-
1
-
-
0035445736
-
Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome
-
Altafaj, X., Dierssen, M., Baamonde, C., Marti, E., Visa, J., Guimera, J., et al. (2001). Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome. Human Molecular Genetics, 10, 1915-1923.
-
(2001)
Human Molecular Genetics
, vol.10
, pp. 1915-1923
-
-
Altafaj, X.1
Dierssen, M.2
Baamonde, C.3
Marti, E.4
Visa, J.5
Guimera, J.6
-
2
-
-
5044234361
-
Chromosome 21 and Down syndrome: From genomics to pathophysiology
-
Antonarakis, S. E., Lyle, R., Dermitzakis, E. T., Reymond, A., & Deutsch, S. (2004). Chromosome 21 and Down syndrome: from genomics to pathophysiology. Nature Review Genetics, 5, 725-738.
-
(2004)
Nature Review Genetics
, vol.5
, pp. 725-738
-
-
Antonarakis, S.E.1
Lyle, R.2
Dermitzakis, E.T.3
Reymond, A.4
Deutsch, S.5
-
3
-
-
0015794093
-
Partial trisomy 21
-
Aula, P., Leisti, J., & Von Koskull, H. (1973). Partial trisomy 21. Clinical Genetics, 4, 241-251.
-
(1973)
Clinical Genetics
, vol.4
, pp. 241-251
-
-
Aula, P.1
Leisti, J.2
Von Koskull, H.3
-
4
-
-
0033978891
-
Discovery and genetic localization of down syndrome cerebellar phenotypes using the Ts65Dn mouse
-
Baxter, L. L., Moran, T. H., Richtsmeier, J. T., Troncoso, J., & Reeves, R. H. (2000). Discovery and genetic localization of down syndrome cerebellar phenotypes using the Ts65Dn mouse. Human Molecular Genetics, 9, 195-202.
-
(2000)
Human Molecular Genetics
, vol.9
, pp. 195-202
-
-
Baxter, L.L.1
Moran, T.H.2
Richtsmeier, J.T.3
Troncoso, J.4
Reeves, R.H.5
-
5
-
-
0038728033
-
Mutational mechanisms of Williams-Beuren syndrome deletions
-
Bayés, M., Magano, L. F., Rivera N., Flores R., & Pérez Jurado L. A. (2003). Mutational mechanisms of Williams-Beuren syndrome deletions. American Journal of Human Genetics, 73, 131-151.
-
(2003)
American Journal of Human Genetics
, vol.73
, pp. 131-151
-
-
Bayés, M.1
Magano, L.F.2
Rivera, N.3
Flores, R.4
Pérez Jurado, L.A.5
-
6
-
-
9644278035
-
Synaptic structural abnormalities in the Ts65Dn mouse model of Down syndrome
-
Belichenko, P. V., Masliah, E., Kleschevnikov, A. M., Villar, A. J., Epstein, C. J., Salehi, A., et al. (2004). Synaptic structural abnormalities in the Ts65Dn mouse model of Down syndrome. Journal of Comparative Neurology, 480, 281-298.
-
(2004)
Journal of Comparative Neurology
, vol.480
, pp. 281-298
-
-
Belichenko, P.V.1
Masliah, E.2
Kleschevnikov, A.M.3
Villar, A.J.4
Epstein, C.J.5
Salehi, A.6
-
7
-
-
0033134860
-
Bridging cognition, the brain and molecular genetics: Evidence from Williams syndrome
-
Bellugi, U., Lichtenberger, L., Mills, D., Galaburda A., & Korenberg, J. R. (1999). Bridging cognition, the brain and molecular genetics: Evidence from Williams syndrome. Trends in Neuroscience, 22, 197-207.
-
(1999)
Trends in Neuroscience
, vol.22
, pp. 197-207
-
-
Bellugi, U.1
Lichtenberger, L.2
Mills, D.3
Galaburda, A.4
Korenberg, J.R.5
-
8
-
-
33645870983
-
Parieto-occipital grey matter abnormalities in children with Williams syndrome
-
Boddaert, N., Mochel, F., Meresse, I., Seidenwurm, D., Cachia, A., Brunelle, F., et al. (2005). Parieto-occipital grey matter abnormalities in children with Williams syndrome. Neuroimage, 30, 721-725.
-
(2005)
Neuroimage
, vol.30
, pp. 721-725
-
-
Boddaert, N.1
Mochel, F.2
Meresse, I.3
Seidenwurm, D.4
Cachia, A.5
Brunelle, F.6
-
9
-
-
0037235547
-
Spatial representation and attention in toddlers with Williams syndrome and Down syndrome
-
Brown, J. H., Johnson, M. H., Paterson, S. J., Gilmore, R., Longhi, E., & Karmiloff-Smith, A. (2003). Spatial representation and attention in toddlers with Williams syndrome and Down syndrome. Neuropsychology, 41, 1037-1046.
