-
1
-
-
0003026374
-
Pathogenesis of multiple sclerosis: Relationship to therapeutic strategies
-
Goodkin, D.E. and Rudnick, R.A. (eds), Springer-Verlag, London
-
Oksenberg, J.R. and Hauser, S.L. (1996) Pathogenesis of multiple sclerosis: relationship to therapeutic strategies. In Goodkin, D.E. and Rudnick, R.A. (eds), Treatments of Multiple Sclerosis: Trial Design, Results and Future Strategies, 2nd edn. Springer-Verlag, London, pp. 17-46.
-
(1996)
Treatments of Multiple Sclerosis: Trial Design, Results and Future Strategies, 2nd Edn.
, pp. 17-46
-
-
Oksenberg, J.R.1
Hauser, S.L.2
-
2
-
-
0028224648
-
The virology of demyelinating disease
-
Johnson, R.T. (1994) The virology of demyelinating disease, Ann. Neurol., 36, S54-S60.
-
(1994)
Ann. Neurol.
, vol.36
-
-
Johnson, R.T.1
-
3
-
-
0000408774
-
Genetic aspects of multiple sclerosis
-
Koetsier, J.C. (ed.), Elsevier Science
-
Myrianthopoulos, N.C. (1985) Genetic aspects of multiple sclerosis. In Koetsier, J.C. (ed.), Handbook of Clinical Neurology: Demyelinating Diseases. Elsevier Science, Vol. 47, pp. 289-317.
-
(1985)
Handbook of Clinical Neurology: Demyelinating Diseases
, vol.47
, pp. 289-317
-
-
Myrianthopoulos, N.C.1
-
4
-
-
0027985358
-
The role of genetic factors in multiple sclerosis susceptibility
-
Ebers, G.C. and Sadovnick, A.D. (1994) The role of genetic factors in multiple sclerosis susceptibility, Neuroimmunol., 54, 1017.
-
(1994)
Neuroimmunol.
, vol.54
, pp. 1017
-
-
Ebers, G.C.1
Sadovnick, A.D.2
-
5
-
-
0030007661
-
Evidence for genetic basis of multiple sclerosis
-
Sadovnick, A.D., Ebers, G.C., Dymenl, D.A. and Risch, N.J. (1996) Evidence for genetic basis of multiple sclerosis. Lancet, 347, 1728-1730.
-
(1996)
Lancet
, vol.347
, pp. 1728-1730
-
-
Sadovnick, A.D.1
Ebers, G.C.2
Dymenl, D.A.3
Risch, N.J.4
-
6
-
-
0029121088
-
A genetic basis for familial aggregation in multiple sclerosis
-
Ebers, G.C., Sadovnick, A.D. and Risch, N.J. (1995) A genetic basis for familial aggregation in multiple sclerosis. Nature, 377, 150-151.
-
(1995)
Nature
, vol.377
, pp. 150-151
-
-
Ebers, G.C.1
Sadovnick, A.D.2
Risch, N.J.3
-
7
-
-
0027537583
-
A population based study of multiple sclerosis in twins: Update
-
Sadovnick, A.D., Armstrong, H., Rice, G.P., Bulman, D., Hashimoto, L., Paly, D.W., Hashimoto, S.A., Warren, S., Hader, W. and Murray, T.J. (1993) A population based study of multiple sclerosis in twins: update. Ann. Neurol., 33, 281-285.
-
(1993)
Ann. Neurol.
, vol.33
, pp. 281-285
-
-
Sadovnick, A.D.1
Armstrong, H.2
Rice, G.P.3
Bulman, D.4
Hashimoto, L.5
Paly, D.W.6
Hashimoto, S.A.7
Warren, S.8
Hader, W.9
Murray, T.J.10
-
8
-
-
0028128084
-
The British Isles survey of multiple sclerosis in twins
-
Mumford, G.L., Wood, N.W., Kellar-Wood, H.F., Thorpe, J.W., Miller, D.H. and Compston, D.A.S. (1994) The British Isles survey of multiple sclerosis in twins. Neurology, 44, 11-15.
