-
1
-
-
77957968873
-
Genetics of early onset cognitive impairment
-
10.1146/annurev-genom-082509-141640, 20822471
-
Ropers HH. Genetics of early onset cognitive impairment. Annu Rev Genomics Hum Genet 2010, 11:161-187. 10.1146/annurev-genom-082509-141640, 20822471.
-
(2010)
Annu Rev Genomics Hum Genet
, vol.11
, pp. 161-187
-
-
Ropers, H.H.1
-
2
-
-
84868543309
-
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
-
10.1016/S0140-6736(12)61480-9, 23020937
-
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet 2012, 380:1674-82. 10.1016/S0140-6736(12)61480-9, 23020937.
-
(2012)
Lancet
, vol.380
, pp. 1674-1682
-
-
Rauch, A.1
Wieczorek, D.2
Graf, E.3
Wieland, T.4
Endele, S.5
Schwarzmayr, T.6
Albrecht, B.7
Bartholdi, D.8
Beygo, J.9
Di Donato, N.10
Dufke, A.11
Cremer, K.12
Hempel, M.13
Horn, D.14
Hoyer, J.15
Joset, P.16
Röpke, A.17
Moog, U.18
Riess, A.19
Thiel, C.T.20
Tzschach, A.21
Wiesener, A.22
Wohlleber, E.23
Zweier, C.24
Ekici, A.B.25
Zink, A.M.26
Rump, A.27
Meisinger, C.28
Grallert, H.29
Sticht, H.30
Schenck, A.31
Engels, H.32
Rappold, G.33
Schröck, E.34
Wieacker, P.35
Riess, O.36
Meitinger, T.37
Reis, A.38
Strom, T.M.39
more..
-
3
-
-
84868686559
-
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
-
10.1056/NEJMoa1206524, 23033978
-
De Ligt J, Willemsen MH, van Bon BWM, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, Del Rosario M, Hoischen A, Scheffer H, De Vries BBA, Brunner HG, Veltman JA, Vissers LELM, De Ligt J, Willemsen MH, van Bon BWM, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, Del Rosario M, Hoischen A, Scheffer H, De Vries BBA, Brunner HG, Veltman JA, Vissers LELM. Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability. N Engl J Med 2012, 367:1921-1929. 10.1056/NEJMoa1206524, 23033978.
-
(2012)
N Engl J Med
, vol.367
, pp. 1921-1929
-
-
De Ligt, J.1
Willemsen, M.H.2
van Bon, B.W.M.3
Kleefstra, T.4
Yntema, H.G.5
Kroes, T.6
Vulto-van Silfhout, A.T.7
Koolen, D.A.8
de Vries, P.9
Gilissen, C.10
Del Rosario, M.11
Hoischen, A.12
Scheffer, H.13
De Vries, B.B.A.14
Brunner, H.G.15
Veltman, J.A.16
Vissers, L.E.L.M.17
De Ligt, J.18
Willemsen, M.H.19
van Bon, B.W.M.20
Kleefstra, T.21
Yntema, H.G.22
Kroes, T.23
Vulto-van Silfhout, A.T.24
Koolen, D.A.25
de Vries, P.26
Gilissen, C.27
Del Rosario, M.28
Hoischen, A.29
Scheffer, H.30
De Vries, B.B.A.31
Brunner, H.G.32
Veltman, J.A.33
Vissers, L.E.L.M.34
more..
-
4
-
-
33751054999
-
The prevalence of psychiatric disorders among people with intellectual disabilities: an analysis of the literature
-
Whitaker S, Read S. The prevalence of psychiatric disorders among people with intellectual disabilities: an analysis of the literature. J Appl Res Intellect Disabil 2006, 19:330-345.
-
(2006)
J Appl Res Intellect Disabil
, vol.19
, pp. 330-345
-
-
Whitaker, S.1
Read, S.2
-
5
-
-
0041698497
-
Emotional and behavioral problems in children and adolescents with and without intellectual disability
-
10.1111/1469-7610.00235, 12455929
-
Dekker MC, Koot HM, van der Ende J, Verhulst FC. Emotional and behavioral problems in children and adolescents with and without intellectual disability. J Child Psychol Psychiatry 2002, 43:1087-98. 10.1111/1469-7610.00235, 12455929.
-
(2002)
J Child Psychol Psychiatry
, vol.43
, pp. 1087-1098
-
-
Dekker, M.C.1
Koot, H.M.2
van der Ende, J.3
Verhulst, F.C.4
-
6
-
-
0037240360
-
Prevalence of psychiatric disorders in children and adolescents with and without intellectual disability
-
Emerson E. Prevalence of psychiatric disorders in children and adolescents with and without intellectual disability. J intellect disability res JIDR 2003, 47:51-8.
