-
1
-
-
0032729834
-
Genetic studies of autistic disorder and chromosome 7
-
Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Ayslworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. 1999. Genetic studies of autistic disorder and chromosome 7. Genomics 61:227-36.
-
(1999)
Genomics
, vol.61
, pp. 227-236
-
-
Ashley-Koch, A.1
Wolpert, C.M.2
Menold, M.M.3
Zaeem, L.4
Basu, S.5
Donnelly, S.L.6
Ravan, S.A.7
Powell, C.M.8
Qumsiyeh, M.B.9
Ayslworth, A.S.10
Vance, J.M.11
Gilbert, J.R.12
Wright, H.H.13
Abramson, R.K.14
DeLong, G.R.15
Cuccaro, M.L.16
Pericak-Vance, M.A.17
-
2
-
-
0019302053
-
Construction of a genetic linkage map in man using restriction fragment length polymorphisms
-
Botstein D, White RL, Skolnick MH, Davies RW. 1980. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet 32:314-31.
-
(1980)
Am J Hum Genet
, vol.32
, pp. 314-331
-
-
Botstein, D.1
White, R.L.2
Skolnick, M.H.3
Davies, R.W.4
-
3
-
-
0033358583
-
Long homozygous chromosomal segments in reference families from the Centre d'Etude du Polymorphisme Humain
-
Broman KW, Weber JL. 1999. Long homozygous chromosomal segments in reference families from the Centre d'Etude du Polymorphisme Humain. Am J Hum Genet 65:1489-92.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1489-1492
-
-
Broman, K.W.1
Weber, J.L.2
-
4
-
-
0033911004
-
Characterization of human crossover interference
-
Broman KW, Weber JL. 2000. Characterization of human crossover interference. Am J Hum Genet 66:1911-26.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1911-1926
-
-
Broman, K.W.1
Weber, J.L.2
-
5
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman KW, Murray JC, Sheffield VC, White RL, Weber JL. 1998. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet 63:861-9.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
6
-
-
0027514896
-
Molecular and statistical approaches to the detection and correction of errors in genotype databases
-
Brzustowicz LM, Mérette C, Xie X, Townsend L, Gilliam TC, Ott J. 1993. Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am J Hum Genet 53:1137-45.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1137-1145
-
-
Brzustowicz, L.M.1
Mérette, C.2
Xie, X.3
Townsend, L.4
Gilliam, T.C.5
Ott, J.6
-
7
-
-
0025942732
-
Influence of aberrant observations on high-resolution linkage analysis outcomes
-
Buetow KH. 1991. Influence of aberrant observations on high-resolution linkage analysis outcomes. Am J Hum Genet 49: 985-94.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 985-994
-
-
Buetow, K.H.1
-
8
-
-
0008771420
-
Gene frequencies in small populations of mutant Drosophilia
-
Buri P. 1956. Gene frequencies in small populations of mutant Drosophilia. Evolution 10:367-402.
-
(1956)
Evolution
, vol.10
, pp. 367-402
-
-
Buri, P.1
-
9
-
-
0022728801
-
Effects of misspecifying genetic parameters in lod score analysis
-
Clerget-Darpoux F, Bonaiti-Pellie C, Hochez J. 1986. Effects of misspecifying genetic parameters in lod score analysis. Biometrics 42:393-9.
-
(1986)
Biometrics
, vol.42
, pp. 393-399
-
-
Clerget-Darpoux, F.1
Bonaiti-Pellie, C.2
Hochez, J.3
-
10
-
-
0031003687
-
Alternative test for linkage between two loci
-
Cleves MA, Elston RC. 1997. Alternative test for linkage between two loci. Genet Epidemiol 14:117-31.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 117-131
-
-
Cleves, M.A.1
Elston, R.C.2
-
11
-
-
0014082426
-
Group inbreeding and coancestry
-
Cockerham CC. 1967. Group inbreeding and coancestry. Genetics 56:89-92.
-
(1967)
Genetics
, vol.56
, pp. 89-92
-
-
Cockerham, C.C.1
-
12
-
-
0002260099
-
Variance of gene frequencies
-
Cockerham CC. 1969. Variance of gene frequencies. Evolution 23:72-84.
-
(1969)
Evolution
, vol.23
, pp. 72-84
-
-
Cockerham, C.C.1
-
13
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES. 2001. High-resolution haplotype structure in the human genome. Nat Genet 29:229-32.