-
(1994)
Neurology
, vol.44
, pp. 11-15
-
-
Mumford, G.L.1
Wood, N.W.2
Kellar-Wood, H.F.3
Thorpe, J.W.4
Miller, D.H.5
Compston, D.A.S.6
-
9
-
-
0028834799
-
Genetic susceptibility in Alzheimer disease
-
Pericak-Vance, M.A. and Haines, J.L. (1995) Genetic susceptibility in Alzheimer disease. Trends Genet., 11, 504-508.
-
(1995)
Trends Genet.
, vol.11
, pp. 504-508
-
-
Pericak-Vance, M.A.1
Haines, J.L.2
-
10
-
-
10544234193
-
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
-
Polymeropoulos, M.H., Higgins, J.J., Golbe, L.I., Johnson, W.G., Ide, S.E., Di Iorio, G., Sanges, G., Stenroos, E.S., Pho, L.T., Schaffer, A.A., Lazzarini, A.M., Nussbaum, R.L. and Duvoisin, R.C. (1996) Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science, 274, 1197-1199.
-
(1996)
Science
, vol.274
, pp. 1197-1199
-
-
Polymeropoulos, M.H.1
Higgins, J.J.2
Golbe, L.I.3
Johnson, W.G.4
Ide, S.E.5
Di Iorio, G.6
Sanges, G.7
Stenroos, E.S.8
Pho, L.T.9
Schaffer, A.A.10
Lazzarini, A.M.11
Nussbaum, R.L.12
Duvoisin, R.C.13
-
11
-
-
0030822568
-
The genetic complexity of Parkinson disease
-
Scott, W.K., Stajich, J.M., Yamaoka, L.H., Speer, M.C., Vance, J.M., Roses, A.D., Pericak-Vance, M.A. and the Deane Laboratory Parkinson Disease Research Group (1997) The genetic complexity of Parkinson disease. Science, 277, 387-388.
-
(1997)
Science
, vol.277
, pp. 387-388
-
-
Scott, W.K.1
Stajich, J.M.2
Yamaoka, L.H.3
Speer, M.C.4
Vance, J.M.5
Roses, A.D.6
Pericak-Vance, M.A.7
-
12
-
-
0015252399
-
HL-A antigen frequencies in multiple sclerosis. Significant increase of HL-A3, HL-A10 and W5, and decrease of HL-A12
-
Bertrams, J. and Kuwert, E. (1972) HL-A antigen frequencies in multiple sclerosis. Significant increase of HL-A3, HL-A10 and W5, and decrease of HL-A12. Eur. Neurol., 7, 74-78.
-
(1972)
Eur. Neurol.
, vol.7
, pp. 74-78
-
-
Bertrams, J.1
Kuwert, E.2
-
13
-
-
0015273990
-
Multiple sclerosis: Association with HL-A3
-
Maito, S., Manerow, N., Mickey, M.R. and Terasaki, P.I. (1972) Multiple sclerosis: association with HL-A3. Tissue Antigens, 2, 1-4.
-
(1972)
Tissue Antigens
, vol.2
, pp. 1-4
-
-
Maito, S.1
Manerow, N.2
Mickey, M.R.3
Terasaki, P.I.4
-
14
-
-
0002621639
-
Multiple sclerosis
-
Tiwari, J.L. and Terasaki, P.I. (eds), Springer-Verlag, New York
-
Tiwari, J.L. and Terasaki, P.I. (1985) Multiple sclerosis. In Tiwari, J.L. and Terasaki, P.I. (eds), HLA and Disease Associations. Springer-Verlag, New York, pp. 152-167.
-
(1985)
HLA and Disease Associations
, pp. 152-167
-
-
Tiwari, J.L.1
Terasaki, P.I.2
-
15
-
-
0025767289
-
HLA class II-associated genetic susceptibility in multiple sclerosis: A critical evaluation
-
Olerup, O. and Hillert, J. (1995) HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation. Tissue Antigens, 38, 1-15.