-
(2003)
Neuropsychology
, vol.41
, pp. 1037-1046
-
-
Brown, J.H.1
Johnson, M.H.2
Paterson, S.J.3
Gilmore, R.4
Longhi, E.5
Karmiloff-Smith, A.6
-
11
-
-
33745027219
-
Laterality in persons with intellectual disability. I. - Do patients with trisomy 21 and williams-beuren syndrome differ from typically developing persons?
-
Carlier, M., Stefanini, S., Deruelle, C., Volterra, V., Doyen, A.-L., Lamard, C., et al. (2006). Laterality in Persons with Intellectual Disability. I. - Do Patients with Trisomy 21 and Williams-Beuren syndrome differ from typically developing persons? Behavior Genetics, 36, 365-376.
-
(2006)
Behavior Genetics
, vol.36
, pp. 365-376
-
-
Carlier, M.1
Stefanini, S.2
Deruelle, C.3
Volterra, V.4
Doyen, A.-L.5
Lamard, C.6
-
12
-
-
29444460122
-
Stability and change in cognitive ability over the life span: A comparison of population with and without Down syndrome
-
Carr, J. (2005). Stability and change in cognitive ability over the life span: A comparison of population with and without Down syndrome. Journal of Intellectual Disability Research, 49, 915-928.
-
(2005)
Journal of Intellectual Disability Research
, vol.49
, pp. 915-928
-
-
Carr, J.1
-
13
-
-
7744237268
-
Functional analysis of genes implicated in Down syndrome: 1. Cognitive abilities in mice transpolygenic for Down syndrome chromosomal region-1 (DCR-1)
-
Chabert, C., Jamon, M., Cherfouh, A., Duquenne, V., Smith, D. J., Rubin, E., et al. (2004). Functional analysis of genes implicated in Down syndrome: 1. Cognitive abilities in mice transpolygenic for Down syndrome chromosomal region-1 (DCR-1). Behavior Genetics, 34, 559-569.
-
(2004)
Behavior Genetics
, vol.34
, pp. 559-569
-
-
Chabert, C.1
Jamon, M.2
Cherfouh, A.3
Duquenne, V.4
Smith, D.J.5
Rubin, E.6
-
15
-
-
0042823394
-
Behavioral assessment of children with Down syndrome using the Reiss psychopathology scale
-
Clark, D., & Wilson, G. N. (2003). Behavioral assessment of children with Down syndrome using the Reiss psychopathology scale. American Journal Medical Genetics, 118, 210-216.
-
(2003)
American Journal Medical Genetics
, vol.118
, pp. 210-216
-
-
Clark, D.1
Wilson, G.N.2
-
17
-
-
0025663975
-
Segmental trisomy of murine chromosome 16: A new model system for studying Down syndrome
-
Davisson, M. T., Schmidt, C., & Akeson, E. C. (1990). Segmental trisomy of murine chromosome 16: A new model system for studying Down syndrome. Progress in Clinical and Biological Research, 360, 263-280.
-
(1990)
Progress in Clinical and Biological Research
, vol.360
, pp. 263-280
-
-
Davisson, M.T.1
Schmidt, C.2
Akeson, E.C.3
-
18
-
-
0027719985
-
Segmental trisomy as a mouse model for Down syndrome
-
Davisson, M. T., Schmidt, C., Reeves, R. H., Irving, N. G., Akeson, E. C., Harris, B. S., & Bronson, R. T. (1993). Segmental trisomy as a mouse model for Down syndrome. Progress in Clinical and Biological Research, 384, 117-133.
-
(1993)
Progress in Clinical and Biological Research
, vol.384
, pp. 117-133
-
-
Davisson, M.T.1
Schmidt, C.2
Reeves, R.H.3
Irving, N.G.4
Akeson, E.C.5
Harris, B.S.6
Bronson, R.T.7
-
19
-
-
0027874350
-
Molecular mapping of twenty-four features of Down syndrome on chromosome 21
-
Delabar, J. M., Theophile, D., Rahmani, Z., Chettouh, Z., Blouin, J. L., Prieur, M., et al. (1993). Molecular mapping of twenty-four features of Down syndrome on chromosome 21. European Journal of Human Genetics, 1, 114-124.
-
(1993)
European Journal of Human Genetics
, vol.1
, pp. 114-124
-
-
Delabar, J.M.1
Theophile, D.2
Rahmani, Z.3
Chettouh, Z.4
Blouin, J.L.5
Prieur, M.6
-
20
-
-
0000922691
-
Observations on an ethnic classification of idiots
-
Down, J. L. H. (1862). Observations on an Ethnic Classification of Idiots. London Hospital Report, 3, 259-262.
