-
1
-
-
0029881013
-
Genomic imprinting and the differential roles of parental genomes in brain development
-
Keverne EB, Fundele R, Narasimha M et al. Genomic imprinting and the differential roles of parental genomes in brain development. Devel Brain Res 1996;92:91-100.
-
(1996)
Devel Brain Res.
, vol.92
, pp. 91-100
-
-
Keverne, E.B.1
Fundele, R.2
Narasimha, M.3
-
2
-
-
0031426323
-
Genomic imprinting in the brain
-
Keverne EB. Genomic imprinting in the brain. Curr Op Neurobiol 1997;7:463-468.
-
(1997)
Curr. Op Neurobiol.
, vol.7
, pp. 463-468
-
-
Keverne, E.B.1
-
3
-
-
0032501220
-
Dissociation of IGF2 and H19 imprinting in human brain
-
Pham NV, Nguyen MT, Hu JF et al. Dissociation of IGF2 and H19 imprinting in human brain. Brain Res 1998;810(1-2):1-8.
-
(1998)
Brain Res.
, vol.810
, Issue.1-2
, pp. 1-8
-
-
Pham, N.V.1
Nguyen, M.T.2
Hu, J.F.3
-
4
-
-
16244411099
-
Imprinted nesp55 influences behavioral reactivity to novel environments
-
Plagge A, Isles AR, Gordon E et al. Imprinted nesp55 influences behavioral reactivity to novel environments. Mol Cell Biol 2005;25(8):3019-3026.
-
(2005)
Mol. Cell. Biol.
, vol.25
, Issue.8
, pp. 3019-3026
-
-
Plagge, A.1
Isles, A.R.2
Gordon, E.3
-
5
-
-
0029074963
-
Parental imprinting effect at the INS-IGF2 diabetes susceptibility locus
-
Polychronakos C, Kukuvitis A, Giannoukakis N et al. Parental imprinting effect at the INS-IGF2 diabetes susceptibility locus. Diabetologia 1995;38(6):715-719.
-
(1995)
Diabetologia
, vol.38
, Issue.6
, pp. 715-719
-
-
Polychronakos, C.1
Kukuvitis, A.2
Giannoukakis, N.3
-
6
-
-
1242320004
-
Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome
-
Whittington J, Holland A, Webb T et al. Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome. J Intellect Disabil Res 2004;48(Pt 2):172-187.
-
(2004)
J. Intellect Disabil Res.
, vol.48
, Issue.2 PART
, pp. 172-187
-
-
Whittington, J.1
Holland, A.2
Webb, T.3
-
7
-
-
0026582561
-
Implications of genomic imprinting for psychiatric genetics
-
Flint J. Implications of genomic imprinting for psychiatric genetics. Psychol Med 1992;22:5-10.
-
(1992)
Psychol. Med.
, vol.22
, pp. 5-10
-
-
Flint, J.1
-
8
-
-
0034827137
-
Imprinted genes and mental dysfunction
-
Davies W, Isles AR, Wilkinson LS. Imprinted genes and mental dysfunction. Ann Med 2001;33(6):428-436.
-
(2001)
Ann. Med.
, vol.33
, Issue.6
, pp. 428-436
-
-
Davies, W.1
Isles, A.R.2
Wilkinson, L.S.3
-
9
-
-
0037043838
-
Evidence for parent of origin effect in late-onset Alzheimer disease
-
Bassett SS, Avramopoulos D, Fallin D. Evidence for parent of origin effect in late-onset Alzheimer disease. Am J Med Genet 2002;114(6):679-686.
-
(2002)
Am. J. Med. Genet.
, vol.114
, Issue.6
, pp. 679-686
-
-
Bassett, S.S.1
Avramopoulos, D.2
Fallin, D.3
-
10
-
-
13444269226
-
Analysis of IMGSAC autism susceptibility loci: Evidence for sex limited and parent of origin specific effects
-
Lamb JA, Barnby G, Bonora E et al. Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. J Med Genet 2005;42(2):132-137.
-
(2005)
J. Med. Genet.
, vol.42
, Issue.2
, pp. 132-137
-
-
Lamb, J.A.1
Barnby, G.2
Bonora, E.3
-
11
-
-
0023806065
-
Higher risk of seizures in offspring of mothers than of fathers with epilepsy
-
Ottman R, Annegers JF, Hauser WA et al. Higher risk of seizures in offspring of mothers than of fathers with epilepsy. Am J Hum Genet 1988;43:257-264.
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 257-264
-
-
Ottman, R.1
Annegers, J.F.2
Hauser, W.A.3
-
12
-
-
0034255591
-
Imprinted genes, cognition and behavior
-
Isles AR, Wilkinson LS. Imprinted genes, cognition and behavior. Trends Cog Sci 2000;4(8):309-318.
-
(2000)
Trends Cog Sci.
, vol.4
, Issue.8
, pp. 309-318
-
-
Isles, A.R.1
Wilkinson, L.S.2
-
13
-
-
0026079591
-
Influence of paternally imprinted genes on development
-
Barton SC, Ferguson-Smith AC, Fundele R et al. Influence of paternally imprinted genes on development. Development 1991;113:679-688.
-
(1991)
Development
, vol.113
, pp. 679-688
-
-
Barton, S.C.1
Ferguson-Smith, A.C.2
Fundele, R.3
-
17
-
-
27244441436
-
Vasopressin/oxytocin and aggression
-
Ferris CF. Vasopressin/oxytocin and aggression. Novartis Found Symp 2005;268:190-198.
-
(2005)
Novartis Found Symp.
, vol.268
, pp. 190-198
-
-
Ferris, C.F.1
-
18
-
-
24144445635
-
Mechanisms underlying epigenetic effects of early social experience: The role of neuropeptides and steroids
-
Cushing BS, Kramer KM. Mechanisms underlying epigenetic effects of early social experience: the role of neuropeptides and steroids. Neurosci Biobehav Rev 2005;29(7):1089-1105.
-
(2005)
Neurosci. Biobehav. Rev.
, vol.29
, Issue.7
, pp. 1089-1105
-
-
Cushing, B.S.1
Kramer, K.M.2
-
19
-
-
28044451047
-
Early experience in humans is associated with changes in neuropeptides critical for regulating social behavior
-
Fries AB, Ziegler TE, Kurian JR et al. Early experience in humans is associated with changes in neuropeptides critical for regulating social behavior. Proc Natl Acad Sci 2005;102(47):17237-17240.
-
(2005)
Proc. Natl. Acad. Sci.
, vol.102
, Issue.47
, pp. 17237-17240
-
-
Fries, A.B.1
Ziegler, T.E.2
Kurian, J.R.3
-
20
-
-
0028832361
-
Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior
-
Allen ND, Logan K, Lally G et al. Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior. Proc Natl Acad Sci 1995;92:10782-10786.
-
(1995)
Proc. Natl. Acad. Sci.
, vol.92
, pp. 10782-10786
-
-
Allen, N.D.1
Logan, K.2
Lally, G.3
-
21
-
-
0028235182
-
Molecular genetic approaches to understanding brain development and behavior
-
Keverne EB. Molecular genetic approaches to understanding brain development and behavior. Psychoneuroendocrinology 1994;19:407-414.
-
(1994)
Psychoneuroendocrinology
, vol.19
, pp. 407-414
-
-
Keverne, E.B.1
-
22
-
-
33745684491
-
The inheritance of cognitive skills. Does genomic imprinting play a role?
-
Goos LM, Silverman I. The inheritance of cognitive skills. Does genomic imprinting play a role? J Neurogenet 2006;20:19-40.
-
(2006)
J. Neurogenet
, vol.20
, pp. 19-40
-
-
Goos, L.M.1
Silverman, I.2
-
23
-
-
0032721892
-
The genetic basis of cognition
-
Flint J. The genetic basis of cognition. Brain Res Bull 1999;122:2015-2031.
-
(1999)
Brain Res. Bull.
, vol.122
, pp. 2015-2031
-
-
Flint, J.1
-
24
-
-
18244402218
-
A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: A five-stage design using DNA pooling and extreme selected groups
-
DOI 10.1023/A:1013385125887
-
Plomin R, Hill L, Craig IW et al. A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: A five stage design using DNA pooling and extreme selected groups. Behav Genet 2001;31(6):497-509. (Pubitemid 34112047)
-
(2001)
Behavior Genetics
, vol.31
, Issue.6
, pp. 497-509
-
-
Plomin, R.1
Hill, L.2
Craig, I.W.3
Mcguffin, P.4
Purcell, S.5
Sham, P.6
Lubinski, D.7
Thompson, L.A.8
Fisher, P.J.9
Turic, D.10
Owen, M.J.11
-
25
-
-
0002706609
-
The puzzle of nongenetic variance
-
Sternberg RJ, Grigorenko EL, eds, Cambridge: Cambridge University Press
-
Jensen AR. The puzzle of nongenetic variance. In: Sternberg RJ, Grigorenko EL, eds. Intelligence, Heredity and Environment. Cambridge: Cambridge University Press, 1998:42-88.
-
(1998)
Intelligence, Heredity and Environment
, pp. 42-88
-
-
Jensen, A.R.1
-
26
-
-
0017175007
-
Parent-offspring resemblance for specific cognitive abilities in two ethnic groups
-
DeFries JC, Ashton GC, Johnson RC et al. Parent-offspring resemblance for specific cognitive abilities in two ethnic groups. Nature 1976;261(5556):131- 133.
-
(1976)
Nature
, vol.261
, Issue.5556
, pp. 131-133
-
-
DeFries, J.C.1
Ashton, G.C.2
Johnson, R.C.3
-
27
-
-
0018351184
-
Familial resemblance for specific cognitive abilities
-
DeFries JC, Johnson RC, Kuse AR et al. Familial resemblance for specific cognitive abilities. Behav Genet 1979;9(1):23-43.
-
(1979)
Behav. Genet.
, vol.9
, Issue.1
, pp. 23-43
-
-
DeFries, J.C.1
Johnson, R.C.2
Kuse, A.R.3
-
28
-
-
0018166375
-
In pursuit of the "spatial gene": A family study
-
Loehlin JC, Sharan S, Jacoby R. In pursuit of the "spatial gene": a family study. Behav Genet 1978;8(1):27-41.
-
(1978)
Behav. Genet.
