-
1
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis GR, Cardon LR, Cookson WO. 2000. A general test of association for quantitative traits in nuclear families. Am J Hum Genet 66:279-292.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
2
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis G, Cherny S, Cookson W, Cardon L. 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.1
Cherny, S.2
Cookson, W.3
Cardon, L.4
-
3
-
-
0024443057
-
Elevated blood serotonin in autistic probands and their first-degree relatives
-
Abramson RK, Wright HH, Carpenter R, Brennan W, Lumpuy O, Cole E, Young SR. 1989. Elevated blood serotonin in autistic probands and their first-degree relatives. J Aut Dev Disord 19:397-407.
-
(1989)
J Aut Dev Disord
, vol.19
, pp. 397-407
-
-
Abramson, R.K.1
Wright, H.H.2
Carpenter, R.3
Brennan, W.4
Lumpuy, O.5
Cole, E.6
Young, S.R.7
-
4
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
-
Alarcon M, Cantor RM, Liu J, Gilliam C, Autism Genetic Research Exchange Consortium, Geschwind DH. 2002. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet 70:60-71.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, C.4
Geschwind, D.H.5
-
5
-
-
0031028361
-
Transmission disequilibrium tests for quantitative traits
-
Allison DB. 1997. Transmission disequilibrium tests for quantitative traits. Am J Hum Genet 60:676-690.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 676-690
-
-
Allison, D.B.1
-
6
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L, Blangero J. 1998. Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 62:1198-1211.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
8
-
-
0036884981
-
Genetics of childhood disorders: XLV. Autism, part 4: Serotonin and autism
-
Anderson GM. 2002. Genetics of childhood disorders: XLV. Autism, part 4: Serotonin and autism. J Am Acad Child Adolsec Psychiatry 41:1513-1516.
-
(2002)
J Am Acad Child Adolsec Psychiatry
, vol.41
, pp. 1513-1516
-
-
Anderson, G.M.1
-
9
-
-
0023440638
-
Whole blood serotonin in autistic and normal subjects
-
Anderson GM, Freedman DX, Cohen DJ, Volkmar FR, Hoder EL, McPhedran P, Minderaa RB, Hansen CR, Young JG. 1987. Whole blood serotonin in autistic and normal subjects. J Child Psychol Psychiatry 28:885-900.
-
(1987)
J Child Psychol Psychiatry
, vol.28
, pp. 885-900
-
-
Anderson, G.M.1
Freedman, D.X.2
Cohen, D.J.3
Volkmar, F.R.4
Hoder, E.L.5
McPhedran, P.6
Minderaa, R.B.7
Hansen, C.R.8
Young, J.G.9
-
10
-
-
0036780698
-
A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-oja T, Sinsheimer JS, Peltonen L, Järvelä I. 2002. A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet 71:777-790.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
Ylisaukko-oja, T.6
Sinsheimer, J.S.7
Peltonen, L.8
Järvelä, I.9
-
11
-
-
0029872978
-
Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey A, Phillips W, Rutter M. 1996. Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J Child Psychol Psychiatry 37:89-126.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
12
-
-
0031897162
-
A clinicopathological study of autism
-
Bailey AP, Luthert P, Dean A, Harding B, Janota I, Montgomery M, Rutter M, Lantos P. 1998. A clinicopathological study of autism. Brain 121:889-905.
-
(1998)
Brain
, vol.121
, pp. 889-905
-
-
Bailey, A.P.1
Luthert, P.2
Dean, A.3
Harding, B.4
Janota, I.5
Montgomery, M.6
Rutter, M.7
Lantos, P.8
-
13
-
-
0033573212
-
An autosomal genomic screen for autism
-
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL, Childress D, Folstein SE, Garcia M, Gardiner MB, Gilman S, Haines JL, Hopkins K, Landa R, Meyer NH, Mullane JA, Nishimura DY, Palmer P, Piven J, Purdy J, Santangelo SL, Searby C, Sheffiled V, Singleton J, Slager S, Struchen T, Svenson S, Vieland V, Wang K, Winklosky B. 1999. An autosomal genomic screen for autism. Am J Med Genet 88:609-615.
-
(1999)
Am J Med Genet
, vol.88
, pp. 609-615
-
-
Barrett, S.1
Beck, J.C.2
Bernier, R.3
Bisson, E.4
Braun, T.A.5
Casavant, T.L.6
Childress, D.7
Folstein, S.E.8
Garcia, M.9
Gardiner, M.B.10
Gilman, S.11
Haines, J.L.12
Hopkins, K.13
Landa, R.14
Meyer, N.H.15
Mullane, J.A.16
Nishimura, D.Y.17
Palmer, P.18
Piven, J.19
Purdy, J.20
Santangelo, S.L.21
Searby, C.22
Sheffiled, V.23
Singleton, J.24
Slager, S.25
Struchen, T.26
Svenson, S.27
Vieland, V.28
Wang, K.29
Winklosky, B.30
more..
-
14
-
-
0036302206
-
A major susceptibility locus for specific language impairment is located on 13q21
-
Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM. 2002. A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet 71:45-55.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 45-55
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Vieland, V.J.4
Bassett, A.S.5
Tallal, P.6
Brzustowicz, L.M.7
-
15
-
-
0034757723
-
Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation
-
Bertrand J, Mars A, Boyle C, Bove F, Yeargin-Allsopp M, Decoufle P. 2001. Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation. Pediatrics 108:1155-1161.
