-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97-101
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
3
-
-
0035163547
-
Extent and distribution of linkage disequilibrium in three genomic regions
-
Abecasis GR, Noguchi E, Heinzmann A, Traherne JA, Bhattacharyya S, Leaves NI, Anderson GG, Zhang Y, Lench NJ, Carey A, Cardon LR, Moffatt MF, Cookson WO (2001) Extent and distribution of linkage disequilibrium in three genomic regions. Am J Hum Genet 68:191-197
-
(2001)
Am J Hum Genet
, vol.68
, pp. 191-197
-
-
Abecasis, G.R.1
Noguchi, E.2
Heinzmann, A.3
Traherne, J.A.4
Bhattacharyya, S.5
Leaves, N.I.6
Anderson, G.G.7
Zhang, Y.8
Lench, N.J.9
Carey, A.10
Cardon, L.R.11
Moffatt, M.F.12
Cookson, W.O.13
-
4
-
-
0345350737
-
Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: Studies of the HLA class II loci
-
Arnheim N, Strange C, Erlich H (1985) Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci. Proc Natl Acad Sci USA 82:6970-6974
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 6970-6974
-
-
Arnheim, N.1
Strange, C.2
Erlich, H.3
-
5
-
-
0030763566
-
Association mapping of disease loci, by use of a pooled DNA genomic screen
-
Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G (1997) Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet 61:734-747
-
(1997)
Am J Hum Genet
, vol.61
, pp. 734-747
-
-
Barcellos, L.F.1
Klitz, W.2
Field, L.L.3
Tobias, R.4
Bowcock, A.M.5
Wilson, R.6
Nelson, M.P.7
Nagatomi, J.8
Thomson, G.9
-
6
-
-
0031949273
-
Genetic association mapping based on discordant sib pairs: The discordant-alleles test
-
Boehnke M, Langefeld CD (1998) Genetic association mapping based on discordant sib pairs: the discordant-alleles test. Am J Hum Genet 62:950-961
-
(1998)
Am J Hum Genet
, vol.62
, pp. 950-961
-
-
Boehnke, M.1
Langefeld, C.D.2
-
7
-
-
0034793167
-
A new nonparametric linkage statistic for mapping both qualitative and quantitative trait loci
-
Camp NJ, Gutin A, Abkevich V, Farnham JM, Cannon-Albright L, Thomas A (2001) A new nonparametric linkage statistic for mapping both qualitative and quantitative trait loci. Genet Epidemiol 21 Suppl 1:S461-S466
-
(2001)
Genet Epidemiol
, vol.21
, Issue.SUPPL. 1
-
-
Camp, N.J.1
Gutin, A.2
Abkevich, V.3
Farnham, J.M.4
Cannon-Albright, L.5
Thomas, A.6
-
8
-
-
0035257236
-
Association study designs for complex diseases
-
Cardon LR, Bell JI (2001) Association study designs for complex diseases. Nat Rev Genet 2:91-99
-
(2001)
Nat Rev Genet
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
9
-
-
0344091561
-
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans
-
Carlson CS, Eberle MA, Rieder MJ, Smith JD, Kruglyak L, Nickerson DA (2003) Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans. Nat Genet 33:518-521
-
(2003)
Nat Genet
, vol.33
, pp. 518-521
-
-
Carlson, C.S.1
Eberle, M.A.2
Rieder, M.J.3
Smith, J.D.4
Kruglyak, L.5
Nickerson, D.A.6
-
10
-
-
0034787677
-
Nonparametric linkage regression. II. Identification of influential pedigrees in tests for linkage
-
Davis CC, Brown WM, Lange EM, Rich SS, Langefeld CD (2001) Nonparametric linkage regression. II. Identification of influential pedigrees in tests for linkage. Genet Epidemiol 21 Suppl 1:S123-S129
-
(2001)
Genet Epidemiol
, vol.21
, Issue.SUPPL. 1
-
-
Davis, C.C.1
Brown, W.M.2
Lange, E.M.3
Rich, S.S.4
Langefeld, C.D.5
-
11
-
-
18444396271
-
A first-generation linkage disequilibrium map of human chromosome 22
-
Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, et al (2002) A first-generation linkage disequilibrium map of human chromosome 22. Nature 418: 544-548
-
(2002)
Nature
, vol.418
, pp. 544-548
-
-
Dawson, E.1
Abecasis, G.R.2
Bumpstead, S.3
Chen, Y.4
Hunt, S.5
Beare, D.M.6
Pabial, J.7
-
12
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D (2002) The structure of haplotype blocks in the human genome. Science 296: 2225-2229
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
13
-
-
0020618874
-
Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis
-
Go RC, King MC, Bailey-Wilson J, Elston RC, Lynch HT (1983) Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis. J Natl Cancer Inst 71:455-461
-
(1983)
J Natl Cancer Inst
, vol.71
, pp. 455-461
-
-
Go, R.C.1
King, M.C.2
Bailey-Wilson, J.3
Elston, R.C.4
Lynch, H.T.5
-
14
-
-
0023179663
-
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. I. Segregation analysis
-