, vol.8
, Issue.1
, pp. 27-41
-
-
Loehlin, J.C.1
Sharan, S.2
Jacoby, R.3
-
29
-
-
0017834926
-
Intrafamilial correlations and heritability estimates for spatial ability in a Minnesota sample
-
McGee MG. Intrafamilial correlations and heritability estimates for spatial ability in a Minnesota sample. Behav Genet 1978;8(1):77-80.
-
(1978)
Behav. Genet.
, vol.8
, Issue.1
, pp. 77-80
-
-
McGee, M.G.1
-
30
-
-
0018179135
-
Parent-offspring resemblance for specific cognitive abilities in Korea
-
Park J, Johnson RC, DeFries JC et al. Parent-offspring resemblance for specific cognitive abilities in Korea. Behav Genet 1978;8(1):43-52.
-
(1978)
Behav. Genet.
, vol.8
, Issue.1
, pp. 43-52
-
-
Park, J.1
Johnson, R.C.2
DeFries, J.C.3
-
31
-
-
0019208920
-
Comparison of parent-offspring resemblance for specific cognitive abilities
-
Spuhler KP, Vandenberg SG. Comparison of parent-offspring resemblance for specific cognitive abilities. Behav Genet 1980;10(4):413-418.
-
(1980)
Behav. Genet.
, vol.10
, Issue.4
, pp. 413-418
-
-
Spuhler, K.P.1
Vandenberg, S.G.2
-
32
-
-
0036265787
-
The correlation between relatives on the supposition of genomic imprinting
-
Spencer HG. The correlation between relatives on the supposition of genomic imprinting. Genetics 2002;161:411-417.
-
(2002)
Genetics
, vol.161
, pp. 411-417
-
-
Spencer, H.G.1
-
33
-
-
1442268529
-
Introduction. In the speciation of modern homo sapiens
-
Crow TJ. Introduction. In The Speciation of Modern Homo sapiens. Proc Br Acad 2002;106:1-20.
-
(2002)
Proc. Br. Acad.
, vol.106
, pp. 1-20
-
-
Crow, T.J.1
-
34
-
-
0032392269
-
Executive function in preschoolers: Links with theory of mind and verbal ability
-
Hughes C. Executive function in preschoolers: links with theory of mind and verbal ability. Brit J Dev Psychol 1998;16:233-253. (Pubitemid 128433616)
-
(1998)
British Journal of Developmental Psychology
, vol.16
, Issue.2
, pp. 233-253
-
-
Hughes, C.1
-
35
-
-
84920591658
-
A normative-developmental study of executive function
-
Welsh M, Pennington B, Groisser D. A normative-developmental study of executive function. Devel Neuropsych 1991;7:131-149.
-
(1991)
Devel Neuropsych.
, vol.7
, pp. 131-149
-
-
Welsh, M.1
Pennington, B.2
Groisser, D.3
-
36
-
-
0018050763
-
Does the chimpanzee have a theory of mind?
-
Premack D, Woodruff G. Does the chimpanzee have a theory of mind? Behav Brain Sci 1978;1:515-526.
-
(1978)
Behav. Brain Sci.
, vol.1
, pp. 515-526
-
-
Premack, D.1
Woodruff, G.2
-
37
-
-
0003616280
-
On the origin of the human mind
-
Caruthers P, Chamberlain A, eds, Cambridge: Cambridge University Press
-
Dunbar R I M. On the origin of the human mind. In: Caruthers P, Chamberlain A, eds. Evolution and the Human Mind: Modularity, Language and Meta-Cognition. Cambridge: Cambridge University Press, 2000:238-253.
-
(2000)
Evolution and the Human Mind: Modularity, Language and Meta-Cognition
, pp. 238-253
-
-
Dunbar, R.I.M.1
-
38
-
-
0036488272
-
Empathy: Its ultimate and proximate bases
-
Preston SD, de Waal FB. Empathy: Its ultimate and proximate bases. Behav Brain Sci 2002;25(1):1-20.
-
(2002)
Behav. Brain Sci.
, vol.25
, Issue.1
, pp. 1-20
-
-
Preston, S.D.1
De Waal, F.B.2
-
39
-
-
0035006759
-
Hemispheric dominance for emotions, empathy and social behavior: Evidence from right and left handers with frontotemporal dementia
-
Perry RJ, Rosen HR, Kramer JH et al. Hemispheric dominance for emotions, empathy and social behavior: evidence from right and left handers with frontotemporal dementia. Neurocase 2001;7(2):145-160.
-
(2001)
Neurocase
, vol.7
, Issue.2
, pp. 145-160
-
-
Perry, R.J.1
Rosen, H.R.2
Kramer, J.H.3
-
40
-
-
0035126473
-
'Theory of mind' and the prefrontal cortex
-
Shallice T. 'Theory of mind' and the prefrontal cortex. Brain 2001;124(Pt 2):247-248.
-
(2001)
Brain
, vol.124
, Issue.2 PART
, pp. 247-248
-
-
Shallice, T.1
-
41
-
-
4444339325
-
A touching sight: SII/PV activation during the observation and experience of touch
-
Keysers C, Wicker B, Gazzola V et al. A touching sight: SII/PV activation during the observation and experience of touch. Neuron 2004;42(2):335-346.
-
(2004)
Neuron
, vol.42
, Issue.2
, pp. 335-346
-
-
Keysers, C.1
Wicker, B.2
Gazzola, V.3
-
42
-
-
0032221027
-
The social brain hypothesis
-
Dunbar R I M. The social brain hypothesis. Evol Anth 1998;6:178-190.
-
(1998)
Evol. Anth
, vol.6
, pp. 178-190
-
-
Dunbar, R.I.M.1
-
43
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychi 1989;30(3):405-416.
-
(1989)
J. Child Psychol. Psychi
, vol.30
, Issue.3
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
-
44
-
-
0036780698
-
A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M, Vanhala R, Varilo T et al. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet 2002;71(4):777-790.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, Issue.4
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
-
45
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum JD, Silverman JM, Smith CJ et al. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 2001;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
-
46
-
-
0033573212
-
An autosomal genomic screen for autism
-
Collaborative Linkage Study of Autism CLSA
-
Collaborative Linkage Study of Autism (CLSA). An autosomal genomic screen for autism. Am J Med Genet (Neuropsychiatric Genetics) 1999;88:609-615.
-
(1999)
Am. J. Med. Genet. (Neuropsychiatric Genetics)
, vol.88
, pp. 609-615
-
-
-
47
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 1998;7:571-578.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 571-578
-
-
-
48
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q and 16p
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q and 16p. Am J Hum Genet 2001;69:570-581.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 570-581
-
-
-
49
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu J, Nyholt DR, Magnussen P et al. A genomewide screen for autism susceptibility loci. Am J Hum Genet 2001;69(2):327-340.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, Issue.2
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
-
50
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris autism research international sibpair study
-
Philippe A, Martinez M, Guilloud-Bataille M et al. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet 1999;8(5):805-812.
-
(1999)
Hum. Mol. Genet.
, vol.8
, Issue.5
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
-
51
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L et al. A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet 1999;65(2):493-507.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, Issue.2
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
-
52
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R et al. A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet 2003;73(4):886-897.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, Issue.4
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
-
53
-
-
23744471663
-
Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs
-
Alarcon M, Yonan AL, Gilliam TC et al. Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Mol Psychiatry, 2005.
-
(2005)
Mol. Psychiatry
-
-
Alarcon, M.1
Yonan, A.L.2
Gilliam, T.C.3
-
54
-
-
18944365556
-
Replication of autism linkage: Fine-mapping peak at 17q21
-
Cantor RM, Kono N, Duvall JA et al. Replication of Autism Linkage: Fine-Mapping Peak at 17q21. Am J Hum Genet 2005;76(6).
-
(2005)
Am. J. Hum. Genet.
, vol.76
, Issue.6
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
-
55
-
-
32844460507
-
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
-
18-28
-
Vorstman JA, Staal WG, van Daalen E et al. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol Psychiatry 2006;11(1):1, 18-28.
-
(2006)
Mol. Psychiatry
, vol.11
, Issue.1
, pp. 1
-
-
Vorstman, J.A.1
Staal, W.G.2
Van Daalen, E.3
-
56
-
-
33745234245
-
Imbalanced genomic imprinting in brain development: An evolutionary basis for the aetiology of autism
-
Badcock C, Crespi B. Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism. J Evol Biol 2006;19(4):1007-1032.
-
(2006)
J. Evol. Biol.
, vol.19
, Issue.4
, pp. 1007-1032
-
-
Badcock, C.1
Crespi, B.2
-
57
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook Jr EH, Lindgren V, Leventhal BL et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 1997;60(4):928-934.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, Issue.4
, pp. 928-934
-
-
Cook Jr., E.H.1
Lindgren, V.2
Leventhal, B.L.3
-
58
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer RJ, Phelan MC, Michaelis RC et al. Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet 1998;76(4):327-336.
-
(1998)
Am. J. Med. Genet.
, vol.76
, Issue.4
, pp. 327-336
-
-
Schroer, R.J.1
Phelan, M.C.2
Michaelis, R.C.3
-
59
-
-
0032169436
-
Interstitial duplications of chromosome region 15q11q13: Clinical and molecular characterization
-
Repetto GM, White LM, Bader PJ et al. Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization. Am J Med Genet 1998;79(2):82-89.
-
(1998)
Am. J. Med. Genet.
, vol.79
, Issue.2
, pp. 82-89
-
-
Repetto, G.M.1
White, L.M.2
Bader, P.J.3
-
60
-
-
0042970462
-
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
-
Nurmi EL, Dowd M, Tadevosyan-Leyfer O et al. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13. J Am Acad Child Adolesc Psychiatry 2003;42(7):856-863.
-
(2003)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.42
, Issue.7
, pp. 856-863
-
-
Nurmi, E.L.1
Dowd, M.2
Tadevosyan-Leyfer, O.3
-
61
-
-
10644257888
-
Microarray analysis of gene/transcript expression in Angelman syndrome: Deletion versus UPD
-
Bittel DC, Kibiryeva N, Talebizadeh Z et al. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Genomics 2005;85(1):85-91.
-
(2005)
Genomics
, vol.85
, Issue.1
, pp. 85-91
-
-
Bittel, D.C.1
Kibiryeva, N.2
Talebizadeh, Z.3
-
62
-
-
0032729834
-
Genetic studies of autistic disorder and chromosome 7
-
Ashley-Koch A, Wolpert CM, Menold MM et al. Genetic studies of autistic disorder and chromosome 7. Genomics 1999;61(3):227-236.