-
(2001)
Pediatrics
, vol.108
, pp. 1155-1161
-
-
Bertrand, J.1
Mars, A.2
Boyle, C.3
Bove, F.4
Yeargin-Allsopp, M.5
Decoufle, P.6
-
16
-
-
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
-
17
-
-
0028359950
-
A case-control family history study of autism
-
Bolton P, Macdonald H, Pickles A, Rios P, Goode S, Crowson M, Bailey A, Rutter M. 1994. A case-control family history study of autism. J Child Psychol Psychiatry 35:877-900.
-
(1994)
J Child Psychol Psychiatry
, vol.35
, pp. 877-900
-
-
Bolton, P.1
Macdonald, H.2
Pickles, A.3
Rios, P.4
Goode, S.5
Crowson, M.6
Bailey, A.7
Rutter, M.8
-
18
-
-
0035830071
-
Incorporating language phenotypes strengthens evidence of linkage to autism
-
Bradford Y, Haines J, Hutcheson H, Gardiner M, Braun T, Sheffield V, Cassavant T, Huang W, Wang K, Vieland V, Folstein S, Santangelo S, Piven J. 2001. Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet 105:539-547.
-
(2001)
Am J Med Genet
, vol.105
, pp. 539-547
-
-
Bradford, Y.1
Haines, J.2
Hutcheson, H.3
Gardiner, M.4
Braun, T.5
Sheffield, V.6
Cassavant, T.7
Huang, W.8
Wang, K.9
Vieland, V.10
Folstein, S.11
Santangelo, S.12
Piven, J.13
-
19
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL. 2001. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 68:1514-1520.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
Lawlor, B.A.7
Fitzgerald, M.8
Greenberg, D.A.9
Davis, K.L.10
-
20
-
-
1542284674
-
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19
-
Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG. 2004. Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. Mol Psychiatry 9:144-150.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 144-150
-
-
Buxbaum, J.D.1
Silverman, J.2
Keddache, M.3
Smith, C.J.4
Hollander, E.5
Ramoz, N.6
Reichert, J.G.7
-
21
-
-
0035958295
-
Pervasive developmental disorders in preschool children
-
Chakrabarti S, Fombonne E. 2001. Pervasive developmental disorders in preschool children. JAMA 285:3093-3099.
-
(2001)
JAMA
, vol.285
, pp. 3093-3099
-
-
Chakrabarti, S.1
Fombonne, E.2
-
22
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D. 1999. A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 65:1170-1177.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
23
-
-
0034132966
-
Reciprocal social behavior in children with and without pervasive developmental disorders
-
Constantino JN, Przybeck T, Friesen D, Todd RD. 2000. Reciprocal social behavior in children with and without pervasive developmental disorders. J Dev Behav Pediatr 21:2-11.
-
(2000)
J Dev Behav Pediatr
, vol.21
, pp. 2-11
-
-
Constantino, J.N.1
Przybeck, T.2
Friesen, D.3
Todd, R.D.4
-
24
-
-
0141539482
-
Validation of a brief quantitative measure of autistic traits: Comparison of the social responsiveness scale with the autism diagnostic interview-revised
-
Constantino JN, Davis SA, Todd RD, Schindler MK, Gross MM, Brophy SL, Metzger LM, Shoushtari CS, Splinter R, Reich W. 2003. Validation of a brief quantitative measure of autistic traits: Comparison of the social responsiveness scale with the autism diagnostic interview-revised. J Aut Dev Disord 33:427-433.
-
(2003)
J Aut Dev Disord
, vol.33
, pp. 427-433
-
-
Constantino, J.N.1
Davis, S.A.2
Todd, R.D.3
Schindler, M.K.4
Gross, M.M.5
Brophy, S.L.6
Metzger, L.M.7
Shoushtari, C.S.8
Splinter, R.9
Reich, W.10
-
26
-
-
0025074929
-
Autistic children and their first-degree relatives: Relationships between serotonin and norepinephrine levels and intelligence
-
Cook EH Jr, Leventhal BL, Heller W, Metz J, Wainwright M, Freedman DX. 1990. Autistic children and their first-degree relatives: Relationships between serotonin and norepinephrine levels and intelligence. J Neuropsychiatry Clin Neurosci 2:268-274.
-
(1990)
J Neuropsychiatry Clin Neurosci
, vol.2
, pp. 268-274
-
-
Cook Jr., E.H.1
Leventhal, B.L.2
Heller, W.3
Metz, J.4
Wainwright, M.5
Freedman, D.X.6
-
27
-
-
0028365630
-
Depressive and obsessive-compulsive symptoms in hyperserotonemic parents of children with autistic disorder
-
Cook EH Jr, Charak DA, Arida J, Spohn JA, Roizen NJ, Leventhal BL. 1994. Depressive and obsessive-compulsive symptoms in hyperserotonemic parents of children with autistic disorder. Psychiatry Res 52:25-33.
-
(1994)
Psychiatry Res
, vol.52
, pp. 25-33
-
-
Cook Jr., E.H.1
Charak, D.A.2
Arida, J.3
Spohn, J.A.4
Roizen, N.J.5
Leventhal, B.L.6
-
28
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Levanthal 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.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Yan, S.5
Lincoln, A.6
Haas, R.7
Courchesne, E.8
Levanthal, B.L.9
-
29
-
-
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 29:229-232.