-
(2001)
Nat Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
14
-
-
0025280026
-
Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome
-
Dausset J, Cann H, Cohen D, Lathrop M, Lalouel JM, White R. 1990. Centre d'Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome. Genomics 6:575-7.
-
(1990)
Genomics
, vol.6
, pp. 575-577
-
-
Dausset, J.1
Cann, H.2
Cohen, D.3
Lathrop, M.4
Lalouel, J.M.5
White, R.6
-
15
-
-
0033711876
-
Bias in multipoint linkage analysis arising from map misspecification
-
Daw EW, Thompson EA, Wijsman EM. 2000. Bias in multipoint linkage analysis arising from map misspecification. Genet Epidemiol 19:366-80.
-
(2000)
Genet Epidemiol
, vol.19
, pp. 366-380
-
-
Daw, E.W.1
Thompson, E.A.2
Wijsman, E.M.3
-
16
-
-
0036444801
-
Map error reduction: Using genetic and sequence-based physical maps to order closely linked markers
-
DeWan AT, Parrado AR, Matise TC, Leal SM. 2002a. Map error reduction: using genetic and sequence-based physical maps to order closely linked markers. Hum Hered 54:34-44.
-
(2002)
Hum Hered
, vol.54
, pp. 34-44
-
-
DeWan, A.T.1
Parrado, A.R.2
Matise, T.C.3
Leal, S.M.4
-
17
-
-
0036139013
-
The map problem: A comparison of genetic and sequence-based physical maps
-
DeWan AT, Parrado AR, Matise TC, Leal SM. 2002b. The map problem: a comparison of genetic and sequence-based physical maps. Am J Hum Genet 70:101-7.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 101-107
-
-
DeWan, A.T.1
Parrado, A.R.2
Matise, T.C.3
Leal, S.M.4
-
18
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J. 1996. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-4.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
19
-
-
0023663060
-
A genetic linkage map of the human genome
-
Donis-Keller H, Green P, Helms C, Cartinhour S, Weiffenbach B, Stephens K, Keith TP, Bowden DW, Smith DR, Lander ES. 1987. A genetic linkage map of the human genome. Cell 51: 319-37.
-
(1987)
Cell
, vol.51
, pp. 319-337
-
-
Donis-Keller, H.1
Green, P.2
Helms, C.3
Cartinhour, S.4
Weiffenbach, B.5
Stephens, K.6
Keith, T.P.7
Bowden, D.W.8
Smith, D.R.9
Lander, E.S.10
-
20
-
-
0008603641
-
The interpretation of lod scores in linkage analysis
-
Edwards JH. 1976. The interpretation of lod scores in linkage analysis. HGM 3:289-93.
-
(1976)
HGM
, vol.3
, pp. 289-293
-
-
Edwards, J.H.1
-
21
-
-
0032870497
-
Exploring the dense mapping of a region of potential linkage in complex disease: An example in multiple sclerosis
-
Feakes R, Sawcer S, Chataway J, Coraddu F, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A. 1999. Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis. Genet Epidemiol 17:51-63.
-
(1999)
Genet Epidemiol
, vol.17
, pp. 51-63
-
-
Feakes, R.1
Sawcer, S.2
Chataway, J.3
Coraddu, F.4
Broadley, S.5
Gray, J.6
Jones, H.B.7
Clayton, D.8
Goodfellow, P.N.9
Compston, A.10
-
22
-
-
0036128504
-
Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers
-
Goddard KA, Wijsman EM 2002. Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Genet Epidemiol 22:205-20.
-
(2002)
Genet Epidemiol
, vol.22
, pp. 205-220
-
-
Goddard, K.A.1
Wijsman, E.M.2
-
23
-
-
0030964440
-
The effects of genotyping errors and interference on estimation of genetic distance
-
Goldstein DR, Zhao H, Speed TP. 1997. The effects of genotyping errors and interference on estimation of genetic distance. Hum Hered 47:86-100.
-
(1997)
Hum Hered
, vol.47
, pp. 86-100
-
-
Goldstein, D.R.1
Zhao, H.2
Speed, T.P.3
-
24
-
-
0034164617
-
Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters
-
Göring HH, Terwilliger JD. 2000. Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters. Am J Hum Genet 66:1298-309.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1298-1309
-
-
Göring, H.H.1
Terwilliger, J.D.2
-
25
-
-
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 8:229-309.
