-
1
-
-
0028206982
-
Parental origin of Robertsonian translocation (15q22q) and Pader Willi syndrome associated with autism
-
Arrieta I, Lobato MN, Martinez B, Criado B. 1994. Parental origin of Robertsonian translocation (15q22q) and Pader Willi syndrome associated with autism. Pychiatric Genet 4:63-65.
-
(1994)
Pychiatric Genet
, vol.4
, pp. 63-65
-
-
Arrieta, I.1
Lobato, M.N.2
Martinez, B.3
Criado, B.4
-
2
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, LeCouteur A, Gottesmati 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
LeCouteur, A.2
Gottesmati, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
3
-
-
0027934165
-
Duplication of chromosome 15q11-13 in two individuals with autistic disorder
-
Baker P, Piven J, Schwartz S, Patil S. 1994. 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
-
4
-
-
0027935295
-
Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia
-
Bundey S, Hardy C, Vickers S, Kilpatrick M, Corbett J. 1994. Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia. Dev Med Child Neurol 36:736-742.
-
(1994)
Dev Med Child Neurol
, vol.36
, pp. 736-742
-
-
Bundey, S.1
Hardy, C.2
Vickers, S.3
Kilpatrick, M.4
Corbett, J.5
-
5
-
-
0029011991
-
Molecular characterization of two proximal deletion breakpoint regions in Both Prader-Willi and Angelman syndrome patients
-
Christian SL, Robinson WP, Huang B, Mutirangura, Line MR, Nakao M, Surti U, Chakravarti A, Ledbetter DH. 1995. Molecular characterization of two proximal deletion breakpoint regions in Both Prader-Willi and Angelman syndrome patients. Am J Hum Genet 57:40-48.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 40-48
-
-
Christian, S.L.1
Robinson, W.P.2
Huang, B.3
Mutirangura4
Line, M.R.5
Nakao, M.6
Surti, U.7
Chakravarti, A.8
Ledbetter, D.H.9
-
6
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autisic disorder
-
Cook Jr EH Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal BL. 1997a. Evidence of linkage between the serotonin transporter and autisic disorder. Mol Psychiatry May 2:3, 247-50.
-
(1997)
Mol Psychiatry May
, vol.2
, Issue.3
, pp. 247-250
-
-
Cook E.H., Jr.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
-
7
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook Jr EH, Lindgren V, Leventhal BL, Courchene R, Lincoln A, Shulman C, Lord C, Courchesne E. 1997b. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 60:928-934.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 928-934
-
-
Cook E.H., Jr.1
Lindgren, V.2
Leventhal, B.L.3
Courchene, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
8
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q1-13 markers
-
Cook Jr EH, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E. 1998. linkage-disequilibrium mapping of autistic disorder, with 15q1-13 markers. Am J Hum Genet 62:1077-1083.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1077-1083
-
-
Cook E.H., Jr.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
-
-
0028821373
-
Supernumerary marker 15 chromosomes: A clinical, molecular and FISH approach to diagnosis and prognosis
-
Crolla J, Harvey J, Sitch F, Dennis N. 1995. Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis. Hum Genet 95:161-170.
-
(1995)
Hum Genet
, vol.95
, pp. 161-170
-
-
Crolla, J.1
Harvey, J.2
Sitch, F.3
Dennis, N.4
-
10
-
-
0030070898
-
Cytogenetic and molecular analysis of inv dupl(15) chromosomes observed in two patients with autistic disorder and mental retardation
-
Flejter WL, Bennet-Baker PE, Ghaziuddin M, McDonald M, Sheldon S, Gorski JL,. 1996. cytogenetic and molecular analysis of inv dupl(15) chromosomes observed in two patients with autistic disorder and mental retardation. Am J Medical Genet 61:182-187.
-
(1996)
Am J Medical Genet
, vol.61
, pp. 182-187
-
-
Flejter, W.L.1
Bennet-Baker, P.E.2
Ghaziuddin, M.3
McDonald, M.4
Sheldon, S.5
Gorski, J.L.6
-
11
-
-
0017530988
-
Infantile autism: A genetic study in 21 twin pairs
-
Folstein SE, Rutter M. 1977. Infantile autism: a genetic study in 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
-
12
-
-
47649096263
-
Autism associated with marker chromosome
-
Gillberg C, Steffenburg S, Wahlstrom J, Gillberg I, Sjostedt A, Martinsson T, Liedgren S et al. 1991. Autism associated with marker chromosome. J Am Acad Child Adolesc Psychiatry 30:489-494.