-
(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
-
30
-
-
0036616585
-
Defining the broader phenotype of autism: Genetic, brain, and behavioral perspectives
-
Dawson G, Webb S, Schellenber GD, Dager S, Friedman S, Aylward E, Richards T. 2002. Defining the broader phenotype of autism: Genetic, brain, and behavioral perspectives. Dev Psychopathol 14:581-611.
-
(2002)
Dev Psychopathol
, vol.14
, pp. 581-611
-
-
Dawson, G.1
Webb, S.2
Schellenber, G.D.3
Dager, S.4
Friedman, S.5
Aylward, E.6
Richards, T.7
-
31
-
-
0035924324
-
The DNA sequence and comparative analysis of human chromosome 20
-
Deloukas P, Matthews LH, Ashurst J, Burton J, Gilbert JG, Jones M, Stavrides G, Almeida JP, Babbage AK, Bagguley CL, Bailey J, Barlow KF, Bates KN, Beard LM, Beare DM, Beasley OP, Bird CP, Blakey SE, Bridgeman AM, Brown AJ, Buck D, Burrill W, Butler AP, Carder C, Carter NP, Chapman JC, Clamp M, Clark G, Clark LN, Clark SY, Clee CM, Clegg S, Cobley VE, Collier RE, Connor R, Corby NR, Coulson A, Coville GJ, Deadman R, Dhami P, Dunn M, Ellington AG, Frankland JA, Fraser A, French L, Garner P, Grafham DV, Griffiths C, Griffiths MN, Gwilliam R, Hall RE, Hammond S, Harley JL, Heath PD, Ho S, Holden JL, Howden PJ, Huckle E, Hunt AR, Hunt SE, Jekosch K, Johnson CM, Johnson D, Kay MP, Kimberley AM, King A, Knights A, Laird GK, Lawlor S, Lehvaslaiho MH, Leversha M, Lloyd C, Lloyd DM, Lovell JD, Marsh VL, Martin SL, McConnachie LJ, McLay K, McMurray AA, Milne S, Mistry D, Moore MJ, Mullikin JC, Nickerson T, Oliver K, Parker A, Patel R, Pearce TA, Peck AI, Phillimore BJ, Prathalingam SR, Plumb RW, Ramsay H, Rice CM, Ross MT, Scott CE, Sehra HK, Shownkeen R, Sims S, Skuce CD, Smith ML, Soderlund C, Steward CA, Sulston JE, Swann M, Sycamore N, Taylor R, Tee L, Thomas DW, Thorpe A, Tracey A, Tromans AC, Vaudin M, Wall M, Wallis JM, Whitehead SL, Whittaker P, Willey DL, Williams L, Williams SA, Wilming L, Wray PW, Hubbard T, Durbin RM, Bentley DR, Beck S, Rogers J. 2001. The DNA sequence and comparative analysis of human chromosome 20. Nature 414:865-871.
-
(2001)
Nature
, vol.414
, pp. 865-871
-
-
Deloukas, P.1
Matthews, L.H.2
Ashurst, J.3
Burton, J.4
Gilbert, J.G.5
Jones, M.6
Stavrides, G.7
Almeida, J.P.8
Babbage, A.K.9
Bagguley, C.L.10
Bailey, J.11
Barlow, K.F.12
Bates, K.N.13
Beard, L.M.14
Beare, D.M.15
Beasley, O.P.16
Bird, C.P.17
Blakey, S.E.18
Bridgeman, A.M.19
Brown, A.J.20
Buck, D.21
Burrill, W.22
Butler, A.P.23
Carder, C.24
Carter, N.P.25
Chapman, J.C.26
Clamp, M.27
Clark, G.28
Clark, L.N.29
Clark, S.Y.30
Clee, C.M.31
Clegg, S.32
Cobley, V.E.33
Collier, R.E.34
Connor, R.35
Corby, N.R.36
Coulson, A.37
Coville, G.J.38
Deadman, R.39
Dhami, P.40
Dunn, M.41
Ellington, A.G.42
Frankland, J.A.43
Fraser, A.44
French, L.45
Garner, P.46
Grafham, D.V.47
Griffiths, C.48
Griffiths, M.N.49
Gwilliam, R.50
Hall, R.E.51
Hammond, S.52
Harley, J.L.53
Heath, P.D.54
Ho, S.55
Holden, J.L.56
Howden, P.J.57
Huckle, E.58
Hunt, A.R.59
Hunt, S.E.60
Jekosch, K.61
Johnson, C.M.62
Johnson, D.63
Kay, M.P.64
Kimberley, A.M.65
King, A.66
Knights, A.67
Laird, G.K.68
Lawlor, S.69
Lehvaslaiho, M.H.70
Leversha, M.71
Lloyd, C.72
Lloyd, D.M.73
Lovell, J.D.74
Marsh, V.L.75
Martin, S.L.76
McConnachie, L.J.77
McLay, K.78
McMurray, A.A.79
Milne, S.80
Mistry, D.81
Moore, M.J.82
Mullikin, J.C.83
Nickerson, T.84
Oliver, K.85
Parker, A.86
Patel, R.87
Pearce, T.A.88
Peck, A.I.89
Phillimore, B.J.90
Prathalingam, S.R.91
Plumb, R.W.92
Ramsay, H.93
Rice, C.M.94
Ross, M.T.95
Scott, C.E.96
Sehra, H.K.97
Shownkeen, R.98
Sims, S.99
more..
