341 related articles for article (PubMed ID: 23665194)
1. The development of next-generation sequencing assays for the mitochondrial genome and 108 nuclear genes associated with mitochondrial disorders.
Dames S; Chou LS; Xiao Y; Wayman T; Stocks J; Singleton M; Eilbeck K; Mao R
J Mol Diagn; 2013 Jul; 15(4):526-34. PubMed ID: 23665194
[TBL] [Abstract][Full Text] [Related]
2. Next generation molecular diagnosis of mitochondrial disorders.
Wong LJ
Mitochondrion; 2013 Jul; 13(4):379-87. PubMed ID: 23473862
[TBL] [Abstract][Full Text] [Related]
3. Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.
Tang S; Wang J; Zhang VW; Li FY; Landsverk M; Cui H; Truong CK; Wang G; Chen LC; Graham B; Scaglia F; Schmitt ES; Craigen WJ; Wong LJ
Hum Mutat; 2013 Jun; 34(6):882-93. PubMed ID: 23463613
[TBL] [Abstract][Full Text] [Related]
4. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing.
Palculict ME; Zhang VW; Wong LJ; Wang J
Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670
[TBL] [Abstract][Full Text] [Related]
5. A high-throughput next-generation sequencing assay for the mitochondrial genome.
Dames S; Eilbeck K; Mao R
Methods Mol Biol; 2015; 1264():77-88. PubMed ID: 25631005
[TBL] [Abstract][Full Text] [Related]
6. Targeted array CGH as a valuable molecular diagnostic approach: experience in the diagnosis of mitochondrial and metabolic disorders.
Wang J; Zhan H; Li FY; Pursley AN; Schmitt ES; Wong LJ
Mol Genet Metab; 2012 Jun; 106(2):221-30. PubMed ID: 22494545
[TBL] [Abstract][Full Text] [Related]
7. Next-generation sequencing for mitochondrial diseases: a wide diagnostic spectrum.
Vasta V; Merritt JL; Saneto RP; Hahn SH
Pediatr Int; 2012 Oct; 54(5):585-601. PubMed ID: 22494076
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial and nuclear disease panel (Mito-aND-Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost-effective and sensitive NGS-based method.
Abicht A; Scharf F; Kleinle S; Schön U; Holinski-Feder E; Horvath R; Benet-Pagès A; Diebold I
Mol Genet Genomic Med; 2018 Nov; 6(6):1188-1198. PubMed ID: 30406974
[TBL] [Abstract][Full Text] [Related]
9. Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.
Sivakumaran TA; Husami A; Kissell D; Zhang W; Keddache M; Black AP; Tinkle BT; Greinwald JH; Zhang K
Otolaryngol Head Neck Surg; 2013 Jun; 148(6):1007-16. PubMed ID: 23525850
[TBL] [Abstract][Full Text] [Related]
10. Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.
Kloss-Brandstätter A; Weissensteiner H; Erhart G; Schäfer G; Forer L; Schönherr S; Pacher D; Seifarth C; Stöckl A; Fendt L; Sottsas I; Klocker H; Huck CW; Rasse M; Kronenberg F; Kloss FR
PLoS One; 2015; 10(8):e0135643. PubMed ID: 26262956
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease.
Wagner M; Berutti R; Lorenz-Depiereux B; Graf E; Eckstein G; Mayr JA; Meitinger T; Ahting U; Prokisch H; Strom TM; Wortmann SB
J Inherit Metab Dis; 2019 Sep; 42(5):909-917. PubMed ID: 31059585
[TBL] [Abstract][Full Text] [Related]
12. Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction.
Nogueira C; Silva L; Pereira C; Vieira L; Leão Teles E; Rodrigues E; Campos T; Janeiro P; Gaspar A; Dupont J; Bandeira A; Martins E; Magalhães M; Sequeira S; Vieira JP; Santos H; Vilarinho S; Vilarinho L
Mitochondrion; 2019 Jul; 47():309-317. PubMed ID: 30831263
[TBL] [Abstract][Full Text] [Related]
13. Targeted multiplex next-generation sequencing: advances in techniques of mitochondrial and nuclear DNA sequencing for population genomics.
Hancock-Hanser BL; Frey A; Leslie MS; Dutton PH; Archer FI; Morin PA
Mol Ecol Resour; 2013 Mar; 13(2):254-68. PubMed ID: 23351075
[TBL] [Abstract][Full Text] [Related]
14. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
[TBL] [Abstract][Full Text] [Related]
15. Validation and clinical performance of a combined nuclear-mitochondrial next-generation sequencing and copy number variant analysis panel in a Canadian population.
Levy MA; Kerkhof J; Belmonte FR; Kaufman BA; Bhai P; Brady L; Bursztyn LLCD; Tarnopolsky M; Rupar T; Sadikovic B
Am J Med Genet A; 2021 Feb; 185(2):486-499. PubMed ID: 33300680
[TBL] [Abstract][Full Text] [Related]
16. mit-o-matic: a comprehensive computational pipeline for clinical evaluation of mitochondrial variations from next-generation sequencing datasets.
Vellarikkal SK; Dhiman H; Joshi K; Hasija Y; Sivasubbu S; Scaria V
Hum Mutat; 2015 Apr; 36(4):419-24. PubMed ID: 25677119
[TBL] [Abstract][Full Text] [Related]
17. New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies.
Legati A; Reyes A; Nasca A; Invernizzi F; Lamantea E; Tiranti V; Garavaglia B; Lamperti C; Ardissone A; Moroni I; Robinson A; Ghezzi D; Zeviani M
Biochim Biophys Acta; 2016 Aug; 1857(8):1326-1335. PubMed ID: 26968897
[TBL] [Abstract][Full Text] [Related]
18. Next-generation sequencing identifies novel mitochondrial variants in pituitary adenomas.
Németh K; Darvasi O; Likó I; Szücs N; Czirják S; Reiniger L; Szabó B; Kurucz PA; Krokker L; Igaz P; Patócs A; Butz H
J Endocrinol Invest; 2019 Aug; 42(8):931-940. PubMed ID: 30684245
[TBL] [Abstract][Full Text] [Related]
19. Plasma-derived cell-free mitochondrial DNA: A novel non-invasive methodology to identify mitochondrial DNA haplogroups in humans.
Newell C; Hume S; Greenway SC; Podemski L; Shearer J; Khan A
Mol Genet Metab; 2018 Dec; 125(4):332-337. PubMed ID: 30361042
[TBL] [Abstract][Full Text] [Related]
20. Clinical validation of targeted next-generation sequencing for inherited disorders.
Yohe S; Hauge A; Bunjer K; Kemmer T; Bower M; Schomaker M; Onsongo G; Wilson J; Erdmann J; Zhou Y; Deshpande A; Spears MD; Beckman K; Silverstein KA; Thyagarajan B
Arch Pathol Lab Med; 2015 Feb; 139(2):204-10. PubMed ID: 25611102
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
