-
1
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner L. Autistic disturbances of affective contact. Nervous Child. 1943;2:217-250.
-
(1943)
Nervous Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
2
-
-
0031563047
-
Autism
-
Rapin I. Autism. NEJM. 1997;337:97-103.
-
(1997)
NEJM
, vol.337
, pp. 97-103
-
-
Rapin, I.1
-
3
-
-
0027101924
-
The validity of autistic spectrum disorders: A literature review
-
Szatmari P. The validity of autistic spectrum disorders: A literature review. J Aut Dev Disord. 1992;22:583-600.
-
(1992)
J Aut Dev Disord.
, vol.22
, pp. 583-600
-
-
Szatmari, P.1
-
6
-
-
0032454027
-
Chromosomal disorders and autism
-
Gillberg C. Chromosomal disorders and autism. J Aut Dev Disord. 1998;28:415-425.
-
(1998)
J Aut Dev Disord.
, vol.28
, pp. 415-425
-
-
Gillberg, C.1
-
7
-
-
0032461803
-
Autism: The point of view from autism studies
-
Feinstein C, Reiss A. Autism: The point of view from autism studies. J Aut Dev Disord. 1998;28:393-405.
-
(1998)
J Aut Dev Disord.
, vol.28
, pp. 393-405
-
-
Feinstein, C.1
Reiss, A.2
-
8
-
-
0032453497
-
Autism and tuberous sclerosis
-
Smalley S.Autism and tuberous sclerosis. J Aut DevDisord. 1998;28:407-414.
-
(1998)
J Aut DevDisord.
, vol.28
, pp. 407-414
-
-
Smalley, S.1
-
12
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from the British twin study
-
Bailey A, LeCouteur A, Bolton P, Simonoff E, Yuzda E, Rutter M. Autism as a strongly genetic disorder: Evidence from the British twin study. Psychol Med. 1995;25:63-77.
-
(1995)
Psychol Med.
, vol.25
, pp. 63-77
-
-
Bailey, A.1
LeCouteur, A.2
Bolton, P.3
Simonoff, E.4
Yuzda, E.5
Rutter, M.6
-
14
-
-
0025008677
-
Linkage studies for genetically complex traits. II. The power of affected sib pairs
-
Risch N. Linkage studies for genetically complex traits. II. The power of affected sib pairs. Am J Human Genet. 1990;46:229-241.
-
(1990)
Am J Human Genet.
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
15
-
-
0025355888
-
Genetic linkage and complex diseases, with special reference to psychiatric disorders
-
Risch N. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genet Epidemiol. 1990;7:1-16.
-
(1990)
Genet Epidemiol.
, vol.7
, pp. 1-16
-
-
Risch, N.1
-
16
-
-
0032461804
-
Finding specific genes that cause autism: A combination of approaches will be needed to maximize power
-
Folstein SE, Bisson E, Santangelo SL, Piven J. Finding specific genes that cause autism: A combination of approaches will be needed to maximize power. J Aut Dev Disord. 1998;28:439-445.
-
(1998)
J Aut Dev Disord.
, vol.28
, pp. 439-445
-
-
Folstein, S.E.1
Bisson, E.2
Santangelo, S.L.3
Piven, J.4
-
17
-
-
0030773652
-
Diagnosing autism: Analyses of data from the Autism Diagnostic Interview
-
Lord C, Pickles A, McLennan J, et al. Diagnosing autism: Analyses of data from the Autism Diagnostic Interview. J Aut Dev Disord. 1997;27:501-517.
-
(1997)
J Aut Dev Disord.
, vol.27
, pp. 501-517
-
-
Lord, C.1
Pickles, A.2
McLennan, J.3
-
18
-
-
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. Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Aut Dev Disord. 1994;24:659-685
-
(1994)
J Aut Dev Disord.
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
LeCouteur, A.3
-
19
-
-
0028012565
-
Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
-
Spiker D, Lotspeich L, Kraemer HC, et al. Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families. Am J Med Genet: Neuropsychia Genet. 1994;54:27-35.
-
(1994)
Am J Med Genet: Neuropsychia Genet.
, vol.54
, pp. 27-35
-
-
Spiker, D.1
Lotspeich, L.2
Kraemer, H.C.3
-
20
-
-
0028171490
-
Molecular analysis and test for linkage between the FMR-1 gene and infantile autism in multiplex families
-
Hallmayer J, Pintado E, Lin A, et al. Molecular analysis and test for linkage between the FMR-1 gene and infantile autism in multiplex families. American Journal of Human Genet. 1994;55:951-959.
-
(1994)
American Journal of Human Genet.
, vol.55
, pp. 951-959
-
-
Hallmayer, J.1
Pintado, E.2
Lin, A.3
-
22
-
-
0041122971
-
Autism and pervasive developmental disorders
-
Bloom FE, Kupfer DJ, eds. New York: Raven Press
-
Lotspeich LJ. Autism and pervasive developmental disorders. In: Bloom FE, Kupfer DJ, eds. Psychopharmacology: The Fourth Generation of Progress. New York: Raven Press; 1995: 1653-1663.