-
(1919)
J Genet
, vol.8
, pp. 229-309
-
-
Haldane, J.B.S.1
-
26
-
-
0032807294
-
Multipoint linkage analysis. A cautionary note
-
Halpern J, Whittemore AS. 1999. Multipoint linkage analysis. A cautionary note. Hum Hered 4:194-6.
-
(1999)
Hum Hered
, vol.4
, pp. 194-196
-
-
Halpern, J.1
Whittemore, A.S.2
-
27
-
-
18444402178
-
Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae. Federated States of Micronesia
-
Han Z, Heath SC, Shmulewitz D, Li W, Auerbach SB, Blundell ML, Lehner T, Ott J, Stoffel M, Friedman JM, Breslow JL. 2002. Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia. Am J Med Genet 110:234-42.
-
(2002)
Am J Med Genet
, vol.110
, pp. 234-242
-
-
Han, Z.1
Heath, S.C.2
Shmulewitz, D.3
Li, W.4
Auerbach, S.B.5
Blundell, M.L.6
Lehner, T.7
Ott, J.8
Stoffel, M.9
Friedman, J.M.10
Breslow, J.L.11
-
28
-
-
9044243415
-
A genome-wide search for non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
-
Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shepard JM, Williams SR, Risch N, Hinds D, Iwasaki N, Ogata M, Omori Y, Petzold C, Rietzch H, Schroder HE, Schulze J, Cox NJ, Menzel S, Boriraj VV, Chen X. 1996. A genome-wide search for non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet 13:161-6.
-
(1996)
Nat Genet
, vol.13
, pp. 161-166
-
-
Hanis, C.L.1
Boerwinkle, E.2
Chakraborty, R.3
Ellsworth, D.L.4
Concannon, P.5
Stirling, B.6
Morrison, V.A.7
Wapelhorst, B.8
Spielman, R.S.9
Gogolin-Ewens, K.J.10
Shepard, J.M.11
Williams, S.R.12
Risch, N.13
Hinds, D.14
Iwasaki, N.15
Ogata, M.16
Omori, Y.17
Petzold, C.18
Rietzch, H.19
Schroder, H.E.20
Schulze, J.21
Cox, N.J.22
Menzel, S.23
Boriraj, V.V.24
Chen, X.25
more..
-
30
-
-
0034795550
-
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
-
Jeffreys AJ, Kauppi L, Neumann R. 2001. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat Genet 29:217-22.
-
(2001)
Nat Genet
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
31
-
-
0034873101
-
An evaluation of the draft human genome sequence
-
Katsanis N, Worley KC, Lupski JR. 2001. An evaluation of the draft human genome sequence. Nat Genet 29:88-91.
-
(2001)
Nat Genet
, vol.29
, pp. 88-91
-
-
Katsanis, N.1
Worley, K.C.2
Lupski, J.R.3
-
32
-
-
0034894422
-
LDB2000: Sequence-based integrated maps of the human genome
-
Ke X, Tapper W, Collins A. 2001. LDB2000: sequence-based integrated maps of the human genome. Bioinformatics 17:581-6.
-
(2001)
Bioinformatics
, vol.17
, pp. 581-586
-
-
Ke, X.1
Tapper, W.2
Collins, A.3
-
33
-
-
0026132133
-
Guidelines for human linkage maps: An international system for human linkage maps (ISLM 1990)
-
Keats BJB, Sherman SL, Morton NE, Robson EB, Buetow KH, Cartwright PE, Chakravarti A, Francke U, Green PP, Ott J. 1991. Guidelines for human linkage maps: an international system for human linkage maps (ISLM 1990). Genomics 9:557-60.
-
(1991)
Genomics
, vol.9
, pp. 557-560
-
-
Keats, B.J.B.1
Sherman, S.L.2
Morton, N.E.3
Robson, E.B.4
Buetow, K.H.5
Cartwright, P.E.6
Chakravarti, A.7
Francke, U.8
Green, P.P.9
Ott, J.10
-
34
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, Richardsson B, Sigurdardottir S, Barnard J, Hallbeck B, Masson G, Shlien A, Palsson ST, Frigge ML, Thorgeirsson TE, Gulcher JR, Stefansson K. 2002. A high-resolution recombination map of the human genome. Nat Genet 31:241-7.