-
(1995)
Tissue Antigens
, vol.38
, pp. 1-15
-
-
Olerup, O.1
Hillert, J.2
-
16
-
-
0020475048
-
HLA typing in sibling pairs with multiple sclerosis
-
Ebers, G.C., Pathy, D., Stiller, C., Nelson, R., Seland, T. and Larsen, B. (1982) HLA typing in sibling pairs with multiple sclerosis. Lancet, 2, 1278 .
-
(1982)
Lancet
, vol.2
, pp. 1278
-
-
Ebers, G.C.1
Pathy, D.2
Stiller, C.3
Nelson, R.4
Seland, T.5
Larsen, B.6
-
17
-
-
0029072687
-
Multiple sclerosis and the HLA-D region: Linkage and association studies
-
Kellar-Wood, H.F., Wood, N.W., Holmans, P., Clayton, D., Robertson, N. and Compston, D.A. (1995) Multiple sclerosis and the HLA-D region: linkage and association studies. J. Neuroimmunol., 58, 183-190.
-
(1995)
J. Neuroimmunol.
, vol.58
, pp. 183-190
-
-
Kellar-Wood, H.F.1
Wood, N.W.2
Holmans, P.3
Clayton, D.4
Robertson, N.5
Compston, D.A.6
-
18
-
-
0027977025
-
Two-locus linkage analysis in multiple sclerosis (MS)
-
Tienari, P.J., Terwilliger, J.D., Ott, J., Palo, J. and Peltonen, L. (1994) Two-locus linkage analysis in multiple sclerosis (MS). Genomics, 19, 320-325.
-
(1994)
Genomics
, vol.19
, pp. 320-325
-
-
Tienari, P.J.1
Terwilliger, J.D.2
Ott, J.3
Palo, J.4
Peltonen, L.5
-
19
-
-
0028153827
-
The HLA-Dw2 haplotype segregates closely with multiple sclerosis in multiplex families
-
Hillert, J., Kall, T., Vrethem, M., Fredrikson, S., Ohlson, M. and Olerup, O. (1994) The HLA-Dw2 haplotype segregates closely with multiple sclerosis in multiplex families. J. Neuroimmunol., 50, 95-100.
-
(1994)
J. Neuroimmunol.
, vol.50
, pp. 95-100
-
-
Hillert, J.1
Kall, T.2
Vrethem, M.3
Fredrikson, S.4
Ohlson, M.5
Olerup, O.6
-
20
-
-
0028810117
-
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex families
-
Eoli, M., Pandolfo, M., Amoroso, A., Salmaggi, A., Zaffaroni, M., Gasparini, P., DiDonato, S., Milanese, C. and Zeviani, M. (1995) Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex families. Eur. J. Hum. Genet., 3, 303-311.
-
(1995)
Eur. J. Hum. Genet.
, vol.3
, pp. 303-311
-
-
Eoli, M.1
Pandolfo, M.2
Amoroso, A.3
Salmaggi, A.4
Zaffaroni, M.5
Gasparini, P.6
DiDonato, S.7
Milanese, C.8
Zeviani, M.9
-
21
-
-
0029899731
-
DR2/DQw1 inheritance and haplotype sharing in affected siblings from multiple sclerosis families
-
Voshkuhl, R.R., Goldstein, A.M., Simonis, T., Davey, R.J. and McFarland, H.F. (1996) DR2/DQw1 inheritance and haplotype sharing in affected siblings from multiple sclerosis families, Ann. Neurol., 39, 804-807.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 804-807
-
-
Voshkuhl, R.R.1
Goldstein, A.M.2
Simonis, T.3
Davey, R.J.4
McFarland, H.F.5
-
22
-
-
15844368830
-
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22
-
Sawcer, S., Jones, H.B., Feakes, R., Gray, J., Smaldon, N., Chataway, J., Robertson, N., Clayton, D., Goodfellow, P.N. and Compslon, A. (1996) A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22. Nature Genet., 13, 464-468.
-
(1996)
Nature Genet.