-
(1862)
London Hospital Report
, vol.3
, pp. 259-262
-
-
Down, J.L.H.1
-
21
-
-
0042207862
-
Observations on an ethnic classification of idiots
-
Down, J. L. H. (1867). Observations on an ethnic classification of idiots. Journal of Mental Science, 13, 121-123.
-
(1867)
Journal of Mental Science
, vol.13
, pp. 121-123
-
-
Down, J.L.H.1
-
22
-
-
0347123261
-
"Everybody in the world is my friend" hypersociability in young children with Williams syndrome
-
Doyle, T. F., Bellugi, U., Korenberg, J. R., & Graham, J. (2004). "Everybody in the world is my friend" hypersociability in young children with Williams syndrome. American Journal of Medical Genetics, 124, 263-273.
-
(2004)
American Journal of Medical Genetics
, vol.124
, pp. 263-273
-
-
Doyle, T.F.1
Bellugi, U.2
Korenberg, J.R.3
Graham, J.4
-
24
-
-
0036724569
-
Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice
-
Fotaki, V., Dierssen, M., Alcantara, S., Martinez, S., Marti, E., Casas, C., et al. (2002). Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice. Molecular and Cellular Biology, 22, 6636-6647.
-
(2002)
Molecular and Cellular Biology
, vol.22
, pp. 6636-6647
-
-
Fotaki, V.1
Dierssen, M.2
Alcantara, S.3
Martinez, S.4
Marti, E.5
Casas, C.6
-
25
-
-
33748573622
-
Laterality in persons with intellectual disability. II. Hand, foot, ear and eye laterality in persons with Trisomy 21 and Williams-Beuren syndrome
-
Gérard-Desplanches, A., Deruelle, C., Stefanini, S., Ayoun, C., Volterra, V., Vicari, S., et al. (2006). Laterality in Persons with Intellectual Disability. II. Hand, foot, ear and eye laterality in persons with Trisomy 21 and Williams-Beuren syndrome. Developmental Psychobiology, 4, 482-497.
-
(2006)
Developmental Psychobiology
, vol.4
, pp. 482-497
-
-
Gérard-Desplanches, A.1
Deruelle, C.2
Stefanini, S.3
Ayoun, C.4
Volterra, V.5
Vicari, S.6
-
26
-
-
18744369030
-
A gene expression map of human chromosome 21 orthologues in the mouse
-
Gitton, Y., Dahmane, N., Baik, S., Ruiz I Altaba, A., Neidhardt, L., Scholze, M., et al. (2002). A gene expression map of human chromosome 21 orthologues in the mouse. Nature, 420, 586-590.
-
(2002)
Nature
, vol.420
, pp. 586-590
-
-
Gitton, Y.1
Dahmane, N.2
Baik, S.3
Altaba, R.I.A.4
Neidhardt, L.5
Scholze, M.6
-
27
-
-
33644659643
-
Indepth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene
-
Gray, V., Karmiloff-Smith, A., Funnell, E., & Tassebehji, M. (2006). Indepth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene. Neuropsychologia, 44, 679-685.
-
(2006)
Neuropsychologia
, vol.44
, pp. 679-685
-
-
Gray, V.1
Karmiloff-Smith, A.2
Funnell, E.3
Tassebehji, M.4
-
28
-
-
0016745165
-
Systematic approach to the study of trisomy in the mouse II
-
Gropp, A., Kolbus, U., & Giers, D. (1975). Systematic approach to the study of trisomy in the mouse II. Cytogenetics and Cell Genetics, 14, 42-62.
-
(1975)
Cytogenetics and Cell Genetics
, vol.14
, pp. 42-62
-
-
Gropp, A.1
Kolbus, U.2
Giers, D.3
-
29
-
-
1642268979
-
Functional and morphological alterations in compound transgenic mice overexpressing Cu/Zn superoxide dismutase and amyloid precursor protein
-
Harris-Cerruti, C., Kamsler, A., Kaplan, B., Lamb, B., Segal, M., & Groner, Y. (2004). Functional and morphological alterations in compound transgenic mice overexpressing Cu/Zn superoxide dismutase and amyloid precursor protein. European Journal of Neuroscience, 19, 1174-1190.
-
(2004)
European Journal of Neuroscience
, vol.19
, pp. 1174-1190
-
-
Harris-Cerruti, C.1
Kamsler, A.2
Kaplan, B.3
Lamb, B.4
Segal, M.5
Groner, Y.6
-
30
-
-
0034001512
-
Down syndrome: Genetic recombination and the origin of the extra chromosome 21
-
Hassold, T., & Sherman, S. (2000). Down syndrome: Genetic recombination and the origin of the extra chromosome 21. Clinical Genetics, 57, 95-100.
-
(2000)
Clinical Genetics
, vol.57
, pp. 95-100
-
-
Hassold, T.1
Sherman, S.2
-
31
-
-
0034682403
-
The DNA sequence of human chromosome 21
-
Hattori, M., Fujiyama, A., Taylor, T. D., Watanabe, H., Yada, T., Park, H. S., et al. (2000). The DNA sequence of human chromosome 21. Nature, 405, 311-319.