-
(1999)
Genomics
, vol.61
, Issue.3
, pp. 227-236
-
-
Ashley-Koch, A.1
Wolpert, C.M.2
Menold, M.M.3
-
63
-
-
0034640697
-
Female with autistic disorder and monosomy X (Turner syndrome):Parent-of- origin effect of the X chromosome
-
Donnelly SL, Wolpert CM, Menold MM et al. Female with autistic disorder and monosomy X (Turner syndrome):parent-of-origin effect of the X chromosome. Am J Med Genet 2000;96(3):312-316.
-
(2000)
Am. J. Med. Genet.
, vol.96
, Issue.3
, pp. 312-316
-
-
Donnelly, S.L.1
Wolpert, C.M.2
Menold, M.M.3
-
64
-
-
23744468693
-
The genetic relationship between individual differences in social and nonsocial behaviors characteristic of autism
-
Ronald A, Happe F, Plomin R. The genetic relationship between individual differences in social and nonsocial behaviors characteristic of autism. Dev Sci 2005;8(5):444-458.
-
(2005)
Dev. Sci.
, vol.8
, Issue.5
, pp. 444-458
-
-
Ronald, A.1
Happe, F.2
Plomin, R.3
-
65
-
-
33744821617
-
Genetic heterogeneity between the three components of the autism spectrum: A twin study
-
Ronald A, Happe F, Bolton P et al. Genetic heterogeneity between the three components of the autism spectrum: a twin study. J Am Acad Child Adolesc Psychiatry 2006;45(6):691-699.
-
(2006)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.45
, Issue.6
, pp. 691-699
-
-
Ronald, A.1
Happe, F.2
Bolton, P.3
-
66
-
-
0033374463
-
Autism in association with Turner syndrome: Genetic implications for male vulnerability to passive developmental disorders
-
Creswell CS, Skuse DH. Autism in association with Turner syndrome: genetic implications for male vulnerability to passive developmental disorders. Neurocase 1999;5:101-108.
-
(1999)
Neurocase
, vol.5
, pp. 101-108
-
-
Creswell, C.S.1
Skuse, D.H.2
-
67
-
-
0142215375
-
Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex and fear recognition in humans
-
Good CD, Lawrence K, Thomas NS et al. Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex and fear recognition in humans. Brain 126 (Pt 11):2431-2446.
-
Brain
, vol.126
, Issue.11 PART
, pp. 2431-2446
-
-
Good, C.D.1
Lawrence, K.2
Thomas, N.S.3
-
68
-
-
0037039037
-
Are you looking at me? Accuracy in processing line-of-sight in Turner syndrome
-
Elgar K, Campbell R, Skuse D. Are you looking at me? Accuracy in processing line-of-sight in Turner syndrome. Proc R Soc Lond B Biol Sci 2002;269(1508):2415-2422.
-
(2002)
Proc. R Soc. Lond. B. Biol. Sci.
, vol.269
, Issue.1508
, pp. 2415-2422
-
-
Elgar, K.1
Campbell, R.2
Skuse, D.3
-
69
-
-
0037210478
-
Being the target of another's emotion: A PET study
-
Wicker B, Perrett DI, Baron-Cohen S et al. Being the target of another's emotion: a PET study. Neuropsychologia 2003;41(2):139-146.
-
(2003)
Neuropsychologia
, vol.41
, Issue.2
, pp. 139-146
-
-
Wicker, B.1
Perrett, D.I.2
Baron-Cohen, S.3
-
70
-
-
0242348826
-
Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome
-
Kesler SR, Blasey CM, Brown WE et al. Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome. Biol Psychiatry 2003;54(6):636-646.
-
(2003)
Biol. Psychiatry
, vol.54
, Issue.6
, pp. 636-646
-
-
Kesler, S.R.1
Blasey, C.M.2
Brown, W.E.3
-
72
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse DH, James RS, Bishop DV et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997;387(6634):705-708.
-
(1997)
Nature
, vol.387
, Issue.6634
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.3
-
73
-
-
0033963470
-
Imprinting, the X-chromosome and the male brain: Explaining sex differences in the liability to autism
-
Skuse DH. Imprinting, the X-chromosome and the male brain: explaining sex differences in the liability to autism. Pediatr Res 2000;47(1):9-16.
-
(2000)
Pediatr. Res.
, vol.47
, Issue.1
, pp. 9-16
-
-
Skuse, D.H.1
-
74
-
-
0035577350
-
A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?
-
Zechner U, Wilda M, Kehrer-Sawatzki H et al. A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution? Trends Genet 2001;17(12):697-701.
-
(2001)
Trends Genet.
, vol.17
, Issue.12
, pp. 697-701
-
-
Zechner, U.1
Wilda, M.2
Kehrer-Sawatzki, H.3
-
75
-
-
20044387409
-
Identification of a cluster of X-linked imprinted genes in mice
-
Raefski AS, O'Neill MJ. Identification of a cluster of X-linked imprinted genes in mice. Nat Genet 2005;37(6):620-624.
-
(2005)
Nat. Genet.
, vol.37
, Issue.6
, pp. 620-624
-
-
Raefski, A.S.1
O'Neill, M.J.2
-
76
-
-
20044386140
-
Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice
-
Davies W, Isles A, Smith R et al. Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice. Nat Genet 2005;37(6):625-629.
-
(2005)
Nat. Genet.
, vol.37
, Issue.6
, pp. 625-629
-
-
Davies, W.1
Isles, A.2
Smith, R.3
-
77
-
-
0001076782
-
Parent specific gene expression and the triploid endosperm
-
Haig D, Westoby M. Parent specific gene expression and the triploid endosperm. Am Nat 1989;134:147-155.
-
(1989)
Am. Nat.
, vol.134
, pp. 147-155
-
-
Haig, D.1
Westoby, M.2
-
79
-
-
0030796284
-
Severe reduction of rat defensive behavior to a predator by discrete hypothalamic chemical lesions
-
Canteras NS, Chiavegatto S, Valle LE et al. Severe reduction of rat defensive behavior to a predator by discrete hypothalamic chemical lesions. Brain Res Bull 1997;44(3):297-305.
-
(1997)
Brain Res. Bull.
, vol.44
, Issue.3
, pp. 297-305
-
-
Canteras, N.S.1
Chiavegatto, S.2
Valle, L.E.3
-
80
-
-
0030732826
-
The structural organization of connections between hypothalamus and cerebral cortex
-
Risold PY, Thompson RH, Swanson LW. The structural organization of connections between hypothalamus and cerebral cortex. Brain Res Rev 1997;24:197-254.
-
(1997)
Brain Res. Rev.
, vol.24
, pp. 197-254
-
-
Risold, P.Y.1
Thompson, R.H.2
Swanson, L.W.3
-
81
-
-
0010188967
-
Social relationships and life history of primates
-
Galloway A, Zihlman AL eds, Princeton, NJ: Princeton University Press
-
Smuts B. Social relationships and life history of primates. In: Galloway A, Zihlman AL eds. The Evolving Female: A Life-History Perspective. Princeton, NJ: Princeton University Press, 1997:60-68.
-
(1997)
The Evolving Female: A Life-History Perspective
, pp. 60-68
-
-
Smuts, B.1
-
82
-
-
0023047808
-
Social relationships and social cognition in nonhuman primates
-
Cheney D, Seyfarth R, Smuts B. Social relationships and social cognition in nonhuman primates. Science 1986;234(4782):1361-1366.
-
(1986)
Science
, vol.234
, Issue.4782
, pp. 1361-1366
-
-
Cheney, D.1
Seyfarth, R.2
Smuts, B.3
-
84
-
-
0027097294
-
Neocortex size as a constraint on group size in primates
-
Dunbar R I M. Neocortex size as a constraint on group size in primates. J Hum Evol 1992;20:469-493.
-
(1992)
J. Hum. Evol.
, vol.20
, pp. 469-493
-
-
Dunbar, R.I.M.1
-
85
-
-
0030818298
-
Visual and socio-cognitive information processing in primate brain evolution
-
Joffe TH, Dunbar RI. Visual and socio-cognitive information processing in primate brain evolution. Proc Biol Sci 1997;264(1386):1303-1307.
-
(1997)
Proc. Biol. Sci.
, vol.264
, Issue.1386
, pp. 1303-1307
-
-
Joffe, T.H.1
Dunbar, R.I.2
-
87
-
-
0031687985
-
Abnormal maternal behavior and growth retardation associated with loss of the imprinted gene Mest
-
Lefebvre L, Viville S, Barton SC et al. Abnormal maternal behavior and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 1998;20:163-169.
-
(1998)
Nat. Genet.
, vol.20
, pp. 163-169
-
-
Lefebvre, L.1
Viville, S.2
Barton, S.C.3
-
88
-
-
33645221829
-
Predicted role of secretin and oxytocin in the treatment of behavioral and developmental disorders: Implications for autism
-
Welch MG, Ruggiero DA. Predicted role of secretin and oxytocin in the treatment of behavioral and developmental disorders: implications for autism. Int Rev Neurobiol 2005;71:273-315.
-
(2005)
Int. Rev. Neurobiol.
, vol.71
, pp. 273-315
-
-
Welch, M.G.1
Ruggiero, D.A.2
-
89
-
-
21344444796
-
Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population
-
Wu S, Jia M, Ruan Y et al. Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Biol Psychiatry 2005;58(1):74-77.
-
(2005)
Biol. Psychiatry
, vol.58
, Issue.1
, pp. 74-77
-
-
Wu, S.1
Jia, M.2
Ruan, Y.3
-
90
-
-
0035886219
-
Oxytocin and autistic disorder: Alterations in peptide forms
-
Green L, Fein D, Modahl C et al. Oxytocin and autistic disorder: alterations in peptide forms. Biol Psychiatry 2001;50(8):609-613.
-
(2001)
Biol. Psychiatry
, vol.50
, Issue.8
, pp. 609-613
-
-
Green, L.1
Fein, D.2
Modahl, C.3
-
91
-
-
0033556679
-
Oxytocin, vasopressin and autism: Is there a connection?
-
Insel TR, O'Brien DJ, Leckman JF. Oxytocin, vasopressin and autism: is there a connection? Biol Psychiatry 1999;45(2):145-157.