, vol.13
, pp. 464-468
-
-
Sawcer, S.1
Jones, H.B.2
Feakes, R.3
Gray, J.4
Smaldon, N.5
Chataway, J.6
Robertson, N.7
Clayton, D.8
Goodfellow, P.N.9
Compslon, A.10
-
23
-
-
0009573338
-
A complete genomic screen for multiple sclerosis, underscores a role for the major histocompatibilily complex
-
Multiple Sclerosis Genetics Group ( 1996) A complete genomic screen for multiple sclerosis, underscores a role for the major histocompatibilily complex. Nature Genet., 13, 469-171.
-
(1996)
Nature Genet.
, vol.13
, pp. 469-1171
-
-
-
24
-
-
0026354602
-
Diagnostic criteria for multiple sclerosis research involving multiply affected families
-
Goodkin, D.E., Doolittle, T.H., Hauser, S.S., Ransohoff, R.M., Roses, A.D. and Rudick, R.A. (1991) Diagnostic criteria for multiple sclerosis research involving multiply affected families. Arch. Neurol., 48, 805-807.
-
(1991)
Arch. Neurol.
, vol.48
, pp. 805-807
-
-
Goodkin, D.E.1
Doolittle, T.H.2
Hauser, S.S.3
Ransohoff, R.M.4
Roses, A.D.5
Rudick, R.A.6
-
25
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell. J.R. and Weeks, D.E. (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nature Genet., 11, 402-408.
-
(1995)
Nature Genet.
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
26
-
-
0030772982
-
Test for linkage and association in nuclear families
-
Martin, E., Kaplan, N. and Weir, B. (1997) Test for linkage and association in nuclear families. Am. J Hum. Genet., 61, 439-448.
-
(1997)
Am. J Hum. Genet.
, vol.61
, pp. 439-448
-
-
Martin, E.1
Kaplan, N.2
Weir, B.3
-
27
-
-
0019787864
-
HLA family studies and multiple sclerosis: A common gene, dominantly expressed
-
Stewart, G.J., McLeod, J.G., Basten, A. and Bashir, H.V. (1981) HLA family studies and multiple sclerosis: a common gene, dominantly expressed. Hum. Immunol., 3, 13-29.
-
(1981)
Hum. Immunol.
, vol.3
, pp. 13-29
-
-
Stewart, G.J.1
McLeod, J.G.2
Basten, A.3
Bashir, H.V.4
-
28
-
-
0031748194
-
Clinical demographics of multiplex families with multiple sclerosis
-
Multiple Sclerosis Genetics Group (1998) Clinical demographics of multiplex families with multiple sclerosis. Ann. Neurol., 43, 530-534.
-
(1998)
Ann. Neurol.
, vol.43
, pp. 530-534
-
-
-
29
-
-
0024533562
-
Extended major histocompatibility complex haplotypes in patients with multiple sclerosis
-
Hauser, S.L., Fleischnick, E., Weiner, H.L., Marcus, D., Awdeh, Z., Yunis, E.J. and Alper, C.A. (1989) Extended major histocompatibility complex haplotypes in patients with multiple sclerosis. Neurology, 39, 275-277.
-
(1989)
Neurology
, vol.39
, pp. 275-277
-
-
Hauser, S.L.1
Fleischnick, E.2
Weiner, H.L.3
Marcus, D.4
Awdeh, Z.5
Yunis, E.J.6
Alper, C.A.7
-
30
-
-
0027492226
-
Multiple sclerosis is associated with genes within or close to the HLA-DR-DQ subregion on a normal DR15, DQ6, Dw2 haplotype
-
Hillert, J. and Olerup, O. (1993) Multiple sclerosis is associated with genes within or close to the HLA-DR-DQ subregion on a normal DR15, DQ6, Dw2 haplotype. Neurology, 43, 63-168.
-
(1993)
Neurology
, vol.43
, pp. 63-168
-
-
Hillert, J.1
Olerup, O.2
-
31
-
-
0025019555
-
Linkage strategies for genetically complex traits. 1. Multilocus models
-
Risch, N. (1990) Linkage strategies for genetically complex traits. 1. Multilocus models. Am .J. Hum. Genet., 46, 222-228.
-
(1990)
Am .J. Hum. Genet.