-
(1991)
J Am Acad Child Adolesc Psychiatry
, vol.30
, pp. 489-494
-
-
Gillberg, C.1
Steffenburg, S.2
Wahlstrom, J.3
Gillberg, I.4
Sjostedt, A.5
Martinsson, T.6
Liedgren, S.7
-
13
-
-
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
-
14
-
-
0028959478
-
A case of autism associated with partial tetrasomy 15
-
Hotof M, Bolton P. 1995. A case of autism associated with partial tetrasomy 15. J Autism Dev Disord 25:41-49.
-
(1995)
J Autism Dev Disord
, vol.25
, pp. 41-49
-
-
Hotof, M.1
Bolton, P.2
-
15
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium. 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet Mar 7:3, 571-578.
-
(1998)
Hum Mol Genet Mar
, vol.7
, Issue.3
, pp. 571-578
-
-
-
16
-
-
0025997752
-
Complex segregation analysis of autism
-
Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A. 1991. Complex segregation analysis of autism. Am J Hum Genet 49:932-938.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 932-938
-
-
Jorde, L.B.1
Hasstedt, S.J.2
Ritvo, E.R.3
Mason-Brothers, A.4
Freeman, B.J.5
Pingree, C.6
McMahon, W.M.7
Petersen, B.8
Jenson, W.R.9
Mo, A.10
-
17
-
-
0031933164
-
A conditional inference framework for extending the transmission-disequilibrium test
-
Lazzeroni LC, Lange K. 1998. A conditional inference framework for extending the transmission-disequilibrium test. Hum Hered 48:67-81.
-
(1998)
Hum Hered
, vol.48
, pp. 67-81
-
-
Lazzeroni, L.C.1
Lange, K.2
-
18
-
-
0028205957
-
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/ Angelman syndrome region: Clinical implications
-
Leana-Cox J, Jenkins L, Palmer C, Plattner R, Shepard L, Flejter W, Zackowski J, Tsien F, Schwartz S. 1994. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/ Angelman syndrome region: clinical implications. Am J Hum Genet 54:748-756.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 748-756
-
-
Leana-Cox, J.1
Jenkins, L.2
Palmer, C.3
Plattner, R.4
Shepard, L.5
Flejter, W.6
Zackowski, J.7
Tsien, F.8
Schwartz, S.9
-
19
-
-
0024430952
-
Autism diagnostic interview: A standardised investigator-based instrument
-
Le Couteur A, Rutter M, Lord C, Rios P, Robertson S, Holdgrafer M, McLennan J. 1989. Autism Diagnostic Interview: a standardised investigator-based instrument. J Aut Devel Discord 19:363-387.
-
(1989)
J Aut Devel Discord
, vol.19
, pp. 363-387
-
-
Le Couteur, A.1
Rutter, M.2
Lord, C.3
Rios, P.4
Robertson, S.5
Holdgrafer, M.6
McLennan, J.7
-
20
-
-
0030773652
-
Diagnosing autism: Analyses of data from the autism diagnostic interview
-
Lord C, Pickles A, McLennan J, Rutter M, Bregman J, Folstein S, Fombonne E, Leboyer M, Minshew N. 1997. Diagnosing autism: analyses of data from the Autism Diagnostic Interview. J Aut Dev Disord 27;501-517.
-
(1997)
J Aut Dev Disord
, vol.27
, pp. 501-517
-
-
Lord, C.1
Pickles, A.2
McLennan, J.3
Rutter, M.4
Bregman, J.5
Folstein, S.6
Fombonne, E.7
Leboyer, M.8
Minshew, N.9
-
21
-
-
0024369122
-
Autism diagnostic observation schedule; a standardised observation of communicative and social behavior
-
Lord C, Rutter M, Goode S, Heemsbergen J, Jordan H, Mahwood L, Schopler E. 1989. Autism Diagnostic Observation Schedule; a standardised observation of communicative and social behavior. J Aut Dev Disord 19;185-212.
-
(1989)
J Aut Dev Disord
, vol.19
, pp. 185-212
-
-
Lord, C.1
Rutter, M.2
Goode, S.3
Heemsbergen, J.4
Jordan, H.5
Mahwood, L.6
Schopler, E.7
-
22
-
-
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 Aut Dev Disord 24;659-685.
-
(1994)
J Aut Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Lecouteur, A.3
-
23
-
-
0030772982
-
Tests for linkage and association in nuclear families
-
Martin ER, Kaplan NL, Weir BS. 1997. Tests 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.R.1
Kaplan, N.L.2
Weir, B.S.3
-
25
-
-
0001777849
-
Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT)
-
Pericak-Vance MA, Wolpert CM, Menold MM, Bass MP, Delong GR, Beaty LM, Zimmerman A, Potter N, Gilbert JR, Vance JM, Wright HH, Abramson RK, Cuccaro ML. 1997. Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT). Am J Hum Genet 40(Suppl A):208.