-
(2000)
Nature
, vol.405
, pp. 311-319
-
-
Hattori, M.1
Fujiyama, A.2
Taylor, T.D.3
Watanabe, H.4
Yada, T.5
Park, H.S.6
-
32
-
-
0002556064
-
Intellectuel development in children with Down syndrome
-
J.-A. Rondal, J. Perera, & L. Nadel Eds., Whurr Publisher: London, U. K
-
Hodapp, R. M., Ewans, D. E., & Gray, F. L. (1999). Intellectuel development in children with Down syndrome. In J.-A. Rondal, J. Perera, & L. Nadel (Eds.), Down Syndrome: A Review of Current Knowledge (pp. 124-132). Whurr Publisher: London, U. K.
-
(1999)
Down Syndrome: A Review of Current Knowledge
, pp. 124-132
-
-
Hodapp, R.M.1
Ewans, D.E.2
Gray, F.L.3
-
33
-
-
0017081784
-
Clinical diagnosis of Down's syndrome
-
Jackson, J. F., North III, E. R., & Thomas, J. G. (1976). Clinical diagnosis of Down's syndrome. Clinical Genetics, 9, 483-487.
-
(1976)
Clinical Genetics
, vol.9
, pp. 483-487
-
-
Jackson, J.F.1
North, E.R.2
Thomas, J.G.3
-
34
-
-
33745029583
-
Gene dosage effect on chromosome 21 transcriptome in trisomy 21: Implication in Down's syndrome cognitive disorders
-
Kahlem, P. (2006). Gene dosage effect on chromosome 21 transcriptome in trisomy 21: Implication in Down's syndrome cognitive disorders. Behavior Genetics, 36, 416-428.
-
(2006)
Behavior Genetics
, vol.36
, pp. 416-428
-
-
Kahlem, P.1
-
35
-
-
3543110316
-
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of Down syndrome
-
Kahlem, P., Sultan, M., Herwig, R., Steinfath, M., Balzereit, D., Eppens, B., et al. (2004). Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of Down syndrome. Genome Research, 14, 1258-1267.
-
(2004)
Genome Research
, vol.14
, pp. 1258-1267
-
-
Kahlem, P.1
Sultan, M.2
Herwig, R.3
Steinfath, M.4
Balzereit, D.5
Eppens, B.6
-
36
-
-
0028341315
-
Down syndrome phenotypes: The consequences of chromosomal imbalance
-
Korenberg, J. R., Chen, X. N., Schipper, R., Sun, Z., Gonsky, R., Gerwehr, S., et al. (1994). Down syndrome phenotypes: The consequences of chromosomal imbalance. Proceedings of the National Academy of Sciences USA, 91, 4997-5001.
-
(1994)
Proceedings of the National Academy of Sciences USA
, vol.91
, pp. 4997-5001
-
-
Korenberg, J.R.1
Chen, X.N.2
Schipper, R.3
Sun, Z.4
Gonsky, R.5
Gerwehr, S.6
-
37
-
-
0036201972
-
Changes in explicit memory associated with early dementia in adults with Down's syndrome
-
Krinsky-McHale, S. J., Devenny, D. A., & Silverman, W. P. (2002). Changes in explicit memory associated with early dementia in adults with Down's syndrome. Journal of Intellectual Disability Research, 46, 198-208.
-
(2002)
Journal of Intellectual Disability Research
, vol.46
, pp. 198-208
-
-
Krinsky-Mc Hale, S.J.1
Devenny, D.A.2
Silverman, W.P.3
-
38
-
-
0042093737
-
Working memory in children and adolescents with Down syndrome: Evidence from a colour memory experiment
-
Laws, G. (2002). Working memory in children and adolescents with Down syndrome: evidence from a colour memory experiment. Journal of Child Psychology and Psychiatry, 43, 353-364.
-
(2002)
Journal of Child Psychology and Psychiatry
, vol.43
, pp. 353-364
-
-
Laws, G.1
-
39
-
-
0002931375
-
Le mongolisme. Premier exemple d'aberration autosomique humaine
-
Lejeune, J., Turpin, R., & Gautier, M. (1958/1959). Le mongolisme. Premier exemple d'aberration autosomique humaine. Annales de génétique, Paris, 1, 41-49.
-
(1958)
Annales de Génétique, Paris
, vol.1
, pp. 41-49
-
-
Lejeune, J.1
Turpin, R.2
Gautier, M.3
-
40
-
-
70449245071
-
Etude des chromosomes somatiques de neuf enfants mongoliens
-
Lejeune, J., Gauthier, M., & Turpin, R. (1959). Etude des chromosomes somatiques de neuf enfants mongoliens. Comptes Rendus de l'Académie des Sciences Paris, 248, 1721-1722.