-
(2002)
Nat Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
Shlien, A.11
Palsson, S.T.12
Frigge, M.L.13
Thorgeirsson, T.E.14
Gulcher, J.R.15
Stefansson, K.16
-
35
-
-
0030861903
-
The use of a genetic map of biallelic markers in linkage studies
-
Kruglyak L. 1997. The use of a genetic map of biallelic markers in linkage studies. Nat Genet 17:21-4.
-
(1997)
Nat Genet
, vol.17
, pp. 21-24
-
-
Kruglyak, L.1
-
36
-
-
0015904613
-
The relation of parental sex and age to recombination fraction in the HLA-A system
-
Lamm LU. 1973. The relation of parental sex and age to recombination fraction in the HLA-A system. Hum Hered 23:197-205.
-
(1973)
Hum Hered
, vol.23
, pp. 197-205
-
-
Lamm, L.U.1
-
38
-
-
0031668654
-
Low-order polynomial trends of trends of female-to-male map distance ratio along human chromosomes
-
Li W, Fann C, Ott J. 1998. Low-order polynomial trends of trends of female-to-male map distance ratio along human chromosomes. Hum Hered 48:266-70.
-
(1998)
Hum Hered
, vol.48
, pp. 266-270
-
-
Li, W.1
Fann, C.2
Ott, J.3
-
39
-
-
0029587470
-
Meiotic recombination hotspots
-
Lichten M, Goldman AS. 1995. Meiotic recombination hotspots. Annu Rev Genet 29:423-44.
-
(1995)
Annu Rev Genet
, vol.29
, pp. 423-444
-
-
Lichten, M.1
Goldman, A.S.2
-
40
-
-
0036094848
-
Systematic evaluation of map quality: Human chromosome 22
-
Matise TC, Porter CJ, Buyske S, Cuttichia AJ, Sulman EP, White PS. 2002a. Systematic evaluation of map quality: human chromosome 22. Am J Hum Genet 70:1398-410.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1398-1410
-
-
Matise, T.C.1
Porter, C.J.2
Buyske, S.3
Cuttichia, A.J.4
Sulman, E.P.5
White, P.S.6
-
41
-
-
0038099592
-
A high resolution human SNP linkage map
-
Matise TC, Sachidanadam, Clark A, Kruglyak L, Wijsman E, Chui B, Cohen C, Detoma C, Ehm M, Glanowski S, He C, Heil J, McMullern I, Stein L, Wagner M, Winik J, Winn-Deen ES, Cann HM, Kai E, Holder HL. 2002b. A high resolution human SNP linkage map. Am J Hum Genet [Suppl] 71:215.
-
(2002)
Am J Hum Genet [Suppl]
, vol.71
, pp. 215
-
-
Matise, T.C.1
Sachidanadam2
Clark, A.3
Kruglyak, L.4
Wijsman, E.5
Chui, B.6
Cohen, C.7
Detoma, C.8
Ehm, M.9
Glanowski, S.10
He, C.11
Heil, J.12
McMullern, I.13
Stein, L.14
Wagner, M.15
Winik, J.16
Winn-Deen, E.S.17
Cann, H.M.18
Kai, E.19
Holder, H.L.20
more..
-
42
-
-
0032518613
-
Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19
-
Mohrenweiser HW, Tsujimoto S, Gordon L, Olsen AS. 1998. Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19. Genomics 47:153-62.
-
(1998)
Genomics
, vol.47
, pp. 153-162
-
-
Mohrenweiser, H.W.1
Tsujimoto, S.2
Gordon, L.3
Olsen, A.S.4
-
43
-
-
0025024612
-
Standard maps of chromosome 10
-
Morton NE, Collins A. 1990. Standard maps of chromosome 10. Ann Hum Genet 54:235-51.
-
(1990)
Ann Hum Genet
, vol.54
, pp. 235-251
-
-
Morton, N.E.1
Collins, A.2
-
44
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
Cooperative Human Linkage Center (CHLC)
-
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J. 1994. A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). Science 265:2049-54.
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
-
45
-
-
0007117724
-
Fallacies of the technique of "haplotyping" two apparently linked loci in multipoint linkage analysis
-
Ott J, Lehner T, Sandkuyl LA. 1988. Fallacies of the technique of "haplotyping" two apparently linked loci in multipoint linkage analysis. Am J Hum Genet 43:154.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 154
-
-
Ott, J.1
Lehner, T.2
Sandkuyl, L.A.3
-
46
-
-
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 5547:1719-23.
