SCOPUS 정보 검색 플랫폼

Volumn 109, Issue 1, 2002, Pages 36-41

Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method

(7) Schutz, Chris K a,b Polley, Diana a,b Robinson, Paula D a Chalifoux, Maryse b,c Macciardi, Fabio d White, Bradley N a Holden, Jeanette J A b,c

a MCMASTER UNIVERSITY (Canada)

b QUEEN S UNIVERSITY (Canada)

c Ongwanada Resource Centre (Canada)

d UNIVERSITY OF TORONTO (Canada)

Author keywords

Autism; Autism spectrum disorders; Genetics; X chromosome

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; AUTISM; CLINICAL ARTICLE; DNA POLYMORPHISM; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; PRIORITY JOURNAL; SIBLING; X CHROMOSOME;

ALLELES; AUTISTIC DISORDER; CHROMOSOME MAPPING; FEMALE; HETEROZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; NUCLEAR FAMILY; X CHROMOSOME;

EID: 0037089946 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10138 Document Type: Article

Times cited : (10)

References (57)

1
- 0004235298
- Washington DC: American Psychiatric Association
- (1994) Diagnostic and statistical manual of mental disorders, 4th edition

2
- 0023081468
- Monoamines in autism: An update of neurochemical research on a pervasive developmental disorder
- (1987) Med Biol , vol.65 , pp. 67-74
- Anderson, G.M.¹

3
- 0028906338
- Autism as a strongly genetic disorder: Evidence from a British twin study
- (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

4
- 0029872978
- Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
- (1996) J Child Psychol Psychiatry , vol.37 , pp. 529-535
- Bailey, A.¹ Phillips, W.² Rutter, M.³

5
- 0032453821
- Autism: The phenotype in relatives
- (1998) J Autism Dev Disord , vol.28 , pp. 369-393
- Bailey, A.¹ Palferman, S.² Heavey, L.³ Le Couteur, A.⁴

6
- 17144456791
- Dinucleotide repeat polymorphism at the MAOA locus
- (1991) Nucleic Acids Res , vol.19 , pp. 689
- Black, G.C.¹ Chen, Z.Y.² Craig, I.W.³ Powell, J.F.⁴

7
- 0344902186
- Genetic influences in autism
- (1990) Int Rev Psychiatry , vol.2 , pp. 67-80
- Bolton, P.¹ Rutter, M.²

8
- 0020477965
- Association of fragile X syndrome with autism
- (1982) Lancet , vol.1 , pp. 100
- Brown, W.T.¹ Friedman, E.² Jenkins, E.C.³ Brooks, J.⁴ Wisniewski, K.⁵ Raguthu, S.⁶ French, J.H.⁷

9
- 0025980843
- Dinucleotide repeat polymorphism at the DXS538 locus
- (1991) Nucleic Acids Res , vol.19 , pp. 1161
- Browne, D.L.¹ Luty, J.A.² Litt, M.³

10
- 0023683047
- First report of a Canadian epidemiological study of autistic syndromes
- (1988) J Child Psychol Psychiatry , vol.29 , pp. 433-446
- Bryson, S.E.¹ Clarke, B.S.² Smith, I.M.³

11
- 0028924329
- The neurobiology of infantile autism
- (1995) Ann Rev Neurosci , vol.18 , pp. 101-128
- Ciaranello, A.L.¹ Ciaranello, R.D.²

12
- 0002986754
- Medical conditions associated with autism
- Cohen DJ, Volkmar FR, editors. New York: Wiley
- (1997) Handbook of autism and pervasive developmental disorders, 2nd edition , pp. 388-410
- Dykens, E.M.¹ Volkmar, F.R.²

13
- 0032461803
- Autism: The point of view from fragile X studies
- (1998) J Autism Dev Disord , vol.28 , pp. 393-405
- Feinstein, C.¹ Reiss, A.L.²

14
- 0033377678
- The screening and diagnosis of autistic spectrum disorders
- (1999) J Autism Dev Disord , vol.29 , pp. 439-484
- Filipek, P.A.¹ Accardo, P.J.² Baranek, G.T.³ Cook Jr., E.H.⁴ Dawson, G.⁵ Gordon, B.⁶ Gravel, J.S.⁷ Johnson, C.P.⁸ Kallen, R.J.⁹ Levy, S.E.¹⁰ Minshew, N.J.¹¹ Ozonoff, S.¹² Prizant, B.M.¹³ Rapin, I.¹⁴ Rogers, S.J.¹⁵ Stone, W.L.¹⁶ Teplin, S.¹⁷ Tuchman, R.F.¹⁸ Volkmar, F.R.¹⁹