-
(2003)
J intellect disability res JIDR
, vol.47
, pp. 51-58
-
-
Emerson, E.1
-
7
-
-
78049329316
-
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
-
10.1038/ng.677, 20890276
-
Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A, Pientka FK, Hellenbroich Y, Kalscheuer VM, Kohlhase J, Moog U, Rappold G, Rauch A, Ropers H-H, von Spiczak S, Tönnies H, Villeneuve N, Villard L, Zabel B, Zenker M, Laube B, Reis A, Wieczorek D, Van Maldergem L, Kutsche K. Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet 2010, 42:1021-6. 10.1038/ng.677, 20890276.
-
(2010)
Nat Genet
, vol.42
, pp. 1021-1026
-
-
Endele, S.1
Rosenberger, G.2
Geider, K.3
Popp, B.4
Tamer, C.5
Stefanova, I.6
Milh, M.7
Kortüm, F.8
Fritsch, A.9
Pientka, F.K.10
Hellenbroich, Y.11
Kalscheuer, V.M.12
Kohlhase, J.13
Moog, U.14
Rappold, G.15
Rauch, A.16
Ropers, H.-H.17
von Spiczak, S.18
Tönnies, H.19
Villeneuve, N.20
Villard, L.21
Zabel, B.22
Zenker, M.23
Laube, B.24
Reis, A.25
Wieczorek, D.26
Van Maldergem, L.27
Kutsche, K.28
more..
-
8
-
-
0035369112
-
NMDA receptor subunits: diversity, development and disease
-
10.1016/S0959-4388(00)00215-4, 11399431
-
Cull-Candy S, Brickley S, Farrant M. NMDA receptor subunits: diversity, development and disease. Curr Opin Neurobiol 2001, 11:327-35. 10.1016/S0959-4388(00)00215-4, 11399431.
-
(2001)
Curr Opin Neurobiol
, vol.11
, pp. 327-335
-
-
Cull-Candy, S.1
Brickley, S.2
Farrant, M.3
-
9
-
-
78049340685
-
Glutamate receptors and learning and memory
-
10.1038/ng1110-925, 20980986
-
Gécz J. Glutamate receptors and learning and memory. Nat Genet 2010, 42:925-6. 10.1038/ng1110-925, 20980986.
-
(2010)
Nat Genet
, vol.42
, pp. 925-926
-
-
Gécz, J.1
-
10
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
10.1038/ng.835, 3115696, 21572417
-
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, Eichler EE. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet 2011, 43:585-9. 10.1038/ng.835, 3115696, 21572417.
-
(2011)
Nat Genet
, vol.43
, pp. 585-589
-
-
O'Roak, B.J.1
Deriziotis, P.2
Lee, C.3
Vives, L.4
Schwartz, J.J.5
Girirajan, S.6
Karakoc, E.7
Mackenzie, A.P.8
Ng, S.B.9
Baker, C.10
Rieder, M.J.11
Nickerson, D.A.12
Bernier, R.13
Fisher, S.E.14
Shendure, J.15
Eichler, E.E.16
-
11
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
10.1038/nature10989, 3350576, 22495309
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012, 485:246-50. 10.1038/nature10989, 3350576, 22495309.
-
(2012)
Nature
, vol.485
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.A.20
Bernier, R.21
Shendure, J.22
Eichler, E.E.23
more..
-
12
-
-
84862689235
-
Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder
-
10.1503/jpn.110109, 3670443, 23766744
-
Alonso P, Gratacós M, Segalàs C, Escaramís G, Real E, Bayés M, Labad J, López-Solà C, Estivill X, Menchón JM. Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder. J psychiatry & neurosci JPN 2012, 37:273-81. 10.1503/jpn.110109, 3670443, 23766744.
-
(2012)
J psychiatry & neurosci JPN
, vol.37
, pp. 273-281
-
-
Alonso, P.1
Gratacós, M.2
Segalàs, C.3
Escaramís, G.4
Real, E.5
Bayés, M.6
Labad, J.7
López-Solà, C.8
Estivill, X.9
Menchón, J.M.10
-
13
-
-
34347407352
-
Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder
-
10.1111/j.1601-183X.2006.00273.x, 17010153
-
Dorval KM, Wigg KG, Crosbie J, Tannock R, Kennedy JL, Ickowicz A, Pathare T, Malone M, Schachar R, Barr CL. Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder. Genes Brain Behav 2007, 6:444-52. 10.1111/j.1601-183X.2006.00273.x, 17010153.
