-
1
-
-
0035653670
-
Genetics of autism: Complex aetiology for a heterogeneous disorder
-
Folstein, S.E. and Rosen-Sheidley, B. (2001) Genetics of autism: Complex aetiology for a heterogeneous disorder. Nat. Rev. Genet., 2, 943-955.
-
(2001)
Nat. Rev. Genet
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
2
-
-
3042775209
-
Autism as a disorder of neural information processing: Directions for research and targets for therapy
-
Belmonte, M.K., Cook, E.H., Jr., Anderson, G.M., Rubenstein, J.L., Greenough, W.T., Beckel-Mitchener, A., Courchesne, E., Boulanger, L.M., Powell, S.B., Levitt, P.R. et al. (2004) Autism as a disorder of neural information processing: Directions for research and targets for therapy. Mol. Psychiatry, 9, 646-663.
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 646-663
-
-
Belmonte, M.K.1
Cook Jr., E.H.2
Anderson, G.M.3
Rubenstein, J.L.4
Greenough, W.T.5
Beckel-Mitchener, A.6
Courchesne, E.7
Boulanger, L.M.8
Powell, S.B.9
Levitt, P.R.10
-
3
-
-
5544306699
-
Autism as a paradigmatic complex genetic disorder
-
Veenstra-Vanderweele, J., Christian, S.L. and Cook, E.H., Jr. (2004) Autism as a paradigmatic complex genetic disorder. Annu. Rev. Genomics Hum. Genet., 5, 379-405.
-
(2004)
Annu. Rev. Genomics Hum. Genet
, vol.5
, pp. 379-405
-
-
Veenstra-Vanderweele, J.1
Christian, S.L.2
Cook Jr., E.H.3
-
4
-
-
3442894480
-
The genetics of autism
-
Muhle, R., Trentacoste, S.V. and Rapin, I. (2004) The genetics of autism. Pediatrics, 113, e472-e486.
-
(2004)
Pediatrics
, vol.113
-
-
Muhle, R.1
Trentacoste, S.V.2
Rapin, I.3
-
5
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu, J., Nyholt, D.R., Magnussen, P., Parano, E., Pavone, P., Geschwind, D., Lord, C., Iversen, P., Hoh, J., Ott, J. et al. (2001) A genomewide screen for autism susceptibility loci. Am. J. Hum. Genet. 69, 327-340.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
Geschwind, D.6
Lord, C.7
Iversen, P.8
Hoh, J.9
Ott, J.10
-
6
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
IMGSAC
-
IMGSAC (2001) A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am. J. Hum. Genet., 69 570-581.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 570-581
-
-
-
7
-
-
0035871209
-
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
-
IMGSAC
-
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
-
-
-
8
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum, J.D., Silverman, J.M., Smith, C.J., Kilifarski, M., Reichert, J., Hollander, E., Lawlor, B.A., Fitzgerald, M., Greenberg, D.A. and Davis, K.L. (2001) Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am. J. Hum. Genet., 68, 1514-1520.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
Lawlor, B.A.7
Fitzgerald, M.8
Greenberg, D.A.9
Davis, K.L.10
-
9
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
-
Alarcon, M., Cantor, R.M., Liu, J., Gilliam, T.C. and Geschwind, D.H. (2002) Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am. J. Hum. Genet., 70, 60-71.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, T.C.4
Geschwind, D.H.5
-
10
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan, A.L., Alarcon, M., Cheng, R., Magnusson, P.K., Spence, S.J., Palmer, A.A., Grunn, A., Juo, S.H., Terwilliger, J.D., Liu, J. et al. (2003) A genomewide screen of 345 families for autism-susceptibility loci. Am. J. Hum. Genet., 73, 886-897.
-
(2003)
Am. J. Hum. Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.4
Spence, S.J.5
Palmer, A.A.6
Grunn, A.7
Juo, S.H.8
Terwilliger, J.D.9
Liu, J.10
-
11
-
-
8844244724
-
Evidence for sex-specific risk alleles in autism spectrum disorder
-
Stone, J.L., Merriman, B., Cantor, R.M., Yonan, A.L., Gilliam, T.C., Geschwind, D.H. and Nelson, S.F. (2004) Evidence for sex-specific risk alleles in autism spectrum disorder. Am. J. Hum. Genet., 75, 1117-1123.
