162 related articles for article (PubMed ID: 21920053)
1. The exome factor.
Stower H
Genome Biol; 2011 Sep; 12(9):407. PubMed ID: 21920053
[TBL] [Abstract][Full Text] [Related]
2. Unlocking Mendelian disease using exome sequencing.
Gilissen C; Hoischen A; Brunner HG; Veltman JA
Genome Biol; 2011 Sep; 12(9):228. PubMed ID: 21920049
[TBL] [Abstract][Full Text] [Related]
3. Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.
Rabbani B; Mahdieh N; Hosomichi K; Nakaoka H; Inoue I
J Hum Genet; 2012 Oct; 57(10):621-32. PubMed ID: 22832387
[TBL] [Abstract][Full Text] [Related]
4. Diagnostic clinical genome and exome sequencing.
Biesecker LG; Green RC
N Engl J Med; 2014 Jun; 370(25):2418-25. PubMed ID: 24941179
[No Abstract] [Full Text] [Related]
5. Reanalysis of Clinical Exome Sequencing Data.
Liu P; Meng L; Normand EA; Xia F; Song X; Ghazi A; Rosenfeld J; Magoulas PL; Braxton A; Ward P; Dai H; Yuan B; Bi W; Xiao R; Wang X; Chiang T; Vetrini F; He W; Cheng H; Dong J; Gijavanekar C; Benke PJ; Bernstein JA; Eble T; Eroglu Y; Erwin D; Escobar L; Gibson JB; Gripp K; Kleppe S; Koenig MK; Lewis AM; Natowicz M; Mancias P; Minor L; Scaglia F; Schaaf CP; Streff H; Vernon H; Uhles CL; Zackai EH; Wu N; Sutton VR; Beaudet AL; Muzny D; Gibbs RA; Posey JE; Lalani S; Shaw C; Eng CM; Lupski JR; Yang Y
N Engl J Med; 2019 Jun; 380(25):2478-2480. PubMed ID: 31216405
[No Abstract] [Full Text] [Related]
6. Computational and statistical approaches to analyzing variants identified by exome sequencing.
Stitziel NO; Kiezun A; Sunyaev S
Genome Biol; 2011 Sep; 12(9):227. PubMed ID: 21920052
[TBL] [Abstract][Full Text] [Related]
7. Next-generation human genetics.
Shendure J
Genome Biol; 2011 Sep; 12(9):408. PubMed ID: 21920048
[TBL] [Abstract][Full Text] [Related]
8. Next-Generation Sequencing to Diagnose Suspected Genetic Disorders.
Adams DR; Eng CM
N Engl J Med; 2018 Oct; 379(14):1353-1362. PubMed ID: 30281996
[No Abstract] [Full Text] [Related]
9. Exome sequencing a review of new strategies for rare genomic disease research.
Brown TL; Meloche TM
Genomics; 2016 Oct; 108(3-4):109-114. PubMed ID: 27387609
[TBL] [Abstract][Full Text] [Related]
10. Genetic diagnosis through whole-exome sequencing.
Jacob HJ
N Engl J Med; 2014 Mar; 370(11):1069. PubMed ID: 24627900
[No Abstract] [Full Text] [Related]
11. Genetic diagnosis through whole-exome sequencing.
Rosen JM
N Engl J Med; 2014 Mar; 370(11):1068. PubMed ID: 24620875
[No Abstract] [Full Text] [Related]
12. Genetic diagnosis through whole-exome sequencing.
Friedman JM; Adam S
N Engl J Med; 2014 Mar; 370(11):1067-8. PubMed ID: 24620874
[No Abstract] [Full Text] [Related]
13. Genetic diagnosis through whole-exome sequencing.
van der Zwaag PA; Jongbloed JD; van Tintelen JP
N Engl J Med; 2014 Mar; 370(11):1067. PubMed ID: 24620873
[No Abstract] [Full Text] [Related]
14. Genetic diagnosis through whole-exome sequencing.
Eng CM; Yang Y; Plon SE
N Engl J Med; 2014 Mar; 370(11):1068. PubMed ID: 24620872
[No Abstract] [Full Text] [Related]
15. Exome sequencing: the expert view.
Biesecker LG; Shianna KV; Mullikin JC
Genome Biol; 2011 Sep; 12(9):128. PubMed ID: 21920051
[TBL] [Abstract][Full Text] [Related]
16. Clinical genetics: exomes in the clinic.
Flintoft L
Nat Rev Genet; 2013 Dec; 14(12):824. PubMed ID: 24145212
[No Abstract] [Full Text] [Related]
17. 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]
18. Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes.
Smith KR; Bromhead CJ; Hildebrand MS; Shearer AE; Lockhart PJ; Najmabadi H; Leventer RJ; McGillivray G; Amor DJ; Smith RJ; Bahlo M
Genome Biol; 2011 Sep; 12(9):R85. PubMed ID: 21917141
[TBL] [Abstract][Full Text] [Related]
19. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
LaDuca H; Farwell KD; Vuong H; Lu HM; Mu W; Shahmirzadi L; Tang S; Chen J; Bhide S; Chao EC
PLoS One; 2017; 12(2):e0170843. PubMed ID: 28152038
[TBL] [Abstract][Full Text] [Related]
20. Next-generation sequencing for clinical diagnostics.
Jacob HJ
N Engl J Med; 2013 Oct; 369(16):1557-8. PubMed ID: 24088040
[No Abstract] [Full Text] [Related]
[Next] [New Search]