-
(1959)
Comptes Rendus de l'Académie des Sciences Paris
, vol.248
, pp. 1721-1722
-
-
Lejeune, J.1
Gauthier, M.2
Turpin, R.3
-
41
-
-
0037168523
-
Genetic variation in the 22q11 locus and susceptibility to schizophrenia
-
Liu, H., Abecasis, G. R., Heath, S. C., Knowles, A., Demars, S., Chen, Y. J., et al. (2002). Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proceedings of the National Academy of Sciences USA, 99, 16859-16864.
-
(2002)
Proceedings of the National Academy of Sciences USA
, vol.99
, pp. 16859-16864
-
-
Liu, H.1
Abecasis, G.R.2
Heath, S.C.3
Knowles, A.4
Demars, S.5
Chen, Y.J.6
-
42
-
-
3543097554
-
Gene expression from the aneuploid chromosome in a trisomy mouse model of Down syndrome
-
Lyle, R., Gehrig, C., Neergaard-Henrichsen, C., Deutsch, S., & Antonarakis, S. E. (2004). Gene expression from the aneuploid chromosome in a trisomy mouse model of Down syndrome. Genome Research, 14, 1268-1274.
-
(2004)
Genome Research
, vol.14
, pp. 1268-1274
-
-
Lyle, R.1
Gehrig, C.2
Neergaard-Henrichsen, C.3
Deutsch, S.4
Antonarakis, S.E.5
-
43
-
-
0037251809
-
Williams syndrome: 15 years of psychological research
-
Mervis, C. B. (2003). Williams syndrome: 15 years of psychological research. Develomental Neuropsychology, 23, 1-12.
-
(2003)
Develomental Neuropsychology
, vol.23
, pp. 1-12
-
-
Mervis, C.B.1
-
44
-
-
4444331998
-
Neural basis of genetically determined visuospatial construction deficit in Williams syndrome
-
Meyer-Lindenberg, A., Kohn, P., Mervis, C. B., Kippenhan, J. S., Olsen, R. K., Morris, C. A., et al. (2004). Neural basis of genetically determined visuospatial construction deficit in Williams syndrome. Neuron, 43, 623-631.
-
(2004)
Neuron
, vol.43
, pp. 623-631
-
-
Meyer-Lindenberg, A.1
Kohn, P.2
Mervis, C.B.3
Kippenhan, J.S.4
Olsen, R.K.5
Morris, C.A.6
-
45
-
-
22144453872
-
Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome
-
Meyer-Lindenberg, A., Mervis, C. B., Sarpal, D., Koch, P., Steele, S., Kohn, P., et al. (2005). Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome. Journal of Clinical Investigation, 115, 1888-1895.
-
(2005)
Journal of Clinical Investigation
, vol.115
, pp. 1888-1895
-
-
Meyer-Lindenberg, A.1
Mervis, C.B.2
Sarpal, D.3
Koch, P.4
Steele, S.5
Kohn, P.6
-
46
-
-
0032032006
-
Cognitive neuroscience and the study of memory
-
Milner, B, Squire, L. R., & Kandel, E. R. (1998). Cognitive neuroscience and the study of memory. Neuron, 20, 445-468.
-
(1998)
Neuron
, vol.20
, pp. 445-468
-
-
Milner, B.1
Squire, L.R.2
Kandel, E.R.3
-
48
-
-
0000432897
-
Neural and cognitive development in Down syndrome
-
L. Nadel & D. Rosenthal Eds., New-York: J. Wiley
-
Nadel, L. (1995). Neural and cognitive development in Down syndrome. In L. Nadel & D. Rosenthal (Eds.), Down syndrome Living and learning in the community (pp. 107-114). New-York: J. Wiley.
-
(1995)
Down Syndrome Living and Learning in the Community
, pp. 107-114
-
-
Nadel, L.1
-
49
-
-
0012555184
-
Learning and memory in Down syndrome
-
J. Rondal, J. Perera, & L. Nadel Eds., London: Whurr Publishers
-
Nadel, L. (1999). Learning and memory in Down syndrome. In J. Rondal, J. Perera, & L. Nadel (Eds.), Down syndrome A review of current knowledge (pp. 133-142). London: Whurr Publishers.
-
(1999)
Down Syndrome a Review of Current Knowledge
, pp. 133-142
-
-
Nadel, L.1
-
50
-
-
25444442381
-
An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes
-
O'Doherty, A., Ruf, S., Mulligan, C., Hildreth, V., Errington, M. L., Cooke, S., et al. (2005). An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science, 309, 2033-2037.
