-
1
-
-
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 25:63-77.
-
(1995)
Psychol Med
, vol.25
, 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
-
2
-
-
21244472348
-
Specific genetic disorders and autism: Clinical contribution towards their identification
-
Cohen D, Pichard N, Tordjman S, Baumann C, Burglen L, Excoffier E, Lazar G, Mazet P, Pinquier C, Verloes A, Heron D (2005) Specific genetic disorders and autism: clinical contribution towards their identification. J Autism Dev Disord 35:103-116.
-
(2005)
J Autism Dev Disord
, vol.35
, pp. 103-116
-
-
Cohen, D.1
Pichard, N.2
Tordjman, S.3
Baumann, C.4
Burglen, L.5
Excoffier, E.6
Lazar, G.7
Mazet, P.8
Pinquier, C.9
Verloes, A.10
Heron, D.11
-
3
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein S, 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.1
Rutter, M.2
-
4
-
-
0035871209
-
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium (IMGSAC) (2001) Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Hum Mol Genet 10:973-982.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 973-982
-
-
-
5
-
-
13444269226
-
Analysis of IMGSAC autism susceptibility loci: Evidence for sex limited and parent of origin specific effects
-
Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E, Blasi F, Maestrini E, Broxholme J, Tzenova J, Weeks D, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC) (2005) Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. J Med Genet 42:132-137.
-
(2005)
J Med Genet
, vol.42
, pp. 132-137
-
-
Lamb, J.A.1
Barnby, G.2
Bonora, E.3
Sykes, N.4
Bacchelli, E.5
Blasi, F.6
Maestrini, E.7
Broxholme, J.8
Tzenova, J.9
Weeks, D.10
Bailey, A.J.11
Monaco, A.P.12
-
6
-
-
0029959476
-
A broader phenotype of autism: The clinical spectrum in twins
-
Le Couteur A, Bailey A, Goode S, Pickles A, Robertson S, Gottesman I, Rutter M (1996) A broader phenotype of autism: the clinical spectrum in twins. J Child Psychol Psychiatry 37:785-801.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 785-801
-
-
Le Couteur, A.1
Bailey, A.2
Goode, S.3
Pickles, A.4
Robertson, S.5
Gottesman, I.6
Rutter, M.7
-
8
-
-
0038752692
-
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: Suggestive linkage on 17p11
-
Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C, Cantor RM, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL (2003) A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. Am J Hum Genet 72:1268-1279.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1268-1279
-
-
Ogdie, M.N.1
Macphie, I.L.2
Minassian, S.L.3
Yang, M.4
Fisher, S.E.5
Francks, C.6
Cantor, R.M.7
McCracken, J.T.8
McGough, J.J.9
Nelson, S.F.10
Monaco, A.P.11
Smalley, S.L.12
-
9
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard JK (2001) Are rare variants responsible for susceptibility to complex diseases? American Journal of Human Genetics 69, 124-137.
-
(2001)
American Journal of Human Genetics
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
10
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of afflicted twins
-
Ritvo ER, Freeman BJ, Mason-Brothers A, Mo A, Ritvo AM (1985) Concordance for the syndrome of autism in 40 pairs of afflicted twins. Am J Psychiatry 142:74-7.
-
(1985)
Am J Psychiatry
, vol.142
, pp. 74-77
-
-
Ritvo, E.R.1
Freeman, B.J.2
Mason-Brothers, A.3
Mo, A.4
Ritvo, A.M.5
-
11
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse DH, James RS, Bishop DV, Coppin B, Dalton P, Aamodt-Leeper G, Bacarese-Hamilton M, Creswell C, McGurk R, Jacobs PA (1997) Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 387:705-708.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.3
Coppin, B.4
Dalton, P.5
Aamodt-Leeper, G.6
Bacarese-Hamilton, M.7
Creswell, C.8
McGurk, R.9
Jacobs, P.A.10
-
12
-
-
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
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