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
32
-
-
0025138302
-
T cells responsive to myelin basic protein in patients with multiple sclerosis
-
Allegrerta, M., Nicklas, J.A., Sriram, S. and Albertini, R.J. (1990) T cells responsive to myelin basic protein in patients with multiple sclerosis. Science, 247, 718-721.
-
(1990)
Science
, vol.247
, pp. 718-721
-
-
Allegrerta, M.1
Nicklas, J.A.2
Sriram, S.3
Albertini, R.J.4
-
33
-
-
0027960893
-
Locus-specific somatic hypermutation in germinal center T cells
-
Zheng, B., Xue, W. and Kelso, G. (1994) Locus-specific somatic hypermutation in germinal center T cells. Nature, 372, 556.
-
(1994)
Nature
, vol.372
, pp. 556
-
-
Zheng, B.1
Xue, W.2
Kelso, G.3
-
34
-
-
0027415561
-
Genomic structure and function in the MHC
-
Trowsdale, J. (1993) Genomic structure and function in the MHC. Trends Genet., 9, 117-122.
-
(1993)
Trends Genet.
, vol.9
, pp. 117-122
-
-
Trowsdale, J.1
-
36
-
-
0028288398
-
Tumor necrosis factor polymorphism in multiple sclerosis: No additional association independent of HLA
-
Roth, M.P., Nogueira, L., Coppin, H., Clanet, M., Clayton, J. and Cambon-Thomsen, A. (1994) Tumor necrosis factor polymorphism in multiple sclerosis: no additional association independent of HLA. J. Neuroimmunol., 51, 93-99.
-
(1994)
J. Neuroimmunol.
, vol.51
, pp. 93-99
-
-
Roth, M.P.1
Nogueira, L.2
Coppin, H.3
Clanet, M.4
Clayton, J.5
Cambon-Thomsen, A.6
-
37
-
-
0030587583
-
Tumor necrosis factor (TNF) microsatellite haplotypes in relation to extended haplotypes. susceptibility to diseases associated with the major histocompatibility complex and TNF secretion
-
Garcia-Merino, A., Alper, C.A., Usuku, K., Marcus-Bagley, D., Lincoln, R., Awdeh, Z., Yunis, E.J., Eisenbarth, G.S., Brink, S.J. and Hauser, S.L. (1996) Tumor necrosis factor (TNF) microsatellite haplotypes in relation to extended haplotypes. susceptibility to diseases usceptibility to diseases associated with the major histocompatibility complex and TNF secretion. Hum. Immunol., 50, 11-21.
-
(1996)
Hum. Immunol.
, vol.50
, pp. 11-21
-
-
Garcia-Merino, A.1
Alper, C.A.2
Usuku, K.3
Marcus-Bagley, D.4
Lincoln, R.5
Awdeh, Z.6
Yunis, E.J.7
Eisenbarth, G.S.8
Brink, S.J.9
Hauser, S.L.10
-
38
-
-
0025604835
-
A gene in the human major histocompatibility complex class II region controlling the class I antigen presentation pathway
-
Spies, T., Bresnahan, M., Bahram, S., Arnold, D., Blanck, G., Mellins, E., Pious, D. and DeMars, R. (1990) A gene in the human major histocompatibility complex class II region controlling the class I antigen presentation pathway. Nature, 348, 744-747.
-
(1990)
Nature
, vol.348
, pp. 744-747
-
-
Spies, T.1
Bresnahan, M.2
Bahram, S.3
Arnold, D.4
Blanck, G.5
Mellins, E.6
Pious, D.7
DeMars, R.8
-
39
-
-
0025688348
-
Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters
-
Trowsdale, J., Hanson, I., Mockridge, I., Beck, S., Townsend, A. and Kelly. A. (1990) Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters. Nature, 348, 741-744.
-
(1990)
Nature
, vol.348
, pp. 741-744
-
-
Trowsdale, J.1
Hanson, I.2
Mockridge, I.3
Beck, S.4
Townsend, A.5
Kelly, A.6
-
40
-
-
0027155587
-
Antigen processing gene polymorphisms in HLA-DR2 multiple sclerosis
-
Liblau, R., van Endert, P.M., Sandberg-Wollheim, M., Patel, S.D., Lopez, M.T., Land, S., Fugger, L. and McDevitt, H.O. (1993) Antigen processing gene polymorphisms in HLA-DR2 multiple sclerosis. Neurology, 43, 1192-1197.