-
32
-
-
0032714352
-
Genomic control for association studies
-
Devlin B, Roeder K. 1999. Genomic control for association studies. Biometrics 55:997-1004.
-
(1999)
Biometrics
, vol.55
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
33
-
-
0036137962
-
Mixture models for linkage analysis of affected sibling pairs and covariates
-
Devlin B, Jones BL, Bacanu SA, Roeder K. 2002. Mixture models for linkage analysis of affected sibling pairs and covariates. Genet Epidemiol 22:52-65.
-
(2002)
Genet Epidemiol
, vol.22
, pp. 52-65
-
-
Devlin, B.1
Jones, B.L.2
Bacanu, S.A.3
Roeder, K.4
-
35
-
-
0025778539
-
Etiology of autism: Genetic influences
-
Folstein SE, Piven J. 1991. Etiology of autism: Genetic influences. Pediatrics 87:767-773.
-
(1991)
Pediatrics
, vol.87
, pp. 767-773
-
-
Folstein, S.E.1
Piven, J.2
-
36
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein SE, Rutter M. 1977. Infantile autism: A genetic study of 21 twin pairs. J Child Psychol Psychiatry 18:297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.E.1
Rutter, M.2
-
37
-
-
0344329866
-
Predictors of cognitive test patterns in autism families
-
Folstein SE, Santangelo SL, Gilman SE, Piven J, Landa R, Lainhart J, Hein J, Wzorek M. 1999. Predictors of cognitive test patterns in autism families. J Child Psychol Psychiatry 40:1117-1128.
-
(1999)
J Child Psychol Psychiatry
, vol.40
, pp. 1117-1128
-
-
Folstein, S.E.1
Santangelo, S.L.2
Gilman, S.E.3
Piven, J.4
Landa, R.5
Lainhart, J.6
Hein, J.7
Wzorek, M.8
-
38
-
-
0032804766
-
The epidemiology of autism: A review
-
Fombonne E. 1999. the epidemiology of autism: A review. Psychol Med 29:767-786.
-
(1999)
Psychol Med
, vol.29
, pp. 767-786
-
-
Fombonne, E.1
-
39
-
-
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. 2002. Altshuler D. 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
-
40
-
-
79959503826
-
The International HapMap Project
-
Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H. 2003. The International HapMap Project. Nature 426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
Gibbs, R.A.1
Belmont, J.W.2
Hardenbol, P.3
Willis, T.D.4
Yu, F.5
Yang, H.6
-
41
-
-
0034098774
-
Allegro, a new computer program for multipoint linkage analysis
-
Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. 2000. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 25:12-13.
-
(2000)
Nat Genet
, vol.25
, pp. 12-13
-
-
Gudbjartsson, D.F.1
Jonasson, K.2
Frigge, M.L.3
Kong, A.4
-
43
-
-
13844313862
-
Whole-genome patterns of common DNA variation in three human populations
-
Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. 2005. Whole-genome patterns of common DNA variation in three human populations. Science 307:1072-1079.
-
(2005)
Science
, vol.307
, pp. 1072-1079
-
-
Hinds, D.A.1
Stuve, L.L.2
Nilsen, G.B.3
Halperin, E.4
Eskin, E.5
Ballinger, D.G.6
Frazer, K.A.7
Cox, D.R.8
-
44
-
-
0033940030
-
The transmission/disequilibrium test for linkage on the X chromosome
-
Ho GY, Bailey-Wilson JE. 2000. The transmission/disequilibrium test for linkage on the X chromosome. Am J Hum Genet 66:1158-1160.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1158-1160
-
-
Ho, G.Y.1
Bailey-Wilson, J.E.2
-
45
-
-
0032470875
-
A discordant-sibship test for disequilibrium and linkage: No need for parental data
-
Horvath S, Laird NM. 1998. A discordant-sibship test for disequilibrium and linkage: No need for parental data. Am J Hum Genet 63:1886-1897.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1886-1897
-
-
Horvath, S.1
Laird, N.M.2
-
46
-
-
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
-
IMGSAC. 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q: International Molecular Genetic Study of Autism Consortium. Hum Mol Genet 7:571-578.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
47
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
IMGSAC
-
IMGSAC. 2001. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 69:570-581.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 570-581
-
-
-
48
-
-
0033782508
-
An EM algorithm for obtaining maximum likelihood estimates in the multi-phenotype variance components linkage model
-
Iturria SJ, Blangero J. 2000. An EM algorithm for obtaining maximum likelihood estimates in the multi-phenotype variance components linkage model. Ann Hum Genet 64:349-362.
-
(2000)
Ann Hum Genet
, vol.64
, pp. 349-362
-
-
Iturria, S.J.1
Blangero, J.2
-
49
-
-
0037043029
-
A risk-factor model of epistatic interaction, focusing on autism
-
Jones MB, Szatmari P. 2002. A risk-factor model of epistatic interaction, focusing on autism. Am J Med Genet 114:558-565.