15
- 0033837083
- Practice parameter: Screening and diagnosis of autism: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society
- (2000) Neurology , vol.55 , pp. 468-479
- Filipek, P.A.¹ Accardo, P.J.² Ashwal, S.³ Baranek, G.T.⁴ Cook Jr., E.H.⁵ Dawson, G.⁶ Gordon, B.⁷ Gravel, J.S.⁸ Johnson, C.P.⁹ Kallen, R.J.¹⁰ Levy, S.E.¹¹ Minshew, N.J.¹² Ozonoff, S.¹³ Prizant, B.M.¹⁴ Rapin, I.¹⁵ Rogers, S.J.¹⁶ Stone, W.L.¹⁷ Teplin, S.W.¹⁸ Tuchman, R.F.¹⁹ Volkmar, F.R.²⁰ more..

16
- 0027160981
- What is associated with the fragile X syndrome?
- (1993) Am J Med Genet , vol.48 , pp. 112-121
- Fisch, G.S.¹

17
- 0032804766
- The epidemiology of autism: A review
- (1999) Psychol Med , vol.29 , pp. 769-786
- Fombonne, E.¹

18
- 0026345716
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
- (1991) Cell , vol.67 , pp. 1047-1058
- Fu, Y.-H.¹ Kuhl, D.P.A.² Pizzuti, A.³ Pieretti, M.⁴ Sutcliffe, J.S.⁵ Richard, S.⁶ Verkerk, A.J.M.H.⁷ Holden, J.J.A.⁸ Fenwick, R.G.⁹ Warren, S.T.¹⁰ Oostra, B.A.¹¹ Nelson, D.L.¹² Caskey, C.T.¹³

19
- 0025780874
- Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26
- (1991) Nucleic Acids Res , vol.19 , pp. 5087
- Gedeon, A.K.¹ Richards, R.I.² Mulley, J.C.³

20
- 0026693979
- Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci
- (1992) Am J Med Genet , vol.43 , pp. 255-260
- Gedeon, A.K.¹ Holman, K.² Richards, R.I.³ Mulley, J.C.⁴

21
- 0032975478
- Autism: Not an extremely rare disorder
- (1999) Acta Psychiatr Scand , vol.99 , pp. 399-406
- Gillberg, C.¹ Wing, L.²

22
- 0026518763
- Dinucleotide repeat (TG)23 in the MAOB gene
- (1992) Nucleic Acids Res , vol.20 , pp. 924
- Grimsby, J.¹ Chen, K.² Devor, E.J.³ Cloninger, C.R.⁴ Shih, J.C.⁵

23
- 0028171490
- Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families
- (1994) Am J Hum Genet , vol.55 , pp. 951-959
- Hallmayer, J.¹ Pintado, E.² Lotspeich, L.³ Spiker, D.⁴ McMahon, W.⁵ Petersen, P.B.⁶ Nichols, P.⁷ Pingree, C.⁸ Kraemer, H.C.⁹ Wong, D.L.¹⁰ Ritvo, E.¹¹ Lin, A.¹² Hebert, J.¹³ Cavalli-Sforza, L.L.¹⁴ Ciaranello, R.D.¹⁵

24
- 85008560109
- Autism and the X chromosome
- (1996) Arch Gen Psychiatry , vol.53 , pp. 985-989
- Hallmayer, J.¹ Hebert, J.M.² Spiker, D.³ Lotspeich, L.⁴ McMahon, W.M.⁵ Petersen, P.B.⁶ Nicholas, P.⁷ Pingree, C.⁸ Lin, A.A.⁹ Cavalli-Sforza, L.L.¹⁰ Risch, N.¹¹ Ciaranello, R.D.¹²

25
- 0026742041
- Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif
- (1992) Genomics , vol.13 , pp. 896-897
- Hinds, H.L.¹ Hendriks, R.W.² Craig, I.W.³ Chen, Z.Y.⁴

26
- 0027449978
- The identification of a third fragile site, FRAXF, in Xq27-q28 distal to both FRAXA and FRAXE
- (1993) Hum Mol Genet , vol.2 , pp. 97-200
- Hirst, M.C.¹ Barnicoat, A.² Flynn, G.³ Wang, Q.⁴ Daker, M.⁵ Buckle, V.J.⁶ Davies, K.E.⁷ Bobrow, M.⁸

