-
1
-
-
84892554874
-
-
Affymetrix. BRLMM: An Improved Genotype Calling Method for the GeneChip Human Mapping 500K Array Set.
-
Affymetrix. 2006. BRLMM: An Improved Genotype Calling Method for the GeneChip Human Mapping 500K Array Set. http://media.affymetrix.com/support/technical/whitepapers/brlmm_whitepaper.pdf.
-
(2006)
-
-
-
2
-
-
0026766161
-
Genetic and clinical correlations of Xp21 muscular dystrophy
-
Bushby KM. 1992. Genetic and clinical correlations of Xp21 muscular dystrophy. J Inherit Metab Dis 15:551-564.
-
(1992)
J Inherit Metab Dis
, vol.15
, pp. 551-564
-
-
Bushby, K.M.1
-
3
-
-
84871969762
-
Large-scale association analysis identifies new risk loci for coronary artery disease
-
CARDIoGRAMplusC4D, and others.
-
CARDIoGRAMplusC4D, Consortium Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J and others. 2013. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet 45:25-33.
-
(2013)
Nat Genet
, vol.45
, pp. 25-33
-
-
Consortium Deloukas, P.1
Kanoni, S.2
Willenborg, C.3
Farrall, M.4
Assimes, T.L.5
Thompson, J.R.6
Ingelsson, E.7
Saleheen, D.8
Erdmann, J.9
-
4
-
-
34147136617
-
Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data
-
Carvalho B, Bengtsson H, Speed TP, Irizarry RA. 2007. Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data. Biostatistics 8:485-499.
-
(2007)
Biostatistics
, vol.8
, pp. 485-499
-
-
Carvalho, B.1
Bengtsson, H.2
Speed, T.P.3
Irizarry, R.A.4
-
5
-
-
52449118475
-
Testing for association on the X chromosome
-
Clayton D. 2008. Testing for association on the X chromosome. Biostatistics 9:593-600.
-
(2008)
Biostatistics
, vol.9
, pp. 593-600
-
-
Clayton, D.1
-
6
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Tregouet DA and others. 2009. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 41:280-282.
-
(2009)
Nat Genet
, vol.41
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
König, I.R.4
Hengstenberg, C.5
Hall, A.S.6
Linsel-Nitschke, P.7
Kathiresan, S.8
Wright, B.9
Tregouet, D.A.10
-
7
-
-
52949089727
-
GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population
-
Giannoulatou E, Yau C, Colella S, Ragoussis J, Holmes CC. 2008. GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population. Bioinformatics 24:2209-2214.
-
(2008)
Bioinformatics
, vol.24
, pp. 2209-2214
-
-
Giannoulatou, E.1
Yau, C.2
Colella, S.3
Ragoussis, J.4
Holmes, C.C.5
-
8
-
-
80054722416
-
X chromosome association testing in genome wide association studies
-
Hickey PF, Bahlo M. 2011. X chromosome association testing in genome wide association studies. Genet Epidemiol 35:664-670.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 664-670
-
-
Hickey, P.F.1
Bahlo, M.2
-
9
-
-
84892558254
-
-
A Catalog of Published Genome-Wide Association Studies
-
Hindorff L, MacArthur J, Morales J, Junkins H, Hall P, Klemm A, Manolio T. 2013. A Catalog of Published Genome-Wide Association Studies. www.genome.gov/gwastudies.
-
(2013)
-
-
Hindorff, L.1
MacArthur, J.2
Morales, J.3
Junkins, H.4
Hall, P.5
Klemm, A.6
Manolio, T.7
-
10
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR. 2012. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet 44:955-959.
-
(2012)
Nat Genet
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
11
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. 2009. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5:e1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
12
-
-
0025881976
-
Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy
-
Ionasescu VV, Trofatter J, Haines JL, Summers AM, Ionasescu R, Searby C. 1991. Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy. Am J Hum Genet 48:1075-1083.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 1075-1083
-
-
Ionasescu, V.V.1
Trofatter, J.2
Haines, J.L.3
Summers, A.M.4
Ionasescu, R.5
Searby, C.6
-
13
-
-
84892538301
-
-
Artificial intelligence and global normalization methods for genotyping.
-
Kermani B. 2008. Artificial intelligence and global normalization methods for genotyping. http://www.patentstorm.us/patents/7467117/fulltext.html.
-
(2008)
-
-
Kermani, B.1
-
14
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
Korn JM, Kuruvilla FG, McCarroll SA, Wysoker A, Nemesh J, Cawley S, Hubbell E, Veitch J, Collins PJ, Darvishi K and others. 2008. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 40:1253-1260.