-
(2002)
Am J Med Genet
, vol.114
, pp. 558-565
-
-
Jones, M.B.1
Szatmari, P.2
-
50
-
-
85047695697
-
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder
-
Kim S-J, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH. 2002. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry 7:278-288.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 278-288
-
-
Kim, S.-J.1
Cox, N.2
Courchesne, R.3
Lord, C.4
Corsello, C.5
Akshoomoff, N.6
Guter, S.7
Leventhal, B.L.8
Courchesne, E.9
Cook, E.H.10
-
51
-
-
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
-
53
-
-
0031014011
-
Macrocephaly in children and adults with autism
-
Lainhart JE, Piven J, Wzorek M, Landa R, Santangelo SL, Coon H, Folstein SE. 1997. Macrocephaly in children and adults with autism. J Am Acad Child Adolsec Psychiatry 36:282-290.
-
(1997)
J Am Acad Child Adolsec Psychiatry
, vol.36
, pp. 282-290
-
-
Lainhart, J.E.1
Piven, J.2
Wzorek, M.3
Landa, R.4
Santangelo, S.L.5
Coon, H.6
Folstein, S.E.7
-
54
-
-
0033814928
-
Implementing a unified approach to family based tests of association
-
Laird NM, Horvath S, Xu X. 2000. Implementing a unified approach to family based tests of association. Genet Epidemiol 19(suppl): 36-42.
-
(2000)
Genet Epidemiol
, vol.19
, Issue.SUPPL.
, pp. 36-42
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
55
-
-
0000803318
-
Construction of multilocus genetic linkage maps in humans
-
Lander ES, Green P. 1987. Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 84:2363-2367.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.S.1
Green, P.2
-
57
-
-
0025244988
-
Relationships of whole blood serotonin and plasma norepinephrine within families
-
Leventhal BL, Cook EH Jr, Morford M, Ravitz A, Freedman D. 1990. Relationships of whole blood serotonin and plasma norepinephrine within families. J Autism Dev Disord 20:499-511.
-
(1990)
J Autism Dev Disord
, vol.20
, pp. 499-511
-
-
Leventhal, B.L.1
Cook Jr., E.H.2
Morford, M.3
Ravitz, A.4
Freedman, D.5
-
58
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu JJ, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC. 2001. A genomewide screen for autism susceptibility loci. Am J Hum Genet 69:327-340.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 327-340
-
-
Liu, J.J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
Geschwind, D.6
Lord, C.7
Iversen, P.8
Hoh, J.9
Ott, J.10
Gilliam, T.C.11
-
59
-
-
2942724284
-
A new method for computing the multipoint posterior probability of linkage
-
Logue MW, Vieland VJ. 2004. A new method for computing the multipoint posterior probability of linkage. Hum Hered 57:90-99.
-
(2004)
Hum Hered
, vol.57
, pp. 90-99
-
-
Logue, M.W.1
Vieland, V.J.2
-
60
-
-
0035825228
-
Quantifying the phenotype in autism spectrum disorders
-
Lord C, Leventhal BL, Cook EH Jr. 2001. Quantifying the phenotype in autism spectrum disorders. Am J Med Genet 105:36-38.
-
(2001)
Am J Med Genet
, vol.105
, pp. 36-38
-
-
Lord, C.1
Leventhal, B.L.2
Cook Jr., E.H.3
-
61
-
-
0033807328
-
Increased density of the platelet serotonin transporter in autism
-
Marazziti D, Muratori F, Cesari A, Masala I, Baroni S, Giannaccini G, Dell'Osso L, Cosenza A, Pfanner P, Cassano GB. 2000. Increased density of the platelet serotonin transporter in autism. Pharmacopsychiatry 33:165-168.
-
(2000)
Pharmacopsychiatry
, vol.33
, pp. 165-168
-
-
Marazziti, D.1
Muratori, F.2
Cesari, A.3
Masala, I.4
Baroni, S.5
Giannaccini, G.6
Dell'Osso, L.7
Cosenza, A.8
Pfanner, P.9
Cassano, G.B.10
-
62
-
-
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
-
63
-
-
24144452995
-
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
-
McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS. 2005. Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet 6:1.
-
(2005)
BMC Med Genet
, vol.6
, pp. 1
-
-
McCauley, J.L.1
Li, C.2
Jiang, L.3
Olson, L.M.4
Crockett, G.5
Gainer, K.6
Folstein, S.E.7
Haines, J.L.8
Sutcliffe, J.S.9
-
64
-
-
0029805972
-
Effects of tryptophan depletion in drug-free adults with autistic disorder
-
McDougle CJ, Naylor ST, Cohen DJ, Aghajanian GK, Heninger GR, Price LH. 1996. Effects of tryptophan depletion in drug-free adults with autistic disorder. Arch Gen Psychiatry 53:993-1000.
-
(1996)
Arch Gen Psychiatry
, vol.53
, pp. 993-1000
-
-
McDougle, C.J.1
Naylor, S.T.2
Cohen, D.J.3
Aghajanian, G.K.4
Heninger, G.R.5
Price, L.H.6
-
66
-
-
0036889590
-
Molecular genetics of speech and language disorders
-
Newbury DF, Monaco AP. 2002. Molecular genetics of speech and language disorders. Curr Opin Pediatr 14:696-701.
-
(2002)
Curr Opin Pediatr
, vol.14
, pp. 696-701
-
-
Newbury, D.F.1
Monaco, A.P.2
-
67
-
-
9444222468
-
Microarray-based comparative genome hybridization and its applications in human genetics
-
Oostlander AE, Meijer GA, Ylstra B. 2004. Microarray-based comparative genome hybridization and its applications in human genetics. Clin Genet 66:488-495.