27
- 0029944243
- Lack of expansion of triplet repeats in the FMR-1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders
- (1996) Am J Med Genet , vol.64 , pp. 399-403
- Holden, J.J.A.¹ Wing, M.² Chalifoux, M.³ Julien-Inalsingh, C.⁴ Schutz, C.⁵ Robinson, P.⁶ Szatmari, P.⁷ White, B.N.⁸

28
- 0029931538
- A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spots
- (1996) Am J Med Genet , vol.64 , pp. 313-318
- Holden, J.J.A.¹ Chalifoux, M.² Wing, M.³ Julien-Inalsingh, C.⁴ White, B.N.⁵

29
- 0002294347
- A simple sequentially rejective multiple test procedure
- (1979) Scand J Stat , vol.6 , pp. 65-70
- Holm, S.¹

30
- 0025859094
- A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD)
- (1991) Nucleic Acids Res , vol.19 , pp. 3159
- Hugnot, J.P.¹ Recan, D.² Jeanpierre, M.³ Kaplan, J.C.⁴ Tolun, A.⁵

31
- 6844251000
- A full genome screen for autism with evidence of linkage to a region of chromosome 7q
- (1998) Hum Mol Genet , vol.7 , pp. 571-578

32
- 0030795260
- Autism and multiple exostoses associated with an X; 8 translocations occurring within the GRPR gene and 3′ to the SDC2 gene
- (1997) Hum Mol Genet , vol.6 , pp. 1241-1250
- Ishikawa-Brush, Y.¹ Powell, J.F.² Bolton, P.³ Miller, A.P.⁴ Francis, F.⁵ Willard, H.F.⁶ Lebrach, H.⁷ Monaco, A.P.⁸

33
- 0033358557
- A note on power approximations for the transmission/disequilibrium test
- (1999) Am J Hum Genet , vol.64 , pp. 1177-1185
- Knapp, M.¹

34
- 0027203684
- Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
- (1993) Cell , vol.74 , pp. 127-134
- Knight, S.J.¹ Flannery, A.V.² Hirst, M.C.³ Campbell, L.⁴ Christodoulou, Z.⁵ Phelps, S.R.⁶ Pointon, J.⁷ Middleton-Price, H.R.⁸ Barnicoat, A.⁹ Pembrey, M.E.¹⁰ Holland, J.¹¹ Oostra, B.A.¹² Bobrow, M.¹³ Davies, K.E.¹⁴

35
- 0018944406
- Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior
- (1980) J Child Psychol Psychiatry , vol.21 , pp. 221-229
- Krug, D.A.¹ Arick, J.² Almond, P.³

36
- 0024430952
- Autism diagnostic interview: A standardized investigator based instrument
- (1989) J Autism Dev Disord , vol.19 , pp. 383-388
- Le Couteur, A.¹ Rutter, M.² Lord, C.³ Rios, P.⁴ Robertson, S.⁵ Holdgrafer, M.⁶ McLennan, J.⁷

37
- 0024369122
- The autism diagnostic observation schedule: A standardized observation of communication and social behavior
- (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

38
- 0025273118
- Five polymorphic microsatellite VNTRs on the human X chromosome
- (1990) Am J Hum Genet , vol.46 , pp. 776-783
- Luty, J.A.¹ Guo, Z.² Willard, H.F.³ Ledbetter, D.H.⁴ Ledbetter, S.⁵ Litt, M.⁶

39
- 0033006510
- Familial factors influence level of functioning in pervasive developmental disorder
- (1999) J Am Acad Child Adolesc Psychiatry , vol.38 , pp. 746-753
- MacLean, J.E.¹ Szatmari, P.² Jones, M.B.³ Bryson, S.E.⁴ Mahoney, W.J.⁵ Bartolucci, G.⁶ Tuff, L.⁷

40
- 0028059776
- Catecholaminergic metabolism and autism
- (1994) Dev Med Child Neurol , vol.36 , pp. 688-697
- Martineau, J.¹ Herault, J.² Petit, E.³ Guerin, P.⁴ Hameury, L.⁵ Perrot, A.⁶ Mallet, J.⁷ Sauvage, D.⁸ Lelord, G.⁹ Muh, J.-P.¹⁰