-
(1999)
Biol. Psychiatry
, vol.45
, Issue.2
, pp. 145-157
-
-
Insel, T.R.1
O'Brien, D.J.2
Leckman, J.F.3
-
92
-
-
33744487635
-
Failing to deactivate: Resting functional abnormalities in autism
-
Kennedy DP, Redcay E, Courchesne E. Failing to deactivate: resting functional abnormalities in autism. Proc Natl Acad Sci 2006;103(21):8275-8280.
-
(2006)
Proc. Natl. Acad. Sci.
, vol.103
, Issue.21
, pp. 8275-8280
-
-
Kennedy, D.P.1
Redcay, E.2
Courchesne, E.3
-
93
-
-
33646501460
-
Monozygotic twins with Asperger syndrome: Differences in behavior reflect variations in brain structure and function
-
Belmonte MK, Carper RA. Monozygotic twins with Asperger syndrome: differences in behavior reflect variations in brain structure and function. Brain Cogn 2006;61(1):110-121.
-
(2006)
Brain Cogn.
, vol.61
, Issue.1
, pp. 110-121
-
-
Belmonte, M.K.1
Carper, R.A.2
-
94
-
-
14644394987
-
Significance of abnormalities in developmental trajectory and asymmetry of cortical serotonin synthesis in autism
-
Chandana SR, Behen ME, Juhasz C et al. Significance of abnormalities in developmental trajectory and asymmetry of cortical serotonin synthesis in autism. Int J Dev Neurosci 2005;23(2-3):171-182.
-
(2005)
Int. J. Dev. Neurosci.
, vol.23
, Issue.2-3
, pp. 171-182
-
-
Chandana, S.R.1
Behen, M.E.2
Juhasz, C.3
-
96
-
-
78049285979
-
-
Great Britain Department of Health Great Britain Department of Health Social Services Inspectorate, ed. Health of the Nation. London, UK: HMSO
-
Mental Illness. What does it mean? In: Great Britain Department of Health Great Britain Department of Health Social Services Inspectorate, ed. Health of the Nation. London, UK: HMSO, 1991.
-
(1991)
Mental Illness. What Does It mean?
-
-
-
97
-
-
33644812110
-
Two new theories of autism: Hyper-systemising and assortative mating
-
Baron-Cohen S. Two new theories of autism: hyper-systemising and assortative mating. Arch Dis Child 2006;91(1):2-5.
-
(2006)
Arch. Dis. Child
, vol.91
, Issue.1
, pp. 2-5
-
-
Baron-Cohen, S.1
-
98
-
-
0031116046
-
Sex differences and non-additivity in heritability of the multidimensional personality questionnaire scales
-
Finkel D, McGue M. Sex differences and non-additivity in heritability of the Multidimensional Personality Questionnaire Scales. J Pers Soc Psychol 1997;72(4):929-938.
-
(1997)
J. Pers Soc. Psychol.
, vol.72
, Issue.4
, pp. 929-938
-
-
Finkel, D.1
McGue, M.2
-
99
-
-
0036357205
-
Behavioral phenotypes in genetic syndromes: Genetic clues to human behavior
-
Cassidy SB, Morris CA. Behavioral phenotypes in genetic syndromes: genetic clues to human behavior. Adv Pediatr 2002;49:59-86.
-
(2002)
Adv. Pediatr.
, vol.49
, pp. 59-86
-
-
Cassidy, S.B.1
Morris, C.A.2
-
100
-
-
0034068335
-
Behavioral phenotypes: What do they teach us?
-
Skuse DH. Behavioral phenotypes: what do they teach us? Arch Dis Child 2000;82(3):222-225.
-
(2000)
Arch. Dis. Child
, vol.82
, Issue.3
, pp. 222-225
-
-
Skuse, D.H.1
-
101
-
-
0025181455
-
Prader-Willi syndrome: Current understanding of cause and diagnosis
-
Butler M. Prader-Willi Syndrome: Current understanding of cause and diagnosis. Am J Med Genet 1990;35:319-332.
-
(1990)
Am. J. Med. Genet.
, vol.35
, pp. 319-332
-
-
Butler, M.1
-
102
-
-
0025958320
-
Genomic imprinting in mammalian development: A parental tug-of-war
-
Moore T, Haig D. Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet 1991;7(2):45-49.
-
(1991)
Trends Genet.
, vol.7
, Issue.2
, pp. 45-49
-
-
Moore, T.1
Haig, D.2
-
103
-
-
0042731249
-
Psychopathology and nonmendelian inheritance
-
M. V. Seeman, eds, Washington, DC: American Psychiatric Press
-
Friend WC. Psychopathology and nonmendelian inheritance. In: M. V. Seeman, ed (s). Gender and Psychopathology. Washington, DC: American Psychiatric Press, 1995:41-61.
-
(1995)
Gender and Psychopathology
, pp. 41-61
-
-
Friend, W.C.1
-
105
-
-
13844253255
-
Possible genomic imprinting of three human obesity-related genetic loci
-
Dong C, Li WD, Geller F et al. Possible genomic imprinting of three human obesity-related genetic loci. Am J Hum Genet 2005;76(3):427-437.
-
(2005)
Am. J. Hum. Genet.
, vol.76
, Issue.3
, pp. 427-437
-
-
Dong, C.1
Li, W.D.2
Geller, F.3
-
106
-
-
0035653510
-
Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians
-
Lindsay RS, Kobes S, Knowler WC et al. Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians. Diabetes 2001;50(12):2850-2857.
-
(2001)
Diabetes
, vol.50
, Issue.12
, pp. 2850-2857
-
-
Lindsay, R.S.1
Kobes, S.2
Knowler, W.C.3
-
107
-
-
0025044079
-
Dissociative analysis of ventromedial hypothalamic obesity syndrome
-
Parkinson WL, Weingarten HP. Dissociative analysis of ventromedial hypothalamic obesity syndrome. Am J Physiol 1990;259(4 Pt 2):R829-835.
-
(1990)
Am. J. Physiol.
, vol.259
, Issue.2-4 PART
-
-
Parkinson, W.L.1
Weingarten, H.P.2
-
108
-
-
0028909857
-
Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors
-
Tecott LH, Sun LM, Akana SF et al. Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors. Nature 1995;374(6522):542-546.
-
(1995)
Nature
, vol.374
, Issue.6522
, pp. 542-546
-
-
Tecott, L.H.1
Sun, L.M.2
Akana, S.F.3
-
109
-
-
0034110321
-
Separate systems for serotonin and leptin in appetite control
-
Halford JC, Blundell JE. Separate systems for serotonin and leptin in appetite control. Ann Med 2000;32(3):222-232.
-
(2000)
Ann. Med.
, vol.32
, Issue.3
, pp. 222-232
-
-
Halford, J.C.1
Blundell, J.E.2
-
110
-
-
0037738698
-
Prader-Willi syndrome and the evolution of human childhood
-
Haig D, Wharton R. Prader-Willi syndrome and the evolution of human childhood. Am J Hum Biol 2003;15(3):320-329.
-
(2003)
Am. J. Hum. Biol.
, vol.15
, Issue.3
, pp. 320-329
-
-
Haig, D.1
Wharton, R.2
-
111
-
-
0034703229
-
Role of brain insulin receptor in control of body weight and reproduction
-
Bruning JC, Gautam D, Burks DJ et al. Role of brain insulin receptor in control of body weight and reproduction. Science 2000;289(5487):2122-2125.
-
(2000)
Science
, vol.289
, Issue.5487
, pp. 2122-2125
-
-
Bruning, J.C.1
Gautam, D.2
Burks, D.J.3
-
112
-
-
16944366697
-
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group
-
Bennett ST, Wilson AJ, Esposito L et al. Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group. Nat Genet 1997;17(3):350-352.
-
(1997)
Nat. Genet.
, vol.17
, Issue.3
, pp. 350-352
-
-
Bennett, S.T.1
Wilson, A.J.2
Esposito, L.3
-
113
-
-
0034874328
-
Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity
-
Le Stunff C, Fallin D, Bougneres P. Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity. Nat Genet 2001;29(1):96-99.
-
(2001)
Nat. Genet.
, vol.29
, Issue.1
, pp. 96-99
-
-
Le Stunff, C.1
Fallin, D.2
Bougneres, P.3
-
114
-
-
1842475324
-
Maternal-fetal interactions and birth order influence insulin variable number of tandem repeats allele class associations with head size at birth and childhood weight gain
-
Ong KK, Petry CJ, Barratt BJ et al. Maternal-fetal interactions and birth order influence insulin variable number of tandem repeats allele class associations with head size at birth and childhood weight gain. Diabetes 2004;53(4):1128-1133.
-
(2004)
Diabetes
, vol.53
, Issue.4
, pp. 1128-1133
-
-
Ong, K.K.1
Petry, C.J.2
Barratt, B.J.3
-
115
-
-
7344254106
-
A catalogue of imprinted genes and parent-of-origin effects in humans and animals
-
Morison IM, Reeve AE. A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum Mol Genet 1998;7(10):1599-1609.
-
(1998)
Hum. Mol. Genet.
, vol.7
, Issue.10
, pp. 1599-1609
-
-
Morison, I.M.1
Reeve, A.E.2
-
116
-
-
0035153058
-
Evidence that insulin is imprinted in the human yolk sac
-
Moore GE, Abu-Amero SN, Bell G et al. Evidence that insulin is imprinted in the human yolk sac. Diabetes 2001;50(1):199-203.
-
(2001)
Diabetes
, vol.50
, Issue.1
, pp. 199-203
-
-
Moore, G.E.1
Abu-Amero, S.N.2
Bell, G.3
-
117
-
-
0028365598
-
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
-
Giddings SJ, King CD, Harman KW et al. Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting. Nat Genet 1994;6(3):310-313.
-
(1994)
Nat. Genet.
, vol.6
, Issue.3
, pp. 310-313
-
-
Giddings, S.J.1
King, C.D.2
Harman, K.W.3
-
118
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara TM, Robertson EJ, Efstratiadis A. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 1991;64(4):849-859.
-
(1991)
Cell.
, vol.64
, Issue.4
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
119
-
-
0026098090
-
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
-
Barlow DP, Stoger R, Herrmann BG et al. The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 1991;349(6304):84-87.
-
(1991)
Nature
, vol.349
, Issue.6304
, pp. 84-87
-
-
Barlow, D.P.1
Stoger, R.2
Herrmann, B.G.3
-
120
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei MS, Zemel S, Tilghman SM. Parental imprinting of the mouse H19 gene. Nature 1991;351(6322):153-155.