-
(2008)
Nat Genet
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
Kuruvilla, F.G.2
McCarroll, S.A.3
Wysoker, A.4
Nemesh, J.5
Cawley, S.6
Hubbell, E.7
Veitch, J.8
Collins, P.J.9
Darvishi, K.10
-
15
-
-
77956242566
-
Quality control and quality assurance in genotypic data for genome-wide association studies
-
Laurie CC, Doheny KF, Mirel DB, Pugh EW, Bierut LJ, Bhangale T, Boehm F, Caporaso NE, Cornelis MC, Edenberg HJ and others. 2010. Quality control and quality assurance in genotypic data for genome-wide association studies. Genet Epidemiol 34:591-602.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 591-602
-
-
Laurie, C.C.1
Doheny, K.F.2
Mirel, D.B.3
Pugh, E.W.4
Bierut, L.J.5
Bhangale, T.6
Boehm, F.7
Caporaso, N.E.8
Cornelis, M.C.9
Edenberg, H.J.10
-
16
-
-
71449112014
-
Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data
-
Ling H, Hetrick K, Bailey-Wilson JE, Pugh EW. 2009. Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data. BMC Proc 3:S57.
-
(2009)
BMC Proc
, vol.3
-
-
Ling, H.1
Hetrick, K.2
Bailey-Wilson, J.E.3
Pugh, E.W.4
-
17
-
-
84892527335
-
Association of X chromosomal variants with coronary heart disease: Results from a meta-analysis. Abstracts from the annual meeting of the International Genetic Epidemiology Society
-
Loley C, Schunkert H, Erdmann J, König IR. 2012. Association of X chromosomal variants with coronary heart disease: Results from a meta-analysis. Abstracts from the annual meeting of the International Genetic Epidemiology Society. Genet Epidemiol 36:720-727.
-
(2012)
Genet Epidemiol
, vol.36
, pp. 720-727
-
-
Loley, C.1
Schunkert, H.2
Erdmann, J.3
König, I.R.4
-
18
-
-
79851513063
-
Association tests for X-chromosomal markers-a comparison of different test statistics
-
Loley C, Ziegler A, König IR. 2011. Association tests for X-chromosomal markers-a comparison of different test statistics. Hum Hered 71:23-36.
-
(2011)
Hum Hered
, vol.71
, pp. 23-36
-
-
Loley, C.1
Ziegler, A.2
König, I.R.3
-
19
-
-
0035822038
-
The hemophilias-from royal genes to gene therapy
-
Mannucci PM, Tuddenham EGD. 2001. The hemophilias-from royal genes to gene therapy. New Engl J Med 344:1773-1779.
-
(2001)
New Engl J Med
, vol.344
, pp. 1773-1779
-
-
Mannucci, P.M.1
Tuddenham, E.G.D.2
-
20
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B. 2010. Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499-511.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
21
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P. 2007. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39:906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
22
-
-
77952668959
-
Coffin-Lowry syndrome
-
Marques Pereira P, Schneider A, Pannetier S, Heron D, Hanauer A. 2010. Coffin-Lowry syndrome. Eur J Hum Genet 18:627-633.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 627-633
-
-
Marques Pereira, P.1
Schneider, A.2
Pannetier, S.3
Heron, D.4
Hanauer, A.5
-
23
-
-
34548292504
-
PLINK: a toolset for whole-genome association and population-based linkage analysis
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D, Maller J, Sklar P, de Bakker PIW, Daly MJ and others. 2007. PLINK: a toolset for whole-genome association and population-based linkage analysis. Am J Hum Genet 81:559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.W.9
Daly, M.J.10
-
24
-
-
84863304598
-
-
R Core Team for the R Foundation for Statistical Computing. Computing RFfS. Vienna, Austria.
-
R Core Team for the R Foundation for Statistical Computing. 2013. R: A Language and Environment for Statistical Computing. Computing RFfS. Vienna, Austria. http://www.R-project.org.
-
(2013)
R: A Language and Environment for Statistical Computing
-
-
-
25
-
-
79952330384
-
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips
-
Ritchie ME, Liu R, Carvalho BS, Irizarry RA. 2011. Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips. BMC Bioinformatics 12:68.
-
(2011)
BMC Bioinformatics
, vol.12
, pp. 68
-
-
Ritchie, M.E.1
Liu, R.2
Carvalho, B.S.3
Irizarry, R.A.4
-
26
-
-
34547623750
-
Genome-wide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann H-E and others. 2007. Genome-wide association analysis of coronary artery disease. N Engl J Med 357:443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.-E.10
-
27
-
-
33644974019
-
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase
-
Scheet P, Stephens M. 2006. A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet 78:629-644.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 629-644
-
-
Scheet, P.1
Stephens, M.2
-
28
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AFR, Barbalic M, Gieger C and others. 2011. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 43:333-338.
-
(2011)
Nat Genet
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
König, I.R.2
Kathiresan, S.3
Reilly, M.P.4
Assimes, T.L.5
Holm, H.6
Preuss, M.7
Stewart, A.F.R.8
Barbalic, M.9
Gieger, C.10
-
29
-
-
34547622688
-
Imputation-based analysis of association studies: candidate regions and quantitative traits
-
Servin B, Stephens M. 2007. Imputation-based analysis of association studies: candidate regions and quantitative traits. PLoS Genet 3:e114.