-
(2004)
Am. J. Hum. Genet
, vol.75
, pp. 1117-1123
-
-
Stone, J.L.1
Merriman, B.2
Cantor, R.M.3
Yonan, A.L.4
Gilliam, T.C.5
Geschwind, D.H.6
Nelson, S.F.7
-
12
-
-
23744471663
-
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
-
Alarcon, M., Yonan, A.L., Gilliam, T.C., Cantor, R.M. and Geschwind, D.H. (2005) Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Mol. Psychiatry, 10, 747-757.
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 747-757
-
-
Alarcon, M.1
Yonan, A.L.2
Gilliam, T.C.3
Cantor, R.M.4
Geschwind, D.H.5
-
13
-
-
18944365556
-
Replication of autism linkage: Fine-mapping peak at 17q21
-
Cantor, R.M., Kono, N., Duvall, J.A., Alvarez-Retuerto, A., Stone, J.L., Alarcon, M., Nelson, S.F. and Geschwind, D.H. (2005) Replication of autism linkage: Fine-mapping peak at 17q21. Am. J. Hum. Genet., 76, 1050-1056.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 1050-1056
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
Alvarez-Retuerto, A.4
Stone, J.L.5
Alarcon, M.6
Nelson, S.F.7
Geschwind, D.H.8
-
14
-
-
24144452995
-
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
-
McCauley, J.L., Li, C., Jiang, L., Olson, L.M., Crockett, G., Gainer, K., Folstein, S.E., Haines, J.L. and Sutcliffe, J.S. (2005) Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med. Genet., 6, 1.
-
(2005)
BMC Med. Genet
, vol.6
, pp. 1
-
-
McCauley, J.L.1
Li, C.2
Jiang, L.3
Olson, L.M.4
Crockett, G.5
Gainer, K.6
Folstein, S.E.7
Haines, J.L.8
Sutcliffe, J.S.9
-
15
-
-
27144517182
-
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism
-
Philippi, A., Roschmann, E., Tores, F., Lindenbaum, P., Benajou, A., Germain-Leclerc, L., Marcaillou, C., Fontaine, K., Vanpeene, M., Roy, S. et al. (2005) Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Mol. Psychiatry, 10, 950-960.
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 950-960
-
-
Philippi, A.1
Roschmann, E.2
Tores, F.3
Lindenbaum, P.4
Benajou, A.5
Germain-Leclerc, L.6
Marcaillou, C.7
Fontaine, K.8
Vanpeene, M.9
Roy, S.10
-
16
-
-
15944397635
-
Effects of updating linkage evidence across subsets of data: Reanalysis of the autism genetic resource exchange data set
-
Bartlett, C.W., Goedken, R. and Vieland, V.J. (2005) Effects of updating linkage evidence across subsets of data: Reanalysis of the autism genetic resource exchange data set. Am. J. Hum. Genet., 76, 688-695.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 688-695
-
-
Bartlett, C.W.1
Goedken, R.2
Vieland, V.J.3
-
17
-
-
31544475931
-
Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder
-
Chen, G.K., Kono, N., Geschwind, D.H. and Cantor, R.M. (2006) Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder. Mol. Psychiatry, 11, 214-220.
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 214-220
-
-
Chen, G.K.1
Kono, N.2
Geschwind, D.H.3
Cantor, R.M.4
-
18
-
-
29944441305
-
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families
-
Ylisaukko-oja, T., Alarcon, M., Cantor, R.M., Auranen, M., Vanhala, R., Kempas, E., von Wendt, L., Jarvela, I., Geschwind, D.H. and Peltonen, L. (2006) Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families. Ann. Neurol., 59, 145-155.
-
(2006)
Ann. Neurol
, vol.59
, pp. 145-155
-
-
Ylisaukko-oja, T.1
Alarcon, M.2
Cantor, R.M.3
Auranen, M.4
Vanhala, R.5
Kempas, E.6
von Wendt, L.7
Jarvela, I.8
Geschwind, D.H.9
Peltonen, L.10
-
19
-
-
0022617471
-
Fragile X and autism: A multicenter survey
-
Brown, W.T., Jenkins, E.C., Cohen, I.L., Fisch, G.S., Wolf-Schein, E.G., Gross, A., Waterhouse, L., Fein, D., Mason-Brothers, A., Ritvo, E. et al. (1986) Fragile X and autism: A multicenter survey. Am. J. Med. Genet., 23, 341-352.