-
(2004)
Clin Genet
, vol.66
, pp. 488-495
-
-
Oostlander, A.E.1
Meijer, G.A.2
Ylstra, B.3
-
69
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes
-
Philippe A, Martinez M, Guilloudbataille M, Gillberg C, Rastam M, Sponheim E, Colemati M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M. 1999. Genome-wide scan for autism susceptibility genes. Hum Mol Genet 8:805-812.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloudbataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Colemati, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
Penet, C.11
Feingold, J.12
Brice, A.13
Leboyer, M.14
-
70
-
-
0029134874
-
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
-
Pickles A, Bolton P, MacDonald H, Bailey A, Le Couteur A, Sim CH, Rutter M. 1995. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism. Am J Hum Genet 57:717-726.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
MacDonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
Rutter, M.7
-
71
-
-
0002020253
-
Psychiatric disorders in the parents of autistic individuals
-
Piven J, Chase GA, Landa R, Wzorek M, Gayle J, Cloud D, Folstein S. 1991. Psychiatric disorders in the parents of autistic individuals. J Am Acad Child Adolsec Psychiatry 30:471-478.
-
(1991)
J Am Acad Child Adolsec Psychiatry
, vol.30
, pp. 471-478
-
-
Piven, J.1
Chase, G.A.2
Landa, R.3
Wzorek, M.4
Gayle, J.5
Cloud, D.6
Folstein, S.7
-
72
-
-
0031035019
-
Broader autism phenotype: Evidence from, a family history study of multiple-incidence autism families
-
Piven J, Palmer P, Jacobi D, Childress D, Arndt S. 1997a. Broader autism phenotype: Evidence from, a family history study of multiple-incidence autism families. Am J Psychiatry 154:185-190.
-
(1997)
Am J Psychiatry
, vol.154
, pp. 185-190
-
-
Piven, J.1
Palmer, P.2
Jacobi, D.3
Childress, D.4
Arndt, S.5
-
73
-
-
0030799999
-
Personality and language characteristics in parents from multiple-incidence autism families
-
Piven J, Palmer P, Landa R, Santangelo S, Jacobi D, Childress D. 1997b. Personality and language characteristics in parents from multiple-incidence autism families. Am J Med Genet 74:398-411.
-
(1997)
Am J Med Genet
, vol.74
, pp. 398-411
-
-
Piven, J.1
Palmer, P.2
Landa, R.3
Santangelo, S.4
Jacobi, D.5
Childress, D.6
-
74
-
-
0029608991
-
Verbal skills in relatives of autistic females
-
Plumet MH, Goldblum MC, Leboyer M. 1995. Verbal skills in relatives of autistic females. Cortex 31:723-733.
-
(1995)
Cortex
, vol.31
, pp. 723-733
-
-
Plumet, M.H.1
Goldblum, M.C.2
Leboyer, M.3
-
75
-
-
0002028461
-
The Role of Serotonin in Autism-Spectrum Disorders
-
Potenza MN, McDougle CJ. 1997. The Role of Serotonin in Autism-Spectrum Disorders. CNS Spectrums 2:25-42.
-
(1997)
CNS Spectrums
, vol.2
, pp. 25-42
-
-
Potenza, M.N.1
McDougle, C.J.2
-
76
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard JK. 2001. Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124-137.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
77
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly PJ. 2000a. Inference of population structure using multilocus genotype data. Genetics 155:945-959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.J.3
-
79
-
-
0030827556
-
A transmission disequilibrium test for quantitative trait loci
-
Rabinowitz D. 1997. A transmission disequilibrium test for quantitative trait loci. Hum Hered 47:342-350.
-
(1997)
Hum Hered
, vol.47
, pp. 342-350
-
-
Rabinowitz, D.1
-
80
-
-
0003201075
-
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
-
Rabinowitz D, Laird NM. 2000. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered 504:227-233.
-
(2000)
Hum Hered
, vol.504
, pp. 227-233
-
-
Rabinowitz, D.1
Laird, N.M.2
-
81
-
-
0029743998
-
Practitioner review: Developmental language disorders: A clinical update
-
Rapin I. 1996. Practitioner review: Developmental language disorders: A clinical update. J Child Psychol Psychiatry 37:643-655.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 643-655
-
-
Rapin, I.1
-
82
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Myers RM. 1999. A genomic screen of autism: Evidence for a multilocus etiology. Am J Hum Genet 65:493-507.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
Kalaydjieva, L.7
McCague, P.8
Dimiceli, S.9
Pitts, T.10
Nguyen, L.11
Yang, J.12
Harper, C.13
Thorpe, D.14
Vermeer, S.15
Young, H.16
Hebert, J.17
Lin, A.18
Ferguson, J.19
Chiotti, C.20
Wiese-Slater, S.21
Rogers, T.22
Salmon, B.23
Nicholas, P.24
Myers, R.M.25
more..
-
83
-
-
0037310257
-
Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity
-
Ritchie MD, Hahn LW, Moore JH. 2003a. Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity. Genet Epidemiol 24:150-157.
-
(2003)
Genet Epidemiol
, vol.24
, pp. 150-157
-
-
Ritchie, M.D.1
Hahn, L.W.2
Moore, J.H.3
-
84
-
-
0642368712
-
Optimization of neural network architecture using genetic programming improves detection and modeling of gene-gene interactions in studies of human diseases
-
Ritchie MD, White BC, Parker JS, Hahn LW, Moore JH. 2003b. Optimization of neural network architecture using genetic programming improves detection and modeling of gene-gene interactions in studies of human diseases. BMC Bioinformatics 4:28.