-
(2007)
PLoS Genet
, vol.3
-
-
Servin, B.1
Stephens, M.2
-
30
-
-
77649126348
-
Coronary heart disease in women: a challenge for the 21st century
-
Solimene MC. 2010. Coronary heart disease in women: a challenge for the 21st century. Clinics (Sao Paulo) 65:99-106.
-
(2010)
Clinics (Sao Paulo)
, vol.65
, pp. 99-106
-
-
Solimene, M.C.1
-
31
-
-
35748941336
-
A genotype calling algorithm for the Illumina BeadArray platform
-
Teo YY, Inouye M, Small KS, Gwilliam R, Deloukas P, Kwiatkowski DP, Clark TG. 2007. A genotype calling algorithm for the Illumina BeadArray platform. Bioinformatics 23:2741-2746.
-
(2007)
Bioinformatics
, vol.23
, pp. 2741-2746
-
-
Teo, Y.Y.1
Inouye, M.2
Small, K.S.3
Gwilliam, R.4
Deloukas, P.5
Kwiatkowski, D.P.6
Clark, T.G.7
-
32
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
The 1000 Genomes Project Consortium.
-
The 1000 Genomes Project Consortium. 2012. An integrated map of genetic variation from 1, 092 human genomes. Nature 491:56-65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
33
-
-
77956635151
-
Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2
-
Thye T, Vannberg FO, Wong SH, Owusu-Dabo E, Osei I, Gyapong J, Sirugo G, Sisay-Joof F, Enimil A, Chinbuah MA and others. 2010. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. Nat Genet 42:739-741.
-
(2010)
Nat Genet
, vol.42
, pp. 739-741
-
-
Thye, T.1
Vannberg, F.O.2
Wong, S.H.3
Owusu-Dabo, E.4
Osei, I.5
Gyapong, J.6
Sirugo, G.7
Sisay-Joof, F.8
Enimil, A.9
Chinbuah, M.A.10
-
34
-
-
84866524806
-
Genome-wide association study indicates two novel resistance loci for severe malaria
-
Timmann C, Thye T, Vens M, Evans J, May J, Ehmen C, Sievertsen J, Muntau B, Ruge G, Loag W and others. 2012. Genome-wide association study indicates two novel resistance loci for severe malaria. Nature 489:443-446.
-
(2012)
Nature
, vol.489
, pp. 443-446
-
-
Timmann, C.1
Thye, T.2
Vens, M.3
Evans, J.4
May, J.5
Ehmen, C.6
Sievertsen, J.7
Muntau, B.8
Ruge, G.9
Loag, W.10
-
35
-
-
79953165427
-
Quality control procedures for genome-wide association studies
-
Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G and others. 2011. Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet 68:1.19.1-1.19.18.
-
(2011)
Curr Protoc Hum Genet
, vol.68
, pp. 1191-11918
-
-
Turner, S.1
Armstrong, L.L.2
Bradford, Y.3
Carlson, C.S.4
Crawford, D.C.5
Crenshaw, A.T.6
de Andrade, M.7
Doheny, K.F.8
Haines, J.L.9
Hayes, G.10
-
36
-
-
84877306707
-
eXclusion: toward integrating the X chromosome in genome-wide association analyses
-
Wise AL, Gyi L, Manolio TA. 2013. eXclusion: toward integrating the X chromosome in genome-wide association analyses. Am J Hum Genet 92:643-647.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 643-647
-
-
Wise, A.L.1
Gyi, L.2
Manolio, T.A.3
-
37
-
-
0037725301
-
Choice of scores in trend tests for case-control studies of candidate-gene associations
-
Zheng G, Freidlin B, Li Z, Gastwirth JL. 2003. Choice of scores in trend tests for case-control studies of candidate-gene associations. Biomed J 45:335-348.
-
(2003)
Biomed J
, vol.45
, pp. 335-348
-
-
Zheng, G.1
Freidlin, B.2
Li, Z.3
Gastwirth, J.L.4
-
39
-
-
71449096845
-
Genome-wide association studies: quality control and population-based measures
-
Ziegler A. 2009. Genome-wide association studies: quality control and population-based measures. Genet Epidemiol 33(Suppl 1):S45-S50.
-
(2009)
Genet Epidemiol
, vol.33
, Issue.SUPPL 1
-
-
Ziegler, A.1
-
41
-
-
41149152918
-
Biostatistical aspects of genome-wide association studies
-
Ziegler A, König IR, Thompson JR. 2008. Biostatistical aspects of genome-wide association studies. Biomed J 50:8-28.
-
(2008)
Biomed J
, vol.50
, pp. 8-28
-
-
Ziegler, A.1
König, I.R.2
Thompson, J.R.3
|