-
(1991)
Nature
, vol.351
, Issue.6322
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
121
-
-
28444441613
-
Association between the insulin-like growth factor 2 gene (IGF2) and scores on the eating attitudes test in nonclinical subjects: A family-based study
-
Bachner-Melman R, Zohar AH, Nemanov L et al. Association between the insulin-like growth factor 2 gene (IGF2) and scores on the Eating Attitudes Test in nonclinical subjects: a family-based study. Am J Psychiatry 2005;162(12):2256-2262.
-
(2005)
Am. J. Psychiatry
, vol.162
, Issue.12
, pp. 2256-2262
-
-
Bachner-Melman, R.1
Zohar, A.H.2
Nemanov, L.3
-
123
-
-
0028863211
-
Structural organization and chromosomal assignment of the human obese gene
-
Isse N, Ogawa Y, Tamura N et al. Structural organization and chromosomal assignment of the human obese gene. J Biol Chem 1995;270(46):27728-27733.
-
(1995)
J. Biol. Chem.
, vol.270
, Issue.46
, pp. 27728-27733
-
-
Isse, N.1
Ogawa, Y.2
Tamura, N.3
-
124
-
-
84882900279
-
Do maternal methyl supplements in mice affect DNA methylation of offspring?
-
author reply 239
-
Waterland RA. Do maternal methyl supplements in mice affect DNA methylation of offspring? J Nutr 2003;133(1):238; author reply 239.
-
(2003)
J. Nutr.
, vol.133
, Issue.1
, pp. 238
-
-
Waterland, R.A.1
-
125
-
-
33144488275
-
Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus
-
Waterland RA, Lin JR, Smith CA et al. Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus. Hum Mol Genet 2006;15(5):705-716.
-
(2006)
Hum. Mol. Genet.
, vol.15
, Issue.5
, pp. 705-716
-
-
Waterland, R.A.1
Lin, J.R.2
Smith, C.A.3
-
126
-
-
15844423514
-
Ex vivo early embryo development and effects on gene expression and imprinting
-
Gardner DK, Lane M. Ex vivo early embryo development and effects on gene expression and imprinting. Reprod Fertil Dev 2005;17(3):361-370.
-
(2005)
Reprod. Fertil. Dev.
, vol.17
, Issue.3
, pp. 361-370
-
-
Gardner, D.K.1
Lane, M.2
-
127
-
-
0032716565
-
Obesity at the age of 50 y in men and women exposed to famine prenatally
-
Ravelli AC, van der Meulen JH, Osmond C et al. Obesity at the age of 50 y in men and women exposed to famine prenatally. Am J Clin Nutr 1999;70(5):811-816.
-
(1999)
Am. J. Clin. Nutr.
, vol.70
, Issue.5
, pp. 811-816
-
-
Ravelli, A.C.1
Van Der Meulen, J.H.2
Osmond, C.3
-
128
-
-
0026772772
-
Type 2 (non-insulin-dependent) diabetes mellitus: The thrifty phenotype hypothesis
-
Hales CN, Barker DJ. Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis. Diabetologia 1992;35(7):595-601.
-
(1992)
Diabetologia
, vol.35
, Issue.7
, pp. 595-601
-
-
Hales, C.N.1
Barker, D.J.2
-
129
-
-
17744386189
-
Nutritionnal epigenomics: Consequences of unbalanced diets on epigenetics processes of programming during lifespan and between generations
-
Junien C, Gallou-Kabani C, Vige A et al. Nutritionnal epigenomics: consequences of unbalanced diets on epigenetics processes of programming during lifespan and between generations. Ann Endocrinol (Paris) 2005;66(2 Pt 3):2S19-2S28.
-
(2005)
Ann. Endocrinol. (Paris)
, vol.66
, Issue.2-3 PART
-
-
Junien, C.1
Gallou-Kabani, C.2
Vige, A.3
-
130
-
-
0024205564
-
The epidemiology of obsessive-compulsive disorder in five US communities
-
Karno M, Golding JM, Sorenson SB et al. The epidemiology of obsessive-compulsive disorder in five US communities. Arch Gen Psychiatry 1988;45(12):1094-1099.
-
(1988)
Arch. Gen. Psychiatry
, vol.45
, Issue.12
, pp. 1094-1099
-
-
Karno, M.1
Golding, J.M.2
Sorenson, S.B.3
-
131
-
-
70350199597
-
Association between the COMT locus and obsessive-compulsive disorder in females but not males
-
Alsobrook 2nd JP, Zohar AH, Leboyer M et al. Association between the COMT locus and obsessive-compulsive disorder in females but not males. Am J Med Genet 2002;114(1):116-120.
-
(2002)
Am. J. Med. Genet.
, vol.114
, Issue.1
, pp. 116-120
-
-
Alsobrook II, J.P.1
Zohar, A.H.2
Leboyer, M.3
-
132
-
-
0033044126
-
Obsessive-compulsive symptoms in Prader-Willi and "Prader-Willi- Like" patients
-
State MW, Dykens EM, Rosner B et al. Obsessive-compulsive symptoms in Prader-Willi and "Prader-Willi-Like" patients. J Am Acad Child Adolesc Psychiatry 1999;38(3):329-334.
-
(1999)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.38
, Issue.3
, pp. 329-334
-
-
State, M.W.1
Dykens, E.M.2
Rosner, B.3
-
133
-
-
0032535656
-
Cerebrospinal fluid levels of oxytocin in Prader-Willi syndrome: A preliminary report
-
Martin A, State M Anderson GM et al. Cerebrospinal fluid levels of oxytocin in Prader-Willi syndrome: a preliminary report. Biol Psychiatry 1998;44(12):1349-1352.
-
(1998)
Biol. Psychiatry
, vol.44
, Issue.12
, pp. 1349-1352
-
-
Martin, A.1
State, M.2
Anderson, G.M.3
-
134
-
-
0027942173
-
Elevated cerebrospinal fluid levels of oxytocin in obsessive-compulsive disorder. Comparison with Tourette's syndrome and healthy controls
-
Leckman JF, Goodman WK, North WG et al. Elevated cerebrospinal fluid levels of oxytocin in obsessive-compulsive disorder. Comparison with Tourette's syndrome and healthy controls. Arch Gen Psychiatry 1994;51(10):782-792.
-
(1994)
Arch. Gen. Psychiatry
, vol.51
, Issue.10
, pp. 782-792
-
-
Leckman, J.F.1
Goodman, W.K.2
North, W.G.3
-
135
-
-
0036930448
-
5-HT2A promoter polymorphism-1438G/A in children and adolescents with obsessive-compulsive disorders
-
Walitza S, Wewetzer C, Warnke A et al. 5-HT2A promoter polymorphism-1438G/A in children and adolescents with obsessive-compulsive disorders. Mol Psychiatry 2002;7(10):1054-1057.
-
(2002)
Mol. Psychiatry
, vol.7
, Issue.10
, pp. 1054-1057
-
-
Walitza, S.1
Wewetzer, C.2
Warnke, A.3
-
136
-
-
0242637392
-
Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype
-
DOI 10.1038/sj.mp.4001415
-
Ozaki N, Goldman D, Kaye WH et al. Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype. Mol Psychiatry 2003;8(11):895, 933-6. (Pubitemid 37421692)
-
(2003)
Molecular Psychiatry
, vol.8
, Issue.11
, pp. 895
-
-
Ozaki, N.1
Goldman, D.2
Kaye, W.H.3
Plotnicov, K.4
Greenberg, B.D.5
Lappalainen, J.6
Rudnick, G.7
Murphy, D.L.8
-
137
-
-
33646032703
-
Current animal models of obsessive compulsive disorder: A critical review
-
Joel D. Current animal models of obsessive compulsive disorder: A critical review. Prog Neuropsychopharmacol Biol Psychiatry, 2006.
-
(2006)
Prog. Neuropsychopharmacol. Biol. Psychiatry
-
-
Joel, D.1
-
138
-
-
0034687740
-
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
-
Cavaillé J, Buiting K, Kiefmann M et al. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc Natl Acad Sci 2000;97(26):14311-14316.
-
(2000)
Proc. Natl. Acad. Sci.
, vol.97
, Issue.26
, pp. 14311-14316
-
-
Cavaillé, J.1
Buiting, K.2
Kiefmann, M.3
-
139
-
-
0034687730
-
Imprinted expression of small nucleolar RNAs in brain: Time for RNomics
-
Filipowicz W. Imprinted expression of small nucleolar RNAs in brain: Time for RNomics. Proc Natl Acad Sci 2000;97(26):14035-14037.
-
(2000)
Proc. Natl. Acad. Sci.
, vol.97
, Issue.26
, pp. 14035-14037
-
-
Filipowicz, W.1
-
140
-
-
0033754151
-
Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from pwcr1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain
-
De Los Santos T, Schweizer J, Rees CA et al. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from pwcr1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain. Am J Hum Genet 2000;67(5):1067-1082.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, Issue.5
, pp. 1067-1082
-
-
De Los Santos, T.1
Schweizer, J.2
Rees, C.A.3
-
141
-
-
0032492176
-
Attention-deficit hyperactivity disorder and hyperkinetic disorder
-
Swanson JM, Sergeant JA, Taylor E et al. Attention-deficit hyperactivity disorder and hyperkinetic disorder. Lancet 1998;351(9100):429-433.
-
(1998)
Lancet
, vol.351
, Issue.9100
, pp. 429-433
-
-
Swanson, J.M.1
Sergeant, J.A.2
Taylor, E.3
-
143
-
-
0242407441
-
Altered midbrain dopaminergic neurotransmission during development in an animal model of ADHD
-
Leo D, Sorrentino E, Volpicelli F et al. Altered midbrain dopaminergic neurotransmission during development in an animal model of ADHD. Neurosci Biobehav Rev 2003;27(7):661-669.
-
(2003)
Neurosci. Biobehav. Rev.
, vol.27
, Issue.7
, pp. 661-669
-
-
Leo, D.1
Sorrentino, E.2
Volpicelli, F.3
-
144
-
-
33644802020
-
Developmental transitions among affective and behavioral disorders in adolescent boys
-
Burke JD, Loeber R, Lahey BB et al. Developmental transitions among affective and behavioral disorders in adolescent boys. J Child Psychol Psychiatry 2005;46(11):1200-1210.