-
(2001)
Science
, vol.5547
, 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..
-
47
-
-
0034977045
-
Linkage disequilibrium in human: Models and data
-
Pritchard JK, Przeworkski M. 2001. Linkage disequilibrium in human: models and data. Am J Hum Genet 69:1-14.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1-14
-
-
Pritchard, J.K.1
Przeworkski, M.2
-
48
-
-
84984084531
-
Male and female recombination rates for nail-patella: ABO linkage in man
-
Renwick J, Schulze J. 1965. Male and female recombination rates for nail-patella: ABO linkage in man. Ann Hum Genet 28: 379-92.
-
(1965)
Ann Hum Genet
, vol.28
, pp. 379-392
-
-
Renwick, J.1
Schulze, J.2
-
49
-
-
0026529005
-
Model misspecification and multipoint linkage analysis
-
Risch N, Giuffra L. 1992. Model misspecification and multipoint linkage analysis. Hum Hered 42:77-92.
-
(1992)
Hum Hered
, vol.42
, pp. 77-92
-
-
Risch, N.1
Giuffra, L.2
-
50
-
-
0035865322
-
A map of human genome squence variation containing 1.42 million single nucleiotide polymorphisms
-
Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, Rogers J, Bentley DR, Kwok PY, Mardis ER, Yeh RT, Schultz B, Cook L, Davenport R, Dante M, Fulton L, Hillier L, Waterston RH, McPherson JD, Gilman B, Schaffner S, Van Etten WJ, Reich D, Higgins J, Daly MJ, Blumenstiel B, Baldwin J, Stange-Thomann N, Zody MC, Linton L, Lander ES, Altshuler D, International SNP Map Working Group. 2001. A map of human genome squence variation containing 1.42 million single nucleiotide polymorphisms. Nature 15:928-33.
-
(2001)
Nature
, vol.15
, 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
Mullikin, J.C.8
Mortimore, B.J.9
Willey, D.L.10
Hunt, S.E.11
Cole, C.G.12
Coggill, P.C.13
Rice, C.M.14
Ning, Z.15
Rogers, J.16
Bentley, D.R.17
Kwok, P.Y.18
Mardis, E.R.19
Yeh, R.T.20
Schultz, B.21
Cook, L.22
Davenport, R.23
Dante, M.24
Fulton, L.25
Hillier, L.26
Waterston, R.H.27
McPherson, J.D.28
Gilman, B.29
Schaffner, S.30
Van Etten, W.J.31
Reich, D.32
Higgins, J.33
Daly, M.J.34
Blumenstiel, B.35
Baldwin, J.36
Stange-Thomann, N.37
Zody, M.C.38
Linton, L.39
Lander, E.S.40
Altshuler, D.41
more..
-
51
-
-
0028865860
-
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps
-
Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL. 1995. A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-44.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1837-1844
-
-
Sheffield, V.C.1
Weber, J.L.2
Buetow, K.H.3
Murray, J.C.4
Even, D.A.5
Wiles, K.6
Gastier, J.M.7
Pulido, J.C.8
Yandava, C.9
Sunden, S.L.10
-
52
-
-
0027999136
-
A PCR-based genetic linkage map of human chromosome 16
-
Shen Y, Kozman HM, Thompson A, Phillips HA, Holman K, Nancarrow J, Lane S, Chen LZ, Apostolou S, Doggett NA. 1994. A PCR-based genetic linkage map of human chromosome 16. Genomics 22:68-76.
-
(1994)
Genomics
, vol.22
, pp. 68-76
-
-
Shen, Y.1
Kozman, H.M.2
Thompson, A.3
Phillips, H.A.4
Holman, K.5
Nancarrow, J.6
Lane, S.7
Chen, L.Z.8
Apostolou, S.9
Doggett, N.A.10
-
53
-
-
0028333697
-
Linkage disequilibrium in growing and stable populations
-
Slatkin M. 1994. Linkage disequilibrium in growing and stable populations. Genetics 137:331-6.
-
(1994)
Genetics
, vol.137
, pp. 331-336
-
-
Slatkin, M.1
-
54
-
-
0027461758
-
A microsatellite genetic linkage map of human chromosome 18
-
Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J, Gilliam TC. 1993. A microsatellite genetic linkage map of human chromosome 18. Genomics 15:48-56.