-
(2005)
Science
, vol.309
, pp. 2033-2037
-
-
O'Doherty, A.1
Ruf, S.2
Mulligan, C.3
Hildreth, V.4
Errington, M.L.5
Cooke, S.6
-
51
-
-
7444231620
-
A chromosome 21 critical region does not cause specific Down syndrome phenotypes
-
Olson, L. E., Richtsmeier J. T., Leszl, J., & Reeves R. H. (2004). A chromosome 21 critical region does not cause specific Down syndrome phenotypes. Science, 306, 687-690.
-
(2004)
Science
, vol.306
, pp. 687-690
-
-
Olson, L.E.1
Richtsmeier, J.T.2
Leszl, J.3
Reeves, R.H.4
-
52
-
-
13144260659
-
Down syndrome and genetics - A case of linked histories
-
Patterson, D., & Costa, A. C. (2005). Down syndrome and genetics - a case of linked histories. Nature Review Genetics, 6, 137-147.
-
(2005)
Nature Review Genetics
, vol.6
, pp. 137-147
-
-
Patterson, D.1
Costa, A.C.2
-
53
-
-
0038687498
-
The neuropsychology of Down syndrome: Evidence for hippocampal dysfunction
-
Pennington, B. F., Moon, J., Edgin, J., Stedron, J., & Nadel, L. (2003). The neuropsychology of Down syndrome: Evidence for hippocampal dysfunction. Child Development, 74, 75-93.
-
(2003)
Child Development
, vol.74
, pp. 75-93
-
-
Pennington, B.F.1
Moon, J.2
Edgin, J.3
Stedron, J.4
Nadel, L.5
-
54
-
-
0028878675
-
Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: Evidence from MRI morphometry
-
Raz, N., Torres, I. J., Briggs, S. D., Spencer, W. D., Thornton, A. E., Loken, W. J., et al. (1995). Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry. Neurology, 45, 356-366.
-
(1995)
Neurology
, vol.45
, pp. 356-366
-
-
Raz, N.1
Torres, I.J.2
Briggs, S.D.3
Spencer, W.D.4
Thornton, A.E.5
Loken, W.J.6
-
55
-
-
18744387970
-
Human chromosome 21 gene expression atlas in the mouse
-
Reymond, A., Marigo, V., Yaylaoglu, M. B., Leoni, A., Ucla, C., Scamuffa, N., et al. (2002). Human chromosome 21 gene expression atlas in the mouse. Nature, 420, 582-586.
-
(2002)
Nature
, vol.420
, pp. 582-586
-
-
Reymond, A.1
Marigo, V.2
Yaylaoglu, M.B.3
Leoni, A.4
Ucla, C.5
Scamuffa, N.6
-
56
-
-
0037433652
-
Down's syndrome
-
Roizen, N. J., & Patterson, D. (2003). Down's syndrome. Lancet, 361, 1281-1289.
-
(2003)
Lancet
, vol.361
, pp. 1281-1289
-
-
Roizen, N.J.1
Patterson, D.2
-
57
-
-
84919644382
-
Language in Down syndrome: Current perspectives
-
J. Rondal, J. Perera, & L. Nadel Eds., London: Whurr Publishers
-
Rondal, J. A. (1999) Language in Down syndrome: Current perspectives. In J. Rondal, J. Perera, & L. Nadel (Eds.), Down syndrome A review of current knowledge (pp. 143-149). London: Whurr Publishers.
-
(1999)
Down Syndrome a Review of Current Knowledge
, pp. 143-149
-
-
Rondal, J.A.1
-
58
-
-
20944439544
-
Functional analysis of genes implicated in Down syndrome: 2. Laterality and corpus callosum size in mice transpolygenic for Down syndrome chromosomal region-1 (DCR-1)
-
Roubertoux, P. L., Bichler, Z., Pinoteau, W., Sérégaza, Z., Fortes, S., Jamon, M., et al. (2005). Functional analysis of genes implicated in Down syndrome: 2. Laterality and corpus callosum size in mice transpolygenic for Down syndrome chromosomal region-1 (DCR-1). Behavior Genetics, 35, 333-341.
-
(2005)
Behavior Genetics
, vol.35
, pp. 333-341
-
-
Roubertoux, P.L.1
Bichler, Z.2
Pinoteau, W.3
Sérégaza, Z.4
Fortes, S.5
Jamon, M.6
-
59
-
-
33745011914
-
Pre-weaning sensorial and motor development in mice transpolygenic for the critical region of trisomy 21
-
Roubertoux, P. L., Bichler, Z., Pinoteau, W., Jamon, M., Sérégaza, Z., Smith, D. J., et al. (2006). Pre-weaning Sensorial and Motor Development in Mice Transpolygenic for the Critical Region of Trisomy 21. Behavior Genetics, 36, 377-386.
-
(2006)
Behavior Genetics
, vol.36
, pp. 377-386
-
-
Roubertoux, P.L.1
Bichler, Z.2
Pinoteau, W.3
Jamon, M.4
Sérégaza, Z.5
Smith, D.J.6
-
60
-
-
34548361243
-
From DNA to the mind
-
Roubertoux, M., & Carlier M. (2007). From DNA to the mind. EMBO Reports, 8, Science & Society, Special Issue, S7-S11.
