-
2
-
-
0021688283
-
Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines
-
Anderson M, Gusella J. 1984. Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines. In Vitro 20: 856-858.
-
(1984)
Vitro
, vol.20
, pp. 856-858
-
-
Anderson, M.1
Gusella, J.2
-
3
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M. 1995. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 25(1):63-77.
-
(1995)
Psychol Med
, vol.25
, Issue.1
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
4
-
-
0027934165
-
Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder
-
Baker P, Piven J, Schwartz S, Patil S. 1994. Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder. J Autism Dev Disord 24:529-535.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 529-535
-
-
Baker, P.1
Piven, J.2
Schwartz, S.3
Patil, S.4
-
5
-
-
0025835296
-
Fast and sensitive silver staining of DNA in polyacrylamide gels
-
Bassam B, Caetano-Anolles G, Gresshoff P. 1991. Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 196:80-83.
-
(1991)
Anal Biochem
, vol.196
, pp. 80-83
-
-
Bassam, B.1
Caetano-Anolles, G.2
Gresshoff, P.3
-
6
-
-
0021957675
-
A comparison of sib-pair linkage tests for disease susceptibility loci
-
[Published erratum appears in Genet Epidemiol 1986; 3:379.]
-
Blackwelder WC, Elston RC. 1985. A comparison of sib-pair linkage tests for disease susceptibility loci. Genet Epidemiol 2:85-97. [Published erratum appears in Genet Epidemiol 1986; 3:379.]
-
(1985)
Genet Epidemiol
, vol.2
, pp. 85-97
-
-
Blackwelder, W.C.1
Elston, R.C.2
-
7
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EHJ, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal, BL. 1997. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 2:247-250.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook, E.H.J.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Yan, S.5
Lincoln, A.6
Haas, R.7
Courchesne, E.8
Leventhal, B.L.9
-
8
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
-
Cook EHJ, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E. 1998. Linkagedisequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Hum Genet 62:1077-1083.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1077-1083
-
-
Cook, E.H.J.1
Courchesne, R.Y.2
Cox, N.J.3
Lord, C.4
Gonen, D.5
Guter, S.J.6
Lincoln, A.7
Nix, K.8
Haas, R.9
Leventhal, B.L.10
Courchesne, E.11
-
9
-
-
0343399663
-
Further evidence for the increased power of LOD scores compared with nonparametric methods
-
Durner M, Vieland VJ, Greenberg DA. 1999. Further evidence for the increased power of LOD scores compared with nonparametric methods. Am J Hum Genet 64:281-289.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 281-289
-
-
Durner, M.1
Vieland, V.J.2
Greenberg, D.A.3
-
10
-
-
15844366743
-
A full genome search in multiple sclerosis
-
Ebers GC, Kukay K, Bulman DE, Sadovnick AD, Rice G, Andersen C, Armstrong H, Cousin K, Bell RB, Hader W, Paty DW, Hashimoto S, Oger J, Duquette P, Warren S, Gray T, P OC, Nath A, Auty A, Metz L, Francis G, Paulseth JE, Murray TJ, Pryse-Phillips W, Risch N, et al. 1996. A full genome search in multiple sclerosis. Nat Genet 13:472-476.
-
(1996)
Nat Genet
, vol.13
, pp. 472-476
-
-
Ebers, G.C.1
Kukay, K.2
Bulman, D.E.3
Sadovnick, A.D.4
Rice, G.5
Andersen, C.6
Armstrong, H.7
Cousin, K.8
Bell, R.B.9
Hader, W.10
Paty, D.W.11
Hashimoto, S.12
Oger, J.13
Duquette, P.14
Warren, S.15
Gray, T.16
P, O.C.17
Nath, A.18
Auty, A.19
Metz, L.20
Francis, G.21
Paulseth, J.E.22
Murray, T.J.23
Pryse-Phillips, W.24
Risch, N.25
more..
-
11
-
-
0031940694
-
Localisation of a gene implicated in a severe speech and language disorder
-
[Published erratum appears in Nat Genet 1998; 18:298.]
-
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. 1998. Localisation of a gene implicated in a severe speech and language disorder. Nat Genet 18:168-170. [Published erratum appears in Nat Genet 1998; 18:298.]
