135 related articles for article (PubMed ID: 21923095)
1. Ayurgenomics: a new way of threading molecular variability for stratified medicine.
Sethi TP; Prasher B; Mukerji M
ACS Chem Biol; 2011 Sep; 6(9):875-80. PubMed ID: 21923095
[No Abstract] [Full Text] [Related]
2. So similar, yet so different.
Check Hayden E
Nature; 2007 Oct; 449(7164):762-3. PubMed ID: 17968406
[No Abstract] [Full Text] [Related]
3. Human genomics: disclosure of variation.
Nielsen R
Nature; 2005 Mar; 434(7031):288-9. PubMed ID: 15772636
[No Abstract] [Full Text] [Related]
4. Genomics. Genetic association by whole-genome analysis?
Kwok PY
Science; 2001 Nov; 294(5547):1669-70. PubMed ID: 11721042
[No Abstract] [Full Text] [Related]
5. Genomics is not enough.
Chakravarti A
Science; 2011 Oct; 334(6052):15. PubMed ID: 21980079
[No Abstract] [Full Text] [Related]
6. Variety of life.
Nature; 2015 Oct; 526(7571):5-6. PubMed ID: 26432202
[No Abstract] [Full Text] [Related]
7. Completing the map of human genetic variation.
; Eichler EE; Nickerson DA; Altshuler D; Bowcock AM; Brooks LD; Carter NP; Church DM; Felsenfeld A; Guyer M; Lee C; Lupski JR; Mullikin JC; Pritchard JK; Sebat J; Sherry ST; Smith D; Valle D; Waterston RH
Nature; 2007 May; 447(7141):161-5. PubMed ID: 17495918
[No Abstract] [Full Text] [Related]
8. Sequencing errors or SNPs at splice-acceptor guanines in dbSNP?
Platzer M; Hiller M; Szafranski K; Jahn N; Hampe J; Schreiber S; Backofen R; Huse K
Nat Biotechnol; 2006 Sep; 24(9):1068-70. PubMed ID: 16964207
[No Abstract] [Full Text] [Related]
9. Genomics: the personal side of genomics.
Blow N
Nature; 2007 Oct; 449(7162):627-30. PubMed ID: 17914399
[No Abstract] [Full Text] [Related]
10. Genomics: Encyclopaedia of humble DNA.
Greally JM
Nature; 2007 Jun; 447(7146):782-3. PubMed ID: 17568731
[No Abstract] [Full Text] [Related]
11. Common sense for our genomes.
Brenner SE
Nature; 2007 Oct; 449(7164):783-4. PubMed ID: 17943102
[No Abstract] [Full Text] [Related]
12. Genomics: The tough new variants.
Nature; 2010 Oct; 467(7319):1136. PubMed ID: 20981104
[No Abstract] [Full Text] [Related]
13. Determination of the clinical significance of an unclassified variant.
Zhang VW; Wang J
Methods Mol Biol; 2012; 837():337-48. PubMed ID: 22215559
[TBL] [Abstract][Full Text] [Related]
14. What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?
Lango H; Weedon MN
J Intern Med; 2008 Jan; 263(1):16-27. PubMed ID: 18088250
[TBL] [Abstract][Full Text] [Related]
15. Human genome variation in health and in neuropsychiatric disorders.
Buretić-Tomljanović A; Tomljanović D
Psychiatr Danub; 2009 Dec; 21(4):562-9. PubMed ID: 19935494
[TBL] [Abstract][Full Text] [Related]
16. Systems medicine and metabolic modelling.
Mardinoglu A; Nielsen J
J Intern Med; 2012 Feb; 271(2):142-54. PubMed ID: 22142312
[TBL] [Abstract][Full Text] [Related]
17. Genome studies: genetics by numbers.
Baker M
Nature; 2008 Jan; 451(7178):516-8. PubMed ID: 18235474
[No Abstract] [Full Text] [Related]
18. How to get the most from a gene test.
Check Hayden E
Nature; 2008 Nov; 456(7218):11. PubMed ID: 18987699
[No Abstract] [Full Text] [Related]
19. The International HapMap Project.
International HapMap Consortium
Nature; 2003 Dec; 426(6968):789-96. PubMed ID: 14685227
[TBL] [Abstract][Full Text] [Related]
20. Genomics: The search for association.
Baker M
Nature; 2010 Oct; 467(7319):1135-8. PubMed ID: 20981103
[No Abstract] [Full Text] [Related]
[Next] [New Search]