-
(2007)
EMBO Reports, 8, Science & Society, Special Issue
, pp. S7-S11
-
-
Roubertoux, M.1
Carlier, M.2
-
61
-
-
33745024585
-
Trisomy 21: From chromosomes to mental retardation
-
Roubertoux, P. L., & Kerdelhué, B. (2006). Trisomy 21: From chromosomes to mental retardation. Behavior Genetics, 36, 434-345.
-
(2006)
Behavior Genetics
, vol.36
, pp. 434-345
-
-
Roubertoux, P.L.1
Kerdelhué, B.2
-
62
-
-
0032568615
-
Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities
-
Sago, H., Carlson, E. J., Smith, D. J., Kilbridge, J., Rubin, E. M., Mobley, W. C., et al. (1998). Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities. Proceedings of the National Academy of Sciences USA, 95, 6256-6261.
-
(1998)
Proceedings of the National Academy of Sciences USA
, vol.95
, pp. 6256-6261
-
-
Sago, H.1
Carlson, E.J.2
Smith, D.J.3
Kilbridge, J.4
Rubin, E.M.5
Mobley, W.C.6
-
63
-
-
0033756144
-
Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome
-
Sago, H., Carlson, E. J., Smith, D. J., Rubin, E. M., Crnic, L. S., Huang, T. T., et al. (2000). Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome. Pediatric Research, 48, 606-613.
-
(2000)
Pediatric Research
, vol.48
, pp. 606-613
-
-
Sago, H.1
Carlson, E.J.2
Smith, D.J.3
Rubin, E.M.4
Crnic, L.S.5
Huang, T.T.6
-
65
-
-
24944583808
-
Origin of the treatment and training of idiots
-
Séguin, E. (1856). Origin of the treatment and training of idiots. American Journal of Education, 2, 145-152.
-
(1856)
American Journal of Education
, vol.2
, pp. 145-152
-
-
Séguin, E.1
-
67
-
-
33745032837
-
Mouse models of cognitive disorders in trisomy 21: A review
-
Sérégaza, Z., Roubertoux, P. L., Jamon, M., & Soumireu-Mourat, B. (2006). Mouse Models of Cognitive Disorders in Trisomy 21: A Review. Behavior Genetics, 36, 387-404.
-
(2006)
Behavior Genetics
, vol.36
, pp. 387-404
-
-
Sérégaza, Z.1
Roubertoux, P.L.2
Jamon, M.3
Soumireu-Mourat, B.4
-
68
-
-
14344275376
-
Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome
-
Shinohara, T., Tomizuka, K., Miyabara, S., Takehara, S., Kazuki, Y., Inoue, J., et al. (2001). Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome. Human Molecular Genetics, 10, 1163-1175.
-
(2001)
Human Molecular Genetics
, vol.10
, pp. 1163-1175
-
-
Shinohara, T.1
Tomizuka, K.2
Miyabara, S.3
Takehara, S.4
Kazuki, Y.5
Inoue, J.6
-
69
-
-
0029075809
-
Construction of a panel of transgenic mice containing a contiguous 2-Mb set of YAC/P1 clones from human chromosome 21q22.2
-
Smith, D. J., Zhu, Y., Zhang, J., Cheng, J. F., & Rubin, E. M. (1995). Construction of a panel of transgenic mice containing a contiguous 2-Mb set of YAC/P1 clones from human chromosome 21q22.2. Genomics, 27, 425-434.
-
(1995)
Genomics
, vol.27
, pp. 425-434
-
-
Smith, D.J.1
Zhu, Y.2
Zhang, J.3
Cheng, J.F.4
Rubin, E.M.5
-
70
-
-
0030915187
-
Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome
-
Smith, D. J., Stevens, M. E., Sudanagunta, S. P., Bronson, R. T., Makhinson, M., Watabe, A. M., et al. (1997). Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome. Nature Genetics, 16, 28-36.
-
(1997)
Nature Genetics
, vol.16
, pp. 28-36
-
-
Smith, D.J.1
Stevens, M.E.2
Sudanagunta, S.P.3
Bronson, R.T.4
Makhinson, M.5
Watabe, A.M.6
-
71
-
-
33745028432
-
Neuroanatomy of Down syndrome in vivo: A model of preclinical Alzheimer's disease
-
Teipel, S. J., & Hampel, H. (2006). Neuroanatomy of Down syndrome in vivo: A model of preclinical Alzheimer's disease. Behavior Genetics, 36, 405-415.