-
(1986)
Am. J. Med. Genet
, vol.23
, pp. 341-352
-
-
Brown, W.T.1
Jenkins, E.C.2
Cohen, I.L.3
Fisch, G.S.4
Wolf-Schein, E.G.5
Gross, A.6
Waterhouse, L.7
Fein, D.8
Mason-Brothers, A.9
Ritvo, E.10
-
20
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A.J., Pieretti, M., Sutcliffe, J.S., Fu, Y.H., Kuhl, D.P., Pizzuti, A., Reiner, O., Richards, S., Victoria, M.F., Zhang, F.P. et al. (1991) Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell, 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.P.10
-
21
-
-
0035675794
-
The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders
-
Rogers, S.J., Wehner, D.E. and Hagerman, R. (2001) The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J. Dev. Behav. Pediatr., 22, 409-417.
-
(2001)
J. Dev. Behav. Pediatr
, vol.22
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, D.E.2
Hagerman, R.3
-
22
-
-
12744260103
-
Autistic spectrum disorder and the fragile X premutation
-
Goodlin-Jones, B.L., Tassone, F., Gane, L.W. and Hagerman, R.J. (2004) Autistic spectrum disorder and the fragile X premutation. J. Dev. Behav. Pediatr., 25, 392-398.
-
(2004)
J. Dev. Behav. Pediatr
, vol.25
, pp. 392-398
-
-
Goodlin-Jones, B.L.1
Tassone, F.2
Gane, L.W.3
Hagerman, R.J.4
-
23
-
-
0029872978
-
Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey, A., Phillips, W. and Rutter, M. (1996) Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J. Child Psychol. Psychiatry, 37 89-126.
-
(1996)
J. Child Psychol. Psychiatry
, vol.37
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
24
-
-
0037317655
-
Genetics of childhood disordeDs: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism
-
Sutcliffe, J.S., Nurmi, E.L. and Lombroso, P.J. (2003) Genetics of childhood disordeDs: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism. J. Am. Acad. Child Adolesc. Psychiatry, 42, 253-256.
-
(2003)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.42
, pp. 253-256
-
-
Sutcliffe, J.S.1
Nurmi, E.L.2
Lombroso, P.J.3
-
25
-
-
3242710286
-
High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage
-
Wang, N.J., Liu, D., Parokonny, A.S. and Schanen, N.C. (2004) High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage. Am. J. Hum. Genet., 75, 267-281.
-
(2004)
Am. J. Hum. Genet
, vol.75
, pp. 267-281
-
-
Wang, N.J.1
Liu, D.2
Parokonny, A.S.3
Schanen, N.C.4
-
26
-
-
0042324104
-
Estimate of the prevalence of chromosome 15q11-q13 duplications
-
Thomas, N.S., Roberts, S.E. and Browne, C.E. (2003) Estimate of the prevalence of chromosome 15q11-q13 duplications. Am. J. Med. Genet. A 120, 596-598.
-
(2003)
Am. J. Med. Genet. A
, vol.120
, pp. 596-598
-
-
Thomas, N.S.1
Roberts, S.E.2
Browne, C.E.3
-
27
-
-
33644759438
-
Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes
-
Baron, C.A., Tepper, C.G., Liu, S.Y., Davis, R.R., Wang, N.J., Schanen, N.C. and Gregg, J.P. (2006) Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes. Hum. Mol. Genet., 15, 853-869.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 853-869
-
-
Baron, C.A.1
Tepper, C.G.2
Liu, S.Y.3
Davis, R.R.4
Wang, N.J.5
Schanen, N.C.6
Gregg, J.P.7
-
28
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Maner, S., Massa, H., Walker, M., Chi, M. et al. (2004) Large-scale copy number polymorphism in the human genome. Science, 305, 525-528.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
-
29
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
Horike, S., Cai, S., Miyano, M., Cheng, J.F. and Kohwi-Shigematsu, T. (2005) Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat. Genet., 37, 31-40.
-
(2005)
Nat. Genet
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
Cheng, J.F.4
Kohwi-Shigematsu, T.5
-
30
-
-
18544386723
-
FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation
-
Meloni, I., Muscettola, M., Raynaud, M., Longo, I., Bruttini, M., Moizard, M.P., Gomot, M., Chelly, J., des Portes, V., Fryns, J.P. et al. (2002) FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. Nat. Genet., 30, 436-440.