-
(1997)
Am J Hum Genet
, vol.40
, Issue.SUPPL. A
, pp. 208
-
-
Pericak-Vance, M.A.1
Wolpert, C.M.2
Menold, M.M.3
Bass, M.P.4
Delong, G.R.5
Beaty, L.M.6
Zimmerman, A.7
Potter, N.8
Gilbert, J.R.9
Vance, J.M.10
Wright, H.H.11
Abramson, R.K.12
Cuccaro, M.L.13
-
26
-
-
0031660251
-
Autistic symptoms among children and young adults with isodicentric chromosome 15
-
Rineer S, Finucane B, Simon EW. 1998. Autistic symptoms among children and young adults with isodicentric chromosome 15. Am J Med Genet 81:428-433.
-
(1998)
Am J Med Genet
, vol.81
, pp. 428-433
-
-
Rineer, S.1
Finucane, B.2
Simon, E.W.3
-
27
-
-
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, 229-239.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 229-239
-
-
Risch, N.1
-
28
-
-
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 142:64-77.
-
(1985)
Am J Psychiatry
, vol.142
, pp. 64-77
-
-
Ritvo, E.R.1
Freeman, B.J.2
Mason-Brothers, A.3
Mo, A.4
Ritvo, A.M.5
-
29
-
-
0027792161
-
Clinical and molecular analysis of five inv dup(15) patients
-
Robinson W, Binkert F, Gine R, Vazquez C, Muller W, Rosenkranz W, Schinzel A. 1993. Clinical and molecular analysis of five inv dup(15) patients. Dur J Hum Genet 1:37-50.
-
(1993)
Dur J Hum Genet
, vol.1
, pp. 37-50
-
-
Robinson, W.1
Binkert, F.2
Gine, R.3
Vazquez, C.4
Muller, W.5
Rosenkranz, W.6
Schinzel, A.7
-
30
-
-
0028081050
-
Intrachromosomal triplication of 15q11-q13
-
Schinzel AA, Brecevic L, Bernasconi F, Binkert G, Berthet F, Wuilloud A, Robinson WP. 1994. Intrachromosomal triplication of 15q11-q13. J Med Genet 31:798-803.
-
(1994)
J Med Genet
, vol.31
, pp. 798-803
-
-
Schinzel, A.A.1
Brecevic, L.2
Bernasconi, F.3
Binkert, G.4
Berthet, F.5
Wuilloud, A.6
Robinson, W.P.7
-
31
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer RJ, Phelan MC, Michaelis RC, Crawford ED, 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.D.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
-
32
-
-
0030977686
-
Genetic influences in childhood-onset psychiatric disorders: Autism and attention-deficit/hyperactivitydisorder
-
Smalley SL. 1997. Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivitydisorder. Am J Hum Genet 60:1276-1282.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1276-1282
-
-
Smalley, S.L.1
-
33
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman R, McGinnis RE, Ewens WJ. 1993. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52:506-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.1
McGinnis, R.E.2
Ewens, W.J.3
-
34
-
-
0028012565
-
Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
-
Spiker D, Lotspeich L, Kraemer HC, Hallmayer J, McMahon W, Peterson PB, Wong DL, Dimiceli S, Ritvo E, Cavalli-Sforza LL, Ciaranello RD. 1994. genetics of autism: characteristics of affected and unaffected children from 37 multiplex families. Am J Med Genet 54:27-35.
-
(1994)
Am J Med Genet
, vol.54
, pp. 27-35
-
-
Spiker, D.1
Lotspeich, L.2
Kraemer, H.C.3
Hallmayer, J.4
McMahon, W.5
Peterson, P.B.6
Wong, D.L.7
Dimiceli, S.8
Ritvo, E.9
Cavalli-Sforza, L.L.10
Ciaranello, R.D.11
-
35
-
-
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
-
36
-
-
0030890115
-
The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localised within a narrowed Angelman syndrome critical region
-
Sutcliffe J, Jiang Y-H, Galjaard R-J, Matsura T, Fang P, Kubota T, Christian S, Bressler J, Cattanach B, Ledbetter DH, Beaudet AL. 1997. The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localised within a narrowed Angelman syndrome critical region. Genome Res 7:367-377.
-
(1997)
Genome Res
, vol.7
, pp. 367-377
-
-
Sutcliffe, J.1
Jiang, Y.-H.2
Galjaard, R.-J.3
Matsura, T.4
Fang, P.5
Kubota, T.6
Christian, S.7
Bressler, J.8
Cattanach, B.9
Ledbetter, D.H.10
Beaudet, A.L.11
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