-
(2006)
Behavior Genetics
, vol.36
, pp. 405-415
-
-
Teipel, S.J.1
Hampel, H.2
-
72
-
-
20244374988
-
Abnormal cortical complexity and thickness profiles mapped in Williams syndrome
-
Thompson, P. M., Lee, A. D., Dutton, R. A., Geaga, J. A., Hayashi, K. M., Eckert, M. A., et al. (2005). Abnormal cortical complexity and thickness profiles mapped in Williams syndrome. Journal of Neuroscience, 25, 4146-4158.
-
(2005)
Journal of Neuroscience
, vol.25
, pp. 4146-4158
-
-
Thompson, P.M.1
Lee, A.D.2
Dutton, R.A.3
Geaga, J.A.4
Hayashi, K.M.5
Eckert, M.A.6
-
73
-
-
0002133864
-
The chromosomes of man
-
Tijo, H., & Levan, A. (1956). The chromosomes of man. Hereditas, 42, 1-6.
-
(1956)
Hereditas
, vol.42
, pp. 1-6
-
-
Tijo, H.1
Levan, A.2
-
74
-
-
0842343353
-
Morphology and morphometry of the corpus callosum in Williams Syndrome: A magnetic resonance imaging analysis
-
Tomaiuolo, F., Di Paola, M., Caravale, B., Vicari, S., Petrides, M., & Caltagirone, C. (2002). Morphology and morphometry of the corpus callosum in Williams Syndrome: A magnetic resonance imaging analysis. NeuroReport, 13, 1-5
-
(2002)
NeuroReport
, vol.13
, pp. 1-5
-
-
Tomaiuolo, F.1
Di Paola, M.2
Caravale, B.3
Vicari, S.4
Petrides, M.5
Caltagirone, C.6
-
75
-
-
0025656521
-
Immunology of Down syndrome: A review
-
Ugazio, A. G, Maccario, R., Notarangelo, L. D., & Burgio, G. R. (1990). Immunology of Down syndrome: A review. American Journal of Medical Genetics, (Suppl.) 7, 204-212.
-
(1990)
American Journal of Medical Genetics, (Suppl.)
, vol.7
, pp. 204-212
-
-
Ugazio, A.G.1
Maccario, R.2
Notarangelo, L.D.3
Burgio, G.R.4
-
76
-
-
33745035951
-
Motor development and neuropsychological patterns in persons with Down syndrome
-
Vicari, S. (2006). Motor development and neuropsychological patterns in persons with Down syndrome. Behavior Genetics, 36, 355-364.
-
(2006)
Behavior Genetics
, vol.36
, pp. 355-364
-
-
Vicari, S.1
-
77
-
-
18644372777
-
Visual and spatial long-term memory: Differential pattern of impairments in Williams and Down syndromes
-
Vicari, S., Belluci, S., & Carlesimo G. A. (2005). Visual and spatial long-term memory: Differential pattern of impairments in Williams and Down syndromes. Developmental Medicine & Child Neurology, 47, 305-311.
-
(2005)
Developmental Medicine & Child Neurology
, vol.47
, pp. 305-311
-
-
Vicari, S.1
Belluci, S.2
Carlesimo, G.A.3
-
78
-
-
2642575083
-
DNA sequence and comparative analysis of chimpanzee chromosome 22
-
Watanabe, H., Fujiyama, A., Hattori, M., Taylor, T. D., Toyoda, A., Kuroki, Y., et al. (2004). DNA sequence and comparative analysis of chimpanzee chromosome 22, Nature, 429, 382-388.
-
(2004)
Nature
, vol.429
, pp. 382-388
-
-
Watanabe, H.1
Fujiyama, A.2
Hattori, M.3
Taylor, T.D.4
Toyoda, A.5
Kuroki, Y.6
-
79
-
-
0035704553
-
Learning and memory in S100-beta transgenic mice: An analysis of impaired and preserved function
-
Winocur, G., Roder, J., & Lobaugh, N. (2001). Learning and memory in S100-beta transgenic mice: an analysis of impaired and preserved function. Neurobiology of Learning and Memory, 75, 230-243.
-
(2001)
Neurobiology of Learning and Memory
, vol.75
, pp. 230-243
-
-
Winocur, G.1
Roder, J.2
Lobaugh, N.3
-
80
-
-
0027248034
-
The development of learning difficulties in children with Down's syndrome
-
Wishart, J. G. (1993). The development of learning difficulties in children with Down's syndrome. Journal of Intellectual Disability Research, 37, 389-403.
-
(1993)
Journal of Intellectual Disability Research
, vol.37
, pp. 389-403
-
-
Wishart, J.G.1
-
81
-
-
0035490099
-
Engineering chromosomal rearrangements in mice
-
Yu, Y., & Bradley, A. (2001). Engineering chromosomal rearrangements in mice. Nature Review Genetics, 10, 780-790.
-
(2001)
Nature Review Genetics
, vol.10
, pp. 780-790
-
-
Yu, Y.1
Bradley, A.2
|