-
(2007)
Genes Brain Behav
, vol.6
, pp. 444-452
-
-
Dorval, K.M.1
Wigg, K.G.2
Crosbie, J.3
Tannock, R.4
Kennedy, J.L.5
Ickowicz, A.6
Pathare, T.7
Malone, M.8
Schachar, R.9
Barr, C.L.10
-
14
-
-
77349127347
-
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia
-
Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P. Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. American j medical genetics Part B Neuropsychiatr genetics official publication Int Society of Psychiatr Genetics 2010, 153B:503-11.
-
(2010)
American j medical genetics Part B Neuropsychiatr genetics official publication Int Society of Psychiatr Genetics
, vol.153 B
, pp. 503-511
-
-
Ludwig, K.U.1
Roeske, D.2
Herms, S.3
Schumacher, J.4
Warnke, A.5
Plume, E.6
Neuhoff, N.7
Bruder, J.8
Remschmidt, H.9
Schulte-Körne, G.10
Müller-Myhsok, B.11
Nöthen, M.M.12
Hoffmann, P.13
-
15
-
-
77950629668
-
Genetic association studies of glutamate, GABA and related genes in schizophrenia and bipolar disorder: a decade of advance
-
10.1016/j.neubiorev.2010.01.002, 20060416
-
Cherlyn SYT, Woon PS, Liu JJ, Ong WY, Tsai GC, Sim K. Genetic association studies of glutamate, GABA and related genes in schizophrenia and bipolar disorder: a decade of advance. Neurosci Biobehav Rev 2010, 34:958-977. 10.1016/j.neubiorev.2010.01.002, 20060416.
-
(2010)
Neurosci Biobehav Rev
, vol.34
, pp. 958-977
-
-
Cherlyn, S.Y.T.1
Woon, P.S.2
Liu, J.J.3
Ong, W.Y.4
Tsai, G.C.5
Sim, K.6
-
16
-
-
0037216407
-
The N-methyl-D-aspartate receptor subunit NR2B: localization, functional properties, regulation, and clinical implications
-
10.1016/S0163-7258(02)00302-9, 12493535
-
Loftis JM, Janowsky A. The N-methyl-D-aspartate receptor subunit NR2B: localization, functional properties, regulation, and clinical implications. Pharmacol Ther 2003, 97:55-85. 10.1016/S0163-7258(02)00302-9, 12493535.
-
(2003)
Pharmacol Ther
, vol.97
, pp. 55-85
-
-
Loftis, J.M.1
Janowsky, A.2
-
17
-
-
84871448593
-
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
-
10.1126/science.1227764, 23160955
-
O'Roak BJ, Vives L, Fu W, Egertson JD, Stanaway IB, Phelps IG, Carvill G, Kumar A, Lee C, Ankenman K, Munson J, Hiatt JB, Turner EH, Levy R, O'Day DR, Krumm N, Coe BP, Martin BK, Borenstein E, Nickerson DA, Mefford HC, Doherty D, Akey JM, Bernier R, Eichler EE, Shendure J. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science 2012, 338(6114):1619-22. 10.1126/science.1227764, 23160955.
-
(2012)
Science
, vol.338
, Issue.6114
, pp. 1619-1622
-
-
O'Roak, B.J.1
Vives, L.2
Fu, W.3
Egertson, J.D.4
Stanaway, I.B.5
Phelps, I.G.6
Carvill, G.7
Kumar, A.8
Lee, C.9
Ankenman, K.10
Munson, J.11
Hiatt, J.B.12
Turner, E.H.13
Levy, R.14
O'Day, D.R.15
Krumm, N.16
Coe, B.P.17
Martin, B.K.18
Borenstein, E.19
Nickerson, D.A.20
Mefford, H.C.21
Doherty, D.22
Akey, J.M.23
Bernier, R.24
Eichler, E.E.25
Shendure, J.26
more..
-
20
-
-
27644525569
-
Der Verhaltensfragebogen für Kinder mit Entwicklungsstörungen: psychometrische Kennwerte und Normierung
-
Steinhausen HC, Winkler Metzke C. Der Verhaltensfragebogen für Kinder mit Entwicklungsstörungen: psychometrische Kennwerte und Normierung. Z Klin Psychol Psychother 2005, 34:266-276.
-
(2005)
Z Klin Psychol Psychother
, vol.34
, pp. 266-276
-
-
Steinhausen, H.C.1
Winkler Metzke, C.2
-
21
-
-
4644291154
-
Differentiating the behavioural profile in autism and mental retardation and testing of a screener
-
Steinhausen H-C, Metzke CW. Differentiating the behavioural profile in autism and mental retardation and testing of a screener. Eur Child Adolesc Psychiatry 2004, 13:214-20.