-
(2005)
J. Child Psychol. Psychiatry
, vol.46
, Issue.11
, pp. 1200-1210
-
-
Burke, J.D.1
Loeber, R.2
Lahey, B.B.3
-
145
-
-
22644444147
-
A systematic evaluation of ADHD and comorbid psychopathology in a population-based twin sample
-
Volk HE, Neuman RJ, Todd RD. A systematic evaluation of ADHD and comorbid psychopathology in a population-based twin sample. J Am Acad Child Adolesc Psychiatry 2005;44(8):768-775.
-
(2005)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.44
, Issue.8
, pp. 768-775
-
-
Volk, H.E.1
Neuman, R.J.2
Todd, R.D.3
-
146
-
-
17644378382
-
Understanding the covariation among childhood externalizing symptoms: Genetic and environmental influences on conduct disorder, attention deficit hyperactivity disorder and oppositional defiant disorder symptoms
-
Dick DM, Viken RJ, Kaprio J et al. Understanding the covariation among childhood externalizing symptoms: genetic and environmental influences on conduct disorder, attention deficit hyperactivity disorder and oppositional defiant disorder symptoms. J Abnorm Child Psychol 2005;33(2):219-229.
-
(2005)
J. Abnorm Child Psychol.
, vol.33
, Issue.2
, pp. 219-229
-
-
Dick, D.M.1
Viken, R.J.2
Kaprio, J.3
-
148
-
-
0034843635
-
Examining the comorbidity of ADHD-related behaviors and conduct problems using a twin study design
-
Thapar A, Harrington R, McGuffin P. Examining the comorbidity of ADHD-related behaviors and conduct problems using a twin study design. Br J Psychiatry 2001;179:224-229.
-
(2001)
Br. J. Psychiatry
, vol.179
, pp. 224-229
-
-
Thapar, A.1
Harrington, R.2
McGuffin, P.3
-
149
-
-
0030762048
-
Do attention deficit hyperactivity disorder and major depression share familial risk factors?
-
Faraone SV, Biederman J. Do attention deficit hyperactivity disorder and major depression share familial risk factors? J Nerv Ment Dis 1997;185(9):533-541.
-
(1997)
J. Nerv. Ment. Dis.
, vol.185
, Issue.9
, pp. 533-541
-
-
Faraone, S.V.1
Biederman, J.2
-
150
-
-
0142219372
-
Association study of a brain-derived neurotrophic-factor genetic polymorphism and major depressive disorders, symptomatology and antidepressant response
-
Tsai SJ, Cheng CY, Yu YW et al. Association study of a brain-derived neurotrophic-factor genetic polymorphism and major depressive disorders, symptomatology and antidepressant response. Am J Med Genet B Neuropsychiatr Genet 2003;123(1):19-22.
-
(2003)
Am. J. Med. Genet. B. Neuropsychiatr Genet.
, vol.123
, Issue.1
, pp. 19-22
-
-
Tsai, S.J.1
Cheng, C.Y.2
Yu, Y.W.3
-
151
-
-
24944534823
-
Children with ADHD and depression: A multisource, multimethod assessment of clinical, social and academic functioning
-
Blackman GL, Ostrander R, Herman KC. Children with ADHD and depression: a multisource, multimethod assessment of clinical, social and academic functioning. J Atten Disord 2005;8(4):195-207.
-
(2005)
J. Atten Disord.
, vol.8
, Issue.4
, pp. 195-207
-
-
Blackman, G.L.1
Ostrander, R.2
Herman, K.C.3
-
152
-
-
4844230613
-
Depressive symptoms and associated factors in children with attention deficit hyperactivity disorder
-
LeBlanc N, Morin D. Depressive symptoms and associated factors in children with attention deficit hyperactivity disorder. J Child Adol Psychiatric Nurs 2004;17(2):49-55.
-
(2004)
J. Child Adol Psychiatric Nurs.
, vol.17
, Issue.2
, pp. 49-55
-
-
LeBlanc, N.1
Morin, D.2
-
153
-
-
0344420293
-
The influence of gender in the familial association between ADHD and major depression
-
Mick E, Biederman J, Santangelo S et al. The influence of gender in the familial association between ADHD and major depression. J Nerv Ment Dis 2003;191(11):699-705.
-
(2003)
J. Nerv. Ment. Dis.
, vol.191
, Issue.11
, pp. 699-705
-
-
Mick, E.1
Biederman, J.2
Santangelo, S.3
-
154
-
-
0030826382
-
Attention-deficit hyperactivity disorder with bipolar disorder: A familial subtype?
-
Faraone SV, Biederman J, Mennin D et al. Attention-deficit hyperactivity disorder with bipolar disorder: a familial subtype? J Am Acad Child Adolesc Psychiatry 1997;36(10):1378-1387.
-
(1997)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.36
, Issue.10
, pp. 1378-1387
-
-
Faraone, S.V.1
Biederman, J.2
Mennin, D.3
-
155
-
-
0025783964
-
Evidence of familial association between attention deficit disorder and major affective disorders
-
Biederman J, Faraone SV, Keenan K et al. Evidence of familial association between attention deficit disorder and major affective disorders. Arch Gen Psychiatry 1991;48(7):633-642.
-
(1991)
Arch. Gen. Psychiatry
, vol.48
, Issue.7
, pp. 633-642
-
-
Biederman, J.1
Faraone, S.V.2
Keenan, K.3
-
156
-
-
0032492214
-
Bipolar and antisocial disorders among relatives of ADHD children: Parsing familial subtypes of illness
-
Faraone SV, Biederman J, Mennin D et al. Bipolar and antisocial disorders among relatives of ADHD children: parsing familial subtypes of illness. Am J Med Genet 1998;81(1):108-116.
-
(1998)
Am. J. Med. Genet.
, vol.81
, Issue.1
, pp. 108-116
-
-
Faraone, S.V.1
Biederman, J.2
Mennin, D.3
-
157
-
-
0043135059
-
Association of ADHD and conduct disorder-brain electrical evidence for the existence of a distinct subtype
-
Banaschewski T, Brandeis D, Heinrich H et al. Association of ADHD and conduct disorder-brain electrical evidence for the existence of a distinct subtype. J Child Psychol Psychiatry 2003;44(3):356-376.
-
(2003)
J. Child Psychol. Psychiatry
, vol.44
, Issue.3
, pp. 356-376
-
-
Banaschewski, T.1
Brandeis, D.2
Heinrich, H.3
-
158
-
-
0036550347
-
Familial links between attention deficit hyperactivity disorder, conduct disorder and bipolar disorder
-
Doyle AE, Faraone SV. Familial links between attention deficit hyperactivity disorder, conduct disorder and bipolar disorder. Curr Psychiatry Rep 2002;4(2):146-152.
-
(2002)
Curr. Psychiatry Rep.
, vol.4
, Issue.2
, pp. 146-152
-
-
Doyle, A.E.1
Faraone, S.V.2
-
159
-
-
0033848774
-
Familial clustering of symptoms and disruptive behaviors in multiplex families with attention-deficit/hyperactivity disorder
-
Smalley SL, McGough JJ, Del'Homme M et al. Familial clustering of symptoms and disruptive behaviors in multiplex families with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2000;39(9):1135-1143.
-
(2000)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.39
, Issue.9
, pp. 1135-1143
-
-
Smalley, S.L.1
McGough, J.J.2
Del'Homme, M.3
-
160
-
-
0034237530
-
Attention-deficit disorder and conduct disorder in girls: Evidence for a familial subtype
-
Faraone SV, Biederman J, Monuteaux MC. Attention-deficit disorder and conduct disorder in girls: evidence for a familial subtype. Biol Psychiatry 2000;48(1):21-29.
-
(2000)
Biol. Psychiatry
, vol.48
, Issue.1
, pp. 21-29
-
-
Faraone, S.V.1
Biederman, J.2
Monuteaux, M.C.3
-
161
-
-
19444368664
-
ADHD symptoms and insistence on sameness in Prader-Willi syndrome
-
Wigren M, Hansen S. ADHD symptoms and insistence on sameness in Prader-Willi syndrome. J Intellect Disabil Res 2005;49(Pt 6):449-456.
-
(2005)
J. Intellect Disabil Res.
, vol.49
, Issue.6 PART
, pp. 449-456
-
-
Wigren, M.1
Hansen, S.2
-
162
-
-
0032837576
-
Prader-Willi syndrome
-
Couper R. Prader-Willi syndrome. J Paediatr Child Health 1999;35(4):331-334.
-
(1999)
J. Paediatr. Child Health
, vol.35
, Issue.4
, pp. 331-334
-
-
Couper, R.1
-
163
-
-
0030788736
-
Recurrent brief depression in Prader-Willi syndrome: A case report
-
Watanabe H, Ohmori O, Abe K. Recurrent brief depression in Prader-Willi syndrome: a case report. Psychiatr Genet 1997;7(1):41-44.
-
(1997)
Psychiatr. Genet.
, vol.7
, Issue.1
, pp. 41-44
-
-
Watanabe, H.1
Ohmori, O.2
Abe, K.3
-
164
-
-
0029587002
-
Correlates of maladaptive behavior in children and adults with Prader-Willi syndrome
-
Dykens EM, Cassidy SB. Correlates of maladaptive behavior in children and adults with Prader-Willi syndrome. Am J Med Genet 1995;60(6):546-549.
-
(1995)
Am. J. Med. Genet.
, vol.60
, Issue.6
, pp. 546-549
-
-
Dykens, E.M.1
Cassidy, S.B.2
-
165
-
-
8844265983
-
Neuropeptides in hypothalamic neuronal disorders
-
Swaab DF. Neuropeptides in hypothalamic neuronal disorders. Int Rev Cytol 2004;240:305-375.
-
(2004)
Int. Rev. Cytol.
, vol.240
, pp. 305-375
-
-
Swaab, D.F.1
-
166
-
-
0034532203
-
Characteristics of two cases with dup (15) (q11.2-q12):One of maternal and one of paternal origin
-
Mao R, Jalal SM, Snow K et al. Characteristics of two cases with dup (15) (q11.2-q12):one of maternal and one of paternal origin. Genet Med 2000;2(2):131-135.
-
(2000)
Genet. Med.
, vol.2
, Issue.2
, pp. 131-135
-
-
Mao, R.1
Jalal, S.M.2
Snow, K.3
-
167
-
-
0022391691
-
Differential activity of maternally and paternally derived chromosome regions in mice
-
Cattanach BM, Kirk M. Differential activity of maternally and paternally derived chromosome regions in mice. Nature 1985;315(6019):496-498.
