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Results: 1 to 20 of 160

Similar articles for PubMed (Select 15900222)

1.

Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.

Vincent JB, Melmer G, Bolton PF, Hodgkinson S, Holmes D, Curtis D, Gurling HM.

Psychiatr Genet. 2005 Jun;15(2):83-90.

PMID:
15900222
2.

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.

Shibayama A, Cook EH Jr, Feng J, Glanzmann C, Yan J, Craddock N, Jones IR, Goldman D, Heston LL, Sommer SS.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):50-3.

PMID:
15211631
3.

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.

Klauck SM, Münstermann E, Bieber-Martig B, Rühl D, Lisch S, Schmötzer G, Poustka A, Poustka F.

Hum Genet. 1997 Aug;100(2):224-9.

PMID:
9254854
4.

Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

Hallmayer J, Pintado E, Lotspeich L, Spiker D, McMahon W, Petersen PB, Nicholas P, Pingree C, Kraemer HC, Wong DL, et al.

Am J Hum Genet. 1994 Nov;55(5):951-9.

5.

Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.

Holden JJ, Wing M, Chalifoux M, Julien-Inalsingh C, Schutz C, Robinson P, Szatmari P, White BN.

Am J Med Genet. 1996 Aug 9;64(2):399-403.

PMID:
8844091
6.

Mutation analysis of the coding sequence of the MECP2 gene in infantile autism.

Beyer KS, Blasi F, Bacchelli E, Klauck SM, Maestrini E, Poustka A; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Hum Genet. 2002 Oct;111(4-5):305-9. Epub 2002 Aug 14. Erratum in: Hum Genet. 2003 Apr;112(4):436.

PMID:
12384770
7.

[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders].

Iurov IIu, Vorsanova SG, Voinova-Ulas VIu, Villard L, Demidova IA, Giunti L, Guivabyccu-Uzielli ML, Budilov AV, Beresheva AK, Novikov PV, Iurov IuV.

Zh Nevrol Psikhiatr Im S S Korsakova. 2005;105(7):4-11. Russian.

PMID:
16117140
8.

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.

Am J Hum Genet. 2002 Oct;71(4):777-90. Epub 2002 Aug 21.

9.

MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications.

Bourdon V, Philippe C, Martin D, Verloès A, Grandemenge A, Jonveaux P.

Mol Diagn. 2003;7(1):3-7.

PMID:
14529314
10.
11.

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families.

Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.

Autism Res. 2010 Apr;3(2):47-52. doi: 10.1002/aur.119.

PMID:
20437600
12.

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

Gauthier J, Joober R, Dubé MP, St-Onge J, Bonnel A, Gariépy D, Laurent S, Najafee R, Lacasse H, St-Charles L, Fombonne E, Mottron L, Rouleau GA.

Mol Psychiatry. 2006 Feb;11(2):206-13.

PMID:
16261168
13.

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.

Vincent JB, Thevarkunnel S, Kolozsvari D, Paterson AD, Roberts W, Scherer SW.

Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):54-6.

PMID:
14755444
14.

Infantile autism--fragile X: molecular findings support genetic heterogeneity.

Malmgren H, Gustavson KH, Wahlström J, Arpi-Henriksson I, Bensch J, Pettersson U, Dahl N.

Am J Med Genet. 1992 Dec 1;44(6):830-3.

PMID:
1481857
15.

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.

Alarcón M, Cantor RM, Liu J, Gilliam TC, Geschwind DH; Autism Genetic Research Exchange Consortium.

Am J Hum Genet. 2002 Jan;70(1):60-71. Epub 2001 Dec 6.

16.
17.

[Genetic study of 20 patients with autism disorders].

Havlovicová M, Propper L, Novotná D, Musová Z, Hrdlicka M, Sedlácek Z.

Cas Lek Cesk. 2002 Jun 21;141(12):381-7. Czech.

PMID:
12238024
18.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79. Epub 2005 Jul 1.

19.

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

Oberlé I, Camerino G, Wrogemann K, Arveiler B, Hanauer A, Raimondi E, Mandel JL.

Hum Genet. 1987 Sep;77(1):60-5.

PMID:
3502701
20.

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.

Thatcher KN, Peddada S, Yasui DH, Lasalle JM.

Hum Mol Genet. 2005 Mar 15;14(6):785-97. Epub 2005 Feb 2.

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