-
(1993)
Genomics
, vol.15
, pp. 48-56
-
-
Straub, R.E.1
Speer, M.C.2
Luo, Y.3
Rojas, K.4
Overhauser, J.5
Ott, J.6
Gilliam, T.C.7
-
55
-
-
0034935574
-
Lod scores for gene mapping in the presence of marker map uncertainty
-
Stringham HM, Boehnke M. 2001. Lod scores for gene mapping in the presence of marker map uncertainty. Genet Epidemiol 21:31-9.
-
(2001)
Genet Epidemiol
, vol.21
, pp. 31-39
-
-
Stringham, H.M.1
Boehnke, M.2
-
56
-
-
0026514890
-
A genetic linkage map of human chromosome 21: Analysis of recombination as a function of sex and age
-
Tanzi RE, Watkins PC, Stewart GD, Wexler NS, Gusella JF, Haines JL. 1992. A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age. Am J Hum Genet 50:551-8.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 551-558
-
-
Tanzi, R.E.1
Watkins, P.C.2
Stewart, G.D.3
Wexler, N.S.4
Gusella, J.F.5
Haines, J.L.6
-
57
-
-
0034912611
-
A sequence-based integrated map of chromosome 22
-
Tapper WJ, Morton NE, Dunham I, Ke X, Collins A. 2001. A sequence-based integrated map of chromosome 22. Genome Res 11:1290-5.
-
(2001)
Genome Res
, vol.11
, pp. 1290-1295
-
-
Tapper, W.J.1
Morton, N.E.2
Dunham, I.3
Ke, X.4
Collins, A.5
-
59
-
-
0026746111
-
On the relative importance of marker heterozygosity and intermarker distance in gene mapping
-
Terwilliger JD, Ding Y, Ott J. 1992. On the relative importance of marker heterozygosity and intermarker distance in gene mapping Genomics 13:951-6.
-
(1992)
Genomics
, vol.13
, pp. 951-956
-
-
Terwilliger, J.D.1
Ding, Y.2
Ott, J.3
-
60
-
-
0027213849
-
Chromosome-based method for rapid computer simulation in human genetic linkage analysis
-
Terwilliger JD, Speer M, Ott J. 1993. Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genet Epidemiol 10:217-24.
-
(1993)
Genet Epidemiol
, vol.10
, pp. 217-224
-
-
Terwilliger, J.D.1
Speer, M.2
Ott, J.3
-
61
-
-
0026742493
-
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors
-
Tomfohrde J, Wood S, Schertzer M, Wagner MJ, Wells DE, Parrish J, Sadler LA, Blanton SH, Daiger SP, Wang Z. 1992. Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors. Genomics 14: 144-52.
-
(1992)
Genomics
, vol.14
, pp. 144-152
-
-
Tomfohrde, J.1
Wood, S.2
Schertzer, M.3
Wagner, M.J.4
Wells, D.E.5
Parrish, J.6
Sadler, L.A.7
Blanton, S.H.8
Daiger, S.P.9
Wang, Z.10
-
62
-
-
0025525784
-
Human DNA polymorphisms and methods of analysis
-
Weber JL. 1990. Human DNA polymorphisms and methods of analysis. Curr Opin Biotechnol 1:166-71.
-
(1990)
Curr Opin Biotechnol
, vol.1
, pp. 166-171
-
-
Weber, J.L.1
-
63
-
-
0036649518
-
The Icelandic map
-
Weber JL. 2002. The Icelandic map. Nat Genet 31:225-226.
-
(2002)
Nat Genet
, vol.31
, pp. 225-226
-
-
Weber, J.L.1
-
64
-
-
0027365391
-
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19
-
Weber JL, Wang Z, Hansen K, Stephenson M, Kappel C, Salzman S, Wilkie PJ, Keats B, Dracopoli NC, Brandriff BF, Olsen AS. 1993. Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19. Am J Hum Genet 53:1079-95.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1079-1095
-
-
Weber, J.L.1
Wang, Z.2
Hansen, K.3
Stephenson, M.4
Kappel, C.5
Salzman, S.6
Wilkie, P.J.7
Keats, B.8
Dracopoli, N.C.9
Brandriff, B.F.10
Olsen, A.S.11
-
65
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop MA. 1992. A second-generation linkage map of the human genome. Nature 359:794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.A.8
-
66
-
-
0015997770
-
Population differences in meiotic recombination frequency between loci on chromosome 1
-
Weitkamp LR. 1974. Population differences in meiotic recombination frequency between loci on chromosome 1. Cytogenet Cell Genet 13:179-82.