-
(2002)
Nat. Genet
, vol.30
, pp. 436-440
-
-
Meloni, I.1
Muscettola, M.2
Raynaud, M.3
Longo, I.4
Bruttini, M.5
Moizard, M.P.6
Gomot, M.7
Chelly, J.8
des Portes, V.9
Fryns, J.P.10
-
31
-
-
2042479398
-
Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders
-
Iwamoto, K., Kakiuchi, C., Bundo, M., Ikeda, K. and Kato, T. (2004) Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders. Mol. Psychiatry, 9, 406-416.
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 406-416
-
-
Iwamoto, K.1
Kakiuchi, C.2
Bundo, M.3
Ikeda, K.4
Kato, T.5
-
32
-
-
18044379515
-
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
-
Brown, V., Jin, P., Ceman, S., Darnell, J.C., O'Donnell, W.T., Tenenbaum, S.A., Jin, X., Feng, Y., Wilkinson, K.D., Keene, J.D. et al. (2001) Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell 107, 477-487.
-
(2001)
Cell
, vol.107
, pp. 477-487
-
-
Brown, V.1
Jin, P.2
Ceman, S.3
Darnell, J.C.4
O'Donnell, W.T.5
Tenenbaum, S.A.6
Jin, X.7
Feng, Y.8
Wilkinson, K.D.9
Keene, J.D.10
-
33
-
-
0034916325
-
The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions
-
Geschwind, D.H., Sowinski, J., Lord, C., Iversen, P., Shestack, J., Jones, P., Ducat, L. and Spence, S.J. (2001) The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions. Am. J. Hum. Genet., 69, 463-466.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 463-466
-
-
Geschwind, D.H.1
Sowinski, J.2
Lord, C.3
Iversen, P.4
Shestack, J.5
Jones, P.6
Ducat, L.7
Spence, S.J.8
-
34
-
-
0037523396
-
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein
-
Schenck, A., Bardoni, B., Langmann, C., Harden, N., Mandel, J.L. and Giangrande, A. (2003) CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein. Neuron, 38, 887-898.
-
(2003)
Neuron
, vol.38
, pp. 887-898
-
-
Schenck, A.1
Bardoni, B.2
Langmann, C.3
Harden, N.4
Mandel, J.L.5
Giangrande, A.6
-
35
-
-
0037276175
-
Statistical tests for differential expression in cDNA microarray experiments
-
Cui, X. and Churchill, G.A. (2003) Statistical tests for differential expression in cDNA microarray experiments. Genome Biol., 4, 210.
-
(2003)
Genome Biol
, vol.4
, pp. 210
-
-
Cui, X.1
Churchill, G.A.2
-
36
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe, J.S., Nelson, D.L., Zhang, F., Pieretti, M., Caskey, C.T., Saxe, D. and Warren, S.T. (1992) DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum. Mol. Genet., 1, 397-400.
-
(1992)
Hum. Mol. Genet
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
Warren, S.T.7
-
37
-
-
0037098954
-
Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11-q13 duplications
-
Herzing, L.B., Cook, E.H., Jr. and Ledbetter, D.H. (2002) Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11-q13 duplications. Hum. Mol. Genet., 11, 1707-1718.
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 1707-1718
-
-
Herzing, L.B.1
Cook Jr., E.H.2
Ledbetter, D.H.3
-
38
-
-
0035942271
-
Significance analysis of microarrays applied to the ionizing radiation response
-
Tusher, V.G., Tibshirani, R. and Chu, G. (2001) Significance analysis of microarrays applied to the ionizing radiation response. Proc. Natl Acad. Sci. USA, 98, 5116-5121.
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 5116-5121
-
-
Tusher, V.G.1
Tibshirani, R.2
Chu, G.3
-
39
-
-
4344571581
-
Rank products: A simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments
-
Breitling, R., Armengaud, P., Amtmann, A. and Herzyk, P. (2004) Rank products: A simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments. FEBS Lett., 573, 83-92.