Goldstein AM, Haile RW, Marazita ML, Paganini-Hill A (1987) A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. I. Segregation analysis. J Natl Cancer Inst 78:911-918
-
(1987)
J Natl Cancer Inst
, vol.78
, pp. 911-918
-
-
Goldstein, A.M.1
Haile, R.W.2
Marazita, M.L.3
Paganini-Hill, A.4
-
15
-
-
0000178021
-
The combination of linkage values and the calculation of distances between the loci of linked factors
-
Haldane JBS (1919) The combination of linkage values and the calculation of distances between the loci of linked factors. J Genet 8:299-309
-
(1919)
J Genet
, vol.8
, pp. 299-309
-
-
Haldane, J.B.S.1
-
16
-
-
0026680687
-
Closing in on a breast cancer gene on chromosome 17q
-
Hall JM, Friedman L, Guenther C, Lee MK, Weber JL, Black DM, King MC (1992) Closing in on a breast cancer gene on chromosome 17q. Am J Hum Genet 50:1235-1242
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1235-1242
-
-
Hall, J.M.1
Friedman, L.2
Guenther, C.3
Lee, M.K.4
Weber, J.L.5
Black, D.M.6
King, M.C.7
-
17
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, et al (2000) Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet 26:163-175
-
(2000)
Nat Genet
, vol.26
, pp. 163-175
-
-
Horikawa, Y.1
Oda, N.2
Cox, N.J.3
Li, X.4
Orho-Melander, M.5
Hara, M.6
Hinokio, Y.7
-
18
-
-
0037458815
-
Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide
-
Kim UK, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D (2003) Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 299:1221-1225
-
(2003)
Science
, vol.299
, pp. 1221-1225
-
-
Kim, U.K.1
Jorgenson, E.2
Coon, H.3
Leppert, M.4
Risch, N.5
Drayna, D.6
-
19
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong A, Cox NJ (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
20
-
-
85030889122
-
Association analysis: Within-sibship sampling variations and solutions
-
Li C, Boehnke M (2001) Association analysis: within-sibship sampling variations and solutions. Am J Hum Genet Suppl 69:A1319
-
(2001)
Am J Hum Genet Suppl
, vol.69
-
-
Li, C.1
Boehnke, M.2
-
21
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
Martin ER, Monks SA, Warren LL, Kaplan NL (2000) A test for linkage and association in general pedigrees: the pedigree disequilibrium test. Am J Hum Genet 67:146-154
-
(2000)
Am J Hum Genet
, vol.67
, pp. 146-154
-
-
Martin, E.R.1
Monks, S.A.2
Warren, L.L.3
Kaplan, N.L.4
-
22
-
-
0032969483
-
Optimal allele-sharing statistics for genetic mapping using affected relatives
-
McPeek MS (1999) Optimal allele-sharing statistics for genetic mapping using affected relatives. Genet Epidemiol 16:225-249
-
(1999)
Genet Epidemiol
, vol.16
, pp. 225-249
-
-
McPeek, M.S.1
-
23
-
-
0037168559
-
High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools
-
Mohlke KL, Erdos MR, Scott LJ, Fingerlin TE, Jackson AU, Silander K, Hollstein P, Boehnke M, Collins FS (2002) High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools. Proc Natl Acad Sci USA 99:16928-16933
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 16928-16933
-
-
Mohlke, K.L.1
Erdos, M.R.2
Scott, L.J.3
Fingerlin, T.E.4
Jackson, A.U.5
Silander, K.6
Hollstein, P.7
Boehnke, M.8
Collins, F.S.9
-
24
-
-
0036275126
-
BeadArray technology: Enabling an accurate, cost-effective approach to high-throughput genotyping
-
Oliphant A, Barker DL, Stuelpnagel JR, Chee MS (2002) BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques Suppl: 56-58, 60-61
-
(2002)
Biotechniques Suppl
, pp. 56-58
-
-
Oliphant, A.1
Barker, D.L.2
Stuelpnagel, J.R.3
Chee, M.S.4
-
25
-
-
0037098634
-
High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology
-
Olivier M, Chuang LM, Chang MS, Chen YT, Pei D, Ranade K, de Witte A, Allen J, Tran N, Curb D, Pratt R, Neefs H, de Arruda Indig M, Law S, Neri B, Wang L, Cox DR (2002) High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology. Nucleic Acids Res 30:e53
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Olivier, M.1
Chuang, L.M.2
Chang, M.S.3
Chen, Y.T.4
Pei, D.5
Ranade, K.6
De Witte, A.7
Allen, J.8
Tran, N.9
Curb, D.10
Pratt, R.11
Neefs, H.12
De Arruda Indig, M.13
Law, S.14
Neri, B.15
Wang, L.16
Cox, D.R.17
-
26
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR (2001) Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294:1719-1723
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
Nguyen, B.T.11
Norris, M.C.12
Sheehan, J.B.13
Shen, N.14
Stern, D.15
Stokowski, R.P.16
Thomas, D.J.17
Trulson, M.O.18
Vyas, K.R.19
Frazer, K.A.20
Fodor, S.P.21
Cox, D.R.22
more..
