-
1
-
-
42149134184
-
Structural genomic variation in ischemic stroke
-
18288507
-
Matarin M Simon-Sanchez J Fung HC Scholz S Gibbs JR Hernandez DG Crews C Britton A Wavrant De Vrieze F Brott TG et al Structural genomic variation in ischemic stroke Neurogenetics 2008, 9(2):101-108. 18288507
-
(2008)
Neurogenetics
, vol.9
, Issue.2
, pp. 101-108
-
-
Matarin, M.1
Simon-Sanchez, J.2
Fung, H.C.3
Scholz, S.4
Gibbs, J.R.5
Hernandez, D.G.6
Crews, C.7
Britton, A.8
Wavrant De Vrieze, F.9
Brott, T.G.10
-
2
-
-
47649090861
-
Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population
-
Bae JS Cheong HS Kim JO Lee SO Kim EM Lee HW Kim S Kim JW Cui T Inoue I et al Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population Biochem Biophys Res Commun 2008.
-
(2008)
Biochem Biophys Res Commun
-
-
Bae, J.S.1
Cheong, H.S.2
Kim, J.O.3
Lee, S.O.4
Kim, E.M.5
Lee, H.W.6
Kim, S.7
Kim, J.W.8
Cui, T.9
Inoue, I.10
-
3
-
-
33749043929
-
Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders
-
17015230
-
Lee JA Lupski JR Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders Neuron 2006, 52(1):103-121. 17015230
-
(2006)
Neuron
, vol.52
, Issue.1
, pp. 103-121
-
-
Lee, J.A.1
Lupski, J.R.2
-
4
-
-
84871979029
-
SNPΠromoter: A database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions
-
2259403 18315851
-
Kim BC Kim WY Park D Chung WH Shin KS Bhak J SNPΠromoter: A database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions BMC Bioinformatics 2008, 9(Suppl 1):S2. 2259403 18315851
-
(2008)
BMC Bioinformatics
, vol.9
, Issue.SUPPL. 1
-
-
Kim, B.C.1
Kim, W.Y.2
Park, D.3
Chung, W.H.4
Shin, K.S.5
Bhak, J.6
-
5
-
-
33747864499
-
SNPΔomain: A web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences
-
(Web Server) 1538855 16845090
-
Han A Kang HJ Cho Y Lee S Kim YJ Gong S SNPΔomain: A web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences Nucleic Acids Res 2006, 34(Web Server :W642-644. 1538855 16845090
-
(2006)
Nucleic Acids Res
-
-
Han, A.1
Kang, H.J.2
Cho, Y.3
Lee, S.4
Kim, Y.J.5
Gong, S.6
-
6
-
-
0035895505
-
The sequence of the human genome
-
11181995
-
Venter JC Adams MD Myers EW Li PW Mural RJ Sutton GG Smith HO Yandell M Evans CA Holt RA et al The sequence of the human genome Science 2001, 291(5507):1304-1351. 11181995
-
(2001)
Science
, vol.291
, Issue.5507
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
-
7
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
12610532
-
Botstein D Risch N Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease Nat Genet 2003, 33(Suppl):228-237. 12610532
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
8
-
-
0345863927
-
The Unified Medical Language System (UMLS): Integrating biomedical terminology
-
(Database) 308795 14681409
-
Bodenreider O The Unified Medical Language System (UMLS): Integrating biomedical terminology Nucleic Acids Res 2004, 32(Database):D267-270. 308795 14681409
-
(2004)
Nucleic Acids Res
-
-
Bodenreider, O.1
-
9
-
-
13444266370
-
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
-
(Database) 539987 15608251
-
Hamosh A Scott AF Amberger JS Bocchini CA McKusick VA Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders Nucleic Acids Res 2005, 33(Database):D514-517. 539987 15608251
-
(2005)
Nucleic Acids Res
-
-
Hamosh, A.1
Scott, A.F.2
Amberger, J.S.3
Bocchini, C.A.4
McKusick, V.A.5
-
11
-
-
0031812897
-
The human gene mutation database
-
147254 9399854
-
Cooper DN Ball EV Krawczak M The human gene mutation database Nucleic Acids Res 1998, 26(1):285-287. 147254 9399854
-
(1998)
Nucleic Acids Res
, vol.26
, Issue.1
, pp. 285-287
-
-
Cooper, D.N.1
Ball, E.V.2
Krawczak, M.3
-
12
-
-
38549092091
-
Database resources of the National Center for Biotechnology Information
-
(Database). 2238880 18045790
-
Wheeler DL Barrett T Benson DA Bryant SH Canese K Chetvernin V Church DM Dicuccio M Edgar R Federhen S et al Database resources of the National Center for Biotechnology Information Nucleic Acids Res 2008, 36(Database):D13-21. 2238880 18045790
-
(2008)
Nucleic Acids Res
-
-
Wheeler, D.L.1
Barrett, T.2
Benson, D.A.3
Bryant, S.H.4
Canese, K.5
Chetvernin, V.6
Church, D.M.7
Dicuccio, M.8
Edgar, R.9
Federhen, S.10
-
15
-
-
33846078622
-