-
(2004)
FEBS Lett
, vol.573
, pp. 83-92
-
-
Breitling, R.1
Armengaud, P.2
Amtmann, A.3
Herzyk, P.4
-
40
-
-
1842690140
-
Marlin-1, a novel RNA-binding protein associates with GABA receptors
-
Couve, A., Restituito, S., Brandon, J.M., Charles, K.J., Bawagan, H., Freeman, K.B., Pangalos, M.N., Calver, A.R. and Moss, S.J. (2004) Marlin-1, a novel RNA-binding protein associates with GABA receptors. J. Biol. Chem., 279, 13934-13943.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 13934-13943
-
-
Couve, A.1
Restituito, S.2
Brandon, J.M.3
Charles, K.J.4
Bawagan, H.5
Freeman, K.B.6
Pangalos, M.N.7
Calver, A.R.8
Moss, S.J.9
-
41
-
-
5644244193
-
Jamip1 (marlin-1) defines a family of proteins interacting with janus kinases and microtubules
-
Steindler, C., Li, Z., Algarte, M., Alcover, A., Libri, V., Ragimbeau, J. and Pellegrini, S. (2004) Jamip1 (marlin-1) defines a family of proteins interacting with janus kinases and microtubules. J. Biol. Chem., 279, 43168-43177.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 43168-43177
-
-
Steindler, C.1
Li, Z.2
Algarte, M.3
Alcover, A.4
Libri, V.5
Ragimbeau, J.6
Pellegrini, S.7
-
42
-
-
0038005018
-
DAVID: Database for Annotation, Visualization, and Integrated Discovery
-
P
-
Dennis, G., Jr., Sherman, B.T., Hosack, D.A., Yang, J., Gao, W., Lane, H.C. and Lempicki, R.A. (2003) DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biol., 4, 3. P.
-
(2003)
Genome Biol
, vol.4
, pp. 3
-
-
Dennis Jr., G.1
Sherman, B.T.2
Hosack, D.A.3
Yang, J.4
Gao, W.5
Lane, H.C.6
Lempicki, R.A.7
-
43
-
-
17844372504
-
From mRNP trafficking to spine dysmorphogenesis: The roots of fragile X syndrome
-
Bagni, C. and Greenough, W.T. (2005) From mRNP trafficking to spine dysmorphogenesis: The roots of fragile X syndrome. Nat. Rev. Neurosci., 6, 376-387.
-
(2005)
Nat. Rev. Neurosci
, vol.6
, pp. 376-387
-
-
Bagni, C.1
Greenough, W.T.2
-
45
-
-
27944502874
-
DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling
-
Millar, J.K., Pickard, B.S., Mackie, S., James, R., Christie, S., Buchanan, S.R., Malloy, M.P., Chubb, J.E., Huston, E., Baillie, G.S. et al. (2005) DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling. Science, 310, 1187-1191.
-
(2005)
Science
, vol.310
, pp. 1187-1191
-
-
Millar, J.K.1
Pickard, B.S.2
Mackie, S.3
James, R.4
Christie, S.5
Buchanan, S.R.6
Malloy, M.P.7
Chubb, J.E.8
Huston, E.9
Baillie, G.S.10
-
46
-
-
0037421721
-
RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice
-
Miyashiro, K.Y., Beckel-Mitchener, A., Purk, T.P., Becker, K.G., Barret, T., Liu, L., Carbonetto, S., Weiler, I.J., Greenough, W.T. and Eberwine, J. (2003) RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice. Neuron, 37, 417-431.
-
(2003)
Neuron
, vol.37
, pp. 417-431
-
-
Miyashiro, K.Y.1
Beckel-Mitchener, A.2
Purk, T.P.3
Becker, K.G.4
Barret, T.5
Liu, L.6
Carbonetto, S.7
Weiler, I.J.8
Greenough, W.T.9
Eberwine, J.10
-
47
-
-
33748646825
-
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes
-
Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Aneey, R., Franke, B., Gill, M., Ebstein, R. et al. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Mol. Psychiatry 10, 934-953.
-
(2006)
Mol. Psychiatry
, vol.10
, pp. 934-953
-
-
Brookes, K.1
Xu, X.2
Chen, W.3
Zhou, K.4
Neale, B.5
Lowe, N.6
Aneey, R.7
Franke, B.8
Gill, M.9
Ebstein, R.10
-
48
-
-
33646145602
-
Lessons from fragile X regarding neurobiology, autism, and neurodegeneration
-
Hagerman, R.J. (2006) Lessons from fragile X regarding neurobiology, autism, and neurodegeneration. J. Dev. Behav. Pediatr., 27, 63-74.
-
(2006)
J. Dev. Behav. Pediatr
, vol.27
, pp. 63-74
-
-
Hagerman, R.J.1
-
49
-
-
0035019948
-
Probing the nature of child psychopathology
-
Todd, R.D. (2001) Probing the nature of child psychopathology. Child Adolesc. Psychiatr. Clin. N. Am., 10, 209-224.