-
(1998)
Nat Genet
, vol.18
, pp. 168-170
-
-
Fisher, S.E.1
Vargha-Khadem, F.2
Watkins, K.E.3
Monaco, A.P.4
Pembrey, M.E.5
-
12
-
-
0024828416
-
Inferring mode of inheritance by comparison of LOD scores
-
Greenberg DA. 1989. Inferring mode of inheritance by comparison of LOD scores. Am J Hum Genet 34:480-486.
-
(1989)
Am J Hum Genet
, vol.34
, pp. 480-486
-
-
Greenberg, D.A.1
-
13
-
-
0028018167
-
Using LOD-score differences to determine mode of inheritance: A simple, robust method even in the presence of heterogeneity and reduced penetrance
-
Greenberg DA, Berger B. 1994. Using LOD-score differences to determine mode of inheritance: a simple, robust method even in the presence of heterogeneity and reduced penetrance. Am J Hum Genet 55:834-840.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 834-840
-
-
Greenberg, D.A.1
Berger, B.2
-
14
-
-
0009573338
-
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex
-
Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR, et al. 1996. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. Nat Genet 13:469-471.
-
(1996)
Nat Genet
, vol.13
, pp. 469-471
-
-
Haines, J.L.1
Ter-Minassian, M.2
Bazyk, A.3
Gusella, J.F.4
Kim, D.J.5
Terwedow, H.6
Pericak-Vance, M.A.7
Rimmler, J.B.8
Haynes, C.S.9
Roses, A.D.10
Lee, A.11
Shaner, B.12
Menold, M.13
Seboun, E.14
Fitoussi, R.P.15
Gartioux, C.16
Reyes, C.17
Ribierre, F.18
Gyapay, G.19
Weissenbach, J.20
Hauser, S.L.21
Goodkin, D.E.22
Lincoln, R.23
Usuku, K.24
Oksenberg, J.R.25
more..
-
15
-
-
0003156643
-
PEDIGENE: A comprehensive data management system to facilitate efficient and rapid disease gene mapping
-
Haynes C, Speer MC, Peedin M, Roses AD, Haines JL, Vance JM, Pericak-Vance MA. 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.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
-
16
-
-
0029996490
-
Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations
-
Hauser ER, Boehnke M, Guo SW, Risch N. 1996. Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet Epidemiol 13:117-137.
-
(1996)
Genet Epidemiol
, vol.13
, pp. 117-137
-
-
Hauser, E.R.1
Boehnke, M.2
Guo, S.W.3
Risch, N.4
-
17
-
-
0031019267
-
Magnitude of type I error when single-locus linkage analysis is maximized over models: A simulation study
-
Hodge SE, Abreu PC, Greenberg DA. 1997. Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study. Am J Hum Genet 60:217-227.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 217-227
-
-
Hodge, S.E.1
Abreu, P.C.2
Greenberg, D.A.3
-
18
-
-
0028029930
-
Lods, wrods, and mods: The interpretation of lod scores calculated under different models
-
Hodge SE, Elston RC. 1994. Lods, wrods, and mods: the interpretation of lod scores calculated under different models. Genet Epidemiol 11:329-342.
-
(1994)
Genet Epidemiol
, vol.11
, pp. 329-342
-
-
Hodge, S.E.1
Elston, R.C.2
-
19
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). 1998a. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 7:571-578.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
20
-
-
0345682694
-
Linkage disequilibrium mapping and candidate gene analysis of autism
-
Abstract 1723
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). 1998b. Linkage disequilibrium mapping and candidate gene analysis of autism. Am J Hum Genet 63(suppl):A298. Abstract 1723.
-
(1998)
Am J Hum Genet
, vol.63
, Issue.SUPPL.
-
-
-
21
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poustka F, Benner A, Lesch KP, Poustka A. 1997. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 6:2233-2238.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
-
22
-
-
0028123781
-
Linkage analysis in nuclear families. 2: Relationship between affected sib-pair tests and lod score analysis
-
Knapp M, Seuchter SA, Baur MP. 1994. Linkage analysis in nuclear families. 2: relationship between affected sib-pair tests and lod score analysis. Hum Hered 44:44-51.