-
(1985)
Nature
, vol.315
, Issue.6019
, pp. 496-498
-
-
Cattanach, B.M.1
Kirk, M.2
-
168
-
-
0029039820
-
Clinical evidence of genomic imprinting in Tourette's Syndrome
-
Lichter DG, Jackson LA, Schachter M. Clinical evidence of genomic imprinting in Tourette's Syndrome. Neurology 1995;45:924-928.
-
(1995)
Neurology
, vol.45
, pp. 924-928
-
-
Lichter, D.G.1
Jackson, L.A.2
Schachter, M.3
-
169
-
-
0029021719
-
Patterns of maternal transmission in bipolar affective disorder
-
McMahon FJ, Stine OC, Meyers DA et al. Patterns of maternal transmission in bipolar affective disorder. Am J Hum Genet 1995;56:1277-1286.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1277-1286
-
-
McMahon, F.J.1
Stine, O.C.2
Meyers, D.A.3
-
170
-
-
0042824074
-
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder
-
Borglum AD, Kirov G, Craddock N et al. Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. Am J Med Genet, B: Neuropsychiatr Genet 2003;117(1):18-22.
-
(2003)
Am. J. Med. Genet, B: Neuropsychiatr Genet.
, vol.117
, Issue.1
, pp. 18-22
-
-
Borglum, A.D.1
Kirov, G.2
Craddock, N.3
-
171
-
-
0036364966
-
Serotonergic system and attention deficit hyperactivity disorder (ADHD):A potential susceptibility locus at the 5-HT (1B) receptor gene in 273 nuclear families from a multi-centre sample
-
Hawi Z, Dring M, Kirley A et al. Serotonergic system and attention deficit hyperactivity disorder (ADHD):a potential susceptibility locus at the 5-HT (1B) receptor gene in 273 nuclear families from a multi-centre sample. Mol Psychiatry 2002;7(7):718-725.
-
(2002)
Mol. Psychiatry
, vol.7
, Issue.7
, pp. 718-725
-
-
Hawi, Z.1
Dring, M.2
Kirley, A.3
-
172
-
-
27144480407
-
Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD
-
Sheehan K, Lowe N, Kirley A et al. Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD. Mol Psychiatry 2005;10(10):944-949.
-
(2005)
Mol. Psychiatry
, vol.10
, Issue.10
, pp. 944-949
-
-
Sheehan, K.1
Lowe, N.2
Kirley, A.3
-
174
-
-
33646688227
-
Possible association between response inhibition and a variant in the brain-expressed tryptophan hydroxylase-2 gene
-
Stoltenberg SF, Glass JM, Chermack ST et al. Possible association between response inhibition and a variant in the brain-expressed tryptophan hydroxylase-2 gene. Psychiatr Genet 2006;16(1):35-38.
-
(2006)
Psychiatr. Genet.
, vol.16
, Issue.1
, pp. 35-38
-
-
Stoltenberg, S.F.1
Glass, J.M.2
Chermack, S.T.3
-
175
-
-
5044238471
-
SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression
-
Zill P, Baghai TC, Zwanzger P et al. SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression. Mol Psychiatry 2004;9(11):1030-1036.
-
(2004)
Mol. Psychiatry
, vol.9
, Issue.11
, pp. 1030-1036
-
-
Zill, P.1
Baghai, T.C.2
Zwanzger, P.3
-
176
-
-
5044237402
-
Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase Isoform (TPH2) gene in suicide victims
-
DOI 10.1016/j.biopsych.2004.07.015, PII S0006322304008054
-
Zill P, Buttner A, Eisenmenger W et al. Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene in suicide victims. Biol Psychiatry 2004;56(8):581-586. (Pubitemid 39336405)
-
(2004)
Biological Psychiatry
, vol.56
, Issue.8
, pp. 581-586
-
-
Zill, P.1
Buttner, A.2
Eisenmenger, W.3
Moller, H.-J.4
Bondy, B.5
Ackenheil, M.6
-
177
-
-
31544454715
-
Enhanced BDNF signaling is associated with an antidepressant-like behavioral response and changes in brain monoamines
-
Koponen E, Rantamaki T, Voikar V et al. Enhanced BDNF signaling is associated with an antidepressant-like behavioral response and changes in brain monoamines. Cell Mol Neurobiol 2005;25(6):973-980.
-
(2005)
Cell. Mol. Neurobiol.
, vol.25
, Issue.6
, pp. 973-980
-
-
Koponen, E.1
Rantamaki, T.2
Voikar, V.3
-
178
-
-
4544328810
-
BDNF and 5-HT: A dynamic duo in age-related neuronal plasticity and neurodegenerative disorders
-
Mattson MP, Maudsley S, Martin B. BDNF and 5-HT: a dynamic duo in age-related neuronal plasticity and neurodegenerative disorders. Trends Neurosci 2004;27(10):589-594.
-
(2004)
Trends Neurosci.
, vol.27
, Issue.10
, pp. 589-594
-
-
Mattson, M.P.1
Maudsley, S.2
Martin, B.3
-
179
-
-
27144502791
-
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD
-
Kent L, Green E, Hawi Z et al. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Mol Psychiatry 2005;10(10):939-943.
-
(2005)
Mol. Psychiatry
, vol.10
, Issue.10
, pp. 939-943
-
-
Kent, L.1
Green, E.2
Hawi, Z.3
-
181
-
-
1242343967
-
Major depression and conduct disorder in youth: Associations with parental psychopathology and parent-child conflict
-
Marmorstein NR, Iacono WG. Major depression and conduct disorder in youth: associations with parental psychopathology and parent-child conflict. J Child Psychol Psychiatry 2004;45(2):377-386.
-
(2004)
J. Child Psychol. Psychiatry
, vol.45
, Issue.2
, pp. 377-386
-
-
Marmorstein, N.R.1
Iacono, W.G.2
-
182
-
-
4444278750
-
Psychiatric disorders among offspring of depressed mothers: Associations with paternal psychopathology
-
Marmorstein NR, Malone SM, Iacono WG. Psychiatric disorders among offspring of depressed mothers: associations with paternal psychopathology. Am J Psychiatry 2004;161(9):1588-1594.
-
(2004)
Am. J. Psychiatry
, vol.161
, Issue.9
, pp. 1588-1594
-
-
Marmorstein, N.R.1
Malone, S.M.2
Iacono, W.G.3
-
183
-
-
4444251068
-
Family transmission and heritability of externalizing disorders: A twin-family study
-
Hicks BM, Krueger RF, Iacono WG et al. Family transmission and heritability of externalizing disorders: a twin-family study. Arch Gen Psychiatry 2004;61(9):922-928.
-
(2004)
Arch. Gen. Psychiatry
, vol.61
, Issue.9
, pp. 922-928
-
-
Hicks, B.M.1
Krueger, R.F.2
Iacono, W.G.3
-
184
-
-
26044439967
-
Family correlates of oppositional and conduct disorders in children with attention deficit/hyperactivity disorder
-
Pfiffner LJ, McBurnett K, Rathouz PJ et al. Family correlates of oppositional and conduct disorders in children with attention deficit/hyperactivity disorder. J Abnorm Child Psychol 2005;33(5):551-563.
-
(2005)
J. Abnorm Child Psychol.
, vol.33
, Issue.5
, pp. 551-563
-
-
Pfiffner, L.J.1
McBurnett, K.2
Rathouz, P.J.3
-
185
-
-
17844385080
-
Paternal alcoholism and offspring conduct disorder: Evidence for the 'common genes' hypothesis
-
Haber JR, Jacob T, Heath AC. Paternal alcoholism and offspring conduct disorder: evidence for the 'common genes' hypothesis. Twin Res Hum Genet 2005;8(2):120-131.
-
(2005)
Twin Res. Hum. Genet.
, vol.8
, Issue.2
, pp. 120-131
-
-
Haber, J.R.1
Jacob, T.2
Heath, A.C.3
-
186
-
-
0034108482
-
Comparison of the role of dopamine, serotonin and noradrenaline genes in ADHD, ODD and conduct disorder: Multivariate regression analysis of 20 genes
-
Comings DE, Gade-Andavolu R, Gonzalez N et al. Comparison of the role of dopamine, serotonin and noradrenaline genes in ADHD, ODD and conduct disorder: multivariate regression analysis of 20 genes. Clin Genet 2000;57(3):178-196.
-
(2000)
Clin. Genet.
, vol.57
, Issue.3
, pp. 178-196
-
-
Comings, D.E.1
Gade-Andavolu, R.2
Gonzalez, N.3
-
187
-
-
0036674495
-
Neuroscience of attention-deficit/hyperactivity disorder: The search for endophenotypes
-
Castellanos FX, Tannock R. Neuroscience of attention-deficit/ hyperactivity disorder: the search for endophenotypes. Nat Rev Neurosci 2002;3(8):617-628.
-
(2002)
Nat. Rev. Neurosci.
, vol.3
, Issue.8
, pp. 617-628
-
-
Castellanos, F.X.1
Tannock, R.2
-
188
-
-
0035171492
-
Deficient inhibition as a marker for familial ADHD
-
Crosbie J, Schachar R. Deficient inhibition as a marker for familial ADHD. Am J Psychiatry 2001;158:1884-1890.
-
(2001)
Am. J. Psychiatry
, vol.158
, pp. 1884-1890
-
-
Crosbie, J.1
Schachar, R.2
-
189
-
-
0034086699
-
Confirmation of an inhibitory control deficit in attention-deficit/ hyperactivity disorder
-
Schachar R, Mota VL, Logan GD et al. Confirmation of an inhibitory control deficit in attention-deficit/hyperactivity disorder. J Abnorm Child Psychol 2000;28(3):227-235.
-
(2000)
J. Abnorm Child Psychol.
, vol.28
, Issue.3
, pp. 227-235
-
-
Schachar, R.1
Mota, V.L.2
Logan, G.D.3
-
190
-
-
0028952250
-
High-resolution genetic mapping of complex traits
-
Kruglyak L, Lander ES. High-resolution genetic mapping of complex traits. Am J Hum Genet 1995;56(5):1212-1223.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, Issue.5
, pp. 1212-1223
-
-
Kruglyak, L.1
Lander, E.S.2
-
191
-
-
0029976062
-
Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees
-
Gershon ES, Badner JA, Detera-Wadleigh SD et al. Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees. Am J Med Genet 1996;67(2):202-207.
-
(1996)
Am. J. Med. Genet.