-
(2001)
Child Adolesc. Psychiatr. Clin. N. Am
, vol.10
, pp. 209-224
-
-
Todd, R.D.1
-
50
-
-
0037403505
-
Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain
-
Mao, R., Zielke, C.L., Zielke, H.R. and Pevsner, J. (2003) Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain. Genomics, 81, 457-467.
-
(2003)
Genomics
, vol.81
, pp. 457-467
-
-
Mao, R.1
Zielke, C.L.2
Zielke, H.R.3
Pevsner, J.4
-
51
-
-
9644289581
-
Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome
-
Tang, Y., Schapiro, M.B., Franz, D.N., Patterson, B.J., Hickey, F.J., Schorry, E.K., Hopkin, R.J., Wylie, M., Narayan, T., Glauser, T.A. et al. (2004) Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome. Ann. Neurol., 56, 808-814.
-
(2004)
Ann. Neurol
, vol.56
, pp. 808-814
-
-
Tang, Y.1
Schapiro, M.B.2
Franz, D.N.3
Patterson, B.J.4
Hickey, F.J.5
Schorry, E.K.6
Hopkin, R.J.7
Wylie, M.8
Narayan, T.9
Glauser, T.A.10
-
52
-
-
21444436743
-
Gene expression analysis of peripheral blood leukocytes from discordant sib-pairs with schizophrenia and bipolar disorder reveals points of convergence between genetic and functional genomic approaches
-
Middleton, F.A., Pato, C.N., Gentile, K.L., McGann, L., Brown, A.M., Trauzzi, M., Diab, H., Morley, C.P., Medeiros, H., Macedo, A. et al. (2005) Gene expression analysis of peripheral blood leukocytes from discordant sib-pairs with schizophrenia and bipolar disorder reveals points of convergence between genetic and functional genomic approaches. Am. J. Med. Genet. B Neuropsychiatr. Genet., 136, 12-25.
-
(2005)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.136
, pp. 12-25
-
-
Middleton, F.A.1
Pato, C.N.2
Gentile, K.L.3
McGann, L.4
Brown, A.M.5
Trauzzi, M.6
Diab, H.7
Morley, C.P.8
Medeiros, H.9
Macedo, A.10
-
53
-
-
10044276811
-
Ca2+ activity at GABAB receptors constitutively promotes metabotropic glutamate signaling in the absence of GABA
-
Tabata, T., Araishi, K., Hashimoto, K., Hashimotodani, Y., van der Putten, H., Bettler, B. and Kano, M. (2004) Ca2+ activity at GABAB receptors constitutively promotes metabotropic glutamate signaling in the absence of GABA. Proc. Natl Acad. Sci. USA, 101, 16952-16957.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 16952-16957
-
-
Tabata, T.1
Araishi, K.2
Hashimoto, K.3
Hashimotodani, Y.4
van der Putten, H.5
Bettler, B.6
Kano, M.7
-
54
-
-
3042647610
-
The mGluR theory of fragile X mental retardation
-
Bear, M.F., Huber, K.M. and Warren, S.T. (2004) The mGluR theory of fragile X mental retardation. Trends Neurosci., 27, 370-377.
-
(2004)
Trends Neurosci
, vol.27
, pp. 370-377
-
-
Bear, M.F.1
Huber, K.M.2
Warren, S.T.3
-
57
-
-
0035900649
-
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function
-
Darnell, J.C., Jensen, K.B., Jin, P., Brown, V., Warren, S.T. and Darnell, R.B. (2001) Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function. Cell, 107, 489-499.
-
(2001)
Cell
, vol.107
, pp. 489-499
-
-
Darnell, J.C.1
Jensen, K.B.2
Jin, P.3
Brown, V.4
Warren, S.T.5
Darnell, R.B.6
-
58
-
-
33747860882
-
QGRS Mapper: A web-based server for predicting G-quadruplexes in nucleotide sequences
-
Kikin, O., D'Antonio, L. and Bagga, P.S. (2006) QGRS Mapper: A web-based server for predicting G-quadruplexes in nucleotide sequences. Nucleic Acids Res., 34, W676-W682.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Kikin, O.1
D'Antonio, L.2
Bagga, P.S.3
-
59
-
-
0037423293
-
The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses
-
Zalfa, F., Giorgi, M., Primerano, B., Moro, A., Di Penta, A., Reis, S., Oostra, B. and Bagni, C. (2003) The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses. Cell, 112, 317-327.