41
- 0024360491
- The fragile X marker and autism in perspective
- (1989) J Am Acad Child Adolesc Psychiatry , vol.28 , pp. 417-421
- Payton, J.B.¹ Steele, M.W.² Wenger, S.L.³ Minshew, N.J.⁴

42
- 0032945941
- Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
- (1999) Hum Mol Genet , vol.8 , pp. 805-812
- Philippe, A.¹ Martinez, M.² Guilloud-Bataille, M.³ Gillbert, C.⁴ Rastam, M.⁵ Sponheim, E.⁶ Coleman, M.⁷ Zappella, M.⁸ Aschauer, H.⁹ Van Maldergem, L.¹⁰ Penet, C.¹¹ Feingold, J.¹² Brice, A.¹³ Lebover, M.¹⁴ Van Malldergerme, L.¹⁵

43
- 0029134874
- Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
- (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

44
- 0027964499
- Molecular cytogenetic analysis of a possible sex influencing region on the X chromosome
- (1994) Hum Genet , vol.94 , pp. 149-153
- Rao, P.N.¹ Klinepeter, K.² Stewart, W.³ Hayworth, R.⁴ Grubs, R.⁵ Pettenati, M.⁶

45
- 0026766989
- Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site
- (1992) Am J Med Genet , vol.43 , pp. 237-243
- Riggins, G.J.¹ Sherman, S.L.² Oostra, B.A.³ Sutcliffe, J.S.⁴ Feitell, D.⁵ Nelson, D.L.⁶ Van Oost, B.A.⁷ Smits, A.P.T.⁸ Ramos, F.J.⁹ Pfendner, E.¹⁰ Kuhl, D.P.A.¹¹ Caskey, C.T.¹² Warren, S.T.¹³

46
- 0025008677
- Linkage strategies for genetically complex traits. II. The power of affected relative pairs
- (1990) Am J Hum Genet , vol.46 , pp. 229-241
- Risch, N.¹

48
- 0021960916
- Concordance for the syndrome of autism in 40 pairs of afflicted twins
- (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

49
- 0028089258
- Autism and known medical conditions: Myth and substance
- (1994) J Child Psychol Psychiatry , vol.35 , pp. 311-322
- Rutter, M.¹ Bailey, A.² Bolton, P.³ Le Couteur, A.⁴

50
- 0025898654
- Genetic influences in autism
- (1991) Psychiatr Clin North Am , vol.14 , pp. 125-139
- Smalley, S.L.¹

51
- 0032453497
- Autism and tuberous sclerosis
- (1998) J Autism Dev Disord , vol.28 , pp. 407-414
- Smalley, S.L.¹

52
- 0025908959
- Polymorphic dinucleotide repeat at the DXS3 locus
- (1991) Nucleic Acids Res , vol.19 , pp. 4793
- Stanier, P.¹ Newton, R.² Forbes, S.A.³ Ivens, A.⁴ Moore, G.E.⁵

53
- 0029813328
- High phenotypic correlations among siblings with autism and pervasive developmental disorders
- (1996) Am J Med Genet , vol.67 , pp. 354-360
- Szatmari, P.¹ Jones, M.B.² Holden, J.³ Bryson, S.⁴ Mahoney, W.⁵ Tuff, L.⁶ MacLean, J.⁷ White, B.⁸ Bartolucci, G.⁹ Schutz, C.¹⁰ Robinson, P.¹¹ Hoult, L.¹²

54
- 0033913088
- The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: A family history study
- (2000) J Child Psychol Psychiatry , vol.41 , pp. 579-586
- Szatmari, P.¹ MacLean, J.E.² Jones, M.B.³ Bryson, S.E.⁴ Zwaigenbaum, L.⁵ Bartolucci, G.⁶ Mahoney, W.J.⁷ Tuff, L.⁸

55
- 0032971826
- Xp deletions associated with autism in three females
- (1999) Hum Genet , vol.104 , pp. 43-48
- Thomas, N.S.¹ Sharp, A.J.²

56
- 0025371201
- Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci
- (1990) Nucleic Acids Res , vol.18 , pp. 4037
- Weber, J.L.¹ Kwitek, A.E.² May, P.E.³ Polymeropoulos, M.H.⁴ Ledbetter, S.⁵

57
- 0027256635
- Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113)
- (1993) Hum Mol Genet , vol.2 , pp. 612
- Weber, C.¹ Oudet, C.² Johnson, S.³ Pilia, G.⁴ Schlessinger, D.⁵ Hanauer, A.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.