-
1
-
-
4444375366
-
As normal as normal can be?
-
Carter NP: As normal as normal can be? Nat Genet 36:931-932 (2004).
-
(2004)
Nat Genet
, vol.36
, pp. 931-932
-
-
Carter, N.P.1
-
2
-
-
27144485366
-
Human genome: Patchwork people
-
Check E: Human genome: patchwork people. Nature 437:1084-1086 (2005).
-
(2005)
Nature
, vol.437
, pp. 1084-1086
-
-
Check, E.1
-
3
-
-
0037837485
-
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence
-
Cheung J, Estivill X, Khaja R, MacDonald JR, Lau K, et al: Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Genome Biol 4:R25 (2003).
-
(2003)
Genome Biol
, vol.4
-
-
Cheung, J.1
Estivill, X.2
Khaja, R.3
MacDonald, J.R.4
Lau, K.5
-
4
-
-
0036107052
-
Time for a unified system of mutation description and reporting: A review of locus-specific mutation databases
-
Claustres M, Horaitis O, Vanevski M, Cotton RG: Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases. Genome Res 12:680-688 (2002).
-
(2002)
Genome Res
, vol.12
, pp. 680-688
-
-
Claustres, M.1
Horaitis, O.2
Vanevski, M.3
Cotton, R.G.4
-
5
-
-
29444441336
-
A high-resolution survey of deletion polymorphism in the human genome
-
Conrad DF, Andrews TD, Carter NP, Hurles ME, Pritchard JK: A high-resolution survey of deletion polymorphism in the human genome. Nat Genet 38:75-81 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 75-81
-
-
Conrad, D.F.1
Andrews, T.D.2
Carter, N.P.3
Hurles, M.E.4
Pritchard, J.K.5
-
6
-
-
29444438167
-
Widening the spectrum of human genetic variation
-
Eichler EE: Widening the spectrum of human genetic variation. Nat Genet 38:9-11 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 9-11
-
-
Eichler, E.E.1
-
8
-
-
33746363353
-
Structural variants: Changing the landscape of chromosomes and design of disease studies
-
Feuk L, Marshall CR, Wintle RF, Scherer SW: Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Genet 15 Spec No 1:R57-66 (2006b).
-
(2006)
Hum Mol Genet
, vol.15
, Issue.SPEC NO 1
-
-
Feuk, L.1
Marshall, C.R.2
Wintle, R.F.3
Scherer, S.W.4
-
9
-
-
3543040014
-
Complex SNP-related sequence variation in segmental genome duplications
-
Fredman D, White SJ, Potter S, Eichler EE, Dunnen JT, Brookes AJ: Complex SNP-related sequence variation in segmental genome duplications. Nat Genet 36:861-866 (2004).
-
(2004)
Nat Genet
, vol.36
, pp. 861-866
-
-
Fredman, D.1
White, S.J.2
Potter, S.3
Eichler, E.E.4
Dunnen, J.T.5
Brookes, A.J.6
-
10
-
-
33746741125
-
Copy number variation: New insights in genome diversity
-
Freeman JL, Perry GH, Feuk L, Redon R, McCarroll SA, et al: Copy number variation: new insights in genome diversity. Genome Res 16:949-961 (2006).
-
(2006)
Genome Res
, vol.16
, pp. 949-961
-
-
Freeman, J.L.1
Perry, G.H.2
Feuk, L.3
Redon, R.4
McCarroll, S.A.5
-
11
-
-
13444259868
-
The Molecular Biology Database Collection: 2005 Update
-
Galperin MY: The Molecular Biology Database Collection: 2005 update. Nucleic Acids Res 33:D5-24 (2005).
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Galperin, M.Y.1
-
12
-
-
20044377204
-
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
-
Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, et al: The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 307:1434-1440 (2005).
-
(2005)
Science
, vol.307
, pp. 1434-1440
-
-
Gonzalez, E.1
Kulkarni, H.2
Bolivar, H.3
Mangano, A.4
Sanchez, R.5
-
13
-
-
29444450702
-
Common deletions and SNPs are in linkage disequilibrium in the human genome
-
Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA: Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet 38:82-85 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 82-85
-
-
Hinds, D.A.1
Kloek, A.P.2
Jen, M.3
Chen, X.4
Frazer, K.A.5
-
14
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, et al: Detection of large-scale variation in the human genome. Nat Genet 36:949-951 (2004).
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
-
15
-
-
33745089349
-
Lafora progressive Myoclonus Epilepsy mutation database- EPM2A and NHLRC1 ( EMP2B ) genes
-
Ianzano L, Zhang J, Chan EM, Zhao XC, Lohi H, et al: Lafora progressive Myoclonus Epilepsy mutation database- EPM2A and NHLRC1 ( EMP2B ) genes. Hum Mutat 26:397 (2005).
-
(2005)
Hum Mutat
, vol.26
, pp. 397
-
-
Ianzano, L.1
Zhang, J.2
Chan, E.M.3
Zhao, X.C.4
Lohi, H.5
-
16
-
-
0037184794
-
Polymorphism of cytochrome P450 and xenobiotic toxicity
-
Ingelman-Sundberg M: Polymorphism of cytochrome P450 and xenobiotic toxicity. Toxicology 181-182:447-452 (2002).
-
(2002)
Toxicology
, vol.181-182
, pp. 447-452
-
-
Ingelman-Sundberg, M.1
-
17
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, et al: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821 (1992).
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
-
18
-
-
22844440839
-
Vive la difference!
-
Lee C: Vive la difference! Nat Genet 37:660-661 (2005).
-
(2005)
Nat Genet
, vol.37
, pp. 660-661
-
-
Lee, C.1
-
19
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, et al: Common deletion polymorphisms in the human genome. Nat Genet 38:86-92 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 86-92
-
-
McCarroll, S.A.1
Hadnott, T.N.2
Perry, G.H.3
Sabeti, P.C.4
Zody, M.C.5
-
20
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, et al: High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211 (1998).
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
-
21
-
-
0038756128
-
Human chromosome 7: DNA sequence and biology
-
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, et al: Human chromosome 7: DNA sequence and biology. Science 300:767-772 (2003).
-
(2003)
Science
, vol.300
, pp. 767-772
-
-
Scherer, S.W.1
Cheung, J.2
MacDonald, J.R.3
Osborne, L.R.4
Nakabayashi, K.5
-
22
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al: Large-scale copy number polymorphism in the human genome. Science 305:525-528 (2004).
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
-
23
-
-
20544462642
-
Segmental duplications and copy-number variation in the human genome
-
Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, et al: Segmental duplications and copy-number variation in the human genome. Am J Hum Genet 77:78-88 (2005).
-
(2005)
Am J Hum Genet
, vol.77
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
-
24
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
Tuzun E, Sharp AJ, Bailey JA, Kaul R, Morrison VA, et al: Fine-scale structural variation of the human genome. Nat Genet 37:727-732 (2005).
-
(2005)
Nat Genet
, vol.37
, pp. 727-732
-
-
Tuzun, E.1
Sharp, A.J.2
Bailey, J.A.3
Kaul, R.4
Morrison, V.A.5
|