-
(2003)
Cell
, vol.112
, pp. 317-327
-
-
Zalfa, F.1
Giorgi, M.2
Primerano, B.3
Moro, A.4
Di Penta, A.5
Reis, S.6
Oostra, B.7
Bagni, C.8
-
60
-
-
7944232720
-
RNA and microRNAs in fragile X mental retardation
-
Jin, P., Alisch, R.S. and Warren, S.T. (2004) RNA and microRNAs in fragile X mental retardation. Nat. Cell Biol., 6, 1048-1053.
-
(2004)
Nat. Cell Biol
, vol.6
, pp. 1048-1053
-
-
Jin, P.1
Alisch, R.S.2
Warren, S.T.3
-
61
-
-
33644750115
-
miRBase: MicroRNA sequences, targets and gene nomenclature
-
Griffiths-Jones, S., Grocock, R.J., van Dongen, S., Bateman, A. and Enright, A.J. (2006) miRBase: MicroRNA sequences, targets and gene nomenclature. Nucleic Acids Res., 34, D140-D144.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Griffiths-Jones, S.1
Grocock, R.J.2
van Dongen, S.3
Bateman, A.4
Enright, A.J.5
-
62
-
-
1842630333
-
Matching strategies in cognitive research with individuals with high-functioning autism: Current practices, instrument biases, and recommendations
-
Mottron, L. (2004) Matching strategies in cognitive research with individuals with high-functioning autism: Current practices, instrument biases, and recommendations. J. Autism Dev. Disord., 34, 19-27.
-
(2004)
J. Autism Dev. Disord
, vol.34
, pp. 19-27
-
-
Mottron, L.1
-
63
-
-
0031225909
-
A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder
-
Yoshikawa, T., Turner, G., Esterling, L.E., Sanders, A.R. and Detera-Wadleigh, S.D. (1997) A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder. Mol. Psychiatry, 2, 393-397.
-
(1997)
Mol. Psychiatry
, vol.2
, pp. 393-397
-
-
Yoshikawa, T.1
Turner, G.2
Esterling, L.E.3
Sanders, A.R.4
Detera-Wadleigh, S.D.5
-
64
-
-
0033047220
-
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
-
Nothen, M.M., Cichon, S., Rohleder, H., Hemmer, S., Franzek, E., Fritze, J., Albus, M., Borrmann-Hassenbach, M., Kreiner, R., Weigelt, B. et al. (1999) Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families. Mol. Psychiatry, 4, 76-84.
-
(1999)
Mol. Psychiatry
, vol.4
, pp. 76-84
-
-
Nothen, M.M.1
Cichon, S.2
Rohleder, H.3
Hemmer, S.4
Franzek, E.5
Fritze, J.6
Albus, M.7
Borrmann-Hassenbach, M.8
Kreiner, R.9
Weigelt, B.10
-
65
-
-
25444438231
-
Assessment of the effect of age at onset on linkage to bipolar disorder: Evidence on chromosomes 18p and 21q
-
Lin, P.I., McInnis, M.G., Potash, J.B., Willour, V.L., Mackinnon, D.F., Miao, K., Depaulo, J.R. and Zandi, P.P. (2005) Assessment of the effect of age at onset on linkage to bipolar disorder: Evidence on chromosomes 18p and 21q. Am. J. Hum. Genet., 77, 545-555.
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 545-555
-
-
Lin, P.I.1
McInnis, M.G.2
Potash, J.B.3
Willour, V.L.4
Mackinnon, D.F.5
Miao, K.6
Depaulo, J.R.7
Zandi, P.P.8
-
66
-
-
0034750695
-
Altered IMPA2 gene expression and calcium homeostasis in bipolar disorder
-
Yoon, I.S., Li, P.P., Siu, K.P., Kennedy, J.L., Cooke, R.G., Parikh, S.V. and Warsh, J.J. (2001) Altered IMPA2 gene expression and calcium homeostasis in bipolar disorder. Mol. Psychiatry, 6, 678-683.
-
(2001)
Mol. Psychiatry
, vol.6
, pp. 678-683
-
-
Yoon, I.S.1
Li, P.P.2
Siu, K.P.3
Kennedy, J.L.4
Cooke, R.G.5
Parikh, S.V.6
Warsh, J.J.7
-
67
-
-
3042763119
-
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: Association between IMPA2 promoter polymorphisms and bipolar disorder
-
Sjoholt, G., Ebstein, R.P., Lie, R.T., Berle, J.O., Mallet, J., Deleuze, J.F., Levinson, D.F., Laurent, C., Mujahed, M., Bannoura, I. et al. (2004) Examination of IMPA1 and IMPA2 genes in manic-depressive patients: Association between IMPA2 promoter polymorphisms and bipolar disorder. Mol. Psychiatry, 9, 621-629.