-
(1993)
Neurology
, vol.43
, pp. 1192-1197
-
-
Liblau, R.1
Van Endert, P.M.2
Sandberg-Wollheim, M.3
Patel, S.D.4
Lopez, M.T.5
Land, S.6
Fugger, L.7
McDevitt, H.O.8
-
41
-
-
0028285712
-
No association of multiple sclerosis to alleles at the TAP2 locus
-
Spurkland, A., Knutsen, I., Undlien, D.E. and Vandal, F. (1994) No association of multiple sclerosis to alleles at the TAP2 locus. Hum. Immunol., 39, 299-301.
-
(1994)
Hum. Immunol.
, vol.39
, pp. 299-301
-
-
Spurkland, A.1
Knutsen, I.2
Undlien, D.E.3
Vandal, F.4
-
42
-
-
0027985360
-
TAP1 and TAP2 transporter gene polymorphisms in multiple sclerosis: No evidence for disease association with TAP
-
Vandevyver, C., Stinissen, P., Cassiman, J.J. and Raus, J. (1994) TAP1 and TAP2 transporter gene polymorphisms in multiple sclerosis: no evidence for disease association with TAP. J. Neuroimmunol., 54, 35-40.
-
(1994)
J. Neuroimmunol.
, vol.54
, pp. 35-40
-
-
Vandevyver, C.1
Stinissen, P.2
Cassiman, J.J.3
Raus, J.4
-
43
-
-
0029039786
-
TAP2 polymorphisms in Australian multiple sclerosis patients
-
Bennetts, B.H., Teutsch, S.M., Heard, R.N., Dunckley, H. and Stewart, G.J. (1995) TAP2 polymorphisms in Australian multiple sclerosis patients. J. Neuroimmunol., 59, 113-121.
-
(1995)
J. Neuroimmunol.
, vol.59
, pp. 113-121
-
-
Bennetts, B.H.1
Teutsch, S.M.2
Heard, R.N.3
Dunckley, H.4
Stewart, G.J.5
-
44
-
-
0028849855
-
Antibody facilitation of multiple sclerosis-like lesions in a nonhuman primate
-
Genain, C.P., Nguyen, M.H., Letvin, N.L., Peral, R., Davis, R.L., Adelman, M., Lees, M.B., Linington, C. and Hauser, S.L. (1995) Antibody facilitation of multiple sclerosis-like lesions in a nonhuman primate. J. Clin. Invest., 96, 2966-2974.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 2966-2974
-
-
Genain, C.P.1
Nguyen, M.H.2
Letvin, N.L.3
Peral, R.4
Davis, R.L.5
Adelman, M.6
Lees, M.B.7
Linington, C.8
Hauser, S.L.9
-
45
-
-
0029052402
-
Characterization of cDNA and genomic clones encoding human myelin oligodendrocyte glycoprotein
-
Hilton, A.A., Slavin, A.J., Hilton, D.J. and Bernard, C.C. (1995) Characterization of cDNA and genomic clones encoding human myelin oligodendrocyte glycoprotein, J Neurochem., 65, 309-318.
-
(1995)
J Neurochem.
, vol.65
, pp. 309-318
-
-
Hilton, A.A.1
Slavin, A.J.2
Hilton, D.J.3
Bernard, C.C.4
-
46
-
-
0028835240
-
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: No evidence of disease association with MOG
-
Roth, M.P., Dolbois, L., Borot, N., Pontarotti, P., Clanet, M. and Coppin, H. (1995) Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG. J. Neuroimmunol., 61, 117-122.