-
(2003)
BMC Bioinformatics
, vol.4
, pp. 28
-
-
Ritchie, M.D.1
White, B.C.2
Parker, J.S.3
Hahn, L.W.4
Moore, J.H.5
-
85
-
-
0038449167
-
Evolutionary-based association analysis using haplotype data
-
Seltman H, Roeder K, Devlin B. 2003. Evolutionary-based association analysis using haplotype data. Genet Epidemiol 25:48-58.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 48-58
-
-
Seltman, H.1
Roeder, K.2
Devlin, B.3
-
86
-
-
18344374001
-
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
-
Shao YJ, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashleykoch AA, Abramson RK, Wright HH, Delong RG, Gilbert JR, Cuccaro ML, Pericakvance MA. 2002. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. Am J Hum Genet 70:1058-1061.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1058-1061
-
-
Shao, Y.J.1
Raiford, K.L.2
Wolpert, C.M.3
Cope, H.A.4
Ravan, S.A.5
Ashleykoch, A.A.6
Abramson, R.K.7
Wright, H.H.8
Delong, R.G.9
Gilbert, J.R.10
Cuccaro, M.L.11
Pericakvance, M.A.12
-
87
-
-
40649113305
-
Symptom domains in autism and related conditions: Evidence for familiality
-
Silverman JM, Smith CJ, Schmeidler J, Hollander E, Lawlor BA, Fitzgerald M, Buxbaum JD, Delaney K, Galvin P, Autism Genetic Research Exchange Consortium. 2002. Symptom domains in autism and related conditions: Evidence for familiality. Am J Med Genet 114:64-73.
-
(2002)
Am J Med Genet
, vol.114
, pp. 64-73
-
-
Silverman, J.M.1
Smith, C.J.2
Schmeidler, J.3
Hollander, E.4
Lawlor, B.A.5
Fitzgerald, M.6
Buxbaum, J.D.7
Delaney, K.8
Galvin, P.9
-
88
-
-
0029944752
-
Brief report: Genetic, prenatal, and immunologic factors
-
Smalley SL, Collins F. 1996. Brief report: Genetic, prenatal, and immunologic factors. J Autism Dev Disord 26:195-198.
-
(1996)
J Autism Dev Disord
, vol.26
, pp. 195-198
-
-
Smalley, S.L.1
Collins, F.2
-
89
-
-
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 HumGenet 62:450-458.
-
(1998)
Am J HumGenet
, vol.62
, pp. 450-458
-
-
Spielman, R.S.1
Ewens, W.J.2
-
90
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. 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
-
91
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M. 1989. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 30:405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
92
-
-
0029116940
-
Parents and collateral relatives of children with pervasive developmental disorders: A family history study
-
Szatmari P, Jones MB, Fisman S, Tuff L, Bartolucci G, Mahoney WJ, Bryson SE. 1995. Parents and collateral relatives of children with pervasive developmental disorders: A family history study. Am J Med Gen 60:60:282-289.
-
(1995)
Am J Med Gen
, vol.60
, Issue.60
, pp. 282-289
-
-
Szatmari, P.1
Jones, M.B.2
Fisman, S.3
Tuff, L.4
Bartolucci, G.5
Mahoney, W.J.6
Bryson, S.E.7
-
94
-
-
0026494911
-
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations
-
Terwilliger JD, Ott J. 1992. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Hum Hered 42:337-346.
-
(1992)
Hum Hered
, vol.42
, pp. 337-346
-
-
Terwilliger, J.D.1
Ott, J.2
-
95
-
-
21344454198
-
Characterizing allelic associations from unphased diploid data by graphical modeling
-
Thomas A. 2005. Characterizing allelic associations from unphased diploid data by graphical modeling. Genet Epidemiol 29:23-35.
-
(2005)
Genet Epidemiol
, vol.29
, pp. 23-35
-
-
Thomas, A.1
-
96
-
-
2442713792
-
Graphical modeling of the joint distribution of alleles at associated loci
-
Thomas A, Camp NJ. 2004. Graphical modeling of the joint distribution of alleles at associated loci. Am J Hum Genet 74:1088-1101.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1088-1101
-
-
Thomas, A.1
Camp, N.J.2
-
97
-
-
0042226484
-
Multipoint linkage analysis by blocked (Gibbs) sampling
-
Thomas A, Gutin A, Abkevich V, Bansai A. 2000. Multipoint linkage analysis by blocked (Gibbs) sampling. Stats Comp 10:259-269.