-
(1994)
Hum Hered
, vol.44
, pp. 44-51
-
-
Knapp, M.1
Seuchter, S.A.2
Baur, M.P.3
-
23
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. 1996. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
24
-
-
17344367913
-
Genome-wide scan of multiple sclerosis in Finnish multiplex families
-
Kuokkanen S, Gschewend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wilstrom J, Palo J, Stein LD, Hudson TJ, Landers ES, Peltonen L. 1997. Genome-wide scan of multiple sclerosis in Finnish multiplex families. Am J Hum Genet 61:1379-1387.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1379-1387
-
-
Kuokkanen, S.1
Gschewend, M.2
Rioux, J.D.3
Daly, M.J.4
Terwilliger, J.D.5
Tienari, P.J.6
Wilstrom, J.7
Palo, J.8
Stein, L.D.9
Hudson, T.J.10
Landers, E.S.11
Peltonen, L.12
-
25
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop GM, Lalouel JM, Julier C, Ott J. 1985. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Med Genet 46:482-253.
-
(1985)
Am J Med Genet
, vol.46
, pp. 482-1253
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
26
-
-
0003055421
-
Language and communication in autism
-
Cohen DJ, Volkmar FR, editors. New York: John Wiley & Sons
-
Lord C, Paul R. 1997. Language and communication in autism. In: Cohen DJ, Volkmar FR, editors. Handbook of autism and pervasive developmental disorders, 2nd ed. New York: John Wiley & Sons, p 195-225.
-
(1997)
Handbook of Autism and Pervasive Developmental Disorders, 2nd Ed.
, pp. 195-225
-
-
Lord, C.1
Paul, R.2
-
27
-
-
0024369122
-
Autism diagnostic observation schedule: A standardized observation of communicative and social behavior
-
Lord C, Rutter M, Goode S, Heemsbergen J, Jordan H, Mawhood L, Schopler E. 1989. Autism diagnostic observation schedule: a standardized observation of communicative and social behavior. J Autism Dev Disord 19:185-212.
-
(1989)
J Autism Dev Disord
, vol.19
, pp. 185-212
-
-
Lord, C.1
Rutter, M.2
Goode, S.3
Heemsbergen, J.4
Jordan, H.5
Mawhood, L.6
Schopler, E.7
-
28
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C, Rutter M, LeCouteur A. 1994. Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24:659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
LeCouteur, A.3
-
29
-
-
0001777849
-
Linkage evidence supports the involvement of chromosome 15 in autistic disorder
-
Abstract 208
-
Pericak-Vance M, Wolpert C, Menold M, Bass M, DeLong G, Beaty L, Zimmerman A, Potter N, Gilbert J, Vance J, Wright H, Abransom R, Cuccaro M. 1997. Linkage evidence supports the involvement of chromosome 15 in autistic disorder. Am J Hum Genet 61(suppl):S40. Abstract 208.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.SUPPL.
-
-
Pericak-Vance, M.1
Wolpert, C.2
Menold, M.3
Bass, M.4
DeLong, G.5
Beaty, L.6
Zimmerman, A.7
Potter, N.8
Gilbert, J.9
Vance, J.10
Wright, H.11
Abransom, R.12
Cuccaro, M.13
-
31
-
-
0024336203
-
The UCLA-University of Utah epidemiologic survey of autism: Recurrence risk estimates and genetic counseling
-
Ritvo ER, Jorde LB, Mason-Brothers A, Freeman BJ, Pingree C, Jones MB, McMahon WM, Petersen PB, Jenson WR, Mo A. 1989. The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling. Am J Psychiatry 146:1032-1036.
-
(1989)
Am J Psychiatry
, vol.146
, pp. 1032-1036
-
-
Ritvo, E.R.1
Jorde, L.B.2
Mason-Brothers, A.3
Freeman, B.J.4
Pingree, C.5
Jones, M.B.6
McMahon, W.M.7
Petersen, P.B.8
Jenson, W.R.9
Mo, A.10
-
33
-
-
15844368830
-
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22
-
Sawcer S, Jones HB, Feakes R, Gray J, Smaldon N, Chataway J, Robertson N, Clayton D, Goodfellow PN, Compston A. 1996. A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22. Nat Genet 13:464-468.