, vol.67
, Issue.2
, pp. 202-207
-
-
Gershon, E.S.1
Badner, J.A.2
Detera-Wadleigh, S.D.3
-
192
-
-
0025756107
-
Comorbidity of attention deficit hyperactivity disorder with conduct, depressive, anxiety and other disorders
-
Biederman J, Newcorn J, Sprich S. Comorbidity of attention deficit hyperactivity disorder with conduct, depressive, anxiety and other disorders. Am J Psychiatry 1991;148(5):564-577.
-
(1991)
Am. J. Psychiatry
, vol.148
, Issue.5
, pp. 564-577
-
-
Biederman, J.1
Newcorn, J.2
Sprich, S.3
-
193
-
-
0026074484
-
A family-genetic study of girls with DSM-III attention deficit disorder
-
Faraone SV, Biederman J, Keenan K et al. A family-genetic study of girls with DSM-III attention deficit disorder. Am J Psychiatr 1991;148(1):112-117.
-
(1991)
Am. J. Psychiatr.
, vol.148
, Issue.1
, pp. 112-117
-
-
Faraone, S.V.1
Biederman, J.2
Keenan, K.3
-
194
-
-
0036860418
-
Neuropsychological performance in DSM-IV ADHD subtypes: An exploratory study with untreated adolescents
-
Schmitz M, Cadore L, Paczko M et al. Neuropsychological performance in DSM-IV ADHD subtypes: an exploratory study with untreated adolescents. Can J Psychiatr 2002;47(9):863-869.
-
(2002)
Can. J. Psychiatr.
, vol.47
, Issue.9
, pp. 863-869
-
-
Schmitz, M.1
Cadore, L.2
Paczko, M.3
-
195
-
-
0036206683
-
Young adults with attention deficit hyperactivity disorder: Subtype differences in comorbidity, educational and clinical history
-
Murphy KR, Barkley RA, Bush T. Young adults with attention deficit hyperactivity disorder: subtype differences in comorbidity, educational and clinical history. J Nerv Ment Dis 2002;190(3):147-157.
-
(2002)
J. Nerv. Ment. Dis.
, vol.190
, Issue.3
, pp. 147-157
-
-
Murphy, K.R.1
Barkley, R.A.2
Bush, T.3
-
196
-
-
0035654422
-
A comparison of the neuropsychological profiles of the DSM-IV subtypes of ADHD
-
Chhabildas N, Pennington BF, Willcutt EG. A comparison of the neuropsychological profiles of the DSM-IV subtypes of ADHD. J Abn Child Psychol 2001;29(6):529-540.
-
(2001)
J. Abn Child Psychol.
, vol.29
, Issue.6
, pp. 529-540
-
-
Chhabildas, N.1
Pennington, B.F.2
Willcutt, E.G.3
-
197
-
-
0035886204
-
A family study of psychiatric comorbidity in girls and boys with attention-deficit/hyperactivity disorder
-
Faraone SV, Biederman J, Mick E et al. A family study of psychiatric comorbidity in girls and boys with attention-deficit/hyperactivity disorder. Biol Psychiatry 2001;50(8):586-592.
-
(2001)
Biol. Psychiatry
, vol.50
, Issue.8
, pp. 586-592
-
-
Faraone, S.V.1
Biederman, J.2
Mick, E.3
-
198
-
-
0036363103
-
Influence of gender on attention deficit hyperactivity disorder in children referred to a psychiatric clinic
-
Biederman J, Mick E, Faraone SV et al. Influence of gender on attention deficit hyperactivity disorder in children referred to a psychiatric clinic. Am J Psychiatr 2002;159(1):36-42.
-
(2002)
Am. J. Psychiatr.
, vol.159
, Issue.1
, pp. 36-42
-
-
Biederman, J.1
Mick, E.2
Faraone, S.V.3
-
200
-
-
0035125285
-
Research in mental retardation: Toward an etiologic approach
-
Dykens EM, Hodapp RM. Research in mental retardation: toward an etiologic approach. J Child Psychol Psychiatry 2001;42(1):49-71.
-
(2001)
J. Child Psychol. Psychiatry
, vol.42
, Issue.1
, pp. 49-71
-
-
Dykens, E.M.1
Hodapp, R.M.2
-
201
-
-
22244471085
-
Genetics and epigenetics in major psychiatric disorders: Dilemmas, achievements, applications and future scope
-
Abdolmaleky HM, Thiagalingam S, Wilcox M. Genetics and epigenetics in major psychiatric disorders: dilemmas, achievements, applications and future scope. Am J Pharmacogenomics 2005;5(3):149-160.
-
(2005)
Am. J. Pharmacogenomics
, vol.5
, Issue.3
, pp. 149-160
-
-
Abdolmaleky, H.M.1
Thiagalingam, S.2
Wilcox, M.3
-
202
-
-
21744434425
-
Deficits in social attribution ability in Prader-Willi syndrome
-
Koenig K, Klin A, Schultz R. Deficits in social attribution ability in Prader-Willi Syndrome. J Autism Dev Disord 2004;34(5).
-
(2004)
J. Autism Dev. Disord.
, vol.34
, Issue.5
-
-
Koenig, K.1
Klin, A.2
Schultz, R.3
-
204
-
-
0033753747
-
Genetics of asthma and allergic disease
-
Cookson WO, Moffatt MF. Genetics of asthma and allergic disease. Hum Mol Genet 2000;9(16):2359-2364.
-
(2000)
Hum. Mol. Genet.
, vol.9
, Issue.16
, pp. 2359-2364
-
-
Cookson, W.O.1
Moffatt, M.F.2
-
205
-
-
0026776492
-
Maternal inheritance of atopic IgE responsiveness on chromosome 11q
-
Cookson WO, Young RP, Sandford AJ et al. Maternal inheritance of atopic IgE responsiveness on chromosome 11q. Lancet 1992;340(8816):381-384.
-
(1992)
Lancet
, vol.340
, Issue.8816
, pp. 381-384
-
-
Cookson, W.O.1
Young, R.P.2
Sandford, A.J.3
-
206
-
-
8744304960
-
The insulin-like growth factor-II receptor gene is associated with type 1 diabetes: Evidence of a maternal effect
-
McCann JA, Xu YQ, Frechette R et al. The insulin-like growth factor-II receptor gene is associated with type 1 diabetes: evidence of a maternal effect. J Clin Endocrinol Metab 2004;89(11):5700-5706.
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, Issue.11
, pp. 5700-5706
-
-
McCann, J.A.1
Xu, Y.Q.2
Frechette, R.3
-
207
-
-
0036856153
-
Parental genomic imprinting in endocrinopathies
-
Polychronakos C, Kukuvitis A. Parental genomic imprinting in endocrinopathies. Eur J Endocrinol 2002;147(5):561-569.
-
(2002)
Eur. J. Endocrinol.
, vol.147
, Issue.5
, pp. 561-569
-
-
Polychronakos, C.1
Kukuvitis, A.2
-
208
-
-
26444531684
-
TP73 allelic expression in human brain and allele frequencies in Alzheimer's disease
-
Li Q, Athan ES, Wei M et al. TP73 allelic expression in human brain and allele frequencies in Alzheimer's disease. BMC Med Genet 2004;5:14.
-
(2004)
BMC Med. Genet.
, vol.5
, pp. 14
-
-
Li, Q.1
Athan, E.S.2
Wei, M.3
-
209
-
-
15244351255
-
Impaired insulin and insulin-like growth factor expression and signaling mechanisms in Alzheimer's disease-is this type 3 diabetes?
-
Steen E, Terry BM, Rivera EJ et al. Impaired insulin and insulin-like growth factor expression and signaling mechanisms in Alzheimer's disease-is this type 3 diabetes? J Alzheimers Dis 2005;7(1):63-80.
-
(2005)
J. Alzheimers Dis.
, vol.7
, Issue.1
, pp. 63-80
-
-
Steen, E.1
Terry, B.M.2
Rivera, E.J.3
-
210
-
-
15244350991
-
Review of insulin and insulin-like growth factor expression, signaling and malfunction in the central nervous system: Relevance to Alzheimer's disease
-
De La Monte SM, Wands JR. Review of insulin and insulin-like growth factor expression, signaling and malfunction in the central nervous system: relevance to Alzheimer's disease. J Alzheimers Dis 2005;7(1):45-61.
-
(2005)
J. Alzheimers Dis.
, vol.7
, Issue.1
, pp. 45-61
-
-
De La Monte, S.M.1
Wands, J.R.2
-
211
-
-
0033959416
-
Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles
-
Huxtable SJ, Saker PJ, Haddad L et al. Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles. Diabetes 2000;49(1):126-130.
-
(2000)
Diabetes
, vol.49
, Issue.1
, pp. 126-130
-
-
Huxtable, S.J.1
Saker, P.J.2
Haddad, L.3
-
212
-
-
0034811734
-
Epigenetic heterogeneity at imprinted loci in normal populations
-
Sakatani T, Wei M, Katoh M et al. Epigenetic heterogeneity at imprinted loci in normal populations. Biochem Biophys Res Commun 2001;283(5):1124-1130.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.283
, Issue.5
, pp. 1124-1130
-
-
Sakatani, T.1
Wei, M.2
Katoh, M.3
-
213
-
-
21044439497
-
Alternative Gnas gene products have opposite effects on glucose and lipid metabolism
-
Chen M, Gavrilova O, Liu J et al. Alternative Gnas gene products have opposite effects on glucose and lipid metabolism. Proc Natl Acad Sci 2005;102(20):7386-7391.
-
(2005)
Proc. Natl. Acad. Sci.
, vol.102
, Issue.20
, pp. 7386-7391
-
-
Chen, M.1
Gavrilova, O.2
Liu, J.3
-
214
-
-
2942694365
-
Insulin resistance syndrome in children
-
Ten S, Maclaren N. Insulin resistance syndrome in children. J Clin Endocrinol Metab 2004;89(6):2526-2539.
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, Issue.6
, pp. 2526-2539
-
-
Ten, S.1
Maclaren, N.2
-
215
-
-
1842533557
-
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits
-
Rodriguez S, Gaunt TR, O'Dell SD et al. Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits. Hum Mol Genet 2004;13(7):715-725.
-
(2004)
Hum. Mol. Genet.
, vol.13
, Issue.7
, pp. 715-725
-
-
Rodriguez, S.1
Gaunt, T.R.2
O'Dell, S.D.3
|