-
(1974)
Cytogenet Cell Genet
, vol.13
, pp. 179-182
-
-
Weitkamp, L.R.1
-
67
-
-
0015904613
-
The relation of parental sex and age to recombination in the HL-A system
-
Weitkamp LR, Van Rood JJ, Thorsby E, Bias W, Fotinio M, Lawler SD, Dausset J, Mayr WR, Bodmer J, Ward FE, Seignalet J, Payne R, Kissmeyer-Nielsen F, Gatti RA, Sachs JA, Lamm LU. 1973. The relation of parental sex and age to recombination in the HL-A system. Hum Hered 23:197-205.
-
(1973)
Hum Hered
, vol.23
, pp. 197-205
-
-
Weitkamp, L.R.1
Van Rood, J.J.2
Thorsby, E.3
Bias, W.4
Fotinio, M.5
Lawler, S.D.6
Dausset, J.7
Mayr, W.R.8
Bodmer, J.9
Ward, F.E.10
Seignalet, J.11
Payne, R.12
Kissmeyer-Nielsen, F.13
Gatti, R.A.14
Sachs, J.A.15
Lamm, L.U.16
-
68
-
-
0037117464
-
Genes on chromosomes 1 and 13 have significant effects on Ascaris infection
-
Williams-Blangero S, VandeBerg JL, Subedi J, Aivaliotis MJ, Rai DR, Upadhayay RP, Jha B, Blangero J. 2002. Genes on chromosomes 1 and 13 have significant effects on Ascaris infection. Proc Natl Acad Sci USA 99:5533-8.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 5533-5538
-
-
Williams-Blangero, S.1
VandeBerg, J.L.2
Subedi, J.3
Aivaliotis, M.J.4
Rai, D.R.5
Upadhayay, R.P.6
Jha, B.7
Blangero, J.8
-
69
-
-
0033926575
-
Equivalence of single- and multilocus markers: Power to detect linkage with composite markers derived from biallelic loci
-
Wilson AF, Sorant AJ. 2000. Equivalence of single- and multilocus markers: power to detect linkage with composite markers derived from biallelic loci. Am J Hum Genet 66:1610-5.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1610-1615
-
-
Wilson, A.F.1
Sorant, A.J.2
-
70
-
-
0001771498
-
Evolution in Mendelian populations
-
Wright S. 1931. Evolution in Mendelian populations. Genetics 16:97-159.
-
(1931)
Genetics
, vol.16
, pp. 97-159
-
-
Wright, S.1
-
71
-
-
0000907353
-
The role of mutation, inbreeding, crossbreeding and selection in evolution
-
Wright S. 1932. The role of mutation, inbreeding, crossbreeding and selection in evolution. Proc 6th Int Cong Genet 1:356-66.
-
(1932)
Proc 6th Int Cong Genet
, vol.1
, pp. 356-366
-
-
Wright, S.1
-
72
-
-
0035865094
-
Comparison of human genetic and sequence-based physical maps
-
Yu A, Zhao C, Fan Y, Jang W, Mungall AJ, Deloukas P, Olsen A, Doggett NA, Ghebranious N, Broman KW, Weber JL. 2001. Comparison of human genetic and sequence-based physical maps. Nature 409:951-3.
-
(2001)
Nature
, vol.409
, pp. 951-953
-
-
Yu, A.1
Zhao, C.2
Fan, Y.3
Jang, W.4
Mungall, A.J.5
Deloukas, P.6
Olsen, A.7
Doggett, N.A.8
Ghebranious, N.9
Broman, K.W.10
Weber, J.L.11
-
73
-
-
0029127079
-
A 37-marker PCR-based genetic linkage map of human chromosome 9: Observations on mutations and positive interference
-
Zahn LM, Kwiatkowski DJ. 1995. A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference. Genomics 28:140-6.
-
(1995)
Genomics
, vol.28
, pp. 140-146
-
-
Zahn, L.M.1
Kwiatkowski, D.J.2
|