-
(1995)
J. Neuroimmunol.
, vol.61
, pp. 117-122
-
-
Roth, M.P.1
Dolbois, L.2
Borot, N.3
Pontarotti, P.4
Clanet, M.5
Coppin, H.6
-
47
-
-
0002303695
-
PCR methods of genotyping
-
Dracopoli, N.C., Haines, J.L., Korf, B.R., Norton, C.C., Seidman, C.E., Seidman, J.G., Moir, D.T. and Smith, D.R. (eds), John Wiley and Sons, New York, Unit 2.5
-
Hudson, T.J., Clark, C.D., Gschwend, M. and Justice-Higgins, E. (1998) PCR methods of genotyping. In Dracopoli, N.C., Haines, J.L., Korf, B.R., Norton, C.C., Seidman, C.E., Seidman, J.G., Moir, D.T. and Smith, D.R. (eds), Current Protocols in Human Genetics. John Wiley and Sons, New York, Unit 2.5.
-
(1998)
Current Protocols in Human Genetics
-
-
Hudson, T.J.1
Clark, C.D.2
Gschwend, M.3
Justice-Higgins, E.4
-
48
-
-
0003156643
-
PEDIGENE: A comprehensive data management system to facilitate efficient and rapid disease gene mapping
-
Haynes, C.S., Speer, M.C., Peedin, M., Roses, A.D., Haines, J.L., Vance, J.M. and Pericak-Vance, M.A. (1995) PEDIGENE: a comprehensive data management system to facilitate efficient and rapid disease gene mapping. Am. J. Hum. Genet., 57, A193.
-
(1995)
Am. J. Hum. Genet.
, vol.57
-
-
Haynes, C.S.1
Speer, M.C.2
Peedin, M.3
Roses, A.D.4
Haines, J.L.5
Vance, J.M.6
Pericak-Vance, M.A.7
-
49
-
-
0029918883
-
Nonparametric simulation-based statistics for detecting linkage in general pedigrees
-
Davis, S., Schroeder, M., Goldin, L.R. and Weeks, D.E. (1996) Nonparametric simulation-based statistics for detecting linkage in general pedigrees. Am. J. Hum. Genet., 58, 867-880.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 867-880
-
-
Davis, S.1
Schroeder, M.2
Goldin, L.R.3
Weeks, D.E.4
-
50
-
-
0025008677
-
Linkage strategies for genetically complex traits. II. The power of affected relative pairs
-
Risch, N. (1990) Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am. J. Hum. Genet., 46, 229-241.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
51
-
-
0025020461
-
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs
-
Risch, N. (1990) Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am. J. Hum. Genet., 46, 242-253.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 242-253
-
-
Risch, N.1
-
52
-
-
0031018304
-
Power studies for the transmission/disequilibrium tests with multiple alleles
-
Kaplan, N.L., Martin, E.R. and Weir, B.S. (1997) Power studies for the transmission/disequilibrium tests with multiple alleles. Am. J. Hum. Genet., 60, 691-702.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 691-702
-
-
Kaplan, N.L.1
Martin, E.R.2
Weir, B.S.3
-
53
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman. R.S., McGinnis, R.E. and Ewens, W.J. (1993) Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet., 52, 506-516.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
54
-
-
0029858544
-
The TDT and other family-based tests for linkage disequilibrium and association
-
Spielman, R.S.and Ewens, W.J. (1996) The TDT and other family-based tests for linkage disequilibrium and association. Am. J. Hum. Genet., 59, 983-989.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 983-989
-
-
Spielman, R.S.1
Ewens, W.J.2
-
55
-
-
7344237478
-
An examination of the TDT for multiple loci
-
McIntyre, L.M., Martin, E.R. and Kaplan, N.L. (1997) An examination of the TDT for multiple loci. Am. J. Hum. Genet., 61, A285.
-
(1997)
Am. J. Hum. Genet.
, vol.61
-
-
McIntyre, L.M.1
Martin, E.R.2
Kaplan, N.L.3
-
56
-
-
0029945706
-
Descent graphs in pedigree analysis: Application to haplotyping, location scores, and marker-sharing statistics
-
Sobel, E. and Lange, K. (1996) Descent graphs in pedigree analysis: application to haplotyping, location scores, and marker-sharing statistics. Am. J. Hum. Genet., 58, 1323-1337.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
|