308 related articles for article (PubMed ID: 20506564)
1. Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics.
Cooper DN; Chen JM; Ball EV; Howells K; Mort M; Phillips AD; Chuzhanova N; Krawczak M; Kehrer-Sawatzki H; Stenson PD
Hum Mutat; 2010 Jun; 31(6):631-55. PubMed ID: 20506564
[TBL] [Abstract][Full Text] [Related]
2. Revealing the human mutome.
Chen JM; Férec C; Cooper DN
Clin Genet; 2010 Oct; 78(4):310-20. PubMed ID: 20569258
[TBL] [Abstract][Full Text] [Related]
3. Comparative genomics for detecting human disease genes.
Moreno C; Lazar J; Jacob HJ; Kwitek AE
Adv Genet; 2008; 60():655-97. PubMed ID: 18358336
[TBL] [Abstract][Full Text] [Related]
4. Association of genes to genetically inherited diseases using data mining.
Perez-Iratxeta C; Bork P; Andrade MA
Nat Genet; 2002 Jul; 31(3):316-9. PubMed ID: 12006977
[TBL] [Abstract][Full Text] [Related]
5. Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genes.
Bjornsson HT; Ellingsen LM; Jonsson JJ
Gene; 2006 Mar; 370():43-50. PubMed ID: 16446059
[TBL] [Abstract][Full Text] [Related]
6. Human Gene Mutation Database (HGMD): 2003 update.
Stenson PD; Ball EV; Mort M; Phillips AD; Shiel JA; Thomas NS; Abeysinghe S; Krawczak M; Cooper DN
Hum Mutat; 2003 Jun; 21(6):577-81. PubMed ID: 12754702
[TBL] [Abstract][Full Text] [Related]
7. Progress in genome-wide association studies of human height.
Hirschhorn JN; Lettre G
Horm Res; 2009 Apr; 71 Suppl 2():5-13. PubMed ID: 19407491
[TBL] [Abstract][Full Text] [Related]
8. [Structural variation in the human genome contributes to variation of traits].
Barøy T; Misceo D; Frengen E
Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1951-5. PubMed ID: 18787571
[TBL] [Abstract][Full Text] [Related]
9. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
10. The mutome and the 100,000 mutation milestone.
Cotton RG
Hum Mutat; 2010 Jun; 31(6):v. PubMed ID: 20513140
[No Abstract] [Full Text] [Related]
11. Highly consistent patterns for inherited human diseases at the molecular level.
López-Bigas N; Blencowe BJ; Ouzounis CA
Bioinformatics; 2006 Feb; 22(3):269-77. PubMed ID: 16287936
[TBL] [Abstract][Full Text] [Related]
12. [Human genome project: a federator program of genomic medicine].
Sfar S; Chouchane L
Pathol Biol (Paris); 2008 May; 56(3):170-5. PubMed ID: 18325690
[TBL] [Abstract][Full Text] [Related]
13. Genome-based prediction of common diseases: advances and prospects.
Janssens AC; van Duijn CM
Hum Mol Genet; 2008 Oct; 17(R2):R166-73. PubMed ID: 18852206
[TBL] [Abstract][Full Text] [Related]
14. Variation in the human genome and the inherited basis of common disease.
Gabriel S
Semin Oncol; 2006 Dec; 33(6 Suppl 11):S46-9. PubMed ID: 17178287
[TBL] [Abstract][Full Text] [Related]
15. Genome annotation past, present, and future: how to define an ORF at each locus.
Brent MR
Genome Res; 2005 Dec; 15(12):1777-86. PubMed ID: 16339376
[TBL] [Abstract][Full Text] [Related]
16. Novel clinico-genome network modeling for revolutionizing genotype-phenotype-based personalized cancer care.
Roukos DH
Expert Rev Mol Diagn; 2010 Jan; 10(1):33-48. PubMed ID: 20014921
[TBL] [Abstract][Full Text] [Related]
17. Druggability of human disease genes.
Sakharkar MK; Sakharkar KR; Pervaiz S
Int J Biochem Cell Biol; 2007; 39(6):1156-64. PubMed ID: 17446117
[TBL] [Abstract][Full Text] [Related]
18. Genetic dissection of diseases: design and methods.
Hoh J; Ott J
Curr Opin Genet Dev; 2004 Jun; 14(3):229-32. PubMed ID: 15172663
[TBL] [Abstract][Full Text] [Related]
19. [Correction of five different types of errors of model REFSEQs appeared in NCBI human gene database only by using two novel human genes C17orf32 and ZNF362].
Zhang DL; Li YD; Ji L
Yi Chuan Xue Bao; 2004 Apr; 31(4):325-34. PubMed ID: 15487498
[TBL] [Abstract][Full Text] [Related]
20. CNVs of noncoding cis-regulatory elements in human disease.
Spielmann M; Klopocki E
Curr Opin Genet Dev; 2013 Jun; 23(3):249-56. PubMed ID: 23601627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]