The UCSC genome browser database: Update 2007
-
(Database). 1669757 17142222
-
Kuhn RM Karolchik D Zweig AS Trumbower H Thomas DJ Thakkapallayil A Sugnet CW Stanke M Smith KE Siepel A et al The UCSC genome browser database: Update 2007 Nucleic Acids Res 2007, 35(Database):D668-673. 1669757 17142222
-
(2007)
Nucleic Acids Res
-
-
Kuhn, R.M.1
Karolchik, D.2
Zweig, A.S.3
Trumbower, H.4
Thomas, D.J.5
Thakkapallayil, A.6
Sugnet, C.W.7
Stanke, M.8
Smith, K.E.9
Siepel, A.10
-
16
-
-
0029919773
-
A World Wide Web (WWW) server database engine for an organelle database, MitoDat
-
8740181
-
Lemkin PF Chipperfield M Merril C Zullo S A World Wide Web (WWW) server database engine for an organelle database, MitoDat Electrophoresis 1996, 17(3):566-572. 8740181
-
(1996)
Electrophoresis
, vol.17
, Issue.3
, pp. 566-572
-
-
Lemkin, P.F.1
Chipperfield, M.2
Merril, C.3
Zullo, S.4
-
18
-
-
0036087166
-
JSNP: A database of common gene variations in the Japanese population
-
99126 11752280
-
Hirakawa M Tanaka T Hashimoto Y Kuroda M Takagi T Nakamura Y JSNP: A database of common gene variations in the Japanese population Nucleic Acids Res 2002, 30(1):158-162. 99126 11752280
-
(2002)
Nucleic Acids Res
, vol.30
, Issue.1
, pp. 158-162
-
-
Hirakawa, M.1
Tanaka, T.2
Hashimoto, Y.3
Kuroda, M.4
Takagi, T.5
Nakamura, Y.6
-
19
-
-
0037250633
-
ALFRED: The ALelle FREquency Database
-
165490 12519999
-
Rajeevan H Osier MV Cheung KH Deng H Druskin L Heinzen R Kidd JR Stein S Pakstis AJ Tosches NP et al ALFRED: The ALelle FREquency Database. Update Nucleic Acids Res 2003, 31(1):270-271. 165490 12519999
-
(2003)
Update Nucleic Acids Res
, vol.31
, Issue.1
, pp. 270-271
-
-
Rajeevan, H.1
Osier, M.V.2
Cheung, K.H.3
Deng, H.4
Druskin, L.5
Heinzen, R.6
Kidd, J.R.7
Stein, S.8
Pakstis, A.J.9
Tosches, N.P.10
-
21
-
-
38649091045
-
Predicting the phenotypic effects of non-synonymous single nucleotide polymorphisms based on support vector machines
-
2216041 18005451
-
Tian J Wu N Guo X Guo J Zhang J Fan Y Predicting the phenotypic effects of non-synonymous single nucleotide polymorphisms based on support vector machines BMC Bioinformatics 2007, 8:450. 2216041 18005451
-
(2007)
BMC Bioinformatics
, vol.8
, pp. 450
-
-
Tian, J.1
Wu, N.2
Guo, X.3
Guo, J.4
Zhang, J.5
Fan, Y.6
-
22
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
168916 12824425
-
Ng PC Henikoff S SIFT: Predicting amino acid changes that affect protein function Nucleic Acids Res 2003, 31(13):3812-3814. 168916 12824425
-
(2003)
Nucleic Acids Res
, vol.31
, Issue.13
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
24
-
-
18644378331
-
The Generic Genome Browser: A Building Block for a Model Organism System Database
-
187535 12368253
-
Stein LD Mungall C Shu S Caudy M Mangone M Day A Nickerson E Stajich JE Harris TW Arva A et al The Generic Genome Browser: A Building Block for a Model Organism System Database Genome Res 2002, 12:1599-1610. 187535 12368253
-
(2002)
Genome Res
, vol.12
, pp. 1599-1610
-
-
Stein, L.D.1
Mungall, C.2
Shu, S.3
Caudy, M.4
Mangone, M.5
Day, A.6
Nickerson, E.7
Stajich, J.E.8
Harris, T.W.9
Arva, A.10
-
25
-
-
34248201577
-
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24
-
17122114
-
Abu A Frydman M Marek D Pras E Stolovitch C Aviram-Goldring A Rienstein S Reznik-Wolf H Pras E Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24 Investigative ophthalmology & visual science 2006, 47(12):5283-5287. 17122114
-
(2006)
Investigative Ophthalmology & Visual Science
, vol.47
, Issue.12
, pp. 5283-5287
-
-
Abu, A.1
Frydman, M.2
Marek, D.3
Pras, E.4
Stolovitch, C.5
Aviram-Goldring, A.6
Rienstein, S.7
Reznik-Wolf, H.8
Pras, E.9
-
26
-
-
0037982811
-
Metabolic effects of the Gly1057Asp polymorphism in IRS-2 and interactions with obesity
-
12765968
-
Stefan N Kovacs P Stumvoll M Hanson RL Lehn-Stefan A Permana PA Baier LJ Tataranni PA Silver K Bogardus C Metabolic effects of the Gly1057Asp polymorphism in IRS-2 and interactions with obesity Diabetes 2003, 52(6):1544-1550. 12765968
-
(2003)
Diabetes
, vol.52
, Issue.6
, pp. 1544-1550
-
-
Stefan, N.1
Kovacs, P.2
Stumvoll, M.3
Hanson, R.L.4
Lehn-Stefan, A.5
Permana, P.A.6
Baier, L.J.7
Tataranni, P.A.8
Silver, K.9
Bogardus, C.10
|