-
1
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat, 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
-
2
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate, A.J. 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
-
3
-
-
20544462642
-
Segmental duplications and copy-number variation in the human genome
-
Sharp, A.J. 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
-
4
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
Tuzun, E. 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
-
5
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium. A haplotype map of the human genome. Nature 437, 1299-1320 (2005).
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
6
-
-
0020656122
-
Deletion mapping of polymorphic loci by apparent parental exclusion
-
Daiger, S.P. & Chakravarti, A. Deletion mapping of polymorphic loci by apparent parental exclusion. Am. J. Med. Genet. 14, 43-48 (1983).
-
(1983)
Am. J. Med. Genet.
, vol.14
, pp. 43-48
-
-
Daiger, S.P.1
Chakravarti, A.2
-
7
-
-
0027509953
-
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
-
Chance, P.F. et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 72, 143-151 (1993).
-
(1993)
Cell
, vol.72
, pp. 143-151
-
-
Chance, P.F.1
-
8
-
-
0037047628
-
Recent segmental duplications in the human genome
-
Bailey, J.A. et al. Recent segmental duplications in the human genome. Science 297, 1003-1007 (2002).
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
-
9
-
-
0010325553
-
Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion
-
Seidegard, J., Vorachek, W.R., Pero, R.W. & Pearson, W.R. Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion. Proc. Natl. Acad. Sci. USA 85, 7293-7297 (1988).
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 7293-7297
-
-
Seidegard, J.1
Vorachek, W.R.2
Pero, R.W.3
Pearson, W.R.4
-
10
-
-
7144257874
-
A new deleted allele in the human cytochrome P450 2A6 (CYP2A6) gene found in individuals showing poor metabolic capacity to coumarin and (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502)
-
Nunoya, K. et al. A new deleted allele in the human cytochrome P450 2A6 (CYP2A6) gene found in individuals showing poor metabolic capacity to coumarin and (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502). Pharmacogenetics 8, 239-249 (1998).
-
(1998)
Pharmacogenetics
, vol.8
, pp. 239-249
-
-
Nunoya, K.1
-
11
-
-
0028231093
-
Human glutathione S-transferase theta (GSTT1): cDNA cloning and the characterization of a genetic polymorphism
-
Pemble, S. et al. Human glutathione S-transferase theta (GSTT1): cDNA cloning and the characterization of a genetic polymorphism. Biochem. J. 300, 271-276 (1994).
-
(1994)
Biochem. J.
, vol.300
, pp. 271-276
-
-
Pemble, S.1
-
12
-
-
4744338923
-
Characterization of a common deletion polymorphism of the UGT2B17 gene linked to UGT2B15
-
Wilson, W. et al. Characterization of a common deletion polymorphism of the UGT2B17 gene linked to UGT2B15. Genomics 84, 707-714 (2005).
-
(2005)
Genomics
, vol.84
, pp. 707-714
-
-
Wilson, W.1
-
13
-
-
8844244726
-
Genetic inheritance of gene expression in human cell lines
-
Monks, S.A. et al. Genetic inheritance of gene expression in human cell lines. Am. J. Hum. Genet. 75, 1094-1105 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 1094-1105
-
-
Monks, S.A.1
-
14
-
-
4043128071
-
Genetic analysis of genome-wide variation in human gene expression
-
Morley, M. et al. Genetic analysis of genome-wide variation in human gene expression. Nature 430, 743-747 (2004).
-
(2004)
Nature
, vol.430
, pp. 743-747
-
-
Morley, M.1
-
15
-
-
27644439141
-
Efficiency and power in genetic association studies
-
in the press
-
de Bakker, P.W. et al. Efficiency and power in genetic association studies. Nat. Genet. (in the press).
-
Nat. Genet.
-
-
De Bakker, P.W.1
-
16
-
-
29444441336
-
A high-resolution survey of deletion polymorphism in the human genome
-
advance online publication 4 December doi:10.1038/ng1697
-
Conrad, D.F., Andrews, T.D., Carter, N.P., Hurles, M.E. & Pritchard, J.K. A high-resolution survey of deletion polymorphism in the human genome. Nat. Genet., advance online publication 4 December 2005 (doi:10.1038/ng1697).
-
(2005)
Nat. Genet.
-
-
Conrad, D.F.1
Andrews, T.D.2
Carter, N.P.3
Hurles, M.E.4
Pritchard, J.K.5
-
17
-
-
29444450702
-
Common deletions and SNPs are in linkage disequilibrium in the human genome
-
advance online publication 4 December doi:10.1038/ng1695
-
Hinds, D.A., Kloek, A.P. & Frazer, K.A. Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat. Genet., advance online publication 4 December 2005 (doi:10.1038/ng1695).
-
(2005)
Nat. Genet.
-
-
Hinds, D.A.1
Kloek, A.P.2
Frazer, K.A.3
-
18
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett, J.C. et al. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics 21, 263-265 (2005).
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
-
19
-
-
37149014152
-
-
Thesis, Massachusetts Institute of Technology
-
Fry, B. Computational Information Design. Thesis, Massachusetts Institute of Technology (2005).
-
(2005)
Computational Information Design
-
-
Fry, B.1
|