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 621-629
-
-
Sjoholt, G.1
Ebstein, R.P.2
Lie, R.T.3
Berle, J.O.4
Mallet, J.5
Deleuze, J.F.6
Levinson, D.F.7
Laurent, C.8
Mujahed, M.9
Bannoura, I.10
-
68
-
-
34547460201
-
-
in press
-
Ohnishi, T., Yamada, K., Ohba, H., Iwayama, Y., Toyota, T., Hattori, E., Inada, T., Kunugi, H., Tatsumi, M., Ozaki, N. et al. (2007) Neuropsychopharmacology, in press.
-
(2007)
Neuropsychopharmacology
-
-
Ohnishi, T.1
Yamada, K.2
Ohba, H.3
Iwayama, Y.4
Toyota, T.5
Hattori, E.6
Inada, T.7
Kunugi, H.8
Tatsumi, M.9
Ozaki, N.10
-
69
-
-
20444411872
-
Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families
-
Romano, V., Cali, F., Seidita, G., Mirisola, M., D'Anna, R.P., Gambino, G., Schinocca, P., Romano, S., Ayala, G.F., Canziani, F. et al. (2005) Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families. Psychiatr. Genet., 15, 149-150.
-
(2005)
Psychiatr. Genet
, vol.15
, pp. 149-150
-
-
Romano, V.1
Cali, F.2
Seidita, G.3
Mirisola, M.4
D'Anna, R.P.5
Gambino, G.6
Schinocca, P.7
Romano, S.8
Ayala, G.F.9
Canziani, F.10
-
70
-
-
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. and Le Couteur, A. (1994) Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J. Autism Dev. Disord., 24, 659-685.
-
(1994)
J. Autism Dev. Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
71
-
-
0035825228
-
Quantifying the phenotype in autism spectrum disorders
-
Lord, C., Leventhal, B.L. and Cook, E.H., Jr. (2001) Quantifying the phenotype in autism spectrum disorders. Am. J. Med. Genet., 105 36-38.
-
(2001)
Am. J. Med. Genet
, vol.105
, pp. 36-38
-
-
Lord, C.1
Leventhal, B.L.2
Cook Jr., E.H.3
-
72
-
-
0037311919
-
TM4: A free, open-source system for microarray data management and analysis
-
Saeed, A.I., Sharov, V., White, J., Li, J., Liang, W., Bhagabati, N., Braisted, J., Klapa, M., Currier, T., Thiagarajan, M. et al. (2003) TM4: A free, open-source system for microarray data management and analysis. Biotechniques, 34, 374-378.
-
(2003)
Biotechniques
, vol.34
, pp. 374-378
-
-
Saeed, A.I.1
Sharov, V.2
White, J.3
Li, J.4
Liang, W.5
Bhagabati, N.6
Braisted, J.7
Klapa, M.8
Currier, T.9
Thiagarajan, M.10
-
73
-
-
28744458859
-
Bioconductor: Open software development for computational biology and bioinformatics
-
Gentleman, R.C., Carey, V.J., Bates, D.M., Bolstad, B., Dettling, M., Dudoit, S., Ellis, B., Gautier, L., Ge, Y., Gentry, J. et al. (2004) Bioconductor: Open software development for computational biology and bioinformatics. Genome Biol., 5, R80.
-
(2004)
Genome Biol
, vol.5
-
-
Gentleman, R.C.1
Carey, V.J.2
Bates, D.M.3
Bolstad, B.4
Dettling, M.5
Dudoit, S.6
Ellis, B.7
Gautier, L.8
Ge, Y.9
Gentry, J.10
-
74
-
-
33747344944
-
Comparison and evaluation of methods for generating differentially expressed gene lists from microarray data
-
Jeffery, I.B., Higgins, D.G. and Culhane, A.C. (2006) Comparison and evaluation of methods for generating differentially expressed gene lists from microarray data. BMC Bioinformatics, 7, 359.
-
(2006)
BMC Bioinformatics
, vol.7
, pp. 359
-
-
Jeffery, I.B.1
Higgins, D.G.2
Culhane, A.C.3
|