-
(2004)
Eur Child Adolesc Psychiatry
, vol.13
, pp. 214-220
-
-
Steinhausen, H.-C.1
Metzke, C.W.2
-
22
-
-
0029065080
-
The developmental behavior checklist: the development and validation of an instrument to assess behavioral and emotional disturbance in children and adolescents with mental retardation
-
10.1007/BF02178498, 7559289
-
Einfeld SL, Tonge BJ. The developmental behavior checklist: the development and validation of an instrument to assess behavioral and emotional disturbance in children and adolescents with mental retardation. J Autism Dev Disord 1995, 25:81-104. 10.1007/BF02178498, 7559289.
-
(1995)
J Autism Dev Disord
, vol.25
, pp. 81-104
-
-
Einfeld, S.L.1
Tonge, B.J.2
-
24
-
-
7344263462
-
The revised Conners' Parent Rating Scale (CPRS-R): factor structure, reliability, and criterion validity
-
10.1023/A:1022602400621, 9700518
-
Conners CK, Sitarenios G, Parker JD, Epstein JN. The revised Conners' Parent Rating Scale (CPRS-R): factor structure, reliability, and criterion validity. J Abnorm Child Psychol 1998, 26:257-68. 10.1023/A:1022602400621, 9700518.
-
(1998)
J Abnorm Child Psychol
, vol.26
, pp. 257-268
-
-
Conners, C.K.1
Sitarenios, G.2
Parker, J.D.3
Epstein, J.N.4
-
25
-
-
7344229200
-
Revision and restandardization of the Conners Teacher Rating Scale (CTRS-R): factor structure, reliability, and criterion validity
-
10.1023/A:1022606501530, 9700520
-
Conners CK, Sitarenios G, Parker JD, Epstein JN. Revision and restandardization of the Conners Teacher Rating Scale (CTRS-R): factor structure, reliability, and criterion validity. J Abnorm Child Psychol 1998, 26:279-91. 10.1023/A:1022606501530, 9700520.
-
(1998)
J Abnorm Child Psychol
, vol.26
, pp. 279-291
-
-
Conners, C.K.1
Sitarenios, G.2
Parker, J.D.3
Epstein, J.N.4
-
26
-
-
0035125640
-
Interkultureller vergleich der conners-skalen: lässt sich die US-amerikanische faktorenstruktur an einer deutschen klinikstichprobe replizieren?
-
10.1024//1422-4917.29.1.16, 11234548
-
Huss M, Iseler A, Lehmkuhl U. Interkultureller vergleich der conners-skalen: lässt sich die US-amerikanische faktorenstruktur an einer deutschen klinikstichprobe replizieren?. Z Kinder Jugendpsychiatr Psychother 2001, 29:16-24. 10.1024//1422-4917.29.1.16, 11234548.
-
(2001)
Z Kinder Jugendpsychiatr Psychother
, vol.29
, pp. 16-24
-
-
Huss, M.1
Iseler, A.2
Lehmkuhl, U.3
-
30
-
-
0023300346
-
Child/adolescent behavioral and emotional problems: implications of cross-informant correlations for situational specificity
-
Achenbach TM, McConaughy SH, Howell CT. Child/adolescent behavioral and emotional problems: implications of cross-informant correlations for situational specificity. Psychol Bull 1987, 101:213-32.
-
(1987)
Psychol Bull
, vol.101
, pp. 213-232
-
-
Achenbach, T.M.1
McConaughy, S.H.2
Howell, C.T.3
-
31
-
-
0019805536
-
Congruence of parents' and teachers' ratings of children's behavior problems
-
10.1007/BF00916839, 7320352
-
Touliatos J, Lindholm BW. Congruence of parents' and teachers' ratings of children's behavior problems. J Abnorm Child Psychol 1981, 9:347-54. 10.1007/BF00916839, 7320352.
-
(1981)
J Abnorm Child Psychol
, vol.9
, pp. 347-354
-
-
Touliatos, J.1
Lindholm, B.W.2
-
32
-
-
0024577908
-
Agreement between parents' and teachers' ratings of behavioral/emotional problems of children aged 4-12
-
10.1111/j.1469-7610.1989.tb00772.x, 2925818
-
Verhulst FC, Akkerhuis GW. Agreement between parents' and teachers' ratings of behavioral/emotional problems of children aged 4-12. J Child Psychol Psychiatry 1989, 30:123-36. 10.1111/j.1469-7610.1989.tb00772.x, 2925818.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 123-136
-
-
Verhulst, F.C.1
Akkerhuis, G.W.2
|