-
27
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch NJ (2000) Searching for genetic determinants in the new millennium. Nature 405:847-856
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
28
-
-
0032427048
-
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling
-
Risch N, Teng J (1998) The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling. Genome Res 8:1273-1288
-
(1998)
Genome Res
, vol.8
, pp. 1273-1288
-
-
Risch, N.1
Teng, J.2
-
29
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, et al (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409:928-933
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
-
30
-
-
0034972488
-
A survey of affected-sibship statistics for nonparametric linkage analysis
-
Sengul H, Weeks DE, Feingold E (2001) A survey of affected-sibship statistics for nonparametric linkage analysis. Am J Hum Genet 69:179-190
-
(2001)
Am J Hum Genet
, vol.69
, pp. 179-190
-
-
Sengul, H.1
Weeks, D.E.2
Feingold, E.3
-
31
-
-
0036077215
-
Powerful regression-based quantitative-trait linkage analysis of general pedigrees
-
Sham PC, Purcell S, Cherny SS, Abecasis GR (2002) Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet 71:238-253
-
(2002)
Am J Hum Genet
, vol.71
, pp. 238-253
-
-
Sham, P.C.1
Purcell, S.2
Cherny, S.S.3
Abecasis, G.R.4
-
32
-
-
0034994415
-
Evaluation of candidate genes in case-control studies: A statistical method to account for related subjects
-
Slager SL, Schaid DJ (2001) Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects. Am J Hum Genet 68:1457-1462
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1457-1462
-
-
Slager, S.L.1
Schaid, D.J.2
-
33
-
-
0031912715
-
A sibship test for linkage in the presence of association: The sib transmission/disequilibrium test
-
Spielman RS, Ewens WJ (1998) A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test. Am J Hum Genet 62:450-458
-
(1998)
Am J Hum Genet
, vol.62
, pp. 450-458
-
-
Spielman, R.S.1
Ewens, W.J.2
-
34
-
-
0035654137
-
Accessing genetic variation: Genotyping single nucleotide polymorphisms
-
Syvanen AC (2001) Accessing genetic variation: genotyping single nucleotide polymorphisms. Nat Rev Genet 2:930-942
-
(2001)
Nat Rev Genet
, vol.2
, pp. 930-942
-
-
Syvanen, A.C.1
-
35
-
-
3643136390
-
Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study
-
Valle T, Tuomilehto J, Bergman RN, Ghosh S, Hauser ER, Eriksson J, Nylund SJ, Kohtamaki K, Toivanen L, Vidgren G, Tuomilehto-Wolf E, Ehnholm C, Blaschak J, Langefeld CD, Watanabe RM, Magnuson V, Ally DS, Hagopian WA, Ross E, Buchanan TA, Collins F, Boehnke M (1998) Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study. Diabetes Care 21:949-958
-
(1998)
Diabetes Care
, vol.21
, pp. 949-958
-
-
Valle, T.1
Tuomilehto, J.2
Bergman, R.N.3
Ghosh, S.4
Hauser, E.R.5
Eriksson, J.6
Nylund, S.J.7
Kohtamaki, K.8
Toivanen, L.9
Vidgren, G.10
Tuomilehto-Wolf, E.11
Ehnholm, C.12
Blaschak, J.13
Langefeld, C.D.14
Watanabe, R.M.15
Magnuson, V.16
Ally, D.S.17
Hagopian, W.A.18
Ross, E.19
Buchanan, T.A.20
Collins, F.21
Boehnke, M.22
more..
-
36
-
-
0037173639
-
Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness
-
Van Eerdewegh P, Little RD, Dupuis J, Del Mastro RG, Falls K, Simon J, Torrey D, et al (2002) Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature 418:426-430
-
(2002)
Nature
, vol.418
, pp. 426-430
-
-
Van Eerdewegh, P.1
Little, R.D.2
Dupuis, J.3
Del Mastro, R.G.4
Falls, K.5
Simon, J.6
Torrey, D.7
-
37
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J (1994) A class of tests for linkage using affected pedigree members. Biometrics 50:118-127
-
(1994)
Biometrics
, vol.50
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
38
-
-
0034537609
-
High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)
-
Wolford JK, Blunt D, Ballecer C, Prochazka M (2000) High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC). Hum Genet 107:483-487
-
(2000)
Hum Genet
, vol.107
, pp. 483-487
-
-
Wolford, J.K.1
Blunt, D.2
Ballecer, C.3
Prochazka, M.4
|