-
(1996)
Nat 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
Compston, A.10
-
34
-
-
0032156583
-
GenoMap; A distributed system for unifying genotyping and genetic linkage analysis
-
Scheetz TE, Braun TA, Munn KJ, Stone EM, Sheffield VC, Casavant TL. 1998. GenoMap; a distributed system for unifying genotyping and genetic linkage analysis. J Parallel Computing.
-
(1998)
J Parallel Computing
-
-
Scheetz, T.E.1
Braun, T.A.2
Munn, K.J.3
Stone, E.M.4
Sheffield, V.C.5
Casavant, T.L.6
-
35
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M, Simensen RJ, Bishop J, Skinner C, Fender D, Stevenson RE. 1998. Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet 76:327-336.
-
(1998)
Am J Med Genet
, vol.76
, pp. 327-336
-
-
Schroer, R.J.1
Phelan, M.C.2
Michaelis, R.C.3
Crawford, E.C.4
Skinner, S.A.5
Cuccaro, M.6
Simensen, R.J.7
Bishop, J.8
Skinner, C.9
Fender, D.10
Stevenson, R.E.11
-
36
-
-
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. et al. 1995. A collection of tri-and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-1844.
-
(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
-
37
-
-
0001395571
-
Testing for heterogeneity of the recombination fraction values in human genetics
-
Smith CAB. 1963. Testing for heterogeneity of the recombination fraction values in human genetics. Ann Hum Genet 27:175-182.
-
(1963)
Ann Hum Genet
, vol.27
, pp. 175-182
-
-
Smith, C.A.B.1
-
38
-
-
0022080849
-
Diagnostic uses of the Vineland adaptive behavior scales
-
Sparrow SS Cicchetti DV. 1985. Diagnostic uses of the Vineland Adaptive Behavior Scales. J Pediatr Psychol 10:215-225.
-
(1985)
J Pediatr Psychol
, vol.10
, pp. 215-225
-
-
Sparrow, S.S.1
Cicchetti, D.V.2
-
39
-
-
0002710362
-
Problems of replicating linkage claims in psychiatry
-
Gershon E, Cloniner C, editors. Washington, DC: American Psychiatric Press
-
Suarez B, Hampe C, Van Eerdewegh P. 1994. Problems of replicating linkage claims in psychiatry. In: Gershon E, Cloniner C, editors. Genetic approaches to mental disorders. Washington, DC: American Psychiatric Press. p 23-46.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 23-46
-
-
Suarez, B.1
Hampe, C.2
Van Eerdewegh, P.3
-
40
-
-
0029919557
-
The problem of ascertainment for linkage analysis
-
Vieland VJ, Hodge SE. 1996. The problem of ascertainment for linkage analysis. Am J Hum Genet 58:1072-1084.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1072-1084
-
-
Vieland, V.J.1
Hodge, S.E.2
-
41
-
-
0026684478
-
Adequacy of single-locus approximations for linkage analyses of oligogenic traits
-
Vieland VJ, Hodge SE, Greenberg DA. 1992. Adequacy of single-locus approximations for linkage analyses of oligogenic traits. Genet Epidemiol 9:45-59.
-
(1992)
Genet Epidemiol
, vol.9
, pp. 45-59
-
-
Vieland, V.J.1
Hodge, S.E.2
Greenberg, D.A.3
-
42
-
-
84878750553
-
A Bayesian approach to replication of linkage studies
-
In press. Goldin L, Amos CI, Chase GA, Goldstein AM, Jarvik GP, Martinez MM, Suarez BK, Weeks DW, Wijsman EM, and MacCluer JW. Genetic Analysis Workshop 11. Analysis of Genetic and Environmental Factors in Common Diseases
-
Wang K, Vieland VJ, Huang J. In press. A Bayesian approach to replication of linkage studies. In: Goldin L, Amos CI, Chase GA, Goldstein AM, Jarvik GP, Martinez MM, Suarez BK, Weeks DW, Wijsman EM, and MacCluer JW. Genetic Analysis Workshop 11. Analysis of Genetic and Environmental Factors in Common Diseases. Genetic Epidemiology.
-
Genetic Epidemiology
-
-
Wang, K.1
Vieland, V.J.2
Huang, J.3
|