-
(2000)
Stats Comp
, vol.10
, pp. 259-269
-
-
Thomas, A.1
Gutin, A.2
Abkevich, V.3
Bansai, A.4
-
98
-
-
0034987571
-
Role of the serotonin transporter in the behavioral expression of autism
-
Tordjman S, Gutneckt L, Carlier M, Spitz E, Antoine C, Slama F, Cohen D, Ferrari P, Roubertoux P, Anderson G. 2001. Role of the serotonin transporter in the behavioral expression of autism. Mol Psychiatry 6:434-439.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 434-439
-
-
Tordjman, S.1
Gutneckt, L.2
Carlier, M.3
Spitz, E.4
Antoine, C.5
Slama, F.6
Cohen, D.7
Ferrari, P.8
Roubertoux, P.9
Anderson, G.10
-
99
-
-
0032231376
-
Bayesian linkage analysis, or: How I learned to stop worrying and love the posterior probability of linkage
-
Vieland VJ. 1998. Bayesian linkage analysis, or: How I learned to stop worrying and love the posterior probability of linkage. Am J Hum Genet 63:947-954.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 947-954
-
-
Vieland, V.J.1
-
101
-
-
0031949066
-
A log-linear approach to case-parent-triad data: Assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
-
Weinberg CR, Wilcox AJ, Lie RT. 1998. A log-linear approach to case-parent-triad data: Assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 62:969-978.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 969-978
-
-
Weinberg, C.R.1
Wilcox, A.J.2
Lie, R.T.3
-
102
-
-
11244294384
-
Joint oligogenic segregation and linkage analysis using bayesian markov chain monte carlo methods
-
Wijsman E, Yu D. 2004. Joint oligogenic segregation and linkage analysis using bayesian markov chain monte carlo methods. Mol Biotechnol 28:205-226.
-
(2004)
Mol Biotechnol
, vol.28
, pp. 205-226
-
-
Wijsman, E.1
Yu, D.2
-
103
-
-
0033747281
-
A phonological investigation of four siblings with childhood autism
-
Wolk L, Giesen J. 2000. A phonological investigation of four siblings with childhood autism. J Commun Disord 33:371-389.
-
(2000)
J Commun Disord
, vol.33
, pp. 371-389
-
-
Wolk, L.1
Giesen, J.2
-
104
-
-
0029778284
-
Head circumference in autism and other pervasive developmental disorders
-
Woodhouse W, Bailey A, Rutter M, Bolton P, Baird G, Le Couleur A. 1996. Head circumference in autism and other pervasive developmental disorders. J Child Psychol Psychiatry 37:665-671.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 665-671
-
-
Woodhouse, W.1
Bailey, A.2
Rutter, M.3
Bolton, P.4
Baird, G.5
Le Couleur, A.6
-
105
-
-
0001200144
-
Testing linkage disequilibrium between a disease gene and marker loci
-
abstr
-
Xie X, Ott J. 1993. Testing linkage disequilibrium between a disease gene and marker loci. Am J Hum Genet 53:1107 [abstr].
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1107
-
-
Xie, X.1
Ott, J.2
-
106
-
-
0032465321
-
TDT statistics for mapping quantitative trait loci
-
Xiong MM, Krushkal J, Boerwinkle E. 1998. TDT statistics for mapping quantitative trait loci. Ann Hum Genet 62:431-452.
-
(1998)
Ann Hum Genet
, vol.62
, pp. 431-452
-
-
Xiong, M.M.1
Krushkal, J.2
Boerwinkle, E.3
-
107
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
Yirmiya N, Pilowsky T, Nemanov L, Arbelle S, Feinsilver T, Fried I, Ebstein RP. 2001. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am J Med Genet 105:381-386.
-
(2001)
Am J Med Genet
, vol.105
, pp. 381-386
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbelle, S.4
Feinsilver, T.5
Fried, I.6
Ebstein, R.P.7
-
108
-
-
1542284670
-
Genome-wide scan for loci of Asperger syndrome
-
Ylisaukkooja T, NieminenvonWendt T, Kempas E, Sarenius S, Varilo T, vonWendt L, Peltonen L, Jarvela I. 2004. Genome-wide scan for loci of Asperger syndrome. Mol Psychiatry 9:161-168.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 161-168
-
-
Ylisaukkooja, T.1
Nieminenvonwendt, T.2
Kempas, E.3
Sarenius, S.4
Varilo, T.5
Vonwendt, L.6
Peltonen, L.7
Jarvela, I.8
-
109
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PKE, Spence SJ, Palmer AA, Grunn A, Juo SHH, Terwilliger JD, Liu JJ, Cantor RM, Geschwind DH, Gilliam TC. 2003. A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet 73:886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.E.4
Spence, S.J.5
Palmer, A.A.6
Grunn, A.7
Juo, S.H.H.8
Terwilliger, J.D.9
Liu, J.J.10
Cantor, R.M.11
Geschwind, D.H.12
Gilliam, T.C.13
-
110
-
-
0037188541
-
A dynamic programming algorithm for haplotype block partitioning
-
Zhang K, Deng M, Chen T, Waterman MS, Sun F. 2002. A dynamic programming algorithm for haplotype block partitioning. Proc Natl Acad Sci USA 99:7335-7339.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 7335-7339
-
-
Zhang, K.1
Deng, M.2
Chen, T.3
Waterman, M.S.4
Sun, F.5
-
111
-
-
0033990339
-
Model-free analysis and permutation test for allelic associations
-
Zhao JH, Curtis D, Sham PC. 2000. Model-free analysis and permutation test for allelic associations. Hum Hered 50:133-139.
-
(2000)
Hum Hered
, vol.50
, pp. 133-139
-
-
Zhao, J.H.1
Curtis, D.2
Sham, P.C.3
-
112
-
-
0036668723
-
Association mapping, using a mixture model for complex traits
-
Zhu X, Zhang S, Zhao H, Cooper RS. 2002. Association mapping, using a mixture model for complex traits. Genet Epidemiol 23:181-196.
-
(2002)
Genet Epidemiol
, vol.23
, pp. 181-196
-
-
Zhu, X.1
Zhang, S.2
Zhao, H.3
Cooper, R.S.4
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