-
(1995)
Psychopharmacology: The Fourth Generation of Progress
, pp. 1653-1663
-
-
Lotspeich, L.J.1
-
23
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook Jr EH, Courchesne RY, Lord C, et. Evidence of linkage between the serotonin transporter and autistic disorder. Mole Psychia. 1997;2:247-250.
-
(1997)
Mole Psychia.
, vol.2
, pp. 247-250
-
-
Cook Jr., E.H.1
Courchesne, R.Y.2
Lord, C.3
-
24
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poustka F, Brenner, Klaus-Peter L, Poustka A. Serotonin transporter (5-HTT) gene variants associated with autism? Human Mole Genet. 1997;6:2233-2238.
-
(1997)
Human Mole Genet.
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Brenner3
Klaus-Peter, L.4
Poustka, A.5
-
25
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook Jr H, Lindgren V, Leventhal BL, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Human Genet. 1997;60:928-934.
-
(1997)
Am J Human Genet.
, vol.60
, pp. 928-934
-
-
Cook Jr., H.1
Lindgren, V.2
Leventhal, B.L.3
-
26
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
-
Cook Jr EH, Courchesne RY, Cox NJ, et al. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Human Genet. 1998;62:1077-1083.
-
(1998)
Am J Human Genet.
, vol.62
, pp. 1077-1083
-
-
Cook Jr., E.H.1
Courchesne, R.Y.2
Cox, N.J.3
-
27
-
-
0001777849
-
Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT)
-
Pericak-Vance MA, Wolpert CM, Menold MM, et al. Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT). Am J Human Genet. Suppl. 1997;A40:208.
-
(1997)
Am J Human Genet.
, vol.A40
, Issue.SUPPL.
, pp. 208
-
-
Pericak-Vance, M.A.1
Wolpert, C.M.2
Menold, M.M.3
-
28
-
-
85034562292
-
Absence of linkage to chromosome 15q11-q13 markers in ninety multiplex families with autism
-
In press
-
Salmon B, Hallmayer J, Rogers T, et al. Absence of linkage to chromosome 15q11-q13 markers in ninety multiplex families with autism. Neuropsychia Genet. In press.
-
Neuropsychia Genet.
-
-
Salmon, B.1
Hallmayer, J.2
Rogers, T.3
-
29
-
-
0030200135
-
Strong association of the third hypervariable region of HLA-DRB1 with autism
-
Warren RP, Odell JD, Warren L, et al. Strong association of the third hypervariable region of HLA-DRB1 with autism. J Neuroimmun. 1996;67:97-102.
-
(1996)
J Neuroimmun.
, vol.67
, pp. 97-102
-
-
Warren, R.P.1
Odell, J.D.2
Warren, L.3
-
31
-
-
0029120604
-
Increased frequency of the extended or ancestral Haplotype B44-SC30-DR4 in autism
-
Daniels WW, Warren RP, Odell J.D, et al. Increased frequency of the extended or ancestral Haplotype B44-SC30-DR4 in autism. Neuropsychobio. 1995;32:120-123.
-
(1995)
Neuropsychobio
, vol.32
, pp. 120-123
-
-
Daniels, W.W.1
Warren, R.P.2
Odell, J.D.3
-
32
-
-
85031582946
-
Exclusion of linkage to the HLA region in ninety multiplex sibships with autism
-
In press
-
Rogers T, Kalaydjieva L, Hallmayer J, et al. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. J Aut Dev Disord. In press.
-
J Aut Dev Disord.
-
-
Rogers, T.1
Kalaydjieva, L.2
Hallmayer, J.3
-
33
-
-
0021994210
-
Gene mapping studies with the syndrome of autism
-
Spence MA, Ritvo ER, Marazita ML, Funderburk SL, Sparkes RS, Freeman BJ. Gene mapping studies with the syndrome of autism. Bebav Genet. 1985;15:1-13.
-
(1985)
Bebav Genet.
, vol.15
, pp. 1-13
-
-
Spence, M.A.1
Ritvo, E.R.2
Marazita, M.L.3
Funderburk, S.L.4
Sparkes, R.S.5
Freeman, B.J.6
-
34
-
-
6844251000
-
A full genome screen for autism with evidence of linkage to a region of chromosome 7p
-
International Molecular Genetic Study of Autism Consortium. A full genome screen for autism with evidence of linkage to a region of chromosome 7p. Human Mole Gene. 1998;7:571-578.
-
(1998)
Human Mole Gene
, vol.7
, pp. 571-578
-
-
-
35
-
-
0033362024
-
A genomic screen of autism: Evidence for polygenic inheritance
-
Risch R, Spiker D, Lotspeich L, et al. A genomic screen of autism: Evidence for polygenic inheritance. Am J Human Genet. 1999;65:493-507.
-
(1999)
Am J Human Genet.
, vol.65
, pp. 493-507
-
-
Risch, R.1
Spiker, D.2
Lotspeich, L.3
|