705 related articles for article (PubMed ID: 26250888)
1. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Genetic and genomic testing for neurologic disease in clinical practice.
Fogel BL
Handb Clin Neurol; 2018; 147():11-22. PubMed ID: 29325607
[TBL] [Abstract][Full Text] [Related]
4. Advances in genomic testing.
Donoghue S; Downie L; Stutterd C
Aust Fam Physician; 2017; 46(4):200-205. PubMed ID: 28376572
[TBL] [Abstract][Full Text] [Related]
5. Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
Hegde M; Santani A; Mao R; Ferreira-Gonzalez A; Weck KE; Voelkerding KV
Arch Pathol Lab Med; 2017 Jun; 141(6):798-805. PubMed ID: 28362156
[TBL] [Abstract][Full Text] [Related]
6. Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.
Worthey EA
Curr Protoc Hum Genet; 2013 Oct; 79():9.24.1-9.24.24. PubMed ID: 24510652
[TBL] [Abstract][Full Text] [Related]
7. Exome sequencing: dual role as a discovery and diagnostic tool.
Ku CS; Cooper DN; Polychronakos C; Naidoo N; Wu M; Soong R
Ann Neurol; 2012 Jan; 71(1):5-14. PubMed ID: 22275248
[TBL] [Abstract][Full Text] [Related]
8. The genetics of neuropsychiatric diseases: looking in and beyond the exome.
Heinzen EL; Neale BM; Traynelis SF; Allen AS; Goldstein DB
Annu Rev Neurosci; 2015 Jul; 38():47-68. PubMed ID: 25840007
[TBL] [Abstract][Full Text] [Related]
9. [Gene mutations; up date].
Nakagawa M
Rinsho Shinkeigaku; 2013; 53(11):903-6. PubMed ID: 24291829
[TBL] [Abstract][Full Text] [Related]
10. Future of whole genome sequencing.
Amor DJ
J Paediatr Child Health; 2015 Mar; 51(3):251-4. PubMed ID: 24893957
[No Abstract] [Full Text] [Related]
11. Genomic Analysis in the Age of Human Genome Sequencing.
Lappalainen T; Scott AJ; Brandt M; Hall IM
Cell; 2019 Mar; 177(1):70-84. PubMed ID: 30901550
[TBL] [Abstract][Full Text] [Related]
12. The Challenge of Analyzing the Results of Next-Generation Sequencing in Children.
Thiffault I; Lantos J
Pediatrics; 2016 Jan; 137 Suppl 1():S3-7. PubMed ID: 26729700
[TBL] [Abstract][Full Text] [Related]
13. The promise of whole-exome sequencing in medical genetics.
Rabbani B; Tekin M; Mahdieh N
J Hum Genet; 2014 Jan; 59(1):5-15. PubMed ID: 24196381
[TBL] [Abstract][Full Text] [Related]
14. [Genetic testing in the fetus and child].
Bartholdi D; Miny P
Ther Umsch; 2013 Nov; 70(11):621-31. PubMed ID: 24168795
[TBL] [Abstract][Full Text] [Related]
15. Technology: Read the instructions.
Scott AR
Nature; 2016 Sep; 537(7619):S54-6. PubMed ID: 27602740
[No Abstract] [Full Text] [Related]
16. Whole exome and whole genome sequencing.
Bick D; Dimmock D
Curr Opin Pediatr; 2011 Dec; 23(6):594-600. PubMed ID: 21881504
[TBL] [Abstract][Full Text] [Related]
17. The DNA of a nation.
Marx V
Nature; 2015 Aug; 524(7566):503-5. PubMed ID: 26310768
[No Abstract] [Full Text] [Related]
18. The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience.
Lawrence L; Sincan M; Markello T; Adams DR; Gill F; Godfrey R; Golas G; Groden C; Landis D; Nehrebecky M; Park G; Soldatos A; Tifft C; Toro C; Wahl C; Wolfe L; Gahl WA; Boerkoel CF
Genet Med; 2014 Oct; 16(10):741-50. PubMed ID: 24784157
[TBL] [Abstract][Full Text] [Related]
19. [Medical genetics and the genome].
Gerdes AM; Vogel I
Ugeskr Laeger; 2014 Nov; 176(46):. PubMed ID: 25394930
[TBL] [Abstract][Full Text] [Related]
20. Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls.
McInerney-Leo AM; Duncan EL
Front Endocrinol (Lausanne); 2020; 11():628946. PubMed ID: 33679611
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
