251 related articles for article (PubMed ID: 17495918)
1. 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]
2. Human genomics: The end of the start for population sequencing.
Birney E; Soranzo N
Nature; 2015 Oct; 526(7571):52-3. PubMed ID: 26432243
[No Abstract] [Full Text] [Related]
3. So similar, yet so different.
Check Hayden E
Nature; 2007 Oct; 449(7164):762-3. PubMed ID: 17968406
[No Abstract] [Full Text] [Related]
4. 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]
5. Mapping a role for SNPs in drug development.
Rothberg BE
Nat Biotechnol; 2001 Mar; 19(3):209-11. PubMed ID: 11231544
[No Abstract] [Full Text] [Related]
6. Genomics: The search for association.
Baker M
Nature; 2010 Oct; 467(7319):1135-8. PubMed ID: 20981103
[No Abstract] [Full Text] [Related]
7. Understanding genome structural variations.
Abyzov A; Li S; Gerstein MB
Oncotarget; 2016 Feb; 7(7):7370-1. PubMed ID: 26657727
[No Abstract] [Full Text] [Related]
8. Human genomics: disclosure of variation.
Nielsen R
Nature; 2005 Mar; 434(7031):288-9. PubMed ID: 15772636
[No Abstract] [Full Text] [Related]
9. An integrated map of structural variation in 2,504 human genomes.
Sudmant PH; Rausch T; Gardner EJ; Handsaker RE; Abyzov A; Huddleston J; Zhang Y; Ye K; Jun G; Fritz MH; Konkel MK; Malhotra A; Stütz AM; Shi X; Casale FP; Chen J; Hormozdiari F; Dayama G; Chen K; Malig M; Chaisson MJP; Walter K; Meiers S; Kashin S; Garrison E; Auton A; Lam HYK; Mu XJ; Alkan C; Antaki D; Bae T; Cerveira E; Chines P; Chong Z; Clarke L; Dal E; Ding L; Emery S; Fan X; Gujral M; Kahveci F; Kidd JM; Kong Y; Lameijer EW; McCarthy S; Flicek P; Gibbs RA; Marth G; Mason CE; Menelaou A; Muzny DM; Nelson BJ; Noor A; Parrish NF; Pendleton M; Quitadamo A; Raeder B; Schadt EE; Romanovitch M; Schlattl A; Sebra R; Shabalin AA; Untergasser A; Walker JA; Wang M; Yu F; Zhang C; Zhang J; Zheng-Bradley X; Zhou W; Zichner T; Sebat J; Batzer MA; McCarroll SA; ; Mills RE; Gerstein MB; Bashir A; Stegle O; Devine SE; Lee C; Eichler EE; Korbel JO
Nature; 2015 Oct; 526(7571):75-81. PubMed ID: 26432246
[TBL] [Abstract][Full Text] [Related]
10. Mapping and sequencing of structural variation from eight human genomes.
Kidd JM; Cooper GM; Donahue WF; Hayden HS; Sampas N; Graves T; Hansen N; Teague B; Alkan C; Antonacci F; Haugen E; Zerr T; Yamada NA; Tsang P; Newman TL; Tüzün E; Cheng Z; Ebling HM; Tusneem N; David R; Gillett W; Phelps KA; Weaver M; Saranga D; Brand A; Tao W; Gustafson E; McKernan K; Chen L; Malig M; Smith JD; Korn JM; McCarroll SA; Altshuler DA; Peiffer DA; Dorschner M; Stamatoyannopoulos J; Schwartz D; Nickerson DA; Mullikin JC; Wilson RK; Bruhn L; Olson MV; Kaul R; Smith DR; Eichler EE
Nature; 2008 May; 453(7191):56-64. PubMed ID: 18451855
[TBL] [Abstract][Full Text] [Related]
11. Human genetics: Individual genomes diversify.
Levy S; Strausberg RL
Nature; 2008 Nov; 456(7218):49-51. PubMed ID: 18987731
[No Abstract] [Full Text] [Related]
12. Genomic copy number variation, human health, and disease.
Wain LV; Armour JA; Tobin MD
Lancet; 2009 Jul; 374(9686):340-50. PubMed ID: 19535135
[TBL] [Abstract][Full Text] [Related]
13. Legal row looms for gene-map firm.
Dalton R
Nature; 2003 May; 423(6939):470. PubMed ID: 12774085
[No Abstract] [Full Text] [Related]
14. Genomics. Genetic association by whole-genome analysis?
Kwok PY
Science; 2001 Nov; 294(5547):1669-70. PubMed ID: 11721042
[No Abstract] [Full Text] [Related]
15. Epigenomic annotation of genetic variants using the Roadmap Epigenome Browser.
Zhou X; Li D; Zhang B; Lowdon RF; Rockweiler NB; Sears RL; Madden PA; Smirnov I; Costello JF; Wang T
Nat Biotechnol; 2015 Apr; 33(4):345-6. PubMed ID: 25690851
[No Abstract] [Full Text] [Related]
16. A haplotype map of the human genome.
Olivier M
Physiol Genomics; 2003 Mar; 13(1):3-9. PubMed ID: 12644628
[No Abstract] [Full Text] [Related]
17. Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
Li MJ; Yan B; Sham PC; Wang J
Brief Bioinform; 2015 May; 16(3):393-412. PubMed ID: 24916300
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Human gene variation: from SNPs to phenotypes.
Ladiges W; Kemp C; Packenham J; Velazquez J
Mutat Res; 2004 Jan; 545(1-2):131-9. PubMed ID: 14698423
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
