Bezuidenhout J; Apffelstaedt JP; Hough FS; Erasmus RT; Schneider JW
Crit Rev Clin Lab Sci; 2015; 52(3):120-37. PubMed ID: 25597499
[TBL] [Abstract][Full Text] [Related]
36. Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype.
Ashrafian H; Watkins H
J Am Coll Cardiol; 2007 Mar; 49(12):1251-64. PubMed ID: 17394955
[TBL] [Abstract][Full Text] [Related]
37. Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing data.
Forni D; Martin D; Abujaber R; Sharp AJ; Sironi M; Hollox EJ
BMC Genomics; 2015 Nov; 16():891. PubMed ID: 26526070
[TBL] [Abstract][Full Text] [Related]
38. Clinical massively parallel sequencing for the diagnosis of myopathies.
Gorokhova S; Biancalana V; Lévy N; Laporte J; Bartoli M; Krahn M
Rev Neurol (Paris); 2015; 171(6-7):558-71. PubMed ID: 26022190
[TBL] [Abstract][Full Text] [Related]
39. Newest Methods for Detecting Structural Variations.
De Coster W; Van Broeckhoven C
Trends Biotechnol; 2019 Sep; 37(9):973-982. PubMed ID: 30902345
[TBL] [Abstract][Full Text] [Related]
40. Mind the Gap: Genetic Variation and Personalized Therapies for Cardiomyopathies.
Zhang Y; MacCosham A
Lifestyle Genom; 2018; 11(2):77-79. PubMed ID: 30231257
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]