-
1
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium, et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447 7145 (2007) 661-678
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
The Wellcome Trust Case Control Consortium1
-
2
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R., Ishikawa S., Fitch K.R., et al. Global variation in copy number in the human genome. Nature 444 7118 (2006) 444-454
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
-
3
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
The International HapMap Consortium, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 449 7164 (2007) 851-861
-
(2007)
Nature
, vol.449
, Issue.7164
, pp. 851-861
-
-
The International HapMap Consortium1
-
4
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll S.A., Kuruvilla F.G., Korn J.M., et al. Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40 (2008) 1166-1174
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
-
5
-
-
57349087268
-
Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder
-
Mick E., Neale B., Middleton F.A., McGough J.J., and Faraone S.V. Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 147B (2008) 1412-1418
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1412-1418
-
-
Mick, E.1
Neale, B.2
Middleton, F.A.3
McGough, J.J.4
Faraone, S.V.5
-
6
-
-
67650261800
-
-
Affymetrix, Inc [http://www.affymetrix.com/index.affx].
-
Affymetrix, Inc [http://www.affymetrix.com/index.affx].
-
-
-
-
7
-
-
33644962095
-
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays
-
Lam CW, To KF, Tong SF. Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays. Clin Biochem 2006;39:187-190.
-
(2006)
Clin Biochem
, vol.39
, pp. 187-190
-
-
Lam, C.W.1
To, K.F.2
Tong, S.F.3
-
8
-
-
0035288338
-
Special features of non-melanoma skin cancer in Hong Kong Chinese patients: 10-year retrospective study
-
Cheng S.Y., Luk N.M., and Chong L.Y. Special features of non-melanoma skin cancer in Hong Kong Chinese patients: 10-year retrospective study. HKMJ 7 (2001) 22-28
-
(2001)
HKMJ
, vol.7
, pp. 22-28
-
-
Cheng, S.Y.1
Luk, N.M.2
Chong, L.Y.3
-
9
-
-
53749101271
-
Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals
-
Nishida N., Koike A., Tajima A., et al. Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals. BMC Genomics 9 (2008) 431
-
(2008)
BMC Genomics
, vol.9
, pp. 431
-
-
Nishida, N.1
Koike, A.2
Tajima, A.3
-
10
-
-
64049087230
-
Analysis of the DYSF mutational spectrum in a large cohort of patients
-
Krahn M., Béroud C., Labelle V., et al. Analysis of the DYSF mutational spectrum in a large cohort of patients. Hum Mutat 29 (2008) e345-375
-
(2008)
Hum Mutat
, vol.29
-
-
Krahn, M.1
Béroud, C.2
Labelle, V.3
-
11
-
-
55149090741
-
Ring chromosome 21 and reproductive pattern: a familial case and review of the literature
-
[2004.e1-5]
-
Bertini V., Valetto A., Uccelli A., Tarntino E., and Simi P. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature. Fertil Steril 90 (2008) [2004.e1-5]
-
(2008)
Fertil Steril
, vol.90
-
-
Bertini, V.1
Valetto, A.2
Uccelli, A.3
Tarntino, E.4
Simi, P.5
-
12
-
-
11944270642
-
DNA-based diagnosis of xeroderma pigmentosum group C by whole-genome scan using single-nucleotide polymorphism microarray
-
Lam C.W., Cheung K.K.T., Luk N.M., Chan S.W., Lo K.K., and Tong S.F. DNA-based diagnosis of xeroderma pigmentosum group C by whole-genome scan using single-nucleotide polymorphism microarray. J Invest Dermatol 124 (2005) 87-91
-
(2005)
J Invest Dermatol
, vol.124
, pp. 87-91
-
-
Lam, C.W.1
Cheung, K.K.T.2
Luk, N.M.3
Chan, S.W.4
Lo, K.K.5
Tong, S.F.6
-
13
-
-
33845903823
-
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: Standardization of molecular investigations of genetic diseases due to consanguinity
-
Lam CW, Tong SF, Wong K, et al. DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity. J Hum Genet 2007;52:98-101.
-
(2007)
J Hum Genet
, vol.52
, pp. 98-101
-
-
Lam, C.W.1
Tong, S.F.2
Wong, K.3
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